1 | NOP56, SCA36
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| Characteristic RNA foci of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan).
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| Liu W, Ikeda Y, Hishikawa N, Yamashita T, Deguchi K, Abe K.
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| Eur J Neurol ur J Neurol. 2014 Jul 2. doi: 10.1111/ene.12491. [Epub ahead of print]
2014
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2 | NOP56, SCA36
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| 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.
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| García-Murias M, Quintáns B, Arias M, Seixas AI, Cacheiro P, Tarrío R, Pardo J, Millán MJ, Arias-Rivas S, Blanco-Arias P, Dapena D, Moreira R, Rodríguez-Trelles F, Sequeiros J, Carracedo A, Silveira I, Sobrido MJ.
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| Brain 135(Pt 5):1423-35. doi: 10.1093/brain/aws069. Epub 2012 Apr 3.
2012
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3 | NOP56, SCA36
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| Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
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| Ikeda Y, Ohta Y, Kobayashi H, Okamoto M, Takamatsu K, Ota T, Manabe Y, Okamoto K, Koizumi A, Abe K.
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| Neurology 79(4):333-41. doi: 10.1212/WNL.0b013e318260436f. Epub 2012 Jun 27.
2012
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4 | FBL, NOP56, NOP58
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| Structurally conserved Nop56/58 N-terminal domain facilitates archaeal box C/D ribonucleoprotein-guided methyltransferase activity.
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| Gagnon KT, Biswas S, Zhang X, Brown BA 2nd, Wollenzien P, Mattos C, Maxwell ES.
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| J Biol Chem 287(23):19418-28. doi: 10.1074/jbc.M111.323253. Epub 2012 Apr 11.
2012
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5 | NOP56, SCA36
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| Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
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| Kobayashi H, Abe K, Matsuura T, Ikeda Y, Hitomi T, Akechi Y, Habu T, Liu W, Okuda H, Koizumi A.
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| Am J Hum Genet 89(1):121-30. doi: 10.1016/j.ajhg.2011.05.015. Epub 2011 Jun 16.
2011
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6 | NHP2L1, NOP56, NOP58, RUVBL1, RUVBL2
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| Evidence that the AAA+ proteins TIP48 and TIP49 bridge interactions between 15.5K and the related NOP56 and NOP58 proteins during box C/D snoRNP biogenesis.
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| McKeegan KS, Debieux CM, Watkins NJ.
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| Mol Cell Biol 29(18):4971-81. doi: 10.1128/MCB.00752-09. Epub 2009 Jul 20.
2009
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7 | FBL, NOP56
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| Fibrillarin and Nop56 interact before being co-assembled in box C/D snoRNPs.
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| Lechertier T, Grob A, Hernandez-Verdun D, Roussel P.
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| Exp Cell Res 315(6):928-42. doi: 10.1016/j.yexcr.2009.01.016. Epub 2009 Jan 30.
2009
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8 | NOP56
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| Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome.
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| Hayano T, Yanagida M, Yamauchi Y, Shinkawa T, Isobe T, Takahashi N.
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| J Biol Chem 278(36):34309-19. Epub 2003 May 30. 2003
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9 | NOP56
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| Nucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesis.
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| Gautier T, Berges T, Tollervey D, Hurt E.
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| Mol Cell Biol 17(12):7088-98. 1997
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10 | NOP56, NOP58
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| Nucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesis.
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| Gautier T, Bergès T, Tollervey D, Hurt E.
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| Mol Cell Biol 17(12):7088-98.
1997
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