WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups | Leukemia
The WT1 Gene – Its Role in Tumourigenesis and Prospects for Immunotherapeutic Advances | In Vivo
DNA Hydroxymethylation Profiling Reveals that WT1 Mutations Result in Loss of TET2 Function in Acute Myeloid Leukemia: Cell Reports
Location of the WT1 gene mutations and their overlap with MRD detection... | Download Scientific Diagram
Frontiers | Oxygen-Dependent Gene Expression in Development and Cancer: Lessons Learned from the Wilms' Tumor Gene, WT1
An integrated genome screen identifies the Wnt signaling pathway as a major target of WT1 | PNAS
Frontiers | Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review
Figure 1 from Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. | Semantic Scholar
A Novel WT1 Gene Mutation Associated with Wilms' Tumor and Congenital Male Genitourinary Malformation | Pediatric Research
WT1: A single gene associated with multiple and severe phenotypes - ScienceDirect
The WT1 Gene – Its Role in Tumourigenesis and Prospects for Immunotherapeutic Advances | In Vivo
Frequency and Clinical Impact of WT1 Mutations in the Context of CEBPA- Mutated Acute Myeloid Leukemia
Frontiers | Wilms' Tumor Protein 1 and Enzymatic Oxidation of 5-Methylcytosine in Brain Tumors: Potential Perspectives
Schematic representation of the WT1 gene and protein structure. All... | Download Scientific Diagram
Wilms tumor 1 mutations in the pathogenesis of acute myeloid leukemia | Haematologica
Acquired WT1 mutations contribute to relapse of NPM1-mutated acute myeloid leukemia following allogeneic hematopoietic stem cell transplant | Bone Marrow Transplantation
Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (WT1) gene | PNAS
Wilms tumor 1 mutations in the pathogenesis of acute myeloid leukemia | Haematologica
Figure 4 from Two molecular subgroups of Wilms' tumors with or without WT1 mutations. | Semantic Scholar
Two Splice Variants of the Wilms' Tumor 1 Gene Have Distinct Functions during Sex Determination and Nephron Formation: Cell
Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report | BMC Nephrology | Full Text
Insights into the physiological role of WT1 from studies of genetically modified mice | Physiological Genomics
JCM | Free Full-Text | The Role of Wilms’ Tumor Gene (WT1) Expression as a Marker of Minimal Residual Disease in Acute Myeloid Leukemia
Isoform-specific and signaling-dependent propagation of acute myeloid leukemia by Wilms tumor 1 - ScienceDirect
Direct sequencing analyses of the WT1 gene. The patient | Open-i
Wilms' Tumor 1 and Dax-1 Modulate the Orphan Nuclear Receptor SF-1 in Sex-Specific Gene Expression: Cell
