CDKN1C protein, human

Known as: KIP2 Protein, P57 protein, human, Beckwith-Wiedemann Syndrome Protein 
Cyclin-dependent kinase inhibitor 1C (316 aa, ~32 kDa) is encoded by the human CDKN1C gene. This protein is involved in the regulation of cell… (More)
National Institutes of Health

Papers overview

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2013
2013
BACKGROUND Russell Silver syndrome (RSS) leads to prenatal and postnatal growth retardation. About 55% of RSS patients present a… (More)
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2013
2013
BACKGROUND Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome associated with an increased risk of pediatric tumors. The… (More)
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Highly Cited
2012
Highly Cited
2012
IMAGe syndrome (intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita and genital anomalies) is an… (More)
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2011
2011
Aim:To investigate the regulatory effect of microRNA-221 (miR-221) on CDKN1C/p57 expression in colorectal carcinoma (CRC).Methods… (More)
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Highly Cited
2009
Highly Cited
2009
CDKN1C (encoding tumor suppressor p57(KIP2)) is a cyclin-dependent kinase (CDK) inhibitor whose family members are often… (More)
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Highly Cited
2008
Highly Cited
2008
The identification of target mRNAs is a key step for assessing the role of aberrantly expressed microRNAs in human cancer. MiR… (More)
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Highly Cited
2005
Highly Cited
2005
PURPOSE Intraductal papillary mucinous neoplasm (IPMN) of the pancreas is an increasingly identified precursor to infiltrating… (More)
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Highly Cited
2005
Highly Cited
2005
Beckwith–Wiedemann Syndrome (BWS) results from mutations or epigenetic events involving imprinted genes at 11p15.5. Most BWS… (More)
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2001
2001
Complex phenotypes and genotypes characterize the human disease, Beckwith--Wiedemann syndrome (BWS). Genetic and epigenetic… (More)
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Highly Cited
1999
Highly Cited
1999
Beckwith-Wiedemann syndrome (BWS) is a human imprinting disorder with a variable phenotype. The major features are anterior… (More)
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