Results 111 to 120 of about 843 (162)

Muscle-specific gene editing improves molecular and phenotypic defects in a mouse model of myotonic dystrophy type 1. [PDF]

Clin Transl Med
Izzo M, Battistini J, Golini E, Voellenkle C, Provenzano C, Orsini T, Strimpakos G, Scavizzi F, Raspa M, Baci D, Frolova S, Tastsoglou S, Zaccagnini G, Garcia-Manteiga JM, Gourdon G, Mandillo S, Cardinali B, Martelli F, Falcone G.   +18 more
europepmc   +1 more source

Correction of RNA-Binding Protein CUGBP1 and GSK3β Signaling as Therapeutic Approach for Congenital and Adult Myotonic Dystrophy Type 1. [PDF]

Int J Mol Sci, 2019
Timchenko L.
europepmc   +1 more source

Amphiphilic Oligonucleotide Derivatives-Promising Tools for Therapeutics. [PDF]

Pharmaceutics
Bauer IA, Dmitrienko EV.
europepmc   +1 more source

Association of Sjögren's syndrome with myotonic dystrophy type 1. [PDF]

BMJ Case Rep, 2019
Kitsis EA, Napier F, Juthani V, Geyer HL.   +3 more
europepmc   +1 more source

Analysis of the DMPK gene CTG repeat in healthy Brazilians [PDF]

, 2007
Ashizawa T, Ashizawa T, Brook JD, Callegri-Jacques SM, Deka R, Gennarelli M, Goldman A, Harley HG, Harper PS, Lewis PO, Luiz Alves Duro, Pedro H. Cabello, Rodrigo Soares Moura-Neto, Siciliano G, Silvia Regina Sampaio Freitas, Tishkoff SA, Yamagata H, Zerylnick C   +17 more
core   +1 more source

A Patient with Myotonic Dystrophy Type 1 Presenting as Parkinsonism. [PDF]

J Mov Disord, 2018
Choi JH, Lee JY, Kim HJ, Jeon B.
europepmc   +1 more source

Is Cardiac Transplantation Still a Contraindication in Patients with Muscular Dystrophy-Related End-Stage Dilated Cardiomyopathy? A Systematic Review. [PDF]

Int J Mol Sci
Politano L.
europepmc   +1 more source

The expression of ion channel mRNAs in skeletal muscles from patients with myotonic muscular dystrophy [PDF]

キムラ, タカシ, 木村, 卓
core  

Expanded CTG repeats in myotonin protein kinase increase susceptibility to oxidative stress

NeuroReport, 1998
The effect of oxidative stress on myogenic cells with expanded CTG repeats in the myotonin protein kinase (MtPK) gene was investigated using MtPK cDNA-transformants in order to investigate the disease process underlying myotonic dystrophy. We employed methylmercury as a model for reagents that produce reactive oxygen species (ROS).
Shoichi Ishiura, Fusako Usuki
openaire   +4 more sources