about
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationSuppression of cell transformation by the cyclin-dependent kinase inhibitor p57KIP2 requires binding to proliferating cell nuclear antigenTumor Suppressor Inactivation in the Pathogenesis of Adult T-Cell LeukemiaTwo novel genes in the center of the 11p15 imprinted domain escape genomic imprintingFetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndromeMyoD regulates p57kip2 expression by interacting with a distant cis-element and modifying a higher order chromatin structureBehavioural abnormalities in a novel mouse model for Silver Russell Syndrome.Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.Genomic imprinting: concept and clinical consequences.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.P27 in cell cycle control and cancer.CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalancep57(KIP2) is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57(KIP2), IGF2, and H19Characterization, tissue expression, and imprinting analysis of the porcine CDKN1C and NAP1L4 genes.CDK inhibitor p57 (Kip2) is downregulated by Akt during HER2-mediated tumorigenicity.Molecular findings in Beckwith-Wiedemann syndrome.p57KIP2 modulates stress-activated signaling by inhibiting c-Jun NH2-terminal kinase/stress-activated protein Kinase.Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome.Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.p57(Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome.Analysis of CDKN1C in Beckwith Wiedemann syndrome.Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques.CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome.
P2860
Q24681734-6D98F0A6-7741-48F5-865E-AED127F28FCDQ24682776-4A48D3BE-F9A8-4EE4-BAE8-2162A25462D0Q28081287-76D771E3-D1CC-4B73-BA6D-3F13F6709E02Q28138506-40F9D95C-44BC-49AB-B58C-08CAD57C7A27Q28505485-BA2A2D08-0544-4AD6-A6C3-926C3E0B29A5Q28512786-624E288B-C53F-4EBD-9C66-6034F855C0DDQ30356916-634F6E85-6DC9-4ADE-A71D-B5E72E7DF2E3Q33285306-8A088F28-F7A4-49EA-BD91-B4A9B373BD35Q33603375-BE7F4859-32D3-433B-B716-F930D981033EQ33927299-2A4E71E1-C8FF-4B99-B237-318124737005Q34024231-F65AF8FC-22CB-4A46-9634-018A5359B99FQ35432995-A859E0AD-059F-4517-81FE-01F06830B454Q35745855-7578A9B6-56E1-4F79-83C5-C43151C1EB16Q35830464-4C6C6B39-071B-438D-9D9E-30FF03FCA798Q36798077-63BC34DA-2041-4EA0-844F-B97DC05C28D4Q38099605-FF625310-077C-4EDB-8E20-6C45D910CADFQ40636332-07E42BC5-1BE2-471C-B78B-52C82E58A676Q41496736-9E4AF285-A38C-4C62-9478-2881043A1F23Q43825017-7225CF89-E3BD-444C-8889-9B341A30E149Q50525407-F4B76A84-782A-48D6-83C1-199EFBD134FDQ52539681-48CA9F52-6075-4705-B9AD-0D193BA9981FQ52984051-62467F45-F6DF-45B3-BA9F-D8A50255B9D3Q53088998-D44732AD-EFE3-43FA-8AEC-DF003F6718B7
P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@ast
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@en
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@nl
type
label
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@ast
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@en
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@nl
prefLabel
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@ast
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@en
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@nl
P2093
P356
P1433
P1476
New p57KIP2 mutations in Beckwith-Wiedemann syndrome
@en
P2093
A Nabetani
E Steichen
H Morisaki
M Nakayama
P2888
P356
10.1007/S004390050573
P407
P577
1997-10-01T00:00:00Z
P6179
1023574549