Results 291 to 300 of about 110,072 (307)

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort

Human Mutation, 2009
Kevin M Flanigan, Payam Soltanzadeh, Anne M Connolly   +2 more
exaly  

Antagonism between DNA hypermethylation and enhancer-blocking activity at the H19 DMD is uncovered by CpG mutations

Nature Genetics, 2004
Nora Engel, Adam G West, Gary Felsenfeld
exaly  

Pharmacological strategies for muscular dystrophy

Nature Reviews Drug Discovery, 2003
Tejvir S Khurana, Kay E Davies
exaly  

DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulate in vitro Human Cardiac Pathophysiology

Frontiers in Bioengineering and Biotechnology, 2020
Sarka Jelinkova, Aleksandra Vilotic, Jan Pribyl   +2 more
exaly  

Protein sequence of DMD gene is related to actin-binding domain of α-actinin

Cell, 1987
Glenn Hammonds
exaly  

Porcine Zygote Injection with Cas9/sgRNA Results in DMD-Modified Pig with Muscle Dystrophy

International Journal of Molecular Sciences, 2016
Hong-Ye Zhao, Hong-Jiang Wei
exaly  

Dystrophin (DMD)

Science-Business eXchange, 2013
openaire   +1 more source

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

Human Mutation, 2009
Sylvie Tuffery-Giraud, Christophe Beroud, Rabah Ben Yaou   +2 more
exaly  

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

Human Mutation, 2007
Christophe Beroud, Sylvie Tuffery-Giraud, Masafumi Matsuo   +2 more
exaly  

Exons 45–55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene

Molecular Therapy, 2019
Yusuke Echigoya, Kenji Rowel Q Lim, Rika Maruyama   +2 more
exaly