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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Genomics
Egile Nagusiak: D’Aurora, Marco, Ferlin, Alberto, Di Nicola, Marta, Garolla, Andrea, De Toni, Luca, Franchi, Sara, Palka, Giandomenico, Foresta, Carlo, Stuppia, Liborio, Gatta, Valentina
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2015
Gaiak:
Research Article
Sarrera elektronikoa: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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