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Article

Sequence alterations in the YBX2 gene are associated with male factor infertility.

Fertility and sterility - 1 Apr 2009

Hammoud Sue, Emery Benjamin R, Dunn Diane, Weiss Robert B, Carrell Douglas T

Abstract excerpt

OBJECTIVE: To investigate YBX2 gene alterations in men with severe defects in spermatogenesis, including azoospermia or severe oligozoospermia, and protamine deregulation. MSY2 has been identified as a central component in the regulation of spermatogenesis in mice, but the potential role of its human orthologue, YBX2 or "Contrin," in human infertility is not known. DESIGN: A prospective cohort study. SETTING:...

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Source

Identifiers

PMID: 18339382
DOI: 10.1016/j.fertnstert.2008.01.009

Genes

YBX2

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.

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Sequence alterations in the YBX2 gene are associated with male factor infertility.PMID 18339382Read ↗

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