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Human Mutation|August 3, 2000
The thermolabile variant 677C-->T can further reduce activity when expressed in cis with severe mutations for human methylenetetrahydrofolate reductaseP Goyette, R Rozen
American Journal of Human Genetics|December 1, 1996
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFRP Goyette, B Christensen, D S Rosenblatt, et al.
American Journal of Human Genetics|May 1, 1995
Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiencyP Goyette, P Frosst, D S Rosenblatt, et al.
The Journal of Biological Chemistry|April 5, 2000
Characterization of retinoic acid receptor-deficient keratinocytesP Goyette, C Feng Chen, W Wang, et al.
Cancer Research|October 18, 2000
Regulation of gli activity by all-trans retinoic acid in mouse keratinocytesP Goyette, D Allan, P Peschard, et al.
Critical Care Medicine|July 1, 1995
In-line microwave blood warming of in-date human packed red blood cellsC G Pappas, H Paddock, P Goyette, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 29, 1998
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)P Goyette, A Pai, R Milos, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 1997
Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery diseaseB Christensen, P Frosst, S Lussier-Cacan, et al.
Nature Genetics|June 1, 1994
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identificationP Goyette, J S Sumner, R Milos, et al.
Human Molecular Genetics|December 1, 1996
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disordersD Leclerc, E Campeau, P Goyette, et al.
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