| 1 | CNBP, LARP1
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| The SARS-CoV-2 RNA-protein interactome in infected human cells
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| Schmidt N, Lareau CA, Keshishian H, Ganskih S, Schneider C, Hennig T, Melanson R, Werner S, Wei Y, Zimmer M, Ade J, Kirschner L, Zielinski S, Dölken L, Lander ES, Caliskan N, Fischer U, Vogel J, Carr SA, Bodem J, Munschauer M.
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| Nat Microbiol. Mar;6(3):339-353. doi: 10.1038/s41564-020-00846-z. Epub 2020 Dec 21 2021
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| 2 | CNBP, SMARCA5, TBX2, WNT5B
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| Beyond the binding site: in vivo identification of tbx2, smarca5 and wnt5b as molecular targets of CNBP during embryonic development.
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| Armas P, Margarit E, Mouguelar VS, Allende ML, Calcaterra NB.
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| PLoS One 8(5):e63234. doi: 10.1371/journal.pone.0063234. Print 2013.
2013
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| 3 | CNBP, DM1, DM2, DMPK
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| Myotonic dystrophy, when simple repeats reveal complex pathogenic entities: new findings and future challenges.
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| Sicot G, Gourdon G, Gomes-Pereira M.
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| Hum Mol Genet 20(R2):R116-23. doi: 10.1093/hmg/ddr343. Epub 2011 Aug 5. Review.
2011
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| 4 | CLCN1, CNBP, DM2, MCB, MCT
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| Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
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| Sun C, Van Ghelue M, Tranebjærg L, Thyssen F, Nilssen Ø, Torbergsen T.
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| Clin Genet 80(6):574-80. doi: 10.1111/j.1399-0004.2010.01616.x. Epub 2011 Jan 19.
2011
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| 5 | CNBP, DM1, DM2
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| Absence of a differentiation defect in muscle satellite cells from DM2 patients.
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| Pelletier R, Hamel F, Beaulieu D, Patry L, Haineault C, Tarnopolsky M, Schoser B, Puymirat J.
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| Neurobiol Dis 36(1):181-90. Epub 2009 Jul 24.PMID: 19632331 2009
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| 6 | CNBP, DM2
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| Reduction of the rate of protein translation in patients with myotonic dystrophy 2.
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| Huichalaf C, Schoser B, Schneider-Gold C, Jin B, Sarkar P, Timchenko L.
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| J Neurosci 29(28):9042-9.PMID: 19605641 2009
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| 7 | CNBP, DM2
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| Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion.
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| Lucchiari S, Pagliarani S, Corti S, Mancinelli E, Servida M, Fruguglietti E, Sansone V, Moggio M, Bresolin N, Comi GP, Meola G.
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| J Neurol Sci 275(1-2):159-63. Epub 2008 Sep 18.PMID: 18804219 2008
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| 8 | CNBP, DM2
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| Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophy.
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| Bassez G, Chapoy E, Bastuji-Garin S, Radvanyi-Hoffman H, Authier FJ, Pellissier JF, Eymard B, Gherardi RK.
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| J Neuropathol Exp Neurol 67(4):319-25.PMID: 18379436 2008
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| 9 | CNBP, DM1, DM2, DMPK
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| Myotonic dystrophy: emerging mechanisms for DM1 and DM2.
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| Cho DH, Tapscott SJ.
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| Biochim Biophys Acta 1772(2):195-204. Epub 2006 Jun 20. Review.
2007
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| 10 | CNBP, PCBP2
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| The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation.
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| Gerbasi VR, Link AJ.
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| Mol Cell Proteomics 6(6):1049-58. Epub 2007 Feb 26.PMID: 17327219 2007
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| 11 | DM2, CNBP
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| DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression.
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| Margolis JM, Schoser BG, Moseley ML, Day JW, Ranum LP.
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| Hum Mol Genet 15(11):1808-15. Epub 2006 Apr 19. 2006
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| 12 | NDUFA5, CNBP
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| Identification of NADH dehydrogenase 1 alpha subcomplex 5 capable to transform murine fibroblasts and overexpressed in human cervical carcinoma cell lines.
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| Shimada T, Moriuchi R, Mori T, Yamada K, Ishimaru T, Katamine S.
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| Biochem Biophys Res Commun 339(3):852-7. Epub 2005 Nov 28. 2006
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| 13 | CNBP, DM2
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| Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population.
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| Vallo L, Bonifazi E, Borgiani P, Novelli G, Botta A.
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| Mol Cell Probes 19(1):71-4. Epub 2004 Nov 12. 2005
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| 14 | FXN, FRDA, FRAXA, FMR1, FRAXE, ATXN1, SCA1, ATXN2, SCA2, ATXN3, MJD, ATXN7, SCA7, SCA6, CACNA1A, SCA17, TBP, DRPLA, ATN1, AR, SBMA, DM1, DMPK, DM2, CNBP, SCA10, ATXN10, SCA12, PPP2R2B, SCA8, ATXN8OS
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| Diseases of unstable repeat expansion: mechanisms and common principles.
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| Gatchel JR, Zoghbi HY.
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| Nat Rev Genet 6(10):743-55. Review. 2005
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| 15 | THRAP3, USP6, CNBP, OMD
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| Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes.
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| Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Chen CJ, Neff JR, Demetri GD, Rosenberg AE, Bridge JA, Fletcher JA.
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| Oncogene 24(21):3419-26. 2005
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| 16 | DM2, CNBP, DM1, DMPK
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| Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease.
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| Maurage CA, Udd B, Ruchoux MM, Vermersch P, Kalimo H, Krahe R, Delacourte A, Sergeant N.
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| Neurology 65(10):1636-8. 2005
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| 17 | CELF1, CNBP, MBNL1, MBNL3
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| Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats.
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| Kino Y, Mori D, Oma Y, Takeshita Y, Sasagawa N, Ishiura S.
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| Hum Mol Genet 13(5):495-507. Epub 2004 Jan 13. 2004
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| 18 | DM2, CNBP
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| Homozygosity for CCTG mutation in myotonic dystrophy type 2.
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| Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmuller H, Ricker K.
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| Brain 127(Pt 8):1868-77. Epub 2004 Jul 1. 2004
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| 19 | DM2, CNBP
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| Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
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| Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, Thornton CA, Moxley RT, Harper PS, Rogers MT, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, Bottani A, Kohler A, Shriver MD, Sallinen R, Wessman M, Zhang S, Wright FA, Krahe R.
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| Am J Hum Genet 73(4):835-48. Epub 2003 Sep 10. 2003
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| 20 | DM2, CNBP
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| Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract.
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| Liquori CL, Ikeda Y, Weatherspoon M, Ricker K, Schoser BG, Dalton JC, Day JW, Ranum LP.
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| Am J Hum Genet 73(4):849-62. Epub 2003 Sep 22. 2003
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| 21 | DM2, CNBP
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| Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.
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| Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP.
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| Neurology 60(4):657-64. 2003
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| 22 | DM2,CNBP
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| Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
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| Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP.
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| Science 293(5531):864-7. 2001
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| 23 | CNBP
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| Linkage of proximal myotonic myopathy to chromosome 3q.
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| Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR.
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| Neurology 52(1):170-1.PMID: 9921867 1999
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| 24 | CNBP
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| Organization of the gene encoding cellular nucleic acid-binding protein.
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| Flink IL, Morkin E.
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| Gene 163(2):279-82. 1995
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| 25 | CNBP
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| Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3-q24.
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| Lusis AJ, et al.
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| Genomics 8 : 411-414. 1990
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| 26 | CNBP
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| Identification of a zinc finger protein that binds to the sterol regulatory element.
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| Rajavashisth TB, et al.
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| Science 245 : 640-643. 1990
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