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1998 1
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2013 1
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2024 1

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PubMed for id: 1653962468

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Page 1
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.
Nashabat M, Nabavizadeh N, Saraçoğlu HP, Sarıbaş B, Avcı Ş, Börklü E, Beillard E, Yılmaz E, Uygur SE, Kayhan CK, Bosco L, Eren ZB, Steindl K, Richter MF, Bademci G, Rauch A, Fattahi Z, Valentino ML, Connolly AM, Bahr A, Viola L, Bergmann AK, Rocha ME, Peart L, Castro-Rojas DL, Bültmann E, Khan S, Giarrana ML, Teleanu RI, Gonzalez JM, Pini A, Schädlich IS, Vill K, Brugger M, Zuchner S, Pinto A, Donkervoort S, Bivona SA, Riza A; Undiagnosed Diseases Network; Streata I, Gläser D, Baquero-Montoya C, Garcia-Restrepo N, Kotzaeridou U, Brunet T, Epure DA, Bertoli-Avella A, Kariminejad A, Tekin M, von Hardenberg S, Bönnemann CG, Stettner GM, Zanni G, Kayserili H, Oflazer ZP, Escande-Beillard N. Nashabat M, et al. Nat Commun. 2024 Feb 27;15(1):1758. doi: 10.1038/s41467-024-45933-5. Nat Commun. 2024. PMID: 38413582 Free PMC article.
The interaction of CRM1 and the nuclear pore protein Tpr.
Zhao CL, Mahboobi SH, Moussavi-Baygi R, Mofrad MR. Zhao CL, et al. PLoS One. 2014 Apr 10;9(4):e93709. doi: 10.1371/journal.pone.0093709. eCollection 2014. PLoS One. 2014. PMID: 24722547 Free PMC article.
Structural determinants and mechanism of mammalian CRM1 allostery.
Dölker N, Blanchet CE, Voß B, Haselbach D, Kappel C, Monecke T, Svergun DI, Stark H, Ficner R, Zachariae U, Grubmüller H, Dickmanns A. Dölker N, et al. Structure. 2013 Aug 6;21(8):1350-60. doi: 10.1016/j.str.2013.05.015. Epub 2013 Jul 11. Structure. 2013. PMID: 23850451 Free article.
CRM1-mediated recycling of snurportin 1 to the cytoplasm.
Paraskeva E, Izaurralde E, Bischoff FR, Huber J, Kutay U, Hartmann E, Lührmann R, Görlich D. Paraskeva E, et al. J Cell Biol. 1999 Apr 19;145(2):255-64. doi: 10.1083/jcb.145.2.255. J Cell Biol. 1999. PMID: 10209022 Free PMC article.