相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications
Mariet Allen et al.
MOLECULAR NEURODEGENERATION (2012)
Genetic Polymorphisms of the TYMS Gene Are Not Associated with Congenital Cardiac Septal Defects in a Han Chinese Population
Jian-Yuan Zhao et al.
PLOS ONE (2012)
NAT1, NOS3, and TYMS Genotypes and the Risk of Conotruncal Cardiac Defects
Philip J. Lupo et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)
The changing epidemiology of congenital heart disease
Teun van der Bom et al.
NATURE REVIEWS CARDIOLOGY (2011)
MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome
Ivana Babic Bozovic et al.
PEDIATRICS INTERNATIONAL (2011)
Head and neck carconogenesis: impact of MTHFD1 G1958A polymorphism
Lidia Maria Rebolho Batista da Silva et al.
REVISTA DA ASSOCIACAO MEDICA BRASILEIRA (2011)
Cancer Chemoprevention Mechanisms Mediated Through the Keap1-Nrf2 Pathway
John D. Hayes et al.
ANTIOXIDANTS & REDOX SIGNALING (2010)
Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects
Frans A Hol et al.
CLINICAL GENETICS (2010)
Transcobalamin C776G genotype modifies the association between vitamin B12 and homocysteine in older Hispanics
M. G. Garrod et al.
EUROPEAN JOURNAL OF CLINICAL NUTRITION (2010)
NFE2L2 Gene Mutation in Male Japanese Squamous Cell Carcinoma of the Lung
Hidefumi Sasaki et al.
JOURNAL OF THORACIC ONCOLOGY (2010)
Association of Reduced Folate Carrier Gene Polymorphism and Maternal Folic Acid Use With Neural Tube Defects
Lijun Pei et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
The Reduced Folate Carrier (SLC19A1) c.80G > A Polymorphism is Associated with Red Cell Folate Concentrations Among Women
Anna Stanislawska-Sachadyn et al.
ANNALS OF HUMAN GENETICS (2009)
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
Gary M. Shaw et al.
BMC MEDICAL GENETICS (2009)
The MTHFD1 p.Arg653Gln Variant Alters Enzyme Function and Increases Risk for Congenital Heart Defects
Karen E. Christensen et al.
HUMAN MUTATION (2009)
Genetic Basis of Neural Tube Defects
Alexander G. Bassuk et al.
SEMINARS IN PEDIATRIC NEUROLOGY (2009)
Prevalence of severe congenital heart disease after folic acid fortification of grain products: time trend analysis in Quebec, Canada
Raluca Ionescu-Ittu et al.
BMJ-BRITISH MEDICAL JOURNAL (2009)
Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts
Abee L. Boyles et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China
Yali Shang et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2008)
Variants of Folate Metabolism Genes and the Risk of Conotruncal Cardiac Defects
Elizabeth Goldmuntz et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2008)
Genetic and lifestyle factors related to the periconception vitamin B12 status and congenital heart defects: A Dutch case-control study
Anna C. Verkleij-Hagoort et al.
MOLECULAR GENETICS AND METABOLISM (2008)
Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects
R. Brouns et al.
PRENATAL DIAGNOSIS (2008)
The MTHFR 677C→T polymorphism and the risk of congenital heart defects:: a literature review and meta-analysis
I. M. van Beynum et al.
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE (2007)
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population
Anne Parle-McDermott et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida
Ivon J. M. van der Linden et al.
MOLECULAR GENETICS AND METABOLISM (2007)
Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations.: Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children
Ana C. M. Alessio et al.
THROMBOSIS RESEARCH (2007)
Abnormal folate metabolism in foetuses affected by neural tube defects
Louisa P. E. Dunlevy et al.
BRAIN (2007)
Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease
A. C. Verkleij-Hagoort et al.
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY (2006)
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population
Anne Parle-McDermott et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Maternal MTHFR 677C>T is a risk factor for congenital heart defects:: effect modification by periconceptional folate supplementation
IM van Beynum et al.
EUROPEAN HEART JOURNAL (2006)
Reduced folate carrier polymorphisms and neural tube defect risk
VB O'Leary et al.
MOLECULAR GENETICS AND METABOLISM (2006)
Study of Four Genes Belonging to the Folate Pathway: Transcobalamin 2 Is Involved in the Onset of Non-Syndromic Cleft Lip With or Without Cleft Palate
Marcella Martinelli et al.
HUMAN MUTATION (2006)
Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene
CA Hobbs et al.
JOURNAL OF MEDICAL GENETICS (2006)
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk
P De Marco et al.
JOURNAL OF HUMAN GENETICS (2006)
Fourteen novel genetic variations and haplotype structures of the TYMS gene encoding human thymidylate synthase (TS)
Su-Ryang Kim et al.
DRUG METABOLISM AND PHARMACOKINETICS (2006)
Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus
WL Zhu et al.
MOLECULAR HUMAN REPRODUCTION (2006)
Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism and the age-at-onset of Alzheimer's and Parkinson's diseases
EM Schmuck et al.
PHARMACOGENETICS AND GENOMICS (2005)
New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?
WG Johnson et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)
Role of polymorphisms in MTHFR and MTHFD1 genes in the outcome of childhood acute lymphoblastic leukemia
M Krajinovic et al.
PHARMACOGENOMICS JOURNAL (2004)
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects
GM Shaw et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2003)
Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans
RM Guéant-Rodriguez et al.
NEUROSCIENCE LETTERS (2003)
Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk
I Morin et al.
MOLECULAR GENETICS AND METABOLISM (2003)
Characterization of the human Omega class glutathione transferase genes and associated polymorphisms
AK Whitbread et al.
PHARMACOGENETICS (2003)
Reduced folate carrier polymorphism (80A → G) and neural tube defects
P De Marco et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Associations between polymorphisms within the thymidylate synthase gene and spina bifida
KA Volcik et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2003)
776C > G polymorphism of the transcobalamin II gene as a risk factor for spina bifida
JJ Pietrzykl et al.
MOLECULAR GENETICS AND METABOLISM (2003)
Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects
S Storti et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2003)
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: Report of the birth defects research group
LC Brody et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Distribution of mutations in human thymidylate synthase yielding resistance to 5-fluorodeoxyuridine
H Kawate et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels
BN Trinh et al.
HUMAN GENETICS (2002)
Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults
JW Miller et al.
BLOOD (2002)
Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects
LA Afman et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2002)
Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida
GM Shaw et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases
GS Zhang et al.
THROMBOSIS RESEARCH (2001)
Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease
R Junker et al.
CARDIOVASCULAR RESEARCH (2001)
Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations
KD Wenstrom et al.
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2001)
Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction
J Chen et al.
ATHEROSCLEROSIS (2001)