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