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You searched for subject:(PBPK). Showing records 1 – 30 of 84 total matches.

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University of Manchester

1. Salem, Farzaneh. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.

Degree: 2014, University of Manchester

 Anticipation of drug-drug interactions (DDIs) in the paediatric population are merely based on data generated in adults. Hence decision on avoiding certain combinations or attempts… (more)

Subjects/Keywords: Paediatric; PBPK

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Salem, F. (2014). APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622

Chicago Manual of Style (16th Edition):

Salem, Farzaneh. “APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.” 2014. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622.

MLA Handbook (7th Edition):

Salem, Farzaneh. “APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.” 2014. Web. 10 Apr 2021.

Vancouver:

Salem F. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622.

Council of Science Editors:

Salem F. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622

2. Salem, Farzaneh. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.

Degree: PhD, 2014, University of Manchester

 Anticipation of drug-drug interactions (DDIs) in the paediatric population are merely based on data generated in adults. Hence decision on avoiding certain combinations or attempts… (more)

Subjects/Keywords: 615.7; Paediatric; PBPK

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Salem, F. (2014). Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991

Chicago Manual of Style (16th Edition):

Salem, Farzaneh. “Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.” 2014. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991.

MLA Handbook (7th Edition):

Salem, Farzaneh. “Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.” 2014. Web. 10 Apr 2021.

Vancouver:

Salem F. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Apr 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991.

Council of Science Editors:

Salem F. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991


University of Georgia

3. Perleberg, Ulrich Reiko. A physiologically based pharmacokinetic model for decane.

Degree: 2014, University of Georgia

 Decane, a 10-carbon n-alkane, was selected to represent the semi-volatile fraction for the initial development of a physiologically-based pharmacokinetic (PBPK) model for Jet Propellant-8. Rats… (more)

Subjects/Keywords: Decane; PBPK Modeling; JP-8

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Perleberg, U. R. (2014). A physiologically based pharmacokinetic model for decane. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/21639

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Perleberg, Ulrich Reiko. “A physiologically based pharmacokinetic model for decane.” 2014. Thesis, University of Georgia. Accessed April 10, 2021. http://hdl.handle.net/10724/21639.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Perleberg, Ulrich Reiko. “A physiologically based pharmacokinetic model for decane.” 2014. Web. 10 Apr 2021.

Vancouver:

Perleberg UR. A physiologically based pharmacokinetic model for decane. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10724/21639.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Perleberg UR. A physiologically based pharmacokinetic model for decane. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/21639

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

4. Tsamandouras, Nikolaos. Development and applications of physiologically-based pharmacokinetic models for population data analyses.

Degree: 2015, University of Manchester

 Physiologically-based pharmacokinetic (PBPK) modelling is traditionally employed to predict drug concentration-time profiles in plasma and tissues using information from physiology / biology, in vitro experiments… (more)

Subjects/Keywords: PBPK modelling; population pharmacokinetics; simvastatin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tsamandouras, N. (2015). Development and applications of physiologically-based pharmacokinetic models for population data analyses. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385

Chicago Manual of Style (16th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385.

MLA Handbook (7th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Web. 10 Apr 2021.

Vancouver:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385.

Council of Science Editors:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385

5. Ball, Kathryn. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.

Degree: Docteur es, Pharmacocinétique, 2014, Université Paris Descartes – Paris V

 Une étape critique au cours du développement de médicaments est la mesure ou la prédiction des concentrations du médicament dans un tissu cible, qui peuvent… (more)

Subjects/Keywords: PBPK; SNC; BHE; Modélisation; Pharmacocinétique; PBPK; CNS; BBB; Modeling; Pharmacokinetics; 615.7

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ball, K. (2014). Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05P630

Chicago Manual of Style (16th Edition):

Ball, Kathryn. “Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed April 10, 2021. http://www.theses.fr/2014PA05P630.

MLA Handbook (7th Edition):

Ball, Kathryn. “Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.” 2014. Web. 10 Apr 2021.

Vancouver:

Ball K. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2014PA05P630.

Council of Science Editors:

Ball K. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05P630


University of Waterloo

6. Park, Hyunjin. Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans.

Degree: 2019, University of Waterloo

 The physiologically based pharmacokinetic (PBPK) modelling has been accepted as one of the most effective mechanistic techniques to analyze pharmacokinetics (PK) of drugs in the… (more)

Subjects/Keywords: pharmacokinetics; PBPK; modelling; cisplatin; chemotherapy; anticancer

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Park, H. (2019). Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/15205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Park, Hyunjin. “Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans.” 2019. Thesis, University of Waterloo. Accessed April 10, 2021. http://hdl.handle.net/10012/15205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Park, Hyunjin. “Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans.” 2019. Web. 10 Apr 2021.

Vancouver:

Park H. Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans. [Internet] [Thesis]. University of Waterloo; 2019. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10012/15205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Park H. Physiologically based Pharmacokinetic (PBPK) Modelling of Cisplatin in Rats and Humans. [Thesis]. University of Waterloo; 2019. Available from: http://hdl.handle.net/10012/15205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

7. Real, Ivan Manuel Reis Sousa. A importância dos parâmetros farmacocinéticos na terapêutica individualizada.

Degree: 2016, RCAAP

Dissertação para obtenção do grau de Mestre no Instituto Superior de Ciências da Saúde Egas Moniz

A terapêutica individualizada é um procedimento que separa os… (more)

Subjects/Keywords: Terapêutica individualizada; Farmacocinética; PBPK; Doenças órfãs

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APA (6th Edition):

Real, I. M. R. S. (2016). A importância dos parâmetros farmacocinéticos na terapêutica individualizada. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Real, Ivan Manuel Reis Sousa. “A importância dos parâmetros farmacocinéticos na terapêutica individualizada.” 2016. Thesis, RCAAP. Accessed April 10, 2021. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Real, Ivan Manuel Reis Sousa. “A importância dos parâmetros farmacocinéticos na terapêutica individualizada.” 2016. Web. 10 Apr 2021.

Vancouver:

Real IMRS. A importância dos parâmetros farmacocinéticos na terapêutica individualizada. [Internet] [Thesis]. RCAAP; 2016. [cited 2021 Apr 10]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Real IMRS. A importância dos parâmetros farmacocinéticos na terapêutica individualizada. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

8. Tsamandouras, Nikolaos. Development and applications of physiologically-based pharmacokinetic models for population data analyses.

Degree: PhD, 2015, University of Manchester

 Physiologically-based pharmacokinetic (PBPK) modelling is traditionally employed to predict drug concentration-time profiles in plasma and tissues using information from physiology/biology, in vitro experiments and in… (more)

Subjects/Keywords: 615.7; PBPK modelling; population pharmacokinetics; simvastatin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tsamandouras, N. (2015). Development and applications of physiologically-based pharmacokinetic models for population data analyses. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748

Chicago Manual of Style (16th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748.

MLA Handbook (7th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Web. 10 Apr 2021.

Vancouver:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748.

Council of Science Editors:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748


University of Washington

9. Zhang, Zufei. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.

Degree: PhD, 2017, University of Washington

 During pregnancy, physiological and ADMET changes in the maternal-fetal dyad can significantly alter drug pharmacokinetics (PK) in the mother and may necessitate dosing regimen adjustments.… (more)

Subjects/Keywords: CYP3A; fetal; PBPK; Pharmacokinetics; Pharmaceutical sciences; Pharmaceutics

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zhang, Z. (2017). Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/38672

Chicago Manual of Style (16th Edition):

Zhang, Zufei. “Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.” 2017. Doctoral Dissertation, University of Washington. Accessed April 10, 2021. http://hdl.handle.net/1773/38672.

MLA Handbook (7th Edition):

Zhang, Zufei. “Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.” 2017. Web. 10 Apr 2021.

Vancouver:

Zhang Z. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1773/38672.

Council of Science Editors:

Zhang Z. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38672


University of Manchester

10. Harwood, Matthew Dillston. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.

Degree: 2015, University of Manchester

 Background: Elucidating the role of intestinal drug transporter function in drug development is crucial, as transporter proteins can impact on drug absorption, efficacy and adverse… (more)

Subjects/Keywords: Transporter proteins; PBPK-IVIVE; Intestine; Absolute Abundance

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APA (6th Edition):

Harwood, M. D. (2015). Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614

Chicago Manual of Style (16th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614.

MLA Handbook (7th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.” 2015. Web. 10 Apr 2021.

Vancouver:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614.

Council of Science Editors:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614


University of Sydney

11. Adiwidjaja, Jeffry. Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation .

Degree: 2020, University of Sydney

 Long-term use of imatinib in patients with Philadelphia chromosome-positive (Ph+) chronic myeloid leukaemia (CML) is effective. Imatinib is given orally at a fixed daily dosing… (more)

Subjects/Keywords: imatinib; bosutinib; PBPK; modelling; simulation; variability

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Adiwidjaja, J. (2020). Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/23217

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Adiwidjaja, Jeffry. “Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation .” 2020. Thesis, University of Sydney. Accessed April 10, 2021. http://hdl.handle.net/2123/23217.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Adiwidjaja, Jeffry. “Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation .” 2020. Web. 10 Apr 2021.

Vancouver:

Adiwidjaja J. Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation . [Internet] [Thesis]. University of Sydney; 2020. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/2123/23217.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Adiwidjaja J. Understanding interindividual variability in response to anti-cancer drugs using modelling and simulation . [Thesis]. University of Sydney; 2020. Available from: http://hdl.handle.net/2123/23217

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

12. Cartiser, Nathalie. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.

Degree: Docteur es, Chimie analytique. Toxicologie médicolégale, 2011, Université Claude Bernard – Lyon I

L'objectif de cette thèse était de faire le point sur la place de l'analyse de la moelle osseuse (MO) en tant que matrice alternative au… (more)

Subjects/Keywords: Toxicologie médicolégale; Moelle Osseuse; Interprétation; Modèle PBPK; Distribution tissulaire; Forensic toxicology; Bone Marrow; Interpretation; PBPK; Tissue distribution; 615.9

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APA (6th Edition):

Cartiser, N. (2011). Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10149

Chicago Manual of Style (16th Edition):

Cartiser, Nathalie. “Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed April 10, 2021. http://www.theses.fr/2011LYO10149.

MLA Handbook (7th Edition):

Cartiser, Nathalie. “Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.” 2011. Web. 10 Apr 2021.

Vancouver:

Cartiser N. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2011LYO10149.

Council of Science Editors:

Cartiser N. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10149

13. Sousa Mendes, Maïlys de. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.

Degree: Docteur es, Pharmacologie, 2016, Sorbonne Paris Cité

Les femmes enceintes sont exposées à de nombreux médicaments et les essais cliniques sont difficilement réalisables dans cette population, c'est pourquoi avoir une méthode qui… (more)

Subjects/Keywords: Pharmacocinétique; PBPK; Grossesse; Foetus; Cotyledon; Placenta; Névirapine; Ténofovir; Emtricitabine; Lamivudine; Pharmacockinetics; PBPK; Pregnancy; Foetus; Cotyledon; Placenta; Nevirapine; Tenofovir; Emtricitabine; Lamivudine; 615.7

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APA (6th Edition):

Sousa Mendes, M. d. (2016). Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB144

Chicago Manual of Style (16th Edition):

Sousa Mendes, Maïlys de. “Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed April 10, 2021. http://www.theses.fr/2016USPCB144.

MLA Handbook (7th Edition):

Sousa Mendes, Maïlys de. “Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.” 2016. Web. 10 Apr 2021.

Vancouver:

Sousa Mendes Md. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2016USPCB144.

Council of Science Editors:

Sousa Mendes Md. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB144

14. Quindroit, Paul. Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Paris, Institut agronomique, vétérinaire et forestier de France

Les pyréthrinoïdes sont des insecticides ubiquitaires utilisés dans de nombreux domaines et par ce fait, les populations humaines sont susceptibles d’y être exposées par plusieurs… (more)

Subjects/Keywords: Modélisation PBPK; Évaluation de l’exposition; Métabolites; Exposition cumulée; Pyréthrinoïdes; Biosurveillance; Exposure assessment; Metabolites; Pyrethroids; Cumulative exposure; PBPK modeling; Biomonitoring; 632.9517

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APA (6th Edition):

Quindroit, P. (2019). Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population. (Doctoral Dissertation). Paris, Institut agronomique, vétérinaire et forestier de France. Retrieved from http://www.theses.fr/2019IAVF0024

Chicago Manual of Style (16th Edition):

Quindroit, Paul. “Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population.” 2019. Doctoral Dissertation, Paris, Institut agronomique, vétérinaire et forestier de France. Accessed April 10, 2021. http://www.theses.fr/2019IAVF0024.

MLA Handbook (7th Edition):

Quindroit, Paul. “Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population.” 2019. Web. 10 Apr 2021.

Vancouver:

Quindroit P. Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population. [Internet] [Doctoral dissertation]. Paris, Institut agronomique, vétérinaire et forestier de France; 2019. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2019IAVF0024.

Council of Science Editors:

Quindroit P. Évaluation des expositions aux pyréthrinoïdes par la modélisation toxicocinétique de données de biosurveillance : application à la population générale française. : Evaluation of pyrethroid exposures by toxicokinetic modeling of biomonitoring data : appliecation to the general French population. [Doctoral Dissertation]. Paris, Institut agronomique, vétérinaire et forestier de France; 2019. Available from: http://www.theses.fr/2019IAVF0024

15. Personne, Stéphane. Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements.

Degree: Docteur es, Biologie Santé. Toxicologie, 2019, Amiens

Les études de biosurveillance ont montré une exposition plus élevée de la population française, y compris les femmes enceintes, aux pyréthrinoïdes par rapport à d'autres… (more)

Subjects/Keywords: Modèle pharmacocinétique basé sur la physiologie; Rat; Grossesse; Permethrin; PBPK model

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APA (6th Edition):

Personne, S. (2019). Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements. (Doctoral Dissertation). Amiens. Retrieved from http://www.theses.fr/2019AMIE0004

Chicago Manual of Style (16th Edition):

Personne, Stéphane. “Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements.” 2019. Doctoral Dissertation, Amiens. Accessed April 10, 2021. http://www.theses.fr/2019AMIE0004.

MLA Handbook (7th Edition):

Personne, Stéphane. “Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements.” 2019. Web. 10 Apr 2021.

Vancouver:

Personne S. Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements. [Internet] [Doctoral dissertation]. Amiens; 2019. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2019AMIE0004.

Council of Science Editors:

Personne S. Développement d'un modèle toxicocinétique basé sur la physiologie pour la perméthrine et ses métabolites chez la rate gestante : 3D radiative transfer modeling over complex vegetation canopies and forest reconstruction from LIDAR measurements. [Doctoral Dissertation]. Amiens; 2019. Available from: http://www.theses.fr/2019AMIE0004


University of Manchester

16. Graham, Helen Sarah. Prediction of drug distribution in rat and human.

Degree: PhD, 2012, University of Manchester

 Many methods exist in the literature for the prediction of pharmacokinetic parameters which describe drug distribution in rat and human, such as tissue-to-plasma partition coefficients… (more)

Subjects/Keywords: 615; Pharmacokinetics; PBPK modelling; Partition coefficients; Volume of distribution

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APA (6th Edition):

Graham, H. S. (2012). Prediction of drug distribution in rat and human. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572

Chicago Manual of Style (16th Edition):

Graham, Helen Sarah. “Prediction of drug distribution in rat and human.” 2012. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572.

MLA Handbook (7th Edition):

Graham, Helen Sarah. “Prediction of drug distribution in rat and human.” 2012. Web. 10 Apr 2021.

Vancouver:

Graham HS. Prediction of drug distribution in rat and human. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Apr 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572.

Council of Science Editors:

Graham HS. Prediction of drug distribution in rat and human. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572

17. Harwood, Matthew Dillston. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.

Degree: PhD, 2015, University of Manchester

 Background: Elucidating the role of intestinal drug transporter function in drug development is crucial, as transporter proteins can impact on drug absorption, efficacy and adverse… (more)

Subjects/Keywords: 615.1; Transporter proteins; PBPK-IVIVE; Intestine; Absolute Abundance

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APA (6th Edition):

Harwood, M. D. (2015). Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832

Chicago Manual of Style (16th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832.

MLA Handbook (7th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.” 2015. Web. 10 Apr 2021.

Vancouver:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832.

Council of Science Editors:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832


East Tennessee State University

18. Forbes, Whitney. Physiologically-Based Pharmacokinetic Model for Ertapenem.

Degree: MS, Mathematical Sciences, 2014, East Tennessee State University

  Ertapenem is a carbapenem used to treat a wide range of bacterial infections. What sets ertapenem apart from other carbapenems is its longer half-life… (more)

Subjects/Keywords: PBPK; Pharmacokinetic; MIC; Ertapenem; ADME; Applied Mathematics; Chemicals and Drugs; Mathematics

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APA (6th Edition):

Forbes, W. (2014). Physiologically-Based Pharmacokinetic Model for Ertapenem. (Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2342

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Forbes, Whitney. “Physiologically-Based Pharmacokinetic Model for Ertapenem.” 2014. Thesis, East Tennessee State University. Accessed April 10, 2021. https://dc.etsu.edu/etd/2342.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Forbes, Whitney. “Physiologically-Based Pharmacokinetic Model for Ertapenem.” 2014. Web. 10 Apr 2021.

Vancouver:

Forbes W. Physiologically-Based Pharmacokinetic Model for Ertapenem. [Internet] [Thesis]. East Tennessee State University; 2014. [cited 2021 Apr 10]. Available from: https://dc.etsu.edu/etd/2342.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Forbes W. Physiologically-Based Pharmacokinetic Model for Ertapenem. [Thesis]. East Tennessee State University; 2014. Available from: https://dc.etsu.edu/etd/2342

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of South Florida

19. Thompson, Zachary John. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.

Degree: 2012, University of South Florida

 Assessment of human exposure to environmental chemicals is inherently subject to uncertainty and variability. There are data gaps concerning the inventory, source, duration, and intensity… (more)

Subjects/Keywords: MCMC; PBPK; Risk assesment; TCDD; American Studies; Arts and Humanities; Biostatistics

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APA (6th Edition):

Thompson, Z. J. (2012). Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4241

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Thompson, Zachary John. “Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.” 2012. Thesis, University of South Florida. Accessed April 10, 2021. https://scholarcommons.usf.edu/etd/4241.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Thompson, Zachary John. “Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.” 2012. Web. 10 Apr 2021.

Vancouver:

Thompson ZJ. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. [Internet] [Thesis]. University of South Florida; 2012. [cited 2021 Apr 10]. Available from: https://scholarcommons.usf.edu/etd/4241.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Thompson ZJ. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4241

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Waterloo

20. Offman, Elliot. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.

Degree: 2016, University of Waterloo

 Prediction of human pharmacokinetics (PK) following subcutaneous (SC) administration to animals is challenged by potential interspecies differences in skin anatomy and physiology. With respect to… (more)

Subjects/Keywords: biologic; subcutaneous; pharmacokinetic; model; simulation; prediction; monkey; lymph; PBPK; mixed-effect

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APA (6th Edition):

Offman, E. (2016). In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10595

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Offman, Elliot. “In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.” 2016. Thesis, University of Waterloo. Accessed April 10, 2021. http://hdl.handle.net/10012/10595.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Offman, Elliot. “In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.” 2016. Web. 10 Apr 2021.

Vancouver:

Offman E. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10012/10595.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Offman E. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10595

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Georgia

21. Martin, Sheppard Allen. Development of a physiologically-based pharmacokinetic model for jet fuels in the rat.

Degree: 2014, University of Georgia

 The pharmacokinetic behavior of the majority of jet fuel constituents has not been previously described in the framework of a physiological-based pharmacokinetic (PBPK) model for… (more)

Subjects/Keywords: Jet Fuel; n-Alkane; Aromatic; Hydrocarbon Mixture; Rat; PBPK Model

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APA (6th Edition):

Martin, S. A. (2014). Development of a physiologically-based pharmacokinetic model for jet fuels in the rat. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26403

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Martin, Sheppard Allen. “Development of a physiologically-based pharmacokinetic model for jet fuels in the rat.” 2014. Thesis, University of Georgia. Accessed April 10, 2021. http://hdl.handle.net/10724/26403.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Martin, Sheppard Allen. “Development of a physiologically-based pharmacokinetic model for jet fuels in the rat.” 2014. Web. 10 Apr 2021.

Vancouver:

Martin SA. Development of a physiologically-based pharmacokinetic model for jet fuels in the rat. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10724/26403.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Martin SA. Development of a physiologically-based pharmacokinetic model for jet fuels in the rat. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26403

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Cincinnati

22. Moorthy, Ganesh. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.

Degree: PhD, Pharmacy: Pharmaceutical Sciences/Biopharmaceutics, 2015, University of Cincinnati

 Dysregulation of PI3K/Akt/mTOR pathway has been implicated in tumorigenesis and malignancy in numerous solid tumors. Everolimus is a potent allosteric inhibitor of mTORC1, and has… (more)

Subjects/Keywords: Pharmaceuticals; pharmacokinetics; Phase I; PBPK; DDI; BEZ235; Everolimus

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Moorthy, G. (2015). Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033

Chicago Manual of Style (16th Edition):

Moorthy, Ganesh. “Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.” 2015. Doctoral Dissertation, University of Cincinnati. Accessed April 10, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033.

MLA Handbook (7th Edition):

Moorthy, Ganesh. “Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.” 2015. Web. 10 Apr 2021.

Vancouver:

Moorthy G. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. [Internet] [Doctoral dissertation]. University of Cincinnati; 2015. [cited 2021 Apr 10]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033.

Council of Science Editors:

Moorthy G. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. [Doctoral Dissertation]. University of Cincinnati; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033

23. Ferreira, Carolina Martins André Oliveira. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.

Degree: 2015, Universidade Fernando Pessoa

Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

Os efeitos adversos decorrentes… (more)

Subjects/Keywords: Estudos toxicológicos; Modelos farmacocinéticos de base fisiológica (PBPK); Farmacocinética; Toxicocinética; Métodos in silico; Toxicological studies; Physiologically-based pharmacokinetic modeling (PBPK); Pharmacokinetics; Toxicokinetics; In silico methods

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APA (6th Edition):

Ferreira, C. M. A. O. (2015). Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. (Thesis). Universidade Fernando Pessoa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ferreira, Carolina Martins André Oliveira. “Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.” 2015. Thesis, Universidade Fernando Pessoa. Accessed April 10, 2021. http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ferreira, Carolina Martins André Oliveira. “Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.” 2015. Web. 10 Apr 2021.

Vancouver:

Ferreira CMAO. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. [Internet] [Thesis]. Universidade Fernando Pessoa; 2015. [cited 2021 Apr 10]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ferreira CMAO. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. [Thesis]. Universidade Fernando Pessoa; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Lorraine

24. Domínguez-Romero, Elena. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.

Degree: Docteur es, Sciences agronomiques, 2016, Université de Lorraine

L’hexabromocyclododécane (HBCD) a été utilisé comme additif dans des polystyrènes (PS). En 2013, l’HBCD a été inclus à la Convention de Stockholm comme Polluant Organique… (more)

Subjects/Keywords: Sécurité Sanitaire des Aliments; HBCD; Modèle PBPK; Poule pondeuse; Caractéristiques physiologiques; Food Safety; HBCD; PBPK model; Laying hen; Physiological features; 636.5; 363.192; 664.07

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Domínguez-Romero, E. (2016). Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2016LORR0167

Chicago Manual of Style (16th Edition):

Domínguez-Romero, Elena. “Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.” 2016. Doctoral Dissertation, Université de Lorraine. Accessed April 10, 2021. http://www.theses.fr/2016LORR0167.

MLA Handbook (7th Edition):

Domínguez-Romero, Elena. “Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.” 2016. Web. 10 Apr 2021.

Vancouver:

Domínguez-Romero E. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. [Internet] [Doctoral dissertation]. Université de Lorraine; 2016. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2016LORR0167.

Council of Science Editors:

Domínguez-Romero E. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. [Doctoral Dissertation]. Université de Lorraine; 2016. Available from: http://www.theses.fr/2016LORR0167

25. Viel, Alexis. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.

Degree: Docteur es, Pharmacie, 2017, Poitiers

La colistine est un vieil antibiotique, utilisé à la fois en médecine humaine et vétérinaire. Cependant, l'arsenal antibiotique étant de plus en plus limité, la… (more)

Subjects/Keywords: Colistine; Antibiorésistance; Pharmacocinétique; Modèle animal; Gène mcr-1; Modèle PBPK; Médecine humaine; Médecine vétérinaire; Colistin; Antibioresistance; Pharmacokinetics; Animal model; Mcr-1; PBPK model; Human medecine; Veterinary medecine; 615.17

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APA (6th Edition):

Viel, A. (2017). Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. (Doctoral Dissertation). Poitiers. Retrieved from http://www.theses.fr/2017POIT1801

Chicago Manual of Style (16th Edition):

Viel, Alexis. “Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.” 2017. Doctoral Dissertation, Poitiers. Accessed April 10, 2021. http://www.theses.fr/2017POIT1801.

MLA Handbook (7th Edition):

Viel, Alexis. “Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.” 2017. Web. 10 Apr 2021.

Vancouver:

Viel A. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. [Internet] [Doctoral dissertation]. Poitiers; 2017. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2017POIT1801.

Council of Science Editors:

Viel A. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. [Doctoral Dissertation]. Poitiers; 2017. Available from: http://www.theses.fr/2017POIT1801


University of Helsinki

26. Järvinen, Hanna. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.

Degree: Farmaceutiska fakulteten, 2017, University of Helsinki

 Lääkeainevasteissa esiintyvä yksilöllinen vaihtelu voi johtaa hankaluuksiin lääkkeen annostuksen määrittämisessä ja lääkkeen käyttöön liittyvien riskien kasvamiseen. Vaihtelua voi esiintyä lääkeaineen farmakokinetiikasta tai farmakodynamiikasta johtuen. Yksi… (more)

Subjects/Keywords: CYP2C19; CYP2D6; interindividual variability; genetic polymorphism; PBPK simulation models; genotyped microsomes; genotype-phenotype correlation; yksilöllinen vaihtelu; geneettinen polymorfia; PBPK-simulaatiomallit; genotyypatut mikrosomit; genotyyppi-fenotyyppi-korrelaatio; Biofarmaci; Biopharmacy; Biofarmasia

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Järvinen, H. (2017). Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/199518

Chicago Manual of Style (16th Edition):

Järvinen, Hanna. “Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.” 2017. Masters Thesis, University of Helsinki. Accessed April 10, 2021. http://hdl.handle.net/10138/199518.

MLA Handbook (7th Edition):

Järvinen, Hanna. “Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.” 2017. Web. 10 Apr 2021.

Vancouver:

Järvinen H. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10138/199518.

Council of Science Editors:

Järvinen H. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/199518

27. M.M. Ulaszewska. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.

Degree: 2010, Università degli Studi di Milano

 Polychlorinated dibenzo-p-dioxins, dibenzofurans (PCDD/Fs) and polychlorinated biphenyls (PCBs) are widespread environmental contaminants. They enter the human body mainly with food and because of lipophilic character… (more)

Subjects/Keywords: dioxin; PCB; PBPK model; human biomonitoring; dietary exposure; Settore AGR/13 - Chimica Agraria

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ulaszewska, M. (2010). THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/150138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ulaszewska, M.M.. “THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.” 2010. Thesis, Università degli Studi di Milano. Accessed April 10, 2021. http://hdl.handle.net/2434/150138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ulaszewska, M.M.. “THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.” 2010. Web. 10 Apr 2021.

Vancouver:

Ulaszewska M. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. [Internet] [Thesis]. Università degli Studi di Milano; 2010. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/2434/150138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ulaszewska M. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. [Thesis]. Università degli Studi di Milano; 2010. Available from: http://hdl.handle.net/2434/150138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Gerard, Cécile. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.

Degree: Docteur es, Recherche clinique, 2012, Université Claude Bernard – Lyon I

En transplantation d'organes solides ou en greffe de moelle osseuse, la ciclosporine et letacrolimus ont prouvé leur efficacité. Ils sont cependant de maniement délicat du… (more)

Subjects/Keywords: Médicaments immunosuppresseurs; Modélisation PBPK; Suivi thérapeutique; Immunosuppressant drugs; PBBK modeling; Therapeutic drug monitoring; 615.1

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APA (6th Edition):

Gerard, C. (2012). Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10265

Chicago Manual of Style (16th Edition):

Gerard, Cécile. “Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed April 10, 2021. http://www.theses.fr/2012LYO10265.

MLA Handbook (7th Edition):

Gerard, Cécile. “Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.” 2012. Web. 10 Apr 2021.

Vancouver:

Gerard C. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2012LYO10265.

Council of Science Editors:

Gerard C. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10265


Freie Universität Berlin

29. Pilari, Sabine. Lumping von PBPK-Modellen und Systembiologie.

Degree: 2011, Freie Universität Berlin

 In der Wirkstofffindung und -entwicklung wird pharmakokinetische und pharmakodynamische Modellierung erfolgreich zur Analyse und Vorhersage des zeitlichen Verlaufes von Wirkstoffkonzentrationen und Wirkstoffeffekten im Patienten genutzt.… (more)

Subjects/Keywords: Pharmacokinetics; Pharmacodynamics; PBPK; Systems Biology; Lumping; Mechanistic Modeling; 500 Naturwissenschaften und Mathematik

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APA (6th Edition):

Pilari, S. (2011). Lumping von PBPK-Modellen und Systembiologie. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/13030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pilari, Sabine. “Lumping von PBPK-Modellen und Systembiologie.” 2011. Thesis, Freie Universität Berlin. Accessed April 10, 2021. https://refubium.fu-berlin.de/handle/fub188/13030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pilari, Sabine. “Lumping von PBPK-Modellen und Systembiologie.” 2011. Web. 10 Apr 2021.

Vancouver:

Pilari S. Lumping von PBPK-Modellen und Systembiologie. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2021 Apr 10]. Available from: https://refubium.fu-berlin.de/handle/fub188/13030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pilari S. Lumping von PBPK-Modellen und Systembiologie. [Thesis]. Freie Universität Berlin; 2011. Available from: https://refubium.fu-berlin.de/handle/fub188/13030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Chicago

30. Kuo, Ilin. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.

Degree: 2012, University of Illinois – Chicago

 Intravenous lipid emulsions (ILE) have been demonstrated to be effective mitigators of systemic toxicity caused by drug overdose, with dramatic resuscitations observed in small animals… (more)

Subjects/Keywords: Lipid rescue; lipid emulsion; lipid sink; bupivacaine; PBPK; drug overdose; intravenous lipid emulsion; intralipid

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APA (6th Edition):

Kuo, I. (2012). Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9151

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kuo, Ilin. “Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.” 2012. Thesis, University of Illinois – Chicago. Accessed April 10, 2021. http://hdl.handle.net/10027/9151.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kuo, Ilin. “Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.” 2012. Web. 10 Apr 2021.

Vancouver:

Kuo I. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10027/9151.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kuo I. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9151

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3]

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