A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
about
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeIdentification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsSmall evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brainIdentification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting controlThe non-coding RNAs as riboregulatorsRegulatory long non-coding RNAs and neuronal disordersEpigenetic principles and mechanisms underlying nervous system functions in health and diseaseThe putatively functional Mkrn1-p1 pseudogene is neither expressed nor imprinted, nor does it regulate its source gene in transAn imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locusComputational discovery of sense-antisense transcription in the human and mouse genomesAn update on the genetic causes of central precocious pubertyA new pathway in the control of the initiation of puberty: the MKRN3 geneNatural antisense transcriptsGenetic & epigenetic approach to human obesityParent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center.Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.Antisense transcripts with FANTOM2 clone set and their implications for gene regulation.Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionCentral precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.The vertebrate makorin ubiquitin ligase gene family has been shaped by large-scale duplication and retroposition from an ancestral gonad-specific, maternal-effect gene.Disruption of the bipartite imprinting center in a family with Angelman syndromePhysical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759.The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.Central precocious puberty caused by mutations in the imprinted gene MKRN3.DNA methylation in genomic imprinting, development, and disease.Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.A novel MKRN3 missense mutation causing familial precocious puberty.The human obesity gene map: the 2001 update.Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.The human obesity gene map: the 2002 update.The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.The role of imprinted genes in fetal growth abnormalities.Distinct phenotypes distinguish the molecular classes of Angelman syndromeThe neurobiology of mouse models syntenic to human chromosome 15q.Temporal and developmental requirements for the Prader-Willi imprinting center.RNAs of the human chromosome 15q11-q13 imprinted regionMakorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans.Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center.
P2860
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P2860
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
description
1999 nî lūn-bûn
@nan
1999 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
A novel imprinted gene, encodi ...... Willi syndrome critical region
@ast
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en-gb
A novel imprinted gene, encodi ...... Willi syndrome critical region
@nl
type
label
A novel imprinted gene, encodi ...... Willi syndrome critical region
@ast
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en-gb
A novel imprinted gene, encodi ...... Willi syndrome critical region
@nl
prefLabel
A novel imprinted gene, encodi ...... Willi syndrome critical region
@ast
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en-gb
A novel imprinted gene, encodi ...... Willi syndrome critical region
@nl
P2093
P2860
P3181
P356
P1476
A novel imprinted gene, encodi ...... Willi syndrome critical region
@en
P2093
D J Driscoll
R D Nicholls
P2860
P304
P3181
P356
10.1093/HMG/8.5.783
P407
P577
1999-05-01T00:00:00Z