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CDKN1C gene

Known as: Cyclin-Dependent Kinase Inhibitor 1C Gene, p57(KIP2), CYCLIN-DEPENDENT KINASE INHIBITOR 1C 
This gene plays a regulatory role in the cell cycle.
National Institutes of Health

Related topics

Related topics

7 relations
Beckwith-Wiedemann SyndromeCDKN1C protein, humanCell Cycle ControlCyclin-Dependent Kinase Inhibitor p57

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CDKN1C wt Allele

Papers overview

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2019
2019
Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case
We present two half siblings with significant short stature who proved a diagnostic challenge for several years. Radiological… 
2015
2015
High Skp2/Low p57Kip2 Expression is Associated with Poor Prognosis in Human Breast Carcinoma
Downregulation of p57Kip2 is involved in tumor progression, and S-phase kinase-associated protein 2 (Skp2) is an E3 ligase that… 
2013
2013
P21‐Activated Kinase 4 Regulates the Cyclin‐Dependent Kinase Inhibitor P57Kip2 in Human Breast Cancer
The p21‐activated kinases have been implicated in the control of cell cycle progression. However, the biological mechanism… 
2013
2013
Knockdown of CDKN1C (p57kip2) and PHLDA2 Results in Developmental Changes in Bovine Pre-implantation Embryos
Imprinted genes have been implicated in early embryonic, placental, and neonatal development and alterations in expression levels… 
2012
2012
Characterization, Tissue Expression, and Imprinting Analysis of the Porcine CDKN1C and NAP1L4 Genes
CDKN1C and NAP1L4 in human CDKN1C/KCNQ1OT1 imprinted domain are two key candidate genes responsible for BWS (Beckwith-Wiedemann… 
2007
2007
Cell Cycle Genes PEDF and CDKN1C in Growing Deer Antlers
Deer antlers are the only mammalian appendage to display an annual cycle of full regeneration. The growth phase in antler… 
2003
2003
Silencing of CDKN 1 C ( p 57 KIP 2 ) is associated with hypomethylation at KvDMR 1 in Beckwith – Wiedemann syndrome
Context: Beckwith–Wiedemann syndrome (BWS) arises by several genetic and epigenetic mechanisms affecting the balance of imprinted… 
2000
2000
Immunohistochemical characterization of p57KIP2 expression in human esophageal squamous cell carcinoma.
Functional defects in the CIP/KIP family of cyclin-dependent kinase inhibitors (CDKIs) have been shown to be associated with… 
2000
2000
Analysis of CDKN1C in Beckwith Wiedemann Syndrome
In this study we have examined 32 patients with Beckwith Wiedemann Syndrome (BWS) for mutations affecting the CDKN1C gene… 
1999
1999
CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance
In this study, we have examined CDKN1C expression in BWS patients with allele imbalance (AI) affecting the 11p15 region. Two of… 
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