Calcium ion in skeletal muscle: its crucial role for muscle function, plasticity, and disease

MW Berchtold, H Brinkmeier… - Physiological …, 2000 - journals.physiology.org
Mammalian skeletal muscle shows an enormous variability in its functional features such as
rate of force production, resistance to fatigue, and energy metabolism, with a wide spectrum …

Dysregulation of calcium homeostasis in muscular dystrophies

A Vallejo-Illarramendi, I Toral-Ojeda… - Expert reviews in …, 2014 - cambridge.org
Muscular dystrophies are a group of diseases characterised by the primary wasting of
skeletal muscle, which compromises patient mobility and in the most severe cases originate …

Meat quality of the longissimus lumborum muscle of Casertana and Large White pigs: Metabolomics and proteomics intertwined

C Marrocco, V Zolla, L Zolla - Journal of proteomics, 2011 - Elsevier
Longissimus lumborum muscles from high fat-deposing Casertana and lean meat Large
White pigs were assayed for meat quality parameters, including early and ultimate post …

Mitochondrial calcium increase induced by RyR1 and IP3R channel activation after membrane depolarization regulates skeletal muscle metabolism

AR Díaz-Vegas, A Cordova, D Valladares… - Frontiers in …, 2018 - frontiersin.org
Aim: We hypothesize that both type-1 ryanodine receptor (RyR1) and IP3-receptor (IP3R)
calcium channels are necessary for the mitochondrial Ca2+ increase caused by membrane …

Drastic reduction of calsequestrin-like proteins and impaired calcium binding in dystrophic mdx muscle

K Culligan, N Banville, P Dowling… - Journal of applied …, 2002 - journals.physiology.org
Although the reduction in dystrophin-associated glycoproteins is the primary
pathophysiological consequence of the deficiency in dystrophin, little is known about the …

Subproteomics analysis of Ca2+‐binding proteins demonstrates decreased calsequestrin expression in dystrophic mouse skeletal muscle

P Doran, P Dowling, J Lohan… - European Journal of …, 2004 - Wiley Online Library
Duchenne muscular dystrophy represents one of the most common hereditary diseases.
Abnormal ion handling is believed to render dystrophin‐deficient muscle fibres more …

Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging

F Chevessier, I Marty, M Paturneau-Jouas… - Neuromuscular …, 2004 - Elsevier
Tubular aggregates are observed in various muscle disorders and appear as densely
packed tubules believed to arise from sarcoplasmic reticulum of striated muscle. They are …

Proteomics and Transcriptomics Investigation on longissimus Muscles in Large White and Casertana Pig Breeds

L Murgiano, A D'Alessandro, MG Egidi… - Journal of proteome …, 2010 - ACS Publications
Consumer complaints against the blandness of modern lean meat and the frequent
reference to the more strongly flavored meat that was available years ago have prompted …

Proteomic profiling of impaired excitation–contraction coupling and abnormal calcium handling in muscular dystrophy

P Dowling, S Gargan, D Swandulla, K Ohlendieck - Proteomics, 2022 - Wiley Online Library
The X‐linked inherited neuromuscular disorder Duchenne muscular dystrophy is
characterised by primary abnormalities in the membrane cytoskeletal component dystrophin …

Sex differences in neuromuscular and biological determinants of isometric maximal force

G Giuriato, MG Romanelli, D Bartolini… - Acta …, 2024 - Wiley Online Library
Aim Force expression is characterized by an interplay of biological and molecular
determinants that are expected to differentiate males and females in terms of maximal …