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

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice

1 Jan 2024

Abstract excerpt

Abstract STUDY QUESTION Are there other pathogenic genes for asthenoteratozoospermia (AT)? SUMMARY ANSWER DNAH3 is a novel candidate gene for AT in humans and mice. WHAT IS KNOWN ALREADY AT is a major cause of male infertility. Several genes underlying AT have been reported; however, the genetic aetiology remains unknown in a majority of affected men. STUDY DESIGN, SIZE, DURATION A total of 432 patients with AT...

Read the complete abstract on PubMed

Topics

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

Share to Hereditary Neurological Disorders
Share to Neurological diseases and metabolism
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38312775
DOI: 10.1093/hropen/hoae003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and micePMID 38312775Read ↗

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia.Semantic proximity Read ↗

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.Semantic proximity Read ↗

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and miceSemantic proximity Read ↗

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.Semantic proximity Read ↗

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.Semantic proximity Read ↗

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility.Semantic proximity Read ↗

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and MiceSemantic proximity Read ↗

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertilitySemantic proximity Read ↗

Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility.Semantic proximity Read ↗

A DNAH17 missense variant causes flagella destabilization and asthenozoospermia.Semantic proximity Read ↗

Novel Variants in DNAH9 Lead to Nonsyndromic Severe AsthenozoospermiaSemantic proximity Read ↗

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagellaSemantic proximity Read ↗

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