Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
about
Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney developmentMutation of the PAX6 gene in patients with autosomal dominant keratitisPaired box mutations in familial and sporadic aniridia predicts truncated aniridia proteinsAnalysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypesRecessive mechanisms of malignancy.Constitutional ring chromosomes and tumour suppressor genes.Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancersGenes and cancerUmbilical cord blood transplantation.The French Wilms' tumour study: no clear evidence for cancer prone families.Microdeletion syndromes, balanced translocations, and gene mappingA FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locusChildhood cancer risk in those with chromosomal and non-chromosomal congenital anomalies in Washington State: 1984-2013Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clonesIdentification of a provirally activated c-Ha-ras oncogene in an avian nephroblastoma via a novel procedure: cDNA cloning of a chimaeric viral-host transcript.The new biomedical technology.Aniridia and mental retardation with deletion of the short arm of chromosome 11.HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumorsA deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization.Wilms's tumour and aniridia: clinical and cytogenetic featuresFine structure analysis of the WT1 gene in sporadic Wilms tumors.Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.Parental origin of de novo constitutional deletions of chromosomal band 11p13Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor.c-Ha-ras-1 oncogene lies between beta-globin and insulin loci on human chromosome 11pThe E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor.Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2ACongenital anomalies and childhood cancer in Great Britain.The use of subchromosome-length unique band sequences in the analysis of prophase chromosomes.Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.The Wilms tumor suppressor WT1 regulates early gonad development by activation of Sf1.Presence of the long chain form of polysialic acid of the neural cell adhesion molecule in Wilms' tumor. Identification of a cell adhesion molecule as an oncodevelopmental antigen and implications for tumor histogenesis.Blastemal cells of nephroblastomatosis complex share an onco-developmental antigen with embryonic kidney and Wilms' tumor. An immunohistochemical study on polysialic acid distributionA probable case of the homozygous condition of the aniridia gene.Expression of the 11p13 Wilms' tumor gene, WT1, correlates with histologic category of Wilms' tumor.Wilms' tumor protein Wt1 is an activator of the anti-Müllerian hormone receptor gene Amhr2.
P2860
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P2860
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年論文
@yue
1978年論文
@zh-hant
1978年論文
@zh-hk
1978年論文
@zh-mo
1978年論文
@zh-tw
1978年论文
@wuu
1978年论文
@zh
1978年论文
@zh-cn
name
Chromosomal imbalance in the A ...... on: 11p interstitial deletion.
@en
type
label
Chromosomal imbalance in the A ...... on: 11p interstitial deletion.
@en
prefLabel
Chromosomal imbalance in the A ...... on: 11p interstitial deletion.
@en
P2093
P1433
P1476
Chromosomal imbalance in the A ...... on: 11p interstitial deletion.
@en
P2093
P304
P407
P577
1978-04-01T00:00:00Z