<p>(A) Calcium staining using Alizarin Red S. No or only few calcium-positive fibers (arrowheads), indicative of abnormal elevated calcium level, were found in DM1 and control biopsies. Calcium deposits were abundant in the DMD sample. DMD muscle sections showed fatty tissue infiltration (asterisks) and fibrosis (stars), which were also detected in some of the DM1 patient biopsies. Scale bars indicate 100 μm. Results from only one of the three controls and three of the six examined DM1 patients are shown. All data are summarized in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0121556#pone.0121556.t002" target="_blank">Table 2</a>. (B) Dystrophin immunostaining. In contrast to the DMD patient biopsy, expression and l...
<p>In (A), intracellular calcium concentrations, [Ca<sup>2+</sup>]i, was assessed by measurement of ...
<p>Immunofluorescence intensities measured in pre-treatment biopsies of different patients with DMD ...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
Duchenne muscular dystrophy, primarily caused by a deficiency in the membrane cytoskeletal protein d...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease caused by toxic RNA from a DMPK gene carr...
<div><p>Myotonic Dystrophy type 1 (DM1) is a multisystemic disease caused by toxic RNA from a <i>DMP...
<p>(A) Representative images of quadriceps sections from DM1 mice and controls after injection with ...
<div><p>Duchenne muscular dystrophy (DMD) is characterized by the absence or reduced levels of dystr...
Duchenne muscular dystrophy (DMD) is characterized by the absence or reduced levels of dystrophin ex...
Abstract Background Duchenne muscular dystrophy (DMD) is a fatal, X-linked genetic disorder. Althoug...
<p><b>A.</b> Representative immunofluorescence images (1 of 10 images) from the tibialis anterior mu...
The present study had the objective of evaluating calcium accumulations in muscle fibers and their c...
1. Duchenne muscular dystrophy (DMD) is a lethal, degenerative muscle disease caused by a genetic mu...
Although the reduction in dystrophin-associated glycoproteins is the primary pathophysiological cons...
The cell biological hypothesis of Duchenne muscular dystrophy assumes that deficiency in the membran...
<p>In (A), intracellular calcium concentrations, [Ca<sup>2+</sup>]i, was assessed by measurement of ...
<p>Immunofluorescence intensities measured in pre-treatment biopsies of different patients with DMD ...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
Duchenne muscular dystrophy, primarily caused by a deficiency in the membrane cytoskeletal protein d...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease caused by toxic RNA from a DMPK gene carr...
<div><p>Myotonic Dystrophy type 1 (DM1) is a multisystemic disease caused by toxic RNA from a <i>DMP...
<p>(A) Representative images of quadriceps sections from DM1 mice and controls after injection with ...
<div><p>Duchenne muscular dystrophy (DMD) is characterized by the absence or reduced levels of dystr...
Duchenne muscular dystrophy (DMD) is characterized by the absence or reduced levels of dystrophin ex...
Abstract Background Duchenne muscular dystrophy (DMD) is a fatal, X-linked genetic disorder. Althoug...
<p><b>A.</b> Representative immunofluorescence images (1 of 10 images) from the tibialis anterior mu...
The present study had the objective of evaluating calcium accumulations in muscle fibers and their c...
1. Duchenne muscular dystrophy (DMD) is a lethal, degenerative muscle disease caused by a genetic mu...
Although the reduction in dystrophin-associated glycoproteins is the primary pathophysiological cons...
The cell biological hypothesis of Duchenne muscular dystrophy assumes that deficiency in the membran...
<p>In (A), intracellular calcium concentrations, [Ca<sup>2+</sup>]i, was assessed by measurement of ...
<p>Immunofluorescence intensities measured in pre-treatment biopsies of different patients with DMD ...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...