Human 45,X fibroblast transcriptome reveals distinct differentially expressed genes including long noncoding RNAs potentially associated with the pathophysiology of Turner syndrome.

Turner syndrome is a chromosomal abnormality characterized by the absence of whole or part of the X chromosome in females. This X aneuploidy condition is associated with a diverse set of clinical phenotypes such as gonadal dysfunction, short stature, osteoporosis and Type II diabetes mellitus, among...

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Autores principales: Shriram N Rajpathak, Shamsudheen Karuthedath Vellarikkal, Ashok Patowary, Vinod Scaria, Sridhar Sivasubbu, Deepti D Deobagkar
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/2603ee93c0ab4638a350e1d2f46aea16
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