Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion-Reference-Cited by-同舟云学术

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Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

Published:1993 Issue:3 Volume:2 Page:259-264
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Little Melissa H.,Williamson Kathleen A.,Mannens Marcel,Kelsey Anna,Gosden Christine,Hastie Nicholas D.,Heyningen Veronica van

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/2/3/259/1946978/2-3-259.pdf

Cited by 145 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. Single‐cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of WT1 kidney disease;The Journal of Pathology;2024-08-23

2. The View of Pediatric Nephrotic Syndrome as a Podocytopathy;Kidney and Dialysis;2023-12-12

3. WT1 regulates expression of DNA repair gene Neil3 during nephrogenesis;American Journal of Physiology-Renal Physiology;2023-03-01

4. A Journey Through Genetics to Biology;Annual Review of Genomics and Human Genetics;2022-08-31

5. WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review;Pediatric Nephrology;2022-02-24

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