X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
5,10-methylenetetrahydrofolate reductase (607) 607
humans (569) 569
female (376) 376
methylenetetrahydrofolate reductase (374) 374
male (317) 317
methylenetetrahydrofolate reductase - genetics (243) 243
common mutation (229) 229
genotype (222) 222
homocysteine (220) 220
adult (219) 219
middle aged (219) 219
risk factors (217) 217
index medicus (186) 186
folate (180) 180
polymorphism, genetic (179) 179
homocysteine - blood (151) 151
aged (149) 149
vascular-disease (147) 147
case-control studies (140) 140
polymorphism (139) 139
mutation (130) 130
mthfr (128) 128
neural-tube defects (125) 125
folic acid (122) 122
genetic predisposition to disease (121) 121
plasma homocysteine (115) 115
genetic aspects (113) 113
risk-factor (113) 113
genetics & heredity (110) 110
risk factor (109) 109
folic acid - blood (92) 92
gene frequency (92) 92
folic-acid (87) 87
hyperhomocysteinemia (85) 85
oxidoreductases acting on ch-nh group donors - genetics (83) 83
methylenetetrahydrofolate reductase gene (82) 82
polymorphism, single nucleotide (82) 82
oncology (81) 81
alleles (79) 79
pregnancy (79) 79
adolescent (73) 73
oxidoreductases - genetics (73) 73
spina-bifida (71) 71
dna methylation (70) 70
genetic polymorphisms (68) 68
folic acid - metabolism (67) 67
risk (66) 66
animals (63) 63
neural tube defects - genetics (63) 63
neural tube defects (61) 61
research (61) 61
biochemistry & molecular biology (60) 60
odds ratio (59) 59
child (56) 56
5,10-methylenetetrahydrofolate reductase - genetics (55) 55
homozygote (54) 54
metabolism (53) 53
gene (52) 52
disease (51) 51
polymerase chain reaction (51) 51
chinese population (49) 49
colorectal-cancer (49) 49
genes (49) 49
peripheral vascular disease (49) 49
physiological aspects (49) 49
c677t polymorphism (48) 48
medicine, research & experimental (47) 47
nutrition & dietetics (47) 47
aged, 80 and over (46) 46
methionine synthase (46) 46
myocardial-infarction (46) 46
methylation (45) 45
mild hyperhomocysteinemia (45) 45
point mutation (45) 45
c677t (44) 44
genetics (43) 43
infant, newborn (43) 43
cardiovascular-disease (42) 42
genetic research (42) 42
meta-analysis (42) 42
child, preschool (41) 41
polymorphism, genetic - genetics (41) 41
vitamin b 12 - blood (41) 41
homocysteine - metabolism (40) 40
prevalence (40) 40
thermolabile variant (40) 40
association (39) 39
hematology (39) 39
pediatrics (39) 39
susceptibility (39) 39
coronary-artery disease (38) 38
enzymes (38) 38
methylenetetrahydrofolate reductase - metabolism (38) 38
polymorphisms (38) 38
analysis (37) 37
hyperhomocysteinemia - genetics (37) 37
vitamin b (37) 37
clinical neurology (36) 36
health aspects (36) 36
cancer (35) 35
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (740) 740
French (9) 9
Chinese (4) 4
Spanish (4) 4
German (2) 2
Polish (2) 2
Russian (2) 2
Japanese (1) 1
Korean (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2006, Volume 27, Issue 2, pp. 334 - 343
Journal Article
Current Pharmaceutical Design, ISSN 1381-6128, 2013, Volume 19, Issue 14, pp. 2574 - 2593
Journal Article
Translational psychiatry, ISSN 2158-3188, 11/2018, Volume 8, Issue 1, pp. 242 - 12
Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme for the critical process of one-carbon metabolism involving folate and homocysteine metabolisms. It... 
FOLATE METABOLIC PATHWAY | HOMOCYSTEINE LEVELS | RISK-FACTOR | PSYCHIATRY | MTHFR C677T POLYMORPHISM | MAJOR DEPRESSIVE DISORDER | 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE | COMMON MUTATION | AUTISM SPECTRUM DISORDERS | GENE POLYMORPHISMS | GENOMIC DNA METHYLATION | Plasma | Enzymes | Vitamin B | DNA methylation | Schizophrenia | Behavior disorders | Polymorphism
Journal Article
Journal Article
American Journal of Epidemiology, ISSN 0002-9262, 11/2009, Volume 170, Issue 10, pp. 1207 - 1221
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2006, Volume 27, Issue 3, pp. 482 - 489
Journal Article
American Journal of Epidemiology, ISSN 0002-9262, 05/2000, Volume 151, Issue 9, pp. 862 - 877
The enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR) is involved in folate metabolism. The MTHFR gene is located on chromosome 1 (1p36.3), and two... 
5,10- methylenetetrahydrofolate reductase | Spinal dysraphism | Abnormalities | Neural tube defects | A1298C | C677T | Genetics | Epidemiology | METHYLENE-TETRAHYDROFOLATE REDUCTASE | spinal dysraphism | CORONARY-ARTERY DISEASE | PLASMA TOTAL HOMOCYSTEINE | abnormalities | NEURAL-TUBE DEFECTS | RISK FACTOR | C677T MUTATION | neural tube defects | COMMON MUTATION | 5,10-methylenetetrahydrofolate reductase | MATERNAL VITAMIN USE | SPINA-BIFIDA | epidemiology | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | genetics | THERMOLABILE METHYLENETETRAHYDROFOLATE REDUCTASE | Africa - epidemiology | Congenital Abnormalities - epidemiology | Gene Frequency - genetics | Age Distribution | Prevalence | Humans | Asian Continental Ancestry Group - genetics | Male | Methylenetetrahydrofolate Reductase (NADPH2) | Case-Control Studies | Americas - epidemiology | Congenital Abnormalities - genetics | Female | African Continental Ancestry Group - genetics | Genetic Linkage | European Continental Ancestry Group - genetics | Reproducibility of Results | Europe - epidemiology | Oxidoreductases Acting on CH-NH Group Donors - genetics | Australia - epidemiology | Pregnancy | Asia - epidemiology | Congenital Abnormalities - ethnology | Alleles | Indians, North American - genetics | Sex Distribution | Dietary Supplements | Neural tube | Analysis | Genetic research | Causes of | Birth defects | Research | Down syndrome | Epidemiological research | Metabolism | Folic acid
Journal Article