Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
about
Sequence-specific transcriptional repression by an MBD2-interacting zinc finger protein MIZFRB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.Synergistic transcriptional activation by hGABP and select members of the activation transcription factor/cAMP response element-binding protein familyCharacterization of a negative retinoic acid response element in the murine Oct4 promoterOncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotypeGenetic predispositions and childhood cancer.Retinoblastoma gene promoter directs transgene expression exclusively to the nervous system.MyoD stimulates RB promoter activity via the CREB/p300 nuclear transduction pathway.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.RB1CC1 activates RB1 pathway and inhibits proliferation and cologenic survival in human cancer.Regulation of RB transcription in vivo by RB family membersMutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counsellingLow penetrance of retinoblastoma for p.V654L mutation of the RB1 gene.Activating transcription factor 3 induces DNA synthesis and expression of cyclin D1 in hepatocytes.Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families.Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing.Mutations in the promoter region of the aldolase B gene that cause hereditary fructose intolerance.A role for epigenetics in hearing: Establishment and maintenance of auditory specific gene expression patterns.Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling.A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice.Visualizing dynamic E2F-mediated repression in vivo.Regulatory mutations and human genetic disease.Reverse genetic system for the analysis of parvovirus telomeres reveals interactions between transcription factor binding sites in the hairpin stemMolecular etiology of low-penetrance retinoblastoma in two pedigrees.Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.Deletion of RB exons 24 and 25 causes low-penetrance retinoblastomaIdentification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisGenetic changes in the transforming growth factor beta (TGF-beta) type II receptor gene in human gastric cancer cells: correlation with sensitivity to growth inhibition by TGF-beta.Exploring the contribution of distal P4 promoter elements to the oncoselectivity of Minute Virus of Mice.A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia.Identification of hepatic nuclear factor 1 binding sites in the 5' flanking region of the human phenylalanine hydroxylase gene: implication of a dual function of phenylalanine hydroxylase stimulator in the phenylalanine hydroxylation system.The spectrum of RB1 germ-line mutations in hereditary retinoblastomaExhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodemaThe genetics of retinoblastoma, revisitedDetection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.How do retinoblastoma tumours form?The RB1 gene mutation in a child with ectopic intracranial retinoblastoma"Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB functionThe transcription factor E2F-1 mediates the autoregulation of RB gene expression.
P2860
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P2860
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
description
1991 nî lūn-bûn
@nan
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
1991年论文
@zh
1991年论文
@zh-cn
name
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
@en
type
label
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
@en
prefLabel
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
@en
P2093
P356
P1433
P1476
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
@en
P2093
P2888
P356
10.1038/353083A0
P407
P577
1991-09-01T00:00:00Z
P6179
1029129601