These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
259 related articles for article (PubMed ID: 24006466)
1. Developmental arrest of Drosophila survival motor neuron (Smn) mutants accounts for differences in expression of minor intron-containing genes. Garcia EL; Lu Z; Meers MP; Praveen K; Matera AG RNA; 2013 Nov; 19(11):1510-6. PubMed ID: 24006466 [TBL] [Abstract][Full Text] [Related]
2. Transcriptomic comparison of Drosophila snRNP biogenesis mutants reveals mutant-specific changes in pre-mRNA processing: implications for spinal muscular atrophy. Garcia EL; Wen Y; Praveen K; Matera AG RNA; 2016 Aug; 22(8):1215-27. PubMed ID: 27268418 [TBL] [Abstract][Full Text] [Related]
3. A Drosophila model of spinal muscular atrophy uncouples snRNP biogenesis functions of survival motor neuron from locomotion and viability defects. Praveen K; Wen Y; Matera AG Cell Rep; 2012 Jun; 1(6):624-31. PubMed ID: 22813737 [TBL] [Abstract][Full Text] [Related]
4. RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns. Doktor TK; Hua Y; Andersen HS; Brøner S; Liu YH; Wieckowska A; Dembic M; Bruun GH; Krainer AR; Andresen BS Nucleic Acids Res; 2017 Jan; 45(1):395-416. PubMed ID: 27557711 [TBL] [Abstract][Full Text] [Related]
5. Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs. Gabanella F; Butchbach ME; Saieva L; Carissimi C; Burghes AH; Pellizzoni L PLoS One; 2007 Sep; 2(9):e921. PubMed ID: 17895963 [TBL] [Abstract][Full Text] [Related]
6. Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins. Huo Q; Kayikci M; Odermatt P; Meyer K; Michels O; Saxena S; Ule J; Schümperli D RNA Biol; 2014; 11(11):1430-46. PubMed ID: 25692239 [TBL] [Abstract][Full Text] [Related]
7. A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle. Rajendra TK; Gonsalvez GB; Walker MP; Shpargel KB; Salz HK; Matera AG J Cell Biol; 2007 Mar; 176(6):831-41. PubMed ID: 17353360 [TBL] [Abstract][Full Text] [Related]
8. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing. Pellizzoni L; Kataoka N; Charroux B; Dreyfuss G Cell; 1998 Nov; 95(5):615-24. PubMed ID: 9845364 [TBL] [Abstract][Full Text] [Related]
9. SMA-causing missense mutations in survival motor neuron (Smn) display a wide range of phenotypes when modeled in Drosophila. Praveen K; Wen Y; Gray KM; Noto JJ; Patlolla AR; Van Duyne GD; Matera AG PLoS Genet; 2014 Aug; 10(8):e1004489. PubMed ID: 25144193 [TBL] [Abstract][Full Text] [Related]
10. An SMN-dependent U12 splicing event essential for motor circuit function. Lotti F; Imlach WL; Saieva L; Beck ES; Hao le T; Li DK; Jiao W; Mentis GZ; Beattie CE; McCabe BD; Pellizzoni L Cell; 2012 Oct; 151(2):440-54. PubMed ID: 23063131 [TBL] [Abstract][Full Text] [Related]
12. Optimization of SMN trans-splicing through the analysis of SMN introns. Shababi M; Lorson CL J Mol Neurosci; 2012 Mar; 46(3):459-69. PubMed ID: 21826391 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Temperature-sensitive spinal muscular atrophy-causing point mutations lead to SMN instability, locomotor defects and premature lethality in Raimer AC; Singh SS; Edula MR; Paris-Davila T; Vandadi V; Spring AM; Matera AG Dis Model Mech; 2020 May; 13(5):. PubMed ID: 32501283 [TBL] [Abstract][Full Text] [Related]
15. Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy. Borg RM; Fenech Salerno B; Vassallo N; Bordonne R; Cauchi RJ Neurobiol Dis; 2016 Oct; 94():245-58. PubMed ID: 27388936 [TBL] [Abstract][Full Text] [Related]
16. Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene. Campion Y; Neel H; Gostan T; Soret J; Bordonné R EMBO J; 2010 Jun; 29(11):1817-29. PubMed ID: 20400941 [TBL] [Abstract][Full Text] [Related]
17. The survival motor neuron gene smn-1 interacts with the U2AF large subunit gene uaf-1 to regulate Caenorhabditis elegans lifespan and motor functions. Gao X; Teng Y; Luo J; Huang L; Li M; Zhang Z; Ma YC; Ma L RNA Biol; 2014; 11(9):1148-60. PubMed ID: 25483032 [TBL] [Abstract][Full Text] [Related]
18. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. Pellizzoni L; Charroux B; Dreyfuss G Proc Natl Acad Sci U S A; 1999 Sep; 96(20):11167-72. PubMed ID: 10500148 [TBL] [Abstract][Full Text] [Related]
19. hnRNP-G promotes exon 7 inclusion of survival motor neuron (SMN) via direct interaction with Htra2-beta1. Hofmann Y; Wirth B Hum Mol Genet; 2002 Aug; 11(17):2037-49. PubMed ID: 12165565 [TBL] [Abstract][Full Text] [Related]
20. SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Zhang Z; Lotti F; Dittmar K; Younis I; Wan L; Kasim M; Dreyfuss G Cell; 2008 May; 133(4):585-600. PubMed ID: 18485868 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]