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

Analysis of PBX1 mutations in 192 Chinese women with Müllerian duct abnormalities.

Fertility and sterility - 30 Jun 2011

Ma Jinlong, Qin Yingying, Liu Wen, Duan Hua, Xia Mingdi, Chen Zi-Jiang

Abstract excerpt

We examined the PBX1 gene in 192 Chinese women with Müllerian duct abnormalities and revealed 2 known single nucleotide polymorphisms: c.61 > A in exon 1 and c.998-1330A>G in intron 7. Future studies in large cohorts of different ethnic populations are warranted to establish definite associations between the PBX1 gene and Müllerian duct abnormalities.

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 China
Share to DNA-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Introns

Share to Mullerian Ducts

Share to Proto-Oncogene Proteins

Share to Urogenital Abnormalities

Source

Identifiers

PMID: 21575942
DOI: 10.1016/j.fertnstert.2011.04.074

Genes

PBX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of PBX1 mutations in 192 Chinese women with Müllerian duct abnormalities.PMID 21575942Read ↗

LHX1 mutation screening in 96 patients with müllerian duct abnormalities.Semantic proximity Read ↗

PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis.Semantic proximity Read ↗

Variants of the WNT7A gene in Chinese patients with müllerian duct abnormalities.Semantic proximity Read ↗

Novel mutations in the TP63 gene are potentially associated with Müllerian duct anomalies.Semantic proximity Read ↗

Mutations in HOXA11 are not responsible for Müllerian duct anomalies in Chinese patients.Semantic proximity Read ↗

Clinical aspects and molecular genetics of the persistent müllerian duct syndrome.Semantic proximity Read ↗

Mutation screening of HOXA7 and HOXA9 genes in Chinese women with Müllerian duct abnormalities.Semantic proximity Read ↗

WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis.Semantic proximity Read ↗

Persistent Mullerian duct syndrome associated with 47,XXY genotype.Semantic proximity Read ↗

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.Semantic proximity Read ↗

Lack of association of WNT5A mutations with Müllerian duct abnormalities.Semantic proximity Read ↗

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.Semantic proximity Read ↗

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