Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
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The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in miceFragile x syndromePrader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterThe emerging landscape of small nucleolar RNAs in cell biologyGeneration of a mouse model with down-regulated U50 snoRNA (SNORD50) expression and its organ-specific phenotypic modulationEpigenetic mechanisms in diurnal cycles of metabolism and neurodevelopmentDo repeated arrays of regulatory small-RNA genes elicit genomic imprinting?: Concurrent emergence of large clusters of small non-coding RNAs and genomic imprinting at four evolutionarily distinct eutherian chromosomal lociThe persistent contributions of RNA to eukaryotic gen(om)e architecture and cellular functionRapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in EuarchontogliresComparative genomics of eukaryotic small nucleolar RNAs reveals deep evolutionary ancestry amidst ongoing intragenomic mobilityLoss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.Alternative processing as evolutionary mechanism for the origin of novel nonprotein coding RNAs.Repertoire of bovine miRNA and miRNA-like small regulatory RNAs expressed upon viral infectionAdult-onset deletion of the Prader-Willi syndrome susceptibility gene Snord116 in mice results in reduced feeding and increased fat mass.The importance of imprinting in the human placenta.The small nucleolar ribonucleoprotein (snoRNP) database.The function of non-coding RNAs in genomic imprinting.Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome.Identification of differentially expressed non-coding RNAs in embryonic stem cell neural differentiationDifferential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus.An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in miceWhen ribosomes go bad: diseases of ribosome biogenesis.A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeSpecies-specific alternative splicing leads to unique expression of sno-lncRNAs.The role of genomic imprinting in biology and disease: an expanding view.Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseasesNon-coding RNAs in imprinted gene clusters.Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.The role of imprinted genes in fetal growth abnormalities.The neurobiology of mouse models syntenic to human chromosome 15q.Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.Temporal and developmental requirements for the Prader-Willi imprinting center.Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs.Hypothalamic expression of snoRNA Snord116 is consistent with a link to the hyperphagia and obesity symptoms of Prader-Willi syndrome.Snord116 is critical in the regulation of food intake and body weightNon-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders.Regulatory RNAs in brain function and disorders.
P2860
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P2860
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@ast
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en-gb
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@nl
type
label
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@ast
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en-gb
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@nl
altLabel
Deletion of the MBII-85 snoRNA ...... n Postnatal Growth Retardation
@en
prefLabel
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@ast
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en-gb
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@nl
P2093
P2860
P3181
P1433
P1476
Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation
@en
P2093
Birte Seeger
Boris V Skryabin
Elena Karpova
Jana Pfeiffer
Jürgen Brosius
Leonid V Gubar
Sergej Handel
Thomas Robeck
P2860
P3181
P356
10.1371/JOURNAL.PGEN.0030235
P407
P577
2007-12-28T00:00:00Z