200 related articles for article (PubMed ID: 33462199)
21. [Alternative splicing and the cure of spinal muscular atrophy].
Marasco LE; Stigliano J; Kornblihtt AR
Medicina (B Aires); 2019; 79(Spec 6/1):582-586. PubMed ID: 31864230
[TBL] [Abstract][Full Text] [Related]
22. HnRNP C1/C2 may regulate exon 7 splicing in the spinal muscular atrophy gene SMN1.
Irimura S; Kitamura K; Kato N; Saiki K; Takeuchi A; Gunadi ; Matsuo M; Nishio H; Lee MJ
Kobe J Med Sci; 2009 Mar; 54(5):E227-36. PubMed ID: 19628962
[TBL] [Abstract][Full Text] [Related]
23. 5-(N-ethyl-N-isopropyl)-amiloride enhances SMN2 exon 7 inclusion and protein expression in spinal muscular atrophy cells.
Yuo CY; Lin HH; Chang YS; Yang WK; Chang JG
Ann Neurol; 2008 Jan; 63(1):26-34. PubMed ID: 17924536
[TBL] [Abstract][Full Text] [Related]
24. Characterization of RNA-Protein Interactions: Lessons from Two RNA-Binding Proteins, SRSF1 and SRSF2.
Skrdlant L; Lin RJ
Methods Mol Biol; 2016; 1421():1-13. PubMed ID: 26965252
[TBL] [Abstract][Full Text] [Related]
25. c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy.
Wu S; Li YL; Cheng NY; Wang C; Dong EL; Lu YQ; Li JJ; Guo XX; Lin X; Lai LL; Liu ZW; Wang N; Chen WJ
J Mol Neurosci; 2018 Jun; 65(2):196-202. PubMed ID: 29799103
[TBL] [Abstract][Full Text] [Related]
26. Synergy between NMR measurements and MD simulations of protein/RNA complexes: application to the RRMs, the most common RNA recognition motifs.
Krepl M; Cléry A; Blatter M; Allain FH; Sponer J
Nucleic Acids Res; 2016 Jul; 44(13):6452-70. PubMed ID: 27193998
[TBL] [Abstract][Full Text] [Related]
27. A-44G transition in SMN2 intron 6 protects patients with spinal muscular atrophy.
Wu X; Wang SH; Sun J; Krainer AR; Hua Y; Prior TW
Hum Mol Genet; 2017 Jul; 26(14):2768-2780. PubMed ID: 28460014
[TBL] [Abstract][Full Text] [Related]
28. Crystal structure of human UP1, the domain of hnRNP A1 that contains two RNA-recognition motifs.
Xu RM; Jokhan L; Cheng X; Mayeda A; Krainer AR
Structure; 1997 Apr; 5(4):559-70. PubMed ID: 9115444
[TBL] [Abstract][Full Text] [Related]
29. SRSF1-Regulated Alternative Splicing in Breast Cancer.
Anczuków O; Akerman M; Cléry A; Wu J; Shen C; Shirole NH; Raimer A; Sun S; Jensen MA; Hua Y; Allain FH; Krainer AR
Mol Cell; 2015 Oct; 60(1):105-17. PubMed ID: 26431027
[TBL] [Abstract][Full Text] [Related]
30. Mechanism of Nonsense-Mediated mRNA Decay Stimulation by Splicing Factor SRSF1.
Aznarez I; Nomakuchi TT; Tetenbaum-Novatt J; Rahman MA; Fregoso O; Rees H; Krainer AR
Cell Rep; 2018 May; 23(7):2186-2198. PubMed ID: 29768215
[TBL] [Abstract][Full Text] [Related]
31. Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1.
Cartegni L; Krainer AR
Nat Genet; 2002 Apr; 30(4):377-84. PubMed ID: 11925564
[TBL] [Abstract][Full Text] [Related]
32. Rescue of spinal muscular atrophy mouse models with AAV9-Exon-specific U1 snRNA.
Donadon I; Bussani E; Riccardi F; Licastro D; Romano G; Pianigiani G; Pinotti M; Konstantinova P; Evers M; Lin S; Rüegg MA; Pagani F
Nucleic Acids Res; 2019 Aug; 47(14):7618-7632. PubMed ID: 31127278
[TBL] [Abstract][Full Text] [Related]
33. Is RNA manipulation a viable therapy for spinal muscular atrophy?
Horne C; Young PJ
J Neurol Sci; 2009 Dec; 287(1-2):27-31. PubMed ID: 19758605
[TBL] [Abstract][Full Text] [Related]
34. Therapeutics that directly increase SMN expression to treat spinal muscular atrophy.
Shababi M; Mattis VB; Lorson CL
Drug News Perspect; 2010 Oct; 23(8):475-82. PubMed ID: 21031163
[TBL] [Abstract][Full Text] [Related]
35. Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophy.
Brichta L; Garbes L; Jedrzejowska M; Grellscheid SN; Holker I; Zimmermann K; Wirth B
Hum Genet; 2008 Mar; 123(2):141-53. PubMed ID: 18172693
[TBL] [Abstract][Full Text] [Related]
36. hnRNP M facilitates exon 7 inclusion of SMN2 pre-mRNA in spinal muscular atrophy by targeting an enhancer on exon 7.
Cho S; Moon H; Loh TJ; Oh HK; Cho S; Choy HE; Song WK; Chun JS; Zheng X; Shen H
Biochim Biophys Acta; 2014; 1839(4):306-15. PubMed ID: 24533984
[TBL] [Abstract][Full Text] [Related]
37. The SMN1 common variant c.22 dupA in Chinese patients causes spinal muscular atrophy by nonsense-mediated mRNA decay in humans.
Bai J; Qu Y; Cao Y; Yang L; Ge L; Jin Y; Wang H; Song F
Gene; 2018 Feb; 644():49-55. PubMed ID: 29080838
[TBL] [Abstract][Full Text] [Related]
38. Isolated pseudo-RNA-recognition motifs of SR proteins can regulate splicing using a noncanonical mode of RNA recognition.
Cléry A; Sinha R; Anczuków O; Corrionero A; Moursy A; Daubner GM; Valcárcel J; Krainer AR; Allain FH
Proc Natl Acad Sci U S A; 2013 Jul; 110(30):E2802-11. PubMed ID: 23836656
[TBL] [Abstract][Full Text] [Related]
39. The SRSF1 linker induces semi-conservative ESE binding by cooperating with the RRMs.
Cho S; Hoang A; Chakrabarti S; Huynh N; Huang DB; Ghosh G
Nucleic Acids Res; 2011 Nov; 39(21):9413-21. PubMed ID: 21852328
[TBL] [Abstract][Full Text] [Related]
40. Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy.
Qu YJ; Bai JL; Cao YY; Wang H; Jin YW; Du J; Ge XS; Zhang WH; Li Y; He SX; Song F
J Mol Diagn; 2016 Sep; 18(5):741-752. PubMed ID: 27425821
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
