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

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

11 Sept 2024

Abstract excerpt

BACKGROUND: Bi-allelic variants in DNAH11 have been identified as causative factors in Primary Ciliary Dyskinesia, leading to abnormal respiratory cilia. Nonetheless, the specific impact of these variants on human sperm flagellar and their involvement in male infertility remain largely unknown. METHODS: A collaborative effort involving two Chinese reproductive centers conducted a study with 975 unrelated...

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis Research Advances
Share to Genetic and Kidney Cyst Diseases
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 39256880
DOI: 10.1186/s40246-024-00658-w

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

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertilityPMID 39256880Read ↗

Association of novel DNAH11 and DNAH 5 variants with oligoasthenoteratozoospermia lead to male infertilitySemantic proximity Read ↗

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

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

Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomesSemantic proximity Read ↗

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

Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and miceSemantic proximity Read ↗

Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure.Semantic proximity Read ↗

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variantsSemantic proximity Read ↗

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

Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella 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 ↗

Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.Semantic proximity Read ↗

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