252 related articles for article (PubMed ID: 35612622)
1. Revealing diverse alternative splicing variants of the highly homologous SMN1 and SMN2 genes by targeted long-read sequencing.
Dai M; Xu Y; Sun Y; Xiao B; Ying X; Liu Y; Jiang W; Zhang J; Liu X; Ji X
Mol Genet Genomics; 2022 Jul; 297(4):1039-1048. PubMed ID: 35612622
[TBL] [Abstract][Full Text] [Related]
2. Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene.
Seo J; Singh NN; Ottesen EW; Sivanesan S; Shishimorova M; Singh RN
PLoS One; 2016; 11(4):e0154390. PubMed ID: 27111068
[TBL] [Abstract][Full Text] [Related]
3. Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.
Harahap NIF; Niba ETE; Ar Rochmah M; Wijaya YOS; Saito T; Saito K; Awano H; Morioka I; Iijima K; Lai PS; Matsuo M; Nishio H; Shinohara M
Brain Dev; 2018 Sep; 40(8):670-677. PubMed ID: 29580671
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Alternative splicing in spinal muscular atrophy underscores the role of an intron definition model.
Singh NN; Singh RN
RNA Biol; 2011; 8(4):600-6. PubMed ID: 21654213
[TBL] [Abstract][Full Text] [Related]
6. A multi-exon-skipping detection assay reveals surprising diversity of splice isoforms of spinal muscular atrophy genes.
Singh NN; Seo J; Rahn SJ; Singh RN
PLoS One; 2012; 7(11):e49595. PubMed ID: 23185376
[TBL] [Abstract][Full Text] [Related]
7. A super minigene with a short promoter and truncated introns recapitulates essential features of transcription and splicing regulation of the SMN1 and SMN2 genes.
Ottesen EW; Seo J; Luo D; Singh NN; Singh RN
Nucleic Acids Res; 2024 Apr; 52(7):3547-3571. PubMed ID: 38214229
[TBL] [Abstract][Full Text] [Related]
8. Splicing of the Survival Motor Neuron genes and implications for treatment of SMA.
Bebee TW; Gladman JT; Chandler DS
Front Biosci (Landmark Ed); 2010 Jun; 15(3):1191-1204. PubMed ID: 20515750
[TBL] [Abstract][Full Text] [Related]
9. SMN transcript stability: could modulation of messenger RNA degradation provide a novel therapy for spinal muscular atrophy?
Heier CR; Gogliotti RG; DiDonato CJ
J Child Neurol; 2007 Aug; 22(8):1013-8. PubMed ID: 17761657
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Heat increases full-length SMN splicing: promise for splice-augmenting therapies for SMA.
Dominguez CE; Cunningham D; Venkataramany AS; Chandler DS
Hum Genet; 2022 Feb; 141(2):239-256. PubMed ID: 35088120
[TBL] [Abstract][Full Text] [Related]
13. Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene.
Niba ETE; Nishio H; Wijaya YOS; Lai PS; Tozawa T; Chiyonobu T; Yamadera M; Okamoto K; Awano H; Takeshima Y; Saito T; Shinohara M
Brain Dev; 2021 Feb; 43(2):294-302. PubMed ID: 33036822
[TBL] [Abstract][Full Text] [Related]
14. Hypoxia is a modifier of SMN2 splicing and disease severity in a severe SMA mouse model.
Bebee TW; Dominguez CE; Samadzadeh-Tarighat S; Akehurst KL; Chandler DS
Hum Mol Genet; 2012 Oct; 21(19):4301-13. PubMed ID: 22763238
[TBL] [Abstract][Full Text] [Related]
15. Genomic Variability in the Survival Motor Neuron Genes (
Butchbach MER
Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360669
[TBL] [Abstract][Full Text] [Related]
16. Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype.
Ruhno C; McGovern VL; Avenarius MR; Snyder PJ; Prior TW; Nery FC; Muhtaseb A; Roggenbuck JS; Kissel JT; Sansone VA; Siranosian JJ; Johnstone AJ; Nwe PH; Zhang RZ; Swoboda KJ; Burghes AHM
Hum Genet; 2019 Mar; 138(3):241-256. PubMed ID: 30788592
[TBL] [Abstract][Full Text] [Related]
17. A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy.
Lorson CL; Hahnen E; Androphy EJ; Wirth B
Proc Natl Acad Sci U S A; 1999 May; 96(11):6307-11. PubMed ID: 10339583
[TBL] [Abstract][Full Text] [Related]
18. A SMN2 Splicing Modifier Rescues the Disease Phenotypes in an In Vitro Human Spinal Muscular Atrophy Model.
Son YS; Choi K; Lee H; Kwon O; Jung KB; Cho S; Baek J; Son B; Kang SM; Kang M; Yoon J; Shen H; Lee S; Oh JH; Lee HA; Lee MO; Cho HS; Jung CR; Kim J; Cho S; Son MY
Stem Cells Dev; 2019 Apr; 28(7):438-453. PubMed ID: 30667343
[TBL] [Abstract][Full Text] [Related]
19. A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.
Monani UR; Lorson CL; Parsons DW; Prior TW; Androphy EJ; Burghes AH; McPherson JD
Hum Mol Genet; 1999 Jul; 8(7):1177-83. PubMed ID: 10369862
[TBL] [Abstract][Full Text] [Related]
20. Advances in therapeutic development for spinal muscular atrophy.
Howell MD; Singh NN; Singh RN
Future Med Chem; 2014 Jun; 6(9):1081-99. PubMed ID: 25068989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]