Swanson MS - Search Results

1

Intron retention induced by microsatellite expansions as a disease biomarker.

Sznajder ŁJ, Thomas JD, Carrell EM, Reid T, McFarland KN, Cleary JD, Oliveira R, Nutter CA, Bhatt K, Sobczak K, Ashizawa T, Thornton CA, Ranum LPW, Swanson MS. Sznajder ŁJ, et al. Among authors: swanson ms. Proc Natl Acad Sci U S A. 2018 Apr 17;115(16):4234-4239. doi: 10.1073/pnas.1716617115. Epub 2018 Apr 2. Proc Natl Acad Sci U S A. 2018. PMID: 29610297 Free PMC article.

2

Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice.

Roberts R, Timchenko NA, Miller JW, Reddy S, Caskey CT, Swanson MS, Timchenko LT. Roberts R, et al. Among authors: swanson ms. Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13221-6. doi: 10.1073/pnas.94.24.13221. Proc Natl Acad Sci U S A. 1997. PMID: 9371827 Free PMC article.

3

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.

Miller JW, Urbinati CR, Teng-Umnuay P, Stenberg MG, Byrne BJ, Thornton CA, Swanson MS. Miller JW, et al. Among authors: swanson ms. EMBO J. 2000 Sep 1;19(17):4439-48. doi: 10.1093/emboj/19.17.4439. EMBO J. 2000. PMID: 10970838 Free PMC article.

4

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, Henderson D, Schalling M, Swanson MS, Thornton CA. Mankodi A, et al. Among authors: swanson ms. Hum Mol Genet. 2001 Sep 15;10(19):2165-70. doi: 10.1093/hmg/10.19.2165. Hum Mol Genet. 2001. PMID: 11590133 Free article.

5

A muscleblind knockout model for myotonic dystrophy.

Kanadia RN, Johnstone KA, Mankodi A, Lungu C, Thornton CA, Esson D, Timmers AM, Hauswirth WW, Swanson MS. Kanadia RN, et al. Among authors: swanson ms. Science. 2003 Dec 12;302(5652):1978-80. doi: 10.1126/science.1088583. Science. 2003. PMID: 14671308

6

Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2.

Mankodi A, Teng-Umnuay P, Krym M, Henderson D, Swanson M, Thornton CA. Mankodi A, et al. Ann Neurol. 2003 Dec;54(6):760-8. doi: 10.1002/ana.10763. Ann Neurol. 2003. PMID: 14681885

7

Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons.

Jiang H, Mankodi A, Swanson MS, Moxley RT, Thornton CA. Jiang H, et al. Among authors: swanson ms. Hum Mol Genet. 2004 Dec 15;13(24):3079-88. doi: 10.1093/hmg/ddh327. Epub 2004 Oct 20. Hum Mol Genet. 2004. PMID: 15496431

8

Nuclear RNA foci in the heart in myotonic dystrophy.

Mankodi A, Lin X, Blaxall BC, Swanson MS, Thornton CA. Mankodi A, et al. Among authors: swanson ms. Circ Res. 2005 Nov 25;97(11):1152-5. doi: 10.1161/01.RES.0000193598.89753.e3. Epub 2005 Oct 27. Circ Res. 2005. PMID: 16254211

9

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.

Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA. Lin X, et al. Among authors: swanson ms. Hum Mol Genet. 2006 Jul 1;15(13):2087-97. doi: 10.1093/hmg/ddl132. Epub 2006 May 22. Hum Mol Genet. 2006. PMID: 16717059

10

Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy.

Kanadia RN, Shin J, Yuan Y, Beattie SG, Wheeler TM, Thornton CA, Swanson MS. Kanadia RN, et al. Among authors: swanson ms. Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11748-53. doi: 10.1073/pnas.0604970103. Epub 2006 Jul 24. Proc Natl Acad Sci U S A. 2006. PMID: 16864772 Free PMC article.

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