• 11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood
• A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region
• A Synopsis of Pediatric Patients With Hepatoblastoma and Wilms Tumor: NSQIP-P 2012-2016
• A Very Long-Acting PARP Inhibitor Suppresses Cancer Cell Growth in DNA Repair-Deficient Tumor Models
• Absence of the TRIP13 c.1060C>T Mutation in Wilms Tumor Patients From Pakistan
• Absence of the TRIP13 c.1060C>T Mutation in Wilms Tumor Patients From Pakistan
• Activation of Hippo Pathway Damages Slit Diaphragm by Deprivation of Ajuba Proteins
• AGORA, a data- and biobank for birth defects and childhood cancer
• An eHealth decision-support tool to prioritize referral practices for genetic evaluation of patients with Wilms tumor
• Analysis of renal lesions in Chinese tuberous sclerosis complex patients with different types of TSC gene mutations
• Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening
• Cafeteria diet induces global and <em>Slc27a3</em>-specific hypomethylation in male Wistar rats
• Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart Association
• Case Report: 2-Year-old With Wilms Tumors, Familial Heterozygous DIS3L2 Mutation, and Cutis Marmorata Telangiectatica Congenita
• Case Report: Two clinical cases of Wilms tumor comorbid to gingival fibromatosis in young children with constitutionally mutated <em>REST</em>
• Case Report: Two clinical cases of Wilms tumor comorbid to gingival fibromatosis in young children with constitutionally mutated REST
• Clinical, Histological, Cytogenetic and Molecular Analysis of Monozygous Twins with Wilms Tumor
• Cost of Treating Pediatric Cancer at the Butaro Cancer Center of Excellence in Rwanda
• Cutaneous metastasis in a case of Wilm's tumor diagnosed on cytology - A rare case report
• Cytotoxic and Antiproliferative Effects of Diarylheptanoids Isolated from <em>Curcuma comosa</em> Rhizomes on Leukaemic Cells
• Cytotoxicity and inhibition of leukemic cell proliferation by sesquiterpenes from rhizomes of Mah-Lueang (Curcuma cf. viridiflora Roxb.)
• Danish Population Based Study of Familial Epilepsy and Childhood Cancer
• Description of mutation spectrum and polymorphism of Wilms' tumor 1 (WT1) gene in hypospadias patients in the Indonesian population
• Detection of TET2 Mutation in Patients with De Novo Acute Myeloid Leukemia: A Mutation Analysis of 51 Iranian Patients
• Development and Validation of a Prediction Model for Kidney Failure in Long-Term Survivors of Childhood Cancer
• DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis
• Diagnosis, clustering, and immune cell infiltration analysis of m6A-related genes in patients with acute myocardial infarction-a bioinformatics analysis
• Environmental exposures related to parental habits in the perinatal period and the risk of Wilms' tumor in children
• Exceptional Response to Cabozantinib in a Patient With Multiply Relapsed Wilms Tumor
• Exonic WT1 pathogenic variants in 46,XY DSD associated with gonadoblastoma
• Factors associated with the latency to diagnosis of childhood cancer in Peru
• Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature
• Flow Cytometry Immunophenotyping for Diagnostic Orientation and Classification of Pediatric Cancer Based on the EuroFlow Solid Tumor Orientation Tube (STOT)
• Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study
• Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches
• Genetic mutational testing of Chinese children with familial hematuria with biopsy-proven FSGS
• Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS
• Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
• Germline variants discovered in lymphoma patients undergoing tumor profiling: a case series
• Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism
• Human Pluripotent Stem Cell-Derived Kidney Model for Nephrotoxicity Studies
• Human umbilical cord mesenchymal stem cells deliver exogenous miR-26a-5p via exosomes to inhibit nucleus pulposus cell pyroptosis through METTL14/NLRP3
• Identification of key genes and validation of key gene aquaporin 1 on Wilms' tumor metastasis
• IGF2BP3 is an essential N⁶-methyladenosine biotarget for suppressing ferroptosis in lung adenocarcinoma cells
• Immune responses against tumour-associated antigen-derived cytotoxic T lymphocyte epitopes in cholangiocarcinoma patients
• Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH
• Incidence and management of pleural effusions in patients with Wilms tumor: A Pediatric Surgical Oncology Research Collaborative study
• ING2-WTAP is a potential therapeutic target in non-small cell lung cancer
• Is there a socioeconomic variation in survival from renal tumours in children and young people resident in northern England (1968-2012)?
• Kidney disease in very long-term survivors of Wilms tumor: A nationwide cohort study with sibling controls
• Late Health Outcomes Among Survivors of Wilms Tumor Diagnosed Over Three Decades: A Report From the Childhood Cancer Survivor Study
• Left atrial metastasis of a Wilms' tumor: A rare occurrence
• Loss of Wilms tumor 1 protein is a marker for apoptosis in response to replicative stress in leukemic cells
• MAPK13 stabilization via m⁶A mRNA modification limits anti-cancer efficacy of rapamycin
• MAPK13 stabilization via m⁶A mRNA modification limits anticancer efficacy of rapamycin
• Maternal and perinatal characteristics, congenital malformations and the risk of wilms tumor: the ESTELLE study
• Maternal lifestyle characteristics and Wilms tumor risk in the offspring: A systematic review and meta-analysis
• Metachronous Wilms Tumor, Glioblastoma, and T-cell Leukemia in an Child With Constitutional Mismatch Repair Deficiency syndrome due to Novel Mutation in MSH6 (c.2590G&gt;T)
• Metachronous Wilms Tumor, Glioblastoma, and T-cell Leukemia in an Child With Constitutional Mismatch Repair Deficiency syndrome due to Novel Mutation in MSH6 (c.2590G>T)
• MicroRNA expression patterns and signalling pathways in the development and progression of childhood solid tumours
• MiT family translocation-associated renal cell carcinoma: A report of two cases in children
• Molecular diagnostics of disorders of sexual development: an Indian survey and systems biology perspective
• Molecular mechanism of Wilms tumour 1-associated protein in diabetes-related dry eye disease by mediating m6A methylation modification of lncRNA NEAT1
• mTORC1 promotes cell growth via m⁶A-dependent mRNA degradation
• Multiple and hereditary renal tumors: a review for radiologists
• MYCN gene polymorphisms and Wilms tumor susceptibility in Chinese children
• New insights into the genetic etiology of Alzheimer's disease and related dementias
• New roles of N6-methyladenosine methylation system regulating the occurrence of non-alcoholic fatty liver disease with N6-methyladenosine-modified MYC
• Novel combined variants of WT1 and TET2 in a refractory and recurrent AML patient
• Novel Intragenic <em>PAX6</em> Deletion in a Pedigree with Aniridia, Morbid Obesity, and Diabetes
• Novel WTX nonsense mutation in a family diagnosed with osteopathia striata with cranial sclerosis: Case report
• Ovarian microcystic stromal tumour: from morphological observations to syndromic associations
• Psychological, educational, and social late effects in adolescent survivors of Wilms tumor: A report from the Childhood Cancer Survivor Study
• Regulation of HtrA2 on WT1 gene expression under imatinib stimulation and its effects on the cell biology of K562 cells
• Relapse of Wilms' tumour and detection methods: a retrospective analysis of the 2001 Renal Tumour Study Group-International Society of Paediatric Oncology Wilms' tumour protocol database
• Renal cell carcinoma in children and adolescents: a retrospective study of a French-Italian series of 93 cases
• Risk of digestive cancers in a cohort of 69 460 five-year survivors of childhood cancer in Europe: the PanCareSurFup study
• Risk of selected childhood cancers and parental employment in painting and printing industries: A register-based case‒control study in Denmark 1968-2015
• Risk of Urological Cancer Among Boys and Men Born with Hypospadias: A Swedish Population-based Study
• RNA methylation machinery and m⁶A target genes as circulating biomarkers of ulcerative colitis and Crohn's disease: Correlation with disease activity, location, and inflammatory cytokines
• Role of m6A RNA methylation in cardiovascular disease (Review)
• Secondary renal neoplasia following chemotherapy or radiation in pediatric patients
• Severe Hepatopathy in National Wilms Tumor Studies 3-5: Prevalence, Clinical Features, and Outcomes After Reintroduction of Chemotherapy
• Social adjustment in adolescent survivors of pediatric central nervous system tumors: A report from the Childhood Cancer Survivor Study
• Sonographic Image of Solitary Kidney in Wilms Tumour Survivors
• TEAD4 is a master regulator of high-risk nasopharyngeal carcinoma
• The COVID-19 pandemic: A rapid global response for children with cancer from SIOP, COG, SIOP-E, SIOP-PODC, IPSO, PROS, CCI, and St Jude Global
• The genetics of aniridia - simple things become complicated
• The pain of survival: Prevalence, patterns, and predictors of pain in survivors of childhood cancer
• The role of N⁶-methyladenosine RNA methylation in the heat stress response of sheep (Ovis aries)
• Toward a methodology for evaluating DNA variants in nuclear families
• Treatment abandonment in children with Wilms tumor at a national referral hospital in Uganda
• TRIM28 inactivation in epithelial nephroblastoma is frequent and often associated with predisposing TRIM28 germline variants
• Using Crowdfunding Campaigns to Examine Financial Toxicity and Logistical Burdens Facing Families of Children With Wilms Tumor
• Wilms Tumor (Nephroblastoma), Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
• Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome
• WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review
• WT1 facilitates the self-renewal of leukemia-initiating cells through the upregulation of BCL2L2: WT1-BCL2L2 axis as a new acute myeloid leukemia therapy target
• WTIP interacts with BRCA2 and is essential for BRCA2 centrosome localization in cervical cancer cell
• Yes-associated protein regulates podocyte cell cycle re-entry and dedifferentiation in adriamycin-induced nephropathy