Genotype/Phenotype Correlation in Nephrotic Syndrome Caused byWT1Mutations-Reference-Cited by-同舟云学术

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Genotype/Phenotype Correlation in Nephrotic Syndrome Caused byWT1Mutations

Published:2010-07-01 Issue:9 Volume:5 Page:1655-1662
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Chernin Gil,Vega-Warner Virginia,Schoeb Dominik S.,Heeringa Saskia F.,Ovunc Bugsu,Saisawat Pawaree,Cleper Roxana,Ozaltin Fatih,Hildebrandt Friedhelm,

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference34 articles.

1. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

2. Donor splice-site mutations in WT1 are responsible for Frasier syndrome

3. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome

4. Mutations in the Wilms' Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9

5. A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

Cited by 95 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. miRNA-193a-mediated WT1 suppression triggers podocyte injury through activation of the EZH2/β-catenin/NLRP3 pathway in children with diabetic nephropathy;Experimental Cell Research;2024-10

2. A review of the genetic background in complicated WT1-related disorders;Clinical and Experimental Nephrology;2024-07-13

3. Nephrotic Syndrome Throughout Childhood: Diagnosing Podocytopathies From the Womb to the Dorm;Pediatric and Developmental Pathology;2024-05-14

4. WT1-related disorders: more than Denys-Drash syndrome;Pediatric Nephrology;2024-02-07

5. Wilms’ tumor gene 1: lessons from the interface between kidney development and cancer;American Journal of Physiology-Renal Physiology;2024-01-01

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