Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation - Test2 - elhamkhani - TriplyDB

Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

http://www.wikidata.org/entity/Q21092489

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The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13 Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice Fragile x syndrome Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster The emerging landscape of small nucleolar RNAs in cell biology Generation of a mouse model with down-regulated U50 snoRNA (SNORD50) expression and its organ-specific phenotypic modulation Epigenetic mechanisms in diurnal cycles of metabolism and neurodevelopment Do 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 loci The persistent contributions of RNA to eukaryotic gen(om)e architecture and cellular function Rapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in Euarchontoglires Comparative genomics of eukaryotic small nucleolar RNAs reveals deep evolutionary ancestry amidst ongoing intragenomic mobility Loss 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 infection Adult-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 differentiation Differential 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 mice When ribosomes go bad: diseases of ribosome biogenesis.A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome Species-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 diseases Non-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 weight Non-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders.Regulatory RNAs in brain function and disorders.

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Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

http://www.wikidata.org/entity/Q21092489

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2007 nî lūn-bûn

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2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n Postnatal Growth Retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Deletion of the MBII-85 snoRNA ...... n postnatal growth retardation

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Birte Seeger

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Boris V Skryabin

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Elena Karpova

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Jana Pfeiffer

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Jürgen Brosius

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Leonid V Gubar

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Sergej Handel

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Thomas Robeck

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P2860

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

Small nucleolar RNAs: an abundant group of noncoding RNAs with diverse cellular functions

Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models

A mouse model for Prader-Willi syndrome imprinting-centre mutations

A mammalian gene with introns instead of exons generating stable RNA products

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

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12

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Timofey S Rozhdestvensky

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2007-12-28T00:00:00Z

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5683737

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