Similar articles for PMID: 28624222

Year	Number of Results
2000	1
2001	4
2002	2
2003	3
2004	3
2005	3
2006	3
2007	4
2008	3
2009	1
2010	4
2011	6
2012	8
2013	11
2014	9
2015	16
2016	6
2017	12
2018	10
2019	16
2020	13
2021	12
2022	15
2023	13
2024	1

1

Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice.

Jauvin D, Chrétien J, Pandey SK, Martineau L, Revillod L, Bassez G, Lachon A, MacLeod AR, Gourdon G, Wheeler TM, Thornton CA, Bennett CF, Puymirat J. Jauvin D, et al. Mol Ther Nucleic Acids. 2017 Jun 16;7:465-474. doi: 10.1016/j.omtn.2017.05.007. Epub 2017 May 17. Mol Ther Nucleic Acids. 2017. PMID: 28624222 Free PMC article.

2

Small Molecules Which Improve Pathogenesis of Myotonic Dystrophy Type 1.

López-Morató M, Brook JD, Wojciechowska M. López-Morató M, et al. Front Neurol. 2018 May 18;9:349. doi: 10.3389/fneur.2018.00349. eCollection 2018. Front Neurol. 2018. PMID: 29867749 Free PMC article. Review.

3

Molecular Effects of the CTG Repeats in Mutant Dystrophia Myotonica Protein Kinase Gene.

Llamusí B, Artero R. Llamusí B, et al. Curr Genomics. 2008 Dec;9(8):509-16. doi: 10.2174/138920208786847944. Curr Genomics. 2008. PMID: 19516957 Free PMC article.

4

Systemic therapy in an RNA toxicity mouse model with an antisense oligonucleotide therapy targeting a non-CUG sequence within the DMPK 3'UTR RNA.

Yadava RS, Yu Q, Mandal M, Rigo F, Bennett CF, Mahadevan MS. Yadava RS, et al. Hum Mol Genet. 2020 Jun 3;29(9):1440-1453. doi: 10.1093/hmg/ddaa060. Hum Mol Genet. 2020. PMID: 32242217 Free PMC article.

5

Enhanced Delivery of Ligand-Conjugated Antisense Oligonucleotides (C16-HA-ASO) Targeting Dystrophia Myotonica Protein Kinase Transcripts for the Treatment of Myotonic Dystrophy Type 1.

Ait Benichou S, Jauvin D, De Serres-Bérard T, Bennett F, Rigo F, Gourdon G, Boutjdir M, Chahine M, Puymirat J. Ait Benichou S, et al. Hum Gene Ther. 2022 Aug;33(15-16):810-820. doi: 10.1089/hum.2022.069. Hum Gene Ther. 2022. PMID: 35794764

6

Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.

Huguet A, Medja F, Nicole A, Vignaud A, Guiraud-Dogan C, Ferry A, Decostre V, Hogrel JY, Metzger F, Hoeflich A, Baraibar M, Gomes-Pereira M, Puymirat J, Bassez G, Furling D, Munnich A, Gourdon G. Huguet A, et al. PLoS Genet. 2012;8(11):e1003043. doi: 10.1371/journal.pgen.1003043. Epub 2012 Nov 29. PLoS Genet. 2012. PMID: 23209425 Free PMC article.

7

Short antisense-locked nucleic acids (all-LNAs) correct alternative splicing abnormalities in myotonic dystrophy.

Wojtkowiak-Szlachcic A, Taylor K, Stepniak-Konieczna E, Sznajder LJ, Mykowska A, Sroka J, Thornton CA, Sobczak K. Wojtkowiak-Szlachcic A, et al. Nucleic Acids Res. 2015 Mar 31;43(6):3318-31. doi: 10.1093/nar/gkv163. Epub 2015 Mar 9. Nucleic Acids Res. 2015. PMID: 25753670 Free PMC article.

8

Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice.

Lo Scrudato M, Poulard K, Sourd C, Tomé S, Klein AF, Corre G, Huguet A, Furling D, Gourdon G, Buj-Bello A. Lo Scrudato M, et al. Mol Ther. 2019 Aug 7;27(8):1372-1388. doi: 10.1016/j.ymthe.2019.05.021. Epub 2019 Jun 5. Mol Ther. 2019. PMID: 31253581 Free PMC article.

9

Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development.

Michel L, Huguet-Lachon A, Gourdon G. Michel L, et al. PLoS One. 2015 Sep 4;10(9):e0137620. doi: 10.1371/journal.pone.0137620. eCollection 2015. PLoS One. 2015. PMID: 26339785 Free PMC article.

10

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

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