Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
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Two distinct and frequently mutated regions of retinoblastoma protein are required for binding to SV40 T antigenSite-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemiaLocalization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.Zinc finger-mediated protein interactions modulate Ikaros activity, a molecular control of lymphocyte developmentOverview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencingCoordinated regulation of intestinal functions in C. elegans by LIN-35/Rb and SLR-2A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancersThe ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.Drosophila as a model system for molecular analysis of tumorigenesis.The retinoblastoma tumor-suppressor gene, the exception that proves the ruleHuman retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutantsApplication of linkage analysis to genetic counselling in families with hereditary retinoblastoma.Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.Molecular mechanism of retinoblastoma gene inactivation in retinoblastoma cell line Y79Three histopathological types of retinoblastoma and their relation to heredity and age of enucleation.A catalog of genes homozygously deleted in human lung cancer and the candidacy of PTPRD as a tumor suppressor gene.Discovering tumor suppressor genes through genome-wide copy number analysis.Trilateral retinoblastoma in transgenic miceMapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.An immunopathologic study of retinoblastoma protein.Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region.The p53 tumour suppressor protein.Role of the retinoblastoma gene in the initiation and progression of human cancerShort, direct repeats at the breakpoints of deletions of the retinoblastoma gene.Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein.Differential occurrence of mutations causative of eye diseases in the Chinese population.Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.Retinoblastoma gene structure and product expression in human gastric carcinomas.Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas.Targeting Rb inactivation in cancers by synthetic lethality.Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencingSomatic mosaicism in a patient with bilateral retinoblastoma.Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.Cervical cancer: is herpes simplex virus type II a cofactor?Genome-wide search for loss of heterozygosity in transgenic mouse tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16.How do retinoblastoma tumours form?Molecular genetics in the pathology and diagnosis of retinoblastoma.Mouse mammary tumor virus/v-Ha-ras transgene-induced mammary tumors exhibit strain-specific allelic loss on mouse chromosome 4Control of junB and extracellular matrix protein expression by transforming growth factor-beta 1 is independent of simian virus 40 T antigen-sensitive growth-sensitive growth-inhibitory eventsInfrequent genomic rearrangement and normal expression of the putative RB1 gene in retinoblastoma tumors.
P2860
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P2860
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 1986
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@en
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@nl
type
label
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@en
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@nl
prefLabel
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@en
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@nl
P2093
P2860
P356
P1476
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
@en
P2093
J M Rapaport
R A Petersen
P2860
P304
P356
10.1073/PNAS.83.19.7391
P407
P577
1986-10-01T00:00:00Z