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

TTY2 genes deletions as genetic risk factor of male infertility.

Cellular and molecular biology (Noisy-le-Grand, France) - 28 Feb 2017

Shaveisi-Zadeh F, Alibakhshi R, Asgari R, Rostami-Far Z, Bakhtiari M, Abdi H, Movafagh A, Mirfakhraie R

Abstract excerpt

Y chromosome has a number of genes that are expressed in testis and have a role in spermatogenesis. TTY2L12A and TTY2L2A are the members of testis transcript Y2 (TTY2) that are Y linked multi-copy gene families, located on Yp11 and Yq11 loci respectively. The aim of this study was to investigate frequency of TTY2L12A and TTY2L2A deletions in azoospermic patients compared with fertile males. This study was...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Y

Share to Gene Deletion

Share to Infertility, Male

Share to Seminal Plasma Proteins

Share to Young Adult

Source

Identifiers

PMID: 28364784
DOI: 10.14715/cmb/2017.63.2.8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

TTY2 genes deletions as genetic risk factor of male infertility.PMID 28364784Read ↗

High frequency of TTTY2-like gene-related deletions in patients with idiopathic oligozoospermia and azoospermia.Semantic proximity Read ↗

Microdeletions and vertical transmission of the Y-chromosome azoospermia factor regionSemantic proximity Read ↗

Association of G/T(rs222859) polymorphism in Exon 1 of YBX2 gene with azoospermia, among Iranian infertile males.Semantic proximity Read ↗

Genetic Risk of Azoospermia Factor (AZF) Microdeletions in Idiopathic Cases of Azoospermia and Oligozoospermia in Central Indian PopulationSemantic proximity Read ↗

Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogram.Semantic proximity Read ↗

Genetics of the human Y chromosome and its association with male infertilitySemantic proximity Read ↗

Cellular and Molecular Genetic Analysis of 1980 Male Infertility PatientsSemantic proximity Read ↗

Population variation in Y-chromosome microdeletion and its role in the evaluation of male infertility management: a systematic reviewSemantic proximity Read ↗

Y-chromosome microdeletions in nonobstructive azoospermia and severe oligozoospermiaSemantic proximity Read ↗

The sperm quality and clinical outcomes were not affected by sY152 deletion in Y chromosome for oligozoospermia or azoospermia men after ICSI treatment.Semantic proximity Read ↗

Prevalence of Y Chromosome Microdeletion Among Mongolian Infertile Men With Azoospermia and Severe OligozoospermiaSemantic proximity Read ↗

Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centreSemantic proximity Read ↗

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