An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome (Q28292249)

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Y Fukushima

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Y Kaneko

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M Inoue

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Y Komoto

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A Okada

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S Ohishi

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A Nabetani

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H Morisaki

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M Nakayama

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N Niikawa

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T Mukai

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

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language of work or name

English

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publication date

October 1996

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171-3

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cites work

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The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases

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Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors

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Differential imprinting and expression of maternal and paternal genomes

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Imprinting: a gamete's point of view

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X-chromosome inactivation: molecular mechanisms and genetic consequences

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DNA methylation and genomic imprinting

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Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors

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Uniparental paternal disomy in a genetic cancer-predisposing syndrome

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Enhanced growth of mice lacking the cyclin-dependent kinase inhibitor function of p27(Kip1).

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A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice

21 January 2018

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Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

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7 January 2021

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

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Impressions of imprints

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Parental imprinting of autosomal mammalian genes

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7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

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7 January 2021

Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome

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Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

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7 January 2021

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

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7 January 2021

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome

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7 January 2021

Chromosome 11 and Beckwith-Wiedemann syndrome

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7 January 2021

The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

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Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females

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Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family

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Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

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Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

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7 January 2021

p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21

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7 January 2021

Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals

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7 January 2021