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You searched for subject:(0369). Showing records 1 – 30 of 525 total matches.

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University of Toronto

1. Mador-House, Kelly Rachel. Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci.

Degree: 2014, University of Toronto

There are over 40 genetic diseases caused by repeat locus-specific instability. The causes of repeat instability are poorly understood and a mechanism that explains their… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Mador-House, K. R. (2014). Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68079

Chicago Manual of Style (16th Edition):

Mador-House, Kelly Rachel. “Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci.” 2014. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/68079.

MLA Handbook (7th Edition):

Mador-House, Kelly Rachel. “Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci.” 2014. Web. 05 Dec 2020.

Vancouver:

Mador-House KR. Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/68079.

Council of Science Editors:

Mador-House KR. Investigation of the Epigenetic Landscape at Disease-causing Polymorphic Repeat Loci. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68079


University of Toronto

2. Chen, Yi-an. Discovery of Problematic Probes in Illumina DNA Methylation Microarrays.

Degree: 2015, University of Toronto

In humans, there are hundreds of cell types, each with specialized functions that make up different tissues and organs. All these cells share the same… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Chen, Y. (2015). Discovery of Problematic Probes in Illumina DNA Methylation Microarrays. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70267

Chicago Manual of Style (16th Edition):

Chen, Yi-an. “Discovery of Problematic Probes in Illumina DNA Methylation Microarrays.” 2015. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/70267.

MLA Handbook (7th Edition):

Chen, Yi-an. “Discovery of Problematic Probes in Illumina DNA Methylation Microarrays.” 2015. Web. 05 Dec 2020.

Vancouver:

Chen Y. Discovery of Problematic Probes in Illumina DNA Methylation Microarrays. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/70267.

Council of Science Editors:

Chen Y. Discovery of Problematic Probes in Illumina DNA Methylation Microarrays. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70267


University of Toronto

3. Lee, Timothy Mendel. Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability.

Degree: 2016, University of Toronto

Cancer is a genetic disease that develops as a result of the acquisition of stable somatic mutations. Many cancers are believed to acquire mutations at… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Lee, T. M. (2016). Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75109

Chicago Manual of Style (16th Edition):

Lee, Timothy Mendel. “Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability.” 2016. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/75109.

MLA Handbook (7th Edition):

Lee, Timothy Mendel. “Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability.” 2016. Web. 05 Dec 2020.

Vancouver:

Lee TM. Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/75109.

Council of Science Editors:

Lee TM. Surveying the Human Genome for Genetic Markers Associated with the Mutator Phenotype and Chromosomal Instability. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/75109


University of Toronto

4. Chernomas, Gregory Simon. Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain.

Degree: 2017, University of Toronto

Adult neural stem cells (NSCs) and neural progenitor cells (NPCs) have been the subject of significant research in recent times. Model organisms, including Drosophila melanogaster,… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Chernomas, G. S. (2017). Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/77787

Chicago Manual of Style (16th Edition):

Chernomas, Gregory Simon. “Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/77787.

MLA Handbook (7th Edition):

Chernomas, Gregory Simon. “Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain.” 2017. Web. 05 Dec 2020.

Vancouver:

Chernomas GS. Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/77787.

Council of Science Editors:

Chernomas GS. Identifying and Characterizing Putative Neural Progenitor Cells within the Adult Drosophila melanogaster Central Brain. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/77787


University of Toronto

5. Mark, Stephanie. Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae.

Degree: 2017, University of Toronto

Discerning the genetic basis of adaptive phenotypes is a fundamental problem in biology that remains an open question. Studies using high-throughput sequencing methods of gene… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Mark, S. (2017). Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/77831

Chicago Manual of Style (16th Edition):

Mark, Stephanie. “Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/77831.

MLA Handbook (7th Edition):

Mark, Stephanie. “Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae.” 2017. Web. 05 Dec 2020.

Vancouver:

Mark S. Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/77831.

Council of Science Editors:

Mark S. Temperature-dependent Patterns of Gene Expression in Caenorhabditis briggsae. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/77831


University of Toronto

6. Alibai, Sabriyeh. Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins.

Degree: 2018, University of Toronto

Molecules that bind to targets with high specificity and affinity are used as therapeutic and diagnostic agents in medicine and research. Protein and non-protein ligands… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Alibai, S. (2018). Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89586

Chicago Manual of Style (16th Edition):

Alibai, Sabriyeh. “Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins.” 2018. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/89586.

MLA Handbook (7th Edition):

Alibai, Sabriyeh. “Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins.” 2018. Web. 05 Dec 2020.

Vancouver:

Alibai S. Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/89586.

Council of Science Editors:

Alibai S. Engineered Protein Scaffolds as Tools for Studying Intracellular Proteins. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89586


University of Toronto

7. Antounians, Lina. An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells.

Degree: 2015, University of Toronto

A major challenge in human genetics is to understand the mechanisms that control gene expression. To identify gene regulatory regions required for vascular homeostasis, we… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Antounians, L. (2015). An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91213

Chicago Manual of Style (16th Edition):

Antounians, Lina. “An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells.” 2015. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/91213.

MLA Handbook (7th Edition):

Antounians, Lina. “An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells.” 2015. Web. 05 Dec 2020.

Vancouver:

Antounians L. An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/91213.

Council of Science Editors:

Antounians L. An Inter-vascular Bed and Inter-species Investigation of Epigenetic Regulatory Elements in Endothelial Cells. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/91213


University of Toronto

8. Tran, Stephanie. Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase.

Degree: 2019, University of Toronto

Our genome is packaged by nucleosomes consisting of ~147 base pairs of DNA wrapped around a histone octamer. Nucleosomes carry post-translational modifications (PTMs) on their… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Tran, S. (2019). Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/101816

Chicago Manual of Style (16th Edition):

Tran, Stephanie. “Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase.” 2019. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/101816.

MLA Handbook (7th Edition):

Tran, Stephanie. “Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase.” 2019. Web. 05 Dec 2020.

Vancouver:

Tran S. Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/101816.

Council of Science Editors:

Tran S. Determining the Mechanism of Nucleosomal Histone Segregation by the CMG Helicase. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/101816


University of Toronto

9. Oh, Yoomi. Identification and Validation of the Regulators of Riboneogenesis.

Degree: 2017, University of Toronto

The riboneogenesis pathway provides yeast with an alternate route for ribose production. Ribose is an essential precursor for nucleotide synthesis. Riboneogenesis connects glycolysis to the… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Oh, Y. (2017). Identification and Validation of the Regulators of Riboneogenesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/97239

Chicago Manual of Style (16th Edition):

Oh, Yoomi. “Identification and Validation of the Regulators of Riboneogenesis.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/97239.

MLA Handbook (7th Edition):

Oh, Yoomi. “Identification and Validation of the Regulators of Riboneogenesis.” 2017. Web. 05 Dec 2020.

Vancouver:

Oh Y. Identification and Validation of the Regulators of Riboneogenesis. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/97239.

Council of Science Editors:

Oh Y. Identification and Validation of the Regulators of Riboneogenesis. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/97239


University of Toronto

10. Raghuram, Nandini. Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context.

Degree: PhD, 2018, University of Toronto

Molecular heterogeneity amongst breast tumors is a major confounding factor in developing effective therapies for patients. Although key oncogenic drivers of breast cancer (BC), like… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Raghuram, N. (2018). Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101660

Chicago Manual of Style (16th Edition):

Raghuram, Nandini. “Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context.” 2018. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/101660.

MLA Handbook (7th Edition):

Raghuram, Nandini. “Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context.” 2018. Web. 05 Dec 2020.

Vancouver:

Raghuram N. Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/101660.

Council of Science Editors:

Raghuram N. Genetic Analysis of Gata4 and RhoC, Modifiers of Her2/Neu Expression and Signaling, in a Mammary Tumor Context. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/101660


University of Toronto

11. Murshedi, Fathiya Al. Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells.

Degree: 2010, University of Toronto

Most immortal human cells maintain their telomeres by up-regulating the enzyme telomerase. Approximately 10-15% of immortal cells maintain their telomere lengths by a recombination-based mechanism… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Murshedi, F. A. (2010). Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24237

Chicago Manual of Style (16th Edition):

Murshedi, Fathiya Al. “Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells.” 2010. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/24237.

MLA Handbook (7th Edition):

Murshedi, Fathiya Al. “Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells.” 2010. Web. 05 Dec 2020.

Vancouver:

Murshedi FA. Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/24237.

Council of Science Editors:

Murshedi FA. Role of FANCM in Alternative Lengthening of Telomeres (ALT) Human Cells. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24237


University of Toronto

12. Abouelkheer, Yasser. MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA.

Degree: 2017, University of Toronto

PRDM14 is an embryonic stem cell pluripotency regulator that is ectopically expressed in human malignancies. The aim of my thesis is to gain insight into… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Abouelkheer, Y. (2017). MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79280

Chicago Manual of Style (16th Edition):

Abouelkheer, Yasser. “MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79280.

MLA Handbook (7th Edition):

Abouelkheer, Yasser. “MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA.” 2017. Web. 05 Dec 2020.

Vancouver:

Abouelkheer Y. MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79280.

Council of Science Editors:

Abouelkheer Y. MODELLING PRDM14 EXPRESSION IN HUMAN ACUTE MYELOID LEUKEMIA. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79280


University of Toronto

13. Vuong, Sandra. Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood.

Degree: 2017, University of Toronto

Congenital heart defects are caused by abnormalities in heart development, which can result from defects in regulation of cardiogenic gene expression by chromatin modifiers. Lethal… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Vuong, S. (2017). Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79285

Chicago Manual of Style (16th Edition):

Vuong, Sandra. “Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79285.

MLA Handbook (7th Edition):

Vuong, Sandra. “Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood.” 2017. Web. 05 Dec 2020.

Vancouver:

Vuong S. Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79285.

Council of Science Editors:

Vuong S. Loss of L3mbtl2 in Cardiac Progenitor Cells Causes Subtle Defects in the Developing Heart Leading to Cardiac Dysfunction in Adulthood. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79285


University of Toronto

14. Sung, Rachel Cheuk Lam. Identifying interacting ligands of human RORγ using transgenic zebrafish.

Degree: 2017, University of Toronto

The retinoic acid receptor-related orphan receptor gamma, or RORγ, is a member of the nuclear receptor ROR family and its activity can be regulated by… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Sung, R. C. L. (2017). Identifying interacting ligands of human RORγ using transgenic zebrafish. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79293

Chicago Manual of Style (16th Edition):

Sung, Rachel Cheuk Lam. “Identifying interacting ligands of human RORγ using transgenic zebrafish.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79293.

MLA Handbook (7th Edition):

Sung, Rachel Cheuk Lam. “Identifying interacting ligands of human RORγ using transgenic zebrafish.” 2017. Web. 05 Dec 2020.

Vancouver:

Sung RCL. Identifying interacting ligands of human RORγ using transgenic zebrafish. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79293.

Council of Science Editors:

Sung RCL. Identifying interacting ligands of human RORγ using transgenic zebrafish. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79293


University of Toronto

15. Bassi, Prabhpreet S. Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A.

Degree: 2017, University of Toronto

Merosin-deficient congenital muscular dystrophy type 1A is an autosomal recessive disease caused by mutations in the LAMA2 gene, which codes for the laminin ⍺2 chain… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Bassi, P. S. (2017). Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79294

Chicago Manual of Style (16th Edition):

Bassi, Prabhpreet S. “Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79294.

MLA Handbook (7th Edition):

Bassi, Prabhpreet S. “Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A.” 2017. Web. 05 Dec 2020.

Vancouver:

Bassi PS. Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79294.

Council of Science Editors:

Bassi PS. Assessing the Therapeutic Potential of CRISPR/Cas9-Mediated Gene Modulation in Merosin-Deficient Congenital Muscular Dystrophy Type 1A. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79294


University of Toronto

16. Lee, Yvonne Kar Man. Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children.

Degree: 2017, University of Toronto

Background: Genetic studies in obesity and eating disorders have identified brain-derived neurotrophic factor (BDNF) and neurotrophic receptor tyrosine kinase 2 (NTRK2) as candidate genes. We… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Lee, Y. K. M. (2017). Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79359

Chicago Manual of Style (16th Edition):

Lee, Yvonne Kar Man. “Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79359.

MLA Handbook (7th Edition):

Lee, Yvonne Kar Man. “Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children.” 2017. Web. 05 Dec 2020.

Vancouver:

Lee YKM. Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79359.

Council of Science Editors:

Lee YKM. Exploring the Role of BDNF and NTRK2 Genetic Polymorphisms on Eating Behaviours in Young Children. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79359


University of Toronto

17. Sinopoli, Vanessa Maria-Teresa. ‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample.

Degree: PhD, 2019, University of Toronto

 Background: Serotonin genes are commonly studied in obsessive-compulsive disorder (OCD), but findings have been inconsistent. OCD is phenotypically heterogeneous, with subgroups reflecting symptom dimensions, sex,… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Sinopoli, V. M. (2019). ‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/97632

Chicago Manual of Style (16th Edition):

Sinopoli, Vanessa Maria-Teresa. “‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample.” 2019. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/97632.

MLA Handbook (7th Edition):

Sinopoli, Vanessa Maria-Teresa. “‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample.” 2019. Web. 05 Dec 2020.

Vancouver:

Sinopoli VM. ‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/97632.

Council of Science Editors:

Sinopoli VM. ‘Long’ Story ‘Short’: Serotonin Genes and Their Association with OC Trait Dimensions and Hoarding in a Community, Pediatric Sample and with Brain Volume Differences in a Clinical, Pediatric OCD Sample. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/97632


University of Toronto

18. Patel, Prital. Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions.

Degree: PhD, 2017, University of Toronto

 Glycogen synthase kinase-3 (GSK-3) α and β are protein-serine threonine kinases that regulate diverse cellular targets. Their substrates range from regulators of cellular metabolism to… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Patel, P. (2017). Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/79417

Chicago Manual of Style (16th Edition):

Patel, Prital. “Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions.” 2017. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/79417.

MLA Handbook (7th Edition):

Patel, Prital. “Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions.” 2017. Web. 05 Dec 2020.

Vancouver:

Patel P. Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/79417.

Council of Science Editors:

Patel P. Multiple Roles of Glycogen Synthase Kinase-3 Genes in Liver Functions. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79417


University of Toronto

19. Allen, Aaron Munro. Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster.

Degree: PhD, 2016, University of Toronto

Pleiotropy is defined as the manifold effects of a gene at the phenotypic level. Understanding the mechanisms of manifold gene action has important implications for… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Allen, A. M. (2016). Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/88980

Chicago Manual of Style (16th Edition):

Allen, Aaron Munro. “Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster.” 2016. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/88980.

MLA Handbook (7th Edition):

Allen, Aaron Munro. “Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster.” 2016. Web. 05 Dec 2020.

Vancouver:

Allen AM. Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/88980.

Council of Science Editors:

Allen AM. Deciphering Pleiotropic Effects: A Molecular Characterisation of the Foraging Gene in Drosophila melanogaster. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/88980


University of Toronto

20. Ho, Ka Ho Eddie. The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence.

Degree: PhD, 2018, University of Toronto

 Understanding the origin, maintenance and distribution of nature’s astonishing diversity of reproductive systems is a major endeavour in evolutionary biology. One of the oldest evolutionary… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Ho, K. H. E. (2018). The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89664

Chicago Manual of Style (16th Edition):

Ho, Ka Ho Eddie. “The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence.” 2018. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/89664.

MLA Handbook (7th Edition):

Ho, Ka Ho Eddie. “The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence.” 2018. Web. 05 Dec 2020.

Vancouver:

Ho KHE. The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/89664.

Council of Science Editors:

Ho KHE. The Effects of Asexuality and Selfing on Genetic Diversity, the Efficacy of Selection and Species Persistence. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89664


University of Toronto

21. Chowdhury, Nabilah Ishrat. The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain.

Degree: PhD, 2015, University of Toronto

 The use of second-generation antipsychotic medications can result in the development of severe side effects such as weight gain and metabolic syndrome. Previous studies have… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Chowdhury, N. I. (2015). The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69267

Chicago Manual of Style (16th Edition):

Chowdhury, Nabilah Ishrat. “The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain.” 2015. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/69267.

MLA Handbook (7th Edition):

Chowdhury, Nabilah Ishrat. “The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain.” 2015. Web. 05 Dec 2020.

Vancouver:

Chowdhury NI. The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/69267.

Council of Science Editors:

Chowdhury NI. The Role of Leptin-melanocortin System Gene Variants in Antipsychotic-Iiduced Weight Gain. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69267


University of Toronto

22. Akef, Abdalla. Investigating mRNA Sequence Features that Regulate Nuclear Export.

Degree: PhD, 2016, University of Toronto

 In eukaryotes, the nucleus divides the cell into two compartments: the nucleoplasm, where RNA is synthesized, processed and packaged, and the cytoplasm, where mature mRNA… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Akef, A. (2016). Investigating mRNA Sequence Features that Regulate Nuclear Export. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/72914

Chicago Manual of Style (16th Edition):

Akef, Abdalla. “Investigating mRNA Sequence Features that Regulate Nuclear Export.” 2016. Doctoral Dissertation, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/72914.

MLA Handbook (7th Edition):

Akef, Abdalla. “Investigating mRNA Sequence Features that Regulate Nuclear Export.” 2016. Web. 05 Dec 2020.

Vancouver:

Akef A. Investigating mRNA Sequence Features that Regulate Nuclear Export. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/72914.

Council of Science Editors:

Akef A. Investigating mRNA Sequence Features that Regulate Nuclear Export. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72914


University of Toronto

23. Nguyen, Charlotte Michelle. Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder.

Degree: 2019, University of Toronto

Short tandem repeats (STRs) may contribute to the genetic etiology of autism spectrum disorder (ASD) since several pathogenic STRs are ASD risk factors. Screening for… (more)

Subjects/Keywords: 0369

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APA (6th Edition):

Nguyen, C. M. (2019). Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/102996

Chicago Manual of Style (16th Edition):

Nguyen, Charlotte Michelle. “Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder.” 2019. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/102996.

MLA Handbook (7th Edition):

Nguyen, Charlotte Michelle. “Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder.” 2019. Web. 05 Dec 2020.

Vancouver:

Nguyen CM. Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/102996.

Council of Science Editors:

Nguyen CM. Genome-wide Investigation of Short Tandem Repeat Variation in Autism Spectrum Disorder. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/102996


University of Toronto

24. Mui, Ryan KY. Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity.

Degree: 2010, University of Toronto

Tubby mice succumb to blindness, deafness, and obesity. Vision and auditory deficits are attributed to neurodegeneration and tubby-associated obesity has been postulated to result from… (more)

Subjects/Keywords: Tubby; 0369

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APA (6th Edition):

Mui, R. K. (2010). Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32207

Chicago Manual of Style (16th Edition):

Mui, Ryan KY. “Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity.” 2010. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/32207.

MLA Handbook (7th Edition):

Mui, Ryan KY. “Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity.” 2010. Web. 05 Dec 2020.

Vancouver:

Mui RK. Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/32207.

Council of Science Editors:

Mui RK. Investigating the Neurobiological Role of Tubby, a Protein Involved in Obesity. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32207


University of Toronto

25. Tkachyova, Ilona. Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity.

Degree: 2013, University of Toronto

Mucopolysaccharidoses result from genetic mutations in lysosomal enzymes required for degradation of glycosaminoglycans. The deficiency in any of eight lysosomal enzymes needed to degrade heparan… (more)

Subjects/Keywords: Mucopolysaccharidoses; NDST1; 0369

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APA (6th Edition):

Tkachyova, I. (2013). Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42963

Chicago Manual of Style (16th Edition):

Tkachyova, Ilona. “Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity.” 2013. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/42963.

MLA Handbook (7th Edition):

Tkachyova, Ilona. “Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity.” 2013. Web. 05 Dec 2020.

Vancouver:

Tkachyova I. Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/42963.

Council of Science Editors:

Tkachyova I. Developing a Potential Substrate Reduction Therapy for Six Mucopolysaccharidoses by Decreasing NDST1 Activity. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42963


University of Toronto

26. Kim, Dennis. Molecular Genetic Analysis of the Mouse Anorexia Mutation.

Degree: 2010, University of Toronto

The serotonergic system regulates numerous behaviours and disruptions in this system have been associated with disorders of mood and mind. Although molecular genetic analysis has… (more)

Subjects/Keywords: serotonin; mouse; 0369

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APA (6th Edition):

Kim, D. (2010). Molecular Genetic Analysis of the Mouse Anorexia Mutation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32211

Chicago Manual of Style (16th Edition):

Kim, Dennis. “Molecular Genetic Analysis of the Mouse Anorexia Mutation.” 2010. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/32211.

MLA Handbook (7th Edition):

Kim, Dennis. “Molecular Genetic Analysis of the Mouse Anorexia Mutation.” 2010. Web. 05 Dec 2020.

Vancouver:

Kim D. Molecular Genetic Analysis of the Mouse Anorexia Mutation. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/32211.

Council of Science Editors:

Kim D. Molecular Genetic Analysis of the Mouse Anorexia Mutation. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32211


University of Toronto

27. Asa, Jonathon S. Probing the Molecular Interactions of ATRX.

Degree: 2017, University of Toronto

Alpha thalassemia/mental retardation syndrome X-linked (ATRX) is linked to both developmental disease and cancer. ATRX functions in coordination with Death Domain Associated Protein 6 (DAXX)… (more)

Subjects/Keywords: ATRX; BioID; 0369

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APA (6th Edition):

Asa, J. S. (2017). Probing the Molecular Interactions of ATRX. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91168

Chicago Manual of Style (16th Edition):

Asa, Jonathon S. “Probing the Molecular Interactions of ATRX.” 2017. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/91168.

MLA Handbook (7th Edition):

Asa, Jonathon S. “Probing the Molecular Interactions of ATRX.” 2017. Web. 05 Dec 2020.

Vancouver:

Asa JS. Probing the Molecular Interactions of ATRX. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/91168.

Council of Science Editors:

Asa JS. Probing the Molecular Interactions of ATRX. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/91168


University of Toronto

28. Benhabib, Hadas. Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks.

Degree: 2014, University of Toronto

Legionnaires' disease is a severe, often fatal pneumonia caused by the intracellular pathogen

M.Sc.

2017-11-18 00:00:00

Advisors/Committee Members: Ensminger, Alexander W, Molecular and Medical Genetics.

Subjects/Keywords: Legionella; Legionnaires; 0369

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APA (6th Edition):

Benhabib, H. (2014). Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80173

Chicago Manual of Style (16th Edition):

Benhabib, Hadas. “Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks.” 2014. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/80173.

MLA Handbook (7th Edition):

Benhabib, Hadas. “Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks.” 2014. Web. 05 Dec 2020.

Vancouver:

Benhabib H. Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/80173.

Council of Science Editors:

Benhabib H. Reconstructing the Evolutionary Trajectory of Legionnaires' Disease Outbreaks. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/80173


University of Toronto

29. McConnell, Murray. Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster.

Degree: 2011, University of Toronto

Egg-laying decisions can have significant fitness consequences. In female Drosophila melanogaster, egg-laying involves foraging-like behaviour. Natural allelic variation in foraging (for) underlies the rover/sitter foraging… (more)

Subjects/Keywords: Oviposition; Drosophila; 0369

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APA (6th Edition):

McConnell, M. (2011). Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29527

Chicago Manual of Style (16th Edition):

McConnell, Murray. “Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster.” 2011. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/29527.

MLA Handbook (7th Edition):

McConnell, Murray. “Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster.” 2011. Web. 05 Dec 2020.

Vancouver:

McConnell M. Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/29527.

Council of Science Editors:

McConnell M. Exploring the Role of the Foraging Gene on Egg-laying Preferences in Drosophila melanogaster. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29527


University of Toronto

30. Malik, Ayesha. The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression.

Degree: 2012, University of Toronto

Background: Antisocial behaviours in adolescents are costly in social and financial terms. These behaviours are heritable and genetic variants may be contributing factors. The purpose… (more)

Subjects/Keywords: genetics of aggression; children; 0369

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APA (6th Edition):

Malik, A. (2012). The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33430

Chicago Manual of Style (16th Edition):

Malik, Ayesha. “The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression.” 2012. Masters Thesis, University of Toronto. Accessed December 05, 2020. http://hdl.handle.net/1807/33430.

MLA Handbook (7th Edition):

Malik, Ayesha. “The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression.” 2012. Web. 05 Dec 2020.

Vancouver:

Malik A. The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1807/33430.

Council of Science Editors:

Malik A. The Role of Genetic Variants Regulating the Oxytocin-­Vasopressin System in Childhood-­onset Aggression. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33430

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