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You searched for subject:(Human Genetics). Showing records 1 – 30 of 632 total matches.

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1. Thomford, Nicholas Ekow. Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation.

Degree: PhD, Division of Human Genetics, 2017, University of Cape Town

 Background: Plants have been used as a source of food and medicine for a very long time, however, recently, there has been a renewed focus… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Thomford, N. E. (2017). Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation. (Doctoral Dissertation). University of Cape Town. Retrieved from http://hdl.handle.net/11427/24457

Chicago Manual of Style (16th Edition):

Thomford, Nicholas Ekow. “Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation.” 2017. Doctoral Dissertation, University of Cape Town. Accessed June 17, 2019. http://hdl.handle.net/11427/24457.

MLA Handbook (7th Edition):

Thomford, Nicholas Ekow. “Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation.” 2017. Web. 17 Jun 2019.

Vancouver:

Thomford NE. Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation. [Internet] [Doctoral dissertation]. University of Cape Town; 2017. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11427/24457.

Council of Science Editors:

Thomford NE. Pharmacogenomics: evaluating induction and inhibition profiles of selected herbal medicinal plants on genes coding for drug metabolising enzymes and cell cycle regulation. [Doctoral Dissertation]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/24457


University of Hawaii

2. Grove, John Sinclair. Aberrant segregation in human populations.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography [142]-147.

ix, 147 l illus

Three cases of aberrant segregation in humans were considered. The first was a possible case of non-random assortment… (more)

Subjects/Keywords: Human genetics

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APA (6th Edition):

Grove, J. S. (2009). Aberrant segregation in human populations. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11493

Chicago Manual of Style (16th Edition):

Grove, John Sinclair. “Aberrant segregation in human populations.” 2009. Doctoral Dissertation, University of Hawaii. Accessed June 17, 2019. http://hdl.handle.net/10125/11493.

MLA Handbook (7th Edition):

Grove, John Sinclair. “Aberrant segregation in human populations.” 2009. Web. 17 Jun 2019.

Vancouver:

Grove JS. Aberrant segregation in human populations. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10125/11493.

Council of Science Editors:

Grove JS. Aberrant segregation in human populations. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11493


McGill University

3. Palenzuela Pulve, Iliana. Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology.

Degree: MS, Department of Human Genetics, 2018, McGill University

The gene named microseminoprotein, prostate-associated (MSMP), also known as PC-3 secreted microseminoprotein, encodes for a small secreted protein with some homology with β-microseminoprotein. Recent studies… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Palenzuela Pulve, I. (2018). Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154852.pdf

Chicago Manual of Style (16th Edition):

Palenzuela Pulve, Iliana. “Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154852.pdf.

MLA Handbook (7th Edition):

Palenzuela Pulve, Iliana. “Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology.” 2018. Web. 17 Jun 2019.

Vancouver:

Palenzuela Pulve I. Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154852.pdf.

Council of Science Editors:

Palenzuela Pulve I. Characterization of the microseminoprotein, prostate-associated (Msmp) gene and its potential role in bone biology. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154852.pdf


McGill University

4. Antonyan, Lilit. Role of FAM57B2 and Lactosylceramide in Chondrogenesis.

Degree: MS, Department of Human Genetics, 2018, McGill University

Chondrogenesis is critical for the healing of fractured bones. After an initial inflammation stage, a "soft callus" composed of chondrocytes bridges the injury site, to… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Antonyan, L. (2018). Role of FAM57B2 and Lactosylceramide in Chondrogenesis. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154689.pdf

Chicago Manual of Style (16th Edition):

Antonyan, Lilit. “Role of FAM57B2 and Lactosylceramide in Chondrogenesis.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154689.pdf.

MLA Handbook (7th Edition):

Antonyan, Lilit. “Role of FAM57B2 and Lactosylceramide in Chondrogenesis.” 2018. Web. 17 Jun 2019.

Vancouver:

Antonyan L. Role of FAM57B2 and Lactosylceramide in Chondrogenesis. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154689.pdf.

Council of Science Editors:

Antonyan L. Role of FAM57B2 and Lactosylceramide in Chondrogenesis. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154689.pdf


McGill University

5. Wong, Cavin. A gene association study to identify novel pancreatic cancer susceptibility genes.

Degree: MS, Department of Human Genetics, 2018, McGill University

 Approximately 10% of pancreatic cancer (PAC) cases are hereditary in nature, however, only a fraction is explained by known susceptibility genes. Recent efforts using Next-Generation… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Wong, C. (2018). A gene association study to identify novel pancreatic cancer susceptibility genes. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154863.pdf

Chicago Manual of Style (16th Edition):

Wong, Cavin. “A gene association study to identify novel pancreatic cancer susceptibility genes.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154863.pdf.

MLA Handbook (7th Edition):

Wong, Cavin. “A gene association study to identify novel pancreatic cancer susceptibility genes.” 2018. Web. 17 Jun 2019.

Vancouver:

Wong C. A gene association study to identify novel pancreatic cancer susceptibility genes. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154863.pdf.

Council of Science Editors:

Wong C. A gene association study to identify novel pancreatic cancer susceptibility genes. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154863.pdf


McGill University

6. Brasell, Emma. Nonsense suppressor therapy of cystinosis.

Degree: PhD, Department of Human Genetics, 2018, McGill University

Cystinosis is a rare, recessive lysosomal storage disorder caused by mutations in the cystinosin (CTNS) gene. CTNS encodes a H+-driven transmembrane transporter responsible for efflux… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Brasell, E. (2018). Nonsense suppressor therapy of cystinosis. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154648.pdf

Chicago Manual of Style (16th Edition):

Brasell, Emma. “Nonsense suppressor therapy of cystinosis.” 2018. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154648.pdf.

MLA Handbook (7th Edition):

Brasell, Emma. “Nonsense suppressor therapy of cystinosis.” 2018. Web. 17 Jun 2019.

Vancouver:

Brasell E. Nonsense suppressor therapy of cystinosis. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154648.pdf.

Council of Science Editors:

Brasell E. Nonsense suppressor therapy of cystinosis. [Doctoral Dissertation]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154648.pdf


McGill University

7. Doha, Zinab. Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome.

Degree: MS, Department of Human Genetics, 2018, McGill University

Capillary Morphogenesis Gene-2 (CMG2) is a transmembrane receptor that shares similarity with integrins and it is thought to be involved in homeostasis of the extracellular… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Doha, Z. (2018). Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154796.pdf

Chicago Manual of Style (16th Edition):

Doha, Zinab. “Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154796.pdf.

MLA Handbook (7th Edition):

Doha, Zinab. “Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome.” 2018. Web. 17 Jun 2019.

Vancouver:

Doha Z. Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154796.pdf.

Council of Science Editors:

Doha Z. Functional characterization of capillary morphogenesis gene 2 and its mutants that cause the hyaline fibromatosis syndrome. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154796.pdf


McGill University

8. Garg, Elika. Examination of pre-processing techniques for NanoString nCounter mRNA data.

Degree: MS, Department of Human Genetics, 2015, McGill University

NanoString is a novel medium-throughput technology which is becoming widely-accepted in the biomedical community for measurement of gene expression. The count data generated by its… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Garg, E. (2015). Examination of pre-processing techniques for NanoString nCounter mRNA data. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile135667.pdf

Chicago Manual of Style (16th Edition):

Garg, Elika. “Examination of pre-processing techniques for NanoString nCounter mRNA data.” 2015. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile135667.pdf.

MLA Handbook (7th Edition):

Garg, Elika. “Examination of pre-processing techniques for NanoString nCounter mRNA data.” 2015. Web. 17 Jun 2019.

Vancouver:

Garg E. Examination of pre-processing techniques for NanoString nCounter mRNA data. [Internet] [Masters thesis]. McGill University; 2015. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile135667.pdf.

Council of Science Editors:

Garg E. Examination of pre-processing techniques for NanoString nCounter mRNA data. [Masters Thesis]. McGill University; 2015. Available from: http://digitool.library.mcgill.ca/thesisfile135667.pdf


McGill University

9. Morad, Kayla. The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model.

Degree: MS, Department of Human Genetics, 2015, McGill University

 Osteocrin (Ostn) encodes a small secreted protein, which is expressed in bone, muscle, tendon, and fat. OSTN shares sequence homology with the natriuretic peptides (NPs:… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Morad, K. (2015). The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile135681.pdf

Chicago Manual of Style (16th Edition):

Morad, Kayla. “The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model.” 2015. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile135681.pdf.

MLA Handbook (7th Edition):

Morad, Kayla. “The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model.” 2015. Web. 17 Jun 2019.

Vancouver:

Morad K. The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model. [Internet] [Masters thesis]. McGill University; 2015. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile135681.pdf.

Council of Science Editors:

Morad K. The effects of osteocrin (Ostn) overexpression on bone growth in a transgenic mouse model. [Masters Thesis]. McGill University; 2015. Available from: http://digitool.library.mcgill.ca/thesisfile135681.pdf


McGill University

10. Bazett, Mark. Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models.

Degree: PhD, Department of Human Genetics, 2015, McGill University

Cystic fibrosis (CF) is a severe, systemic disease that impacts multiple organs, including the lungs, bones and intestine. In the lungs, in addition to reoccurring… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Bazett, M. (2015). Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile135564.pdf

Chicago Manual of Style (16th Edition):

Bazett, Mark. “Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models.” 2015. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile135564.pdf.

MLA Handbook (7th Edition):

Bazett, Mark. “Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models.” 2015. Web. 17 Jun 2019.

Vancouver:

Bazett M. Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models. [Internet] [Doctoral dissertation]. McGill University; 2015. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile135564.pdf.

Council of Science Editors:

Bazett M. Airway mechanics, the intestinal microbiome and their interaction in cystic fibrosis mouse models. [Doctoral Dissertation]. McGill University; 2015. Available from: http://digitool.library.mcgill.ca/thesisfile135564.pdf


McGill University

11. Miller, Julie Ann. ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment.

Degree: MS, Department of Human Genetics, 2015, McGill University

The alpha chain of the nascent polypeptide associated complex (alphaNAC) functions as a transcriptional coregulator in osteoblasts. When osteoblasts are stimulated by parathyroid hormone (PTH),… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Miller, J. A. (2015). ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile135655.pdf

Chicago Manual of Style (16th Edition):

Miller, Julie Ann. “ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment.” 2015. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile135655.pdf.

MLA Handbook (7th Edition):

Miller, Julie Ann. “ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment.” 2015. Web. 17 Jun 2019.

Vancouver:

Miller JA. ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment. [Internet] [Masters thesis]. McGill University; 2015. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile135655.pdf.

Council of Science Editors:

Miller JA. ChIP-seq identifies Lrp6 as a novel αNAC gene target following PTH treatment. [Masters Thesis]. McGill University; 2015. Available from: http://digitool.library.mcgill.ca/thesisfile135655.pdf


McGill University

12. Gerges, Amanda. The αNAC transcriptional coregulator is a substrate of p38α MAP kinase.

Degree: MS, Department of Human Genetics, 2016, McGill University

The alpha chain of the nascent polypeptide associated complex, abridged to αNAC, plays an important role as a transcriptional coregulator in bones. Its activity is… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Gerges, A. (2016). The αNAC transcriptional coregulator is a substrate of p38α MAP kinase. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143952.pdf

Chicago Manual of Style (16th Edition):

Gerges, Amanda. “The αNAC transcriptional coregulator is a substrate of p38α MAP kinase.” 2016. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile143952.pdf.

MLA Handbook (7th Edition):

Gerges, Amanda. “The αNAC transcriptional coregulator is a substrate of p38α MAP kinase.” 2016. Web. 17 Jun 2019.

Vancouver:

Gerges A. The αNAC transcriptional coregulator is a substrate of p38α MAP kinase. [Internet] [Masters thesis]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile143952.pdf.

Council of Science Editors:

Gerges A. The αNAC transcriptional coregulator is a substrate of p38α MAP kinase. [Masters Thesis]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143952.pdf


McGill University

13. Leblicq, Coralie. Autosomal recessive insulin-dependent diabetes.

Degree: MS, Department of Human Genetics, 2016, McGill University

 Background and hypothesis: Type 1 diabetes (T1DM) is due to the autoimmune destruction of the insulin-producing pancreatic beta-cells. T1DM is a multifactorial disease with a… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Leblicq, C. (2016). Autosomal recessive insulin-dependent diabetes. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143955.pdf

Chicago Manual of Style (16th Edition):

Leblicq, Coralie. “Autosomal recessive insulin-dependent diabetes.” 2016. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile143955.pdf.

MLA Handbook (7th Edition):

Leblicq, Coralie. “Autosomal recessive insulin-dependent diabetes.” 2016. Web. 17 Jun 2019.

Vancouver:

Leblicq C. Autosomal recessive insulin-dependent diabetes. [Internet] [Masters thesis]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile143955.pdf.

Council of Science Editors:

Leblicq C. Autosomal recessive insulin-dependent diabetes. [Masters Thesis]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143955.pdf


McGill University

14. Lopez Buitrago, Juan Pablo. The role of microRNA in major depression and antidepressant treatment.

Degree: PhD, Department of Human Genetics, 2016, McGill University

Major depressive disorder (MDD) affects between 6.4 and 10.1% of the population and despite its prevalence and considerable burden, our understanding of its pathophysiology remains… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Lopez Buitrago, J. P. (2016). The role of microRNA in major depression and antidepressant treatment. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143761.pdf

Chicago Manual of Style (16th Edition):

Lopez Buitrago, Juan Pablo. “The role of microRNA in major depression and antidepressant treatment.” 2016. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile143761.pdf.

MLA Handbook (7th Edition):

Lopez Buitrago, Juan Pablo. “The role of microRNA in major depression and antidepressant treatment.” 2016. Web. 17 Jun 2019.

Vancouver:

Lopez Buitrago JP. The role of microRNA in major depression and antidepressant treatment. [Internet] [Doctoral dissertation]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile143761.pdf.

Council of Science Editors:

Lopez Buitrago JP. The role of microRNA in major depression and antidepressant treatment. [Doctoral Dissertation]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143761.pdf


McGill University

15. Yuki, Kyoko. Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis.

Degree: PhD, Department of Human Genetics, 2016, McGill University

Salmonella infections in humans are responsible for two major clinical diseases, typhoid fever and salmonellosis, a self-limiting gastroenteritis. Salmonella infections are transmitted by a fecal-oral… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Yuki, K. (2016). Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143583.pdf

Chicago Manual of Style (16th Edition):

Yuki, Kyoko. “Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis.” 2016. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile143583.pdf.

MLA Handbook (7th Edition):

Yuki, Kyoko. “Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis.” 2016. Web. 17 Jun 2019.

Vancouver:

Yuki K. Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis. [Internet] [Doctoral dissertation]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile143583.pdf.

Council of Science Editors:

Yuki K. Identification of novel salmonella susceptibility loci using ENU chemical mutagenesis. [Doctoral Dissertation]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143583.pdf

16. Eva, Megan. Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen.

Degree: PhD, Department of Human Genetics, 2016, McGill University

Salmonella is a ubiquitous Gram-negative bacterium that causes both food and waterborne illnesses. Infection outcome can vary between individuals within the population and result in… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Eva, M. (2016). Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143635.pdf

Chicago Manual of Style (16th Edition):

Eva, Megan. “Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen.” 2016. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile143635.pdf.

MLA Handbook (7th Edition):

Eva, Megan. “Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen.” 2016. Web. 17 Jun 2019.

Vancouver:

Eva M. Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen. [Internet] [Doctoral dissertation]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile143635.pdf.

Council of Science Editors:

Eva M. Mouse genetic determinants of Salmonella Typhimurium susceptibility identified in a chemical mutagenesis screen. [Doctoral Dissertation]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143635.pdf


McGill University

17. Laverde Duarte, Maria. Characterization of temporal claudin expression and analysis of sequence variants in early kidney development.

Degree: MS, Department of Human Genetics, 2018, McGill University

Congenital Anomalies in the Kidney and Urinary Tract (CAKUT) refer to a range of phenotypes in the kidney and the urinary tract. CAKUT is present… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Laverde Duarte, M. (2018). Characterization of temporal claudin expression and analysis of sequence variants in early kidney development. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154871.pdf

Chicago Manual of Style (16th Edition):

Laverde Duarte, Maria. “Characterization of temporal claudin expression and analysis of sequence variants in early kidney development.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154871.pdf.

MLA Handbook (7th Edition):

Laverde Duarte, Maria. “Characterization of temporal claudin expression and analysis of sequence variants in early kidney development.” 2018. Web. 17 Jun 2019.

Vancouver:

Laverde Duarte M. Characterization of temporal claudin expression and analysis of sequence variants in early kidney development. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154871.pdf.

Council of Science Editors:

Laverde Duarte M. Characterization of temporal claudin expression and analysis of sequence variants in early kidney development. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154871.pdf


McGill University

18. Rahimi, Sophia. Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction.

Degree: MS, Department of Human Genetics, 2018, McGill University

 In Canada, the use of assisted reproductive technologies (ARTs) has risen within the last decade due to the increased prevalence of infertility. Although the majority… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Rahimi, S. (2018). Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154608.pdf

Chicago Manual of Style (16th Edition):

Rahimi, Sophia. “Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile154608.pdf.

MLA Handbook (7th Edition):

Rahimi, Sophia. “Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction.” 2018. Web. 17 Jun 2019.

Vancouver:

Rahimi S. Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile154608.pdf.

Council of Science Editors:

Rahimi S. Effect of folic acid supplementation on adverse morphological and epigenetic outcomes in offspring conceived using assisted reproduction. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile154608.pdf


McGill University

19. Feulner, Lara Michele. Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications.

Degree: MS, Department of Human Genetics, 2018, McGill University

Renal cell carcinoma (RCC) is known to occur across a wide age spectrum traversing age-related organismal changes, however little is known as to how the… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Feulner, L. M. (2018). Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile160544.pdf

Chicago Manual of Style (16th Edition):

Feulner, Lara Michele. “Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile160544.pdf.

MLA Handbook (7th Edition):

Feulner, Lara Michele. “Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications.” 2018. Web. 17 Jun 2019.

Vancouver:

Feulner LM. Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile160544.pdf.

Council of Science Editors:

Feulner LM. Age related variations in gene expression patterns of renal cell carcinoma - Biological and translational implications. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile160544.pdf


McGill University

20. Martel, Rosalie. Optimization of an antibody microarray platform for exosome proteomics.

Degree: M. Eng., Biological & Biomedical Engineering, 2018, McGill University

Extracellular vesicles (EVs) are a heterogeneous ensemble of membrane bodies released by all cell types into their environment. Initially dismissed as cell debris, they have… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Martel, R. (2018). Optimization of an antibody microarray platform for exosome proteomics. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile161283.pdf

Chicago Manual of Style (16th Edition):

Martel, Rosalie. “Optimization of an antibody microarray platform for exosome proteomics.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile161283.pdf.

MLA Handbook (7th Edition):

Martel, Rosalie. “Optimization of an antibody microarray platform for exosome proteomics.” 2018. Web. 17 Jun 2019.

Vancouver:

Martel R. Optimization of an antibody microarray platform for exosome proteomics. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile161283.pdf.

Council of Science Editors:

Martel R. Optimization of an antibody microarray platform for exosome proteomics. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile161283.pdf


McGill University

21. Lean, Graham. «Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation.

Degree: MS, Department of Human Genetics, 2018, McGill University

Regeneration of adult skeletal muscle depends on rare skeletal muscle stem cells (MuSCs) that reside in a quiescent state underneath the basal lamina of the… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Lean, G. (2018). «Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile161379.pdf

Chicago Manual of Style (16th Edition):

Lean, Graham. “«Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation.” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile161379.pdf.

MLA Handbook (7th Edition):

Lean, Graham. “«Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation.” 2018. Web. 17 Jun 2019.

Vancouver:

Lean G. «Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation. [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile161379.pdf.

Council of Science Editors:

Lean G. «Ex vivo» expansion of skeletal muscle stem cells with a novel inhibitor of eIF1α dephosphorylation. [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile161379.pdf


McGill University

22. Bahous, Renata. Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function.

Degree: PhD, Department of Human Genetics, 2018, McGill University

Folate is a B vitamin that plays an essential role in normal brain/cognitive function and homocysteine/methionine (methyl) metabolism. Disturbances in folate metabolism can be either… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Bahous, R. (2018). Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile160663.pdf

Chicago Manual of Style (16th Edition):

Bahous, Renata. “Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function.” 2018. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile160663.pdf.

MLA Handbook (7th Edition):

Bahous, Renata. “Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function.” 2018. Web. 17 Jun 2019.

Vancouver:

Bahous R. Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile160663.pdf.

Council of Science Editors:

Bahous R. Impact of folate and homocysteine metabolism disturbances on brain biochemistry and cognitive function. [Doctoral Dissertation]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile160663.pdf


McGill University

23. Crouse, Alanna. A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo».

Degree: MS, Department of Human Genetics, 2018, McGill University

Over the past 50 years, Canadians have increased their consumption of fresh fruits and vegetables. Over this same time period, foodborne related illness caused by… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Crouse, A. (2018). A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo». (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile161282.pdf

Chicago Manual of Style (16th Edition):

Crouse, Alanna. “A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo».” 2018. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile161282.pdf.

MLA Handbook (7th Edition):

Crouse, Alanna. “A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo».” 2018. Web. 17 Jun 2019.

Vancouver:

Crouse A. A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo». [Internet] [Masters thesis]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile161282.pdf.

Council of Science Editors:

Crouse A. A syst-OMICS approach to food safety: identifying genetic determinants of «Salmonella» virulence «in vivo». [Masters Thesis]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile161282.pdf


McGill University

24. Leung, Vicki. The role of the planar cell polarity protein Vangl2 in retinal axon guidance.

Degree: PhD, Department of Human Genetics, 2018, McGill University

Van-Gogh-like 2 (Vangl2), a critical player in the establishment of planar cell polarity (PCP), is well known for its crucial role in vertebrate neural tube… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Leung, V. (2018). The role of the planar cell polarity protein Vangl2 in retinal axon guidance. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile160599.pdf

Chicago Manual of Style (16th Edition):

Leung, Vicki. “The role of the planar cell polarity protein Vangl2 in retinal axon guidance.” 2018. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile160599.pdf.

MLA Handbook (7th Edition):

Leung, Vicki. “The role of the planar cell polarity protein Vangl2 in retinal axon guidance.” 2018. Web. 17 Jun 2019.

Vancouver:

Leung V. The role of the planar cell polarity protein Vangl2 in retinal axon guidance. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile160599.pdf.

Council of Science Editors:

Leung V. The role of the planar cell polarity protein Vangl2 in retinal axon guidance. [Doctoral Dissertation]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile160599.pdf


McGill University

25. Argyriou, Catherine. Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum.

Degree: PhD, Department of Human Genetics, 2018, McGill University

Zellweger spectrum disorder (ZSD) usually results from biallelic mutations in PEX genes required for peroxisome biogenesis. PEX1-G843D is a common hypomorphic allele associated with milder… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Argyriou, C. (2018). Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile160694.pdf

Chicago Manual of Style (16th Edition):

Argyriou, Catherine. “Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum.” 2018. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile160694.pdf.

MLA Handbook (7th Edition):

Argyriou, Catherine. “Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum.” 2018. Web. 17 Jun 2019.

Vancouver:

Argyriou C. Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile160694.pdf.

Council of Science Editors:

Argyriou C. Developing drug and gene therapies for peroxisome biogenesis disorders of the Zellweger Spectrum. [Doctoral Dissertation]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile160694.pdf


McGill University

26. Monlong, Jean Marcel Maurice. Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts.

Degree: PhD, Department of Human Genetics, 2018, McGill University

 Copy number variation (CNV) affects genomic regions from 50 bp up to entire chromosomes. In addition to being one of the major forms of genomic… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Monlong, J. M. M. (2018). Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile160984.pdf

Chicago Manual of Style (16th Edition):

Monlong, Jean Marcel Maurice. “Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts.” 2018. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile160984.pdf.

MLA Handbook (7th Edition):

Monlong, Jean Marcel Maurice. “Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts.” 2018. Web. 17 Jun 2019.

Vancouver:

Monlong JMM. Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile160984.pdf.

Council of Science Editors:

Monlong JMM. Population-based approaches to characterize copy number variation from whole-genome sequencing in healthy individuals and disease cohorts. [Doctoral Dissertation]. McGill University; 2018. Available from: http://digitool.library.mcgill.ca/thesisfile160984.pdf


McGill University

27. Karimzadeh Reghbati, Mehran. Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks.

Degree: MS, Department of Human Genetics, 2015, McGill University

Next generation sequencing and complementary DNA (cDNA) microarrays are ableto identify aberrations in the structure of DNA and levels of RNA respectively. Whilemany bioinformatics tools… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Karimzadeh Reghbati, M. (2015). Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile135668.pdf

Chicago Manual of Style (16th Edition):

Karimzadeh Reghbati, Mehran. “Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks.” 2015. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile135668.pdf.

MLA Handbook (7th Edition):

Karimzadeh Reghbati, Mehran. “Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks.” 2015. Web. 17 Jun 2019.

Vancouver:

Karimzadeh Reghbati M. Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks. [Internet] [Masters thesis]. McGill University; 2015. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile135668.pdf.

Council of Science Editors:

Karimzadeh Reghbati M. Investigating enrichment patterns of cancer genomic aberrations in protein interaction networks. [Masters Thesis]. McGill University; 2015. Available from: http://digitool.library.mcgill.ca/thesisfile135668.pdf

28. Akoury, Elie. Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles.

Degree: PhD, Department of Human Genetics, 2016, McGill University

 A molar pregnancy or hydatidiform mole (HM) is a human pregnancy with no embryo, but cystic degeneration of chorionic villi and excessive proliferation of the… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Akoury, E. (2016). Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile141420.pdf

Chicago Manual of Style (16th Edition):

Akoury, Elie. “Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles.” 2016. Doctoral Dissertation, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile141420.pdf.

MLA Handbook (7th Edition):

Akoury, Elie. “Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles.” 2016. Web. 17 Jun 2019.

Vancouver:

Akoury E. Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles. [Internet] [Doctoral dissertation]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile141420.pdf.

Council of Science Editors:

Akoury E. Role of the nucleotide oligomerization domain-like receptor protein 7 in the pathology of recurrent hydatidiform moles. [Doctoral Dissertation]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile141420.pdf


McGill University

29. Alsuwailem, Abdulaziz Abdul. Improved drug activity in high-content screening of the microtubule network.

Degree: MS, Department of Human Genetics, 2016, McGill University

High-Content Screening (HCS) is a technology based on the automation of fluorescence microscopy, to screen and analyze the spatial and morphological properties of individual cells.… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Alsuwailem, A. A. (2016). Improved drug activity in high-content screening of the microtubule network. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile141536.pdf

Chicago Manual of Style (16th Edition):

Alsuwailem, Abdulaziz Abdul. “Improved drug activity in high-content screening of the microtubule network.” 2016. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile141536.pdf.

MLA Handbook (7th Edition):

Alsuwailem, Abdulaziz Abdul. “Improved drug activity in high-content screening of the microtubule network.” 2016. Web. 17 Jun 2019.

Vancouver:

Alsuwailem AA. Improved drug activity in high-content screening of the microtubule network. [Internet] [Masters thesis]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile141536.pdf.

Council of Science Editors:

Alsuwailem AA. Improved drug activity in high-content screening of the microtubule network. [Masters Thesis]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile141536.pdf


McGill University

30. Wang, Zibo. Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology.

Degree: MS, Department of Human Genetics, 2016, McGill University

In recent years, the global study of expression quantitative trait loci (eQTLs) has been driven by the advances of next generation sequencing (NGS) combined with… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Wang, Z. (2016). Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile139842.pdf

Chicago Manual of Style (16th Edition):

Wang, Zibo. “Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology.” 2016. Masters Thesis, McGill University. Accessed June 17, 2019. http://digitool.library.mcgill.ca/thesisfile139842.pdf.

MLA Handbook (7th Edition):

Wang, Zibo. “Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology.” 2016. Web. 17 Jun 2019.

Vancouver:

Wang Z. Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology. [Internet] [Masters thesis]. McGill University; 2016. [cited 2019 Jun 17]. Available from: http://digitool.library.mcgill.ca/thesisfile139842.pdf.

Council of Science Editors:

Wang Z. Dissecting the regulation of expression quantitative trait loci using RNA sequencing technology. [Masters Thesis]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile139842.pdf

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