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Results: 1-16 |
Results: 16

Authors: GOYETTE P PAI A MILOS R FROSST P TRAN P CHEN ZT CHAN M ROZEN R
Citation: P. Goyette et al., GENE STRUCTURE OF HUMAN AND MOUSE METHYLENETETRAHYDROFOLATE REDUCTASE(MTHFR), Mammalian genome, 9(8), 1998, pp. 652-656

Authors: GOYETTE P ROSENBLATT D ROZEN R
Citation: P. Goyette et al., HOMOCYSTINURIA (METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY) AND MUTATION OF FACTOR-V GENE, Journal of inherited metabolic disease, 21(6), 1998, pp. 690-691

Authors: CHRISTENSEN B FROSST P LUSSIERCACAN S SELHUB J GOYETTE P ROSENBLATT DS GENEST J ROZEN R
Citation: B. Christensen et al., CORRELATION OF A COMMON MUTATION IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE WITH PLASMA HOMOCYSTEINE IN PATIENTS WITH PREMATURE CORONARY-ARTERY DISEASE, Arteriosclerosis, thrombosis, and vascular biology, 17(3), 1997, pp. 569-573

Authors: SHEPPARD CA GOYETTE P FROSST P ROZEN R GUENTHER B LUDWIG M MATTHEWS RG
Citation: Ca. Sheppard et al., STUDIES OF A MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE - A RISKFACTOR FOR CARDIOVASCULAR-DISEASE AND NEURAL-TUBE DEFECTS, The FASEB journal, 11(9), 1997, pp. 926-926

Authors: LECLERC D CAMPEAU E GOYETTE P ADJALLA CE CHRISTENSEN B ROSS M EYDOUX P ROSENBLATT DS ROZEN R GRAVEL RA
Citation: D. Leclerc et al., HUMAN METHIONINE SYNTHASE - CDNA CLONING AND IDENTIFICATION OF MUTATIONS IN PATIENTS OF THE CBLG COMPLEMENTATION GROUP OF FOLATE COBALAMIN DISORDERS/, Human molecular genetics, 5(12), 1996, pp. 1867-1874

Authors: CHRISTENSEN B GOYETTE P ALHENDY A ROSENBLATT DS ROZEN R
Citation: B. Christensen et al., NEW MUTATION IDENTIFIED IN 4 UNRELATED PATIENTS WITH METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY, Pediatric research, 39(4), 1996, pp. 843-843

Authors: GOYETTE P CHRISTENSEN B ROSENBLATT DS ROZEN R
Citation: P. Goyette et al., SEVERE AND MILD MUTATIONS IN CIS FOR THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE, AND DESCRIPTION OF 5 NOVEL MUTATIONS IN MTHFR, American journal of human genetics, 59(6), 1996, pp. 1268-1275

Authors: FROSST P BLOM HJ MILOS R GOYETTE P SHEPPARD CA MATTHEWS RG BOERS GJH DENHEIJER M KLUIJTMANS LAJ VANDENHEUVEL LP ROZEN R
Citation: P. Frosst et al., A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE, Nature genetics, 10(1), 1995, pp. 111-113

Authors: PAPPAS CG PADDOCK H GOYETTE P GRABOWY R CONNOLLY RJ SCHWAITZBERG SD
Citation: Cg. Pappas et al., IN-LINE MICROWAVE BLOOD WARMING OF IN-DATE HUMAN PACKED RED-BLOOD-CELLS, Critical care medicine, 23(7), 1995, pp. 1243-1250

Authors: GOYETTE P FROSST P CHRISTENSEN B ALHENDY A ROSENBLATT DS ROZEN R
Citation: P. Goyette et al., A COMMON MUTATION RESULTING IN A THERMOLABILE ENZYME CAN BE PRESENT ON THE SAME ALLELE AS MUTATIONS FOR SEVERE DEFICIENCY OF METHYLENETETRAHYDROFOLATE REDUCTASE, Pediatric research, 37(4), 1995, pp. 148-148

Authors: CHRISTENSEN B FROSST P GOYETTE P SELHUB J ROSENBLATT DS GENEST J ROZEN R
Citation: B. Christensen et al., METHYLENETETRAHYDROFOLATE REDUCTASE IN PREMATURE CAD - CORRELATION OFENZYMATIC-ACTIVITY AND THERMOLABILITY WITH GENOTYPE AND PLASMA HOMOCYSTEINE, Circulation, 92(8), 1995, pp. 485-485

Authors: GOYETTE P PAI A MILOS R ROZEN R
Citation: P. Goyette et al., GENOMIC STRUCTURE OF HUMAN AND MOUSE METHYLENETETRAHYDROFOLATE REDUCTASE, American journal of human genetics, 57(4), 1995, pp. 813-813

Authors: GOYETTE P FROSST P ROSENBLATT DS ROZEN R
Citation: P. Goyette et al., 7 NOVEL MUTATIONS IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE ANDGENOTYPE-PHENOTYPE CORRELATIONS IN SEVERE METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY, American journal of human genetics, 56(5), 1995, pp. 1052-1059

Authors: GOYETTE P SUMNER JS MILOS R DUNCAN AMV ROSENBLATT DS MATTHEWS RG ROZEN R
Citation: P. Goyette et al., HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION (VOL 7, PG 195, 1994), Nature genetics, 7(4), 1994, pp. 551-551

Authors: GOYETTE P SUMNER JS MILOS R DUNCAN AMV ROSENBLATT DS MATTHEWS RG ROZEN R
Citation: P. Goyette et al., HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION, Nature genetics, 7(2), 1994, pp. 195-200

Authors: GOYETTE P SUMNER J MILOS R DUNCAN A ROSENBLATT D MATTHEWS R ROZEN R
Citation: P. Goyette et al., ISOLATION OF A CDNA FOR HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) AND IDENTIFICATION OF MUTATIONS IN MTHFR-DEFICIENT PATIENTS, American journal of human genetics, 53(3), 1993, pp. 153-153
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