Similar articles for PMID: 24354850

Year	Number of Results
1954	1
1967	1
2003	1
2004	4
2005	5
2006	6
2007	8
2008	8
2009	10
2010	9
2011	12
2012	17
2013	10
2014	17
2015	13
2016	9
2017	10
2018	9
2019	11
2020	17
2021	12
2022	10
2023	8
2024	0

1

Transcriptionally correlated subcellular dynamics of MBNL1 during lens development and their implication for the molecular pathology of myotonic dystrophy type 1.

Coleman SM, Prescott AR, Sleeman JE. Coleman SM, et al. Biochem J. 2014 Mar 1;458(2):267-80. doi: 10.1042/BJ20130870. Biochem J. 2014. PMID: 24354850 Free article.

2

Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.

Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA. Ho TH, et al. J Cell Sci. 2005 Jul 1;118(Pt 13):2923-33. doi: 10.1242/jcs.02404. Epub 2005 Jun 16. J Cell Sci. 2005. PMID: 15961406

3

MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.

de Haro M, Al-Ramahi I, De Gouyon B, Ukani L, Rosa A, Faustino NA, Ashizawa T, Cooper TA, Botas J. de Haro M, et al. Hum Mol Genet. 2006 Jul 1;15(13):2138-45. doi: 10.1093/hmg/ddl137. Epub 2006 May 24. Hum Mol Genet. 2006. PMID: 16723374

4

Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).

Santoro M, Modoni A, Masciullo M, Gidaro T, Broccolini A, Ricci E, Tonali PA, Silvestri G. Santoro M, et al. Exp Mol Pathol. 2010 Oct;89(2):158-68. doi: 10.1016/j.yexmp.2010.05.007. Epub 2010 Jun 1. Exp Mol Pathol. 2010. PMID: 20685272

5

Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2.

Cardani R, Mancinelli E, Rotondo G, Sansone V, Meola G. Cardani R, et al. Eur J Histochem. 2006 Jul-Sep;50(3):177-82. Eur J Histochem. 2006. PMID: 16920640 Free article.

6

Gain of RNA function in pathological cases: Focus on myotonic dystrophy.

Klein AF, Gasnier E, Furling D. Klein AF, et al. Biochimie. 2011 Nov;93(11):2006-12. doi: 10.1016/j.biochi.2011.06.028. Epub 2011 Jul 13. Biochimie. 2011. PMID: 21763392 Review.

7

Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy.

Mootha VV, Hansen B, Rong Z, Mammen PP, Zhou Z, Xing C, Gong X. Mootha VV, et al. Invest Ophthalmol Vis Sci. 2017 Sep 1;58(11):4579-4585. doi: 10.1167/iovs.17-22350. Invest Ophthalmol Vis Sci. 2017. PMID: 28886202 Free PMC article.

8

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. 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

9

Muscleblind-like 1 knockout mice reveal novel splicing defects in the myotonic dystrophy brain.

Suenaga K, Lee KY, Nakamori M, Tatsumi Y, Takahashi MP, Fujimura H, Jinnai K, Yoshikawa H, Du H, Ares M Jr, Swanson MS, Kimura T. Suenaga K, et al. PLoS One. 2012;7(3):e33218. doi: 10.1371/journal.pone.0033218. Epub 2012 Mar 13. PLoS One. 2012. PMID: 22427994 Free PMC article.

10

Overexpression of MBNL1 fetal isoforms and modified splicing of Tau in the DM1 brain: two individual consequences of CUG trinucleotide repeats.

Dhaenens CM, Schraen-Maschke S, Tran H, Vingtdeux V, Ghanem D, Leroy O, Delplanque J, Vanbrussel E, Delacourte A, Vermersch P, Maurage CA, Gruffat H, Sergeant A, Mahadevan MS, Ishiura S, Buée L, Cooper TA, Caillet-Boudin ML, Charlet-Berguerand N, Sablonnière B, Sergeant N. Dhaenens CM, et al. Exp Neurol. 2008 Apr;210(2):467-78. doi: 10.1016/j.expneurol.2007.11.020. Epub 2007 Dec 4. Exp Neurol. 2008. PMID: 18177861

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