Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The significance of 1793G>A polymorphism in MTHFR gene in women with first trimester recurrent miscarriages.

Neuro endocrinology letters - 1 Jan 2010

Seremak-Mrozikiewicz Agnieszka, Drews Krzysztof, Kurzawinska Grazyna, Bogacz Anna, Grzeskowiak Edmund, Mrozikiewicz Przemyslaw M

Abstract excerpt

BACKGROUND: Recurrent miscarriages (RM) are significant social and clinical problem. One of suggested reason of RM is hyperhomocysteinemia. Polymorphic genes involved in homocysteine and folate metabolism, including 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, are considered as an important risk factors for homocysteine accumulation and modulator of RM susceptibility. Therefore the aim of this study was...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Habitual
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Poland

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Polymorphism, Single Nucleotide

Share to Pregnancy

Share to Pregnancy Trimester, First

Source

Identifiers

PMID: 21173738

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The significance of 1793G>A polymorphism in MTHFR gene in women with first trimester recurrent miscarriages.PMID 21173738Read ↗

[Genetic conditioned changes in activity of 5,10-methylenetetrahydrofolate reductase (MTHFR) and recurrent miscarriages].Semantic proximity Read ↗

An Association Study of the SLC19A1 Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian Population.Semantic proximity Read ↗

Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.Semantic proximity Read ↗

Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase gene A1298C polymorphism and susceptibility to recurrent pregnancy loss: a meta-analysis.Semantic proximity Read ↗

Plasma homocysteine and vitamin B12 serum levels, red blood cell folate concentrations, C677T methylenetetrahydrofolate reductase gene mutation and risk of recurrent miscarriage: a case-control study in Spain.Semantic proximity Read ↗

MTHFR C677T polymorphism and recurrent early pregnancy loss risk in north Indian population.Semantic proximity Read ↗

The C677T polymorphism of the methylenetetrahydrofolate reductase gene and idiopathic recurrent miscarriage.Semantic proximity Read ↗

MTHFR C677T polymorphism, folate, vitamin B12 and homocysteine in recurrent pregnancy losses: a case control study among North Indian women.Semantic proximity Read ↗

Association of histidine-rich glycoprotein C633T single nucleotide polymorphism and recurrent miscarriage in Iranian women.Semantic proximity Read ↗

A woman with five consecutive fetal deaths: case report and retrospective analysis of hyperhomocysteinemia prevalence in 100 consecutive women with recurrent miscarriages.Semantic proximity Read ↗

Contribution of inherited thrombophilia to recurrent miscarriage in the Polish population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.