"Genes, Wilms Tumor" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Genes at loci that are involved in the development of WILMS TUMOR. Included are human WT1 at 11p13 and human WT2 (MTACR1) at 11p15.
| Descriptor ID |
D016162
|
| MeSH Number(s) |
G05.360.340.024.340.375.249.420 G05.360.340.024.340.415.400.420
|
| Concept/Terms |
Genes, Wilms Tumor- Genes, Wilms Tumor
- Tumor Genes, Wilms
- Wilms' Tumor Genes
- Genes, Wilms' Tumor
- Tumor Genes, Wilms'
- Genes, Wilms
- Wilms Genes
- Wilms Tumor Genes
- Genes, Wilms'
- Genes, Wilm
- Genes, Wilm's
- Wilms' Genes
Genes, WT2 Wilms Tumor- Genes, WT2 Wilms Tumor
- MTACR1 Genes
- Gene, MTACR1
- Genes, MTACR1
- MTACR1 Gene
- WT2 Genes, Human
- Gene, Human WT2
- Genes, Human WT2
- Human WT2 Gene
- Human WT2 Genes
- WT2 Gene, Human
- Multiple Tumor-Associated Chromosome Region 1 Genes
- Multiple Tumor Associated Chromosome Region 1 Genes
|
Below are MeSH descriptors whose meaning is more general than "Genes, Wilms Tumor".
Below are MeSH descriptors whose meaning is more specific than "Genes, Wilms Tumor".
This graph shows the total number of publications written about "Genes, Wilms Tumor" by people in this website by year, and whether "Genes, Wilms Tumor" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Wilms Tumor" by people in Profiles.
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The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromes. Pediatr Blood Cancer. 2023 05; 70 Suppl 2:e29984.
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Origins of DNA methylation defects in Wilms tumors. Cancer Lett. 2019 08 10; 457:119-128.
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Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation. J Clin Invest. 2011 Jan; 121(1):174-83.
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Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature. Am J Med Genet A. 2010 Mar; 152A(3):732-6.
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Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome. Pediatr Blood Cancer. 2009 Dec 15; 53(7):1349-51.
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Nephroblastic neoplasms. Clin Lab Med. 2005 Jun; 25(2):341-61, vi-vii.
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A mutant form of the Wilms' tumor suppressor gene WT1 observed in Denys-Drash syndrome interferes with glomerular capillary development. J Am Soc Nephrol. 2002 Aug; 13(8):2058-67.
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Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins. Pediatr Nephrol. 2001 Mar; 16(3):227-31.
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Frequent association of beta-catenin and WT1 mutations in Wilms tumors. Cancer Res. 2000 Nov 15; 60(22):6288-92.
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Familial Wilms' tumor with neural elements: characterization by histology, immunohistochemistry, and genetic analysis. Pediatr Dev Pathol. 2000 Nov-Dec; 3(6):561-7.