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

Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS).

Reproduction in domestic animals = Zuchthygiene - 1 Jun 2024

Rozynek Jedrzej, Nowacka-Woszuk Joanna, Stachowiak Monika, Sowinska Natalia, Lukomska Anna, Gruss Michal, Switonski Marek, Szczerbal Izabela

Abstract excerpt

A 1-year-old European shorthair male cat with a normally developed penis was subjected to genetic, endocrinological and histological studies due to unilateral cryptorchidism. The blood testosterone level was typical for males, while the level of anti-Mullerian hormone (AMH) was very low. Surgical removal of internal reproductive organs was followed by a histological study, which revealed inactive testicles with...

Read the complete abstract on PubMed

Topics

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

Share to Anti-Mullerian Hormone
Share to Cat Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cryptorchidism

Share to Disorder of Sex Development, 46,XY

Share to Mutation, Missense

Share to Receptors, Peptide

Share to Receptors, Transforming Growth Factor beta

Source

Identifiers

PMID: 38837470
DOI: 10.1111/rda.14635

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS).PMID 38837470Read ↗

Persistent Mullerian duct syndrome in dogs – a new insight into organization of <i>AMH</i> and <i>AMHR2</i> genesSemantic proximity Read ↗

Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome.Semantic proximity Read ↗

Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Müllerian duct syndrome.Semantic proximity Read ↗

A novel mutation of AMHR2 in two brothers with persistent Müllerian duct syndrome and their intracytoplasmic sperm injection outcome.Semantic proximity Read ↗

AMH gene mutations in two Egyptian families with persistent müllerian duct syndrome.Semantic proximity Read ↗

The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.Semantic proximity Read ↗

A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct SyndromeSemantic proximity Read ↗

A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome.Semantic proximity Read ↗

AMH and AMHR2 Involvement in Congenital Disorders of Sex DevelopmentSemantic proximity Read ↗

Persistent Müllerian duct syndrome: an update.Semantic proximity Read ↗

Identification of AMH and AMHR2 Variants Led to the Diagnosis of Persistent Müllerian Duct Syndrome in Three Cases.Semantic proximity Read ↗

Persistent Mï¿½llerian duct syndrome: A case report and reviewSemantic proximity Read ↗

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