about
The regions of the retinoblastoma protein needed for binding to adenovirus E1A or SV40 large T antigen are common sites for mutationsTwo distinct and frequently mutated regions of retinoblastoma protein are required for binding to SV40 T antigenPurification, biochemical characterization, and biological function of human esterase DCloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13Molecular cloning of the human esterase D gene, a genetic marker of retinoblastomaThe ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.Constitutional ring chromosomes and tumour suppressor genes.Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningiomaConstruction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.Interstitial deletion of distal 13q associated with Hirschsprung's diseaseApplication 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 Y7913q-/r(13) mosaicismFamily studies on the chromosomal location of the retinoblastoma gene (Rb-1).Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.Abnormalities in structure and expression of the human retinoblastoma gene in SCLC.Trilateral retinoblastoma in transgenic miceRetinoblastoma and partial deletion of the long arm of chromosome 13Role of the retinoblastoma gene in the initiation and progression of human cancerExpression of the functional cone phototransduction cascade in retinoblastomaRestriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumorsPharmacokinetics and molecular detoxicationThe incidence and epidemiology of retinoblastoma in New Zealand: A 30-year surveyLoss of the retinoblastoma susceptibility gene (RB1) is a frequent and early event in prostatic tumorigenesis.Abnormal chromosome repair and risk of developing cancer.Oncogenes and tumor-suppressor genes.The diagnosis of retinoblastomaIsolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2AFamilial retinoblastoma: segregation of chromosome 13 in four families.Eight closely linked loci place the Wilson disease locus within 13q14-q21.Chromosomal aberrations and schizophrenia. Autosomes.An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom.Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind studyStructural alterations of the RB1 gene in human soft tissue tumours.The location and appearance of second malignancies in patients with bilateral retinoblastoma.Isolation and characterisation of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridisationMolecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus.Multivariate analyses of DNA index, p62c-myc, and clinicopathological status of patients with ovarian cancer.
P2860
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P2860
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh-hant
name
Retinoblastoma and subband deletion of chromosome 13.
@en
Retinoblastoma and subband deletion of chromosome 13.
@nl
type
label
Retinoblastoma and subband deletion of chromosome 13.
@en
Retinoblastoma and subband deletion of chromosome 13.
@nl
prefLabel
Retinoblastoma and subband deletion of chromosome 13.
@en
Retinoblastoma and subband deletion of chromosome 13.
@nl
P1476
Retinoblastoma and subband deletion of chromosome 13.
@en
P2093
P304
P577
1978-02-01T00:00:00Z