Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
about
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeRhabdomyosarcoma-associated locus and MYOD1 are syntenic but separate loci on the short arm of human chromosome 11Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney developmentHomozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancyGenetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphismTranscriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesAnalysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationLoss 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 imprintingAntioncogenes and human cancer.Common and specific roles of the related CDK inhibitors p27 and p57 revealed by a knock-in mouse modelGenome-wide association study identifies multiple risk loci for chronic lymphocytic leukemiaGenomic imprinting: review and relevance to human diseases.Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesisProviral rearrangements and overexpression of a new cellular gene (nov) in myeloblastosis-associated virus type 1-induced nephroblastomasThe importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes.Genetic polymorphisms of p21 and risk of second primary malignancy in patients with index squamous cell carcinoma of the head and neckMosaic uniparental disomy in Beckwith-Wiedemann syndrome.Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndromeMultiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsPediatric oncology.The yin and yang of kidney development and Wilms' tumorsA radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease lociConstitutional 1p36 deletion in a child with neuroblastoma.Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromesOppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumorsLow frequency of p57KIP2 mutation in Beckwith-Wiedemann syndromeDiagnosing Friedreich's ataxia.The molecular basis of nephrogenesis and congenital kidney diseaseExpression of the 11p13 Wilms' tumor gene, WT1, correlates with histologic category of Wilms' tumor.Morphology and growth characteristics of epithelial cells from classic Wilms' tumors.Genomic imprinting: mechanism and role in human pathology.The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome.Uniparental disomy occurs infrequently in Wilms tumor patients.Genetic variants of p27 and p21 as predictors for risk of second primary malignancy in patients with index squamous cell carcinoma of head and neck.Long non-coding RNAs: versatile master regulators of gene expression and crucial players in cancer.Molecular genetic analysis of chromosome 11p in familial Wilms tumour.
P2860
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P2860
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
description
1989 nî lūn-bûn
@nan
1989 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@ast
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@en
type
label
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@ast
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@en
prefLabel
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@ast
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@en
P2093
P2860
P1476
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
@en
P2093
Cavenee WK
Kalbakji A
Lampkin BC
P2860
P304
P407
P577
1989-05-01T00:00:00Z