Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants
about
Cloning and sequence of the human adrenodoxin reductase geneLoss of heterozygosity at 13q14 and 13q21 in high grade, high stage prostate cancerThe ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.Molecular mechanisms of cancer.Isolation of DNA sequences deleted in lung cancer by genomic difference cloning.Molecular mechanism of retinoblastoma gene inactivation in retinoblastoma cell line Y79Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.Structure of the human retinoblastoma gene.Cloning and chromosomal localization of the gene coding for human protein kinase CK1.Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling.Molecular etiology of low-penetrance retinoblastoma in two pedigrees.Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencingExclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer.Malignant tumors during the first 2 decades of life in the offspring of atomic bomb survivorsSomatic mosaicism in a patient with bilateral retinoblastoma.Molecular mechanisms in the evolution of chronic myelocytic leukemia.p21WAF-1 reorganizes the nucleus in tumor suppression.Loss of heterozygosity on chromosome 17p13 in breast carcinomas identifies tumors with high proliferation indexFollow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 geneHuman retinoblastoma gene: long-range mapping and analysis of its deletion in a breast cancer cell lineMolecular genetics in the pathology and diagnosis of retinoblastoma.The transcription factor E2F-1 mediates the autoregulation of RB gene expression.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.Mutations in the RB1 gene and their effects on transcription.Recombination by sequence repeats with formation of suppressive or residual mitochondrial DNA in Neurospora.C-terminal truncation of the retinoblastoma gene product leads to functional inactivation.One hundred years of retinoblastoma research. From the clinic to the gene and back again.The Histochemistry and Cell Biology omnium-gatherum: the year 2015 in review.Re-characterization of established human retinoblastoma cell lines.PCR-based detection of a polymorphic BamHI site in intron 1 of the human retinoblastoma (RB) gene.Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneDevelopmental rescue of an embryonic-lethal mutation in the retinoblastoma gene in chimeric miceRetinoblastoma cell lines Y79, RB355 and WERI-Rb27 are genetically related.The Retinoblastoma Gene in Myeloid Leukaemias.Molecular Diagnostics in Clinical Oncology
P2860
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P2860
Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants
description
1988 nî lūn-bûn
@nan
1988 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@ast
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@en
Human retinoblastoma susceptib ...... s intragenic deletion mutants.
@nl
type
label
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@ast
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@en
Human retinoblastoma susceptib ...... s intragenic deletion mutants.
@nl
prefLabel
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@ast
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@en
Human retinoblastoma susceptib ...... s intragenic deletion mutants.
@nl
P2093
P2860
P356
P1476
Human retinoblastoma susceptib ...... us intragenic deletion mutants
@en
P2093
Bookstein R
Friedmann T
P2860
P304
P356
10.1073/PNAS.85.7.2210
P407
P577
1988-04-01T00:00:00Z