Astronauts returning from space shuttle missions or the International Space Station have
been diagnosed with various health problems such as bone demineralization, muscle …

Centronuclear myopathies (CNM) are rare congenital disorders characterized by muscle
weakness and structural defects including fiber hypotrophy and organelle mispositioning …

Mitochondria–cytoskeleton interactions modulate cellular physiology by regulating
mitochondrial transport, positioning, and immobilization. However, there is very little …

The ability of a mitochondrion to undergo fission and fusion, and to be transported and
localized within a cell are central not just to proper functioning of mitochondria, but also to …

Mitochondrial dysfunction is considered the major contributor to skeletal muscle wasting in
different conditions. Genetically determined neuromuscular disorders occur as a result of …

Patients with pulmonary emphysema often develop locomotor muscle dysfunction, which is
independently associated with disability and higher mortality in that population. Muscle …

Simple Summary The objective of this study is to examine the effects of T-2 toxin (T-2) and
green tea powders (GTP) on growth performance, hematology, and pathology parameters in …

Introduction: Mitral regurgitation (MR) imposes volume overload on the left ventricle (LV) and
elevates wall stress, triggering its adverse remodeling. Pronounced LV dilation, minimal wall …

The desmin-associated protein myospryn, encoded by the cardiomyopathy-associated gene
5 (CMYA5), is a TRIM-like protein associated to the BLOC-1 (Biogenesis of Lysosomes …

Until recently restricted to hereditary mitochondrial diseases, mitochondrial dysfunction is
now recognized as a key player and strategic factor in the pathophysiological of many …