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

PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis.

Reproductive biomedicine online - 1 Aug 2012

Wang Peng, Zhao Han, Sun Mei, Li Yuan, Chen Zi-Jiang

Abstract excerpt

The paired box gene 2 (PAX2) has been proven to be a crucial gene during organogenesis of the urogenital system in mice models. This study was aimed to explore the relationship between PAX2 mutations and human Müllerian duct abnormalities (MDA). A total of 192 Chinese MDA patients (15 cases of ut...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to China
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Molecular Sequence Data

Share to Mullerian Ducts

Share to PAX2 Transcription Factor

Share to Point Mutation

Share to Pregnancy

Source

Identifiers

PMID: 22683154
DOI: 10.1016/j.rbmo.2012.04.010

Genes

PAX2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22683154-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis.PMID 22683154Read ↗

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

A novel mutation of HOXA11 in a patient with septate uterus.Semantic proximity Read ↗

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

Management and Molecular Diagnosis of Persistent Müllerian Duct Syndrome in Chinese PatientsSemantic proximity Read ↗

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

Studying Müllerian duct anomalies - from cataloguing phenotypes to discovering causation.Semantic proximity Read ↗

Unraveling the Mysteries of PAX8 in Reproductive Tract CancersSemantic proximity Read ↗

Sequence variant in the CDC42BPB gene is potentially associated with Mullerian duct anomalies.Semantic proximity Read ↗

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

Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.Semantic proximity Read ↗

Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?Semantic proximity Read ↗

Paired-Box Gene 8 (PAX8) and Its Association With Epithelial CarcinomasSemantic proximity Read ↗

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