Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
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Induction of p57(KIP2) expression by p73beta.Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeInactivation of p57KIP2 by regional promoter hypermethylation and histone deacetylation in human tumorsIdentification and functional characterization of an intragenic DNA binding site for the spumaretroviral trans-activator in the human p57Kip2 geneIntrinsic structural disorder and sequence features of the cell cycle inhibitor p57Kip2CDKN1C/p57kip2 is a candidate tumor suppressor gene in human breast cancer.Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumorsLow frequency of p57KIP2 mutation in Beckwith-Wiedemann syndromeCDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalancep57(KIP2) is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57(KIP2), IGF2, and H19Binding sites for adeno-associated virus Rep proteins within the human genome.Decreased expression of p57(KIP2)mRNA in human bladder cancer.Epigenetic Characterization of CDKN1C in Placenta Samples from Non-syndromic Intrauterine Growth Restriction.Transforming growth factor beta-induced cell cycle arrest of human hematopoietic cells requires p57KIP2 up-regulation.The multiple roles of the cyclin-dependent kinase inhibitory protein p57(KIP2) in cerebral cortical neurogenesis.Induction of cellular genes is mediated by the Bel1 transactivator in foamy virus-infected human cells.My road to alternative splicing control: from simple paths to loops and interconnections.Differential regulation of HIC1 target genes by CtBP and NuRD, via an acetylation/SUMOylation switch, in quiescent versus proliferating cells.Differential tumor suppressor properties and transforming growth factor-beta responsiveness of p57KIP2 in leukemia cells with aberrant p57KIP2 promoter DNA methylation.A novel p21WAF1/CIP1 transcript is highly dependent on p53 for its basal expression in mouse tissues.Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.p21B, a variant of p21(Waf1/Cip1), is induced by the p53 family.A human-specific polymorphism in the coding region of the aggrecan gene. Variable number of tandem repeats produce a range of core protein sizes in the general population.Analysis of CDKN1C in Beckwith Wiedemann syndrome.p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas
P2860
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P2860
Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
description
1996 nî lūn-bûn
@nan
1996 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Characterization of the human ...... egion, and mutational analysis
@ast
Characterization of the human ...... egion, and mutational analysis
@en
Characterization of the human ...... egion, and mutational analysis
@nl
type
label
Characterization of the human ...... egion, and mutational analysis
@ast
Characterization of the human ...... egion, and mutational analysis
@en
Characterization of the human ...... egion, and mutational analysis
@nl
prefLabel
Characterization of the human ...... egion, and mutational analysis
@ast
Characterization of the human ...... egion, and mutational analysis
@en
Characterization of the human ...... egion, and mutational analysis
@nl
P2093
P3181
P1433
P1476
Characterization of the human ...... egion, and mutational analysis
@en
P2093
M Matsushima
T Furuhata
Y Nakamura
P2888
P304
P3181
P356
10.1007/BF02281873
10.1007/S004390050106
P407
P577
1996-05-01T00:00:00Z
P6179
1025315267