SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
about
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in miceCritical association of ncRNA with intronsPrader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterA deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadismThe 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 lociLoss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviourDeletion of PREPl causes growth impairment and hypotonia in miceThe 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.Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice.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.Non-coding RNAs: a key to future personalized molecular therapy?Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome.Necdin controls proliferation of white adipocyte progenitor cells.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 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.Neuronal chromatin dynamics of imprinting in development and diseaseGlobal 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.Epigenetic regulation of neuronal dendrite and dendritic spine developmentImpaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.The neurobiology of mouse models syntenic to human chromosome 15q.Prader-Willi syndrome and autism spectrum disorders: an evolving story.Noncoding RNAs in mental retardationReactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCsTemporal and developmental requirements for the Prader-Willi imprinting center.
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P2860
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
description
2008 nî lūn-bûn
@nan
2008 թուականին հրատարակուած գիտական յօդուած
@hyw
2008 թվականին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@ast
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en-gb
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@nl
type
label
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@ast
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en-gb
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@nl
altLabel
SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
@en
prefLabel
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@ast
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en-gb
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@nl
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P2860
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SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
@en
P2093
Hong Hua Li
Nicola M Solomon
Shengwen Zhang
Uta Francke
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P3181
P356
10.1371/JOURNAL.PONE.0001709
P407
P577
2008-01-01T00:00:00Z