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

2

0 references

Y Fukushima

3

0 references

Y Kaneko

4

0 references

M Inoue

5

0 references

Y Komoto

6

0 references

A Okada

7

0 references

S Ohishi

8

0 references

A Nabetani

9

0 references

H Morisaki

10

0 references

M Nakayama

11

0 references

N Niikawa

12

0 references

T Mukai

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

13

0 references

language of work or name

English

0 references

publication date

October 1996

0 references

published in

Nature Genetics

0 references

volume

14

0 references

issue

2

0 references

page(s)

171-3

0 references

cites work

1 reference

https://api.crossref.org/works/10.1038/NG1096-171

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1096-171

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

Differential imprinting and expression of maternal and paternal genomes

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

Imprinting: a gamete's point of view

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

X-chromosome inactivation: molecular mechanisms and genetic consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

DNA methylation and genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

Impressions of imprints

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

Parental imprinting of autosomal mammalian genes

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

Chromosome 11 and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-171

7 January 2021