Associated Papers
Clonal architecture of FLT3-ITD and acquired 13q uniparental disomy define prognostic heterogeneity and therapeutic vulnerabilities in acute myeloid leukemia.
Lai A et al.
Neoplasia (new York, N.y.), 2025
41411742 (PubMed )
Supplement: mmc2.xlsx › Sheet1
Potential involvement of abnormal splicing in severe WT1-related disorders.
Nagano C et al.
Clinical and Experimental Nephrology, 2025
Impact of myelodysplasia-related gene mutations and residual mutations at remission in venetoclax/azacitidine for AML.
Ikoma Y et al.
Leukemia, 2025
40259101 (PubMed )
Supplement: 41375_2025_2625_MOESM2_ESM.xlsx › Sheet5
Nuclear Phase Separation Drives NPM1-mutant Acute Myeloid Leukemia.
Datar GK et al.
Biorxiv : the Preprint Server for Biology, 2025
40501735 (PubMed )
Supplement: NIHPP2025.05.23.655671v1-supplement-1.pdf
Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children.
Glénisson M et al.
Kidney International Reports, 2025
40303223 (PubMed )
Supplement: mmc1.pdf
Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant.
Nguyen TTT et al.
Frontiers in Pediatrics, 2025
Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset Phenotypes.
van Peer SE et al.
Kidney International Reports, 2024
Association of Atypical Hemolytic Uremic Syndrome With Wilms' Tumor 1 Gene Mutations: A Case Series and Literature Review.
Al Zabali S et al.
Cureus, 2024
High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Smith C et al.
Kidney International Reports, 2023
37850022 (PubMed )
Supplement: mmc1.pdf
Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children.
Chen H et al.
Frontiers in Pediatrics, 2023
Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children.
Bezdicka M et al.
Scientific Reports, 2022
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
34386660 (PubMed )
Supplement: mmc1.pdf
Case Report: Denys-Drash Syndrome With WT1 Causative Variant Presenting as Atypical Hemolytic Uremic Syndrome.
Cheng C et al.
Frontiers in Pediatrics, 2020
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