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Author Details
Full Name
Christopher R McMaster
Affiliation
Dalhousie University
ORCID
Career Start Year
1989
Papers
104
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35322809
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism.
Nat Commun
2022
35447137
Choline kinase inhibition promotes ER-phagy.
J Lipid Res
2022
36379551
Core elements of participant consent documents for Canadian human genomics research and the National Human Genome Library: guidance for policy.
CMAJ
2022
35951321
Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4.
JAMA Ophthalmol
2022
35151687
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia.
J Biol Chem
2022
35202461
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Brain
2022
33454747
Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.
Brain
2021
33734376
Genetic analysis of Pycr1 and Pycr2 in mice.
Genetics
2021
33381478
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations.
Front Pediatr
2020
32032513
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms.
Am J Hum Genet
2020
33454021
Genetic diseases of the Kennedy pathways for membrane synthesis.
J Biol Chem
2020
31566834
Frizzled 4 regulates ventral blood vessel remodeling in the zebrafish retina.
Dev Dyn
2019
29178478
From yeast to humans - roles of the Kennedy pathway for phosphatidylcholine synthesis.
FEBS Lett
2018
30053067
Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.
Nucleic Acids Res
2018
29905858
Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.
Nucleic Acids Res
2018
29487144
How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases.
Genetics
2018
28052917
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis.
Brain
2017
28404662
SLC25 Family Member Genetic Interactions Identify a Role for <i>HEM25</i> in Yeast Electron Transport Chain Stability.
G3 (Bethesda)
2017
26821380
Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia.
PLoS Genet
2016
27521373
Lipid synthesis and membrane contact sites: a crossroads for cellular physiology.
J Lipid Res
2016
27489958
Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy.
PLoS One
2016
27038157
Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.
Pediatr Blood Cancer
2016
25572853
Phosphorylation of caveolin-1 on tyrosine-14 induced by ROS enhances palmitate-induced death of beta-pancreatic cells.
Biochim Biophys Acta
2015
26352440
Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study.
Public Health Genomics
2015
26415690
Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome.
Chem Phys Lipids
2015
25688091
The mitochondrial quality control protein Yme1 is necessary to prevent defective mitophagy in a yeast model of Barth syndrome.
J Biol Chem
2015
24434691
Attitudes of parents toward the return of targeted and incidental genomic research findings in children.
Genet Med
2014
27896114
Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of <i>UBIAD1</i> gene expression.
Mol Genet Metab Rep
2014
25340522
Germline mutations in MAP3K6 are associated with familial gastric cancer.
PLoS Genet
2014
25124931
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
JAMA Ophthalmol
2014
23335509
Drug uptake, lipid rafts, and vesicle trafficking modulate resistance to an anticancer lysophosphatidylcholine analogue in yeast.
J Biol Chem
2013
24187140
Choline transport activity regulates phosphatidylcholine synthesis through choline transporter Hnm1 stability.
J Biol Chem
2013
23593226
The yeast oxysterol binding protein Kes1 maintains sphingolipid levels.
PLoS One
2013
23793442
A novel rearrangement of occludin causes brain calcification and renal dysfunction.
Hum Genet
2013
23383173
Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14.
PLoS One
2013
23344949
Alteration of plasma membrane organization by an anticancer lysophosphatidylcholine analogue induces intracellular acidification and internalization of plasma membrane transporters in yeast.
J Biol Chem
2013
22334669
A detour for yeast oxysterol binding proteins.
J Biol Chem
2012
22966490
Guidelines for the use and interpretation of assays for monitoring autophagy.
Autophagy
2012
22704758
A generalizable pre-clinical research approach for orphan disease therapy.
Orphanet J Rare Dis
2012
21358631
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.
Nat Genet
2011
20651827
Surprising roles for phospholipid binding proteins revealed by high throughput genetics.
Biochem Cell Biol
2010
20729555
Lipid binding requirements for oxysterol-binding protein Kes1 inhibition of autophagy and endosome-trans-Golgi trafficking pathways.
J Biol Chem
2010
19129178
Phospholipid transfer protein Sec14 is required for trafficking from endosomes and regulates distinct trans-Golgi export pathways.
J Biol Chem
2009
19841481
NTE1-encoded phosphatidylcholine phospholipase b regulates transcription of phospholipid biosynthetic genes.
J Biol Chem
2009
19141610
The Kap60-Kap95 karyopherin complex directly regulates phosphatidylcholine synthesis.
J Biol Chem
2009
17938859
Emerging roles of the oxysterol-binding protein family in metabolism, transport, and signaling.
Cell Mol Life Sci
2008
18773978
Tryptophan fluorescence reveals induced folding of Vibrio harveyi acyl carrier protein upon interaction with partner enzymes.
Biochim Biophys Acta
2008
16731034
Phosphatidylcholine synthesis and its catabolism by yeast neuropathy target esterase 1.
Biochim Biophys Acta
2007
17601877
Regulation of phosphoinositide levels by the phospholipid transfer protein Sec14p controls Cdc42p/p21-activated kinase-mediated cell cycle progression at cytokinesis.
Eukaryot Cell
2007
17881569
The oxysterol binding protein Kes1p regulates Golgi apparatus phosphatidylinositol-4-phosphate function.
Proc Natl Acad Sci U S A
2007
1 - 50 of 104
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Suzhou Institute of Nano-Tech and Nano-Bionics (SINANO), Chinese Academy of Sciences
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University of Otago
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University at Albany
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