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We report here the identification of an apparent zebrafish orthologue of the human dystrophin gene that expresses a 400-kDa protein that is localised to the muscle membrane surface.
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This signaling is usually done on muscle cell receptors that are located at the membrane surface of the muscle cell.
Muscular tension, mitochondria volume density (Vv) and compared membrane surface (δm) of the four muscles were significantly lower in COPD + Saline group compared to Control + Saline group, while fatigue index, mitochondria surface area, Bnip3 and Cyto C were higher (P < 0.05).
So, at least in some of usual preys of the cobra hunt (like rats, bird eggs, etc)., blood and muscle cells contain small or even considerable amounts of PS on their outer membrane surface.
Diverse laboratory conditions have been used in surface electromyography (sEMG) studies in order to gain insights into the neural regulatory strategies and muscle membrane alterations.
In mammals, the membrane-associated network of surface proteins known as dystrophin glycoprotein complex (DGC) helps maintain plasma membrane integrity by stabilizing the muscle membrane and limiting any physical damage caused by contraction.
Electrophysiological results indicate nonexcitable muscle membrane, but not necessarily ICUAW.
Duchenne muscular dystrophy is a lethal X-linked muscle disease resulting from a defect in the muscle membrane protein dystrophin.
The absence of dystrophin leads to muscle membrane fragility, muscle death (necrosis) and eventual replacement of skeletal muscle by fat and fibrous connective tissue.
Peptide-induced membrane permeabilization follows binding to the membrane surface.
This marked reduction is necessary to affect muscle membrane repair.
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