Study on skeletal muscle dystrophin and neuromuscular junction in adult and young mdx mice
<p><strong>Objective</strong> To observe the skeletal muscle dystrophin expression and neuromuscular junction (NMJ) morphology in adult and young mdx mice. <strong>Methods </strong> Select eight 8-week-old specific pathogen free (SPF) C57BL/6 mice, four 8-week-old adul...
Main Authors: | Yu-ling ZHU, Yi-ming SUN, Hui-li ZHANG, Yu ZHANG, Ya-qin LI, Meng-long CHEN, Liang WANG, Cheng ZHANG |
---|---|
Format: | Article |
Language: | English |
Published: |
Tianjin Huanhu Hospital
2015-05-01
|
Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
Subjects: | |
Online Access: | http://www.cjcnn.org/index.php/cjcnn/article/view/1192 |
Similar Items
-
Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in mdx Mice
by: Timothy M. Moore, et al.
Published: (2020-06-01) -
Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles
by: Sandra Murphy, et al.
Published: (2015-09-01) -
Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies
by: Elisabeth Le Rumeur
Published: (2015-07-01) -
Expression of dystrophin-glycoprotein complex at the skeletal muscle sarcolemma in Duchenne muscular dystrophy
by: Lei ZHAO, et al.
Published: (2015-06-01) -
Peptide Nucleic Acid Promotes Systemic Dystrophin Expression and Functional Rescue in Dystrophin-deficient mdx Mice
by: Xianjun Gao, et al.
Published: (2015-01-01)