Similar articles for PMID: 18078930

Year	Number of Results
1954	1
1957	2
1958	1
1997	1
1998	3
1999	12
2000	11
2001	28
2002	28
2003	30
2004	31
2005	43
2006	41
2007	58
2008	43
2009	23
2010	15
2011	9
2012	13
2013	8
2014	8
2015	12
2016	7
2017	19
2018	10
2019	8
2020	7
2021	5
2022	6
2023	4
2024	0

1

Genetic conversion of an SMN2 gene to SMN1: a novel approach to the treatment of spinal muscular atrophy.

DiMatteo D, Callahan S, Kmiec EB. DiMatteo D, et al. Exp Cell Res. 2008 Feb 15;314(4):878-86. doi: 10.1016/j.yexcr.2007.10.012. Epub 2007 Oct 24. Exp Cell Res. 2008. PMID: 18078930

2

Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy.

Thurmond J, Butchbach ME, Palomo M, Pease B, Rao M, Bedell L, Keyvan M, Pai G, Mishra R, Haraldsson M, Andresson T, Bragason G, Thosteinsdottir M, Bjornsson JM, Coovert DD, Burghes AH, Gurney ME, Singh J. Thurmond J, et al. J Med Chem. 2008 Feb 14;51(3):449-69. doi: 10.1021/jm061475p. Epub 2008 Jan 19. J Med Chem. 2008. PMID: 18205293

3

Stimulating full-length SMN2 expression by delivering bifunctional RNAs via a viral vector.

Baughan T, Shababi M, Coady TH, Dickson AM, Tullis GE, Lorson CL. Baughan T, et al. Mol Ther. 2006 Jul;14(1):54-62. doi: 10.1016/j.ymthe.2006.01.012. Epub 2006 Mar 31. Mol Ther. 2006. PMID: 16580882 Free article.

4

A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy.

Vezain M, Saugier-Veber P, Melki J, Toutain A, Bieth E, Husson M, Pedespan JM, Viollet L, Pénisson-Besnier I, Fehrenbach S, Bou J, Frébourg T, Tosi M. Vezain M, et al. Eur J Hum Genet. 2007 Oct;15(10):1054-62. doi: 10.1038/sj.ejhg.5201885. Epub 2007 Jul 4. Eur J Hum Genet. 2007. PMID: 17609673

5

Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test.

Su YN, Hung CC, Li H, Lee CN, Cheng WF, Tsao PN, Chang MC, Yu CL, Hsieh WS, Lin WL, Hsu SM. Su YN, et al. Hum Mutat. 2005 May;25(5):460-7. doi: 10.1002/humu.20160. Hum Mutat. 2005. PMID: 15832310

6

A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels.

Wolstencroft EC, Mattis V, Bajer AA, Young PJ, Lorson CL. Wolstencroft EC, et al. Hum Mol Genet. 2005 May 1;14(9):1199-210. doi: 10.1093/hmg/ddi131. Epub 2005 Mar 24. Hum Mol Genet. 2005. PMID: 15790598

7

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B. Sun Y, et al. Hum Mutat. 2005 Jan;25(1):64-71. doi: 10.1002/humu.20111. Hum Mutat. 2005. PMID: 15580564

8

Spinal muscular atrophy: from gene to therapy.

Wirth B, Brichta L, Hahnen E. Wirth B, et al. Semin Pediatr Neurol. 2006 Jun;13(2):121-31. doi: 10.1016/j.spen.2006.06.008. Semin Pediatr Neurol. 2006. PMID: 17027862 Review.

9

Diverse small-molecule modulators of SMN expression found by high-throughput compound screening: early leads towards a therapeutic for spinal muscular atrophy.

Jarecki J, Chen X, Bernardino A, Coovert DD, Whitney M, Burghes A, Stack J, Pollok BA. Jarecki J, et al. Hum Mol Genet. 2005 Jul 15;14(14):2003-18. doi: 10.1093/hmg/ddi205. Epub 2005 Jun 8. Hum Mol Genet. 2005. PMID: 15944201

10

Genetic study of SMA patients without homozygous SMN1 deletions: identification of compound heterozygotes and characterisation of novel intragenic SMN1 mutations.

Martín Y, Valero A, del Castillo E, Pascual SI, Hernández-Chico C. Martín Y, et al. Hum Genet. 2002 Mar;110(3):257-63. doi: 10.1007/s00439-002-0681-y. Epub 2002 Feb 8. Hum Genet. 2002. PMID: 11935338

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