Past Defences
2021 l 2022 l 2023 l 2024
2020 |2019 |2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2008 | 2007 | 2006
2005 | 2004 | 2003 | 2001 | 2000 | 1999 | 1998 | 1997 | 1996 | 1995 |
2024
| Doctoral |
|
| Porter, Vanessa |
Discovery of HPV-associated genomic alterations in cervical cancer |
2023
| Doctoral |
|
| Scott, Erika |
Elucidating genetic predictors for anthracycline-induced cardiotoxicity and cisplatin-induced ototoxicity in pediatric and adult cancer patients to improve patient treatment decisions |
| Carlaw, Tiffany |
Therapeutic genome editing for the treatment of genetic diseases: Testing the safety and effectiveness of CRISPR/cas9 therapeutic base editing |
| Cyrus, Sharri |
Polycomb Repressive Complex 2 Related Syndromes: Functional Studies of Human Gene Variants in Drosophila |
| Shortill, Shawn |
Identification and Functional Analysis of the Endosomal vine complex in Saccharomyces cerevisiae |
| Schaffner, Samantha |
Associations of DNA Methylation with Individual Differences in Parkinson’s Disease Susceptibility |
| Dziurdzik, Samantha |
Membrane contact site targeting and functions of Vps13 and related bridging lipid transporters |
| Thomson, Sarah |
Novel approaches for therapeutic modulation of gene expression in Huntington’s disease |
| Gibson, Kristen |
Assessment of biological markers to aid subtype classification in pediatric primary systemic vasculitis |
| Mirjalili, Zeinab |
Successful Gene Editing in a Novel Mouse Model of Aniridia Towards Prevention of Blindness |
| Kumar, Arun |
Analytic models for carrier sense multiple access networks |
| Akbari, Vahid |
Detecting DNA methylation using nanopore sequencing : from genome-wide analysis to haplotype-resolved and parent-of-origin phasing |
| Master’s |
|
| Jenkins, Kyle |
Simulating chromoanagenesis for tool development and testing |
| Cheung, Chun Wai |
Characterization of DPP4⁺ fibroadipogenic progenitors in skeletal muscle |
| Lin, Dorothy |
Dispersed measures of cord blood DNA methylation do not reflect third trimester bisphenol exposure |
| Sabatino, Brendil |
Characterization of the transcriptomic response to acute starvation in the C. elegans hypodermis |
| Adair, Bethany |
Development of a CRISPR gene correction strategy for aniridia employing a minimally humanized mouse embryonic stem cell-based disease model |
2022
| Doctoral |
|
| Doering, Kelsie |
The Caenorhabditis elegans nuclear hormone receptor NHR-49 functions in stress response pathway regulation |
| Eskandari-Nasab, Ebrahim |
Prosurvival role of CASPASE3 in normal and malignant human mammary cells |
| Wang, Fangwu |
Characterization of the lympho-neutrophil/monocyte restriction process in human cells |
| Ha, Amanda |
Functional characterization of Mest and its imprinted gametic differentially methylated region. |
| Hasbullah, Jafar |
An investigation of the role of pharmacogenetics in the development and prevention of anthracycline-induced cardiotoxicity |
| |
|
| Master’s |
|
| Dawo, Sebastian |
Salmonella Typhimurium Based Genome-Wide CRISPR/CAS 9 Knockout Screen to Study p16 Degradation |
| Elazabbi, Nairuz |
Allele-specific expression differences in the mouse embryonic hindbrain following prenatal alcohol exposure |
| Theberge, Emilie |
Investigating sex differences in the polygenic risk of major depressive disorder and shared associations with cardiovascular disease |
| Horbach Marodin, Rafaela |
Genetic interactions between cohesin and DNA damage response pathways in Saccharomyces cerevisiae |
2021
| Doctoral |
|
| Amitzi, Leanne |
DDX11 Helicase as a Synthetic Lethal Cancer Therapy Target |
| Pillsworth, Jessica |
Adult-Type Granulosa Cell Tumours of the Ovary: A Foxl2-Centric Disease |
| |
|
| Master’s |
|
| Newman-Simmons, Avery |
Investigating the Genetic Contributions to Familial Intracranial Aneurysms in a First Nation from Northwestern British Columbia |
| Riyadh, Omer |
Uncovering factors implicated in oncogenic NRAS modification by analyzing large scale functional genomic data sets |
| Grant, Peter |
Investigating Trends in Out-of-Pocket Pay for Out-of-Province Genetic Testing in British Columbia |
2020
| Doctoral |
|
| Refaeli, Ido |
Generation, characterization and optimization of mouse models for genetic glomerular disease |
| Dixon-McDougall, Thomas |
Functionality of domains of XIST and their role in establishing chromosome inactivation |
| Brown, Joshua |
Diverse functions of Rtt107 in the Saccharomyces cerevisiae DNA damage response |
| Canals Hernaez, Diana |
Investigation of the Role of Podocalyxin in Cancer Progression and Its Potential as a Cancer Therapeutic |
| Del Gobbo, Giulia |
Genomic Profiling in the Placenta: Toward a Greater Understanding of Genetic Variation Contributing to Placental Insufficiency and Fetal Growth Restriction |
| Master’s |
|
| Dever, Kristy |
A broader role for the RNAPII phosphatase, FCP1, in transcription regulation |
| Lin, Jennifer |
The pharmacogenomics of hepatitis C: optimizing efficacy and safety on treatment |
| Farag, Roula |
Molecular mechanisms of BAP1 mutations in uveal melanoma |
2019
| Doctoral |
|
| Collins, Sorcha |
The role of the carnitine palmitoyltransferase 1A (CPT1A) p.P479L variant in Inuit infant and child health outcomes in Nunavut |
| Kadhim, Alexandre |
Investigating the role of transcriptional coactivator MED15 in beta cell maturation |
| Al Shekaili, Hilal Hamed |
Investigating vitamin B6-dependent epileptic encephalopathies in human patients and a mouse model |
| Dixon, Katherine |
Molecular characterization and genetic diagnosis of cancer predisposition syndromes using genome and transcriptome sequencing |
| Richard Albert, Julien |
Application of an allele-specific pipeline to study DNA methylation inheritance and dynamics in the early embryo |
| Jones, Samantha |
Characterization of environmental and genetic factors in multiple-case lymphoid cancer families |
| Tam, Annie S. |
The conserved role of RNA splicing factors in genome maintenance |
| Urtatiz Gongora, Oscar |
Oncogenic GNAQ and BRAF in epidermal versus non-epidermal melanocytes |
| Goodman, Sarah |
Contributions of intrinsic and environmental factors to early life DNA methylation |
| Master’s |
|
| Jain, Fagun |
Two novel genetically engineered mouse models for uveal melanoma with liver metastasis |
| Kwan, Harwood |
An investigation into the non-coding genomic landscape and effects of chemotherapeutics in pre-treated advanced cancers |
| Jensen, Kristoffer |
HP1-mediated transcriptional silencing of ERVs and genes in mouse embryonic stem cells |
| Soundara Rajan, Jeffy |
Investigating mouse motor activity and learning behavior using quantitative trait locus (QTL) analysis to elucidate the genetic underpinnings of developmental coordination disorder (DCD) |
| Gupta, Ishita |
Spatiotemporal characterisation of some transcriptional signatures in early cerebellar development |
| Vermeulen, Michael |
Improving and estimating Y chromosome loss in blood and brain tissues using high-throughput sequencing |
2018
| Doctoral |
|
| Barbaian, Artem |
Endogenous retroviruses drive transcriptional innovation in human cancer |
| Peeters, Samantha |
Modelling human escape from X-chromosome inactivation in mouse |
| Konwar, Chaini |
Molecular profiling of acute chorioamnionitis-affected placentas: insights into genomic variation underlying a common preterm birth condition |
| Singh, Chaahat S. B. |
Mechanism underlying dysregulated cerebral vessel growth in Alzheimer’s disease |
| Hickmott, Jack |
rAAV9 mediated PAX6 gene transfer temporarily reverses corneal epithelial thinning in a mouse model of aniridia |
| Islam, Sumaiya |
Tissue-specific investigations on DNA methylation variation in human neurobiological diseases |
| McEwen, Lisa |
DNA methylation variation across the human life course |
| Wong, Chi Kin |
The role of p300 transcriptional coactivators in pancreatic beta cells |
| Master’s |
|
| Porter, Vanessa |
Targeting Autophagy in Chronic Myeloid Leukemia Through Inhibition of the Core Autophagy Protein ATG4B |
| Shomer, Naomi |
A Regulatory Mechanism of Zinc Homeostasis Involving the Mediator Subunit MDT-15 and the Transcription Factor HIZR-1 |
2017
| Doctoral |
|
| Chen, Carol |
Interphase Histone H3 Serine 10 Phosphorylation in Mouse Embryonic Stem Cells |
| Cohen, Ana |
Detailed Phenotyping and Next-Generation Sequencing for Characterization of Rare Overgrowth Syndromes |
| Fam, Andrew |
Tyrosol-DNA Phosphodiesterase1 (TDP1): From Spinocerebellar Ataxia to Roles in Mitochondrial DNA Repair and Cancer Therapy |
| Kay, Christopher |
Population Genetics and Allele-Specific Silencing of the Huntington Disease Mutation |
| Lussier, Alexandre Andre |
Epigenetic Signatures of Prenatal Alcohol Exposure |
| Wilson, Samantha |
Genetic and Epigenetic Profiling of Placental Insufficiency: Identifying Biomarkers of Preeclampsia and Intrauterine Growth Restriction |
| Zhang, Peter |
Transcriptional Regulation in the Development of the Cerebellum and Cerebellar Granule Cells |
| Zhang, Regan-Heng |
The Lysine Methyltransferase EHMT2/G9a in Mesenchymal Development |
| Master’s |
|
| Ellis, Samantha |
Introduction of the Antigen Presentation Machinery Using Novel Small Molecules |
| Hitchcock, Emma |
Next Generation Sequencing to Determine a Genetic Cause of Familial Intracranial Aneurysms |
| Little, Natasha |
Characterization of IAPLTR1 Subclasses and Bidirectional Promoter Activity: “Making Sense of it All” |
| Reytan, Sivan |
Identification of Cancer Relevant Synthetic Genetic Interactions with Cohesin Mutations in Saccharomyces Cerevisiae |
| Segovia Ugarte, Romulo |
Synthetic Hypermutation: Gene-Drug Mutation Rate Synergy Reveals a Translesion |
| Selmer, Laura |
Intracranial Manifestations in Neurofibromatosis 1 |
| Szetzo, Rochelle |
Telomere Position Effect in Embryonic Stem Cells: Heterogeneity, Imprinting, and Modifier Screen |
| Turner, Kelly |
Assessment of a Potential Therapeutic Target in the Hedgehog Pathway for the Eradication of Primitive Chronic Myeloid Leukemia Cells |
| Yuen, Michael |
Mapping Complex Genomic Translocations Using Strand-seq |
2016
| Doctoral |
|
Chung, George Chih Hsuen
|
Genetic Determinants of Genome Stability and Crossover Distribution in the Nematode Caenorhabditis elegans |
| Connolly, Colum |
Microglial Dysfunction Induced by Mutant Huntingtin |
| Dastan, Jila |
Exome Sequencing for Understanding Phenotypic Variability in Subjects with 16p11.2 CNV |
| Grants, Jennifer |
Roles of the Mediator Subunit CDK-8 in Developmental and Physiological Responses in Caenorhabditis elegans |
| Kaurah, Pardeep |
Hereditary Diffuse Gastric: Cancer Risk and the Personal Cost of Preventative Surgery |
| Ladha, Safia |
Impact of Caspase-6 Modulation on Huntington Disease Phenotypes in the YAC128 Mouse Model |
| Trinh, Joanne |
Identification of Genetic Modifiers in Lrrks2 Parkinsonism |
| Yeung, Joanna |
The Role of Pax6 and Wls in Rhombic Lip Compartmentation and Cerebellar Development |
| Master’s |
|
| de Goede, Olivia |
Identifying Epigenetic Associations with Cell Type and Gestational Age in the Neonatal Immune System |
| Lee, Ka Young |
Functional Characterization of Gene Regulation by NHR-49 |
| Pilsworth, Jessica |
Gene Expression and Mutation Profiles Define Novel Subclasses of Cytogenetically Normal Acute Myeloid Leukemia |
2015
| Doctoral |
|
| DeSouza, Rebecca |
Characterization of the Huntingtin Gene Promoter and Huntingtin Transcriptional Regulation |
| Heppner, Jonathan |
Early Disruption of the Extracellular Matrix in Murine Mucopolysaccharidosis I |
| Lin, David Tse-Shen |
Characterization of Novel Regulatory Components in the Dynamic Protein Palmitolytion Cycle |
| Liu, Sheng |
Transcriptional Repression of Retrotransposons in Mouse Germline |
| Rothe, Katharina |
Characterization of Novel Therapeutic Targets in Chronic Meyloid Leukemia |
| Tharmarajah, Grace |
The Role of Adamts9 in Melanoblast Migration and Modification of the Skin Proteome |
| Thompson, Peter |
Transcriptional Silencing of Endogenous Retroviruses by the Novel Lysine Methytransferase Co-repressor hnRNP K |
| Master’s |
|
| Ang, Sidney |
Identification and Characterization of Dosage Mutator Genes in Saccharomyces cerevisiae |
| Huff, Ryan |
Generation and Characterization of a Lysine (K)-specific Methyltransferase 2D Knockout Human Cell Line |
2014
| Doctoral |
|
| Esmailzadeh, Sharmin |
The role of BIN1 in the Regulation of Cell Proliferation, Apoptosis and Tumor Formation in Cutaneous T-Cell Lymphoma |
| Jett, Kimberly |
Vascular Function in Neurofibromatosis 1 |
| Lee, Joshua |
Multiple Sclerosis in Asian Populations : The Genetic and Environmental Determinants of Variable Susceptibility and Clinical Profile |
| Miller, Michelle |
Validation of Two Novel Mouse Models of Conditional Meis1 Deletion to Study Roles in Adult Mouse Hematopoiesis |
| Poon, Anna Fong-Yee |
Genetic Architecture of Neurogenesis in the Adult Mouse Forebrain: Insights from Quantitative Trait Locus Analyses |
| Master’s |
|
| Billings, Raewyn |
Stimulating Human Tumour Heterogeneity using Cancer Cell Line Mixtures |
| Greenwood, Talitha |
Gene Discovery in Individuals from Families Indicative of Mendelian Forms of Late-Onset Alzheimer Disease |
| Huang, Jenny Li-Ying |
Ocular Melanocytes respond to Oncogenic GNAQQ209L differently compared to Epidermal and Dermal Melanocytes in Mice |
| Kaur, Achint |
The Role of Sterol 12α- hydroxylase (Cyp8b1) in Glucose Homeostasis |
| Lee, Jong Wook |
A Genome-Wide Association Study of Cisplatin-Induced Hearing Loss in Children |
| Moshgabadi, Noushin |
Identification of Synthetic Cytotoxic Interactions to Improve the Efficacy of DNA Damaging Therapeutic Agents |
| Tam, Annie |
Whole Genome Mutational Profiling of the Chemotherapeutic Agent Mitomycin C |
| Ye, Xin |
Mapping a New Locus for Non-Syndromic Strabismus with High-Throughput Genome Analysis |
2013
| Doctoral |
|
| Baradaran-Heravi, Alireza |
Schimke Immuno-osseous Dysplasia: Association of SMARCAL1 Mutations with Genetics and Environmental Disturbances of Gene Expression |
| de Leeuw, Charles |
Development of Tools in Mouse for Future Gene Therapy: Promoters for the CNS, and Novel Expression Models of Neural Stem Cell Regulator, NR2E1 |
| Hanna, Courtney |
Patterns of DNA Methylation on the Human X Chromosome and Use in Analyzing X-Chromosome Inactivation |
| MacIsaac, Julia |
Developmental Consequences of Imprinted Transcription at the Mest Locus |
| Mazarei, Gelareh |
Investigating the role of Indoleamine 2,3 dioxygenase in Huntington disease |
| Master’s |
|
| Blair, John |
DNA methylation studies of preeclamsia and related conditions |
| Chapman, Andrew |
Transcriptional regulation of the XIST locus |
| Jacob, Karen |
The function of the imprinted transcription factor ASCL2 in mouse trophoblast development |
| Kelsey, Angela |
Mechanisms for XIST RNA cis-localisation |
| Stepien, Katarzyna |
Prenatal Alcohol Exposure Programs Steady-State Gene Expression and the Gene Expression Response to Inflammation in the Adult Rat Brain |
| Yoo, Janice |
The effects of cerebellar hemorrhage on the development of the postnatal cerebellum |
2012
| Doctoral |
|
| Cotton, Allison |
Patterns of DNA Methylation on the Human X Chromosome and Use in Analyzing X-Chromosome Inactivation |
| Earp, Madalene |
Genetic Studies to Discover Common Variants Associated with Epithelial Ovarian Cancer Risk and Variation in Age of Natural Menopause |
| Kang, Martin |
Post-transcriptional Regulation of ABCA1 |
| Minks, Jakub |
Role of XIST RNA and Its Interacting Protein Partners in Gene Silencing |
| Semaka, Alicia |
Genetic Counselling Implications for Intermediate Allele Predictive Test Results for Huntington Disease |
| Master’s |
|
| Chowdhury, Miraj |
Tyrosyl-DNA Phosphodiesterase 1 (TDP1): A Rhabdomyosarcoma Therapeutic Target and Mitochondrial DNA Repair Enzyme |
| Chun, Stella |
Identification and validation of CDK13 interacting proteins |
| Fisher, Emily |
The Epidemiology of Huntington Disease in British Columbia |
| Fornika, Dan |
Mitochondrial Genome Variation and Healthy Aging |
| Lepage, Sarah |
Analysis of the Mechanism of Maintenance of the H3K27 Trimethylation Mark Using a Novel Chromatin Targeting System |
| Yang, Christine |
DNA methylation demonstrates spread of X-chromosome inactivation to human transgenes |
2011
| Doctoral |
|
| Burston, Helen |
Genome-wide Analysis of Endocytic Recycling inS. cerevisiae |
| Deo, Mugdha |
Role of Nf1 Signaling in Regulating Pigmentation in Mice |
| Lee, Connie |
The role of imprinted genes in mouse models of IUGR |
| Leung, Danny |
Transcriptional Silencing of Endogenous Retroviruses: Interplay Between Histone H3K9 Methylation and DNA Methylation |
| McLellan, Jessica |
A Cross Species Approach to Identify Potential Therapeutic Targets through Synthetic Lethal Interactions |
| Oh-McGinnis, Rosemary |
Regulation of Genomic Imprinting in the Mouse Placenta |
| Yuen, Ryan |
Epigenetics of Human Fetal and Placental Development |
Zahir, Farah
|
The Pathogenicity of Copy Number Variants in Children with Intellectual Disability |
| Master’s |
|
| Brind’Amour, Julie |
Analysis of the Mechanism of Maintenance of the H3K27 Trimethylation Mark Using a Novel Chromatin Targeting System |
| Decker, Michelle |
Telomere Length and Dynamics in Hutchinson-Gilford Progeria Syndrome |
| Miceli, Katharine |
Who’s the Boss? An Investigation into the Complex Relationship between Endogenous Retroviruses and Nearby Genes |
| Sekulovic, Sanja |
Analysis of the Mechanism of Maintenance of the H3K27 Trimethylation Mark Using a Novel Chromatin Targeting System |
2010
| Doctoral |
|
| Alwan, Sura |
Risk Assessment of Birth Defects in Human Pregnancy |
| Degeer, Donna |
Characterization of a Novel Fluorescent Reporter of Genomic Imprinting in the Mouse |
| Gallo, Marco |
Misc/OCG is a New Stress Response Gene and Regulator of Apoptosis, Germline Stem Cell Proliferation and Insulin Secretion |
| Jensen, Victor |
Novel Components of the Dauer Larva Developmental Signaling Pathway in Caenorhabditis elegans |
| Schuetz, Johanna |
Genetic Variation in Lymphocyte Life and Death Genes and Risk of non-Hodgkin Lymphomas |
| Jones, Meaghan |
XIST/Xist Induced Epigenetic Events in Somatic Cells |
| Long, Michael |
Development of Strategies to Enhance the Contribution of Hematopoietic Cells to Skeletal Muscle Repair. |
| Morrissy, Anca |
Bioinformatic Analysis of Cis-Encoded Antisense Transcription |
| Pouladi, Mahmoud |
On the Modulation of Excitotoxicity as a Therapeutic Approach for the Treatment of Huntington Disease |
| Thorogood, Nancy |
XIST/Xist Induced Epigenetic Events in Somatic Cells |
| Vrljicak, Pavel |
Genomic Analysis of Embryonic Heart Development in the Mouse |
| Young, Fiona |
The Biology and Expression of Huntingtin-Interacting Protein 14 |
|
|
| Master’s |
|
| Bourque, Danielle |
Imprinted Genes in the Placenta and Obstetrical Complications |
| Degeer, Donna |
Characterization of a Novel Fluorescent Reporter of Genomic Imprinting in the Mouse |
| Hirukawa, Alison |
The role of SHIP1 in modulating disease severity in the K/BxN serum transfer model of rheumatoid arthritis |
| Huang, Jim |
The characterization of atm-1 in Caenorhabditis elegans |
| Lohn, Zoe |
A New Role for the Tumour Suppressor, lin-35, During Meiotic Recombination in Caenorhabditis elegans |
| Ngai, Tiffany |
The Low-density Lipoprotein Receptor Knock-out Mouse: A Model for the Study of Energy Balance |
| Plamondon, Jenna |
Genetic and Epigenetic Factors in a Mouse Model for Multifactorial Cleft Lip |
| Thiele, Jenny |
Generation and characterization of embryonic stem cell lines derived from the YAC128 mouse model of Huntington disease |
2009
| Doctoral |
|
| Chang, Samuel |
Identification and characterization of cis-acting regulatory elements for human XIST |
| Griffith, Malachi |
Methods for Transcript Variant Discovery and Alternative Expression Analysis – Application to the Study of Fluorouracil Resistance in Colorectal Cancer |
| Haddon, Jamie |
Mast cells : homeostatic regulation, activation, gene expression, surface antigens, and role in allergic disease |
| Lam, Karen |
The role of palmitoylation in endoplasmic reticulum transport and quality control of the yeast polytopic protein Chs3 |
| Pugh, Trevor |
Analysis of primary human cancers: from single genes to whole transcriptomes |
| Wong, Bibiana |
Evaluating the Effects of Variable NR2E1 Levels on Gene Expression, Behaviour, and Neural and Ocular Development |
| Master’s |
|
| Borrie, Adrienne |
A mutational screen of NR2E1 in patients with Aniridia, Peters’ Anomaly, and related eye disorders. |
| Riendeau, Noemie |
Autism Spectrum Disorders: Identification of Novel Microdeletions and Microduplications and their Associated Phenotypes |
| Tkac, Jan |
Detection of Telomeric DNA Circles in Human ALT Cells Using Rolling Circle Amplification |
| Toub, Omid |
Initial characterization and Intracellular localization of two suppressors of position effect variegation in Drosophila melanogaster, S2214 and puckered |
2008
| Doctoral |
|
| Bretherick, Karla |
Genetic factors in premature ovarian failure |
| Griffith, Obi |
Identification of gene expression changes in human cancer using bioinformatic approaches |
| Rouhi, Arefeh |
A role for epigenetic modifications in the maintenance of mouse Ly49 receptor expression |
| Ryan, Jane |
A Genome-Wide Linkage Scan and Targeted Family-Based Association Analysis of Dyslexia |
| Master’s |
|
| Elves, Rachel |
Consequences of mitotic loss of heterozygosiy on genomic imprinting in mouse embryonic stem cells |
| Kennah, Erin |
Identification of differentially expressed genes in AHL-1-mediated leukemic transformation in human cutaneous T-cell lymphoma |
| Koochek, Maryam |
Sub-microscopic chromosomal imbalances in idiopathic autism spectrum disorder (ASD) |
| Mazarei, Gelareh |
Identification of Novel Striatal-Enriched Transcripts and their Analysis in Huntington Disease |
| Miller, Shelley |
Development of embryonic stem cells expressing endogenous levels of a fluorescent protein fused to the telomere binding protein TRF1 |
| Wagner, Laura |
Silencing mutant huntington by RNA interference for the treatment of Huntington disease |
2007
| Doctoral |
|
| Bakovic, Silvia |
Ex vivo expansion of hematopoietic stem cells for use in nonmyeloablative transplantation |
| Brunham, Liam |
The impact of genetic variation in ABCA1 on cholesterol metabolism, atherosclerosis and diabetes |
| Tarailo, Maja |
Spindle assembly checkpoint and chromosome stability in Caenorhabditis elegans |
| Youds, Jillian |
Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans |
| Master’s |
|
| Harbord, Sara |
X Chromosome Abnormalities in Breast and Ovarian Cancer |
2006
| Doctoral |
|
| Graham, Rona |
In vivo characterization of caspase resistant huntingtin: Insights into the pathogenic mechanism of Huntington disease |
| Kumar, Ravinesh |
Ex vivo expansion of hematopoietic stem cells for use in nonmyeloablative transplantation |
| Mar, Lynn |
Role of TGIF in cell cycle control and establishment of laterality |
| Nielsen, Julie |
The role of podocalyxin in adhesion and cell morphogenesis |
| Tucker, Tracy |
Pathogenesis of neurofibromatosis 1 associated neurofibromas |
| Yuen, Karen |
Identification and characterization of chromosome instability mutants in the yeast Saccharomyces cerevisiae and implications to human cancer |
| Master’s |
|
| Randall, Derrick |
Identification of a Serum Biomarker for Mucopolysaccharidosis |
| Sipahimalani, Payal |
Variation in ATM and genetic susceptibility to non-Hodgkin lymphoma |
| Quint, Desiree |
Aberrant Hypermethylation of Xq12 in Lymphoma |
| Wu, Joyce |
YB-1 is a Downstream Component of the PI3K/Akt Signaling Pathway and Regulates EGFR in Breast Carcinoma: A Mechanism for Breast Cancer Growth |
2005
| Doctoral |
|
| Cheng, Benjamin |
Identificaton of novel factors required for chromosome segregation in budding yeast |
| Cheung, Iris |
Instability of G-rich DNA in Caenorhabditis elegans |
| Gair, Jane |
Genetic mechanismss of nondisjunction in humans |
| Gurevich, Rhonna |
Functional analysis of the NUP98- Topoisoerase 1 (NUP98-TOP1) fusion gene in the pathogenesis of leukemia |
| Murray, Angus |
Functional genomics of the A600 locus in Leishmania mexicana |
| Pleasance, Erin |
Identification and analysis of programmed cell death genes in Drosophila melanogaster and human cancer using bioinformatic analysis of gene expression data |
| Van Raamsdonk, J. |
Characterization and treatment of mouse models in Huntington disease |
| Master’s |
|
| Schnerch, Angelique |
Analysis of Undifferentiated Human Embryonic Stem Cell Lines Using Serial Analysis of Gene Expression |
| Hoscheit, Julia |
Multifactorial genetics of exencephaly in the SELH/Bc mouse strain |
| Yen, Ziny |
Comparative sudies of X inactivation within Eutheria |
2004
| Doctoral |
|
| Dickstein, Dara |
The Role of Inflammation and amyloid beta in Alzeimer Disease Pathology |
2003
| Doctoral |
|
| Chopra, Vikramjit |
The HIP1 family of cytoskeletal-associated proteins |
| Chow, Jennifer |
XIST and its role in X-chromosome inactivation |
| Chu, Pak-Yan (Pat) |
Effect of c-kit and flt-3 overexpression on primitive hematopoietic cells |
| Penaherrera, Maria |
X-chromosome inactivation pattern in human extraembryonic and fetal tissues |
| Russell, Chris |
Transgenic expression of human alpha-L-iduronidase in mouse and characterization of the long term pathophysiology of murine alpha |
| Wilhelm, Brian |
The genomic organization and transcriptional regulation of natural killer receptor genes |
| Master’s |
|
| Lee, Tsz Kin |
Bioinformatic analysis on NF1 transcriptional regulation |
2002
| Doctoral |
|
| Anderson, Cathy |
Variable X inactivation of the human TIMP1 gene |
| Faulkes, Sharlene |
Site-directed integration using the Cre/lox system in hematopoietic and embryonic stem cells |
Master’s
|
|
| Kwok, Ed |
XIST and macroH2A1.2 in hybrid cells |
2001
| Doctoral |
|
| Szudek, Jacek |
Analysis of variable expressivity in Neurofibromatosis |
| Parker, Jodey |
The Caenorhabditis elegans homologue of huntingtin interacting protein 1 has multiple roles in development |
2000
| Doctoral |
|
| Moslehi, Roxana |
Genetic studies of ovarian cancer in Jewish women |
1999
| Doctoral |
|
| Hodgson, John |
Production and characterization of YAC transgenic mice expressing the normal and mutant Huntington’s disease gene |
| Bruskiewich, R. |
Genetic mapping, functional analysis and bioinformatics of Werner syndrome locus (WRN) |
1998
| Doctoral |
|
| Gagne, Eric |
Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease |
| Nelson, Tanya |
Molecular and genetic analysis of human 8p inversion duplication chromosomes |
| Kowalski, Paul |
Novel genetic effects of a human endogenous retrovirus inserion |
1997
| Doctoral |
|
| Ginzinger, David |
Lipoprotein lipase deficiency in a colony of domestic cats |
1996
| Doctoral |
|
| Pawliuk, Robert |
Growth properties and genetic manipulation of murine hemopoietic stem cells |
1995
| Doctoral |
|
| Biaoyang, Lin |
Cloning and characterization of genes in the proximal candidate region for the Huntington disease in mouse and human |