Gladman JT - Search Results

1

Development of an AP-FRET based analysis for characterizing RNA-protein interactions in myotonic dystrophy (DM1).

Rehman S, Gladman JT, Periasamy A, Sun Y, Mahadevan MS. Rehman S, et al. Among authors: gladman jt. PLoS One. 2014 Apr 29;9(4):e95957. doi: 10.1371/journal.pone.0095957. eCollection 2014. PLoS One. 2014. PMID: 24781112 Free PMC article.

2

Age of onset of RNA toxicity influences phenotypic severity: evidence from an inducible mouse model of myotonic dystrophy (DM1).

Gladman JT, Mandal M, Srinivasan V, Mahadevan MS. Gladman JT, et al. PLoS One. 2013 Sep 5;8(9):e72907. doi: 10.1371/journal.pone.0072907. eCollection 2013. PLoS One. 2013. PMID: 24039817 Free PMC article.

3

TWEAK Regulates Muscle Functions in a Mouse Model of RNA Toxicity.

Yadava RS, Foff EP, Yu Q, Gladman JT, Zheng TS, Mahadevan MS. Yadava RS, et al. Among authors: gladman jt. PLoS One. 2016 Feb 22;11(2):e0150192. doi: 10.1371/journal.pone.0150192. eCollection 2016. PLoS One. 2016. PMID: 26901467 Free PMC article.

4

MBNL1 overexpression is not sufficient to rescue the phenotypes in a mouse model of RNA toxicity.

Yadava RS, Kim YK, Mandal M, Mahadevan K, Gladman JT, Yu Q, Mahadevan MS. Yadava RS, et al. Among authors: gladman jt. Hum Mol Genet. 2019 Jul 15;28(14):2330-2338. doi: 10.1093/hmg/ddz065. Hum Mol Genet. 2019. PMID: 30997488 Free PMC article.

5

NKX2-5, a modifier of skeletal muscle pathology due to RNA toxicity.

Gladman JT, Yadava RS, Mandal M, Yu Q, Kim YK, Mahadevan MS. Gladman JT, et al. Hum Mol Genet. 2015 Jan 1;24(1):251-64. doi: 10.1093/hmg/ddu443. Epub 2014 Aug 28. Hum Mol Genet. 2015. PMID: 25168381 Free PMC article.

6

TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy.

Yadava RS, Foff EP, Yu Q, Gladman JT, Kim YK, Bhatt KS, Thornton CA, Zheng TS, Mahadevan MS. Yadava RS, et al. Among authors: gladman jt. Hum Mol Genet. 2015 Apr 1;24(7):2035-48. doi: 10.1093/hmg/ddu617. Epub 2014 Dec 11. Hum Mol Genet. 2015. PMID: 25504044 Free PMC article.

7

A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype.

Gladman JT, Bebee TW, Edwards C, Wang X, Sahenk Z, Rich MM, Chandler DS. Gladman JT, et al. Hum Mol Genet. 2010 Nov 1;19(21):4239-52. doi: 10.1093/hmg/ddq343. Epub 2010 Aug 12. Hum Mol Genet. 2010. PMID: 20705738 Free PMC article.

8

Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype.

Pierson CR, Dulin-Smith AN, Durban AN, Marshall ML, Marshall JT, Snyder AD, Naiyer N, Gladman JT, Chandler DS, Lawlor MW, Buj-Bello A, Dowling JJ, Beggs AH. Pierson CR, et al. Among authors: gladman jt. Hum Mol Genet. 2012 Feb 15;21(4):811-25. doi: 10.1093/hmg/ddr512. Epub 2011 Nov 7. Hum Mol Genet. 2012. PMID: 22068590 Free PMC article.

9

Intron 7 conserved sequence elements regulate the splicing of the SMN genes.

Gladman JT, Chandler DS. Gladman JT, et al. Hum Genet. 2009 Dec;126(6):833-41. doi: 10.1007/s00439-009-0733-7. Hum Genet. 2009. PMID: 19701774 Free PMC article.

10

Splicing of the Survival Motor Neuron genes and implications for treatment of SMA.

Bebee TW, Gladman JT, Chandler DS. Bebee TW, et al. Among authors: gladman jt. Front Biosci (Landmark Ed). 2010 Jun 1;15(3):1191-1204. doi: 10.2741/3670. Front Biosci (Landmark Ed). 2010. PMID: 20515750 Free PMC article. Review.

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