A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
about
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardationMolecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromePrader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterGenetics of Prader-Willi syndrome and Prader-Will-Like syndromeAlternative processing as evolutionary mechanism for the origin of novel nonprotein coding RNAs.RNA hairpins in noncoding regions of human brain and Caenorhabditis elegans mRNA are edited by adenosine deaminases that act on RNA.A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeThe human obesity gene map: the 2001 update.Non-coding RNAs in imprinted gene clusters.The human obesity gene map: the 2002 update.Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain.Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome.Imprinted small RNA genes.Snord116 is critical in the regulation of food intake and body weightModes of imprinted gene action in learning disability.Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome.Box C/D small nucleolar RNA genes and the Prader-Willi syndrome: a complex interplay.Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.The Human Obesity Gene Map: The 2004 UpdateFamilial interstitial 570 kbp deletion of theUBE3Agene region causing Angelman syndrome but not Prader-Willi syndrome
P2860
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P2860
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A translocation breakpoint clu ...... cription unit on chromosome 15
@ast
A translocation breakpoint clu ...... cription unit on chromosome 15
@en
A translocation breakpoint clu ...... cription unit on chromosome 15
@nl
type
label
A translocation breakpoint clu ...... cription unit on chromosome 15
@ast
A translocation breakpoint clu ...... cription unit on chromosome 15
@en
A translocation breakpoint clu ...... cription unit on chromosome 15
@nl
prefLabel
A translocation breakpoint clu ...... cription unit on chromosome 15
@ast
A translocation breakpoint clu ...... cription unit on chromosome 15
@en
A translocation breakpoint clu ...... cription unit on chromosome 15
@nl
P2093
P3181
P356
P1476
A translocation breakpoint clu ...... cription unit on chromosome 15
@en
P2093
A Hüttenhofer
A Schinzel
B Horsthemke
H G Nothwang
H H Ropers
P304
P3181
P356
10.1093/HMG/10.3.201
P407
P577
2001-02-01T00:00:00Z