Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
about
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeFunctional characterization of ORCTL2--an organic cation transporter expressed in the renal proximal tubulesImprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesLoss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprintingMultiple complementary transcripts of pCMa1, a novel gene located at chromosome 11p15.1-2, and melanocytic cell transformation.Genomic imprinting: concept and clinical consequences.Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndromeMultiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.Wilms tumor genetics.Chest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors.Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumorsMaternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression.Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.Caveolins in rhabdomyosarcomaRhabdomyosarcomas: an overview on the experimental animal models.Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters.Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast.Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.DNA methylation of imprinted genes at birth is associated with child weight status at birth, 1 year, and 3 years.
P2860
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P2860
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Multiple genetic loci within 1 ...... mosomal transferable fragments
@ast
Multiple genetic loci within 1 ...... mosomal transferable fragments
@en
type
label
Multiple genetic loci within 1 ...... mosomal transferable fragments
@ast
Multiple genetic loci within 1 ...... mosomal transferable fragments
@en
prefLabel
Multiple genetic loci within 1 ...... mosomal transferable fragments
@ast
Multiple genetic loci within 1 ...... mosomal transferable fragments
@en
P2093
P2860
P50
P356
P1476
Multiple genetic loci within 1 ...... mosomal transferable fragments
@en
P2093
A Westerveld
C Lengauer
D Schlessinger
J M Hoovers
L A Johnson
L M Kalikin
P2860
P304
12456-12460
P356
10.1073/PNAS.92.26.12456
P407
P577
1995-12-01T00:00:00Z