Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(HepaRG). Showing records 1 – 23 of 23 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of Edinburgh

1. Morgan, Frances Katie. Formulating an improved in vitro hepatic model for drug development and toxicity testing.

Degree: PhD, 2019, University of Edinburgh

 There is a need in the pharmaceutical industry for more informative and functional in vitro human models for drug testing as the currently used animal… (more)

Subjects/Keywords: nanopattern; ECIS; impedance; HepaRG; C3A

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Morgan, F. K. (2019). Formulating an improved in vitro hepatic model for drug development and toxicity testing. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35899

Chicago Manual of Style (16th Edition):

Morgan, Frances Katie. “Formulating an improved in vitro hepatic model for drug development and toxicity testing.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed April 15, 2021. http://hdl.handle.net/1842/35899.

MLA Handbook (7th Edition):

Morgan, Frances Katie. “Formulating an improved in vitro hepatic model for drug development and toxicity testing.” 2019. Web. 15 Apr 2021.

Vancouver:

Morgan FK. Formulating an improved in vitro hepatic model for drug development and toxicity testing. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1842/35899.

Council of Science Editors:

Morgan FK. Formulating an improved in vitro hepatic model for drug development and toxicity testing. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35899


Universidade Nova

2. Rebelo, Sofia Raquel Paulo. Development of 3D in vitro models for prediction of hepatic metabolism and toxicity.

Degree: 2015, Universidade Nova

The development of human cell models that recapitulate hepatic functionality allows the study of metabolic pathways involved in toxicity and disease. The increased biological relevance,… (more)

Subjects/Keywords: 3D; Hepatic; Microencapsulation; Bioreactor; Co-culture; HepaRG

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rebelo, S. R. P. (2015). Development of 3D in vitro models for prediction of hepatic metabolism and toxicity. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15268

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):

Rebelo, Sofia Raquel Paulo. “Development of 3D in vitro models for prediction of hepatic metabolism and toxicity.” 2015. Thesis, Universidade Nova. Accessed April 15, 2021. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15268.

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

MLA Handbook (7th Edition):

Rebelo, Sofia Raquel Paulo. “Development of 3D in vitro models for prediction of hepatic metabolism and toxicity.” 2015. Web. 15 Apr 2021.

Vancouver:

Rebelo SRP. Development of 3D in vitro models for prediction of hepatic metabolism and toxicity. [Internet] [Thesis]. Universidade Nova; 2015. [cited 2021 Apr 15]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15268.

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

Council of Science Editors:

Rebelo SRP. Development of 3D in vitro models for prediction of hepatic metabolism and toxicity. [Thesis]. Universidade Nova; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15268

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

3. Al-Attrache, Houssein. Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation.

Degree: Docteur es, Biologie et sciences de la santé, 2016, Rennes 1; Université libanaise

Chez l’homme, de nombreux médicaments ne sont toxiques que chez un petit nombre de patients traités. Divers facteurs de susceptibilité, génétiques et autres (doses quotidiennes,… (more)

Subjects/Keywords: Médicaments; Cellules HepaRG; Levure; Inflammation; Toxicité; Drugs; HepaRG cells; Yeast; Inflammation; Toxicity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Al-Attrache, H. (2016). Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation. (Doctoral Dissertation). Rennes 1; Université libanaise. Retrieved from http://www.theses.fr/2016REN1B049

Chicago Manual of Style (16th Edition):

Al-Attrache, Houssein. “Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation.” 2016. Doctoral Dissertation, Rennes 1; Université libanaise. Accessed April 15, 2021. http://www.theses.fr/2016REN1B049.

MLA Handbook (7th Edition):

Al-Attrache, Houssein. “Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation.” 2016. Web. 15 Apr 2021.

Vancouver:

Al-Attrache H. Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation. [Internet] [Doctoral dissertation]. Rennes 1; Université libanaise; 2016. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2016REN1B049.

Council of Science Editors:

Al-Attrache H. Etude de la toxicité idiosyncratique de médicaments sur cellules HepaRG et levure : influence du stress inflammatoire et de la biotransformation : Study of the idiosyncratic toxicity of drugs in HepaRG and yeast : influence of inflammatory stress and biotransformation. [Doctoral Dissertation]. Rennes 1; Université libanaise; 2016. Available from: http://www.theses.fr/2016REN1B049

4. Michaut, Anaïs. Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity.

Degree: Docteur es, Biologie et sciences de la santé, 2015, Rennes 1

 L'obésité et les maladies du foie associées (NAFLD) augmentent le risque et la sévérité de l’hépatotoxicité induite par certains xénobiotiques, mais les mécanismes impliqués sont… (more)

Subjects/Keywords: Obésité; Stéatose; Nafld; Paracétamol; Cyp2e1; Cyp3a4; Acide gras; HepaRG; Obésity; Steatosis; Nafld; Acetaminophen; Cyp2e1; Cyp3a4; Fatty acid; HepaRG

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Michaut, A. (2015). Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2015REN1B015

Chicago Manual of Style (16th Edition):

Michaut, Anaïs. “Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity.” 2015. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2015REN1B015.

MLA Handbook (7th Edition):

Michaut, Anaïs. “Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity.” 2015. Web. 15 Apr 2021.

Vancouver:

Michaut A. Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity. [Internet] [Doctoral dissertation]. Rennes 1; 2015. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2015REN1B015.

Council of Science Editors:

Michaut A. Mise au point d'un modèle de stéatose hépatique liée à l'obésité : application à l'étude de la toxicité du paracétamol : Development of e cell model of liver steatosis related to obesity : application to the study of acetaminophen toxicity. [Doctoral Dissertation]. Rennes 1; 2015. Available from: http://www.theses.fr/2015REN1B015

5. Savary, Camille. Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells.

Degree: Docteur es, Biologie et Sciences de la Santé, 2014, Rennes 1

L’Homme est exposé tout au long de sa vie à de nombreux contaminants présents dans l’environnement et l’alimentation généralement à faibles doses et en mélanges.… (more)

Subjects/Keywords: Contaminants de l’environnement; Toxicité chronique; Mélanges; Cancérogenèse; Cellules HepaRG; Environmental contaminants; Chronic toxicity; Chemical mixture; Carcinogenesis; HepaRG cells

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Savary, C. (2014). Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2014REN1B007

Chicago Manual of Style (16th Edition):

Savary, Camille. “Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells.” 2014. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2014REN1B007.

MLA Handbook (7th Edition):

Savary, Camille. “Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells.” 2014. Web. 15 Apr 2021.

Vancouver:

Savary C. Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells. [Internet] [Doctoral dissertation]. Rennes 1; 2014. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2014REN1B007.

Council of Science Editors:

Savary C. Étude de la toxicité chronique et du potentiel cancérogène de contaminants de l’environnement séparément et en mélange sur les cellules HepaRG : Study of chronic toxicity and carcinogenic potential of environmental contaminants separately and in mixture in HepaRG cells. [Doctoral Dissertation]. Rennes 1; 2014. Available from: http://www.theses.fr/2014REN1B007

6. Launey, Yoann. Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines.

Degree: Docteur es, Biologie et sciences de la santé, 2015, Rennes 1

Le sepsis sévère est un problème majeur de santé publique mondiale. Sa mortalité élevée résulte d’une réponse dérégulée de l’hôte au sepsis, associant hyper inflammation… (more)

Subjects/Keywords: Sepsis; Dysfonction hépatocellulaire; Catécholamines; Co-Culture cellulaire; HepaRG; Sepsis; Liver dysfunction; Catecholamines; Cell co-Culture; HepaRG

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Launey, Y. (2015). Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2015REN1B023

Chicago Manual of Style (16th Edition):

Launey, Yoann. “Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines.” 2015. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2015REN1B023.

MLA Handbook (7th Edition):

Launey, Yoann. “Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines.” 2015. Web. 15 Apr 2021.

Vancouver:

Launey Y. Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines. [Internet] [Doctoral dissertation]. Rennes 1; 2015. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2015REN1B023.

Council of Science Editors:

Launey Y. Dysfonction hépatique septique : rôle des catécholamines : Sepsis Liver dysfunction : role of catecholamines. [Doctoral Dissertation]. Rennes 1; 2015. Available from: http://www.theses.fr/2015REN1B023

7. Lu, Heng. Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer.

Degree: Docteur es, Biologie moléculaire, 2016, Sorbonne Paris Cité

 Ce projet de thèse portait sur le développement d’outils microfluidiques pour la toxicologie et la recherche contre le cancer. En permettant l’analyse simultanée d’un très… (more)

Subjects/Keywords: Microfluidique en gouttes; Cytochrome P450; HepaRG; Syndromes myélodysplasiques; Droplet-based microfluidics; Cytochrome P450; HepaRG; Myelodysplastic syndrome; 571.95

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lu, H. (2016). Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB064

Chicago Manual of Style (16th Edition):

Lu, Heng. “Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed April 15, 2021. http://www.theses.fr/2016USPCB064.

MLA Handbook (7th Edition):

Lu, Heng. “Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer.” 2016. Web. 15 Apr 2021.

Vancouver:

Lu H. Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2016USPCB064.

Council of Science Editors:

Lu H. Development of droplet-based microfluidic tools for toxicology and cancer research : Systèmes microfluidiques de crillage à haut débit en microgouttelettes pour la toxicologie et la recherche sur cancer. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB064

8. Bouezzedine, Fidaa. Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6.

Degree: Docteur es, Biologie et sciences de la santé, 2015, Rennes 1

L’hépatite B est une maladie infectieuse grave et extrêmement contagieuse. Malgré l’existence d’un vaccin efficace plus de 240 millions de personnes souffrent d’une infection hépatique… (more)

Subjects/Keywords: Entrée virale; Fusion; HepaRG; Phh; Il-6; Ntcp; Vhb

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bouezzedine, F. (2015). Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2015REN1B003

Chicago Manual of Style (16th Edition):

Bouezzedine, Fidaa. “Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6.” 2015. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2015REN1B003.

MLA Handbook (7th Edition):

Bouezzedine, Fidaa. “Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6.” 2015. Web. 15 Apr 2021.

Vancouver:

Bouezzedine F. Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6. [Internet] [Doctoral dissertation]. Rennes 1; 2015. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2015REN1B003.

Council of Science Editors:

Bouezzedine F. Analyse de l'entrée du virus de l'hépatite B : Etude du processus de fusion et de l'effet de l'interleukine 6 : Hepatitis B virus entry analysis : Study of the fusion process and effect of interleukin 6. [Doctoral Dissertation]. Rennes 1; 2015. Available from: http://www.theses.fr/2015REN1B003

9. Burbank, Matthew. Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis.

Degree: Docteur es, Biologie et sciences de la santé, 2016, Rennes 1

La cholestase intrahépatique est une manifestation fréquente des lésions hépatiques induites par les médicaments; Cependant, les mécanismes impliqués sont peu connus. Nous avons cherché à… (more)

Subjects/Keywords: Rock/mlck; Antagonistes des récepteurs à l'endothéline; Cholestase; Hépatotoxicité; Canalicule biliaire; Cellules HepaRG; Rock/mlck; Endothelin receptor antagonists; Cholestasis; Hepatotoxicity; Bile canaliculi; HepaRG cells

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Burbank, M. (2016). Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2016REN1B024

Chicago Manual of Style (16th Edition):

Burbank, Matthew. “Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis.” 2016. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2016REN1B024.

MLA Handbook (7th Edition):

Burbank, Matthew. “Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis.” 2016. Web. 15 Apr 2021.

Vancouver:

Burbank M. Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis. [Internet] [Doctoral dissertation]. Rennes 1; 2016. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2016REN1B024.

Council of Science Editors:

Burbank M. Altération de la dynamique des canalicules biliaires in vitro : une nouvelle approche de la prédiction de la cholestase intrahépatique d'origine médicamenteuse : Alterations of bile canaliculi dynamics : a new approach in the prediction of drug-induced intrahepatic cholestasis. [Doctoral Dissertation]. Rennes 1; 2016. Available from: http://www.theses.fr/2016REN1B024


University of Saskatchewan

10. Hawsawi, Ahlam Ahmad 1982-. Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG.

Degree: 2018, University of Saskatchewan

 High blood cholesterol (HBC) is an important risk factor of cardiovascular disease (CVD), which is associated with high morbidity and mortality worldwide. Lifestyle changes and… (more)

Subjects/Keywords: Cholesterol Trafficking; HepaRG; Flaxseed Lignan Metabolites; Enterolactone; Enterolactone Glucuronide; OATP hepatic uptake transporters; OATP1B1; OATP1B3.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hawsawi, A. A. 1. (2018). Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/10065

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):

Hawsawi, Ahlam Ahmad 1982-. “Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG.” 2018. Thesis, University of Saskatchewan. Accessed April 15, 2021. http://hdl.handle.net/10388/10065.

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

MLA Handbook (7th Edition):

Hawsawi, Ahlam Ahmad 1982-. “Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG.” 2018. Web. 15 Apr 2021.

Vancouver:

Hawsawi AA1. Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10388/10065.

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

Council of Science Editors:

Hawsawi AA1. Flaxseed Lignan Metabolites Modulate Hepatocellular Cholesterol Trafficking In HepaRG. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/10065

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


Universiteit Utrecht

11. Paskel, R.F. Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs.

Degree: 2013, Universiteit Utrecht

 Unfavorable drug metabolism is the main reason for attrition of new chemical entities and withdrawal of drugs from the market, costing pharmaceutical companies a great… (more)

Subjects/Keywords: in vitro systems; hepatic clearance; in vivo; human; predicting; liver microsomes; liver slices; hepatocytes; primary hepatocytes; HepaRG

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Paskel, R. F. (2013). Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/281238

Chicago Manual of Style (16th Edition):

Paskel, R F. “Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs.” 2013. Masters Thesis, Universiteit Utrecht. Accessed April 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/281238.

MLA Handbook (7th Edition):

Paskel, R F. “Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs.” 2013. Web. 15 Apr 2021.

Vancouver:

Paskel RF. Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2021 Apr 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/281238.

Council of Science Editors:

Paskel RF. Human-Based In Vitro Systems for Predicting In Vivo Hepatic Clearance of Drugs. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/281238

12. Ferreira, Ana Filipa da Silva. Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação.

Degree: 2012, Universidade da Beira Interior

 O período de estágio final, inserido no Plano de Estudos do Mestrado em Ciências Farmacêuticas da Universidade da Beira Interior, surge como o culminar da… (more)

Subjects/Keywords: Amiodarona - Fármacos - Avaliação; Células HepaRG; Farmácia comunitária - Gestão - Estágio pedagógico; Farmácia hospitalar - Gestão - Estágio pedagógico; Farmacêutico - Utente - Medicamento

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ferreira, A. F. d. S. (2012). Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação. (Thesis). Universidade da Beira Interior. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/1137

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, Ana Filipa da Silva. “Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação.” 2012. Thesis, Universidade da Beira Interior. Accessed April 15, 2021. http://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/1137.

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

MLA Handbook (7th Edition):

Ferreira, Ana Filipa da Silva. “Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação.” 2012. Web. 15 Apr 2021.

Vancouver:

Ferreira AFdS. Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação. [Internet] [Thesis]. Universidade da Beira Interior; 2012. [cited 2021 Apr 15]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/1137.

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

Council of Science Editors:

Ferreira AFdS. Avaliação da interação de fármacos com a amiodarona em células HepaRG : experiência profissionalizante na vertente de farmácia comunitária, hospitalar e investigação. [Thesis]. Universidade da Beira Interior; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/1137

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


North-West University

13. Crous, Ané. The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous.

Degree: 2013, North-West University

 Sulforaphane is an isothiocyanate found in high concentrations in cruciferous vegetables like broccoli. Sulforaphane has received much attention due to the evidence that it inhibits… (more)

Subjects/Keywords: Sulforaphane; oxidative stress; t-BHP; MTT; phase I and phase II; biotransformation; LC-ESI-MS/MS; HepaRG cells

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Crous, A. (2013). The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous. (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/9642

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):

Crous, Ané. “The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous. ” 2013. Thesis, North-West University. Accessed April 15, 2021. http://hdl.handle.net/10394/9642.

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

MLA Handbook (7th Edition):

Crous, Ané. “The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous. ” 2013. Web. 15 Apr 2021.

Vancouver:

Crous A. The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous. [Internet] [Thesis]. North-West University; 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10394/9642.

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

Council of Science Editors:

Crous A. The effect of sulforaphane on oxidative stress and biotransformation in HepaRG cells / A. Crous. [Thesis]. North-West University; 2013. Available from: http://hdl.handle.net/10394/9642

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

14. SUN MIN. ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION.

Degree: 2020, National University of Singapore

Subjects/Keywords: Hepatocyte differentiation; Hepatocyte maturation; Physical microenvironment; HepaRG; Topographies; Materiomics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

MIN, S. (2020). ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION. (Thesis). National University of Singapore. Retrieved from https://scholarbank.nus.edu.sg/handle/10635/164906

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):

MIN, SUN. “ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION.” 2020. Thesis, National University of Singapore. Accessed April 15, 2021. https://scholarbank.nus.edu.sg/handle/10635/164906.

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

MLA Handbook (7th Edition):

MIN, SUN. “ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION.” 2020. Web. 15 Apr 2021.

Vancouver:

MIN S. ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION. [Internet] [Thesis]. National University of Singapore; 2020. [cited 2021 Apr 15]. Available from: https://scholarbank.nus.edu.sg/handle/10635/164906.

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

Council of Science Editors:

MIN S. ENGINEERING PHYSICAL MICROENVIRONMENTS FOR HEPATOCYTE DIFFERENTIATION AND MATURATION. [Thesis]. National University of Singapore; 2020. Available from: https://scholarbank.nus.edu.sg/handle/10635/164906

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

15. Smith, Marie-Caroline. Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach.

Degree: Docteur es, Biochimie, biologie moléculaire et cellulaire, 2017, Brest

Les céréales et les produits issus de leur transformation sont susceptibles d’être contaminés par des espèces fongiques capables de produire des mycotoxines. L’Homme est ainsi… (more)

Subjects/Keywords: Fusariotoxines; Mélanges; Toxicité aigüe; Toxicité chronique; Toxico-protéomique; THP-1; Caco-2; HepaRG; Cocultures; Fusariotoxins; Mixtures; Acute toxicity; Chronic toxicity; Toxico-protéomic; THP-1; Caco-2; HepaRG; Co-culture; 579.567 7; 615.952 95

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, M. (2017). Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach. (Doctoral Dissertation). Brest. Retrieved from http://www.theses.fr/2017BRES0084

Chicago Manual of Style (16th Edition):

Smith, Marie-Caroline. “Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach.” 2017. Doctoral Dissertation, Brest. Accessed April 15, 2021. http://www.theses.fr/2017BRES0084.

MLA Handbook (7th Edition):

Smith, Marie-Caroline. “Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach.” 2017. Web. 15 Apr 2021.

Vancouver:

Smith M. Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach. [Internet] [Doctoral dissertation]. Brest; 2017. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2017BRES0084.

Council of Science Editors:

Smith M. Incidence de la multi-contamination aux mycotoxines de Fusarium sur cellules humaines : évaluation de la cytotoxicité et approche toxico-protéomique : Incidence of Fusarium mycotoxins multicontamination on human cells : cytotoxicity evaluation and toxicoproteomic approach. [Doctoral Dissertation]. Brest; 2017. Available from: http://www.theses.fr/2017BRES0084

16. Pivert, Adeline. Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research.

Degree: Docteur es, Microbiologie, 2017, Angers

L’infection par le virus de l’hépatite B (VHB) reste un problème de santé publique avec plus de 880 000 décès chaque année dans le monde.… (more)

Subjects/Keywords: Virus de l’hépatite B; Mutations du promoteur basal du core et precore; Technologie lentivirale; HepaRG; Fibrose hépatique; Hepatitis B virus; Basal core promotor and precore mutations; Lentiviral technology; HepaRG; Liver fibrosis; 616.91; 616.3

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pivert, A. (2017). Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research. (Doctoral Dissertation). Angers. Retrieved from http://www.theses.fr/2017ANGE0075

Chicago Manual of Style (16th Edition):

Pivert, Adeline. “Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research.” 2017. Doctoral Dissertation, Angers. Accessed April 15, 2021. http://www.theses.fr/2017ANGE0075.

MLA Handbook (7th Edition):

Pivert, Adeline. “Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research.” 2017. Web. 15 Apr 2021.

Vancouver:

Pivert A. Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research. [Internet] [Doctoral dissertation]. Angers; 2017. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2017ANGE0075.

Council of Science Editors:

Pivert A. Mutations dans la région précore du virus de l’hépatite B et fibrose hépatique : approche épidémiologique et application fondamentale : HBV precore mutations and liver fibrosis : epidemiologic approach and basic research. [Doctoral Dissertation]. Angers; 2017. Available from: http://www.theses.fr/2017ANGE0075

17. Pasqua, Mattia. Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel.

Degree: Docteur es, Biomatériaux et Bio-ingénierie : Unité de Recherche Biomécanique et Bio-ingénierie (UMR-7338), 2020, Compiègne

Pour tous les patients souffrant d'une insuffisance hépatique aigue, il existe un besoin urgent de solutions alternatives à la transplantation du foie. En raison de… (more)

Subjects/Keywords: Insuffisance hépatique aigue; HepaRG; Billes d’alginate; Encapsulation de cellules hépatiques; Foie bioartificiel; Culture cellulaire 3D; Activités métaboliques; Sphéroïdes; Acute liver failure; HepaRG; Alginate beads; Hepatic cell encapsulation; Bioartificial liver; 3D cell culture; Cell differentiation; Bioreactors; Metabolic activities; Spheroids; Extracorporeal circulation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pasqua, M. (2020). Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel. (Doctoral Dissertation). Compiègne. Retrieved from http://www.theses.fr/2020COMP2557

Chicago Manual of Style (16th Edition):

Pasqua, Mattia. “Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel.” 2020. Doctoral Dissertation, Compiègne. Accessed April 15, 2021. http://www.theses.fr/2020COMP2557.

MLA Handbook (7th Edition):

Pasqua, Mattia. “Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel.” 2020. Web. 15 Apr 2021.

Vancouver:

Pasqua M. Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel. [Internet] [Doctoral dissertation]. Compiègne; 2020. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2020COMP2557.

Council of Science Editors:

Pasqua M. Preclinical studies on an extracorporeal bioartificial liver : Études précliniques sur un foie extracorporel bioartificiel. [Doctoral Dissertation]. Compiègne; 2020. Available from: http://www.theses.fr/2020COMP2557

18. Casajus, Hubert. Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates.

Degree: Docteur es, Chimie, 2017, Rennes 1

Les polyesters aliphatiques, comme le poly(acide malique) et ses dérivés, sont une famille de polymères aux propriétés de bio(comptabilité) et de bio(dégradabilité) remarquables, qui en… (more)

Subjects/Keywords: Polymérisation enzymatique; Lipases; Plan d’expérience; Malolactonate de benzyle; Poly(malate de benzyle); Nanoparticules; Vectorisation de principes actifs; Cellules hépatiques HepaRG; Cytoxicités aigüe et chronique; Métabolisme cellulaire; Enzymatic polymerization; Lipases; Design of experiments; Benzyl malolactonate; Poly(benzyl malate); Nanoparticles; Drug delivery systems; HepaRG hepatic cells line; Acute and chronic cytotoxicities; Cellular metabolismEnzymatic polymerization; Lipases; Design of experiments; Benzyl malolactonate; Poly(benzyl malate); Nanoparticles; Drug delivery systems; HepaRG hepatic cells line; Acute and chronic cytotoxicities; Cellular metabolism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Casajus, H. (2017). Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2017REN1S090

Chicago Manual of Style (16th Edition):

Casajus, Hubert. “Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates.” 2017. Doctoral Dissertation, Rennes 1. Accessed April 15, 2021. http://www.theses.fr/2017REN1S090.

MLA Handbook (7th Edition):

Casajus, Hubert. “Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates.” 2017. Web. 15 Apr 2021.

Vancouver:

Casajus H. Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates. [Internet] [Doctoral dissertation]. Rennes 1; 2017. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2017REN1S090.

Council of Science Editors:

Casajus H. Étude de la polymérisation enzymatique de la malolactonates en présence de lipases : Study of the lipase-catalyzed polymerization of malolactonates. [Doctoral Dissertation]. Rennes 1; 2017. Available from: http://www.theses.fr/2017REN1S090

19. Gomes, Ana Inês Pacheco Vaz. In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model.

Degree: 2016, RCAAP

 Pharmacokinetics information, especially regarding the drug metabolic profile, is a requirement during the preclinical and clinical development. In vitro methodologies represent more and more useful… (more)

Subjects/Keywords: Cyp2c9 Inhibition; Drug Interactions; Flavonoids; Heparg Cells; Highperformance Liquid Chromatography; In Vitro Studies; Tolbutamide; Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gomes, A. I. P. V. (2016). In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5808

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):

Gomes, Ana Inês Pacheco Vaz. “In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model.” 2016. Thesis, RCAAP. Accessed April 15, 2021. https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5808.

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

MLA Handbook (7th Edition):

Gomes, Ana Inês Pacheco Vaz. “In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model.” 2016. Web. 15 Apr 2021.

Vancouver:

Gomes AIPV. In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model. [Internet] [Thesis]. RCAAP; 2016. [cited 2021 Apr 15]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5808.

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

Council of Science Editors:

Gomes AIPV. In vitro assessment of cytochrome P450 2C9 inhibition: tolbutamide as probe substrate and HepaRG cells as human hepatic model. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5808

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

20. Santos, João Pedro Ladeira. Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro.

Degree: 2014, RCAAP

 O estágio curricular realizado no final dos 5 anos do Mestrado Integrado em Ciências Farmacêuticas apresenta-se como uma ferramenta fundamental na aplicação de todos os… (more)

Subjects/Keywords: Caco-2; Farmácia Comunitária; Farmácia Hospitalar; Gp-P; Heparg; Kb-C2; Mcf-7/Adr; Mdck-Mdr1; Rodamina 123; Domínio/Área Científica::Ciências Médicas::Ciências da Saúde

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Santos, J. P. L. (2014). Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5142

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):

Santos, João Pedro Ladeira. “Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro.” 2014. Thesis, RCAAP. Accessed April 15, 2021. https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5142.

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

MLA Handbook (7th Edition):

Santos, João Pedro Ladeira. “Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro.” 2014. Web. 15 Apr 2021.

Vancouver:

Santos JPL. Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro. [Internet] [Thesis]. RCAAP; 2014. [cited 2021 Apr 15]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5142.

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

Council of Science Editors:

Santos JPL. Inibição da glicoproteína-P: modelos celulares para ensaios de screening in vitro. [Thesis]. RCAAP; 2014. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5142

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

21. Weemhoff, James Lawrence. Mechanistic Biomarkers in Acute Liver Injury.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2017, University of Kansas

 Acute liver failure continues to be a major medical problem. There are many underlying causes of acute liver failure, but drug induced liver injury is… (more)

Subjects/Keywords: Toxicology; Acetaminophen; Biomarkers; HepaRG; Hypoxic Hepatitis; Liver Injury; Liver Transplantation

…50 4. COMPARISON OF FRESHLY DIFFERENTIATED AND CRYOPRESERVED PREDIFFERENTIATED HEPARG… …UNDIFFERENTIATED VS. PRE-DIFFERENTIATED CRYOPRESERVED HEPARG CELLS… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Weemhoff, J. L. (2017). Mechanistic Biomarkers in Acute Liver Injury. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27044

Chicago Manual of Style (16th Edition):

Weemhoff, James Lawrence. “Mechanistic Biomarkers in Acute Liver Injury.” 2017. Doctoral Dissertation, University of Kansas. Accessed April 15, 2021. http://hdl.handle.net/1808/27044.

MLA Handbook (7th Edition):

Weemhoff, James Lawrence. “Mechanistic Biomarkers in Acute Liver Injury.” 2017. Web. 15 Apr 2021.

Vancouver:

Weemhoff JL. Mechanistic Biomarkers in Acute Liver Injury. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1808/27044.

Council of Science Editors:

Weemhoff JL. Mechanistic Biomarkers in Acute Liver Injury. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/27044

22. -6532-9152. Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture.

Degree: MS, Baylor University. Dept. of Environmental Science., 2019, Baylor University

 In vitro bioassays have been useful in predicting mechanisms of toxicity; however, conventional cell-based assays grown in monolayers are unavoidably poor models for human tissues… (more)

Subjects/Keywords: Co-culture. Caco-2. HepaRG. Cytotoxicity. Antioxidant enzymes. Galveston Bay. Red Drum. Black Drum. Spotted Trout. Oyster.

…organotypic co-culture system, using intestinal (Caco-2) and hepatic (HepaRG)… …extracts led to significant cell mortality in monocultures. HepaRG cells in monoculture expressed… …lower levels of glutathione peroxidase and superoxide dismutase than HepaRG cells in coculture… …adenocarcinoma cell line, Caco-2, and the hepatic cell line, HepaRG, were utilized. Caco-2 cells… …The HepaRG cell line exhibits particularly unique qualities; confluent HepaRG cells can be… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

-6532-9152. (2019). Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture. (Masters Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/10765

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6532-9152. “Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture.” 2019. Masters Thesis, Baylor University. Accessed April 15, 2021. http://hdl.handle.net/2104/10765.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-6532-9152. “Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture.” 2019. Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-6532-9152. Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture. [Internet] [Masters thesis]. Baylor University; 2019. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2104/10765.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-6532-9152. Biological responses from contaminants accumulated in seafood using an in vitro human intestinal and liver co-culture. [Masters Thesis]. Baylor University; 2019. Available from: http://hdl.handle.net/2104/10765

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

23. Song, Yang. ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development.

Degree: 2012, University of Illinois – Chicago

 Tuberculosis (TB) is among the top three life-threatening infectious diseases in developing countries. Therefore, there is a great need to discover and develop novel anti-TB… (more)

Subjects/Keywords: Tuberculosis; Metabolism; Assay development; LC-MS; Method development; HepaRG cells; Active metabolites; Cytochrome P450 induction; liquid chromatography mass spectrometry

…108 5. HARNESSING HepaRG CELLS FOR CYTOCHROME P450 INDUCTION STUDIES… …111 5.2.2. Culturing of HepaRG cells in customized medium for induction study… …111 5.2.3. Establish methods to evaluate CYP activity and expression in HepaRG cells… …HepaRG cells.......................................................................128 5.3.6… …114 TABLE XXV. HYDROCORTISONE CONCENTRATION-DEPENDENCE OF CYP ENZYME INDUCTION IN HEPARG… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Song, Y. (2012). ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9044

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):

Song, Yang. “ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development.” 2012. Thesis, University of Illinois – Chicago. Accessed April 15, 2021. http://hdl.handle.net/10027/9044.

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

MLA Handbook (7th Edition):

Song, Yang. “ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development.” 2012. Web. 15 Apr 2021.

Vancouver:

Song Y. ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10027/9044.

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

Council of Science Editors:

Song Y. ADMEt Evaluation of Anti-tuberculosis Compounds and New Methodologies Development. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9044

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

.