Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
about
sameAs
Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studiesGenetics of human neural tube defectsCharacterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatmentNutrition, One-Carbon Metabolism and Neural Tube Defects: A Review118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defectsEvaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.Prevalence of MTHFR C677T and MS A2756G polymorphisms in major depressive disorder, and their impact on response to fluoxetine treatment.Geographical distribution of MTHFR C677T, A1298C and MTRR A66G gene polymorphisms in China: findings from 15357 adults of Han nationality.Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature.Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK populationAssociation between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers.Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?Identifying women who might benefit from higher doses of folic acid in pregnancy.Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningoceleGenetic variation in genes of folate metabolism and neural-tube defect risk.Etiology, pathogenesis and prevention of neural tube defects.Folic acid supplementation for pregnant women and those planning pregnancy: 2015 update.Acquired and inherited disorders of cobalamin and folate in children.Influence of combined methionine synthase (MTR 2756A > G) and methylenetetrahydrofolate reductase (MTHFR 677C > T) polymorphisms to plasma homocysteine levels in Korean patients with ischemic stroke.Neural tube defects, folic acid and methylationThe search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma.Pharmacogenetics of drug-induced birth defects: what is known so far?Human neural tube defects: genetic causes and prevention."Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis".Association between MTHFR C677T polymorphism and venous thromboembolism risk in the Chinese population: a meta-analysis of 24 case-controlled studies.Polycystic ovary syndrome and the single nucleotide polymorphisms of methylenetetrahydrofolate reductase: a pilot observational study.Association Between MTHFR Genetic Variants and Multiple Sclerosis in a Southern Iranian Population.Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects.Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms.Variants in MTHFR gene and neural tube defects susceptibility in China.Metabolic and genetic risk factors for migraine in children.No evidence for association of MTHFR 677C>T and 1298A>C variants with placental DNA methylation.The 677C>T mutation of the MTHFR gene increases the risk of venous thromboembolism in Koreans and a meta-analysis from Asian population.
P2860
Q21089859-CF9494C8-420E-4552-A128-F1F635E21988Q22337140-D7D44244-26D8-4CF8-A8DB-B3F2D104A90EQ24316931-7A12A0B9-B0FA-47C5-9E37-8A3AA4D35209Q28066331-A656D5EB-16E5-4A1E-A9C7-DC1415B4C487Q33459545-71DBE916-17B9-447C-9FC4-AEF412BBDC75Q33638091-55BBB67B-07A6-4D18-B336-03DF4972B80DQ33981170-4F3B8128-DEB2-4D9C-8918-13B13572C59DQ34614550-7FBDA66F-02E0-4EBC-9083-F9F6539E1CC9Q34672452-BB29CB86-3B40-4EFF-83E2-40139C9AA98BQ35113186-BB8A4B17-6F0F-4EB3-9A90-3776604C5C8AQ35311051-1583F617-FE8E-4D82-8892-52F55DA175E5Q35445213-34FE016A-F666-43CD-8494-AC25B8256EFFQ35586626-82C422D4-80FE-4E35-AAEB-004E35954C13Q35600454-95BD1902-D944-4C6D-9FB7-E0EDD5C7A21BQ35886420-922BDDBD-E00A-45B9-A5B2-2423049B0938Q35891898-5E5D77EF-5C07-4DAD-851D-B26352ABBAB8Q36467477-E3B72A72-CE60-4571-BBEF-F3598A29BCC7Q36491874-A009D029-29DC-4EED-B1DB-BDB7834F1D13Q36536655-4F6AE990-2AD3-4C0A-B7E4-1BA79481F65BQ36538527-4D264EF2-5F59-4060-B587-36DCB25733B9Q37065550-EEC2374C-BC4B-415E-BBAA-65B03FEAF224Q37236998-41E234AD-73D9-4900-BA99-FEF4F54544B8Q37399043-2C956E5B-2121-4627-A432-96A60D49F93CQ37418975-C4A0D76D-0447-4F03-8E08-55CBD004A814Q37869124-8BDD9C1C-6F2D-49B6-B088-6CE89C02BA78Q37889823-B4D3C534-C997-4576-BEB1-77D077FCBB6FQ38227383-767421F3-D4F1-4871-8940-2E9E3183C729Q38242424-076A2859-A562-40FC-90B7-DCAB6294DBDFQ40220435-CC778D12-15D0-4138-A021-C030BE5DB6D3Q41114527-9FE7D8A1-B90B-4F0D-AA35-58D1691DAFC4Q44409883-944EB30C-45A8-4551-B48B-72BFE2A5BE9FQ46388221-D15849D2-FD09-469C-8D0B-24B8BE69313BQ48239565-F7D8ABE8-E916-4825-99E0-B91F19CF9072Q51498300-2E26F21F-41C2-4DD7-B58F-EB951B53E46AQ52689990-41F1C2CC-2ECB-4CA1-928C-7D9538BAA276Q53665117-D393D9D2-B3BF-41F9-A0F5-5AEFD291C995
P2860
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
description
2002 թուականին հրատարակուած գիտական յօդուած
@hyw
2002 թվականին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Januar 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 2002)
@en
vedecký článok (publikovaný 2002)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd in 2002)
@nl
наукова стаття, опублікована у 2002
@uk
مقالة علمية (نشرت عام 2002)
@ar
name
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@ast
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@en
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@nl
type
label
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@ast
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@en
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@nl
prefLabel
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@ast
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@en
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@nl
P2093
P50
P356
P1476
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
@en
P2093
Anna Moroni
Armando Cama
Elisa Merello
Huiping Zhu
Lorenza Arata
Luciano Andreussi
Patrizia De Marco
P2888
P304
P356
10.1007/S100380200043
P407
P577
2002-01-01T00:00:00Z