p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas (Q57499701)

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8 January 2020

title

p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas (English)

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8 January 2020

5

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author name string

Tamara Potikha

1

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8 January 2020

Sameer Kassem

2

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8 January 2020

Esther P Haber

3

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8 January 2020

Ilana Ariel

4

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publication date

1 March 2005

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8 January 2020

published in

Laboratory Investigation

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8 January 2020

volume

85

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page(s)

364-375

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issue

3

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https://scigraph.springernature.com/pub.10.1038/labinvest.3700229

8 January 2020

exact match

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cites work

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

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

21 January 2018

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

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

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Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

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Beckwith-Wiedemann syndrome: imprinting in clusters revisited

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Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

21 January 2018

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Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors

21 January 2018

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Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome

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

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Decreased expression of p57(KIP2)mRNA in human bladder cancer

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Expression of p57(KIP2) potently blocks the growth of human astrocytomas and induces cell senescence

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Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

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Hyperinsulinism of the newborn

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Hyperinsulinism in infancy: from basic science to clinical disease.

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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

21 January 2018

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Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

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Hyperinsulinism: molecular aetiology of focal disease

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Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy

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p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.

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Monoclonal antibodies against recombinant parts of the Ki-67 antigen (MIB 1 and MIB 3) detect proliferating cells in microwave-processed formalin-fixed paraffin sections

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Adherence to the first-AUG rule when a second AUG codon follows closely upon the first

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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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Stabilization of MyoD by direct binding to p57(Kip2)

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Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes.

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Genomic imprinting in the rat: linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis.

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A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice

21 January 2018

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Spatial and temporal expression patterns of the cyclin-dependent kinase (CDK) inhibitors p27Kip1 and p57Kip2 during mouse development.

21 January 2018

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p57Kip2 expression is enhanced during mid-cardiac murine development and is restricted to trabecular myocardium

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Dynamic temporal and spatial regulation of the cdk inhibitor p57(kip2) during embryo morphogenesis.

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p57Kip2 regulates actin dynamics by binding and translocating LIM-kinase 1 to the nucleus

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Podocyte expression of the CDK-inhibitor p57 during development and disease

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Negative regulators of cyclin-dependent kinases and their roles in cancers

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Cooperation between the Cdk inhibitors p27(KIP1) and p57(KIP2) in the control of tissue growth and development

21 January 2018

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Modulation of the expression of the Cip/Kip family of cyclin-dependent kinase inhibitors in foetal developing lungs of hamsters

21 January 2018

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Beckwith-Wiedemann syndrome: a quantitative, immunohistochemical study of pancreatic islet cell populations

21 January 2018

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Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

21 January 2018

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Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour

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7 January 2021

Mice lacking a CDK inhibitor, p57Kip2, exhibit skeletal abnormalities and growth retardation

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7 January 2021

Role of p27(Kip1) in human intestinal cell differentiation

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Differential expression of cyclin-dependent kinase inhibitors in human glomerular disease: role in podocyte proliferation and maturation

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Age-dependent changes of p57(Kip2) and p21(Cip1/Waf1) expression in skeletal muscle and lung of mice

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7 January 2021

10.1038/LABINVEST.3700229

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8 January 2020

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