Deregulation of sertoli and leydig cells function in patients with klinefelter syndrome as evidenced by testis transcriptome analysis

BACKGROUND: Klinefelter Syndrome (KS) is the most common abnormality of sex chromosomes (47,XXY) and represents the first genetic cause of male infertility. Mechanisms leading to KS testis degeneration are still not completely defined but considered to be mainly the result of germ cells loss. In ord...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:BMC Genomics
Prif Awduron: D’Aurora, Marco, Ferlin, Alberto, Di Nicola, Marta, Garolla, Andrea, De Toni, Luca, Franchi, Sara, Palka, Giandomenico, Foresta, Carlo, Stuppia, Liborio, Gatta, Valentina
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2015
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4362638/
https://ncbi.nlm.nih.gov/pubmed/25879484
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1356-0
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