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Items: 1 to 20 of 116

1.

Long noncoding RNAs with snoRNA ends.

Yin QF, Yang L, Zhang Y, Xiang JF, Wu YW, Carmichael GG, Chen LL.

Mol Cell. 2012 Oct 26;48(2):219-30. doi: 10.1016/j.molcel.2012.07.033. Epub 2012 Sep 6.

2.

Species-specific alternative splicing leads to unique expression of sno-lncRNAs.

Zhang XO, Yin QF, Wang HB, Zhang Y, Chen T, Zheng P, Lu X, Chen LL, Yang L.

BMC Genomics. 2014 Apr 16;15:287. doi: 10.1186/1471-2164-15-287.

3.

Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM.

Hum Mol Genet. 2009 Nov 15;18(22):4227-38. doi: 10.1093/hmg/ddp373. Epub 2009 Aug 5.

4.

Coiled bodies are predisposed to a spatial association with genes that contain snoRNA sequences in their introns.

Schul W, Adelaar B, van Driel R, de Jong L.

J Cell Biochem. 1999 Dec 1;75(3):393-403.

PMID:
10536363
5.

Maturation of mammalian H/ACA box snoRNAs: PAPD5-dependent adenylation and PARN-dependent trimming.

Berndt H, Harnisch C, Rammelt C, Stöhr N, Zirkel A, Dohm JC, Himmelbauer H, Tavanez JP, Hüttelmaier S, Wahle E.

RNA. 2012 May;18(5):958-72. doi: 10.1261/rna.032292.112. Epub 2012 Mar 22. Erratum in: RNA. 2014 Aug;20(8):1349.

6.

Long noncoding RNAs: Re-writing dogmas of RNA processing and stability.

Wilusz JE.

Biochim Biophys Acta. 2016 Jan;1859(1):128-38. doi: 10.1016/j.bbagrm.2015.06.003. Epub 2015 Jun 11. Review.

7.

A computational screen for C/D box snoRNAs in the human genomic region associated with Prader-Willi and Angelman syndromes.

Sridhar P, Gan HH, Schlick T.

J Biomed Sci. 2008 Nov;15(6):697-705. doi: 10.1007/s11373-008-9271-x. Epub 2008 Jul 27.

PMID:
18661287
8.
10.

Sno/scaRNAbase: a curated database for small nucleolar RNAs and cajal body-specific RNAs.

Xie J, Zhang M, Zhou T, Hua X, Tang L, Wu W.

Nucleic Acids Res. 2007 Jan;35(Database issue):D183-7. Epub 2006 Nov 11.

11.

Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region.

Cavaillé J, Seitz H, Paulsen M, Ferguson-Smith AC, Bachellerie JP.

Hum Mol Genet. 2002 Jun 15;11(13):1527-38.

PMID:
12045206
12.

Biogenesis and intranuclear trafficking of human box C/D and H/ACA RNPs.

Kiss T, Fayet E, Jády BE, Richard P, Weber M.

Cold Spring Harb Symp Quant Biol. 2006;71:407-17. Review.

PMID:
17381323
13.

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

Ding F, Prints Y, Dhar MS, Johnson DK, Garnacho-Montero C, Nicholls RD, Francke U.

Mamm Genome. 2005 Jun;16(6):424-31.

PMID:
16075369
14.

The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing.

Kishore S, Khanna A, Zhang Z, Hui J, Balwierz PJ, Stefan M, Beach C, Nicholls RD, Zavolan M, Stamm S.

Hum Mol Genet. 2010 Apr 1;19(7):1153-64. doi: 10.1093/hmg/ddp585. Epub 2010 Jan 6.

15.
16.

Plant U13 orthologues and orphan snoRNAs identified by RNomics of RNA from Arabidopsis nucleoli.

Kim SH, Spensley M, Choi SK, Calixto CP, Pendle AF, Koroleva O, Shaw PJ, Brown JW.

Nucleic Acids Res. 2010 May;38(9):3054-67. doi: 10.1093/nar/gkp1241. Epub 2010 Jan 16.

17.

Processing of snoRNAs as a new source of regulatory non-coding RNAs: snoRNA fragments form a new class of functional RNAs.

Falaleeva M, Stamm S.

Bioessays. 2013 Jan;35(1):46-54. doi: 10.1002/bies.201200117. Epub 2012 Nov 26. Review.

18.
19.

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

Runte M, Varon R, Horn D, Horsthemke B, Buiting K.

Hum Genet. 2005 Feb;116(3):228-30. Epub 2004 Nov 23.

PMID:
15565282
20.

Unusual Processing Generates SPA LncRNAs that Sequester Multiple RNA Binding Proteins.

Wu H, Yin QF, Luo Z, Yao RW, Zheng CC, Zhang J, Xiang JF, Yang L, Chen LL.

Mol Cell. 2016 Nov 3;64(3):534-548. doi: 10.1016/j.molcel.2016.10.007. Epub 2016 Oct 27.

PMID:
27871485

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