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You searched for subject:(0307). Showing records 31 – 60 of 386 total matches.

[1] [2] [3] [4] [5] … [13]

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University of Toronto

31. Rajendran, Dushyandi. Identification of Novel Regulators of Numb Alternative Splicing.

Degree: 2014, University of Toronto

Alternative splicing (AS) is a post-transcriptional mechanism resulting in the production of multiple mRNA and protein isoforms from a single gene. The endocytic adaptor protein… (more)

Subjects/Keywords: Cancer; Development; Protein; RNA; 0307

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APA (6th Edition):

Rajendran, D. (2014). Identification of Novel Regulators of Numb Alternative Splicing. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72370

Chicago Manual of Style (16th Edition):

Rajendran, Dushyandi. “Identification of Novel Regulators of Numb Alternative Splicing.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/72370.

MLA Handbook (7th Edition):

Rajendran, Dushyandi. “Identification of Novel Regulators of Numb Alternative Splicing.” 2014. Web. 24 Aug 2019.

Vancouver:

Rajendran D. Identification of Novel Regulators of Numb Alternative Splicing. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/72370.

Council of Science Editors:

Rajendran D. Identification of Novel Regulators of Numb Alternative Splicing. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/72370


University of Toronto

32. Rajendran, Dushyandi. Identification of Novel Regulators of Numb Alternative Splicing.

Degree: 2014, University of Toronto

Alternative splicing (AS) is a post-transcriptional mechanism resulting in the production of multiple mRNA and protein isoforms from a single gene. The endocytic adaptor protein… (more)

Subjects/Keywords: Cancer; Development; Protein; RNA; 0307

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APA (6th Edition):

Rajendran, D. (2014). Identification of Novel Regulators of Numb Alternative Splicing. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72378

Chicago Manual of Style (16th Edition):

Rajendran, Dushyandi. “Identification of Novel Regulators of Numb Alternative Splicing.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/72378.

MLA Handbook (7th Edition):

Rajendran, Dushyandi. “Identification of Novel Regulators of Numb Alternative Splicing.” 2014. Web. 24 Aug 2019.

Vancouver:

Rajendran D. Identification of Novel Regulators of Numb Alternative Splicing. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/72378.

Council of Science Editors:

Rajendran D. Identification of Novel Regulators of Numb Alternative Splicing. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/72378


University of Toronto

33. Lee, Jennifer PY. Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1.

Degree: 2016, University of Toronto

The Hedgehog (Hh)-pathway is a critical signalling cascade that determines cell fate and is required for embryonic and postnatal development. A central component of this… (more)

Subjects/Keywords: Hedgehog; Hh-signalling; Ptch1; 0307

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APA (6th Edition):

Lee, J. P. (2016). Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75114

Chicago Manual of Style (16th Edition):

Lee, Jennifer PY. “Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1.” 2016. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/75114.

MLA Handbook (7th Edition):

Lee, Jennifer PY. “Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1.” 2016. Web. 24 Aug 2019.

Vancouver:

Lee JP. Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/75114.

Council of Science Editors:

Lee JP. Characterizing the Structure and Function of the Cytoplasmic Domains of Ptch1. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/75114


University of Toronto

34. Ali, Mehrab. Chemical Genetic Interactions for Antibiotics in Escherichia coli.

Degree: 2012, University of Toronto

The discovery of penicillin ushered in the era of the mass use of antibiotics in clinical settings. Today the development of antibiotic resistance and lack… (more)

Subjects/Keywords: Escherichia coli; chemical genetics; 0307

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APA (6th Edition):

Ali, M. (2012). Chemical Genetic Interactions for Antibiotics in Escherichia coli. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32516

Chicago Manual of Style (16th Edition):

Ali, Mehrab. “Chemical Genetic Interactions for Antibiotics in Escherichia coli.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/32516.

MLA Handbook (7th Edition):

Ali, Mehrab. “Chemical Genetic Interactions for Antibiotics in Escherichia coli.” 2012. Web. 24 Aug 2019.

Vancouver:

Ali M. Chemical Genetic Interactions for Antibiotics in Escherichia coli. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/32516.

Council of Science Editors:

Ali M. Chemical Genetic Interactions for Antibiotics in Escherichia coli. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32516


University of Toronto

35. Bhattacharya, Anandi. Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells.

Degree: 2012, University of Toronto

Distal regulatory elements (DREs) have been identified upstream of the hematopoietic regulator Lim domain only 2 (Lmo2) gene in the human and mouse genomes. In… (more)

Subjects/Keywords: Molecular Biology; Cell Biology; 0307

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APA (6th Edition):

Bhattacharya, A. (2012). Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33337

Chicago Manual of Style (16th Edition):

Bhattacharya, Anandi. “Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/33337.

MLA Handbook (7th Edition):

Bhattacharya, Anandi. “Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells.” 2012. Web. 24 Aug 2019.

Vancouver:

Bhattacharya A. Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/33337.

Council of Science Editors:

Bhattacharya A. Distal Enhancer – Gene Interactions at the Lmo2 locus in Mouse Erythroid cells. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33337


University of Toronto

36. Wan, Mark H. The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification.

Degree: 2013, University of Toronto

Introduction: Activation of Runt Related Transcription Factor 2 (RUNX2) is required for transdifferentiation of Vascular Smooth Muscle Cells (VSMCs) into a calcifying osteoblast-like phenotype. Our… (more)

Subjects/Keywords: Pathology; Molecular; 0571; 0307

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APA (6th Edition):

Wan, M. H. (2013). The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/35146

Chicago Manual of Style (16th Edition):

Wan, Mark H. “The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification.” 2013. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/35146.

MLA Handbook (7th Edition):

Wan, Mark H. “The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification.” 2013. Web. 24 Aug 2019.

Vancouver:

Wan MH. The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/35146.

Council of Science Editors:

Wan MH. The Mechanism of Discoidin Domain Receptor 1 Mediated Vascular Calcification. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35146


University of Toronto

37. Smith, Lindsay. Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation.

Degree: 2018, University of Toronto

The triad, formed by the close apposition of the T-tubule and terminal sarcoplasmic reticulum, is an important skeletal muscle substructure that regulates excitation-contraction coupling and… (more)

Subjects/Keywords: muscle; phosphoinositide; triad; zebrafish; 0307

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APA (6th Edition):

Smith, L. (2018). Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91418

Chicago Manual of Style (16th Edition):

Smith, Lindsay. “Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation.” 2018. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/91418.

MLA Handbook (7th Edition):

Smith, Lindsay. “Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation.” 2018. Web. 24 Aug 2019.

Vancouver:

Smith L. Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/91418.

Council of Science Editors:

Smith L. Investigating the Role of Phosphoinositides in Skeletal Muscle Development and Substructure Formation. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91418


University of Toronto

38. Acharya, Durga. Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages.

Degree: 2018, University of Toronto

Macrophages are able to recognize, bind and internalize pathogens through two types of phagocytic receptors; the Fc receptors (FcγR) and the complement receptors (CR). FcγRs… (more)

Subjects/Keywords: Inflammation; Macrophages; Phagocytosis; 0307

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APA (6th Edition):

Acharya, D. (2018). Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91479

Chicago Manual of Style (16th Edition):

Acharya, Durga. “Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages.” 2018. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/91479.

MLA Handbook (7th Edition):

Acharya, Durga. “Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages.” 2018. Web. 24 Aug 2019.

Vancouver:

Acharya D. Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/91479.

Council of Science Editors:

Acharya D. Interplay between phagocytosis and pro-inflammatory cytokine production in macrophages. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91479


University of Toronto

39. D'Ambrosio, Lisa. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.

Degree: 2010, University of Toronto

Reversible protein phosphorylation is an essential regulatory mechanism used by eukaryotes to coordinate the biochemical processes of the cell. The PP2A phosphatase functions to dephosphorylate… (more)

Subjects/Keywords: phosphatase; mass spectrometry; 0307

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APA (6th Edition):

D'Ambrosio, L. (2010). Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24554

Chicago Manual of Style (16th Edition):

D'Ambrosio, Lisa. “Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/24554.

MLA Handbook (7th Edition):

D'Ambrosio, Lisa. “Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.” 2010. Web. 24 Aug 2019.

Vancouver:

D'Ambrosio L. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/24554.

Council of Science Editors:

D'Ambrosio L. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24554


University of Toronto

40. Sturgeon, Kendra. Refining Positional Identity in the Vertebrate Hindbrain.

Degree: 2010, University of Toronto

The vertebrate hindbrain is divided early in embryogenesis along its anterior-posterior axis into eight segments known as rhombomeres. This provides an excellent model for studying… (more)

Subjects/Keywords: hindbrain development; segmentation; 0369; 0307

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APA (6th Edition):

Sturgeon, K. (2010). Refining Positional Identity in the Vertebrate Hindbrain. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32209

Chicago Manual of Style (16th Edition):

Sturgeon, Kendra. “Refining Positional Identity in the Vertebrate Hindbrain.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/32209.

MLA Handbook (7th Edition):

Sturgeon, Kendra. “Refining Positional Identity in the Vertebrate Hindbrain.” 2010. Web. 24 Aug 2019.

Vancouver:

Sturgeon K. Refining Positional Identity in the Vertebrate Hindbrain. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/32209.

Council of Science Editors:

Sturgeon K. Refining Positional Identity in the Vertebrate Hindbrain. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32209


University of Toronto

41. Bertrand, Kelsey C. The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma.

Degree: 2010, University of Toronto

Medulloblastoma is the most common pediatric brain tumour, yet many of the underlying genetic and epigenetic factors have yet to be discovered. After a genome… (more)

Subjects/Keywords: medulloblastoma; PCDH10; 0307; 0369

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APA (6th Edition):

Bertrand, K. C. (2010). The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/27544

Chicago Manual of Style (16th Edition):

Bertrand, Kelsey C. “The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/27544.

MLA Handbook (7th Edition):

Bertrand, Kelsey C. “The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma.” 2010. Web. 24 Aug 2019.

Vancouver:

Bertrand KC. The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/27544.

Council of Science Editors:

Bertrand KC. The Role of Cell Adhesion Genes in the Pathogenesis of Medulloblastoma. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/27544


University of Toronto

42. Vojvodic, Milijana. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.

Degree: 2010, University of Toronto

Neuroblastoma (NB) is the most common extra-cranial solid tumor in children. Recently discovered neuroblastoma tumor-initiating cells (NB-TICs) have many properties of cancer stem cells and… (more)

Subjects/Keywords: Neuroblastoma; Phospho-proteomics; 0307

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APA (6th Edition):

Vojvodic, M. (2010). Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30136

Chicago Manual of Style (16th Edition):

Vojvodic, Milijana. “Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/30136.

MLA Handbook (7th Edition):

Vojvodic, Milijana. “Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets.” 2010. Web. 24 Aug 2019.

Vancouver:

Vojvodic M. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/30136.

Council of Science Editors:

Vojvodic M. Phospho-proteomic Analysis of Neuroblastoma Tumor Initiating Cell Signaling Pathways: Identification of Src Family and B Cell Receptor Signaling as Novel Drug Targets. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/30136


University of Toronto

43. Fung, Thomas Anthony. Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer.

Degree: 2017, University of Toronto

Abstract WDR5 is a core subunit of the MLL-WRAD methyltransferases, NSL-MOF acetyltransferases and MYC-MAX transcription factors. Dysregulation of these complexes has been implicated in numerous… (more)

Subjects/Keywords: Colorectal Cancer; Epigenetics; WDR5; 0307

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APA (6th Edition):

Fung, T. A. (2017). Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79378

Chicago Manual of Style (16th Edition):

Fung, Thomas Anthony. “Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer.” 2017. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/79378.

MLA Handbook (7th Edition):

Fung, Thomas Anthony. “Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer.” 2017. Web. 24 Aug 2019.

Vancouver:

Fung TA. Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/79378.

Council of Science Editors:

Fung TA. Characterizing effects of small molecule inhibition of WDR5 in colorectal cancer. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79378


University of Toronto

44. Scaife, Matthew. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.

Degree: 2010, University of Toronto

Lentivirus-mediated gene therapy has curative potential for a variety of disorders, however, insertional oncogenesis still remains a concern. One approach to increase safety of such… (more)

Subjects/Keywords: gene therapy; fabry disease; 0307

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APA (6th Edition):

Scaife, M. (2010). Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25794

Chicago Manual of Style (16th Edition):

Scaife, Matthew. “Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/25794.

MLA Handbook (7th Edition):

Scaife, Matthew. “Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.” 2010. Web. 24 Aug 2019.

Vancouver:

Scaife M. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/25794.

Council of Science Editors:

Scaife M. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25794


University of Toronto

45. Stevenson, James. Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes.

Degree: 2010, University of Toronto

The bacterial protein H-NS acts to silence horizontally acquired genes. H-NS physically interacts via its N-terminus with two paralogous proteins, Hha and YdgT. Deletion of… (more)

Subjects/Keywords: H-NS; Salmonella; 0307; 0410

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APA (6th Edition):

Stevenson, J. (2010). Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25812

Chicago Manual of Style (16th Edition):

Stevenson, James. “Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/25812.

MLA Handbook (7th Edition):

Stevenson, James. “Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes.” 2010. Web. 24 Aug 2019.

Vancouver:

Stevenson J. Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/25812.

Council of Science Editors:

Stevenson J. Hha and YdgT Act Through H-NS to Repress Horizontally Acquired Genes. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25812


University of Toronto

46. Graham, Cassandra. A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas.

Degree: 2011, University of Toronto

Paediatric undifferentiated soft tissue sarcomas (USTSs) are a diagnostically challenging group of neoplasms. We hypothesized that USTSs contain distinct subgroups that can be identified based… (more)

Subjects/Keywords: Sarcoma; Molecular Biology; 0307; 0369

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APA (6th Edition):

Graham, C. (2011). A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29551

Chicago Manual of Style (16th Edition):

Graham, Cassandra. “A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas.” 2011. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/29551.

MLA Handbook (7th Edition):

Graham, Cassandra. “A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas.” 2011. Web. 24 Aug 2019.

Vancouver:

Graham C. A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/29551.

Council of Science Editors:

Graham C. A Detailed Genomic and Transcriptomic Analysis of Paediatric Undifferentiate Sarcomas. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29551


University of Toronto

47. Ng, Mark. Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties.

Degree: 2016, University of Toronto

The Bacille Calmette-GuĂŠrin (BCG) vaccine is the only vaccine for tuberculosis (TB) control. Although effective in preventing disseminated forms of TB in children, its efficacy… (more)

Subjects/Keywords: BCG; BCG-Russia; RecA; 0307

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APA (6th Edition):

Ng, M. (2016). Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72769

Chicago Manual of Style (16th Edition):

Ng, Mark. “Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties.” 2016. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/72769.

MLA Handbook (7th Edition):

Ng, Mark. “Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties.” 2016. Web. 24 Aug 2019.

Vancouver:

Ng M. Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/72769.

Council of Science Editors:

Ng M. Investigating the Role of a Natural RecA Mutation on BCG-Russia Vaccine Properties. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72769


University of Toronto

48. Curak, Jasna. Investigating the ERBB Protein Interactome.

Degree: 2010, University of Toronto

The erythroblastoma (ErbB) receptor family consists of four members that are implicated in many human cancers. To gain insight into their biological function, we investigated… (more)

Subjects/Keywords: ErbB receptors; LUMIER; 0307

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APA (6th Edition):

Curak, J. (2010). Investigating the ERBB Protein Interactome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29983

Chicago Manual of Style (16th Edition):

Curak, Jasna. “Investigating the ERBB Protein Interactome.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/29983.

MLA Handbook (7th Edition):

Curak, Jasna. “Investigating the ERBB Protein Interactome.” 2010. Web. 24 Aug 2019.

Vancouver:

Curak J. Investigating the ERBB Protein Interactome. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/29983.

Council of Science Editors:

Curak J. Investigating the ERBB Protein Interactome. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/29983


University of Toronto

49. Jayakumaran, Gowtham. Molecular Mechanisms Regulating Somatic Reprogramming.

Degree: 2014, University of Toronto

In reprogramming, cellular transition to pluripotency only occurs in few cells. My thesisis focused on exploring the mechanisms underlying the successful transition of somatic cells… (more)

Subjects/Keywords: Cell plasticity; NGS; Reprogramming; Stem cells; 0307

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APA (6th Edition):

Jayakumaran, G. (2014). Molecular Mechanisms Regulating Somatic Reprogramming. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67955

Chicago Manual of Style (16th Edition):

Jayakumaran, Gowtham. “Molecular Mechanisms Regulating Somatic Reprogramming.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/67955.

MLA Handbook (7th Edition):

Jayakumaran, Gowtham. “Molecular Mechanisms Regulating Somatic Reprogramming.” 2014. Web. 24 Aug 2019.

Vancouver:

Jayakumaran G. Molecular Mechanisms Regulating Somatic Reprogramming. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/67955.

Council of Science Editors:

Jayakumaran G. Molecular Mechanisms Regulating Somatic Reprogramming. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67955


University of Toronto

50. Florjanczyk, Ursula. Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens.

Degree: 2014, University of Toronto

Cholera outbreaks, caused by surges in pathogenic Vibrio cholerae, recur frequently in areas with water reservoirs around unsanitary living conditions. Phage therapy is being pursued… (more)

Subjects/Keywords: mathematical modeling; phage therapy; synthetic biology; 0307

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APA (6th Edition):

Florjanczyk, U. (2014). Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68010

Chicago Manual of Style (16th Edition):

Florjanczyk, Ursula. “Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/68010.

MLA Handbook (7th Edition):

Florjanczyk, Ursula. “Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens.” 2014. Web. 24 Aug 2019.

Vancouver:

Florjanczyk U. Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/68010.

Council of Science Editors:

Florjanczyk U. Design of Engineered Bacteria for Regulated Phage Release: Progress Towards Targeted Elimination of Pathogens. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68010


University of Toronto

51. Lee, Richard Heungki. An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors.

Degree: 2015, University of Toronto

Peroxisome proliferator-activated receptors (PPARs) are a group of nuclear receptors (NRs) that play major roles in metabolism and development and, when disrupted, lead to disorders… (more)

Subjects/Keywords: Coenzyme Q10; Nuclear Receptor; PPAR; 0307

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APA (6th Edition):

Lee, R. H. (2015). An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70369

Chicago Manual of Style (16th Edition):

Lee, Richard Heungki. “An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors.” 2015. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/70369.

MLA Handbook (7th Edition):

Lee, Richard Heungki. “An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors.” 2015. Web. 24 Aug 2019.

Vancouver:

Lee RH. An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/70369.

Council of Science Editors:

Lee RH. An In Vivo System for the Identification of Ligands for Peroxisome Proliferator-activated Receptors. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70369


University of Toronto

52. Lau, Garnet Jean. Analysis of Naked in the Canonical Wnt Pathway.

Degree: 2008, University of Toronto

Wnt signalling is involved throughout development and is inappropriately activated in a variety of human cancers. In the canonical pathway, secreted Wnt proteins induce the… (more)

Subjects/Keywords: Naked; Wnt; 0307

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APA (6th Edition):

Lau, G. J. (2008). Analysis of Naked in the Canonical Wnt Pathway. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/17191

Chicago Manual of Style (16th Edition):

Lau, Garnet Jean. “Analysis of Naked in the Canonical Wnt Pathway.” 2008. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/17191.

MLA Handbook (7th Edition):

Lau, Garnet Jean. “Analysis of Naked in the Canonical Wnt Pathway.” 2008. Web. 24 Aug 2019.

Vancouver:

Lau GJ. Analysis of Naked in the Canonical Wnt Pathway. [Internet] [Masters thesis]. University of Toronto; 2008. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/17191.

Council of Science Editors:

Lau GJ. Analysis of Naked in the Canonical Wnt Pathway. [Masters Thesis]. University of Toronto; 2008. Available from: http://hdl.handle.net/1807/17191


University of Toronto

53. Zheng, Yiyu Terrence. The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium.

Degree: 2009, University of Toronto

Autophagy, a cellular degradative pathway, plays a key role in protecting the cytosol from bacterial colonization, but the mechanisms of bacterial recognition by this pathway… (more)

Subjects/Keywords: Autophagy; Salmonella; 0307

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APA (6th Edition):

Zheng, Y. T. (2009). The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25697

Chicago Manual of Style (16th Edition):

Zheng, Yiyu Terrence. “The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium.” 2009. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/25697.

MLA Handbook (7th Edition):

Zheng, Yiyu Terrence. “The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium.” 2009. Web. 24 Aug 2019.

Vancouver:

Zheng YT. The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/25697.

Council of Science Editors:

Zheng YT. The Role of P62 in Autophagy of Salmonella Enterica Serovar Typhimurium. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/25697


University of Toronto

54. Shalev, Zvi. Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection.

Degree: 2009, University of Toronto

The pathogenic subgroup C feline leukemia virus (C virus) arises in infected cats by mutations in the envelope gene (env) of subgroup A FeLV (A… (more)

Subjects/Keywords: FeLV; retrovirus; 0307

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APA (6th Edition):

Shalev, Z. (2009). Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18871

Chicago Manual of Style (16th Edition):

Shalev, Zvi. “Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection.” 2009. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/18871.

MLA Handbook (7th Edition):

Shalev, Zvi. “Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection.” 2009. Web. 24 Aug 2019.

Vancouver:

Shalev Z. Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/18871.

Council of Science Editors:

Shalev Z. Identification of Feline Leukemia Virus Variant That Uses THTR1, FLVCR1 and FLVCR2 as Receptors for Infection. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18871


University of Toronto

55. Oliveri, Stefanie. Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death.

Degree: 2011, University of Toronto

Cullin 7 (Cul7) is a member of the cullin protein family that is emerging as a complex anti-apoptotic player in tumourigenesis. We hypothesize that by… (more)

Subjects/Keywords: Cul7; Myc; Cell Death; 0307; 0992

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APA (6th Edition):

Oliveri, S. (2011). Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31376

Chicago Manual of Style (16th Edition):

Oliveri, Stefanie. “Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death.” 2011. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/31376.

MLA Handbook (7th Edition):

Oliveri, Stefanie. “Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death.” 2011. Web. 24 Aug 2019.

Vancouver:

Oliveri S. Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/31376.

Council of Science Editors:

Oliveri S. Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31376


University of Toronto

56. DiLabio, Julia Alexandra Maria. Reprogramming Mouse Glioma Stem Cells with Defined Factors.

Degree: 2012, University of Toronto

This thesis shows that p53-deficient mouse glioma brain tumour stem cells (BTSCs), which fail to express pluripotency factors, can be reprogrammed with specific transcription factors… (more)

Subjects/Keywords: cancer; glioma; reprogramming; stem cells; iPS; 0307

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APA (6th Edition):

DiLabio, J. A. M. (2012). Reprogramming Mouse Glioma Stem Cells with Defined Factors. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42904

Chicago Manual of Style (16th Edition):

DiLabio, Julia Alexandra Maria. “Reprogramming Mouse Glioma Stem Cells with Defined Factors.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/42904.

MLA Handbook (7th Edition):

DiLabio, Julia Alexandra Maria. “Reprogramming Mouse Glioma Stem Cells with Defined Factors.” 2012. Web. 24 Aug 2019.

Vancouver:

DiLabio JAM. Reprogramming Mouse Glioma Stem Cells with Defined Factors. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/42904.

Council of Science Editors:

DiLabio JAM. Reprogramming Mouse Glioma Stem Cells with Defined Factors. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42904


University of Toronto

57. Kop, Anna. DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation.

Degree: 2011, University of Toronto

This study examined DNA methylation patterns at promoters of endothelial cell (EC)-enriched genes during differentiation of mouse ES cells towards the EC. We have previously… (more)

Subjects/Keywords: endothelial cell; epigenetics; DNA methylation; differentiation; 0307

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APA (6th Edition):

Kop, A. (2011). DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31285

Chicago Manual of Style (16th Edition):

Kop, Anna. “DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation.” 2011. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/31285.

MLA Handbook (7th Edition):

Kop, Anna. “DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation.” 2011. Web. 24 Aug 2019.

Vancouver:

Kop A. DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/31285.

Council of Science Editors:

Kop A. DNA Methylation Changes at Promoters of Endothelial Cell-enriched Genes during in vitro Differentiation. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31285


University of Toronto

58. Siddiqui, Tamjeed. Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration.

Degree: 2012, University of Toronto

Microglia, immune cells of the central nervous system, activate in response to pathophysiological stimuli. One of their reactive phenotypes is to migrate to site of… (more)

Subjects/Keywords: microglia; podosomes; migration; Ca2+; 0719; 0379; 0307

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APA (6th Edition):

Siddiqui, T. (2012). Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32286

Chicago Manual of Style (16th Edition):

Siddiqui, Tamjeed. “Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/32286.

MLA Handbook (7th Edition):

Siddiqui, Tamjeed. “Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration.” 2012. Web. 24 Aug 2019.

Vancouver:

Siddiqui T. Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/32286.

Council of Science Editors:

Siddiqui T. Microglia Podosomes: Characterization, Ca2+ Regulation and Potential Role in Migration. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32286


University of Toronto

59. Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).

Degree: 2012, University of Toronto

Shiga-like toxin 1 (SLT-1) is produced by Escherichia coli strains like the pathogenic strain O157:H7. These bacterial strains are responsible for worldwide cases of food… (more)

Subjects/Keywords: protein toxin; shiga-like toxin 1; 0307

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APA (6th Edition):

Wei. (2012). Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32501

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Wei. “Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/32501.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Wei. “Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).” 2012. Web. 24 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/32501.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32501

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Toronto

60. Jarvis, Jordan. Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis.

Degree: 2012, University of Toronto

3BP2 was originally identified through its interaction with the ABL kinase. Fusion of ABL with the BCR gene forms the BCR-ABL onco-protein, which is causative… (more)

Subjects/Keywords: leukemia; signal transduction; BCR-ABL; 3BP2; 0307

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APA (6th Edition):

Jarvis, J. (2012). Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33254

Chicago Manual of Style (16th Edition):

Jarvis, Jordan. “Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/33254.

MLA Handbook (7th Edition):

Jarvis, Jordan. “Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis.” 2012. Web. 24 Aug 2019.

Vancouver:

Jarvis J. Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/33254.

Council of Science Editors:

Jarvis J. Role of the Adapter Protein 3BP2 in BCR-ABL-mediated Signal Transduction and Leukemogenesis. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33254

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