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Level: thesis

You searched for subject:(Liver). Showing records 1 – 21 of 21 total matches.

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1. Wilson, Gayle. Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase.

Degree: MS, 1980, Oregon Health Sciences University

Subjects/Keywords: Electron Transport Complex IV  – biosynthesis; Liver  – cytology; Mitochondria, Liver

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APA (6th Edition):

Wilson, G. (1980). Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4PZ571X ; http://digitalcommons.ohsu.edu/etd/2301

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):

Wilson, Gayle. “Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase.” 1980. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4PZ571X ; http://digitalcommons.ohsu.edu/etd/2301.

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

MLA Handbook (7th Edition):

Wilson, Gayle. “Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase.” 1980. Web. 22 Jul 2019.

Vancouver:

Wilson G. Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase. [Internet] [Thesis]. Oregon Health Sciences University; 1980. [cited 2019 Jul 22]. Available from: doi:10.6083/M4PZ571X ; http://digitalcommons.ohsu.edu/etd/2301.

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

Council of Science Editors:

Wilson G. Mitochondrial protein biosynthesis in cultured rat hepatocytes, cytochrome c oxidase. [Thesis]. Oregon Health Sciences University; 1980. Available from: doi:10.6083/M4PZ571X ; http://digitalcommons.ohsu.edu/etd/2301

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

2. Thienes, Clinton H. Hepatic circulation and associated veins in a six millimeter pig embryo.

Degree: MS, 1923, Oregon Health Sciences University

Subjects/Keywords: Liver Circulation; Hepatic Veins

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APA (6th Edition):

Thienes, C. H. (1923). Hepatic circulation and associated veins in a six millimeter pig embryo. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4BG2KXN ; http://digitalcommons.ohsu.edu/etd/183

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):

Thienes, Clinton H. “Hepatic circulation and associated veins in a six millimeter pig embryo.” 1923. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4BG2KXN ; http://digitalcommons.ohsu.edu/etd/183.

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

MLA Handbook (7th Edition):

Thienes, Clinton H. “Hepatic circulation and associated veins in a six millimeter pig embryo.” 1923. Web. 22 Jul 2019.

Vancouver:

Thienes CH. Hepatic circulation and associated veins in a six millimeter pig embryo. [Internet] [Thesis]. Oregon Health Sciences University; 1923. [cited 2019 Jul 22]. Available from: doi:10.6083/M4BG2KXN ; http://digitalcommons.ohsu.edu/etd/183.

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

Council of Science Editors:

Thienes CH. Hepatic circulation and associated veins in a six millimeter pig embryo. [Thesis]. Oregon Health Sciences University; 1923. Available from: doi:10.6083/M4BG2KXN ; http://digitalcommons.ohsu.edu/etd/183

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

3. Mesch, Joan A. Quality of life following liver transplantation.

Degree: MS, 1992, Oregon Health Sciences University

Subjects/Keywords: Liver Transplantation; Quality of Life

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APA (6th Edition):

Mesch, J. A. (1992). Quality of life following liver transplantation. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4DB7ZXB ; http://digitalcommons.ohsu.edu/etd/1746

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):

Mesch, Joan A. “Quality of life following liver transplantation.” 1992. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4DB7ZXB ; http://digitalcommons.ohsu.edu/etd/1746.

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

MLA Handbook (7th Edition):

Mesch, Joan A. “Quality of life following liver transplantation.” 1992. Web. 22 Jul 2019.

Vancouver:

Mesch JA. Quality of life following liver transplantation. [Internet] [Thesis]. Oregon Health Sciences University; 1992. [cited 2019 Jul 22]. Available from: doi:10.6083/M4DB7ZXB ; http://digitalcommons.ohsu.edu/etd/1746.

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

Council of Science Editors:

Mesch JA. Quality of life following liver transplantation. [Thesis]. Oregon Health Sciences University; 1992. Available from: doi:10.6083/M4DB7ZXB ; http://digitalcommons.ohsu.edu/etd/1746

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

4. Cowens, Kylie Rose. EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM.

Degree: MS, 2015, University of New Hampshire

 Polybrominated diphenyl ethers (PBDEs) are flame-retardant chemicals that contaminate the environment. Through ingestion and inhalation, these chemicals get into the human body, where they affect… (more)

Subjects/Keywords: Fat Metabolism; Glyceroneogenesis; Liver; Phosphoenolpyruvate carboxykinase; Biochemistry; Nutrition

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APA (6th Edition):

Cowens, K. R. (2015). EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM. (Thesis). University of New Hampshire. Retrieved from https://scholars.unh.edu/thesis/1013

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):

Cowens, Kylie Rose. “EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM.” 2015. Thesis, University of New Hampshire. Accessed July 22, 2019. https://scholars.unh.edu/thesis/1013.

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

MLA Handbook (7th Edition):

Cowens, Kylie Rose. “EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM.” 2015. Web. 22 Jul 2019.

Vancouver:

Cowens KR. EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM. [Internet] [Thesis]. University of New Hampshire; 2015. [cited 2019 Jul 22]. Available from: https://scholars.unh.edu/thesis/1013.

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

Council of Science Editors:

Cowens KR. EFFECT OF IN VIVO POLYBROMINATED DIPHENYL ETHER (PBDE) TREATMENT ON HEPATIC GLYCERONEOGENESIS AND LIPID METABOLISM. [Thesis]. University of New Hampshire; 2015. Available from: https://scholars.unh.edu/thesis/1013

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

5. Schlansky, Barry. Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry.

Degree: M.P.H., 2013, Oregon Health Sciences University

Subjects/Keywords: Liver  – Transplantation; Liver  – Cancer; Liver  – Cirrhosis; Hospitals  – Waiting lists; Survival analysis (Biometry); Liver Transplantation; Carcinoma, Hepatocellular; Liver Cirrhosis; Waiting Lists; Survival Analysis

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APA (6th Edition):

Schlansky, B. (2013). Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4513W7R ; http://digitalcommons.ohsu.edu/etd/943

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):

Schlansky, Barry. “Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry.” 2013. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4513W7R ; http://digitalcommons.ohsu.edu/etd/943.

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

MLA Handbook (7th Edition):

Schlansky, Barry. “Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry.” 2013. Web. 22 Jul 2019.

Vancouver:

Schlansky B. Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry. [Internet] [Thesis]. Oregon Health Sciences University; 2013. [cited 2019 Jul 22]. Available from: doi:10.6083/M4513W7R ; http://digitalcommons.ohsu.edu/etd/943.

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

Council of Science Editors:

Schlansky B. Waitlist time predicts survival after liver transplantation for hepatocellular carcinoma : a cohort study in the United Network for Organ Sharing registry. [Thesis]. Oregon Health Sciences University; 2013. Available from: doi:10.6083/M4513W7R ; http://digitalcommons.ohsu.edu/etd/943

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


Virginia Commonwealth University

6. Fassnacht, Ryan. Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis.

Degree: MS, Physiology, 2010, Virginia Commonwealth University

 The leading causes of liver disease are Hepatitis C virus infection and chronic alcohol abuse. Alcohol accelerates liver disease in HCV but the mechanisms are… (more)

Subjects/Keywords: liver cirrhosis; hepatitis c virus; alcoholic cirrhosis; gene expression; microarrays; Life Sciences; Physiology

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APA (6th Edition):

Fassnacht, R. (2010). Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2246

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):

Fassnacht, Ryan. “Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis.” 2010. Thesis, Virginia Commonwealth University. Accessed July 22, 2019. https://scholarscompass.vcu.edu/etd/2246.

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

MLA Handbook (7th Edition):

Fassnacht, Ryan. “Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis.” 2010. Web. 22 Jul 2019.

Vancouver:

Fassnacht R. Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Jul 22]. Available from: https://scholarscompass.vcu.edu/etd/2246.

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

Council of Science Editors:

Fassnacht R. Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2246

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


University of Illinois – Urbana-Champaign

7. Shahzad, Khuram. Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database.

Degree: MS, 4026, 2013, University of Illinois – Urbana-Champaign

 To-date bovine liver and adipose tissues have been investigated through several molecular techniques. However, for the most part molecular work in these tissues has been… (more)

Subjects/Keywords: Bioinformatics; Systems Biology; Transcriptome profiling; Enrichment analysis; Bovine liver; Bovine adipose tissue; Transition cows

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APA (6th Edition):

Shahzad, K. (2013). Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42472

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):

Shahzad, Khuram. “Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database.” 2013. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/42472.

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

MLA Handbook (7th Edition):

Shahzad, Khuram. “Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database.” 2013. Web. 22 Jul 2019.

Vancouver:

Shahzad K. Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/42472.

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

Council of Science Editors:

Shahzad K. Bioinformatics analysis of liver and adipose tissue microarray data from periparturient dairy cattle and development of a web-based ruminant specific microarray database. [Thesis]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42472

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

8. Polonoff, Ethel S. In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats.

Degree: MS, 1975, Oregon Health Sciences University

Subjects/Keywords: Pharmaceutical Preparations  – metabolism; Phenytoin  – metabolism; Microsomes, Liver  – enzymology

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APA (6th Edition):

Polonoff, E. S. (1975). In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M42805T1 ; http://digitalcommons.ohsu.edu/etd/2484

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):

Polonoff, Ethel S. “In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats.” 1975. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M42805T1 ; http://digitalcommons.ohsu.edu/etd/2484.

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

MLA Handbook (7th Edition):

Polonoff, Ethel S. “In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats.” 1975. Web. 22 Jul 2019.

Vancouver:

Polonoff ES. In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats. [Internet] [Thesis]. Oregon Health Sciences University; 1975. [cited 2019 Jul 22]. Available from: doi:10.6083/M42805T1 ; http://digitalcommons.ohsu.edu/etd/2484.

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

Council of Science Editors:

Polonoff ES. In vitro metabolism of drug substrates by liver microsomal enzymes from male, pregnant and nonpregnant female rats. [Thesis]. Oregon Health Sciences University; 1975. Available from: doi:10.6083/M42805T1 ; http://digitalcommons.ohsu.edu/etd/2484

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


University of Illinois – Urbana-Champaign

9. Kaylan, Kerim Berk. Engineered microenvironments for studying liver progenitor differentiation.

Degree: MS, Bioengineering, 2016, University of Illinois – Urbana-Champaign

 The bipotential differentiation of liver progenitor cells underlies liver development and bile duct formation as well as liver regeneration and disease. Both TGFβ and Notch… (more)

Subjects/Keywords: liver progenitors; bipotential liver progenitors; hepatoblasts; hepatocytes; cholangiocytes; bile duct cells; liver progenitor differentiation; osteopontin; Opn; Spp1; albumin; Alb; morphogenesis; tissue morphogenesis; bile duct morphogenesis; bile duct formation; liver development; Notch; Notch signaling; Jagged-1; Jag1; Delta-like 1; Dll1; Delta-like 4; Dll4; transforming growth factor β; TGFβ; TGFβ signaling; TGFβ1; Extracellular matrix proteins (ECM); collagen I; collagen III; collagen IV; laminin; fibronectin; co-cultures; Green fluorescent protein (GFP); microenvironment; microenvironmental regulation; cell microenvironment; cellular microenvironment; cell microarrays; cellular microarrays; engineered microenvironments

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APA (6th Edition):

Kaylan, K. B. (2016). Engineered microenvironments for studying liver progenitor differentiation. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90492

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):

Kaylan, Kerim Berk. “Engineered microenvironments for studying liver progenitor differentiation.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/90492.

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

MLA Handbook (7th Edition):

Kaylan, Kerim Berk. “Engineered microenvironments for studying liver progenitor differentiation.” 2016. Web. 22 Jul 2019.

Vancouver:

Kaylan KB. Engineered microenvironments for studying liver progenitor differentiation. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/90492.

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

Council of Science Editors:

Kaylan KB. Engineered microenvironments for studying liver progenitor differentiation. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90492

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

10. Hayman, Amanda Verienna. Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population.

Degree: M.P.H., 2006, Oregon Health Sciences University

Subjects/Keywords: Obesity; Fatty Liver  – epidemiology; Fibrosis  – epidemiology; Hepatitis C, Chronic  – complications

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APA (6th Edition):

Hayman, A. V. (2006). Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4PV6HM6 ; http://digitalcommons.ohsu.edu/etd/2897

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):

Hayman, Amanda Verienna. “Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population.” 2006. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4PV6HM6 ; http://digitalcommons.ohsu.edu/etd/2897.

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

MLA Handbook (7th Edition):

Hayman, Amanda Verienna. “Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population.” 2006. Web. 22 Jul 2019.

Vancouver:

Hayman AV. Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population. [Internet] [Thesis]. Oregon Health Sciences University; 2006. [cited 2019 Jul 22]. Available from: doi:10.6083/M4PV6HM6 ; http://digitalcommons.ohsu.edu/etd/2897.

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

Council of Science Editors:

Hayman AV. Effect of obesity on hepatic steatosis and fibrosis in a hepatitis-C infected population. [Thesis]. Oregon Health Sciences University; 2006. Available from: doi:10.6083/M4PV6HM6 ; http://digitalcommons.ohsu.edu/etd/2897

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

11. Zaman, Atif. Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis.

Degree: M.P.H., 2000, Oregon Health Sciences University

Subjects/Keywords: Liver Cirrhosis; Esophageal and Gastric Varices; Gastrointestinal Hemorrhage; Risk Factors

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APA (6th Edition):

Zaman, A. (2000). Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4QR4VD5 ; http://digitalcommons.ohsu.edu/etd/3308

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):

Zaman, Atif. “Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis.” 2000. Thesis, Oregon Health Sciences University. Accessed July 22, 2019. doi:10.6083/M4QR4VD5 ; http://digitalcommons.ohsu.edu/etd/3308.

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

MLA Handbook (7th Edition):

Zaman, Atif. “Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis.” 2000. Web. 22 Jul 2019.

Vancouver:

Zaman A. Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis. [Internet] [Thesis]. Oregon Health Sciences University; 2000. [cited 2019 Jul 22]. Available from: doi:10.6083/M4QR4VD5 ; http://digitalcommons.ohsu.edu/etd/3308.

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

Council of Science Editors:

Zaman A. Risk factors for the presence of varices in cirrhotic patients without a history of variceal hemorrage : thesis. [Thesis]. Oregon Health Sciences University; 2000. Available from: doi:10.6083/M4QR4VD5 ; http://digitalcommons.ohsu.edu/etd/3308

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


SUNY College at Brockport

12. Scarpulla, Richard Carl. Transfer RNA Associated with Rat Liver Plasma Membranes.

Degree: MS, Biology, 1974, SUNY College at Brockport

  Plasma membranes were isolated by differential and gradient centrifugation of rat liver homogenates. The isolation was monitored by assay of the plasma membrane marker… (more)

Subjects/Keywords: THESIS 171; Brockport Thesis Collection; Transfer RNA; cell membranes; liver cells; BTC; Biology

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APA (6th Edition):

Scarpulla, R. C. (1974). Transfer RNA Associated with Rat Liver Plasma Membranes. (Thesis). SUNY College at Brockport. Retrieved from https://digitalcommons.brockport.edu/env_theses/27

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):

Scarpulla, Richard Carl. “Transfer RNA Associated with Rat Liver Plasma Membranes.” 1974. Thesis, SUNY College at Brockport. Accessed July 22, 2019. https://digitalcommons.brockport.edu/env_theses/27.

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

MLA Handbook (7th Edition):

Scarpulla, Richard Carl. “Transfer RNA Associated with Rat Liver Plasma Membranes.” 1974. Web. 22 Jul 2019.

Vancouver:

Scarpulla RC. Transfer RNA Associated with Rat Liver Plasma Membranes. [Internet] [Thesis]. SUNY College at Brockport; 1974. [cited 2019 Jul 22]. Available from: https://digitalcommons.brockport.edu/env_theses/27.

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

Council of Science Editors:

Scarpulla RC. Transfer RNA Associated with Rat Liver Plasma Membranes. [Thesis]. SUNY College at Brockport; 1974. Available from: https://digitalcommons.brockport.edu/env_theses/27

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


Virginia Commonwealth University

13. Whitehill, Benjamin Cameron. Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation.

Degree: MS, Physiology, 2007, Virginia Commonwealth University

 Hepatitis C Virus (HCV) infection represents a worldwide pandemic and is currently the leading cause of cirrhosis and liver transplantation. After transplantation recurrence is almost… (more)

Subjects/Keywords: liver transplantation; OAS1; ISG15; IFNB1; interferon; hepatitis C virus; HCV; Life Sciences; Physiology

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APA (6th Edition):

Whitehill, B. C. (2007). Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1210

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):

Whitehill, Benjamin Cameron. “Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation.” 2007. Thesis, Virginia Commonwealth University. Accessed July 22, 2019. https://scholarscompass.vcu.edu/etd/1210.

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

MLA Handbook (7th Edition):

Whitehill, Benjamin Cameron. “Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation.” 2007. Web. 22 Jul 2019.

Vancouver:

Whitehill BC. Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation. [Internet] [Thesis]. Virginia Commonwealth University; 2007. [cited 2019 Jul 22]. Available from: https://scholarscompass.vcu.edu/etd/1210.

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

Council of Science Editors:

Whitehill BC. Genetic Variations in Interferon-Induced Genes and HCV Recurrence after Liver Transplantation. [Thesis]. Virginia Commonwealth University; 2007. Available from: https://scholarscompass.vcu.edu/etd/1210

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

14. Zhang, Xiyuan. A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats.

Degree: MS, 0037, 2011, University of Illinois – Urbana-Champaign

 Maternal high fat (HF) diet feeding is associated with increased risk of developing metabolism-related diseases in adult offspring, including chronic liver disease. The present study… (more)

Subjects/Keywords: Aging; Cancer; Oxidative stress; Non-alcoholic fatty liver disease; Lipid

…non-alcoholic fatty liver disease NEFA non-esterified fatty acid ng nanogram (s… …weanlings (Koukkou et al., 1998). Liver, as an important organ in regulating metabolism… …2009). Chronic liver diseases, like non-alcoholic fatty liver disease, can be induced in… …hypertension, hyperlipidemia, impaired insulin tolerance, fatty liver disease and other chronic… …5 and chronic liver diseases. It was reported that offspring from dams fed a diet high… 

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APA (6th Edition):

Zhang, X. (2011). A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24049

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):

Zhang, Xiyuan. “A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/24049.

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

MLA Handbook (7th Edition):

Zhang, Xiyuan. “A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats.” 2011. Web. 22 Jul 2019.

Vancouver:

Zhang X. A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/24049.

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

Council of Science Editors:

Zhang X. A maternal high fat diet represses the expression of antioxidant defense genes and induces the cellular senescence pathway in the liver of male offspring rats. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24049

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


California State University – San Bernardino

15. Hooks, Deborah Jane. The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning.

Degree: MSin Psychology, Psychology, 1993, California State University – San Bernardino

Subjects/Keywords: Learning in animals; Rats  – Training; Rats  – Physiology; Phenols  – Physiological effect; Liver function tests; Psychology

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APA (6th Edition):

Hooks, D. J. (1993). The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning. (Thesis). California State University – San Bernardino. Retrieved from http://scholarworks.lib.csusb.edu/etd-project/718

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):

Hooks, Deborah Jane. “The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning.” 1993. Thesis, California State University – San Bernardino. Accessed July 22, 2019. http://scholarworks.lib.csusb.edu/etd-project/718.

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

MLA Handbook (7th Edition):

Hooks, Deborah Jane. “The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning.” 1993. Web. 22 Jul 2019.

Vancouver:

Hooks DJ. The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning. [Internet] [Thesis]. California State University – San Bernardino; 1993. [cited 2019 Jul 22]. Available from: http://scholarworks.lib.csusb.edu/etd-project/718.

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

Council of Science Editors:

Hooks DJ. The effect of phenol denervation of the hepatic portal vein nerves on taste aversion learning. [Thesis]. California State University – San Bernardino; 1993. Available from: http://scholarworks.lib.csusb.edu/etd-project/718

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


Virginia Commonwealth University

16. Schwartz, Joseph D. The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004.

Degree: MPH, Epidemiology & Community Health, 2005, Virginia Commonwealth University

 Objective: Chronic disease comorbidities, on the rise in the U.S. and Virginia, represent a new challenge to the way medicine is practiced and prescribed. This… (more)

Subjects/Keywords: cerebrovascular degeneration; diabetes; liver; renal; aging; descriptive study; cardiovascular; Epidemiology; Medicine and Health Sciences; Public Health

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APA (6th Edition):

Schwartz, J. D. (2005). The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/894

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):

Schwartz, Joseph D. “The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004.” 2005. Thesis, Virginia Commonwealth University. Accessed July 22, 2019. https://scholarscompass.vcu.edu/etd/894.

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

MLA Handbook (7th Edition):

Schwartz, Joseph D. “The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004.” 2005. Web. 22 Jul 2019.

Vancouver:

Schwartz JD. The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004. [Internet] [Thesis]. Virginia Commonwealth University; 2005. [cited 2019 Jul 22]. Available from: https://scholarscompass.vcu.edu/etd/894.

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

Council of Science Editors:

Schwartz JD. The Prevalence of Comorbid Chronic Disease in Virginia's Adult Patient Population during the Years 2001 and 2004. [Thesis]. Virginia Commonwealth University; 2005. Available from: https://scholarscompass.vcu.edu/etd/894

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

17. Jones, Jennifer. Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age.

Degree: MS, 0002, 2013, University of Illinois – Urbana-Champaign

 A set of growth regulating genes has been identified that decline in expression in organs with age. This downregulation is thought to coordinate organ growth… (more)

Subjects/Keywords: Ezh2; Gpc3; Mdk; Mest; Mycn; Peg3; Plagl1; growth; gene expression; downregulation; muscle; heart; liver

…lung, kidney, liver, and heart of male C57BL/6 mice and Sprague Dawley rats through 8 weeks… …expression of Ezh2 and Mycn in mouse liver was downregulated more in embryonic stages than… …fetal mouse liver resulted in reduced proliferation. In contrast, Gpc3 knockdown resulted in… …of age observed in the promoter regions of Mdk, Peg3, and Plagl1 in the kidney, liver, and… …hepatocyte growth and liver regeneration (Liu et al., 2009). In hepatocytes, a reduction… 

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APA (6th Edition):

Jones, J. (2013). Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42308

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):

Jones, Jennifer. “Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age.” 2013. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/42308.

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

MLA Handbook (7th Edition):

Jones, Jennifer. “Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age.” 2013. Web. 22 Jul 2019.

Vancouver:

Jones J. Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/42308.

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

Council of Science Editors:

Jones J. Reductions in expression of growth regulating genes are observed in skeletal muscle and organs with age. [Thesis]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42308

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

18. Sulzberger, Saige. Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows.

Degree: MS, Animal Sciences, 2016, University of Illinois – Urbana-Champaign

 Oral supplementation of clay has been reported to function as buffer, an adsorbent, and aid in immune function. However, clays come in a variety of… (more)

Subjects/Keywords: Clay; Buffer; Acute and subacute ruminal acidosis (SARA); Aflatoxin; Liver; Gene Expression

…because the liver is a predominantly lipophilic organ, they increased risks of hepatocellular… …2014). For dairy cows, aflatoxins have been found to impair liver activity and suppress… …number of responses, but in the liver, they trigger the release of acute phase proteins such as… …Applegate. 2014. Growth, serum biochemistry, complement activity, and liver gene expression… 

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APA (6th Edition):

Sulzberger, S. (2016). Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95393

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):

Sulzberger, Saige. “Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/95393.

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

MLA Handbook (7th Edition):

Sulzberger, Saige. “Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows.” 2016. Web. 22 Jul 2019.

Vancouver:

Sulzberger S. Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/95393.

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

Council of Science Editors:

Sulzberger S. Effects of clay supplementation on rumen environment, metabolism, inflammation, and performance in dairy cows. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95393

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

19. Blackmore, Katherine Anne. Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism.

Degree: MS, Animal Sciences, 2016, University of Illinois – Urbana-Champaign

 Obesity is the leading cause of preventable chronic disease, such as diabetes, heart disease and cancer. The most significant factor driving obesity and the development… (more)

Subjects/Keywords: Stem cell; Crypt; Food intake; Symmetric division; Liver Kinase B; AMP kinase pathway

…Physiology. Gastrointestinal and Liver Physiology 302.10 (2012): G1111-32. Print. 42. Van… …adaptational growth of several tissues, including bone, skin, adipose, liver and the small intestinal… 

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APA (6th Edition):

Blackmore, K. A. (2016). Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92752

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):

Blackmore, Katherine Anne. “Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/92752.

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

MLA Handbook (7th Edition):

Blackmore, Katherine Anne. “Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism.” 2016. Web. 22 Jul 2019.

Vancouver:

Blackmore KA. Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/92752.

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

Council of Science Editors:

Blackmore KA. Nutritional status dictates the rate and mode of intestinal epithelial stem cell proliferation through an AMPK dependent mechanism. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92752

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


California State University – San Bernardino

20. Wardak, Mohammad Alif. Survival analysis.

Degree: MAin Mathematics, Mathematics, 2005, California State University – San Bernardino

 Survival analysis pertains to a statistical approach designed to take into account the amount of time an experimental unit contributes to a study. A Mayo… (more)

Subjects/Keywords: Survival analysis (Biometry); Multivariate analysis; Analysis of variance; Mathematical analysis; Liver Cirrhosis Research; Analysis of variance; Mathematical analysis; Multivariate analysis; Survival analysis (Biometry); Mathematics

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APA (6th Edition):

Wardak, M. A. (2005). Survival analysis. (Thesis). California State University – San Bernardino. Retrieved from https://scholarworks.lib.csusb.edu/etd-project/2810

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):

Wardak, Mohammad Alif. “Survival analysis.” 2005. Thesis, California State University – San Bernardino. Accessed July 22, 2019. https://scholarworks.lib.csusb.edu/etd-project/2810.

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

MLA Handbook (7th Edition):

Wardak, Mohammad Alif. “Survival analysis.” 2005. Web. 22 Jul 2019.

Vancouver:

Wardak MA. Survival analysis. [Internet] [Thesis]. California State University – San Bernardino; 2005. [cited 2019 Jul 22]. Available from: https://scholarworks.lib.csusb.edu/etd-project/2810.

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

Council of Science Editors:

Wardak MA. Survival analysis. [Thesis]. California State University – San Bernardino; 2005. Available from: https://scholarworks.lib.csusb.edu/etd-project/2810

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

21. Ceddia, Ryan Patrick. Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid.

Degree: MS, Animal Science, 2008, North Carolina State University

 Obesity is rapidly becoming a major problem in the United States and throughout the world. Polygenic models of obesity are most similar to human obesity… (more)

Subjects/Keywords: Fatty Acid; Obesity; Mice; Adipose; Real-Time RT-PCR; Body Size; Conjugated Linoleic Acid; CLA; Epididymal Fat; Liver; Breeding; Gene Expression; <; I>; Mus musculus<; /I>;

…10, CIS-12-CONJUGATED LINOLEIC ACID REGULATION OF GENE EXPRESSION IN THE LIVER OF A… …Histology ….116 Fatty Acid Composition of Liver 117… …2.4 Liver Microarray Results ...102 Table 2.5 Real-Time RT-PCR Results… …Composition of Liver Tissue from Mice Fed LA or CLA …...131 Table 3.3 Microarray and Real-time RT… …biosynthesis in the liver of these mice (151). These mice have a QTL, a region of DNA that… 

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APA (6th Edition):

Ceddia, R. P. (2008). Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/944

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):

Ceddia, Ryan Patrick. “Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid.” 2008. Thesis, North Carolina State University. Accessed July 22, 2019. http://www.lib.ncsu.edu/resolver/1840.16/944.

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

MLA Handbook (7th Edition):

Ceddia, Ryan Patrick. “Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid.” 2008. Web. 22 Jul 2019.

Vancouver:

Ceddia RP. Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid. [Internet] [Thesis]. North Carolina State University; 2008. [cited 2019 Jul 22]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/944.

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

Council of Science Editors:

Ceddia RP. Genomic Characterization of Two Models of Obesity in Mice: Divergent Selection for Epididymal Fat and the Effects of trans-10, cis-12-Conjugated Linoleic Acid. [Thesis]. North Carolina State University; 2008. Available from: http://www.lib.ncsu.edu/resolver/1840.16/944

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

.