Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.
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Inhibition of cellular proliferation by the Wilms tumor suppressor WT1 requires association with the inducible chaperone Hsp70Zinc finger point mutations within the WT1 gene in Wilms tumor patientsEpicardial Epithelial-to-Mesenchymal Transition in Heart Development and DiseaseThe Denys-Drash syndromeTumor-suppressor genes: cardinal factors in inherited predisposition to human cancersRealizing the promise of cancer predisposition genes.Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.A dominant mutation in the Wilms tumor gene WT1 cooperates with the viral oncogene E1A in transformation of primary kidney cells.Oxygen-Dependent Gene Expression in Development and Cancer: Lessons Learned from the Wilms' Tumor Gene, WT1The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans.Fine structure analysis of the WT1 gene in sporadic Wilms tumors.Reprogramming of Sertoli cells to fetal-like Leydig cells by Wt1 ablationWT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences.Genomic changes in the WT-gene (WT1) in Wilms' tumors and their correlation with histologyExpression of the 11p13 Wilms' tumor gene, WT1, correlates with histologic category of Wilms' tumor.Clear cell sarcoma of the kidney expresses insulinlike growth factor-II but not WT1 transcripts.Uniparental disomy occurs infrequently in Wilms tumor patients.Molecular genetic analysis of chromosome 11p in familial Wilms tumour.Towards an understanding of Wilms' tumour.Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor.Copy number variations and cancer.Alternative splicing and genomic structure of the Wilms tumor gene WT1Sequence and structural requirements for high-affinity DNA binding by the WT1 gene product.Wilms Tumor Suppressor, WT1, Cooperates with MicroRNA-26a and MicroRNA-101 to Suppress Translation of the Polycomb Protein, EZH2, in Mesenchymal Stem Cells.Transcriptional Control of Cell Lineage Development in Epicardium-Derived Cells.Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene.Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.Genomic organization of the human WT1 gene.
P2860
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P2860
Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.
description
1991 nî lūn-bûn
@nan
1991 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@ast
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@en
type
label
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@ast
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@en
prefLabel
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@ast
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@en
P2093
P2860
P1476
Evidence for WT1 as a Wilms tu ...... inal deletion in bilateral WT.
@en
P2093
Saunders GF
P2860
P304
P407
P577
1991-05-01T00:00:00Z