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2. Splicing of a critical exon of human Survival Motor Neuron is regulated by a unique silencer element located in the last intron. Singh NK; Singh NN; Androphy EJ; Singh RN Mol Cell Biol; 2006 Feb; 26(4):1333-46. PubMed ID: 16449646 [TBL] [Abstract][Full Text] [Related]
3. hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing. Kashima T; Rao N; David CJ; Manley JL Hum Mol Genet; 2007 Dec; 16(24):3149-59. PubMed ID: 17884807 [TBL] [Abstract][Full Text] [Related]
4. Antisense masking of an hnRNP A1/A2 intronic splicing silencer corrects SMN2 splicing in transgenic mice. Hua Y; Vickers TA; Okunola HL; Bennett CF; Krainer AR Am J Hum Genet; 2008 Apr; 82(4):834-48. PubMed ID: 18371932 [TBL] [Abstract][Full Text] [Related]
5. Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2. Cartegni L; Hastings ML; Calarco JA; de Stanchina E; Krainer AR Am J Hum Genet; 2006 Jan; 78(1):63-77. PubMed ID: 16385450 [TBL] [Abstract][Full Text] [Related]
6. The regulation and regulatory activities of alternative splicing of the SMN gene. Singh NN; Androphy EJ; Singh RN Crit Rev Eukaryot Gene Expr; 2004; 14(4):271-85. PubMed ID: 15663357 [TBL] [Abstract][Full Text] [Related]
7. An extended inhibitory context causes skipping of exon 7 of SMN2 in spinal muscular atrophy. Singh NN; Androphy EJ; Singh RN Biochem Biophys Res Commun; 2004 Mar; 315(2):381-8. PubMed ID: 14766219 [TBL] [Abstract][Full Text] [Related]
9. In vivo selection reveals combinatorial controls that define a critical exon in the spinal muscular atrophy genes. Singh NN; Androphy EJ; Singh RN RNA; 2004 Aug; 10(8):1291-305. PubMed ID: 15272122 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. An intronic element contributes to splicing repression in spinal muscular atrophy. Kashima T; Rao N; Manley JL Proc Natl Acad Sci U S A; 2007 Feb; 104(9):3426-31. PubMed ID: 17307868 [TBL] [Abstract][Full Text] [Related]
13. A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy. Kashima T; Manley JL Nat Genet; 2003 Aug; 34(4):460-3. PubMed ID: 12833158 [TBL] [Abstract][Full Text] [Related]
14. The RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) gene. Chen HH; Chang JG; Lu RM; Peng TY; Tarn WY Mol Cell Biol; 2008 Nov; 28(22):6929-38. PubMed ID: 18794368 [TBL] [Abstract][Full Text] [Related]
15. Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes. Singh RN; Singh NN Adv Neurobiol; 2018; 20():31-61. PubMed ID: 29916015 [TBL] [Abstract][Full Text] [Related]
16. Htra2-beta 1 stimulates an exonic splicing enhancer and can restore full-length SMN expression to survival motor neuron 2 (SMN2). Hofmann Y; Lorson CL; Stamm S; Androphy EJ; Wirth B Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9618-23. PubMed ID: 10931943 [TBL] [Abstract][Full Text] [Related]
17. Bifunctional antisense oligonucleotides provide a trans-acting splicing enhancer that stimulates SMN2 gene expression in patient fibroblasts. Skordis LA; Dunckley MG; Yue B; Eperon IC; Muntoni F Proc Natl Acad Sci U S A; 2003 Apr; 100(7):4114-9. PubMed ID: 12642665 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Modulating role of RNA structure in alternative splicing of a critical exon in the spinal muscular atrophy genes. Singh NN; Singh RN; Androphy EJ Nucleic Acids Res; 2007; 35(2):371-89. PubMed ID: 17170000 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]