A clinical overview of WT1 gene mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference118 articles.
1. A point mutation found in the WT1 gene in a sporadic Wilms' tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome
2. Homozygous intragenic deletion in the WT1 gene in a sporadic Wilms' tumour associated with high levels of expression of a truncated transcript
3. , , , , (1996) A WT1 antisense oligonucleotide inhibits proliferation and induces apoptosis in lyeloid leukemia cell lines. Oncogene (in press).
4. The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo
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1. Single‐cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of WT1 kidney disease;The Journal of Pathology;2024-08-23
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5. Appropriate Amounts and Activity of the Wilms’ Tumor Suppressor Gene, wt1, Are Required for Normal Pronephros Development of Xenopus Embryos;Journal of Developmental Biology;2022-10-29
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