Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects.
about
Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailtyTranscobalamin C776G genotype modifies the association between vitamin B12 and homocysteine in older HispanicsConcept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions.Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.Vitamin B-12 status during pregnancy and child's IQ at age 8: a Mendelian randomization study in the Avon longitudinal study of parents and children.Maternal folate-related gene environment interactions and congenital heart defects.Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?Genetic variation in genes of folate metabolism and neural-tube defect risk.Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.Neural tube defects, folic acid and methylationGene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis.Association of genetic variants of methionine metabolism with methotrexate-induced CNS white matter changes in patients with primary CNS lymphoma.Markers of B-vitamin deficiency and frailty in older womenEnvironmental influence on the worldwide prevalence of a 776C->G variant in the transcobalamin gene (TCN2).Pharmacogenetics of drug-induced birth defects: what is known so far?Association of ulcerative colitis with transcobalamin II gene polymorphisms and serum homocysteine, vitamin B12, and folate levels in Chinese patients.A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin.Analysis of the transcobalamin II 776C>G (259P>R) single nucleotide polymorphism by denaturing HPLC in healthy elderly: associations with cobalamin, homocysteine and holo-transcobalamin II.Transcobalamin 776C→G polymorphism is associated with peripheral neuropathy in elderly individuals with high folate intake.A80G polymorphism of reduced folate carrier 1 (RFC1) and C776G polymorphism of transcobalamin 2 (TC2) genes in Down's syndrome etiology.A candidate gene study of one-carbon metabolism pathway genes and colorectal cancer risk.Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studies.Should vitamin B12 status be considered in assessing risk of neural tube defects?Pyrosequencing assay for genotyping of the Transcobalamin II 776C>G polymorphism.Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.MTHFD1 G1958A, BHMT G742A, TC2 C776G and TC2 A67G polymorphisms and head and neck squamous cell carcinoma risk.Transcobalamin Polymorphism 67A->G, but Not 776C->G, Affects Serum Holotranscobalamin in a Cohort of Healthy Middle-Aged Men and Women
P2860
Q24618116-5265EC04-574A-4C8A-AC84-A97BB315B2E9Q24628651-8D17AFCA-7876-448C-8F65-5F4F044126DCQ27780078-F841CD05-203A-49BB-92C8-A6EE69AD8674Q33958199-C3C48573-B43F-43A2-AD2D-DC8F5E8A4888Q34507227-F709E7BF-BFFE-4AAE-940F-7D0D3080FCF3Q34521969-C2474AA9-B712-4085-A372-A322D3162DAEQ35600454-5B9877FE-406D-4BA4-8A36-69AA3FF4C3B5Q36467477-6A5D1DF0-3797-4E98-B334-F50C64CEA152Q37029453-1200A848-C6C0-4CA5-BF65-4D50CDE0F39BQ37236998-58D38DAA-781E-4646-93D1-54A13C2F87B9Q37246148-5C8119EB-C779-4603-BDC8-F88D4AC93CB6Q37284222-1CFB1E67-36E1-4570-BC20-DE148217F142Q37337021-DB366B57-0806-45D7-BBED-7E35E5B7073FQ37340010-15225A76-8A0B-4609-887F-5FAF6F316036Q37869124-F86379A0-2BF7-49EE-814C-09B2EC599A81Q40193336-A7F7DA76-ADC4-4018-A66B-8FBAB545F633Q41549089-DF274A19-2DFD-462A-8129-A902D3EB954CQ44680024-5D074D13-0FF6-4E90-9917-C4A436959D89Q46053162-893E7D8C-AE21-4453-8B67-4A89A71B8532Q46094011-E92732D8-942C-4699-956A-51F259313FA2Q47386572-36FD38F4-EEC2-4F45-BD3A-3872FFB2148EQ47944759-112061AE-A2E8-4AB1-91B4-E34EF980AB85Q48521095-908354FD-FCCC-454D-A05C-183689A7A15CQ50775343-E695ACD0-80DA-43C6-B45C-ACB656BAC771Q50967534-E679E53F-1A34-49FB-A6AD-4148C7DE2710Q54368104-7F95FCF0-67EC-48E2-8F2D-1C6905D33ED3Q57677507-216946B6-5C06-49BA-9E2E-50FB8336C939
P2860
Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Single nucleotide polymorphism ...... risk for neural tube defects.
@en
Single nucleotide polymorphism ...... risk for neural tube defects.
@nl
type
label
Single nucleotide polymorphism ...... risk for neural tube defects.
@en
Single nucleotide polymorphism ...... risk for neural tube defects.
@nl
prefLabel
Single nucleotide polymorphism ...... risk for neural tube defects.
@en
Single nucleotide polymorphism ...... risk for neural tube defects.
@nl
P2093
P2860
P356
P1476
Single nucleotide polymorphism ...... risk for neural tube defects.
@en
P2093
Frans J M Trijbels
Karin J A Lievers
Lydia A Afman
Nathalie M J van der Put
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5200830
P50
P577
2002-07-01T00:00:00Z