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

Haplotype and mutation analysis of the TGFBR3 gene in Chinese women with idiopathic premature ovarian failure.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology - 1 Jan 2012

Qin Chun-rong, Chen Shi-ling, Yao Ji-long, Li Tao, Wu Wei-qing

Abstract excerpt

This study screened the TGFBR3 mutations in Chinese patients with idiopathic premature ovarian failure (POF) to gain a better understanding the genetic aetiology of POF. One hundred twelve Chinese patients with idiopathic POF and 110 women from normal controls were examined. The coding region and respective flanking intronic regions of the TGFBR3 gene were amplified by the PCR, and the DNA fragments were directly...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Genetic Association Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Haplotypes

Share to Models, Biological

Share to Mutation, Missense

Share to Primary Ovarian Insufficiency

Share to Proteoglycans

Share to Receptors, Transforming Growth Factor beta

Source

Identifiers

PMID: 21756058
DOI: 10.3109/09513590.2011.583954

Genes

TGFBR3

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Haplotype and mutation analysis of the TGFBR3 gene in Chinese women with idiopathic premature ovarian failure.PMID 21756058Read ↗

[Application of DHPLC screening TGFBR-3 gene in Chinese women with idiopathic premature ovarian failure].Semantic proximity Read ↗

Association between TGF-β/BMP signaling pathway polymorphisms and the risk of primary ovarian insufficiency in Korean women.Semantic proximity Read ↗

Association study of TGFBR2 and miR-518 gene polymorphisms with age at natural menopause, premature ovarian failure, and early menopause among Chinese Han women.Semantic proximity Read ↗

Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing.Semantic proximity Read ↗

Genetic Etiologic Analysis in 74 Chinese Han Women with Idiopathic Premature Ovarian Insufficiency by Combined Molecular Genetic TestingSemantic proximity Read ↗

Mutational analysis of the betaglycan gene-coding region in susceptibility for ovarian failure.Semantic proximity Read ↗

Epistasis between the HSD17B4 and TG polymorphisms is associated with premature ovarian failure.Semantic proximity Read ↗

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure.Semantic proximity Read ↗

Genetic variants in TGF-β pathway are associated with ovarian cancer risk.Semantic proximity Read ↗

Novel WT1 Missense Mutations in Han Chinese Women with Premature Ovarian Failure.Semantic proximity Read ↗

Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.Semantic proximity Read ↗

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.Semantic proximity Read ↗

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