Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations
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Title
Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations
Authors
Keywords
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Journal
Cancers
Volume 13, Issue 1, Pages 60
Publisher
MDPI AG
Online
2020-12-28
DOI
10.3390/cancers13010060
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Related references
Note: Only part of the references are listed.- WT1-Mutant Wilms Tumor Progression Is Associated With Diverting Clonal Mutations of CTNNB1
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- Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15
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- Senescence Process in Primary Wilms' Tumor Cell Culture Induced by p53 Independent p21 Expression
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- Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm
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- Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation
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- Fast and accurate short read alignment with Burrows-Wheeler transform
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- Clinical relevance of mutations in the Wilms tumor suppressor 1 geneWT1and the cadherin-associated protein β1 geneCTNNB1for patients with Wilms tumors
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