Skip to Main Content

Author Details

Christopher R McMaster
Dalhousie University
1989
104
38
PMIDPaper TitleJournal TitlePublished Year
35322809Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism.Nat Commun2022
35447137Choline kinase inhibition promotes ER-phagy.J Lipid Res2022
36379551Core elements of participant consent documents for Canadian human genomics research and the National Human Genome Library: guidance for policy.CMAJ2022
35951321Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4.JAMA Ophthalmol2022
35151687A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia.J Biol Chem2022
35202461Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.Brain2022
33454747Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.Brain2021
33734376Genetic analysis of Pycr1 and Pycr2 in mice.Genetics2021
33381478Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations.Front Pediatr2020
32032513The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms.Am J Hum Genet2020
33454021Genetic diseases of the Kennedy pathways for membrane synthesis.J Biol Chem2020
31566834Frizzled 4 regulates ventral blood vessel remodeling in the zebrafish retina.Dev Dyn2019
29178478From yeast to humans - roles of the Kennedy pathway for phosphatidylcholine synthesis.FEBS Lett2018
30053067Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.Nucleic Acids Res2018
29905858Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.Nucleic Acids Res2018
29487144How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases.Genetics2018
28052917A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis.Brain2017
28404662SLC25 Family Member Genetic Interactions Identify a Role for <i>HEM25</i> in Yeast Electron Transport Chain Stability.G3 (Bethesda)2017
26821380Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia.PLoS Genet2016
27521373Lipid synthesis and membrane contact sites: a crossroads for cellular physiology.J Lipid Res2016
27489958Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy.PLoS One2016
27038157Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.Pediatr Blood Cancer2016
25572853Phosphorylation of caveolin-1 on tyrosine-14 induced by ROS enhances palmitate-induced death of beta-pancreatic cells.Biochim Biophys Acta2015
26352440Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study.Public Health Genomics2015
26415690Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome.Chem Phys Lipids2015
25688091The mitochondrial quality control protein Yme1 is necessary to prevent defective mitophagy in a yeast model of Barth syndrome.J Biol Chem2015
24434691Attitudes of parents toward the return of targeted and incidental genomic research findings in children.Genet Med2014
27896114Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of <i>UBIAD1</i> gene expression.Mol Genet Metab Rep2014
25340522Germline mutations in MAP3K6 are associated with familial gastric cancer.PLoS Genet2014
25124931Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.JAMA Ophthalmol2014
23335509Drug uptake, lipid rafts, and vesicle trafficking modulate resistance to an anticancer lysophosphatidylcholine analogue in yeast.J Biol Chem2013
24187140Choline transport activity regulates phosphatidylcholine synthesis through choline transporter Hnm1 stability.J Biol Chem2013
23593226The yeast oxysterol binding protein Kes1 maintains sphingolipid levels.PLoS One2013
23793442A novel rearrangement of occludin causes brain calcification and renal dysfunction.Hum Genet2013
23383173Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14.PLoS One2013
23344949Alteration of plasma membrane organization by an anticancer lysophosphatidylcholine analogue induces intracellular acidification and internalization of plasma membrane transporters in yeast.J Biol Chem2013
22334669A detour for yeast oxysterol binding proteins.J Biol Chem2012
22966490Guidelines for the use and interpretation of assays for monitoring autophagy.Autophagy2012
22704758A generalizable pre-clinical research approach for orphan disease therapy.Orphanet J Rare Dis2012
21358631Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.Nat Genet2011
20651827Surprising roles for phospholipid binding proteins revealed by high throughput genetics.Biochem Cell Biol2010
20729555Lipid binding requirements for oxysterol-binding protein Kes1 inhibition of autophagy and endosome-trans-Golgi trafficking pathways.J Biol Chem2010
19129178Phospholipid transfer protein Sec14 is required for trafficking from endosomes and regulates distinct trans-Golgi export pathways.J Biol Chem2009
19841481NTE1-encoded phosphatidylcholine phospholipase b regulates transcription of phospholipid biosynthetic genes.J Biol Chem2009
19141610The Kap60-Kap95 karyopherin complex directly regulates phosphatidylcholine synthesis.J Biol Chem2009
17938859Emerging roles of the oxysterol-binding protein family in metabolism, transport, and signaling.Cell Mol Life Sci2008
18773978Tryptophan fluorescence reveals induced folding of Vibrio harveyi acyl carrier protein upon interaction with partner enzymes.Biochim Biophys Acta2008
16731034Phosphatidylcholine synthesis and its catabolism by yeast neuropathy target esterase 1.Biochim Biophys Acta2007
17601877Regulation of phosphoinositide levels by the phospholipid transfer protein Sec14p controls Cdc42p/p21-activated kinase-mediated cell cycle progression at cytokinesis.Eukaryot Cell2007
17881569The oxysterol binding protein Kes1p regulates Golgi apparatus phosphatidylinositol-4-phosphate function.Proc Natl Acad Sci U S A2007
  • 1 - 50 of 104

Recommended Authors

Morgridge Institute for Research
Career Start Year 2011
Number of shared co-authors 0
Lukasiewicz Research Network-PORT Polish Center for Technology Development
Career Start Year 2009
Number of shared co-authors 2
Center for Global Infectious Disease Research, Seattle Children's Research Institute
Career Start Year 2008
Number of shared co-authors 2
Institut fur Werkstoffkunde (Materials Science), Leibniz Universitat Hannover
Career Start Year 2008
Number of shared co-authors 3
Osnabruck University Department of Biology/Chemistry Bioanalytical Chemistry section
Career Start Year 2007
Number of shared co-authors 3
VILLUM Center for Bioanalytical Sciences, University of Southern Denmark
Career Start Year 2003
Number of shared co-authors 1
The Weizmann Institute of Science
Career Start Year 2000
Number of shared co-authors 2
University of Pittsburgh
Career Start Year 2000
Number of shared co-authors 0
Harvard T. H. Chan School of Public Health
Career Start Year 1999
Number of shared co-authors 2
Instituto de Fisiologia
Career Start Year 1998
Number of shared co-authors 0
Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark
Career Start Year 1996
Number of shared co-authors 1
Max Planck Institute of Molecular Cell Biology and Genetics
Career Start Year 1996
Number of shared co-authors 0
AstraZeneca Oncology R&D
Career Start Year 1995
Number of shared co-authors 2
Ottawa Institute of Systems Biology, University of Ottawa, University of Calgary
Career Start Year 1994
Number of shared co-authors 1
University of Toronto, Canada Mediterranean Institute for Life Sciences
Career Start Year 1993
Number of shared co-authors 2
Duke University Medical Center
Career Start Year 1993
Number of shared co-authors 0
Johns Hopkins University School of Medicine
Career Start Year 1992
Number of shared co-authors 0
School of Pharmacy, University of Nottingham
Career Start Year 1989
Number of shared co-authors 0
Yale School of Medicine
Career Start Year 1989
Number of shared co-authors 2
Center for Global Infectious Disease Research, Seattle Children's Research Institute
Career Start Year 1988
Number of shared co-authors 2
Chungnam National University
Career Start Year 1987
Number of shared co-authors 1
Sanford Burnham Prebys Medical Discovery Institute
Career Start Year 1987
Number of shared co-authors 0
Institute for Research in Immunology and Cancer (IRIC), Universite de Montreal
Career Start Year 1986
Number of shared co-authors 9
Medical Research Council Laboratory of Molecular Biology
Career Start Year 1984
Number of shared co-authors 1
University of California San Diego
Career Start Year 1980
Number of shared co-authors 0
Weill Institute for Cell and Molecular Biology, Cornell University
Career Start Year 1978
Number of shared co-authors 2
Saarland University, Center for Molecular Signaling
Career Start Year 1978
Number of shared co-authors 0
University of Cambridge
Career Start Year 1976
Number of shared co-authors 0
University of California San Diego
Career Start Year 1975
Number of shared co-authors 3
University of Texas Health Science Center at San Antonio Texas78229 USA.
Career Start Year 1973
Number of shared co-authors 0

Collaborators

Children's Hospital of Eastern Ontario
Co-authored papers 3
Hospital for Sick Children
Co-authored papers 3
Canadian Institutes of Health Research Institute of Genetics
Co-authored papers 2
Institute of Neurology, University College London (UCL)
Co-authored papers 2
McGill University
Co-authored papers 2
Yale University
Co-authored papers 1
Harvard Medical School
Co-authored papers 1
Whitehead Institute for Biomedical Research and Massachusetts Institute of Technology
Co-authored papers 1
Suzhou Institute of Nano-Tech and Nano-Bionics (SINANO), Chinese Academy of Sciences
Co-authored papers 1
New York State Psychiatric Institute, Research Foundation for Mental Hygiene
Co-authored papers 1
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 1
University of Otago
Co-authored papers 1
University at Albany
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
Instituto Universitario de Oncologia, Universidad de Oviedo
Co-authored papers 1
Co-authored papers 1
University of Pennsylvania
Co-authored papers 1
University of British Columbia
Co-authored papers 1
CNRS UMR9018, Institut Gustave Roussy, Universite Paris-Saclay
Co-authored papers 1
Institute for Neurodegenerative Diseases, University of California San Francisco
Co-authored papers 1
King Edward Memorial Hospital
Co-authored papers 1
Children's Hospital of Philadelphia
Co-authored papers 1
Co-authored papers 1
National Centre for Indigenous Genomics, Australian National University
Co-authored papers 1
Te Kotahi Research Institute, University of Waikato
Co-authored papers 1
Co-authored papers 1
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill
Co-authored papers 1
Co-authored papers 1
North-West University
Co-authored papers 1
University College Dublin
Co-authored papers 1