Therapeutic Potential for CFTR Correctors in Autosomal Recessive Polycystic Kidney Disease-Reference-Cited by-同舟云学术

Therapeutic Potential for CFTR Correctors in Autosomal Recessive Polycystic Kidney Disease

Published:2021 Issue:5 Volume:12 Page:1517-1529
ISSN:2352-345X
Container-title:Cellular and Molecular Gastroenterology and Hepatology
language:en
Short-container-title:Cellular and Molecular Gastroenterology and Hepatology

Author:

Yanda Murali K.,Tomar Vartika,Cebotaru Liudmila^ORCID

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference67 articles.

1. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein;Ward;Nat Genet,2002

2. Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene;Nagasawa;J Am Soc Nephrol,2002

3. Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD);Sweeney;Cell Tissue Res,2006

4. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology;Zerres;Am J Med Genet,1998

5. The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling;Guay-Woodford;Am J Hum Genet,1995

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1. STUB1 exacerbates calcium oxalate-induced kidney injury by modulating reactive oxygen species-mediated cellular autophagy via regulating CFTR ubiquitination;Urolithiasis;2024-04-02

2. CFTR and PC2, partners in the primary cilia in autosomal dominant polycystic kidney disease;American Journal of Physiology-Cell Physiology;2023-09-01

3. Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model;American Journal of Physiology-Gastrointestinal and Liver Physiology;2023-05-01

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