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You searched for subject:(cholesterol synthesis). Showing records 1 – 22 of 22 total matches.

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University of British Columbia

1. Dendy, Shauneen Marguerite. Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals.

Degree: MS- MSc, Human Nutrition, 1990, University of British Columbia

 The purpose of this study was to investigate whether increased endogenous cholesterol synthesis contributes to the elevated plasma cholesterol levels observed in type III hyperlipoproteinemia… (more)

Subjects/Keywords: Cholesterol  – Synthesis; Hyperlipoproteinemia; Cholesterol  – biosynthesis

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APA (6th Edition):

Dendy, S. M. (1990). Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals. (Masters Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/28979

Chicago Manual of Style (16th Edition):

Dendy, Shauneen Marguerite. “Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals.” 1990. Masters Thesis, University of British Columbia. Accessed April 15, 2021. http://hdl.handle.net/2429/28979.

MLA Handbook (7th Edition):

Dendy, Shauneen Marguerite. “Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals.” 1990. Web. 15 Apr 2021.

Vancouver:

Dendy SM. Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals. [Internet] [Masters thesis]. University of British Columbia; 1990. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2429/28979.

Council of Science Editors:

Dendy SM. Cholesterol synthesis in type III hyperlipoproteinemic and non-hyperlipidemic individuals. [Masters Thesis]. University of British Columbia; 1990. Available from: http://hdl.handle.net/2429/28979


University of British Columbia

2. Kroeger, Steven Hugh. The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats.

Degree: MS- MSc, Human Nutrition, 1984, University of British Columbia

 This study was performed to determine the rates of in vitro cholesterol synthesis, as measured by ³H incorporation into cholesterol, in gluteal white adipose tissue… (more)

Subjects/Keywords: Cholesterol - Synthesis; Cholesterol - biosynthesis

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APA (6th Edition):

Kroeger, S. H. (1984). The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats. (Masters Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/24834

Chicago Manual of Style (16th Edition):

Kroeger, Steven Hugh. “The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats.” 1984. Masters Thesis, University of British Columbia. Accessed April 15, 2021. http://hdl.handle.net/2429/24834.

MLA Handbook (7th Edition):

Kroeger, Steven Hugh. “The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats.” 1984. Web. 15 Apr 2021.

Vancouver:

Kroeger SH. The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats. [Internet] [Masters thesis]. University of British Columbia; 1984. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2429/24834.

Council of Science Editors:

Kroeger SH. The effect of litter size on the developmental pattern of cholesterol synthesis in intestinal and white adipose tissue of neonatal rats. [Masters Thesis]. University of British Columbia; 1984. Available from: http://hdl.handle.net/2429/24834


University of New South Wales

3. Chua, Ngee Kiat. Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis.

Degree: UNSW, 2020, University of New South Wales

Cholesterol is an essential lipid associated with many important biological functions. At both the cellular and physiological levels, cholesterol is acquired through two main sources.… (more)

Subjects/Keywords: Degron; Cholesterol; Cholesterol synthesis; Endoplasmic reticulum-associated degradation (ERAD); Protein degradation; Squalene monooxygenase; Ubiquitin

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APA (6th Edition):

Chua, N. K. (2020). Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/65592 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:65027/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Chua, Ngee Kiat. “Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis.” 2020. Doctoral Dissertation, University of New South Wales. Accessed April 15, 2021. http://handle.unsw.edu.au/1959.4/65592 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:65027/SOURCE02?view=true.

MLA Handbook (7th Edition):

Chua, Ngee Kiat. “Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis.” 2020. Web. 15 Apr 2021.

Vancouver:

Chua NK. Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis. [Internet] [Doctoral dissertation]. University of New South Wales; 2020. [cited 2021 Apr 15]. Available from: http://handle.unsw.edu.au/1959.4/65592 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:65027/SOURCE02?view=true.

Council of Science Editors:

Chua NK. Degron features of the regulatory domain of squalene monooxygenase - a rate limiting enzyme in cholesterol synthesis. [Doctoral Dissertation]. University of New South Wales; 2020. Available from: http://handle.unsw.edu.au/1959.4/65592 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:65027/SOURCE02?view=true


University of Manitoba

4. Wang, Yanan. Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans.

Degree: Human Nutritional Sciences, 2015, University of Manitoba

 The cholesterol-lowering effect of mixed linkage (1→3) (1→4)-β-D-glucans (β-glucan) from barley has been documented, yet the underlying mechanism responsible for this action and factors influencing… (more)

Subjects/Keywords: β-glucan; molecular weight; viscosity; cholesterol; CYP7A1; bile acid; mechanism; microbiota; cardiovascular disease; cholesterol absorption; cholesterol synthesis

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APA (6th Edition):

Wang, Y. (2015). Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31048

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):

Wang, Yanan. “Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans.” 2015. Thesis, University of Manitoba. Accessed April 15, 2021. http://hdl.handle.net/1993/31048.

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

MLA Handbook (7th Edition):

Wang, Yanan. “Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans.” 2015. Web. 15 Apr 2021.

Vancouver:

Wang Y. Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans. [Internet] [Thesis]. University of Manitoba; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1993/31048.

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

Council of Science Editors:

Wang Y. Effect of β-glucan molecular weight and viscosity on the mechanism of cholesterol lowering in humans. [Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/31048

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


University of Alberta

5. Lambert, Jennifer E. Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention.

Degree: PhD, Department of Agricultural, Food, and Nutritional Science, 2011, University of Alberta

 Elevated plasma lipids are risk factors for cardiovascular disease (CVD). In certain conditions plasma lipids are normal yet individuals experience increased morbidity. Type 1 diabetes… (more)

Subjects/Keywords: Transplant; Diet; Type 1 diabetes; Deuterium; Cholesterol synthesis; Liver; Lipogenesis

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APA (6th Edition):

Lambert, J. E. (2011). Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/xw42n7888

Chicago Manual of Style (16th Edition):

Lambert, Jennifer E. “Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention.” 2011. Doctoral Dissertation, University of Alberta. Accessed April 15, 2021. https://era.library.ualberta.ca/files/xw42n7888.

MLA Handbook (7th Edition):

Lambert, Jennifer E. “Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention.” 2011. Web. 15 Apr 2021.

Vancouver:

Lambert JE. Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2021 Apr 15]. Available from: https://era.library.ualberta.ca/files/xw42n7888.

Council of Science Editors:

Lambert JE. Investigation of fatty acid and cholesterol synthesis using stable isotopes in type 1 diabetes, liver failure, islet and liver transplant, and effect of dietary intervention. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/xw42n7888


University of Cambridge

6. Dickson, Anna. Regulation of Protein Degradation at the Endoplasmic Reticulum.

Degree: PhD, 2020, University of Cambridge

 Endoplasmic reticulum (ER) associated degradation (ERAD) is important for removing damaged or misfolded proteins at the ER membrane, and is central to the physiological regulation… (more)

Subjects/Keywords: Endoplasmic reticulum; protein degradation; Cholesterol synthesis; Hypoxia; CRISPR Cas9 genetic screens

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APA (6th Edition):

Dickson, A. (2020). Regulation of Protein Degradation at the Endoplasmic Reticulum. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/312261

Chicago Manual of Style (16th Edition):

Dickson, Anna. “Regulation of Protein Degradation at the Endoplasmic Reticulum.” 2020. Doctoral Dissertation, University of Cambridge. Accessed April 15, 2021. https://www.repository.cam.ac.uk/handle/1810/312261.

MLA Handbook (7th Edition):

Dickson, Anna. “Regulation of Protein Degradation at the Endoplasmic Reticulum.” 2020. Web. 15 Apr 2021.

Vancouver:

Dickson A. Regulation of Protein Degradation at the Endoplasmic Reticulum. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Apr 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/312261.

Council of Science Editors:

Dickson A. Regulation of Protein Degradation at the Endoplasmic Reticulum. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/312261


University of British Columbia

7. Mazier, Marie Jeanne Patricia. Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men.

Degree: PhD, Human Nutrition, 1994, University of British Columbia

 To examine the effect of diet fat type on rates of cholesterol synthesis and esterification during feeding and fasting, nine healthy male subjects were fed… (more)

Subjects/Keywords: Fat  – Physiological effect; Cholesterol  – Synthesis; Cholesterol  – Metabolism

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APA (6th Edition):

Mazier, M. J. P. (1994). Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men. (Doctoral Dissertation). University of British Columbia. Retrieved from http://hdl.handle.net/2429/8877

Chicago Manual of Style (16th Edition):

Mazier, Marie Jeanne Patricia. “Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men.” 1994. Doctoral Dissertation, University of British Columbia. Accessed April 15, 2021. http://hdl.handle.net/2429/8877.

MLA Handbook (7th Edition):

Mazier, Marie Jeanne Patricia. “Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men.” 1994. Web. 15 Apr 2021.

Vancouver:

Mazier MJP. Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men. [Internet] [Doctoral dissertation]. University of British Columbia; 1994. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2429/8877.

Council of Science Editors:

Mazier MJP. Influence of diet fat saturation on rates of cholesterol synthesis and esterification in healthy young men. [Doctoral Dissertation]. University of British Columbia; 1994. Available from: http://hdl.handle.net/2429/8877


East Carolina University

8. Wercholuk, Ashley N. Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp.

Degree: MS, Chemistry, 2014, East Carolina University

 Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB) disease, is the leading cause of death due to bacterial infection worldwide, claiming nearly two million… (more)

Subjects/Keywords: Chemistry, Biochemistry; Chemistry, Organic; Microbiology; Cholesterol – metabolism; Fluorescence; M. smegmatis; Naphthalimide; Synthesis; Biology, Microbiology; Organic chemistry; Biochemistry; Mycobacterium tuberculosis; Cholesterol

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APA (6th Edition):

Wercholuk, A. N. (2014). Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4528

Chicago Manual of Style (16th Edition):

Wercholuk, Ashley N. “Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp.” 2014. Masters Thesis, East Carolina University. Accessed April 15, 2021. http://hdl.handle.net/10342/4528.

MLA Handbook (7th Edition):

Wercholuk, Ashley N. “Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp.” 2014. Web. 15 Apr 2021.

Vancouver:

Wercholuk AN. Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp. [Internet] [Masters thesis]. East Carolina University; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10342/4528.

Council of Science Editors:

Wercholuk AN. Elucidating "Consumption" : Using Fluorescent Steroid Probes to Understand Host Cholesterol Utilization by Mycobacterium spp. [Masters Thesis]. East Carolina University; 2014. Available from: http://hdl.handle.net/10342/4528


University of Manitoba

9. Mintarno, Melinda. Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals.

Degree: Human Nutritional Sciences, 2011, University of Manitoba

 Global obesity is linked to chronic diseases including hypercholesterolemia, a cardiovascular disease risk factor, thus weight reduction in obesity is a key priority for combatting… (more)

Subjects/Keywords: weight loss; BMI; DEXA; body composition; fat mass; fat free mass; cholesterol absorption; cholesterol synthesis; HDL-C; LDL-C; total cholesterol; triglyceride; SNP; NPC1L1; ABCG5; ABCG8; diet; physical activity

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APA (6th Edition):

Mintarno, M. (2011). Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4506

Chicago Manual of Style (16th Edition):

Mintarno, Melinda. “Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals.” 2011. Masters Thesis, University of Manitoba. Accessed April 15, 2021. http://hdl.handle.net/1993/4506.

MLA Handbook (7th Edition):

Mintarno, Melinda. “Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals.” 2011. Web. 15 Apr 2021.

Vancouver:

Mintarno M. Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals. [Internet] [Masters thesis]. University of Manitoba; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1993/4506.

Council of Science Editors:

Mintarno M. Effects of weight loss and phenotype traits on changes in body composition and cholesterol metabolism in overweight individuals. [Masters Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4506


Texas Tech University

10. King, Steven Robert. Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein.

Degree: Accounting and Information Systems, 1998, Texas Tech University

 While the first step in the production of steroid hormones in the body is the conversion of cholesterol to pregnenolone by the cholesterol side-chain cleavage… (more)

Subjects/Keywords: Cholesterol  – Synthesis; Proteins; Steroid hormones  – Synthesis; Cholesterol  – Metabolism; Mitochondrial membranes

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APA (6th Edition):

King, S. R. (1998). Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/22254

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):

King, Steven Robert. “Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein.” 1998. Thesis, Texas Tech University. Accessed April 15, 2021. http://hdl.handle.net/2346/22254.

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

MLA Handbook (7th Edition):

King, Steven Robert. “Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein.” 1998. Web. 15 Apr 2021.

Vancouver:

King SR. Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein. [Internet] [Thesis]. Texas Tech University; 1998. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2346/22254.

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

Council of Science Editors:

King SR. Biochemical Characterizations of the Steroidogenic Acute Regulatory (StAR) Protein. [Thesis]. Texas Tech University; 1998. Available from: http://hdl.handle.net/2346/22254

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

11. Alam, Mohd. Gulfam. Synthesis and characterization of some cholesterol derivatives;.

Degree: Chemistry, 2008, Aligarh Muslim University

Abstract not available newline newline

Summary p.i-viii

Advisors/Committee Members: Shams-uz-Zaman.

Subjects/Keywords: Synthesis; Cholesterol; Derivatives; 1; 3; 4-thiazolidinones; Steroidal

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APA (6th Edition):

Alam, M. G. (2008). Synthesis and characterization of some cholesterol derivatives;. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/53151

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):

Alam, Mohd Gulfam. “Synthesis and characterization of some cholesterol derivatives;.” 2008. Thesis, Aligarh Muslim University. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/53151.

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

MLA Handbook (7th Edition):

Alam, Mohd Gulfam. “Synthesis and characterization of some cholesterol derivatives;.” 2008. Web. 15 Apr 2021.

Vancouver:

Alam MG. Synthesis and characterization of some cholesterol derivatives;. [Internet] [Thesis]. Aligarh Muslim University; 2008. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53151.

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

Council of Science Editors:

Alam MG. Synthesis and characterization of some cholesterol derivatives;. [Thesis]. Aligarh Muslim University; 2008. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53151

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


Indian Institute of Science

12. Biswas, Joydeep. Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

 The thesis entitled “Novel Cationic Gemini Lipids, Click Chemistry Based Adducts and Amphiphile-Capped Silver Nanostructures: Synthesis, Aggregation and Biological Properties” elucidates the design, synthesis, aggregation… (more)

Subjects/Keywords: Gemini Lipids; Amphiphile Silver Nanostructures; Gemini Cationic Lipids - Synthesis; Cationic Liposomes - Synthesis; Cholesterol-Based Cationic Lipids; Cholesterol-Based Gemini Lipids; Cationic Pseudoglyceryl Gemini Lipids; Click Chemistry; Silver Nanoparticle Loaded Liposomes; Gemini Cationic Surfactants; Ag-Nanorods; Cholesterol Based System; Ag-Nanoparticles; Biochemistry

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APA (6th Edition):

Biswas, J. (2013). Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/1894

Chicago Manual of Style (16th Edition):

Biswas, Joydeep. “Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed April 15, 2021. http://etd.iisc.ac.in/handle/2005/1894.

MLA Handbook (7th Edition):

Biswas, Joydeep. “Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties.” 2013. Web. 15 Apr 2021.

Vancouver:

Biswas J. Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2021 Apr 15]. Available from: http://etd.iisc.ac.in/handle/2005/1894.

Council of Science Editors:

Biswas J. Novel Cationic Gemini Lipids, Click Chemistry Based Adducts And Amphiphile-Capped Silver Nanostructures : Synthesis, Aggregation And Biological Properties. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/1894


Univerzitet u Beogradu

13. Vladimirov, Sandra, 1987-, 34229607. Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom.

Degree: Farmaceutski fakultet, 2020, Univerzitet u Beogradu

Medicinske nauke - Farmacija - Medicinska biohemija / Medical sciences - Pharmacy - Medical biochemistry

Kolorektalni karcinom (CRC) je maligno oboljenje sa visokom prevalencijom u… (more)

Subjects/Keywords: colorectal cancer; non-cholesterol sterols in serum and HDL fraction; changes in cholesterol synthesis and absorption; vitamin D metabolites; independent predictors of colorectal cancer

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APA (6th Edition):

Vladimirov, Sandra, 1987-, 3. (2020). Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:21578/bdef:Content/get

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):

Vladimirov, Sandra, 1987-, 34229607. “Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom.” 2020. Thesis, Univerzitet u Beogradu. Accessed April 15, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:21578/bdef:Content/get.

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

MLA Handbook (7th Edition):

Vladimirov, Sandra, 1987-, 34229607. “Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom.” 2020. Web. 15 Apr 2021.

Vancouver:

Vladimirov, Sandra, 1987- 3. Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom. [Internet] [Thesis]. Univerzitet u Beogradu; 2020. [cited 2021 Apr 15]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:21578/bdef:Content/get.

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

Council of Science Editors:

Vladimirov, Sandra, 1987- 3. Ispitivanje biomarkera homeostaze holesterola i metabolizma vitamina D kod pacijenata sa kolorektalnim karcinomom. [Thesis]. Univerzitet u Beogradu; 2020. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:21578/bdef:Content/get

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


University of Cincinnati

14. SCHMID, KARA E. ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT.

Degree: PhD, Medicine : Pathobiology and Molecular Medicine, 2003, University of Cincinnati

Cholesterol is essential for proper fetal development. Defects in fetal cholesterol metabolism can cause developmental abnormalities, including mental retardation and stunted growth as demonstrated by… (more)

Subjects/Keywords: Biophysics, Medical; fetal cholesterol metabolism; placental transport; cholesterol synthesis; Smith-Lemli-Optiz

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APA (6th Edition):

SCHMID, K. E. (2003). ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1061304521

Chicago Manual of Style (16th Edition):

SCHMID, KARA E. “ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT.” 2003. Doctoral Dissertation, University of Cincinnati. Accessed April 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1061304521.

MLA Handbook (7th Edition):

SCHMID, KARA E. “ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT.” 2003. Web. 15 Apr 2021.

Vancouver:

SCHMID KE. ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT. [Internet] [Doctoral dissertation]. University of Cincinnati; 2003. [cited 2021 Apr 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1061304521.

Council of Science Editors:

SCHMID KE. ENDOGENOUS AND EXOGENOUS SOURCES OF CHOLESTEROL DURING FETAL DEVELOPMENT. [Doctoral Dissertation]. University of Cincinnati; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1061304521


McMaster University

15. Zhang, Jing. Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide).

Degree: MSc, 1999, McMaster University

Poly(N-isopropylacrylamides) and copolymers of N-(isopropylacrylamide) and N(tetrahydrofurfurylacrylamide) bearing cholesterol substituents were prepared and their solution properties in water and in methanol were studied by… (more)

Subjects/Keywords: synthesis; solution properties; cholesterol; methanol; chemistry; spectroscopy

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APA (6th Edition):

Zhang, J. (1999). Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide). (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/19281

Chicago Manual of Style (16th Edition):

Zhang, Jing. “Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide).” 1999. Masters Thesis, McMaster University. Accessed April 15, 2021. http://hdl.handle.net/11375/19281.

MLA Handbook (7th Edition):

Zhang, Jing. “Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide).” 1999. Web. 15 Apr 2021.

Vancouver:

Zhang J. Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide). [Internet] [Masters thesis]. McMaster University; 1999. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11375/19281.

Council of Science Editors:

Zhang J. Synthesis, Characterization and Solution Properties of Cholesterol Substituted Poly(N-isopropylacrylamide). [Masters Thesis]. McMaster University; 1999. Available from: http://hdl.handle.net/11375/19281


George Mason University

16. Khan, Hameed A. Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia .

Degree: 2013, George Mason University

 Cardiovascular disease (CVD) is ranked as the number one cause of mortality and morbidity worldwide. High blood cholesterol is the number one risk factor for… (more)

Subjects/Keywords: variation to statins response; HMGCR isoforms and hypercholesterolemia; Duet Vectors for co-expression; Screeing for HMGCR inhibitors; Regulating cholesterol synthesis; Use of Cobalt Column for Bioprospecting

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APA (6th Edition):

Khan, H. A. (2013). Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8007

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):

Khan, Hameed A. “Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia .” 2013. Thesis, George Mason University. Accessed April 15, 2021. http://hdl.handle.net/1920/8007.

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

MLA Handbook (7th Edition):

Khan, Hameed A. “Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia .” 2013. Web. 15 Apr 2021.

Vancouver:

Khan HA. Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia . [Internet] [Thesis]. George Mason University; 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1920/8007.

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

Council of Science Editors:

Khan HA. Variation in Interpersonal Response to Statin Drugs in Hypercholesterolemia . [Thesis]. George Mason University; 2013. Available from: http://hdl.handle.net/1920/8007

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


University of Gothenburg / Göteborgs Universitet

17. Friberg, Anders. Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor.

Degree: 2009, University of Gothenburg / Göteborgs Universitet

 Ovarian follicle atresia caused by granulosa cell apoptosis is a central process in normal female physiology. Progesterone has been reported to be a survival factor… (more)

Subjects/Keywords: ovary; granulosa cells; ovulation; luteinization; progesterone; apoptosis; cholesterol synthesis; isoprenylation

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APA (6th Edition):

Friberg, A. (2009). Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/19404

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):

Friberg, Anders. “Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor.” 2009. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed April 15, 2021. http://hdl.handle.net/2077/19404.

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

MLA Handbook (7th Edition):

Friberg, Anders. “Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor.” 2009. Web. 15 Apr 2021.

Vancouver:

Friberg A. Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2009. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2077/19404.

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

Council of Science Editors:

Friberg A. Granulosa cell apoptosis: Transcriptional regulation by the nuclear progesterone receptor. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2009. Available from: http://hdl.handle.net/2077/19404

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


University of Kentucky

18. Mokashi, Vishwesh. SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE.

Degree: 2004, University of Kentucky

 Supernatant protein factor (SPF) is a 46-kDa cytosolic protein that stimulates squalene monooxygenase, which catalyses the second committed step in cholesterol biosynthesis. The mechanism by… (more)

Subjects/Keywords: Supernatant protein factor; cholesterol synthesis; squalene monooxygenase; phosphorylation; protein kinase A

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APA (6th Edition):

Mokashi, V. (2004). SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/gradschool_diss/469

Chicago Manual of Style (16th Edition):

Mokashi, Vishwesh. “SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE.” 2004. Doctoral Dissertation, University of Kentucky. Accessed April 15, 2021. https://uknowledge.uky.edu/gradschool_diss/469.

MLA Handbook (7th Edition):

Mokashi, Vishwesh. “SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE.” 2004. Web. 15 Apr 2021.

Vancouver:

Mokashi V. SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE. [Internet] [Doctoral dissertation]. University of Kentucky; 2004. [cited 2021 Apr 15]. Available from: https://uknowledge.uky.edu/gradschool_diss/469.

Council of Science Editors:

Mokashi V. SUPERNATANT PROTEIN FACTOR: INSIGHTS INTO ITS REGULATION AND ABILITY TO STIMULATE CHOLESTEROL SYNTHESIS IN VITRO AND IN CELL CULTURE. [Doctoral Dissertation]. University of Kentucky; 2004. Available from: https://uknowledge.uky.edu/gradschool_diss/469


Miami University

19. Ghimire, Harishchandra. Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques.

Degree: PhD, Chemistry, 2010, Miami University

 EPR spectroscopic techniques provide powerful methods to study the structural dynamics, topology, and distance measurements of peptides/proteins in membranes and solutions. Cholesterol containing bicelles were… (more)

Subjects/Keywords: Analytical Chemistry; Biochemistry; Biophysics; Chemistry; SDSL; TOAC spin labeling; EPR spectroscopy; DEER spectroscopy; X-band and Q-band EPR; Solid Phase Peptide Synthesis; Fmoc-TOAC Synthesis; Optimizing Solid Phase Peptide Synthesis for TOAC labeling; HPLC; Membrane Alignment; Cholesterol Bicelle Study

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APA (6th Edition):

Ghimire, H. (2010). Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1291739688

Chicago Manual of Style (16th Edition):

Ghimire, Harishchandra. “Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques.” 2010. Doctoral Dissertation, Miami University. Accessed April 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1291739688.

MLA Handbook (7th Edition):

Ghimire, Harishchandra. “Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques.” 2010. Web. 15 Apr 2021.

Vancouver:

Ghimire H. Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques. [Internet] [Doctoral dissertation]. Miami University; 2010. [cited 2021 Apr 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1291739688.

Council of Science Editors:

Ghimire H. Structure, Dynamics, and Distance Measurements in Membrane Proteins and Peptides using EPR Spectroscopic Techniques. [Doctoral Dissertation]. Miami University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1291739688

20. Penque, Brent A. Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Excess caloric intake and/or obesity currently remain the largest predisposing risk factors for the development of type 2 diabetes. Discerning… (more)

Subjects/Keywords: Chromium  – Therapeutic use  – Research; Hexosamines  – Synthesis; Amino sugars; Diabetes  – Pathophysiology; Obesity; Insulin resistance  – Physiological effect; Biosynthesis; Adipose tissues  – Pathophysiology; Glucosamine; Cholesterol  – Metabolism; Actin; Cardiovascular system  – Diseases; Lipid membranes  – Metabolism  – Research

…45 II.A. Increased HBP Activity Provokes Cholesterol Synthesis, Cytoskeletal Dysfunction… …activation of cholesterol synthesis impairs glucose and cholesterol transport. I will further… …Improves Cellular Cholesterol Efflux, ABCA1 Functionality, and Rab8 Cycling Rendered Defective by… …Hyperinsulinemia in Adipocytes .... 65 II.C. Chromium Protects Against Hexosamine-Induced Cholesterol… …cholesterol acyltransferase LDL Low density lipoprotein LF Low fat LKB1 Liver kinase B1 LMWCr… 

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APA (6th Edition):

Penque, B. A. (2014). Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/3805

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):

Penque, Brent A. “Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium.” 2014. Thesis, IUPUI. Accessed April 15, 2021. http://hdl.handle.net/1805/3805.

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

MLA Handbook (7th Edition):

Penque, Brent A. “Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium.” 2014. Web. 15 Apr 2021.

Vancouver:

Penque BA. Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium. [Internet] [Thesis]. IUPUI; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1805/3805.

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

Council of Science Editors:

Penque BA. Mechanisms of hexosamine-induced cholesterol accumulation and therapeutic actions of chromium. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/3805

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


Penn State University

21. Boonyarattanakalin, Siwarutt. SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS.

Degree: 2008, Penn State University

 Receptors on the surface of mammalian cells function as sensors and mediators of uptake of specific ligands in the extracellular environment. These biomolecules reside on… (more)

Subjects/Keywords: chemistry; synthetic organic; synthesis; organic; bioorganic; medicinal; chemical biology; biological chemistry; synthetic receptors; receptors; delivery; drug delivery; fluorescence; fluorescent; probes; cellular probes; cellular surface; protein uptake; synthetic receptor targeting; endocytosis; lipid rafts; fluorescent probes; his tag; receptor-mediated endocytosis; vancomycin; IgG; Fc; Pennsylvania Green; lipid bilayers; biomolecules; cholesterylamine; cholesterol; steroids; 3ƒÒ-cholesterylamine; endosomes; lysosomes; listeria; mimicking; mimic; design and synthesis; antibody; antibodies

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APA (6th Edition):

Boonyarattanakalin, S. (2008). SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6960

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):

Boonyarattanakalin, Siwarutt. “SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS.” 2008. Thesis, Penn State University. Accessed April 15, 2021. https://submit-etda.libraries.psu.edu/catalog/6960.

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

MLA Handbook (7th Edition):

Boonyarattanakalin, Siwarutt. “SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS.” 2008. Web. 15 Apr 2021.

Vancouver:

Boonyarattanakalin S. SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS. [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 15]. Available from: https://submit-etda.libraries.psu.edu/catalog/6960.

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

Council of Science Editors:

Boonyarattanakalin S. SYNTHETIC MIMICS OF MAMMALIAN CELL SURFACE RECEPTORS. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6960

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

22. Kamani, Mustafa. Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism.

Degree: 2013, University of Toronto

Glycosphingolipid (GSL) metabolism is a complex process involving proteins and enzymes at distinct locations within the cell. Mammalian GSLs are typically based on glucose or… (more)

Subjects/Keywords: Sphingolipids; Metabolism; Lysosomal storage disorders; adamantane; Glucosylceramide; Lactosylceramide; P-glycoprotein; MDR1; Gaucher disease; Fabry disease; siRNA; Gb2 galabiosylceramide; Glycolipids; Inhibitors; Knockout mouse; Crossbreeding; Glucosylceramide synthase; Lactosylceramide synthase; Ganglioside; Globo-series; Gb3 synthase; pharmacological chaperone; Glucocerebrosidase; Substrate reduction therapy; ATP8B1; Cholesterol; ABC transporters; P-type ATPase; Flippase; FAPP2; GLTP; Glycosyltransferase; Glycolipid analogues; ERAD; ABCB1; knockdown; GM3 and EGFR; GM3 and insulin receptor; Glycolipid synthesis; Glycolipid metabolism; enzyme enhancement therapy; 0487; 0307; 0491; 0379; 0306

…95 3.3.2 Adamantyl glycosphingolipid synthesis… …104 3.4.1 AdaGSL synthesis… …114 3.4.7 AdaGalCer prevents Gb3 synthesis in Fabry disease (FD) cells… …120 3.5.1 AdaGalCer selectively inhibits globo-series GSL synthesis in normal and Fabry… …120 3.5.2 AdaGlcCer both stimulates and inhibits GSL synthesis… 

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

APA (6th Edition):

Kamani, M. (2013). Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35860

Chicago Manual of Style (16th Edition):

Kamani, Mustafa. “Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism.” 2013. Doctoral Dissertation, University of Toronto. Accessed April 15, 2021. http://hdl.handle.net/1807/35860.

MLA Handbook (7th Edition):

Kamani, Mustafa. “Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism.” 2013. Web. 15 Apr 2021.

Vancouver:

Kamani M. Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1807/35860.

Council of Science Editors:

Kamani M. Novel Intrinsic and Extrinsic Approaches to Selectively Regulate Glycosphingolipid Metabolism. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35860

.