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You searched for subject:(Liver fibrosis). Showing records 1 – 30 of 241 total matches.

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University of Sydney

1. EL Sharkawy, Rasha. MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis .

Degree: 2020, University of Sydney

 Background and aims: More than 90% of liver-related morbidity and mortality is a consequence of hepatic fibrosis that culminates in cirrhosis. Since anti-fibrotic drugs are… (more)

Subjects/Keywords: Liver; Fibrosis; MERTK

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

APA (6th Edition):

EL Sharkawy, R. (2020). MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/23249

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):

EL Sharkawy, Rasha. “MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis .” 2020. Thesis, University of Sydney. Accessed April 15, 2021. http://hdl.handle.net/2123/23249.

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

MLA Handbook (7th Edition):

EL Sharkawy, Rasha. “MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis .” 2020. Web. 15 Apr 2021.

Vancouver:

EL Sharkawy R. MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis . [Internet] [Thesis]. University of Sydney; 2020. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2123/23249.

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

Council of Science Editors:

EL Sharkawy R. MERTK receptor tyrosine kinase: A novel therapeutic target for liver fibrosis . [Thesis]. University of Sydney; 2020. Available from: http://hdl.handle.net/2123/23249

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


University of Edinburgh

2. Ramachandran, Prakash. Identification and characterisation of the restorative hepatic macrophage.

Degree: PhD, 2014, University of Edinburgh

 Long thought to be irreversible, it is now clear that liver fibrogenesis is a dynamic process, with scar tissue capable of being remodelled as well… (more)

Subjects/Keywords: 616.3; liver fibrosis; macrophage

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APA (6th Edition):

Ramachandran, P. (2014). Identification and characterisation of the restorative hepatic macrophage. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9555

Chicago Manual of Style (16th Edition):

Ramachandran, Prakash. “Identification and characterisation of the restorative hepatic macrophage.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed April 15, 2021. http://hdl.handle.net/1842/9555.

MLA Handbook (7th Edition):

Ramachandran, Prakash. “Identification and characterisation of the restorative hepatic macrophage.” 2014. Web. 15 Apr 2021.

Vancouver:

Ramachandran P. Identification and characterisation of the restorative hepatic macrophage. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1842/9555.

Council of Science Editors:

Ramachandran P. Identification and characterisation of the restorative hepatic macrophage. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/9555


IUPUI

3. Hamang, Matthew J. The Roles of Activin A and B in Liver Inflammation and Fibrosis.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Liver fibrosis is the result of different types of chronic liver diseases, such as cholestatic liver disease and nonalcoholic steatohepatitis,… (more)

Subjects/Keywords: Activin; Inflammation; Liver fibrosis

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APA (6th Edition):

Hamang, M. J. (2019). The Roles of Activin A and B in Liver Inflammation and Fibrosis. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/19008

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):

Hamang, Matthew J. “The Roles of Activin A and B in Liver Inflammation and Fibrosis.” 2019. Thesis, IUPUI. Accessed April 15, 2021. http://hdl.handle.net/1805/19008.

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

MLA Handbook (7th Edition):

Hamang, Matthew J. “The Roles of Activin A and B in Liver Inflammation and Fibrosis.” 2019. Web. 15 Apr 2021.

Vancouver:

Hamang MJ. The Roles of Activin A and B in Liver Inflammation and Fibrosis. [Internet] [Thesis]. IUPUI; 2019. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1805/19008.

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

Council of Science Editors:

Hamang MJ. The Roles of Activin A and B in Liver Inflammation and Fibrosis. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/19008

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


University of New South Wales

4. Torpy, James. An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis.

Degree: Biotechnology & Biomolecular Sciences, 2013, University of New South Wales

Fibrosis of the lungs and liver, characterised by excessive extra-cellular matrix (ECM) deposition and scarring following injury, has a significant negative impact on health worldwide.… (more)

Subjects/Keywords: Liver/Lung Fibrosis; CXCR7

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APA (6th Edition):

Torpy, J. (2013). An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52886 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11564/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Torpy, James. “An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis.” 2013. Masters Thesis, University of New South Wales. Accessed April 15, 2021. http://handle.unsw.edu.au/1959.4/52886 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11564/SOURCE01?view=true.

MLA Handbook (7th Edition):

Torpy, James. “An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis.” 2013. Web. 15 Apr 2021.

Vancouver:

Torpy J. An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis. [Internet] [Masters thesis]. University of New South Wales; 2013. [cited 2021 Apr 15]. Available from: http://handle.unsw.edu.au/1959.4/52886 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11564/SOURCE01?view=true.

Council of Science Editors:

Torpy J. An investigation of the cellular mechanisms regulated by CXCR7 during hepatic and pulmonary fibrosis. [Masters Thesis]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52886 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11564/SOURCE01?view=true


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 REQUEST OF AUTHOR.] Nonalcoholic steatohepatitis (NASH) is a liver disease that is associated with obesity and is… (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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Linden MA. Aerobic exercise training as a mitigator of nonalcoholic fatty liver disease related fibrosis. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2021 Apr 15]. 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 Illinois – Chicago

6. Mendoza-Elias, Nasya. Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model.

Degree: 2018, University of Illinois – Chicago

Liver disease affects ten percent of the world’s population, and estimates show that this yearly incidence is growing each year. Liver fibrosis is a key… (more)

Subjects/Keywords: porcine model; oncopig; cirrhosis; liver fibrosis; liver disease; alcohol liver disease

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APA (6th Edition):

Mendoza-Elias, N. (2018). Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/23042

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):

Mendoza-Elias, Nasya. “Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model.” 2018. Thesis, University of Illinois – Chicago. Accessed April 15, 2021. http://hdl.handle.net/10027/23042.

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

MLA Handbook (7th Edition):

Mendoza-Elias, Nasya. “Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model.” 2018. Web. 15 Apr 2021.

Vancouver:

Mendoza-Elias N. Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10027/23042.

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

Council of Science Editors:

Mendoza-Elias N. Laboratory and Clinical Profile of Alcohol-Induced Liver Fibrosis in a Transgenic Porcine Model. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/23042

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

7. Patel, Gaurang G. Functionalized nanocarriers for effective treatment of liver fibrosis;.

Degree: Pharmacy, 2011, Maharaja Sayajirao University of Baroda

None

Summary p. 285-297, References included in chapters

Advisors/Committee Members: Misra, Ambikanandan.

Subjects/Keywords: Pharmacy; Liver fibrosis

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APA (6th Edition):

Patel, G. G. (2011). Functionalized nanocarriers for effective treatment of liver fibrosis;. (Thesis). Maharaja Sayajirao University of Baroda. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/7482

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):

Patel, Gaurang G. “Functionalized nanocarriers for effective treatment of liver fibrosis;.” 2011. Thesis, Maharaja Sayajirao University of Baroda. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/7482.

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

MLA Handbook (7th Edition):

Patel, Gaurang G. “Functionalized nanocarriers for effective treatment of liver fibrosis;.” 2011. Web. 15 Apr 2021.

Vancouver:

Patel GG. Functionalized nanocarriers for effective treatment of liver fibrosis;. [Internet] [Thesis]. Maharaja Sayajirao University of Baroda; 2011. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/7482.

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

Council of Science Editors:

Patel GG. Functionalized nanocarriers for effective treatment of liver fibrosis;. [Thesis]. Maharaja Sayajirao University of Baroda; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/7482

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

8. Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada, Kiyoshi. Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。.

Degree: 博士(医学), 2017, Nara Medical University / 奈良県立医科大学

BACKGROUND: It is widely understood that insulin resistance (IR) critically correlates with the development of liver fibrosis in several types of chronic liver injuries. Several… (more)

Subjects/Keywords: SGLT2 inhibitor; Liver fibrosis; Insulin resistance

Page 1

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APA (6th Edition):

Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada, K. (2017). Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/3318

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):

Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada, Kiyoshi. “Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。.” 2017. Thesis, Nara Medical University / 奈良県立医科大学. Accessed April 15, 2021. http://hdl.handle.net/10564/3318.

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

MLA Handbook (7th Edition):

Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada, Kiyoshi. “Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。.” 2017. Web. 15 Apr 2021.

Vancouver:

Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada K. Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10564/3318.

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

Council of Science Editors:

Nishimura, Norihisa; Kitade, Mitsuteru; Noguchi, Ryuichi; Namisaki, Tadashi; Moriya, Kei; Takeda, Kosuke; Okura, Yasushi; Aihara, Yosuke; Douhara, Akitoshi; Kawaratani, Hideto; Asada K. Ipragliflozin, a sodium-glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka Long-Evans Tokushima fatty rats. : SGLT2阻害薬であるイプラグリフロジンは2型糖尿病自然発症モデルであるOLETFラットにおいて肝線維化進展を抑制する。. [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. Available from: http://hdl.handle.net/10564/3318

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


University of Toronto

9. Sadri, Ali-Reza. The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury.

Degree: 2017, University of Toronto

Liver fibrosis is known to become problematic after persistent injury. However, little is known about its response after an acute insult. Myeloid lineage cells, specifically,… (more)

Subjects/Keywords: fibrosis; Kupffer; liver; macrophage; myeloid; serotonin; 0982

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APA (6th Edition):

Sadri, A. (2017). The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/81182

Chicago Manual of Style (16th Edition):

Sadri, Ali-Reza. “The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury.” 2017. Masters Thesis, University of Toronto. Accessed April 15, 2021. http://hdl.handle.net/1807/81182.

MLA Handbook (7th Edition):

Sadri, Ali-Reza. “The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury.” 2017. Web. 15 Apr 2021.

Vancouver:

Sadri A. The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1807/81182.

Council of Science Editors:

Sadri A. The Spatiotemporal Accumulation of Myeloid Lineage Cells Is Mapping Out Fibrosis in the Liver after Acute and Chronic Injury. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/81182


University of Illinois – Chicago

10. Liu, Jennifer Sue. Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis.

Degree: 2018, University of Illinois – Chicago

 The liver executes a plethora of functions such as drug metabolism, plasma protein secretion, and urea synthesis. Additionally, drug toxicity to the liver is a… (more)

Subjects/Keywords: Hepatocellular carcinoma; liver model; cholangiocyte; fibrosis

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APA (6th Edition):

Liu, J. S. (2018). Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22620

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, Jennifer Sue. “Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis.” 2018. Thesis, University of Illinois – Chicago. Accessed April 15, 2021. http://hdl.handle.net/10027/22620.

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

MLA Handbook (7th Edition):

Liu, Jennifer Sue. “Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis.” 2018. Web. 15 Apr 2021.

Vancouver:

Liu JS. Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10027/22620.

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

Council of Science Editors:

Liu JS. Engineering Culture Platforms to Study Human Liver Cancer and Fibrosis. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22620

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


IUPUI

11. Culver, Alexander. TGF-beta signaling in an in vivo model of NASH.

Degree: 2016, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

A burgeoning area of focus within liver disease research is centered on the concomitant muscle atrophy present in end stage… (more)

Subjects/Keywords: NASH; Activin; Nonalcoholic steatohepatitis; liver; fibrosis; gdf8

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APA (6th Edition):

Culver, A. (2016). TGF-beta signaling in an in vivo model of NASH. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/11829

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):

Culver, Alexander. “TGF-beta signaling in an in vivo model of NASH.” 2016. Thesis, IUPUI. Accessed April 15, 2021. http://hdl.handle.net/1805/11829.

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

MLA Handbook (7th Edition):

Culver, Alexander. “TGF-beta signaling in an in vivo model of NASH.” 2016. Web. 15 Apr 2021.

Vancouver:

Culver A. TGF-beta signaling in an in vivo model of NASH. [Internet] [Thesis]. IUPUI; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1805/11829.

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

Council of Science Editors:

Culver A. TGF-beta signaling in an in vivo model of NASH. [Thesis]. IUPUI; 2016. Available from: http://hdl.handle.net/1805/11829

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


University of Melbourne

12. Nadebaum, David. Shear wave elastography in the assessment of liver fibrosis.

Degree: 2017, University of Melbourne

 The accurate quantification of liver fibrosis is essential to the prognostication and clinical management of patients with chronic liver disease (CLD). Whilst liver biopsy remains… (more)

Subjects/Keywords: liver; fibrosis; cirrhosis; elastography; shear wave; obesity

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APA (6th Edition):

Nadebaum, D. (2017). Shear wave elastography in the assessment of liver fibrosis. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/219873

Chicago Manual of Style (16th Edition):

Nadebaum, David. “Shear wave elastography in the assessment of liver fibrosis.” 2017. Masters Thesis, University of Melbourne. Accessed April 15, 2021. http://hdl.handle.net/11343/219873.

MLA Handbook (7th Edition):

Nadebaum, David. “Shear wave elastography in the assessment of liver fibrosis.” 2017. Web. 15 Apr 2021.

Vancouver:

Nadebaum D. Shear wave elastography in the assessment of liver fibrosis. [Internet] [Masters thesis]. University of Melbourne; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11343/219873.

Council of Science Editors:

Nadebaum D. Shear wave elastography in the assessment of liver fibrosis. [Masters Thesis]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/219873


University of Sydney

13. Henderson, James Matthew. Dipeptidyl peptidases in experimental hepatocellular carcinoma .

Degree: 2018, University of Sydney

 The urgent unmet need to develop hepatocellular carcinoma (HCC) therapies is addressed here by characterising a novel mouse model of HCC in the context of… (more)

Subjects/Keywords: hepatocellular carcinoma; dipeptidyl peptidase; fibrosis; liver disease

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APA (6th Edition):

Henderson, J. M. (2018). Dipeptidyl peptidases in experimental hepatocellular carcinoma . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20017

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):

Henderson, James Matthew. “Dipeptidyl peptidases in experimental hepatocellular carcinoma .” 2018. Thesis, University of Sydney. Accessed April 15, 2021. http://hdl.handle.net/2123/20017.

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

MLA Handbook (7th Edition):

Henderson, James Matthew. “Dipeptidyl peptidases in experimental hepatocellular carcinoma .” 2018. Web. 15 Apr 2021.

Vancouver:

Henderson JM. Dipeptidyl peptidases in experimental hepatocellular carcinoma . [Internet] [Thesis]. University of Sydney; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2123/20017.

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

Council of Science Editors:

Henderson JM. Dipeptidyl peptidases in experimental hepatocellular carcinoma . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/20017

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


University of Sydney

14. Metwally, Mayada. Role of novel genetic variations on tissue fibrosis .

Degree: University of Sydney

 Tissue fibrosis is a highly heritable complex phenotype that has both core and disease-specific pathways and is responsible for nearly half of all deaths worldwide.… (more)

Subjects/Keywords: fibrosis; liver; genetic

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APA (6th Edition):

Metwally, M. (n.d.). Role of novel genetic variations on tissue fibrosis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/21713

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Metwally, Mayada. “Role of novel genetic variations on tissue fibrosis .” Thesis, University of Sydney. Accessed April 15, 2021. http://hdl.handle.net/2123/21713.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Metwally, Mayada. “Role of novel genetic variations on tissue fibrosis .” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Metwally M. Role of novel genetic variations on tissue fibrosis . [Internet] [Thesis]. University of Sydney; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2123/21713.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Metwally M. Role of novel genetic variations on tissue fibrosis . [Thesis]. University of Sydney; Available from: http://hdl.handle.net/2123/21713

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Aberdeen

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

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 https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152910390005941 ; https://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 April 15, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152910390005941 ; https://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. 15 Apr 2021.

Vancouver:

Tachtatzis PM. Accelerated ageing, senescence and the natural history of chronic hepatitis B virus infection. [Internet] [Doctoral dissertation]. University of Aberdeen; 2015. [cited 2021 Apr 15]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152910390005941 ; https://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: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152910390005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680959


Columbia University

16. Zhu, Changyu. Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer.

Degree: 2019, Columbia University

 Non-alcoholic steatohepatitis (NASH) is a chronic liver disease associated with the worldwide spread of obesity. NASH predisposes development of fibrosis and hepatocellular carcinoma (HCC), but… (more)

Subjects/Keywords: Biology; Medicine; Liver – Diseases; Notch proteins; Liver – Fibrosis

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APA (6th Edition):

Zhu, C. (2019). Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-877b-v389

Chicago Manual of Style (16th Edition):

Zhu, Changyu. “Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer.” 2019. Doctoral Dissertation, Columbia University. Accessed April 15, 2021. https://doi.org/10.7916/d8-877b-v389.

MLA Handbook (7th Edition):

Zhu, Changyu. “Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer.” 2019. Web. 15 Apr 2021.

Vancouver:

Zhu C. Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2021 Apr 15]. Available from: https://doi.org/10.7916/d8-877b-v389.

Council of Science Editors:

Zhu C. Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-877b-v389


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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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 Edinburgh

18. Zou, Xiantong. The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease.

Degree: PhD, 2014, University of Edinburgh

 Non-alcoholic fatty liver disease (NAFLD) is a worldwide health problem which includes steatosis (triglyceride accumulation alone), non-alcoholic steatohepatitis (NASH, with liver inflammation), fibrosis, cirrhosis and… (more)

Subjects/Keywords: 616.3; 11ß-HSD1; liver fibrosis; NAFLD; Non-alcoholic fatty liver disease

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APA (6th Edition):

Zou, X. (2014). The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/18748

Chicago Manual of Style (16th Edition):

Zou, Xiantong. “The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed April 15, 2021. http://hdl.handle.net/1842/18748.

MLA Handbook (7th Edition):

Zou, Xiantong. “The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease.” 2014. Web. 15 Apr 2021.

Vancouver:

Zou X. The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1842/18748.

Council of Science Editors:

Zou X. The role of 11β-hydroxysteroid dehydrogenase type 1 in liver fibrosis and inflammation in non-alcoholic fatty liver disease. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/18748

19. Androutsakos, Theodoros. HIV και ήπαρ.

Degree: 2020, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

The introduction of antiretroviral treatment (ART) for HIV-infected patients has led to a change of these patients' life expectancy, making HIV infection a chronic rather… (more)

Subjects/Keywords: HIV λοίμωξη; Ηπατική ίνωση; Ήπαρ; Μη επεμβατικοί δείκτες ηπατικής ίνωσης; HIV infection; Liver fibrosis; Liver; Non invasive biomarkers of liver fibrosis

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

APA (6th Edition):

Androutsakos, T. (2020). HIV και ήπαρ. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/46948

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):

Androutsakos, Theodoros. “HIV και ήπαρ.” 2020. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 15, 2021. http://hdl.handle.net/10442/hedi/46948.

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

MLA Handbook (7th Edition):

Androutsakos, Theodoros. “HIV και ήπαρ.” 2020. Web. 15 Apr 2021.

Vancouver:

Androutsakos T. HIV και ήπαρ. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10442/hedi/46948.

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

Council of Science Editors:

Androutsakos T. HIV και ήπαρ. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. Available from: http://hdl.handle.net/10442/hedi/46948

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


Universiteit Utrecht

20. Poll, D. van. Stem cells in liver disease.

Degree: 2008, Universiteit Utrecht

 Failure of the liver, the largest vital organ in the body, unequivocally results in death. Hepatic failure most commonly evolves over a period of several… (more)

Subjects/Keywords: Geneeskunde; liver; stem cells; liver fibrosis; fulminant hepatic failure; transplantation; inflammation; regeneration; cell death

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APA (6th Edition):

Poll, D. v. (2008). Stem cells in liver disease. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/27630

Chicago Manual of Style (16th Edition):

Poll, D van. “Stem cells in liver disease.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed April 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/27630.

MLA Handbook (7th Edition):

Poll, D van. “Stem cells in liver disease.” 2008. Web. 15 Apr 2021.

Vancouver:

Poll Dv. Stem cells in liver disease. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2021 Apr 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/27630.

Council of Science Editors:

Poll Dv. Stem cells in liver disease. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/27630


University of Edinburgh

21. Haideri, Sharmin Shabbir. Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy.

Degree: PhD, 2017, University of Edinburgh

 The difference between the number of patients needing transplantation for chronic liver disease and the number of organ donors is growing, drawing attention to the… (more)

Subjects/Keywords: bone marrow-derived macrophages; BMDM; liver fibrosis; mouse model; liver regeneration; macrophages; stem cells

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APA (6th Edition):

Haideri, S. S. (2017). Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28848

Chicago Manual of Style (16th Edition):

Haideri, Sharmin Shabbir. “Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed April 15, 2021. http://hdl.handle.net/1842/28848.

MLA Handbook (7th Edition):

Haideri, Sharmin Shabbir. “Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy.” 2017. Web. 15 Apr 2021.

Vancouver:

Haideri SS. Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1842/28848.

Council of Science Editors:

Haideri SS. Embryonic stem cell derived macrophages as a model for studying liver fibrosis and a potential source of cells for therapy. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28848

22. Zanten, R.A.A. Serum parameters of liver fibrosis.

Degree: Department of Gastroenterology & Hepatology, 1991, Erasmus University Medical Center

 textabstractChronic liver disease is often associated with deposition of fibrous tissue, a process which together with the destruction of normal liver and liver cell regeneration,… (more)

Subjects/Keywords: liver; chronic liver disease; fibrosis; cirrhosis

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APA (6th Edition):

Zanten, R. A. A. (1991). Serum parameters of liver fibrosis. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/50757

Chicago Manual of Style (16th Edition):

Zanten, R A A. “Serum parameters of liver fibrosis.” 1991. Doctoral Dissertation, Erasmus University Medical Center. Accessed April 15, 2021. http://hdl.handle.net/1765/50757.

MLA Handbook (7th Edition):

Zanten, R A A. “Serum parameters of liver fibrosis.” 1991. Web. 15 Apr 2021.

Vancouver:

Zanten RAA. Serum parameters of liver fibrosis. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1991. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1765/50757.

Council of Science Editors:

Zanten RAA. Serum parameters of liver fibrosis. [Doctoral Dissertation]. Erasmus University Medical Center; 1991. Available from: http://hdl.handle.net/1765/50757


Virginia Tech

23. Ford, Andrew Joseph. Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro.

Degree: PhD, Chemical Engineering, 2018, Virginia Tech

 The cellular microenvironment in vivo consists of both mechanical and chemical signals, which drive cell function and fate. These signals include the composition, architecture, and… (more)

Subjects/Keywords: inflammation; ECM remodeling; liver fibrosis; liver sinusoidal endothelial cells; cytoplasmic stiffness; macrophage fibroblast co-culture

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APA (6th Edition):

Ford, A. J. (2018). Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/96711

Chicago Manual of Style (16th Edition):

Ford, Andrew Joseph. “Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro.” 2018. Doctoral Dissertation, Virginia Tech. Accessed April 15, 2021. http://hdl.handle.net/10919/96711.

MLA Handbook (7th Edition):

Ford, Andrew Joseph. “Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro.” 2018. Web. 15 Apr 2021.

Vancouver:

Ford AJ. Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10919/96711.

Council of Science Editors:

Ford AJ. Investigating the Interplay between Inflammation and Matrix Stiffness: Evaluation of Cell Phenotype and Cytoplasmic Stiffness In Vitro. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/96711


University of Sydney

24. Rauff, Bisma. In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis .

Degree: 2016, University of Sydney

 Chronic liver disease (CLD) is a leading cause of mortality around the world and can arise from a range of injuries or insults. Untreated CLD… (more)

Subjects/Keywords: Chronic liver disease (CLD); liver fibrosis; cholestasis; HCV; NF-KB signalling; cholangiocarcinoma

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APA (6th Edition):

Rauff, B. (2016). In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16717

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):

Rauff, Bisma. “In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis .” 2016. Thesis, University of Sydney. Accessed April 15, 2021. http://hdl.handle.net/2123/16717.

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

MLA Handbook (7th Edition):

Rauff, Bisma. “In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis .” 2016. Web. 15 Apr 2021.

Vancouver:

Rauff B. In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis . [Internet] [Thesis]. University of Sydney; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2123/16717.

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

Council of Science Editors:

Rauff B. In vitro and in vivo models to investigate the mechanisms of liver fibrosis and cholestasis . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/16717

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

25. Γριμπίλας, Γεώργιος. Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση.

Degree: 2013, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Liver fibrosis is a wound healing process activated in cases of chronic liverdamage, as in the case of alcohol abuse or chronic viral hepatitis. The… (more)

Subjects/Keywords: Ήπαρ; Ηπατική διεγερτικότητα; Ηπατική αναγέννηση; Κίρρωση; Ηπατική ίνωση; Θειοακεταμίδη; Liver; Liver regeneration; Cirrhosis; Liver fibrosis; Thioacetamide; Hepatic stimulation substance

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APA (6th Edition):

Γριμπίλας, . . (2013). Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/29494

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):

Γριμπίλας, Γεώργιος. “Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση.” 2013. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 15, 2021. http://hdl.handle.net/10442/hedi/29494.

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

MLA Handbook (7th Edition):

Γριμπίλας, Γεώργιος. “Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση.” 2013. Web. 15 Apr 2021.

Vancouver:

Γριμπίλας . Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10442/hedi/29494.

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

Council of Science Editors:

Γριμπίλας . Διερεύνηση του μηχανισμού δράσης της ηπατικής διεγερτικής ουσίας ( HSS) στην κίρρωση. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2013. Available from: http://hdl.handle.net/10442/hedi/29494

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


NSYSU

26. 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 April 15, 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. 15 Apr 2021.

Vancouver:

Kao Y. Investigation on the Pathological Role of Hepatoma-Derived Growth Factor in Hepatic Fibrogenesis. [Internet] [Doctoral dissertation]. NSYSU; 2009. [cited 2021 Apr 15]. 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


NSYSU

27. Wu, Li-chuan. Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice.

Degree: Master, Biological Sciences, 2009, NSYSU

 Typically chronic injury leads to hepatic fibrosis. No effective antifibrotic drugs have been approved, but herbal drugs have potential on the therapy of hepatic fibrosis.… (more)

Subjects/Keywords: Hydroxyproline; Sirius red staining; Thioacetamide; Liver fibrosis; Pluchea indica

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

APA (6th Edition):

Wu, L. (2009). Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0908109-170256

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):

Wu, Li-chuan. “Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice.” 2009. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0908109-170256.

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

MLA Handbook (7th Edition):

Wu, Li-chuan. “Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice.” 2009. Web. 15 Apr 2021.

Vancouver:

Wu L. Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice. [Internet] [Thesis]. NSYSU; 2009. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0908109-170256.

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

Council of Science Editors:

Wu L. Hepatoprotective Effects of Pluchea indica (L.) Less. Aqueous Extract against Thioacetamide-induced Liver Fibrosis in Mice. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0908109-170256

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


NSYSU

28. Tai, Chun-pao. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.

Degree: Master, Biological Sciences, 2013, NSYSU

 Abstract MiRNAs are an emerging class of highly conserved non-coding small RNAs that regulate gene expression at the post-transcriptional level. Most miRNAs are generated by… (more)

Subjects/Keywords: liver fibrosis; miRNA; Drosha; gene-specific reverse transcriptase-PCR; Dicer

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

APA (6th Edition):

Tai, C. (2013). Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547

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):

Tai, Chun-pao. “Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.” 2013. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547.

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

MLA Handbook (7th Edition):

Tai, Chun-pao. “Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice.” 2013. Web. 15 Apr 2021.

Vancouver:

Tai C. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547.

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

Council of Science Editors:

Tai C. Detection of microRNA expression in the blood of CCl4-induced liver fibrotic mice. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0810113-130547

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


NSYSU

29. Su, Pei-xuan. CB1 Antisense in the Treatment of Liver Fibrosis.

Degree: Master, Institute of Biomedical Sciences, 2014, NSYSU

Liver fibrosis results from chronic injury to the liver and inflammation activation of hepatic stellate cells produce excessive accumulation of type I collagen proteins, ultimately… (more)

Subjects/Keywords: AM251; Collagen type I; Liver fibrosis; CB1 antisense oligonucleotide; CB1 receptor

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

APA (6th Edition):

Su, P. (2014). CB1 Antisense in the Treatment of Liver Fibrosis. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801114-161740

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):

Su, Pei-xuan. “CB1 Antisense in the Treatment of Liver Fibrosis.” 2014. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801114-161740.

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

MLA Handbook (7th Edition):

Su, Pei-xuan. “CB1 Antisense in the Treatment of Liver Fibrosis.” 2014. Web. 15 Apr 2021.

Vancouver:

Su P. CB1 Antisense in the Treatment of Liver Fibrosis. [Internet] [Thesis]. NSYSU; 2014. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801114-161740.

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

Council of Science Editors:

Su P. CB1 Antisense in the Treatment of Liver Fibrosis. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801114-161740

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


NSYSU

30. Chen, Tian-zong. Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat.

Degree: Master, Institute of Biomedical Sciences, 2016, NSYSU

Liver fibrosis is the excessive accumulation of extracellular matrix proteins including collagen that occurs in most types of chronic liver diseases. Several studies indicated liver(more)

Subjects/Keywords: ECSW; Anti-oxidative stress; Liver fibrosis; Proliferation; Inflammatory

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

APA (6th Edition):

Chen, T. (2016). Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604116-132259

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):

Chen, Tian-zong. “Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat.” 2016. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604116-132259.

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

MLA Handbook (7th Edition):

Chen, Tian-zong. “Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat.” 2016. Web. 15 Apr 2021.

Vancouver:

Chen T. Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604116-132259.

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

Council of Science Editors:

Chen T. Extracorporeal Shock Wave Therapy Attenuates CCl4 induced Liver Fibrosis in Rat. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604116-132259

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

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