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

Diagnostic genetic screening for assisted reproductive technologies patients with macrozoospermia

10 Feb 2017

Abstract excerpt

Macrozoospermia is characterized by a high proportion of abnormal spermatozoa with enlarged heads. So far, it has been associated with mutations only in the Aurora Kinase C gene (AURKC) in some cases. Although many publications have reported failure to conceive in couples with macrozoospermia, a few others have described successful pregnancies, thus raising questions as to whether ICSI and AURKC genetic screening...

Read the complete abstract on PubMed

Topics

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

Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Reproductive Health and Technologies
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 28187507
DOI: 10.1111/andr.12311

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Diagnostic genetic screening for assisted reproductive technologies patients with macrozoospermiaPMID 28187507Read ↗

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermiaSemantic proximity Read ↗

Two frequent loss-of-function mutations in Aurora Kinase C gene in Algerian infertile men with macrozoospermia.Semantic proximity Read ↗

Successful intracytoplasmic sperm injection in a macrozoospermia case with novel compound heterozygous aurora kinase C (AURKC) mutations.Semantic proximity Read ↗

Compound heterozygosity for novel AURKC mutations in an infertile man with macrozoospermia.Semantic proximity Read ↗

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.Semantic proximity Read ↗

Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermiaSemantic proximity Read ↗

Genetic aspects of monomorphic teratozoospermia: a review.Semantic proximity Read ↗

Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men.Semantic proximity Read ↗

Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.Semantic proximity Read ↗

Sperm macrocephaly syndrome in a patient without AURKC mutations and with a history of recurrent miscarriage.Semantic proximity Read ↗

Characterization of macrozoospermia-associated AURKC mutations in a mammalian meiotic system.Semantic proximity Read ↗

Teratozoospermia: spotlight on the main genetic actors in the human.Semantic proximity Read ↗

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