The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs.
about
Prader-Willi, Angelman, and 15q11-q13 Duplication SyndromesThe emerging landscape of small nucleolar RNAs in cell biologyRegulation of alternative splicing by local histone modifications: potential roles for RNA-guided mechanismsRapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in EuarchontogliresIdentification and functional analysis of long non-coding RNAs in human and mouse early embryos based on single-cell transcriptome dataSmall non-coding RNA signature in multiple sclerosis patients after treatment with interferon-β.Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus.DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks.Paternal sperm DNA methylation associated with early signs of autism risk in an autism-enriched cohortC/D-box snoRNA-derived RNA production is associated with malignant transformation and metastatic progression in prostate cancer.Non-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders.The expression pattern of small nucleolar and small Cajal body-specific RNAs characterizes distinct molecular subtypes of multiple myeloma.RNAs of the human chromosome 15q11-q13 imprinted regionDual function of C/D box small nucleolar RNAs in rRNA modification and alternative pre-mRNA splicing.An updated human snoRNAome.Processing of snoRNAs as a new source of regulatory non-coding RNAs: snoRNA fragments form a new class of functional RNAs.Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?The Role of Noncoding RNAs in Neurodevelopmental Disorders: The Case of Rett Syndrome.Box C/D small nucleolar RNA genes and the Prader-Willi syndrome: a complex interplay.Regulatory role of small nucleolar RNAs in human diseases.SNORD116 and SNORD115 change expression of multiple genes and modify each other's activity.Potential applications of MEG3 in cancer diagnosis and prognosis.Recommendations for the investigation of animal models of Prader-Willi syndrome.Evidence for rRNA 2'-O-methylation plasticity: Control of intrinsic translational capabilities of human ribosomes.SNORD126 promotes HCC and CRC cell growth by activating the PI3K-AKT pathway through FGFR2.Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.
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P2860
The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@ast
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@en
type
label
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@ast
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@en
prefLabel
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@ast
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@en
P2860
P356
P1476
The SNORD115 (H/MBII-52) and S ...... ate canonical box C/D snoRNAs.
@en
P2093
Jérôme Cavaillé
Marie-Line Bortolin-Cavaillé
P2860
P304
P356
10.1093/NAR/GKS321
P407
P577
2012-04-11T00:00:00Z