Results 161 to 170 of about 23,715 (235)

Unlocking the genetic blueprint of duchenne muscular dystrophy: A personalized approach with MLPA and WES. [PDF]

Glob Med Genet
Mathur P, Kaur A, Agarwal KK, Agarwal LK, Mathur A, Choudhary D.   +5 more
europepmc   +1 more source

Becker muscular dystrophy mice showed site-specific decay of type IIa fibers with capillary change in skeletal muscle. [PDF]

Elife
Miyazaki D, Sato M, Shiba N, Yoshizawa T, Nakamura A.   +4 more
europepmc   +1 more source

A <i>de novo TNNI3K</i> variant aggravates the pathogenicity of <i>DMD</i>-associated early-onset cardiomyopathy: a case report. [PDF]

Front Genet
Qie D, Zhai Y, Yang F, Li Y, Xu R.
europepmc   +1 more source

Distinct Patterns of Dystrophin Organization in Myocyte Sarcolemma and Transverse Tubules of Normal and Diseased Human Myocardium [PDF]

, 2000
Raffi Kaprielian, Shirley Stevenson, Stephen Rothery, Michael J. Cullen, Nicholas J. Severs   +4 more
openalex   +1 more source

Lost in Transition: Challenges in the Journey from Pediatric to Adult Care for a Romanian <i>DMD</i> Patient. [PDF]

Healthcare (Basel)
Lupu M, Marcu MA, Epure DA, Vladacenco OA, Severin EM, Teleanu RI.   +5 more
europepmc   +1 more source

Engineered human myogenic cells in hydrogels generate innervated vascularized myofibers within dystrophic mouse muscle on long-term engraftment. [PDF]

Cell Rep Med
Kowala A, Boot J, Meng J, Mein CA, Pourquié O, Connelly JT, Morgan JE, Lin YY.   +7 more
europepmc   +1 more source

Titin fragment is a sensitive biomarker in Duchenne muscular dystrophy model mice carrying full-length human dystrophin gene on human artificial chromosome. [PDF]

Sci Rep
Hiramuki Y, Hosokawa M, Osawa K, Shirakawa T, Watanabe Y, Hanajima R, Kugoh H, Awano H, Matsuo M, Kazuki Y.   +9 more
europepmc   +1 more source

Binding of LncDACH1 to dystrophin impairs the membrane trafficking of Nav1.5 protein and increases ventricular arrhythmia susceptibility. [PDF]

Elife
Xue G, Yang J, Zhang Y, Yang Y, Zhang R, Li D, Tian T, Li J, Zhang X, Li C, Li X, Yang J, Shen K, Guo Y, Liu X, Yang G, Xuan L, Shan H, Lu Y, Baofeng Y, Pan Z.   +20 more
europepmc   +1 more source

Incidental finding of a <i>DMD</i> exons 48-55 deletion during prenatal diagnosis. [PDF]

Front Pediatr
Zhang M, Lin Z, Chen M, Guo D, Yang Q, He Q, Mao B, Liang B, Chen L, Cai M, Huang H, Xu L.   +11 more
europepmc   +1 more source

Differential expression of dystrophin isoforms and utrophin during dibutyryl-cAMP-induced morphological differentiation of rat brain astrocytes

, 1998
Michihiro Imamura, Eijiro Ozawa
openalex   +1 more source