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You searched for subject:(Hepatocytes). Showing records 1 – 30 of 217 total matches.

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1. Striz, Anneliese. Rab17 regulation of vesicle trafficking in hepatocytes.

Degree: 2017, The Catholic University of America

A major focus of our laboratory is identifying the molecules and mechanisms that regulate polarized protein sorting in hepatocytes, the major epithelial cells of the… (more)

Subjects/Keywords: hepatocytes; rab17

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APA (6th Edition):

Striz, A. (2017). Rab17 regulation of vesicle trafficking in hepatocytes. (Thesis). The Catholic University of America. Retrieved from http://hdl.handle.net/1961/cuislandora:64708

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):

Striz, Anneliese. “Rab17 regulation of vesicle trafficking in hepatocytes.” 2017. Thesis, The Catholic University of America. Accessed January 25, 2021. http://hdl.handle.net/1961/cuislandora:64708.

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

MLA Handbook (7th Edition):

Striz, Anneliese. “Rab17 regulation of vesicle trafficking in hepatocytes.” 2017. Web. 25 Jan 2021.

Vancouver:

Striz A. Rab17 regulation of vesicle trafficking in hepatocytes. [Internet] [Thesis]. The Catholic University of America; 2017. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1961/cuislandora:64708.

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

Council of Science Editors:

Striz A. Rab17 regulation of vesicle trafficking in hepatocytes. [Thesis]. The Catholic University of America; 2017. Available from: http://hdl.handle.net/1961/cuislandora:64708

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


University of Alberta

2. Kharaud, Gagandeep. Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes.

Degree: Masters of Science in Pharmaceutical Sciences, Faculty of Pharmacy and Pharmaceutical Sciences, 2010, University of Alberta

 The purpose of this project was to formulate, modify and evaluate nanoparticles for targeting asialoglycoprotein receptor found in large numbers exclusively on hepatocyte surfaces. Our… (more)

Subjects/Keywords: asialofetuin; hepatocytes; nanoparticles

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APA (6th Edition):

Kharaud, G. (2010). Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/2f75r9133

Chicago Manual of Style (16th Edition):

Kharaud, Gagandeep. “Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes.” 2010. Masters Thesis, University of Alberta. Accessed January 25, 2021. https://era.library.ualberta.ca/files/2f75r9133.

MLA Handbook (7th Edition):

Kharaud, Gagandeep. “Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes.” 2010. Web. 25 Jan 2021.

Vancouver:

Kharaud G. Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2021 Jan 25]. Available from: https://era.library.ualberta.ca/files/2f75r9133.

Council of Science Editors:

Kharaud G. Asialofetuin-coated PLGA Nanoparticles for Targeting Hepatocytes. [Masters Thesis]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/2f75r9133


University of Alberta

3. Roggenbeck, Barbara A. Hepatobiliary Transport of Arsenic.

Degree: PhD, Department of Physiology, 2016, University of Alberta

 Arsenic is a proven human carcinogen and associated with a myriad of other adverse health effects. This metalloid is methylated in human liver to monomethylarsonic… (more)

Subjects/Keywords: hepatocytes; arsenic; transport

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APA (6th Edition):

Roggenbeck, B. A. (2016). Hepatobiliary Transport of Arsenic. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c1j92g751z

Chicago Manual of Style (16th Edition):

Roggenbeck, Barbara A. “Hepatobiliary Transport of Arsenic.” 2016. Doctoral Dissertation, University of Alberta. Accessed January 25, 2021. https://era.library.ualberta.ca/files/c1j92g751z.

MLA Handbook (7th Edition):

Roggenbeck, Barbara A. “Hepatobiliary Transport of Arsenic.” 2016. Web. 25 Jan 2021.

Vancouver:

Roggenbeck BA. Hepatobiliary Transport of Arsenic. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2021 Jan 25]. Available from: https://era.library.ualberta.ca/files/c1j92g751z.

Council of Science Editors:

Roggenbeck BA. Hepatobiliary Transport of Arsenic. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/c1j92g751z

4. Suresh Kumar, N. Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;.

Degree: 2015, University of Kerala

newline

Advisors/Committee Members: Kurup, P.A..

Subjects/Keywords: hepatocytes; lipoproteins

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APA (6th Edition):

Suresh Kumar, N. (2015). Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;. (Thesis). University of Kerala. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54515

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):

Suresh Kumar, N. “Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;.” 2015. Thesis, University of Kerala. Accessed January 25, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54515.

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

MLA Handbook (7th Edition):

Suresh Kumar, N. “Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;.” 2015. Web. 25 Jan 2021.

Vancouver:

Suresh Kumar N. Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;. [Internet] [Thesis]. University of Kerala; 2015. [cited 2021 Jan 25]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54515.

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

Council of Science Editors:

Suresh Kumar N. Metabolism of very low density lipoproteins in primary cultures of rat hepatocytes;. [Thesis]. University of Kerala; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54515

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


Universidade Nova

5. Tostões, Rui Manuel Lucas Gameiro Domingues. Process engineering of liver cells for drug testing applications.

Degree: 2012, Universidade Nova

Dissertação para obtenção do Grau de Doutor em Bioengenharia

The primary culture of human hepatocytes is a requirement in drug development tests. This application is… (more)

Subjects/Keywords: CYP450; Hepatocytes; 3D; Long term

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APA (6th Edition):

Tostões, R. M. L. G. D. (2012). Process engineering of liver cells for drug testing applications. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7612

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):

Tostões, Rui Manuel Lucas Gameiro Domingues. “Process engineering of liver cells for drug testing applications.” 2012. Thesis, Universidade Nova. Accessed January 25, 2021. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7612.

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

MLA Handbook (7th Edition):

Tostões, Rui Manuel Lucas Gameiro Domingues. “Process engineering of liver cells for drug testing applications.” 2012. Web. 25 Jan 2021.

Vancouver:

Tostões RMLGD. Process engineering of liver cells for drug testing applications. [Internet] [Thesis]. Universidade Nova; 2012. [cited 2021 Jan 25]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7612.

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

Council of Science Editors:

Tostões RMLGD. Process engineering of liver cells for drug testing applications. [Thesis]. Universidade Nova; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7612

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


University of Manchester

6. Wood, Francesca Leanne. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.

Degree: 2016, University of Manchester

 As a critical parameter in pharmacokinetics, prediction of clearance is an integral aspect of drug discovery programmes. Since the liver is the major site of… (more)

Subjects/Keywords: hepatocytes; hepatic clearance; drug metabolism

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APA (6th Edition):

Wood, F. L. (2016). Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576

Chicago Manual of Style (16th Edition):

Wood, Francesca Leanne. “Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 25, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576.

MLA Handbook (7th Edition):

Wood, Francesca Leanne. “Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.” 2016. Web. 25 Jan 2021.

Vancouver:

Wood FL. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 25]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576.

Council of Science Editors:

Wood FL. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576


University of Manchester

7. Harrison, James Andrew Roy. Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance.

Degree: 2018, University of Manchester

 Predictive pharmacokinetics now forms a critical part of the drug discovery process. However, metabolic data has been demonstrated to under-predict in vivo clearance, while no… (more)

Subjects/Keywords: Hepatocytes; Pharmacokinetics; In vivo prediction

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APA (6th Edition):

Harrison, J. A. R. (2018). Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313017

Chicago Manual of Style (16th Edition):

Harrison, James Andrew Roy. “Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance.” 2018. Doctoral Dissertation, University of Manchester. Accessed January 25, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313017.

MLA Handbook (7th Edition):

Harrison, James Andrew Roy. “Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance.” 2018. Web. 25 Jan 2021.

Vancouver:

Harrison JAR. Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Jan 25]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313017.

Council of Science Editors:

Harrison JAR. Utility of hepatocellular systems to measure drug transport and metabolism for prediction of in vivo drug clearance. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313017


University of Cambridge

8. Geti, Imbisaat. Production of hepatocytes from human pluripotent stem cells for cell-based therapy.

Degree: PhD, 2019, University of Cambridge

 Human pluripotent stem cells (hPSCs) can self-renew indefinitely in vitro while maintaining the capacity to differentiate into diverse cell types, including hepatocytes. Thus, hPSCs allow… (more)

Subjects/Keywords: Hepatocytes; Cell based therapy; regenerative medicine; liver; liver differentiation; hepatocytes differentiation

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APA (6th Edition):

Geti, I. (2019). Production of hepatocytes from human pluripotent stem cells for cell-based therapy. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291327

Chicago Manual of Style (16th Edition):

Geti, Imbisaat. “Production of hepatocytes from human pluripotent stem cells for cell-based therapy.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 25, 2021. https://www.repository.cam.ac.uk/handle/1810/291327.

MLA Handbook (7th Edition):

Geti, Imbisaat. “Production of hepatocytes from human pluripotent stem cells for cell-based therapy.” 2019. Web. 25 Jan 2021.

Vancouver:

Geti I. Production of hepatocytes from human pluripotent stem cells for cell-based therapy. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 25]. Available from: https://www.repository.cam.ac.uk/handle/1810/291327.

Council of Science Editors:

Geti I. Production of hepatocytes from human pluripotent stem cells for cell-based therapy. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291327


University of Cambridge

9. Geti, Imbisaat. Production of hepatocytes from human pluripotent stem cells for cell-based therapy.

Degree: PhD, 2019, University of Cambridge

 Human pluripotent stem cells (hPSCs) can self-renew indefinitely in vitro while maintaining the capacity to differentiate into diverse cell types, including hepatocytes. Thus, hPSCs allow… (more)

Subjects/Keywords: Hepatocytes; Cell based therapy; regenerative medicine; liver; liver differentiation; hepatocytes differentiation

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APA (6th Edition):

Geti, I. (2019). Production of hepatocytes from human pluripotent stem cells for cell-based therapy. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.38508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774691

Chicago Manual of Style (16th Edition):

Geti, Imbisaat. “Production of hepatocytes from human pluripotent stem cells for cell-based therapy.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 25, 2021. https://doi.org/10.17863/CAM.38508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774691.

MLA Handbook (7th Edition):

Geti, Imbisaat. “Production of hepatocytes from human pluripotent stem cells for cell-based therapy.” 2019. Web. 25 Jan 2021.

Vancouver:

Geti I. Production of hepatocytes from human pluripotent stem cells for cell-based therapy. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 25]. Available from: https://doi.org/10.17863/CAM.38508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774691.

Council of Science Editors:

Geti I. Production of hepatocytes from human pluripotent stem cells for cell-based therapy. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.38508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774691

10. Suresh Kumar N. Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;.

Degree: 2015, University of Kerala

newline

Advisors/Committee Members: Kurup P A, Sudhakaran P R.

Subjects/Keywords: Hepatocytes; Lipoproteins; Metabolism

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APA (6th Edition):

N, S. K. (2015). Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;. (Thesis). University of Kerala. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/45876

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):

N, Suresh Kumar. “Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;.” 2015. Thesis, University of Kerala. Accessed January 25, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/45876.

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

MLA Handbook (7th Edition):

N, Suresh Kumar. “Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;.” 2015. Web. 25 Jan 2021.

Vancouver:

N SK. Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;. [Internet] [Thesis]. University of Kerala; 2015. [cited 2021 Jan 25]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/45876.

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

Council of Science Editors:

N SK. Metabolism of Very Low Density Lipoproteins in Primary Cultures of Rat Hepatocytes;. [Thesis]. University of Kerala; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/45876

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


Cornell University

11. Qian, Lichuan. THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS.

Degree: 2006, Cornell University

 This thesis explored the influence of culture environment on proliferation and hepatic differentiation of fetal liver cells. Specifically, signals provided by soluble factors and culture… (more)

Subjects/Keywords: hepatocytes; tissue engineering

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APA (6th Edition):

Qian, L. (2006). THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/2868

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):

Qian, Lichuan. “THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS.” 2006. Thesis, Cornell University. Accessed January 25, 2021. http://hdl.handle.net/1813/2868.

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

MLA Handbook (7th Edition):

Qian, Lichuan. “THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS.” 2006. Web. 25 Jan 2021.

Vancouver:

Qian L. THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS. [Internet] [Thesis]. Cornell University; 2006. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1813/2868.

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

Council of Science Editors:

Qian L. THREE-DIMENSIONAL CULTURE OF FETAL LIVER CELLS. [Thesis]. Cornell University; 2006. Available from: http://hdl.handle.net/1813/2868

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


University of Guelph

12. Morgan, Larry. The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress.

Degree: MS, Department of Biomedical Sciences, 2014, University of Guelph

 Cytochrome P450 2A5 (CYP2A5) is a murine orthologue of human CYP2A6 and is predominantly found within the endoplasmic reticulum (ER) of the liver. CYP2A5 differs… (more)

Subjects/Keywords: CYP2A5; ER Stress; Hepatocytes; Nrf2; Heme; Bilirubin

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APA (6th Edition):

Morgan, L. (2014). The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7827

Chicago Manual of Style (16th Edition):

Morgan, Larry. “The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress.” 2014. Masters Thesis, University of Guelph. Accessed January 25, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7827.

MLA Handbook (7th Edition):

Morgan, Larry. “The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress.” 2014. Web. 25 Jan 2021.

Vancouver:

Morgan L. The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress. [Internet] [Masters thesis]. University of Guelph; 2014. [cited 2021 Jan 25]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7827.

Council of Science Editors:

Morgan L. The Role of Cytochrome P450 2A5 During Endoplasmic Reticulum Stress. [Masters Thesis]. University of Guelph; 2014. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7827


Vytautas Magnus University

13. Matulevičiūtė, Kristina. Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties.

Degree: Master, Biochemistry, 2008, Vytautas Magnus University

Šiais laikais vėžys yra viena iš dažniausiai diagnozuojamų vyrų ir moterų ligų. Todėl labai svarbu sukurti naujus vėžio gydymo būdus, didinančius žmonių išgyvenamumą, palengvinančius gijimo… (more)

Subjects/Keywords: Hipertermija; Hepatocitai; Mitochondrija; Hyperthermia; Hepatocytes; Mitochondria

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APA (6th Edition):

Matulevičiūtė, Kristina. (2008). Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties. (Masters Thesis). Vytautas Magnus University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20080628_092239-70148 ;

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

Chicago Manual of Style (16th Edition):

Matulevičiūtė, Kristina. “Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties.” 2008. Masters Thesis, Vytautas Magnus University. Accessed January 25, 2021. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20080628_092239-70148 ;.

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

MLA Handbook (7th Edition):

Matulevičiūtė, Kristina. “Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties.” 2008. Web. 25 Jan 2021.

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

Vancouver:

Matulevičiūtė, Kristina. Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties. [Internet] [Masters thesis]. Vytautas Magnus University; 2008. [cited 2021 Jan 25]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20080628_092239-70148 ;.

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

Council of Science Editors:

Matulevičiūtė, Kristina. Kepenų ląstelių ir mitochondrijų atsakas į hipertermijos poveikį. Priklausomybė nuo eksperimentinio gyvūno lyties. [Masters Thesis]. Vytautas Magnus University; 2008. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20080628_092239-70148 ;

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


Queen Mary, University of London

14. Shephard, Matthew T. Targeted differentiation of pluripotent stem cells to hepatocytes.

Degree: PhD, 2018, Queen Mary, University of London

 Pluripotent stem cells (PSCs) possess the ability to differentiate to virtually any cell type whilst retaining the capacity to self-renew. There is an unmet need… (more)

Subjects/Keywords: Pluripotent Stem Cells; hepatocytes; cell differentiation

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APA (6th Edition):

Shephard, M. T. (2018). Targeted differentiation of pluripotent stem cells to hepatocytes. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338

Chicago Manual of Style (16th Edition):

Shephard, Matthew T. “Targeted differentiation of pluripotent stem cells to hepatocytes.” 2018. Doctoral Dissertation, Queen Mary, University of London. Accessed January 25, 2021. http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338.

MLA Handbook (7th Edition):

Shephard, Matthew T. “Targeted differentiation of pluripotent stem cells to hepatocytes.” 2018. Web. 25 Jan 2021.

Vancouver:

Shephard MT. Targeted differentiation of pluripotent stem cells to hepatocytes. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2018. [cited 2021 Jan 25]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338.

Council of Science Editors:

Shephard MT. Targeted differentiation of pluripotent stem cells to hepatocytes. [Doctoral Dissertation]. Queen Mary, University of London; 2018. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338


University of Surrey

15. Jones, Richard A. Dissection of the Fas mediated apoptosis pathway.

Degree: PhD, 2000, University of Surrey

 The mechanism of Fas antigen-induced hepatocyte apoptosis was investigated. Using a monoclonal antibody directed against the Fas antigen, apoptosis was induced in freshly isolated murine… (more)

Subjects/Keywords: 572; Hepatocytes; Antibodies

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APA (6th Edition):

Jones, R. A. (2000). Dissection of the Fas mediated apoptosis pathway. (Doctoral Dissertation). University of Surrey. Retrieved from http://epubs.surrey.ac.uk/855648/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340415

Chicago Manual of Style (16th Edition):

Jones, Richard A. “Dissection of the Fas mediated apoptosis pathway.” 2000. Doctoral Dissertation, University of Surrey. Accessed January 25, 2021. http://epubs.surrey.ac.uk/855648/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340415.

MLA Handbook (7th Edition):

Jones, Richard A. “Dissection of the Fas mediated apoptosis pathway.” 2000. Web. 25 Jan 2021.

Vancouver:

Jones RA. Dissection of the Fas mediated apoptosis pathway. [Internet] [Doctoral dissertation]. University of Surrey; 2000. [cited 2021 Jan 25]. Available from: http://epubs.surrey.ac.uk/855648/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340415.

Council of Science Editors:

Jones RA. Dissection of the Fas mediated apoptosis pathway. [Doctoral Dissertation]. University of Surrey; 2000. Available from: http://epubs.surrey.ac.uk/855648/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340415


University of Manchester

16. Wood, Francesca. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.

Degree: PhD, 2016, University of Manchester

 As a critical parameter in pharmacokinetics, prediction of clearance is an integral aspect of drug discovery programmes. Since the liver is the major site of… (more)

Subjects/Keywords: 610; drug metabolism; hepatocytes; hepatic clearance

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APA (6th Edition):

Wood, F. (2016). Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443

Chicago Manual of Style (16th Edition):

Wood, Francesca. “Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 25, 2021. https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443.

MLA Handbook (7th Edition):

Wood, Francesca. “Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.” 2016. Web. 25 Jan 2021.

Vancouver:

Wood F. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 25]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443.

Council of Science Editors:

Wood F. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443


University of Bath

17. Sangan, Caroline Beth. Reprogramming of hepatic and pancreatic cells.

Degree: PhD, 2012, University of Bath

 Cell therapy involving treatment of diseases with the body’s own cells would benefit both liver diseases and Type 1 diabetes. Liver diseases are associated with… (more)

Subjects/Keywords: 616.362; transdifferentiation; liver; oval cells; hepatocytes; pancreas

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APA (6th Edition):

Sangan, C. B. (2012). Reprogramming of hepatic and pancreatic cells. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/reprogramming-of-hepatic-and-pancreatic-cells(bf928893-1169-48e9-8498-3325a46bead8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582549

Chicago Manual of Style (16th Edition):

Sangan, Caroline Beth. “Reprogramming of hepatic and pancreatic cells.” 2012. Doctoral Dissertation, University of Bath. Accessed January 25, 2021. https://researchportal.bath.ac.uk/en/studentthesis/reprogramming-of-hepatic-and-pancreatic-cells(bf928893-1169-48e9-8498-3325a46bead8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582549.

MLA Handbook (7th Edition):

Sangan, Caroline Beth. “Reprogramming of hepatic and pancreatic cells.” 2012. Web. 25 Jan 2021.

Vancouver:

Sangan CB. Reprogramming of hepatic and pancreatic cells. [Internet] [Doctoral dissertation]. University of Bath; 2012. [cited 2021 Jan 25]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/reprogramming-of-hepatic-and-pancreatic-cells(bf928893-1169-48e9-8498-3325a46bead8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582549.

Council of Science Editors:

Sangan CB. Reprogramming of hepatic and pancreatic cells. [Doctoral Dissertation]. University of Bath; 2012. Available from: https://researchportal.bath.ac.uk/en/studentthesis/reprogramming-of-hepatic-and-pancreatic-cells(bf928893-1169-48e9-8498-3325a46bead8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582549


University of Minnesota

18. Chau, David. A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes.

Degree: PhD, Biomedical Engineering, 2017, University of Minnesota

 The recent advancements in stem cell biology have allowed for new and exciting opportunities to use stem cells in clinical and industrial applications. Stem cells… (more)

Subjects/Keywords: Differentiation; Hepatocytes; Metabolism; Stem Cells; Transcriptomics

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APA (6th Edition):

Chau, D. (2017). A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/209039

Chicago Manual of Style (16th Edition):

Chau, David. “A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes.” 2017. Doctoral Dissertation, University of Minnesota. Accessed January 25, 2021. http://hdl.handle.net/11299/209039.

MLA Handbook (7th Edition):

Chau, David. “A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes.” 2017. Web. 25 Jan 2021.

Vancouver:

Chau D. A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/11299/209039.

Council of Science Editors:

Chau D. A Systems Approach to Studying the Differentiation of Stem Cells Towards Hepatocytes. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/209039

19. Harper, Tod 1982-. Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2.

Degree: Doctoral, Molecular Toxicology, 2013, The University of Texas Medical Branch at Galveston

 Proper hepatocyte function is vital for survival; hence unrepaired destruction of the parenchymal tissue leading to liver decompensation is devastating. Therefore, understanding the homeostatic process… (more)

Subjects/Keywords: AhR; Stc2; Hepatocytes; Apoptosis; ER Stress

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APA (6th Edition):

Harper, T. 1. (2013). Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2. (Doctoral Dissertation). The University of Texas Medical Branch at Galveston. Retrieved from http://hdl.handle.net/2152.3/542

Chicago Manual of Style (16th Edition):

Harper, Tod 1982-. “Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2.” 2013. Doctoral Dissertation, The University of Texas Medical Branch at Galveston. Accessed January 25, 2021. http://hdl.handle.net/2152.3/542.

MLA Handbook (7th Edition):

Harper, Tod 1982-. “Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2.” 2013. Web. 25 Jan 2021.

Vancouver:

Harper T1. Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2. [Internet] [Doctoral dissertation]. The University of Texas Medical Branch at Galveston; 2013. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/2152.3/542.

Council of Science Editors:

Harper T1. Novel Insights Into Normal Aryl Hydrocarbon Receptor Biology Through the Regulation of Stanniocalcin 2. [Doctoral Dissertation]. The University of Texas Medical Branch at Galveston; 2013. Available from: http://hdl.handle.net/2152.3/542

20. Borel Rinkes, Inne. Hepatocytes in the development of liver support systems.

Degree: 1993, Erasmus University Medical Center

 This thesis focuses on the development of alternative strategies in the treatment of patients with acute fulminant hepatic failure and inborn errors of metabolism, using… (more)

Subjects/Keywords: hepatocytes; liver support

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APA (6th Edition):

Borel Rinkes, I. (1993). Hepatocytes in the development of liver support systems. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/39513

Chicago Manual of Style (16th Edition):

Borel Rinkes, Inne. “Hepatocytes in the development of liver support systems.” 1993. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 25, 2021. http://hdl.handle.net/1765/39513.

MLA Handbook (7th Edition):

Borel Rinkes, Inne. “Hepatocytes in the development of liver support systems.” 1993. Web. 25 Jan 2021.

Vancouver:

Borel Rinkes I. Hepatocytes in the development of liver support systems. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1993. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1765/39513.

Council of Science Editors:

Borel Rinkes I. Hepatocytes in the development of liver support systems. [Doctoral Dissertation]. Erasmus University Medical Center; 1993. Available from: http://hdl.handle.net/1765/39513


University of Alberta

21. Alsagheir, Ali I. Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production.

Degree: MS, Department of Surgery, 2014, University of Alberta

 Abstract Introduction: Chronic hepatitis C virus (HCV) infection is a global problem. The World Health Organization estimates that about 170 million individuals around the world… (more)

Subjects/Keywords: Human embryonic stem cells; Differentiated hepatocytes; Hepatitis C virus; Stem cells; Hepatocytes-like cells

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APA (6th Edition):

Alsagheir, A. I. (2014). Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c2j62s516f

Chicago Manual of Style (16th Edition):

Alsagheir, Ali I. “Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production.” 2014. Masters Thesis, University of Alberta. Accessed January 25, 2021. https://era.library.ualberta.ca/files/c2j62s516f.

MLA Handbook (7th Edition):

Alsagheir, Ali I. “Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production.” 2014. Web. 25 Jan 2021.

Vancouver:

Alsagheir AI. Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2021 Jan 25]. Available from: https://era.library.ualberta.ca/files/c2j62s516f.

Council of Science Editors:

Alsagheir AI. Differentiation of human embryonic stem cells into hepatocytes and their in vivo application for hepatitis C viral production. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/c2j62s516f


Universiteit Utrecht

22. 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

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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 January 25, 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. 25 Jan 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 Jan 25]. 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

23. Agnetti, Jean. Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Université Paris-Saclay (ComUE)

La phosphoinositide 3-kinase p110δ (PI3Kδ) est principalement exprimée dans les cellules hématopoïétiques et son inhibiteur, l'idélalisib est approuvé pour le traitement de la leucémie et… (more)

Subjects/Keywords: PI3Kδ; Polarité; Hepatocytes; Cellules souches; Matrice extracellulaire; Hepatoblastome; PI3Kδ; Polarity; Hepatocytes; Stem cells; Extracellular matrix; Hepatoblastoma

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APA (6th Edition):

Agnetti, J. (2019). Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS363

Chicago Manual of Style (16th Edition):

Agnetti, Jean. “Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 25, 2021. http://www.theses.fr/2019SACLS363.

MLA Handbook (7th Edition):

Agnetti, Jean. “Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ.” 2019. Web. 25 Jan 2021.

Vancouver:

Agnetti J. Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2019SACLS363.

Council of Science Editors:

Agnetti J. Etude de la polarité cellulaire et du microenvironnement dans la morphogenèse et les cancers du foie : rôle de la PI3Kδ : Study of Cell Polarity and Extracellular Matrix in Liver Morphogenesis and Cancer Development : Role of PI3Kδ. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS363


University of Florida

24. Biel, Thomas G. Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury.

Degree: PhD, Medical Sciences - Physiology and Pharmacology (IDP), 2014, University of Florida

 Hepatic ischemia/reperfusion (I/R) injury causes organ damage that can lead to liver failure and mortality after resection and transplantation surgeries. Currently, there are no therapeutic… (more)

Subjects/Keywords: Acetylation; Cell death; Cytoprotection; Death; Hepatocytes; Ischemia; Liver; Mitochondria; Physical trauma; Reperfusion; autophagy  – hepatocytes  – ischemia  – liver  – mitofusin2  – reperfusion  – resection  – sirtuin1

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APA (6th Edition):

Biel, T. G. (2014). Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0047316

Chicago Manual of Style (16th Edition):

Biel, Thomas G. “Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury.” 2014. Doctoral Dissertation, University of Florida. Accessed January 25, 2021. https://ufdc.ufl.edu/UFE0047316.

MLA Handbook (7th Edition):

Biel, Thomas G. “Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury.” 2014. Web. 25 Jan 2021.

Vancouver:

Biel TG. Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury. [Internet] [Doctoral dissertation]. University of Florida; 2014. [cited 2021 Jan 25]. Available from: https://ufdc.ufl.edu/UFE0047316.

Council of Science Editors:

Biel TG. Mitofusin 2 Mediates Sirtuin 1 Induced Autophagy to Suppress Liver Ischemia/Reperfusion Injury. [Doctoral Dissertation]. University of Florida; 2014. Available from: https://ufdc.ufl.edu/UFE0047316


NSYSU

25. Kao, Ying-hsien. Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis.

Degree: PhD, Biological Sciences, 2009, NSYSU

 Liver fibrosis, a major medical problem with significant morbidity and mortality, is considered as a wound-healing response to a variety of chronic stimuli. It is… (more)

Subjects/Keywords: hepatoma-derived growth factor; liver fibrosis; hepatocytes; transforming growth factor-beta

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APA (6th Edition):

Kao, Y. (2009). Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0825109-033053

Chicago Manual of Style (16th Edition):

Kao, Ying-hsien. “Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis.” 2009. Doctoral Dissertation, NSYSU. Accessed January 25, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0825109-033053.

MLA Handbook (7th Edition):

Kao, Ying-hsien. “Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis.” 2009. Web. 25 Jan 2021.

Vancouver:

Kao Y. Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis. [Internet] [Doctoral dissertation]. NSYSU; 2009. [cited 2021 Jan 25]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0825109-033053.

Council of Science Editors:

Kao Y. Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis. [Doctoral Dissertation]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0825109-033053

26. Baimakhanov, Zhassulan. Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果.

Degree: 博士(医学), 2016, Nagasaki University / 長崎大学

 Although cell sheet technology has recently been developed for use in both animal experiments and in the clinical setting, it remains unclear whether transplanted hepatocyte… (more)

Subjects/Keywords: Hepatocytes; Cell sheet; Transplantation; Rat diseased model; Metabolic support

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APA (6th Edition):

Baimakhanov, Z. (2016). Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/36836

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):

Baimakhanov, Zhassulan. “Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果.” 2016. Thesis, Nagasaki University / 長崎大学. Accessed January 25, 2021. http://hdl.handle.net/10069/36836.

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

MLA Handbook (7th Edition):

Baimakhanov, Zhassulan. “Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果.” 2016. Web. 25 Jan 2021.

Vancouver:

Baimakhanov Z. Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2016. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10069/36836.

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

Council of Science Editors:

Baimakhanov Z. Efficacy of Multilayered Hepatocyte Sheet Transplantation for Radiation-Induced Liver Damage and Partial Hepatectomy in a Rat Model : 放射線性肝障害と肝切除を組み合わせたラットモデルに対する多層化肝細胞シートの移植効果. [Thesis]. Nagasaki University / 長崎大学; 2016. Available from: http://hdl.handle.net/10069/36836

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


Dalhousie University

27. Savage, Kimberley. THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES.

Degree: MS, Department of Pathology, 2011, Dalhousie University

 Transplantation is the optimal form of therapy for patients with end-stage liver disease; however, the use of organs with hepatic steatosis is often associated with… (more)

Subjects/Keywords: In vitro ischemia reperfusion; Gene therapy; Hepatocytes; MMP-9; HO-1

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APA (6th Edition):

Savage, K. (2011). THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14249

Chicago Manual of Style (16th Edition):

Savage, Kimberley. “THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES.” 2011. Masters Thesis, Dalhousie University. Accessed January 25, 2021. http://hdl.handle.net/10222/14249.

MLA Handbook (7th Edition):

Savage, Kimberley. “THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES.” 2011. Web. 25 Jan 2021.

Vancouver:

Savage K. THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10222/14249.

Council of Science Editors:

Savage K. THE DEVELOPMENT OF AN IN VITRO MODEL TO EXAMINE AND MODULATE HEPATIC ISCHEMIA AND REPERFUSION RESPONSES. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14249

28. Kyriakou, Loukas. Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς.

Degree: 2015, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Cadmium is a known industrial and environmental pollutant. It causes hepatotoxicity uponacute administration.Features of cadmium-induced acute hepatoxicity encompass necrosis,apoptosis, peliosis and inflammatory infiltration.Gadolinium chloride (GdCl3)… (more)

Subjects/Keywords: Ηπατοτοξικότητα; Κάδμιο; Γαδολίνιο; Νέκρωση; Ηπατοκύτταρα; Hepatotoxicity; Cadmium; Gadolinium; Necrosis; Hepatocytes

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

APA (6th Edition):

Kyriakou, L. (2015). Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42861

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):

Kyriakou, Loukas. “Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς.” 2015. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed January 25, 2021. http://hdl.handle.net/10442/hedi/42861.

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

MLA Handbook (7th Edition):

Kyriakou, Loukas. “Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς.” 2015. Web. 25 Jan 2021.

Vancouver:

Kyriakou L. Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10442/hedi/42861.

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

Council of Science Editors:

Kyriakou L. Μελέτη του μηχανισμού ηπατοτοξικής δράσης του καδμίου σε επίμυς. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. Available from: http://hdl.handle.net/10442/hedi/42861

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


University of Saskatchewan

29. Jamwal, Ankur 1986-. Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss).

Degree: 2018, University of Saskatchewan

 The existing scientific literature suggests that selenium can modify arsenite or cadmium toxicity in fish; however, our current understanding of the biochemical pathways involved in… (more)

Subjects/Keywords: Arsenite; Cadmium; Selenite; Selenomethionine; Hepatocytes; Interaction; Oxidative stress; Redox homeostasis

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

APA (6th Edition):

Jamwal, A. 1. (2018). Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss). (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/8331

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):

Jamwal, Ankur 1986-. “Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss).” 2018. Thesis, University of Saskatchewan. Accessed January 25, 2021. http://hdl.handle.net/10388/8331.

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

MLA Handbook (7th Edition):

Jamwal, Ankur 1986-. “Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss).” 2018. Web. 25 Jan 2021.

Vancouver:

Jamwal A1. Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss). [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10388/8331.

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

Council of Science Editors:

Jamwal A1. Interactive effects of selenium on arsenic and cadmium induced toxicity in rainbow trout (Oncorhynchus mykiss). [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/8331

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


Penn State University

30. Goyak, Katy M. O. Expression profiling of interindividual and interspecies variability in hepatic models. .

Degree: 2009, Penn State University

 Although in vivo rodent models are a necessary part of the risk assessment process, incorporation of human models is necessary in order to evaluate whether… (more)

Subjects/Keywords: DNA microarrays; human hepatocytes

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

APA (6th Edition):

Goyak, K. M. O. (2009). Expression profiling of interindividual and interspecies variability in hepatic models. . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9046

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):

Goyak, Katy M O. “Expression profiling of interindividual and interspecies variability in hepatic models. .” 2009. Thesis, Penn State University. Accessed January 25, 2021. https://submit-etda.libraries.psu.edu/catalog/9046.

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

MLA Handbook (7th Edition):

Goyak, Katy M O. “Expression profiling of interindividual and interspecies variability in hepatic models. .” 2009. Web. 25 Jan 2021.

Vancouver:

Goyak KMO. Expression profiling of interindividual and interspecies variability in hepatic models. . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Jan 25]. Available from: https://submit-etda.libraries.psu.edu/catalog/9046.

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

Council of Science Editors:

Goyak KMO. Expression profiling of interindividual and interspecies variability in hepatic models. . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9046

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

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