Found: 24
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Universal Nephroblastomatosis with Bilateral Hyperplastic Nephromegaly in Siblings.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 1, p. 47, doi. 10.2350/07-11-0380.1
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- Publication type:
- Article
Familial Wilms' Tumor with Neural Elements: Characterization by Histology, Immunohistochemistry, and Genetic Analysis.
- Published in:
- Pediatric & Developmental Pathology, 2000, v. 3, n. 6, p. 561, doi. 10.1007/s100240010106
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- Publication type:
- Article
RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology.
- Published in:
- JNCI: Journal of the National Cancer Institute, 1992, v. 84, n. 3, p. 181
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- Publication type:
- Article
Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation.
- Published in:
- 2011
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- Publication type:
- journal article
Wilms tumor 1 (WT1) regulates KRAS-driven oncogenesis and senescence in mouse and human models.
- Published in:
- 2010
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- Publication type:
- journal article
Left-sided cryptorchidism in mice with Wilms' tumour 1 gene deletion in gubernaculum testis.
- Published in:
- Journal of Pathology, 2013, v. 230, n. 1, p. 39, doi. 10.1002/path.4161
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- Publication type:
- Article
Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study.
- Published in:
- Journal of Pathology, 2012, v. 228, n. 1, p. 119, doi. 10.1002/path.4010
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- Publication type:
- Article
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43730-0
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- Publication type:
- Article
Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13.
- Published in:
- Nature, 1988, v. 336, n. 6197, p. 377, doi. 10.1038/336377a0
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- Publication type:
- Article
Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors.
- Published in:
- Oncogene, 2003, v. 22, n. 24, p. 3821, doi. 10.1038/sj.onc.1206597
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- Publication type:
- Article
Wilm's tumor 1 promotes memory flexibility.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11781-x
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- Publication type:
- Article
Absence of PPP2R1A mutations in Wilms tumor.
- Published in:
- Oncogene, 2001, v. 20, n. 16, p. 2050, doi. 10.1038/sj.onc.1204301
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- Publication type:
- Article
Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma.
- Published in:
- Oncogene, 1999, v. 18, n. 50, p. 7063, doi. 10.1038/sj.onc.1203192
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- Publication type:
- Article
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.
- Published in:
- Nature Communications, 2015, v. 6, n. 12, p. 10013, doi. 10.1038/ncomms10013
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- Publication type:
- Article
Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 3, p. 227, doi. 10.1007/s004670000537
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- Publication type:
- Article
Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 2, p. 333, doi. 10.1093/hmg/ddt423
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- Publication type:
- Article
Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 6, p. 461, doi. 10.1002/gcc.20553
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- Publication type:
- Article
Genome-wide loss of heterozygosity analysis of WT1wild-type and WT1-mutant Wilms tumors.
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 43, n. 2, p. 172
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- Publication type:
- Article
Children's Oncology Group's 2013 blueprint for research: Renal tumors.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 6, p. 994, doi. 10.1002/pbc.24419
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- Publication type:
- Article
Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome.
- Published in:
- Pediatric Blood & Cancer, 2009, v. 53, n. 7, p. 1349, doi. 10.1002/pbc.22152
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- Publication type:
- Article
A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208936
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- Publication type:
- Article
Mutation in the PAX6 gene in twenty patients with aniridia.
- Published in:
- Human Mutation, 2000, v. 15, n. 4, p. 332, doi. 10.1002/(SICI)1098-1004(200004)15:4<332::AID-HUMU5>3.0.CO;2-1
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- Publication type:
- Article
Wilms' tumours: about tumour suppressor genes, an oncogene and a chameleon gene.
- Published in:
- 2011
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- Publication type:
- journal article
Monitoring Therapy with MEK Inhibitor U0126 in a Novel Wilms Tumor Model in Wt1 Knockout Igf2 Transgenic Mice Using F-FDG PET with Dual-Contrast Enhanced CT and MRI: Early Metabolic Response Without Inhibition of Tumor Growth.
- Published in:
- Molecular Imaging & Biology, 2013, v. 15, n. 2, p. 175, doi. 10.1007/s11307-012-0588-5
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- Publication type:
- Article