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Universitat Autònoma de Barcelona

1. Clotet i Codina, Imma. Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1.

Degree: Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia, 2007, Universitat Autònoma de Barcelona

 Over 40 million people worldwide are infected with human immunodeficiency virus (HIV). Five million people were new infected and three million were killed by the… (more)

Subjects/Keywords: VIH-1; Inhibidors; Hit; Ciències Experimentals; 615

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

APA (6th Edition):

Clotet i Codina, I. (2007). Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/286170

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):

Clotet i Codina, Imma. “Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1.” 2007. Thesis, Universitat Autònoma de Barcelona. Accessed September 25, 2020. http://hdl.handle.net/10803/286170.

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

MLA Handbook (7th Edition):

Clotet i Codina, Imma. “Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1.” 2007. Web. 25 Sep 2020.

Vancouver:

Clotet i Codina I. Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2007. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10803/286170.

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

Council of Science Editors:

Clotet i Codina I. Determinació de l’activitat antiviral de nous compostos inhibidors del VIH-1. [Thesis]. Universitat Autònoma de Barcelona; 2007. Available from: http://hdl.handle.net/10803/286170

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


University of Bath

2. Dhami, Archana. Approaches to new DNA-repair inhibitors for applications in cancer therapy.

Degree: PhD, 2008, University of Bath

 5-Aminoisoquinolin-1(2H)-one hydrochloride (5-AIQ.HCI) is a potent, water-soluble PARP-1 inhibitor that exhibits outstanding activity in a wide range of disease models in vivo. The aim of… (more)

Subjects/Keywords: 615; 5-amino isoquinolin-1-one; H-substitute

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APA (6th Edition):

Dhami, A. (2008). Approaches to new DNA-repair inhibitors for applications in cancer therapy. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/approaches-to-new-dnarepair-inhibitors-for-applications-in-cancer-therapy(cd734853-b380-490e-a0b7-2e733ad03921).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512320

Chicago Manual of Style (16th Edition):

Dhami, Archana. “Approaches to new DNA-repair inhibitors for applications in cancer therapy.” 2008. Doctoral Dissertation, University of Bath. Accessed September 25, 2020. https://researchportal.bath.ac.uk/en/studentthesis/approaches-to-new-dnarepair-inhibitors-for-applications-in-cancer-therapy(cd734853-b380-490e-a0b7-2e733ad03921).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512320.

MLA Handbook (7th Edition):

Dhami, Archana. “Approaches to new DNA-repair inhibitors for applications in cancer therapy.” 2008. Web. 25 Sep 2020.

Vancouver:

Dhami A. Approaches to new DNA-repair inhibitors for applications in cancer therapy. [Internet] [Doctoral dissertation]. University of Bath; 2008. [cited 2020 Sep 25]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/approaches-to-new-dnarepair-inhibitors-for-applications-in-cancer-therapy(cd734853-b380-490e-a0b7-2e733ad03921).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512320.

Council of Science Editors:

Dhami A. Approaches to new DNA-repair inhibitors for applications in cancer therapy. [Doctoral Dissertation]. University of Bath; 2008. Available from: https://researchportal.bath.ac.uk/en/studentthesis/approaches-to-new-dnarepair-inhibitors-for-applications-in-cancer-therapy(cd734853-b380-490e-a0b7-2e733ad03921).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512320


Freie Universität Berlin

3. Kuntzsch, Dana. Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC).

Degree: 2013, Freie Universität Berlin

 In recent years, the interest in phytotherapy steadily increased. Today research is focused on enlightening the phytopharmaceutical effects of medicinal plants, in order to establish… (more)

Subjects/Keywords: Epithelialer Natriumkanal (ENaC); Sgk-1; MAPK; Glucocorticoidrezeptor; TNF-alpha; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik

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APA (6th Edition):

Kuntzsch, D. (2013). Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC). (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/13517

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):

Kuntzsch, Dana. “Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC).” 2013. Thesis, Freie Universität Berlin. Accessed September 25, 2020. https://refubium.fu-berlin.de/handle/fub188/13517.

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

MLA Handbook (7th Edition):

Kuntzsch, Dana. “Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC).” 2013. Web. 25 Sep 2020.

Vancouver:

Kuntzsch D. Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC). [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Sep 25]. Available from: https://refubium.fu-berlin.de/handle/fub188/13517.

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

Council of Science Editors:

Kuntzsch D. Characterization of plant-derived glucocorticoid receptor modulators and their effects on the epithelial sodium channel (ENaC). [Thesis]. Freie Universität Berlin; 2013. Available from: https://refubium.fu-berlin.de/handle/fub188/13517

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


Universitat de Barcelona

4. Gris Ormo, Georgia. Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies.

Degree: 2015, Universitat de Barcelona

 La presente Tesis Doctoral se centra en el estudio del receptor sigma-11) en el campo del dolor. Esta investigación ha sido parte de un… (more)

Subjects/Keywords: Dolor; Pain; Proteïnes de membrana; Proteínas de membranas; Membrane proteins; Receptor Sigma-1; Sigma-1 receptor; Algesia; Algèsia; Medicina del dolor; Pain medicine; Ciències de la Salut; 615

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

APA (6th Edition):

Gris Ormo, G. (2015). Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/361398

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):

Gris Ormo, Georgia. “Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies.” 2015. Thesis, Universitat de Barcelona. Accessed September 25, 2020. http://hdl.handle.net/10803/361398.

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

MLA Handbook (7th Edition):

Gris Ormo, Georgia. “Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies.” 2015. Web. 25 Sep 2020.

Vancouver:

Gris Ormo G. Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies. [Internet] [Thesis]. Universitat de Barcelona; 2015. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10803/361398.

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

Council of Science Editors:

Gris Ormo G. Selective blockade of the sigma-1 receptor for the treatment of pain of different aetiology: Preclinical studies. [Thesis]. Universitat de Barcelona; 2015. Available from: http://hdl.handle.net/10803/361398

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

5. Lesage, Julien. Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression.

Degree: Docteur es, Médecine - STS, 2016, Reims

Au cours de la conversion métastatique des tumeurs épithéliales, les cellules tumorales acquièrent des capacités invasives/migratoires nouvelles. Ce changement phénotypique est associé au processus de… (more)

Subjects/Keywords: Zo-1; Cancers broncho-Pulmonaires; Transition épithélio-Mésenchymateuse (TEM); NF-KappaB; Progression tumorale; Cxcl8/il-8; Zo-1; Lung cancer; Epithelial-To-Mesenchymal transition (EMT); NF-KappaB; Tumor progression; Cxcl8/il-8; 615

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

APA (6th Edition):

Lesage, J. (2016). Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2016REIMM201

Chicago Manual of Style (16th Edition):

Lesage, Julien. “Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression.” 2016. Doctoral Dissertation, Reims. Accessed September 25, 2020. http://www.theses.fr/2016REIMM201.

MLA Handbook (7th Edition):

Lesage, Julien. “Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression.” 2016. Web. 25 Sep 2020.

Vancouver:

Lesage J. Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression. [Internet] [Doctoral dissertation]. Reims; 2016. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2016REIMM201.

Council of Science Editors:

Lesage J. Implication des Zonula Occludens dans la progression métastatique des cancers broncho-pulmonaires : Involvement of Zonula Occludens proteins in metastatic lung cancer progression. [Doctoral Dissertation]. Reims; 2016. Available from: http://www.theses.fr/2016REIMM201


University of Bath

6. Sunderland, Peter T. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.

Degree: PhD, 2010, University of Bath

Subjects/Keywords: 615; 5-AIQ; poly(ADP-ribose)polymerase; isoform selectivity; DNA repair; isoquinolin-1-ones

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APA (6th Edition):

Sunderland, P. T. (2010). Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/design-and-synthesis-of-selective-inhibitors-of-polyadpribosepolymerase2(8636312c-cb9c-4e67-89ed-ab73a86a8195).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371

Chicago Manual of Style (16th Edition):

Sunderland, Peter T. “Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.” 2010. Doctoral Dissertation, University of Bath. Accessed September 25, 2020. https://researchportal.bath.ac.uk/en/studentthesis/design-and-synthesis-of-selective-inhibitors-of-polyadpribosepolymerase2(8636312c-cb9c-4e67-89ed-ab73a86a8195).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371.

MLA Handbook (7th Edition):

Sunderland, Peter T. “Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.” 2010. Web. 25 Sep 2020.

Vancouver:

Sunderland PT. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. [Internet] [Doctoral dissertation]. University of Bath; 2010. [cited 2020 Sep 25]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/design-and-synthesis-of-selective-inhibitors-of-polyadpribosepolymerase2(8636312c-cb9c-4e67-89ed-ab73a86a8195).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371.

Council of Science Editors:

Sunderland PT. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. [Doctoral Dissertation]. University of Bath; 2010. Available from: https://researchportal.bath.ac.uk/en/studentthesis/design-and-synthesis-of-selective-inhibitors-of-polyadpribosepolymerase2(8636312c-cb9c-4e67-89ed-ab73a86a8195).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371


Universitat Pompeu Fabra

7. Llop Escorihuela, Esther. Structural analysis of eythropoietin glycans.

Degree: Departament de Ciències Experimentals i de la Salut, 2008, Universitat Pompeu Fabra

 Erythropoietin (EPO) is a glycoprotein hormone secreted primarily by adult kidneys in response to tissue hypoxia. It is involved in the maturation and ultimately regulation… (more)

Subjects/Keywords: Aminoacids; Alkylation; Acetyllactosamine; Acetylation; 2-DE; 2-aminobenzamide; 5-methylene-dioxybenzene; 2-diamino-4; 1; Aminoácidos; Alquilación; Agencia Mundial Antidopaje; Aclaramiento; Ácido siálico; Ácido neuramínico; Acetillactosamina; Acetilación; 2-DE; 2-aminobenzamida; 5-metileno-dioxybenzeno; 2-diamino-4; 1; Analysis; Antennae; Antibody; Antigen; Asialo-receptor; Band; 615

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APA (6th Edition):

Llop Escorihuela, E. (2008). Structural analysis of eythropoietin glycans. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7129

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):

Llop Escorihuela, Esther. “Structural analysis of eythropoietin glycans.” 2008. Thesis, Universitat Pompeu Fabra. Accessed September 25, 2020. http://hdl.handle.net/10803/7129.

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

MLA Handbook (7th Edition):

Llop Escorihuela, Esther. “Structural analysis of eythropoietin glycans.” 2008. Web. 25 Sep 2020.

Vancouver:

Llop Escorihuela E. Structural analysis of eythropoietin glycans. [Internet] [Thesis]. Universitat Pompeu Fabra; 2008. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10803/7129.

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

Council of Science Editors:

Llop Escorihuela E. Structural analysis of eythropoietin glycans. [Thesis]. Universitat Pompeu Fabra; 2008. Available from: http://hdl.handle.net/10803/7129

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


Universitat Pompeu Fabra

8. Fonseca Casals, Francina. Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals.

Degree: Departament de Ciències Experimentals i de la Salut, 2010, Universitat Pompeu Fabra

 Els programes de manteniment amb metadona (PMM) han demostrat eficàcia en el tractament del trastorn per dependència d'opiacis malgrat la persistència de pacients amb mala… (more)

Subjects/Keywords: genotip; haplotip; gen resistència multisubstància (ABCB1); gen miocardina (MYOCD); gen; gen candidat; farmacogenòmica; fenotip; farmacogenètica; farmacodinàmica; farmacocinètica; estereoselectivitat; epistaxi; enzim; enantiòmer; 3-diphenyl-1-pyrrolidine; 5-dimethyl-3; 3-diphenylpyrrolidine; electroforesi; EMDP; 2-ethyl-5-methyl-3; 2-ethylidene-1; dopamina; EDDP; criptocrom 1 (CRY1); desintoxicació; comorbiditat psiquiàtrica; Citocrom P4503A5; Citocrom P4503A4; Citocrom P4502D6; Citocrom P4502B6; Citocrom P4502C19; Citocrom P4502C9; Citocrom P4501A2; Citocrom P450; biodisponibilitat; Alel; addicció; abstinència; withdrawal; vulnerability; stereoselectivity; substance abuse; single nucleotide polymorphism (SNP); psychiatric comorbidity; replacement therapy; polymorphism; pharmacogenomics; pharmacokinetics; phenotype; pharmacogenetics; pharmacodynamics; opioid dependence; opioid; opiate; neurotrophins; neurotransmitter; Myocardin gene (MYOCD); resistant gene 1 (ABCB1); multidrug; methadone; mu opioid receptor; metabotropic glutamate receptors; maintenance treatment; Isomers; heroin (diacetylmorphine); Haplotype; Genotype; gene; Epistasis; Enzyme; Enantiomer; 3-diphenyl-1-pyrrolidine; 2-ethyl-5-methyl-3; EMDP; Electrophoresis; 3-diphenylpyrrolidine; 5-dimethyl-3; dopamine; EDDP; 2-ethylidene-1; detoxification; Cytochrome P4503A5; Cytochrome P4503A4; Cytochrome P4502D6; Cytochrome P4502C9; Cytochrome P4502C19; Cytochrome P4502B6; Cytochrome P4501A2; Cytochrome P450; Cryptochrome 1 gene (CRY1); craving; Complex Disease; candidate gene; allele; Brain Derived Neurotrophic factor (BDNF); addiction; heroïna (diacetilmorfina); isòmers; metadona; neurotransmissor; neurotrofines; opiacis; polimorfisme; polimorfisme de nucleòtid únic (SNP); receptor metabotròpic del glutamat; receptor opioide mu; tractament de manteniment; tractament substitutiu; trastorn per ús de substàncies; vulnerabilitat; 615

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APA (6th Edition):

Fonseca Casals, F. (2010). Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7234

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):

Fonseca Casals, Francina. “Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals.” 2010. Thesis, Universitat Pompeu Fabra. Accessed September 25, 2020. http://hdl.handle.net/10803/7234.

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

MLA Handbook (7th Edition):

Fonseca Casals, Francina. “Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals.” 2010. Web. 25 Sep 2020.

Vancouver:

Fonseca Casals F. Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals. [Internet] [Thesis]. Universitat Pompeu Fabra; 2010. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10803/7234.

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

Council of Science Editors:

Fonseca Casals F. Pharmacogenomic study of oppioid addicts in methadone treatment / Francina Fonseca Casals. [Thesis]. Universitat Pompeu Fabra; 2010. Available from: http://hdl.handle.net/10803/7234

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

.