Results 271 to 280 of about 796,652 (317)
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MUSCLE ACTIVITY and MUSCLE PROTEINS
Biological Reviews, 1950Summary1. If it were experimentally possible to examine muscle extracts made during defined phases of the contraction cycle, the relation of muscular work to changes in the composition of such extracts might then be elucidated. The changes of normal muscle proteins in relation to muscular function, could then be considered from a truly physiological ...
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Muscle Spindles in the Digastric Muscle of the Rabbit
Journal of Dental Research, 1988The digastric muscle of the rabbit was studied for the presence of muscle spindles. One of the 19 adult digastric muscles we examined contained in excess of 12 spindles scattered throughout the belly. No spindles were found in the contralateral muscle, or in any of the digastric muscles from other animals. Although jaw depressor muscles of most mammals
Z F, Muhl, O, Kotov
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Water in normal muscle and muscle with a tumor
Biochimica et Biophysica Acta (BBA) - General Subjects, 1975The total water content, the amount of non-freezable water, and the Na-+ and K-+ contents in the gastrocnemius muscle of albino mice with and without a solid tumor were determined. The spin-lattice relaxation time (T1) for the water protons in the two kinds of muscle were measured at six resonance frequencies ranging from 4.5 to 60 MHz over the ...
Fung, B M +5 more
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Continuum, 2006
In recent years the term CHANNELOPATHY has been adopted to describe neurological disorders caused by mutations in different ion channel genes. Myopathic channelopathies include two main groups: nondystrophic myotonias and periodic paralyses. This article reviews the clinical features, diagnostic approach, molecular causes, and management of patients ...
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In recent years the term CHANNELOPATHY has been adopted to describe neurological disorders caused by mutations in different ion channel genes. Myopathic channelopathies include two main groups: nondystrophic myotonias and periodic paralyses. This article reviews the clinical features, diagnostic approach, molecular causes, and management of patients ...
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Journal of Inherited Metabolic Disease, 1990
SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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Muscle spindles in the mylohyoid muscle of rats
International Journal of Oral and Maxillofacial Surgery, 1992The mylohyoid muscle has several functions in relation to respiration, deglutition, and phonation, but these functions are not fully understood. The interaction of the mylohyoid nerve and muscle in 25 rats was studied by neurophysiologic and histologic methods.
M, Yamaoka +4 more
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Muscle Filament Structure and Muscle Contraction
Annual Review of Biophysics and Bioengineering, 1975Research into the mechanism of muscle contraction has reached a very intriguing stage. It now seems likely that all types of muscle may operate in basically the same way. But despite the present detailed knowledge of the molecular arrangements in certain muscles, the precise way in which a muscle generates force is still a mystery. According to the now
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Dystrobrevins in muscle and non-muscle tissues
Neuromuscular Disorders, 2007The alpha- and beta-dystrobrevins belong to the family of dystrophin-related and dystrophin-associated proteins. As constituents of the dystrophin-associated protein complex, alpha-dystrobrevin was believed to have a role predominantly in muscles and beta-dystrobrevin in non-muscle tissues.
Rees, M., Lien, Chun, Gorecki, Darek
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Muscle Contraction and Fibrous Muscle Proteins
1952Publisher Summary This chapter deals with the contraction of different kinds of muscle that show differences with respect to the amount of tension developed, the maximum shortening, the rate of shortening, and the fuel requirement. These differences not only reflect the varying levels of evolutionary development, but also a considerable adaptation to
H H, WEBER, H, PORTZEHL
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Muscle physiology in spasticity and muscle stiffness
ToxiconThis paper examines the physiological changes in spastic muscles contributing to spasticity and muscle stiffness, focusing on the underlying mechanisms and their clinical implications. Spasticity, which is prevalent in neurological conditions such as multiple sclerosis, cerebral palsy, spinal cord injury, stroke, and traumatic brain injury, is ...
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