Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies-Reference-Cited by-同舟云学术

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Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies

Published:2023-12 Issue:12 Volume:25 Page:100983
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Martino Jeremiah,Liu Qingxue,Vukojevic Katarina,Ke Juntao,Lim Tze Y.,Khan Atlas,Gupta Yask,Perez Alejandra,Yan Zonghai,Milo Rasouly Hila,Vena Natalie,Lippa Natalie,Giordano Jessica L.,Saraga Marijan,Saraga-Babic Mirna,Westland Rik,Bodria Monica,Piaggio Giorgio,Bendapudi Pavan K.,Iglesias Alejandro D.,Wapner Ronald J.,Tasic Velibor,Wang Fan,Ionita-Laza Iuliana,Ghiggeri Gian Marco,Kiryluk Krzysztof,Sampogna Rosemary V.,Mendelsohn Cathy L.,D’Agati Vivette D.,Gharavi Ali G.,Sanna-Cherchi Simone^ORCID

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

American Urological Association

Nierstichting

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference56 articles.

1. Epidemiology of chronic renal failure in children: data from the ItalKid project;Ardissino;Pediatrics,2003

2. State-specific trends in chronic kidney failure—United States, 1990-2001;MMWR Morb Mortal Wkly Rep,2004

3. Renal outcome in patients with congenital anomalies of the kidney and urinary tract;Sanna-Cherchi;Kidney Int,2009

4. Genetic basis of human congenital anomalies of the kidney and urinary tract;Sanna-Cherchi;J Clin Invest,2018

5. Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations;Khan;Kidney Int,2022

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