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.
151 related articles for article (PubMed ID: 23477310)
1. SMN1 gene duplications are more frequent in patients with progressive muscular atrophy. Kuźma-Kozakiewicz M; Jędrzejowska M; Kaźmierczak B Amyotroph Lateral Scler Frontotemporal Degener; 2013 Sep; 14(5-6):457-62. PubMed ID: 23477310 [TBL] [Abstract][Full Text] [Related]
2. Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients. Yamamoto T; Sato H; Lai PS; Nurputra DK; Harahap NI; Morikawa S; Nishimura N; Kurashige T; Ohshita T; Nakajima H; Yamada H; Nishida Y; Toda S; Takanashi J; Takeuchi A; Tohyama Y; Kubo Y; Saito K; Takeshima Y; Matsuo M; Nishio H Brain Dev; 2014 Nov; 36(10):914-20. PubMed ID: 24359787 [TBL] [Abstract][Full Text] [Related]
3. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS. Veldink JH; Kalmijn S; Van der Hout AH; Lemmink HH; Groeneveld GJ; Lummen C; Scheffer H; Wokke JH; Van den Berg LH Neurology; 2005 Sep; 65(6):820-5. PubMed ID: 16093455 [TBL] [Abstract][Full Text] [Related]
4. Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients. Gamez J; Also E; Alias L; Corbera-Bellalta M; Barceló MJ; Centeno M; Raguer N; Gratacós M; Baiget M; Tizzano EF Clin Neurol Neurosurg; 2007 Dec; 109(10):844-8. PubMed ID: 17850955 [TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy. He J; Zhang QJ; Lin QF; Chen YF; Lin XZ; Lin MT; Murong SX; Wang N; Chen WJ Gene; 2013 Apr; 518(2):325-9. PubMed ID: 23352792 [TBL] [Abstract][Full Text] [Related]
6. The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study. Zhang Y; He J; Zhang Y; Li L; Tang X; Wang L; Guo J; Jin C; Tighe S; Zhang Y; Zhu Y; Zhu B Medicine (Baltimore); 2020 Jan; 99(3):e18809. PubMed ID: 32011487 [TBL] [Abstract][Full Text] [Related]
7. Telomeric Region of the Spinal Muscular Atrophy Locus Is Susceptible to Structural Variations. Noguchi Y; Onishi A; Nakamachi Y; Hayashi N; Harahap NI; Rochmah MA; Shima A; Yanagisawa S; Morisada N; Nakagawa T; Iijima K; Kasagi S; Saegusa J; Kawano S; Shinohara M; Tairaku S; Saito T; Kubo Y; Saito K; Nishio H Pediatr Neurol; 2016 May; 58():83-9. PubMed ID: 27268759 [TBL] [Abstract][Full Text] [Related]
8. Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1. Ogino S; Gao S; Leonard DG; Paessler M; Wilson RB Eur J Hum Genet; 2003 Mar; 11(3):275-7. PubMed ID: 12673282 [TBL] [Abstract][Full Text] [Related]
9. The importance of the SMN genes in the genetics of sporadic ALS. Corcia P; Camu W; Praline J; Gordon PH; Vourch P; Andres C Amyotroph Lateral Scler; 2009; 10(5-6):436-40. PubMed ID: 19922137 [TBL] [Abstract][Full Text] [Related]
10. [Analysis of survival motor neuron gene conversion in patients with spinal muscular atrophy]. He SX; Ge XS; Qu YJ; Jin YW; Wang H; Bai JL; Song F Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):606-11. PubMed ID: 22161088 [TBL] [Abstract][Full Text] [Related]
11. Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants. Milligan JN; Larson JL; Filipovic-Sadic S; Laosinchai-Wolf W; Huang YW; Ko TM; Abbott KM; Lemmink HH; Toivonen M; Schleutker J; Gentile C; Van Deerlin VM; Zhu H; Latham GJ J Mol Diagn; 2021 Jun; 23(6):753-764. PubMed ID: 33798739 [TBL] [Abstract][Full Text] [Related]
12. Universal fluorescent multiplex PCR and capillary electrophoresis for evaluation of gene conversion between SMN1 and SMN2 in spinal muscular atrophy. Wang CC; Jong YJ; Chang JG; Chen YL; Wu SM Anal Bioanal Chem; 2010 Jul; 397(6):2375-83. PubMed ID: 20563565 [TBL] [Abstract][Full Text] [Related]
13. [Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy]. Zhang YH; Zhang YQ; Zhu BS; He J; Wang L; Tang XH; Guo JJ; Jin CC; Chen H; Zhang J; Zhang JM; Li L Zhongguo Dang Dai Er Ke Za Zhi; 2019 Mar; 21(3):239-243. PubMed ID: 30907347 [TBL] [Abstract][Full Text] [Related]
14. [Quantitative analysis of the genes determining spinal muscular atrophy]. Nagymihály M; Herczegfalvi A; Tímár L; Karcagi V Ideggyogy Sz; 2009 Nov; 62(11-12):390-7. PubMed ID: 20025129 [TBL] [Abstract][Full Text] [Related]
16. SMN1 gene, but not SMN2, is a risk factor for sporadic ALS. Corcia P; Camu W; Halimi JM; Vourc'h P; Antar C; Vedrine S; Giraudeau B; de Toffol B; Andres CR; Neurology; 2006 Oct; 67(7):1147-50. PubMed ID: 16931506 [TBL] [Abstract][Full Text] [Related]
17. [Detection of homozygous deletions in spinal muscular atrophy with genomic DNA sequencing]. Cao YY; Qu YJ; Song F; Bai JL; Jin YW; Wang H; Li Y; Zhang WH Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):410-4. PubMed ID: 23926006 [TBL] [Abstract][Full Text] [Related]
18. A genetic and phenotypic analysis in Spanish spinal muscular atrophy patients with c.399_402del AGAG, the most frequently found subtle mutation in the SMN1 gene. Cuscó I; López E; Soler-Botija C; Jesús Barceló M; Baiget M; Tizzano EF Hum Mutat; 2003 Aug; 22(2):136-43. PubMed ID: 12872254 [TBL] [Abstract][Full Text] [Related]
19. Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: simultaneous detection of SMN1 and SMN2 deletion. Baris I; Etlik O; Koksal V; Arican-Baris ST Mol Cell Probes; 2010 Jun; 24(3):138-41. PubMed ID: 20025960 [TBL] [Abstract][Full Text] [Related]
20. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Wirth B Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]