Detalhe da pesquisa
1.
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.
Nat Genet
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Artigo
em Inglês
| MEDLINE | ID: mdl-7920641
2.
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.
Nat Genet
; 10(1): 111-3, 1995 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-7647779
3.
A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles.
Genes Immun
; 12(1): 51-8, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20962850
4.
Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis.
Gut
; 58(6): 799-804, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19201773
5.
MAST3: a novel IBD risk factor that modulates TLR4 signaling.
Genes Immun
; 9(7): 602-12, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18650832
6.
Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.
Nat Genet
; 7(4): 551, 1994 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-7951330
7.
Regulation of gli activity by all-trans retinoic acid in mouse keratinocytes.
Cancer Res
; 60(19): 5386-9, 2000 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11034076
8.
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
Mucosal Immunol
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Artigo
em Inglês
| MEDLINE | ID: mdl-19079170
9.
The thermolabile variant 677C-->T can further reduce activity when expressed in cis with severe mutations for human methylenetetrahydrofolate reductase.
Hum Mutat
; 16(2): 132-8, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10923034
10.
Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.
Am J Hum Genet
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Artigo
em Inglês
| MEDLINE | ID: mdl-7726158
11.
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.
Am J Hum Genet
; 59(6): 1268-75, 1996 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-8940272
12.
Characterization of retinoic acid receptor-deficient keratinocytes.
J Biol Chem
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Artigo
em Inglês
| MEDLINE | ID: mdl-10748128
13.
Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.
Arterioscler Thromb Vasc Biol
; 17(3): 569-73, 1997 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9102178
14.
In-line microwave blood warming of in-date human packed red blood cells.
Crit Care Med
; 23(7): 1243-50, 1995 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-7600834
15.
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)
Mamm Genome
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Artigo
em Inglês
| MEDLINE | ID: mdl-9680386
16.
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Hum Mol Genet
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Artigo
em Inglês
| MEDLINE | ID: mdl-8968737
17.
Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene.
J Inherit Metab Dis
; 21(6): 690-1, 1998 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-9762613