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You searched for subject:(Liver cells ). Showing records 1 – 30 of 297 total matches.

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California State University – Sacramento

1. Lessa, Nataly Carneiro. Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes.

Degree: MA, Biological Sciences (Stem Cell, 2011, California State University – Sacramento

Liver disease is one of the leading causes of death worldwide, and over 25,000 people per year die in the U.S. Often the only option… (more)

Subjects/Keywords: hESC; Liver cells; Liver disease

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APA (6th Edition):

Lessa, N. C. (2011). Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/1268

Chicago Manual of Style (16th Edition):

Lessa, Nataly Carneiro. “Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes.” 2011. Masters Thesis, California State University – Sacramento. Accessed June 16, 2019. http://hdl.handle.net/10211.9/1268.

MLA Handbook (7th Edition):

Lessa, Nataly Carneiro. “Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes.” 2011. Web. 16 Jun 2019.

Vancouver:

Lessa NC. Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes. [Internet] [Masters thesis]. California State University – Sacramento; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10211.9/1268.

Council of Science Editors:

Lessa NC. Role of decellularized liver matrix on human embryonic stem cell differentiation into functional hepatocytes. [Masters Thesis]. California State University – Sacramento; 2011. Available from: http://hdl.handle.net/10211.9/1268


University of Western Australia

2. Tirnitz-Parker, Janina Elke Eleonore. Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells.

Degree: PhD, 2007, University of Western Australia

 [Truncated abstract] Oval cells are adult liver progenitor cells that regenerate the liver when hepatocyte replication is inhibited following chronic or carcinogenic injury. They have… (more)

Subjects/Keywords: Liver cells; Cytokines; Liver; Liver; Liver diseases; Stem cells; Cell transplantation; Liver; Liver regeneration; Cytokines; Liver stem cells; TWEAK/Fn14 signalling

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APA (6th Edition):

Tirnitz-Parker, J. E. E. (2007). Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=9527&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Tirnitz-Parker, Janina Elke Eleonore. “Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells.” 2007. Doctoral Dissertation, University of Western Australia. Accessed June 16, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=9527&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Tirnitz-Parker, Janina Elke Eleonore. “Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells.” 2007. Web. 16 Jun 2019.

Vancouver:

Tirnitz-Parker JEE. Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells. [Internet] [Doctoral dissertation]. University of Western Australia; 2007. [cited 2019 Jun 16]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=9527&local_base=GEN01-INS01.

Council of Science Editors:

Tirnitz-Parker JEE. Primary culture and immortal cell lines as in vitro models to evaluate the role of TWEAK signalling in hepatic oval cells. [Doctoral Dissertation]. University of Western Australia; 2007. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=9527&local_base=GEN01-INS01


University of Western Australia

3. Viebahn, Cornelia Sabine. Interaction between the immune system and liver progenitor cells.

Degree: PhD, 2009, University of Western Australia

Liver progenitor cells (LPCs) play a major role in the regeneration process following chronic liver damage. LPCs can differentiate into hepatocytes and cholangiocytes and thus… (more)

Subjects/Keywords: Chemokines; Cytokines; Inflammation; Liver; Liver; Liver cells; Stem cells; Liver progenitor cells/liver stem cells; Inflammation; Liver regeneration; Cytokines and chemokines

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APA (6th Edition):

Viebahn, C. S. (2009). Interaction between the immune system and liver progenitor cells. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12806&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Viebahn, Cornelia Sabine. “Interaction between the immune system and liver progenitor cells.” 2009. Doctoral Dissertation, University of Western Australia. Accessed June 16, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12806&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Viebahn, Cornelia Sabine. “Interaction between the immune system and liver progenitor cells.” 2009. Web. 16 Jun 2019.

Vancouver:

Viebahn CS. Interaction between the immune system and liver progenitor cells. [Internet] [Doctoral dissertation]. University of Western Australia; 2009. [cited 2019 Jun 16]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12806&local_base=GEN01-INS01.

Council of Science Editors:

Viebahn CS. Interaction between the immune system and liver progenitor cells. [Doctoral Dissertation]. University of Western Australia; 2009. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12806&local_base=GEN01-INS01


University of Edinburgh

4. Kung, Janet Wui Cheung. Investigating the liver progenitor cell niche in the developing human liver.

Degree: PhD, 2016, University of Edinburgh

Liver cirrhosis places an increasing burden on healthcare worldwide. Currently the only treatment is liver transplantation. Whilst liver transplant has a relatively good five-year survival,… (more)

Subjects/Keywords: foetal liver; liver progenitor cells; LPCs; microarray

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APA (6th Edition):

Kung, J. W. C. (2016). Investigating the liver progenitor cell niche in the developing human liver. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25953

Chicago Manual of Style (16th Edition):

Kung, Janet Wui Cheung. “Investigating the liver progenitor cell niche in the developing human liver.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed June 16, 2019. http://hdl.handle.net/1842/25953.

MLA Handbook (7th Edition):

Kung, Janet Wui Cheung. “Investigating the liver progenitor cell niche in the developing human liver.” 2016. Web. 16 Jun 2019.

Vancouver:

Kung JWC. Investigating the liver progenitor cell niche in the developing human liver. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1842/25953.

Council of Science Editors:

Kung JWC. Investigating the liver progenitor cell niche in the developing human liver. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25953


University of Missouri – Columbia

5. Linden, Melissa A. Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis.

Degree: 2015, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Nonalcoholic steatohepatitis (NASH) is a liver disease that is associated with obesity and is characterized… (more)

Subjects/Keywords: Liver cells; Liver  – Fibrosis; Obesity  – Health aspects

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APA (6th Edition):

Linden, M. A. (2015). Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/47149

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):

Linden, Melissa A. “Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis.” 2015. Thesis, University of Missouri – Columbia. Accessed June 16, 2019. http://hdl.handle.net/10355/47149.

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

MLA Handbook (7th Edition):

Linden, Melissa A. “Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis.” 2015. Web. 16 Jun 2019.

Vancouver:

Linden MA. Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10355/47149.

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

Council of Science Editors:

Linden MA. Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis. [Thesis]. University of Missouri – Columbia; 2015. Available from: http://hdl.handle.net/10355/47149

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


University of Western Australia

6. Lim, Rebecca. Roles of interferon α and γ in the hepatic progenitor (oval) cell response.

Degree: PhD, 2007, University of Western Australia

[Truncated abstract] Hepatic progenitor cells (HPC) are becoming increasingly recognized as facultative stem cells capable of regenerating the liver during chronic liver injury and also… (more)

Subjects/Keywords: Liver; Stem cells; Liver cells; Interferon; Hepatic progenitor cells

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APA (6th Edition):

Lim, R. (2007). Roles of interferon α and γ in the hepatic progenitor (oval) cell response. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34868&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Lim, Rebecca. “Roles of interferon α and γ in the hepatic progenitor (oval) cell response.” 2007. Doctoral Dissertation, University of Western Australia. Accessed June 16, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34868&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Lim, Rebecca. “Roles of interferon α and γ in the hepatic progenitor (oval) cell response.” 2007. Web. 16 Jun 2019.

Vancouver:

Lim R. Roles of interferon α and γ in the hepatic progenitor (oval) cell response. [Internet] [Doctoral dissertation]. University of Western Australia; 2007. [cited 2019 Jun 16]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34868&local_base=GEN01-INS01.

Council of Science Editors:

Lim R. Roles of interferon α and γ in the hepatic progenitor (oval) cell response. [Doctoral Dissertation]. University of Western Australia; 2007. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34868&local_base=GEN01-INS01


University of Edinburgh

7. Hsieh, Wei-Chen. Role of galectin-3 in liver progenitor cell proliferation and differentiation.

Degree: PhD, 2011, University of Edinburgh

Liver progenitor cells (LPCs) respond to hepatic injury when hepatocyte division is impaired in chronic or severe injury. The LPCs are intimately surrounded by myofibroblasts,… (more)

Subjects/Keywords: Liver progenitor cells; Galectin-3

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APA (6th Edition):

Hsieh, W. (2011). Role of galectin-3 in liver progenitor cell proliferation and differentiation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8754

Chicago Manual of Style (16th Edition):

Hsieh, Wei-Chen. “Role of galectin-3 in liver progenitor cell proliferation and differentiation.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed June 16, 2019. http://hdl.handle.net/1842/8754.

MLA Handbook (7th Edition):

Hsieh, Wei-Chen. “Role of galectin-3 in liver progenitor cell proliferation and differentiation.” 2011. Web. 16 Jun 2019.

Vancouver:

Hsieh W. Role of galectin-3 in liver progenitor cell proliferation and differentiation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1842/8754.

Council of Science Editors:

Hsieh W. Role of galectin-3 in liver progenitor cell proliferation and differentiation. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/8754


NSYSU

8. Liu, Ren-Chao. A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells.

Degree: Master, Biological Sciences, 2009, NSYSU

 Rogdi was a novel gene with unknown function. According to GeneBank database, the gene is located on chromsome 10q12 and the length of coding regeion… (more)

Subjects/Keywords: hepatic stellate cells; fibrotic liver

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APA (6th Edition):

Liu, R. (2009). A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909109-115746

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):

Liu, Ren-Chao. “A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells.” 2009. Thesis, NSYSU. Accessed June 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909109-115746.

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

MLA Handbook (7th Edition):

Liu, Ren-Chao. “A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells.” 2009. Web. 16 Jun 2019.

Vancouver:

Liu R. A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells. [Internet] [Thesis]. NSYSU; 2009. [cited 2019 Jun 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909109-115746.

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

Council of Science Editors:

Liu R. A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909109-115746

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


Oregon State University

9. Perdew, Gary H. Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s].

Degree: PhD, Food Science and Technology, 1984, Oregon State University

 Cyclopropenoid fatty acids (CPFA) are unique compounds that contain a highly strained and reactive cyclopropene ring structure. These compounds have been shown to cause a… (more)

Subjects/Keywords: Liver cells

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APA (6th Edition):

Perdew, G. H. (1984). Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s]. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/27241

Chicago Manual of Style (16th Edition):

Perdew, Gary H. “Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s].” 1984. Doctoral Dissertation, Oregon State University. Accessed June 16, 2019. http://hdl.handle.net/1957/27241.

MLA Handbook (7th Edition):

Perdew, Gary H. “Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s].” 1984. Web. 16 Jun 2019.

Vancouver:

Perdew GH. Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s]. [Internet] [Doctoral dissertation]. Oregon State University; 1984. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1957/27241.

Council of Science Editors:

Perdew GH. Alteration in levels and synthesis of proteins in trout hepatocytes due to dietary cyclopropenoid fatty acid[s]. [Doctoral Dissertation]. Oregon State University; 1984. Available from: http://hdl.handle.net/1957/27241


University of Hong Kong

10. Sung, Ying-ju, Cecilia. Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma.

Degree: PhD, 2014, University of Hong Kong

 Hepatocellular carcinoma (HCC) is the sixth most common cancer and the second leading cause of cancer-related deaths in the world. It is a disease with… (more)

Subjects/Keywords: Liver - Cancer - Treatment; T cells

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APA (6th Edition):

Sung, Ying-ju, C. (2014). Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. (Doctoral Dissertation). University of Hong Kong. Retrieved from Sung, Y. C. [宋穎如]. (2014). Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387993 ; http://dx.doi.org/10.5353/th_b5387993 ; http://hdl.handle.net/10722/208577

Chicago Manual of Style (16th Edition):

Sung, Ying-ju, Cecilia. “Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed June 16, 2019. Sung, Y. C. [宋穎如]. (2014). Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387993 ; http://dx.doi.org/10.5353/th_b5387993 ; http://hdl.handle.net/10722/208577.

MLA Handbook (7th Edition):

Sung, Ying-ju, Cecilia. “Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma.” 2014. Web. 16 Jun 2019.

Vancouver:

Sung, Ying-ju C. Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Jun 16]. Available from: Sung, Y. C. [宋穎如]. (2014). Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387993 ; http://dx.doi.org/10.5353/th_b5387993 ; http://hdl.handle.net/10722/208577.

Council of Science Editors:

Sung, Ying-ju C. Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Sung, Y. C. [宋穎如]. (2014). Reuglation of T helper 17 by bacteria : an approach for the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387993 ; http://dx.doi.org/10.5353/th_b5387993 ; http://hdl.handle.net/10722/208577


Drexel University

11. Cirillo, Joseph N. Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model.

Degree: 2011, Drexel University

An authentic human liver model has the potential to be a revolutionary development in the field of biotechnology, and the progress of microtechnology has made… (more)

Subjects/Keywords: Mechanical engineering; Liver cells; Biotechnology

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APA (6th Edition):

Cirillo, J. N. (2011). Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/3877

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):

Cirillo, Joseph N. “Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model.” 2011. Thesis, Drexel University. Accessed June 16, 2019. http://hdl.handle.net/1860/3877.

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

MLA Handbook (7th Edition):

Cirillo, Joseph N. “Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model.” 2011. Web. 16 Jun 2019.

Vancouver:

Cirillo JN. Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model. [Internet] [Thesis]. Drexel University; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1860/3877.

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

Council of Science Editors:

Cirillo JN. Fundamental studies of liver cell culture microtechnology and techniques for the purpose of designing a liver model. [Thesis]. Drexel University; 2011. Available from: http://hdl.handle.net/1860/3877

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


University of Edinburgh

12. Lu, Wei-Yu. Defining the liver repopulating capacities of hepatic progenitor cells.

Degree: PhD, 2014, University of Edinburgh

 The liver has the ability to regenerate rapidly during acute liver injury by activating mature hepatocytes to divide and restore the damaged liver mass. In… (more)

Subjects/Keywords: 616.3; liver regeneration; stem cells

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APA (6th Edition):

Lu, W. (2014). Defining the liver repopulating capacities of hepatic progenitor cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17875

Chicago Manual of Style (16th Edition):

Lu, Wei-Yu. “Defining the liver repopulating capacities of hepatic progenitor cells.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed June 16, 2019. http://hdl.handle.net/1842/17875.

MLA Handbook (7th Edition):

Lu, Wei-Yu. “Defining the liver repopulating capacities of hepatic progenitor cells.” 2014. Web. 16 Jun 2019.

Vancouver:

Lu W. Defining the liver repopulating capacities of hepatic progenitor cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1842/17875.

Council of Science Editors:

Lu W. Defining the liver repopulating capacities of hepatic progenitor cells. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/17875


Rutgers University

13. Yang, Hong, 1976-. Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:.

Degree: PhD, Chemical and Biochemical Engineering, 2010, Rutgers University

Extracorporeal bioartificial liver (BAL) devices, involving primary hepatocytes, represent a promising option to provide temporary support for patients with liver failure. Current use of BAL… (more)

Subjects/Keywords: Amino acids; Liver cells

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APA (6th Edition):

Yang, Hong, 1. (2010). Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052170

Chicago Manual of Style (16th Edition):

Yang, Hong, 1976-. “Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:.” 2010. Doctoral Dissertation, Rutgers University. Accessed June 16, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052170.

MLA Handbook (7th Edition):

Yang, Hong, 1976-. “Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:.” 2010. Web. 16 Jun 2019.

Vancouver:

Yang, Hong 1. Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Jun 16]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052170.

Council of Science Editors:

Yang, Hong 1. Design and analysis of amino acid supplementation in hepatocyte culture using in vitro experiment and mathematical modeling:. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052170


University of Hong Kong

14. Kwan, Hoi-tung. Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma.

Degree: PhD, 2014, University of Hong Kong

 Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. While HCC patients at early stages are eligible for liver resection and liver transplantation,… (more)

Subjects/Keywords: Cancer cells; Liver - Cancer - Treatment; Stem cells

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APA (6th Edition):

Kwan, H. (2014). Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. (Doctoral Dissertation). University of Hong Kong. Retrieved from Kwan, H. [關愷彤]. (2014). Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719483 ; http://hdl.handle.net/10722/223620

Chicago Manual of Style (16th Edition):

Kwan, Hoi-tung. “Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed June 16, 2019. Kwan, H. [關愷彤]. (2014). Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719483 ; http://hdl.handle.net/10722/223620.

MLA Handbook (7th Edition):

Kwan, Hoi-tung. “Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma.” 2014. Web. 16 Jun 2019.

Vancouver:

Kwan H. Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Jun 16]. Available from: Kwan, H. [關愷彤]. (2014). Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719483 ; http://hdl.handle.net/10722/223620.

Council of Science Editors:

Kwan H. Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Kwan, H. [關愷彤]. (2014). Gremlin2 promotes the enrichment of CD44+ cancer stem cells after transarterial chemoembolization in the treatment of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719483 ; http://hdl.handle.net/10722/223620


University of Hong Kong

15. Tang, Kwan-ho. Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma.

Degree: PhD, 2011, University of Hong Kong

 A novel theory in the field of tumor biology postulates that cancer growth is driven by a population of stem-like cells, called tumor-initiating cells (TICs).… (more)

Subjects/Keywords: Stem cells.; Liver - Cancer.; Cancer cells.

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APA (6th Edition):

Tang, K. (2011). Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tang, K. [鄧鈞豪]. (2011). Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784978 ; http://dx.doi.org/10.5353/th_b4784978 ; http://hdl.handle.net/10722/174536

Chicago Manual of Style (16th Edition):

Tang, Kwan-ho. “Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed June 16, 2019. Tang, K. [鄧鈞豪]. (2011). Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784978 ; http://dx.doi.org/10.5353/th_b4784978 ; http://hdl.handle.net/10722/174536.

MLA Handbook (7th Edition):

Tang, Kwan-ho. “Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma.” 2011. Web. 16 Jun 2019.

Vancouver:

Tang K. Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Jun 16]. Available from: Tang, K. [鄧鈞豪]. (2011). Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784978 ; http://dx.doi.org/10.5353/th_b4784978 ; http://hdl.handle.net/10722/174536.

Council of Science Editors:

Tang K. Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Tang, K. [鄧鈞豪]. (2011). Significance of IL-8 signaling in CD133 mediated tumor initiation and progression of hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784978 ; http://dx.doi.org/10.5353/th_b4784978 ; http://hdl.handle.net/10722/174536


University of Hong Kong

16. 何永源; Ho, Wing-yuen. Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma.

Degree: PhD, 2013, University of Hong Kong

 Hepatocellular carcinoma (HCC) is one of the most devastating malignancies worldwide with increasing incidences in both developed and developing countries. Survival rates have not been… (more)

Subjects/Keywords: Stem cells; Cancer cells; Liver - Cancer - Treatment

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APA (6th Edition):

何永源; Ho, W. (2013). Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ho, W. [何永源]. (2013). Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108670 ; http://dx.doi.org/10.5353/th_b5108670 ; http://hdl.handle.net/10722/193521

Chicago Manual of Style (16th Edition):

何永源; Ho, Wing-yuen. “Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed June 16, 2019. Ho, W. [何永源]. (2013). Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108670 ; http://dx.doi.org/10.5353/th_b5108670 ; http://hdl.handle.net/10722/193521.

MLA Handbook (7th Edition):

何永源; Ho, Wing-yuen. “Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma.” 2013. Web. 16 Jun 2019.

Vancouver:

何永源; Ho W. Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Jun 16]. Available from: Ho, W. [何永源]. (2013). Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108670 ; http://dx.doi.org/10.5353/th_b5108670 ; http://hdl.handle.net/10722/193521.

Council of Science Editors:

何永源; Ho W. Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Ho, W. [何永源]. (2013). Identification and characterization of CD90⁺ cancer stem cells in hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108670 ; http://dx.doi.org/10.5353/th_b5108670 ; http://hdl.handle.net/10722/193521


Université Catholique de Louvain

17. Berardis, Silvia. Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells.

Degree: 2014, Université Catholique de Louvain

Cirrhosis represents a major health issue for which no effective treatment is available so far, except liver transplantation, hardly accessible for patients because of a… (more)

Subjects/Keywords: Liver fibrosis; Hepatic stellate cells; Liver stem/progenitor cells

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APA (6th Edition):

Berardis, S. (2014). Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/151994

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):

Berardis, Silvia. “Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells.” 2014. Thesis, Université Catholique de Louvain. Accessed June 16, 2019. http://hdl.handle.net/2078.1/151994.

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

MLA Handbook (7th Edition):

Berardis, Silvia. “Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells.” 2014. Web. 16 Jun 2019.

Vancouver:

Berardis S. Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells. [Internet] [Thesis]. Université Catholique de Louvain; 2014. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/2078.1/151994.

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

Council of Science Editors:

Berardis S. Evaluation of the anti-fibrotic properties of adult-derived human liver stem/progenitor cells. [Thesis]. Université Catholique de Louvain; 2014. Available from: http://hdl.handle.net/2078.1/151994

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


University of Western Australia

18. Low, Jasmine. Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation.

Degree: PhD, 2010, University of Western Australia

Liver progenitor cells are a subpopulation of liver cells with bipotentiality, that is, they have the ability to differentiate into hepatocytes or cholangiocytes. In certain… (more)

Subjects/Keywords: Liver; Liver; Liver cells; Stem cells; Gene expression; Carcinogenesis; Microarray; Mouse liver; Liver progenitor cells; Transcriptome; Marker genes; Gene signatures; Neoplastic transformation

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APA (6th Edition):

Low, J. (2010). Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=23620&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Low, Jasmine. “Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation.” 2010. Doctoral Dissertation, University of Western Australia. Accessed June 16, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=23620&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Low, Jasmine. “Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation.” 2010. Web. 16 Jun 2019.

Vancouver:

Low J. Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation. [Internet] [Doctoral dissertation]. University of Western Australia; 2010. [cited 2019 Jun 16]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=23620&local_base=GEN01-INS01.

Council of Science Editors:

Low J. Transcriptomic analyses of mouse liver progenitor cells : establishing their signature and defining gene expression patterns associated with neoplastic transformation. [Doctoral Dissertation]. University of Western Australia; 2010. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=23620&local_base=GEN01-INS01


University of Arizona

19. MASSE, JUDITH LEE PETERS. A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE.

Degree: 1982, University of Arizona

 A single injection of thioacetamide (TAA) induces a significant increase in hepatocytes' DNA synthesis and mitosis within 48 hours without accompanying pathology. The present study… (more)

Subjects/Keywords: Liver cells.; Liver  – Growth.

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APA (6th Edition):

MASSE, J. L. P. (1982). A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE. (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/184225

Chicago Manual of Style (16th Edition):

MASSE, JUDITH LEE PETERS. “A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE. ” 1982. Doctoral Dissertation, University of Arizona. Accessed June 16, 2019. http://hdl.handle.net/10150/184225.

MLA Handbook (7th Edition):

MASSE, JUDITH LEE PETERS. “A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE. ” 1982. Web. 16 Jun 2019.

Vancouver:

MASSE JLP. A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE. [Internet] [Doctoral dissertation]. University of Arizona; 1982. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10150/184225.

Council of Science Editors:

MASSE JLP. A MORPHOLOGICAL STUDY OF THE HEPATIC RESPONSE TO A SINGLE INJECTION OF THIOACETAMIDE. [Doctoral Dissertation]. University of Arizona; 1982. Available from: http://hdl.handle.net/10150/184225

20. Cazares, Tareian Alonzo. Characterization of the effects of NRG-1 on HepG2 cell metabolism.

Degree: Thesis (M.S.), 2015, Ball State University

 Neuregulin-1 (NRG-1) is an epidermal growth factor-like ligand that binds to the human epidermal growth factor receptor 3 (HER3) resulting in increased glucose uptake, mitochondrial… (more)

Subjects/Keywords: Ligands (Biochemistry); Epidermal growth factor  – Receptors.; Liver cells.; Liver  – Physiology.

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APA (6th Edition):

Cazares, T. A. (2015). Characterization of the effects of NRG-1 on HepG2 cell metabolism. (Masters Thesis). Ball State University. Retrieved from http://cardinalscholar.bsu.edu/handle/123456789/200064

Chicago Manual of Style (16th Edition):

Cazares, Tareian Alonzo. “Characterization of the effects of NRG-1 on HepG2 cell metabolism.” 2015. Masters Thesis, Ball State University. Accessed June 16, 2019. http://cardinalscholar.bsu.edu/handle/123456789/200064.

MLA Handbook (7th Edition):

Cazares, Tareian Alonzo. “Characterization of the effects of NRG-1 on HepG2 cell metabolism.” 2015. Web. 16 Jun 2019.

Vancouver:

Cazares TA. Characterization of the effects of NRG-1 on HepG2 cell metabolism. [Internet] [Masters thesis]. Ball State University; 2015. [cited 2019 Jun 16]. Available from: http://cardinalscholar.bsu.edu/handle/123456789/200064.

Council of Science Editors:

Cazares TA. Characterization of the effects of NRG-1 on HepG2 cell metabolism. [Masters Thesis]. Ball State University; 2015. Available from: http://cardinalscholar.bsu.edu/handle/123456789/200064


University of Southern California

21. Chen, Wan-Ting. The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 Cancer progression is characterized by the overriding of growth arrest and rapid cell proliferation, which require increased protein synthesis. Additionally, the poor vascularization of cancer… (more)

Subjects/Keywords: ER chaperones; GRP94; GRP78; liver cancer; liver progenitor cells

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APA (6th Edition):

Chen, W. (2014). The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/459118/rec/7275

Chicago Manual of Style (16th Edition):

Chen, Wan-Ting. “The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis.” 2014. Doctoral Dissertation, University of Southern California. Accessed June 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/459118/rec/7275.

MLA Handbook (7th Edition):

Chen, Wan-Ting. “The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis.” 2014. Web. 16 Jun 2019.

Vancouver:

Chen W. The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Jun 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/459118/rec/7275.

Council of Science Editors:

Chen W. The roles of endoplasmic reticulum chaperones in regulating liver homeostasis and tumorigenesis. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/459118/rec/7275

22. Allam, Heba Samir Esmaeil. Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy.

Degree: PhD, Biological Sciences, 2011, U of Denver

  Hepatitis C virus (HCV) is an important human pathogen that causes chronic hepatitis cirrhosis, steatosis and hepatocellular carcinoma (HCC) worldwide. Although current FDA-approved drugs… (more)

Subjects/Keywords: Hepatitis C virus; Liver cancer; Stem cells

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APA (6th Edition):

Allam, H. S. E. (2011). Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/746

Chicago Manual of Style (16th Edition):

Allam, Heba Samir Esmaeil. “Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy.” 2011. Doctoral Dissertation, U of Denver. Accessed June 16, 2019. https://digitalcommons.du.edu/etd/746.

MLA Handbook (7th Edition):

Allam, Heba Samir Esmaeil. “Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy.” 2011. Web. 16 Jun 2019.

Vancouver:

Allam HSE. Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy. [Internet] [Doctoral dissertation]. U of Denver; 2011. [cited 2019 Jun 16]. Available from: https://digitalcommons.du.edu/etd/746.

Council of Science Editors:

Allam HSE. Hepatitis C Virus-Induced Hepatocellular Carcinoma: cancer stem cell and gene therapy. [Doctoral Dissertation]. U of Denver; 2011. Available from: https://digitalcommons.du.edu/etd/746


University of Aberdeen

23. Tachtatzis, Phaedra Maria. Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection.

Degree: Thesis (M.D.), 2015, University of Aberdeen

 Hepatitis B virus infection (HBV) is an important health problem worldwide, with a significant rate of chronic infection, which can lead to cirrhosis and hepatocellular… (more)

Subjects/Keywords: 616.9; Hepatitis B virus; Liver cells; Fibrosis

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APA (6th Edition):

Tachtatzis, P. M. (2015). Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=228557 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680959

Chicago Manual of Style (16th Edition):

Tachtatzis, Phaedra Maria. “Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection.” 2015. Doctoral Dissertation, University of Aberdeen. Accessed June 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=228557 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680959.

MLA Handbook (7th Edition):

Tachtatzis, Phaedra Maria. “Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection.” 2015. Web. 16 Jun 2019.

Vancouver:

Tachtatzis PM. Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection. [Internet] [Doctoral dissertation]. University of Aberdeen; 2015. [cited 2019 Jun 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=228557 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680959.

Council of Science Editors:

Tachtatzis PM. Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection. [Doctoral Dissertation]. University of Aberdeen; 2015. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=228557 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680959

24. Fekir, Karim. Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma.

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

Le cancer primitif du foie, ou carcinome hépatocellulaire (CHC), est l’un des premiers cancers dans le monde chez l’homme adulte. L'identité des cellules à l'origine… (more)

Subjects/Keywords: Foie; Cancer; Cellules souches; Liver cells; Cancer

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APA (6th Edition):

Fekir, K. (2015). Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2015REN1B007

Chicago Manual of Style (16th Edition):

Fekir, Karim. “Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma.” 2015. Doctoral Dissertation, Rennes 1. Accessed June 16, 2019. http://www.theses.fr/2015REN1B007.

MLA Handbook (7th Edition):

Fekir, Karim. “Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma.” 2015. Web. 16 Jun 2019.

Vancouver:

Fekir K. Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma. [Internet] [Doctoral dissertation]. Rennes 1; 2015. [cited 2019 Jun 16]. Available from: http://www.theses.fr/2015REN1B007.

Council of Science Editors:

Fekir K. Biomarqueurs et nouvelles approches thérapeutiques ciblant les cellules souches cancéreuses dans le carcinome hépatocellulaire : Biomarkers and new therapeutic approches targeting cancer stem cells in hepatocellular carcinoma. [Doctoral Dissertation]. Rennes 1; 2015. Available from: http://www.theses.fr/2015REN1B007


University of Western Australia

25. Tonkin, Joanne. Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies.

Degree: PhD, 2011, University of Western Australia

[Truncated abstract] There is great interest in the field of liver progenitor (oval) cells which are a bipotential compartment of cells responding to chronic liver(more)

Subjects/Keywords: Liver disease; Stem cells; Bone marrow

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APA (6th Edition):

Tonkin, J. (2011). Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30858&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Tonkin, Joanne. “Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies.” 2011. Doctoral Dissertation, University of Western Australia. Accessed June 16, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30858&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Tonkin, Joanne. “Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies.” 2011. Web. 16 Jun 2019.

Vancouver:

Tonkin J. Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies. [Internet] [Doctoral dissertation]. University of Western Australia; 2011. [cited 2019 Jun 16]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30858&local_base=GEN01-INS01.

Council of Science Editors:

Tonkin J. Establishing a relationship between bone marrow cells and liver progenitor cells by expression profiling and cell tracing studies. [Doctoral Dissertation]. University of Western Australia; 2011. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30858&local_base=GEN01-INS01


University of Aberdeen

26. Banks, Ruth. An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells.

Degree: PhD, 2013, University of Aberdeen

 Genes involved in xenobiotic metabolism and antioxidant signaling are enhanced in the liver of long-lived models, suggesting that a link exists between increased stress resistance… (more)

Subjects/Keywords: 570; Liver cells; Stress (Physiology); Vitamin E

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APA (6th Edition):

Banks, R. (2013). An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=205386 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600096

Chicago Manual of Style (16th Edition):

Banks, Ruth. “An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells.” 2013. Doctoral Dissertation, University of Aberdeen. Accessed June 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=205386 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600096.

MLA Handbook (7th Edition):

Banks, Ruth. “An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells.” 2013. Web. 16 Jun 2019.

Vancouver:

Banks R. An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells. [Internet] [Doctoral dissertation]. University of Aberdeen; 2013. [cited 2019 Jun 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=205386 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600096.

Council of Science Editors:

Banks R. An investigation into putative mechanisms underlying the effects of α-tocopherol and its metabolites on the adaptive stress response in HepG2 cells. [Doctoral Dissertation]. University of Aberdeen; 2013. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=205386 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600096


University of Southern California

27. Galicia Medina, Vivian A. PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer.

Degree: PhD, Systems Biology & Disease, 2011, University of Southern California

 Progenitor or tumor initiating cells (TICs) are “altered” stem cells with the capacity to form solid tumors. Tumor suppressor PTEN (phosphatase and tensin homologue deleted… (more)

Subjects/Keywords: Pten; tumor initiating cells; liver cancer

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

APA (6th Edition):

Galicia Medina, V. A. (2011). PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/470211/rec/5315

Chicago Manual of Style (16th Edition):

Galicia Medina, Vivian A. “PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer.” 2011. Doctoral Dissertation, University of Southern California. Accessed June 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/470211/rec/5315.

MLA Handbook (7th Edition):

Galicia Medina, Vivian A. “PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer.” 2011. Web. 16 Jun 2019.

Vancouver:

Galicia Medina VA. PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Jun 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/470211/rec/5315.

Council of Science Editors:

Galicia Medina VA. PTEN deletion induced tumor initiating cells: Strategies to accelerate the disease progression of liver cancer. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/470211/rec/5315


University of Bath

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

APA (6th Edition):

Sangan, C. B. (2012). Reprogramming of hepatic and pancreatic cells. (Doctoral Dissertation). University of Bath. Retrieved from 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 June 16, 2019. 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. 16 Jun 2019.

Vancouver:

Sangan CB. Reprogramming of hepatic and pancreatic cells. [Internet] [Doctoral dissertation]. University of Bath; 2012. [cited 2019 Jun 16]. Available from: 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://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582549


University of Aberdeen

29. Cowie, David. Differential induction of organic anion transporting polypeptides in rat liver.

Degree: School of Medicine and Dentistry., 2008, University of Aberdeen

Subjects/Keywords: Liver cells.; Anions.

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

APA (6th Edition):

Cowie, D. (2008). Differential induction of organic anion transporting polypeptides in rat liver. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25707 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25707&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Cowie, David. “Differential induction of organic anion transporting polypeptides in rat liver.” 2008. Doctoral Dissertation, University of Aberdeen. Accessed June 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25707 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25707&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Cowie, David. “Differential induction of organic anion transporting polypeptides in rat liver.” 2008. Web. 16 Jun 2019.

Vancouver:

Cowie D. Differential induction of organic anion transporting polypeptides in rat liver. [Internet] [Doctoral dissertation]. University of Aberdeen; 2008. [cited 2019 Jun 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25707 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25707&custom_att_2=simple_viewer.

Council of Science Editors:

Cowie D. Differential induction of organic anion transporting polypeptides in rat liver. [Doctoral Dissertation]. University of Aberdeen; 2008. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25707 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25707&custom_att_2=simple_viewer

30. Blachley, Jon David. A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice.

Degree: 1972, North Texas State University

Liver cells from lymphosarcoma-bearing DBA/1J mice were shown, by parabiotic culture with normal liver cells from isologous mice, to elaborate an agent which could pass a 25 mu filter and transform the normal cells to a malignant state. Advisors/Committee Members: Scholes, Vernon E., Norton, S. J..

Subjects/Keywords: carcinogens; liver cells

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

APA (6th Edition):

Blachley, J. D. (1972). A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice. (Thesis). North Texas State University. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc131529/

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):

Blachley, Jon David. “A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice.” 1972. Thesis, North Texas State University. Accessed June 16, 2019. https://digital.library.unt.edu/ark:/67531/metadc131529/.

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

MLA Handbook (7th Edition):

Blachley, Jon David. “A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice.” 1972. Web. 16 Jun 2019.

Vancouver:

Blachley JD. A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice. [Internet] [Thesis]. North Texas State University; 1972. [cited 2019 Jun 16]. Available from: https://digital.library.unt.edu/ark:/67531/metadc131529/.

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

Council of Science Editors:

Blachley JD. A Carcinogenic Agent Elaborated by Liver Cells from Lymphosarcoma-Bearing Mice. [Thesis]. North Texas State University; 1972. Available from: https://digital.library.unt.edu/ark:/67531/metadc131529/

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

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