Inactivation of Bardet-Biedl syndrome genes causes kidney defects

Bardet-Biedl syndrome (BBS) is a rare hereditary autosomal recessive disease associated with several features including obesity, hypertension, and renal abnormalities. The underlying mechanisms of renal defects associated with BBS remain poorly defined. We examined the histological, molecular, and f...

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Detaylı Bibliyografya
Asıl Yazarlar: Guo, Deng-Fu, Beyer, Andreas M., Yang, Baoli, Nishimura, Darryl Y., Sheffield, Val C., Rahmouni, Kamal
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Physiological Society 2011
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3043995/
https://ncbi.nlm.nih.gov/pubmed/21106857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00150.2010
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