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University: McGill University

You searched for subject:( GTPase Activating Proteins metabolism 60). Showing records 1 – 30 of 422 total matches.

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McGill University

1. Kalantari, Fariba. A cellular and molecular approach to investigate pathological calcification in liver.

Degree: PhD, Department of Anatomy and Cell Biology., 2008, McGill University

The liver is a vital organ, playing numerous critical roles in the body. The liver's ability to perform essential functions is disturbed by injuries that… (more)

Subjects/Keywords: Calcinosis  – etiology.; Liver Diseases  – pathology.; Liver Transplantation  – pathology.; ras GTPase-Activating Proteins  – metabolism.

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APA (6th Edition):

Kalantari, F. (2008). A cellular and molecular approach to investigate pathological calcification in liver. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111907.pdf

Chicago Manual of Style (16th Edition):

Kalantari, Fariba. “A cellular and molecular approach to investigate pathological calcification in liver.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111907.pdf.

MLA Handbook (7th Edition):

Kalantari, Fariba. “A cellular and molecular approach to investigate pathological calcification in liver.” 2008. Web. 12 Nov 2019.

Vancouver:

Kalantari F. A cellular and molecular approach to investigate pathological calcification in liver. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111907.pdf.

Council of Science Editors:

Kalantari F. A cellular and molecular approach to investigate pathological calcification in liver. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111907.pdf


McGill University

2. Danek, Eric Ian. Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42.

Degree: PhD, Department of Anatomy and Cell Biology., 2008, McGill University

 The Rho GTPases form a diverse family of proteins which regulates numerous cell processes from cytoskeletal reorganization to control of gene expression. They are negatively… (more)

Subjects/Keywords: GTPase-Activating Proteins  – metabolism.; Mitogen-Activated Protein Kinase 3  – metabolism.; Glycogen Synthase Kinase 3  – metabolism.; Phosphorylation.; rac1 GTP-Binding Protein  – metabolism.; cdc42 GTP-Binding Protein  – metabolism.

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APA (6th Edition):

Danek, E. I. (2008). Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile113853.pdf

Chicago Manual of Style (16th Edition):

Danek, Eric Ian. “Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile113853.pdf.

MLA Handbook (7th Edition):

Danek, Eric Ian. “Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42.” 2008. Web. 12 Nov 2019.

Vancouver:

Danek EI. Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile113853.pdf.

Council of Science Editors:

Danek EI. Characterization of regulatory mechanisms of CdGAP, a negative regulator of the small GTPases Rac1 and Cdc42. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile113853.pdf


McGill University

3. Fok, Patrick Terrence. The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration.

Degree: PhD, Division of Experimental Medicine., 2008, McGill University

Cancer cells commonly lose expression of cell adhesion molecules, such as E-cadherin and CEACAM1, with disease progression. Re-introduction of these molecules into high-grade tumor cells… (more)

Subjects/Keywords: Cell Movement.; Cell Adhesion.; Transcription Factors.; Receptors, Cytoplasmic and Nuclear.; Receptors, Virus  – physiology.; Tubulin.; beta Catenin.; ras GTPase-Activating Proteins.

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APA (6th Edition):

Fok, P. T. (2008). The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile113861.pdf

Chicago Manual of Style (16th Edition):

Fok, Patrick Terrence. “The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile113861.pdf.

MLA Handbook (7th Edition):

Fok, Patrick Terrence. “The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration.” 2008. Web. 12 Nov 2019.

Vancouver:

Fok PT. The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile113861.pdf.

Council of Science Editors:

Fok PT. The identification of protein-protein interactors of the Coxsackievirus and Adenovirus Receptor (CAR) and their impact on cell migration. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile113861.pdf


McGill University

4. Charest-Marcotte, Alexis, 1984-. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.

Degree: MS, Department of Biochemistry., 2009, McGill University

 Nuclear receptors play crucial roles in the transcriptional regulation of many biological processes such as development and cellular differentiation. ERRalpha is known, along with coactivator… (more)

Subjects/Keywords: Liver  – metabolism.; Homeodomain Proteins  – metabolism.; Receptors, Estrogen  – metabolism.; Heat-Shock Proteins  – metabolism.

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APA (6th Edition):

Charest-Marcotte, Alexis, 1. (2009). Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111571.pdf

Chicago Manual of Style (16th Edition):

Charest-Marcotte, Alexis, 1984-. “Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.” 2009. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111571.pdf.

MLA Handbook (7th Edition):

Charest-Marcotte, Alexis, 1984-. “Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.” 2009. Web. 12 Nov 2019.

Vancouver:

Charest-Marcotte, Alexis 1. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. [Internet] [Masters thesis]. McGill University; 2009. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111571.pdf.

Council of Science Editors:

Charest-Marcotte, Alexis 1. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. [Masters Thesis]. McGill University; 2009. Available from: http://digitool.library.mcgill.ca/thesisfile111571.pdf


McGill University

5. Buscarlet, Manuel. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.

Degree: PhD, Division of Neuroscience., 2008, McGill University

Groucho/transducin-like Enhancer of split (Gro/TLE) family proteins are corepressors found as part of multiple transcriptional complexes that play significant roles during many developmental processes, including… (more)

Subjects/Keywords: Neurons  – metabolism.; Cerebral Cortex  – metabolism.; Repressor Proteins  – metabolism.

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APA (6th Edition):

Buscarlet, M. (2008). The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115670.pdf

Chicago Manual of Style (16th Edition):

Buscarlet, Manuel. “The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile115670.pdf.

MLA Handbook (7th Edition):

Buscarlet, Manuel. “The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.” 2008. Web. 12 Nov 2019.

Vancouver:

Buscarlet M. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile115670.pdf.

Council of Science Editors:

Buscarlet M. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115670.pdf


McGill University

6. Faubert, Amélie. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.

Degree: PhD, Division of Experimental Medicine., 2007, McGill University

Self-renewal is central to the expansion of normal and cancerous stem cells. Its understanding is therefore critical for future advances in transplantation-based therapies and cancer… (more)

Subjects/Keywords: Hematopoietic Stem Cells  – metabolism.; Homeodomain Proteins  – metabolism.; Proto-Oncogene Proteins  – metabolism.

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APA (6th Edition):

Faubert, A. (2007). Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile103195.pdf

Chicago Manual of Style (16th Edition):

Faubert, Amélie. “Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.” 2007. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile103195.pdf.

MLA Handbook (7th Edition):

Faubert, Amélie. “Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.” 2007. Web. 12 Nov 2019.

Vancouver:

Faubert A. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. [Internet] [Doctoral dissertation]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile103195.pdf.

Council of Science Editors:

Faubert A. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. [Doctoral Dissertation]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile103195.pdf


McGill University

7. Jani, Klodiana. The role of integrin-dependent cell matrix adhesion in muscle development.

Degree: PhD, Department of Biology., 2009, McGill University

Cell adhesion is essential to cell motility and tissue integrity and is regulated by the Integrin family of transmembrane receptors. Integrin binds to ligand extracellularly… (more)

Subjects/Keywords: Striated muscle  – Metabolism.; Integrins  – Metabolism.; Cell adhesion.; Muscle, Skeletal  – metabolism.; Integrins  – metabolism.; Drosophila Proteins  – metabolism.; Carrier Proteins  – metabolism.; Adaptor Proteins, Signal Transducing  – metabolism.; Cell Adhesion  – physiology.

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APA (6th Edition):

Jani, K. (2009). The role of integrin-dependent cell matrix adhesion in muscle development. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115688.pdf

Chicago Manual of Style (16th Edition):

Jani, Klodiana. “The role of integrin-dependent cell matrix adhesion in muscle development.” 2009. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile115688.pdf.

MLA Handbook (7th Edition):

Jani, Klodiana. “The role of integrin-dependent cell matrix adhesion in muscle development.” 2009. Web. 12 Nov 2019.

Vancouver:

Jani K. The role of integrin-dependent cell matrix adhesion in muscle development. [Internet] [Doctoral dissertation]. McGill University; 2009. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile115688.pdf.

Council of Science Editors:

Jani K. The role of integrin-dependent cell matrix adhesion in muscle development. [Doctoral Dissertation]. McGill University; 2009. Available from: http://digitool.library.mcgill.ca/thesisfile115688.pdf


McGill University

8. Beauchamp, Pascal. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.

Degree: MS, Department of Biochemistry., 2008, McGill University

 Muscle tissue development (myogenesis) involves the formation of specific fibers (myotubes) from muscle cells (myoblasts). For this to occur, the sequential expression of Myogenic Regulatory… (more)

Subjects/Keywords: Myoblasts  – cytology.; Myoblasts  – metabolism.; RNA-Binding Proteins  – metabolism.; Antigens, Surface  – metabolism.; Caspases  – metabolism.

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APA (6th Edition):

Beauchamp, P. (2008). The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111586.pdf

Chicago Manual of Style (16th Edition):

Beauchamp, Pascal. “The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111586.pdf.

MLA Handbook (7th Edition):

Beauchamp, Pascal. “The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.” 2008. Web. 12 Nov 2019.

Vancouver:

Beauchamp P. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111586.pdf.

Council of Science Editors:

Beauchamp P. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111586.pdf


McGill University

9. Ainsworth, Julia. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.

Degree: MS, Department of Microbiology and Immunology., 2007, McGill University

The HPV E6-p53 interaction is well-understood, but not for all high-risk HPV types. In addition, HPV E6 p53-independent functions are gaining recognition for their importance… (more)

Subjects/Keywords: Viral Envelope Proteins  – metabolism.; Oncogene Proteins, Viral  – metabolism.; Papillomaviridae  – physiology.; Tumor Suppressor Protein p53  – metabolism.; Membrane Proteins  – metabolism.

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APA (6th Edition):

Ainsworth, J. (2007). Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112368.pdf

Chicago Manual of Style (16th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile112368.pdf.

MLA Handbook (7th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Web. 12 Nov 2019.

Vancouver:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf.

Council of Science Editors:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf


McGill University

10. Martel-Lorion, Chloe. Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library.

Degree: MS, Department of Biochemistry, 2004, McGill University

Note:

The unfolded protein response (UPR) signaling pathway is activated by an accumulation of unfolded proteins in the lumen of the endoplasmic reticulum (ER). Irelp… (more)

Subjects/Keywords: Protein Folding.; Endoplasmic Reticulum  – metabolism.; Saccharomyces cerevisiae Proteins  – metabolism.

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APA (6th Edition):

Martel-Lorion, C. (2004). Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile161940.pdf

Chicago Manual of Style (16th Edition):

Martel-Lorion, Chloe. “Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library.” 2004. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile161940.pdf.

MLA Handbook (7th Edition):

Martel-Lorion, Chloe. “Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library.” 2004. Web. 12 Nov 2019.

Vancouver:

Martel-Lorion C. Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library. [Internet] [Masters thesis]. McGill University; 2004. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile161940.pdf.

Council of Science Editors:

Martel-Lorion C. Unfolded Protein Response Inhibitors Identified by High Throughput Screening of a Combinatorial Chemistry Compound Library. [Masters Thesis]. McGill University; 2004. Available from: http://digitool.library.mcgill.ca/thesisfile161940.pdf


McGill University

11. Lattermann, Ralph. Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state.

Degree: MS, School of Dietetics and Human Nutrition., 2002, McGill University

The present project investigated the effect of epidural blockade with local anesthetic on the catabolic stress response during and immediately after abdominal surgery in fasting… (more)

Subjects/Keywords: Surgery  – Nutritional aspects.; Peridural anesthesia.; Proteins  – Metabolism.; Glucose  – Metabolism.

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APA (6th Edition):

Lattermann, R. (2002). Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile29451.pdf

Chicago Manual of Style (16th Edition):

Lattermann, Ralph. “Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state.” 2002. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile29451.pdf.

MLA Handbook (7th Edition):

Lattermann, Ralph. “Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state.” 2002. Web. 12 Nov 2019.

Vancouver:

Lattermann R. Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state. [Internet] [Masters thesis]. McGill University; 2002. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile29451.pdf.

Council of Science Editors:

Lattermann R. Epidural blockade and the catabolic response to surgery : an integrated analysis of perioperative protein and glucose metabolism using stable isotope kinetics in the fasted and fed state. [Masters Thesis]. McGill University; 2002. Available from: http://digitool.library.mcgill.ca/thesisfile29451.pdf


McGill University

12. Smith, Douglas W., 1961-. The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts.

Degree: MS, Department of Biology., 1986, McGill University

Subjects/Keywords: Fibroblasts.; Amino acids  – Metabolism.; Proteins  – Metabolism  – Disorders.; Cells  – Permeability.

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APA (6th Edition):

Smith, Douglas W., 1. (1986). The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile65416.pdf

Chicago Manual of Style (16th Edition):

Smith, Douglas W., 1961-. “The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts.” 1986. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile65416.pdf.

MLA Handbook (7th Edition):

Smith, Douglas W., 1961-. “The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts.” 1986. Web. 12 Nov 2019.

Vancouver:

Smith, Douglas W. 1. The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts. [Internet] [Masters thesis]. McGill University; 1986. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile65416.pdf.

Council of Science Editors:

Smith, Douglas W. 1. The lysinuric protein intolerance phenotype : amino acid transport in cultured skin fibroblasts. [Masters Thesis]. McGill University; 1986. Available from: http://digitool.library.mcgill.ca/thesisfile65416.pdf


McGill University

13. Gordon, Cedric Ivanhoe. The effect of dietary pectin on protein utilization in weaning rats.

Degree: MS, Department of Animal Science, 1982, McGill University

Subjects/Keywords: Pectin; Proteins  – Metabolism; Food  – Fiber content

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APA (6th Edition):

Gordon, C. I. (1982). The effect of dietary pectin on protein utilization in weaning rats. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile57384.pdf

Chicago Manual of Style (16th Edition):

Gordon, Cedric Ivanhoe. “The effect of dietary pectin on protein utilization in weaning rats.” 1982. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile57384.pdf.

MLA Handbook (7th Edition):

Gordon, Cedric Ivanhoe. “The effect of dietary pectin on protein utilization in weaning rats.” 1982. Web. 12 Nov 2019.

Vancouver:

Gordon CI. The effect of dietary pectin on protein utilization in weaning rats. [Internet] [Masters thesis]. McGill University; 1982. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile57384.pdf.

Council of Science Editors:

Gordon CI. The effect of dietary pectin on protein utilization in weaning rats. [Masters Thesis]. McGill University; 1982. Available from: http://digitool.library.mcgill.ca/thesisfile57384.pdf


McGill University

14. Purkey, Robert Michael. Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution.

Degree: PhD, Department of Chemistry., 1972, McGill University

Subjects/Keywords: Proteins  – Analysis; Tryptophan  – Metabolism.; Electron spectroscopy

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APA (6th Edition):

Purkey, R. M. (1972). Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile70726.pdf

Chicago Manual of Style (16th Edition):

Purkey, Robert Michael. “Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution.” 1972. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile70726.pdf.

MLA Handbook (7th Edition):

Purkey, Robert Michael. “Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution.” 1972. Web. 12 Nov 2019.

Vancouver:

Purkey RM. Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution. [Internet] [Doctoral dissertation]. McGill University; 1972. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile70726.pdf.

Council of Science Editors:

Purkey RM. Electronic spectroscopy as a probe of heterogeneity in the local environment of polar aromatic chromophores in proteins and free solution. [Doctoral Dissertation]. McGill University; 1972. Available from: http://digitool.library.mcgill.ca/thesisfile70726.pdf


McGill University

15. Yamani, Lama. Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism.

Degree: MS, Department of Human Genetics., 2008, McGill University

 Cobalamin must be metabolized intracellularly in order to bind two enzymes: methionine synthase in cytoplasm and methylmalonyl-CoA mutase in mitochondria. Defects in this process cause… (more)

Subjects/Keywords: Metabolism, Inborn Errors  – metabolism.; Fibroblasts  – metabolism.; Mitochondrial Proteins  – metabolism.; Transcobalamins  – metabolism.; Vitamin B 12  – metabolism.

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APA (6th Edition):

Yamani, L. (2008). Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112320.pdf

Chicago Manual of Style (16th Edition):

Yamani, Lama. “Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile112320.pdf.

MLA Handbook (7th Edition):

Yamani, Lama. “Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism.” 2008. Web. 12 Nov 2019.

Vancouver:

Yamani L. Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile112320.pdf.

Council of Science Editors:

Yamani L. Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile112320.pdf


McGill University

16. Dolatshahi, Marjan. Conformational changes of polyomavirus during cell entry.

Degree: MS, Department of Anatomy and Cell Biology., 2008, McGill University

 Similar to other non-enveloped viruses, the mechanism of cell entry for polyomaviruses is poorly understood. The polyomavirus capsid is an icosahedron composed of 72 pentamers… (more)

Subjects/Keywords: Polyomavirus  – physiology.; Capsid Proteins  – metabolism.; Receptors, Virus  – metabolism.; N-Acetylneuraminic Acid  – metabolism.; Mice.

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APA (6th Edition):

Dolatshahi, M. (2008). Conformational changes of polyomavirus during cell entry. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111604.pdf

Chicago Manual of Style (16th Edition):

Dolatshahi, Marjan. “Conformational changes of polyomavirus during cell entry.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111604.pdf.

MLA Handbook (7th Edition):

Dolatshahi, Marjan. “Conformational changes of polyomavirus during cell entry.” 2008. Web. 12 Nov 2019.

Vancouver:

Dolatshahi M. Conformational changes of polyomavirus during cell entry. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111604.pdf.

Council of Science Editors:

Dolatshahi M. Conformational changes of polyomavirus during cell entry. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111604.pdf


McGill University

17. Sundaram, Priyanka. The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells.

Degree: MS, Department of Biochemistry., 2008, McGill University

 Muscle wasting is a significant complication of many diseases including diabetes mellitus, renal and liver failure, HIV/AIDS, and cancer. Sustained loss of skeletal muscle can… (more)

Subjects/Keywords: Muscle Proteins  – biosynthesis.; Endopeptidases  – metabolism.; Muscle, Skeletal  – metabolism.; Muscular Atrophy  – metabolism.

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APA (6th Edition):

Sundaram, P. (2008). The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111547.pdf

Chicago Manual of Style (16th Edition):

Sundaram, Priyanka. “The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111547.pdf.

MLA Handbook (7th Edition):

Sundaram, Priyanka. “The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells.” 2008. Web. 12 Nov 2019.

Vancouver:

Sundaram P. The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111547.pdf.

Council of Science Editors:

Sundaram P. The deubiquitinating enzyme USP19 negatively regulates the expression of muscle-specific genes in L6 muscle cells. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111547.pdf


McGill University

18. Marini, Wanda. Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours.

Degree: MS, Department of Microbiology and Immunology., 2009, McGill University

 One of the major unresolved questions in cancer biology is why the majority of tumour cells express mutant p53 proteins. p53 is considered the prototype… (more)

Subjects/Keywords: Tumor Suppressor Protein p53  – genetics.; Tumor Suppressor Protein p53  – metabolism.; Intracellular Signaling Peptides and Proteins  – metabolism.; Nuclear Proteins  – metabolism.; Alternative Splicing.

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APA (6th Edition):

Marini, W. (2009). Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile116033.pdf

Chicago Manual of Style (16th Edition):

Marini, Wanda. “Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours.” 2009. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile116033.pdf.

MLA Handbook (7th Edition):

Marini, Wanda. “Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours.” 2009. Web. 12 Nov 2019.

Vancouver:

Marini W. Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours. [Internet] [Masters thesis]. McGill University; 2009. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile116033.pdf.

Council of Science Editors:

Marini W. Comparing mutant p53 and a wild-type p53 isoform, p47 : rationale for the selection of mutant p53 in tumours. [Masters Thesis]. McGill University; 2009. Available from: http://digitool.library.mcgill.ca/thesisfile116033.pdf


McGill University

19. Frigault, Melanie M. (Melanie Mae), 1979-. The role of the Gab family of docking proteins in Met mediated membrane ruffle formation.

Degree: PhD, Department of Biochemistry., 2008, McGill University

In response to extra-cellular cues, cells activate signal transduction pathways to elicit a biological response. Cell surface growth factor receptors such as the Met receptor… (more)

Subjects/Keywords: Epithelial Cells  – cytology.; Cell Membrane  – metabolism.; Cell Shape.; Proto-Oncogene Proteins c-met  – metabolism.; Adaptor Proteins, Signal Transducing  – metabolism.

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APA (6th Edition):

Frigault, Melanie M. (Melanie Mae), 1. (2008). The role of the Gab family of docking proteins in Met mediated membrane ruffle formation. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115673.pdf

Chicago Manual of Style (16th Edition):

Frigault, Melanie M. (Melanie Mae), 1979-. “The role of the Gab family of docking proteins in Met mediated membrane ruffle formation.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile115673.pdf.

MLA Handbook (7th Edition):

Frigault, Melanie M. (Melanie Mae), 1979-. “The role of the Gab family of docking proteins in Met mediated membrane ruffle formation.” 2008. Web. 12 Nov 2019.

Vancouver:

Frigault, Melanie M. (Melanie Mae) 1. The role of the Gab family of docking proteins in Met mediated membrane ruffle formation. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile115673.pdf.

Council of Science Editors:

Frigault, Melanie M. (Melanie Mae) 1. The role of the Gab family of docking proteins in Met mediated membrane ruffle formation. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115673.pdf


McGill University

20. Ring, Giselle Natasha. Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast.

Degree: MS, Division of Experimental Medicine., 2007, McGill University

 The ability to evade apoptosis is an acquired characteristic associated with many normal and pathophysiological processes. TMEM 85 represents a novel transmembrane domain containing human… (more)

Subjects/Keywords: Apoptosis  – physiology.; bcl-2-Associated X Protein  – metabolism.; Membrane Proteins  – metabolism.; Saccharomyces cerevisiae Proteins  – metabolism.

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APA (6th Edition):

Ring, G. N. (2007). Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112352.pdf

Chicago Manual of Style (16th Edition):

Ring, Giselle Natasha. “Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast.” 2007. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile112352.pdf.

MLA Handbook (7th Edition):

Ring, Giselle Natasha. “Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast.” 2007. Web. 12 Nov 2019.

Vancouver:

Ring GN. Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile112352.pdf.

Council of Science Editors:

Ring GN. Identification and characterization of TMEM 85, a novel suppressor of bax-mediated cell death in yeast. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112352.pdf


McGill University

21. Laberge, Marie-Kristine. Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling.

Degree: MS, Division of Experimental Medicine., 2008, McGill University

 Activation of the Unfolded Protein Response (UPR) following stress in the Endoplasmic Reticulum (ER) is an important mechanism by which obesity results in insulin resistance… (more)

Subjects/Keywords: Insulin  – metabolism.; Insulin Resistance.; Insulin Receptor Substrate Proteins; Protein Folding.; Endoplasmic Reticulum  – metabolism.; Adaptor Proteins, Signal Transducing  – metabolism.

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APA (6th Edition):

Laberge, M. (2008). Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111950.pdf

Chicago Manual of Style (16th Edition):

Laberge, Marie-Kristine. “Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111950.pdf.

MLA Handbook (7th Edition):

Laberge, Marie-Kristine. “Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling.” 2008. Web. 12 Nov 2019.

Vancouver:

Laberge M. Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111950.pdf.

Council of Science Editors:

Laberge M. Nck1 is required for ER stress-induced insulin resistance and regulation of IRS1-dependent insulin signalling. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111950.pdf


McGill University

22. Cardin, Eric. Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity.

Degree: PhD, Division of Experimental Medicine., 2008, McGill University

 Phosphorylation of the alpha-subunit of the eukaryotic initiation factor 2 (eIF2alpha) on Serine 51 (Ser51) is an early event associated with downregulation of protein synthesis… (more)

Subjects/Keywords: Eukaryotic Initiation Factor-2  – metabolism.; eIF-2 Kinase  – metabolism.; Serine  – metabolism.; Oncogene Proteins  – physiology.; Adaptor Proteins, Signal Transducing  – physiology.

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APA (6th Edition):

Cardin, E. (2008). Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111905.pdf

Chicago Manual of Style (16th Edition):

Cardin, Eric. “Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111905.pdf.

MLA Handbook (7th Edition):

Cardin, Eric. “Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity.” 2008. Web. 12 Nov 2019.

Vancouver:

Cardin E. Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111905.pdf.

Council of Science Editors:

Cardin E. Function of Nck-1 adaptor protein as modulator of elF2alpha phosphorylation by specific elF2alpha kinases and PKR activity. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111905.pdf


McGill University

23. Drolet, Jessica Ann. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.

Degree: MS, Department of Microbiology and Immunology., 2007, McGill University

 Saccharomyces cerevisiae has developed mechanisms in order to survive harsh environmental conditions. This species responds to stresses such as ethanol, heat, and weak acid exposure… (more)

Subjects/Keywords: Saccharomyces cerevisiae Proteins  – metabolism.; Gene Expression Regulation, Fungal  – genetics.; Zinc  – metabolism.; Zinc Fingers.

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APA (6th Edition):

Drolet, J. A. (2007). Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112617.pdf

Chicago Manual of Style (16th Edition):

Drolet, Jessica Ann. “Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.” 2007. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile112617.pdf.

MLA Handbook (7th Edition):

Drolet, Jessica Ann. “Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.” 2007. Web. 12 Nov 2019.

Vancouver:

Drolet JA. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile112617.pdf.

Council of Science Editors:

Drolet JA. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112617.pdf


McGill University

24. Li, Ying, 1972, Mar. 31-. The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro.

Degree: MS, Division of Experimental Medicine., 2007, McGill University

 Cyclic guanosine 3', 5'-monophosphate (cGMP) has recently emerged as an endogenous regulator for controlling or reversing cardiac hypertrophy. Increased protein accumulation is a key feature… (more)

Subjects/Keywords: Myocytes, Cardiac  – metabolism.; Proteins  – metabolism.; Cyclic GMP  – analogs & derivatives.; Cardiomegaly  – etiology.

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APA (6th Edition):

Li, Ying, 1972, M. 3. (2007). The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile101863.pdf

Chicago Manual of Style (16th Edition):

Li, Ying, 1972, Mar 31-. “The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro.” 2007. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile101863.pdf.

MLA Handbook (7th Edition):

Li, Ying, 1972, Mar 31-. “The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro.” 2007. Web. 12 Nov 2019.

Vancouver:

Li, Ying, 1972 M3. The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile101863.pdf.

Council of Science Editors:

Li, Ying, 1972 M3. The effects of cyclic guanosine 3', 5'-monophosphate analog on protein accumulation in adult rat cardiomyocytes in vitro. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile101863.pdf


McGill University

25. Kafaie, Jafar. Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability.

Degree: PhD, Division of Experimental Medicine., 2008, McGill University

 In the past three decades, various steps of the human immunodeficiency virus type 1 (HIV-1) life cycle have been thoroughly studied. Many of these steps,… (more)

Subjects/Keywords: HIV-1  – physiology.; Nucleocapsid Proteins  – metabolism.; RNA, Viral  – metabolism.; Dimerization.

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APA (6th Edition):

Kafaie, J. (2008). Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111914.pdf

Chicago Manual of Style (16th Edition):

Kafaie, Jafar. “Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111914.pdf.

MLA Handbook (7th Edition):

Kafaie, Jafar. “Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability.” 2008. Web. 12 Nov 2019.

Vancouver:

Kafaie J. Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111914.pdf.

Council of Science Editors:

Kafaie J. Role of the NC protein of human immunodeficiency virus type 1 in viral RNA dimerization and packaging, as well as in virus replication and stability. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111914.pdf


McGill University

26. Hamadeh, Mazen Jamal. Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus.

Degree: PhD, School of Dietetics and Human Nutrition., 2001, McGill University

 Postprandial urea production in subjects with insulin dependent diabetes mellitus (IDDM) on conventional insulin therapy is normal when the previous diet is high in protein,… (more)

Subjects/Keywords: Diabetes  – Nutritional aspects.; Amino acids  – Metabolism.; Proteins  – Metabolism  – Disorders.; Low-protein diet.

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APA (6th Edition):

Hamadeh, M. J. (2001). Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile36948.pdf

Chicago Manual of Style (16th Edition):

Hamadeh, Mazen Jamal. “Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus.” 2001. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile36948.pdf.

MLA Handbook (7th Edition):

Hamadeh, Mazen Jamal. “Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus.” 2001. Web. 12 Nov 2019.

Vancouver:

Hamadeh MJ. Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus. [Internet] [Doctoral dissertation]. McGill University; 2001. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile36948.pdf.

Council of Science Editors:

Hamadeh MJ. Methods for detecting abnormal adaptation to protein restriction in humans with special reference to insulin-dependent diabetes mellitus. [Doctoral Dissertation]. McGill University; 2001. Available from: http://digitool.library.mcgill.ca/thesisfile36948.pdf


McGill University

27. Huynh, Carl. The cytoprotective role of Ras signaling in glomerular epithelial cell injury.

Degree: MS, Department of Physiology., 2007, McGill University

 In experimental membranous nephropathy, complement C5b-9-induced glomerular epithelial cell (GEC) injury leads to breakdown of glomerular peimselectivity and proteinuria. This study addresses mechanisms that limit… (more)

Subjects/Keywords: Kidney Glomerulus  – metabolism.; Epithelium  – metabolism.; Complement Membrane Attack Complex.; Cytoprotection  – physiology.; ras Proteins  – metabolism.; 1-Phosphatidylinositol 3-Kinase  – metabolism.

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APA (6th Edition):

Huynh, C. (2007). The cytoprotective role of Ras signaling in glomerular epithelial cell injury. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112639.pdf

Chicago Manual of Style (16th Edition):

Huynh, Carl. “The cytoprotective role of Ras signaling in glomerular epithelial cell injury.” 2007. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile112639.pdf.

MLA Handbook (7th Edition):

Huynh, Carl. “The cytoprotective role of Ras signaling in glomerular epithelial cell injury.” 2007. Web. 12 Nov 2019.

Vancouver:

Huynh C. The cytoprotective role of Ras signaling in glomerular epithelial cell injury. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile112639.pdf.

Council of Science Editors:

Huynh C. The cytoprotective role of Ras signaling in glomerular epithelial cell injury. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112639.pdf


McGill University

28. Goyette, Nathalie. The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster.

Degree: MS, School of Dietetics and Human Nutrition., 1993, McGill University

 Dietary fats and animal proteins have been shown to exert different lipidemic responses in many animals, including humans. Oxidative stress has been associated with the… (more)

Subjects/Keywords: Cholesterol  – Metabolism.; Proteins in nutrition.; Lipids in nutrition.

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APA (6th Edition):

Goyette, N. (1993). The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile26020.pdf

Chicago Manual of Style (16th Edition):

Goyette, Nathalie. “The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster.” 1993. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile26020.pdf.

MLA Handbook (7th Edition):

Goyette, Nathalie. “The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster.” 1993. Web. 12 Nov 2019.

Vancouver:

Goyette N. The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster. [Internet] [Masters thesis]. McGill University; 1993. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile26020.pdf.

Council of Science Editors:

Goyette N. The effects of dietary protein and fat on cholesterol metabolism in the golden Syrian hamster. [Masters Thesis]. McGill University; 1993. Available from: http://digitool.library.mcgill.ca/thesisfile26020.pdf


McGill University

29. Behmoaram, Emy. Biological studies of fascin function in cancer cell invasion and cancer progression.

Degree: MS, Division of Experimental Medicine., 2008, McGill University

 The process of metastasis is initiated through the acquisition of inherent and autonomous motile and invasive properties by tumor cells. These phenomena are initiated through… (more)

Subjects/Keywords: Neoplasm Invasiveness.; Prostatic Neoplasms  – metabolism.; Breast Neoplasms  – metabolism.; Carrier Proteins  – physiology.; Microfilament Proteins  – physiology.

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APA (6th Edition):

Behmoaram, E. (2008). Biological studies of fascin function in cancer cell invasion and cancer progression. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111596.pdf

Chicago Manual of Style (16th Edition):

Behmoaram, Emy. “Biological studies of fascin function in cancer cell invasion and cancer progression.” 2008. Masters Thesis, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile111596.pdf.

MLA Handbook (7th Edition):

Behmoaram, Emy. “Biological studies of fascin function in cancer cell invasion and cancer progression.” 2008. Web. 12 Nov 2019.

Vancouver:

Behmoaram E. Biological studies of fascin function in cancer cell invasion and cancer progression. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile111596.pdf.

Council of Science Editors:

Behmoaram E. Biological studies of fascin function in cancer cell invasion and cancer progression. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111596.pdf


McGill University

30. Chénard, Carol Anne. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.

Degree: PhD, Department of Microbiology and Immunology., 2008, McGill University

For the past 45 years, QKI has been studied for its role in the processes of development and central nervous system myelination using the qkv… (more)

Subjects/Keywords: RNA-Binding Proteins  – physiology.; Oligodendroglia  – cytology.; Heterogeneous-Nuclear Ribonucleoprotein K  – metabolism.; Protein-Arginine N-Methyltransferase  – metabolism.; Methylation.; Poly(A)-Binding Proteins  – metabolism.; Myelin Basic Proteins  – metabolism.; Mice.; Mice, Quaking.

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APA (6th Edition):

Chénard, C. A. (2008). Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115894.pdf

Chicago Manual of Style (16th Edition):

Chénard, Carol Anne. “Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.” 2008. Doctoral Dissertation, McGill University. Accessed November 12, 2019. http://digitool.library.mcgill.ca/thesisfile115894.pdf.

MLA Handbook (7th Edition):

Chénard, Carol Anne. “Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.” 2008. Web. 12 Nov 2019.

Vancouver:

Chénard CA. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Nov 12]. Available from: http://digitool.library.mcgill.ca/thesisfile115894.pdf.

Council of Science Editors:

Chénard CA. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115894.pdf

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