Variations in folate pathway genes are associated with unexplained female infertility.
about
Intercultural Usage of Mori Folium: Comparison Review from a Korean Medical PerspectiveReview on autoimmune reactions in female infertility: antibodies to follicle stimulating hormoneThe effects of oxidative stress on female reproduction: a reviewThe association of idiopathic recurrent early pregnancy loss with polymorphisms in folic acid metabolism-related genesEffect of folate deficiency on promoter methylation and gene expression of Esr1, Cav1, and Elavl1, and its influence on spermatogenesisPreconception interventions in infertile couples.Maternal characteristics and pregnancy outcomes after assisted reproductive technology by infertility diagnosis: ovulatory dysfunction versus tubal obstruction.Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms in Male Partners of Recurrent Miscarriage Couples.Combination of thrombophilic gene polymorphisms as a cause of increased the risk of recurrent pregnancy loss.Improvement of gamete quality by stimulating and feeding the endogenous antioxidant system: mechanisms, clinical results, insights on gene-environment interactions and the role of diet.May Underdiagnosed Nutrition Imbalances Be Responsible for a Portion of So-Called Unexplained Infertility? From Diagnosis to Potential Treatment Options.Maternally Contributed Folate Receptor 1 Is Expressed in Ovarian Follicles and Contributes to Preimplantation Development.Folic acid supplementation and methylenetetrahydrofolate reductase (MTHFR) gene variations in relation to in vitro fertilization pregnancy outcome.Effects of Subacute Administration of Co-Trimoxazole and Folic Acid on Ovarian Tissue in Adult Female Rats.A folate receptor alpha double-mutated haplotype 1816delC-1841A is distributed throughout Eurasia and associated with lower erythrocyte folate levels.Low-molecular-weight heparin in women with repeated implantation failure.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.Variation in hyaluronan-binding protein 2 (HABP2) promoter region is associated with unexplained female infertility.Association of GSTM1 and GSTT1 gene polymorphisms and in-vitro fertilisation outcome in a population in northern Iran.Solute Carrier Family 19, member 1 (SLC19A1) polymorphisms (-43T>C, 80G>A, and 696C>T), and haplotypes in idiopathic recurrent spontaneous abortion in a Korean population.Analysis of plasminogen activator inhibitor-1, integrin beta3, beta fibrinogen, and methylenetetrahydrofolate reductase polymorphisms in Iranian women with recurrent pregnancy loss.
P2860
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P2860
Variations in folate pathway genes are associated with unexplained female infertility.
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Variations in folate pathway genes are associated with unexplained female infertility.
@ast
Variations in folate pathway genes are associated with unexplained female infertility.
@en
Variations in folate pathway genes are associated with unexplained female infertility.
@nl
type
label
Variations in folate pathway genes are associated with unexplained female infertility.
@ast
Variations in folate pathway genes are associated with unexplained female infertility.
@en
Variations in folate pathway genes are associated with unexplained female infertility.
@nl
prefLabel
Variations in folate pathway genes are associated with unexplained female infertility.
@ast
Variations in folate pathway genes are associated with unexplained female infertility.
@en
Variations in folate pathway genes are associated with unexplained female infertility.
@nl
P2093
P50
P1476
Variations in folate pathway genes are associated with unexplained female infertility.
@en
P2093
Margit Laanpere
Tiina Syvänen
Torbjörn K Nilsson
P304
P356
10.1016/J.FERTNSTERT.2009.02.025
P407
P577
2009-03-26T00:00:00Z