A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling-Reference-Cited by-同舟云学术

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling

Published:2017-04-05 Issue:8 Volume:28 Page:2364-2376
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Vivante Asaf,Mann Nina,Yonath Hagith,Weiss Anna-Carina,Getwan Maike,Kaminski Michael M.,Bohnenpoll Tobias,Teyssier Catherine,Chen Jing,Shril Shirlee,van der Ven Amelie T.,Ityel Hadas,Schmidt Johanna Magdalena,Widmeier Eugen,Bauer Stuart B.,Sanna-Cherchi Simone,Gharavi Ali G.,Lu Weining,Magen Daniella,Shukrun Rachel,Lifton Richard P.,Tasic Velibor,Stanescu Horia C.,Cavaillès Vincent,Kleta Robert,Anikster Yair,Dekel Benjamin,Kispert Andreas,Lienkamp Soeren S.,Hildebrandt Friedhelm

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

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5. Congenital anomalies of the kidney and urinary tract genetics in mice and men

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