Results 41 to 50 of about 255,284 (355)

Novel individualized power training protocol preserves physical function in adult and older mice [PDF]

open access: yes, 2019
Sarcopenia, the age-related loss of muscle mass and strength, contributes to frailty, functional decline, and reduced quality of life in older adults. Exercise is a recognized therapy for sarcopenia and muscle dysfunction, though not a cure. Muscle power
Fandrey, Katie R.   +2 more
core   +1 more source

Hoff Mann′s syndrome with unusually long duration: Report on clinical, laboratory and muscle imaging findings in two cases

open access: yesAnnals of Indian Academy of Neurology, 2014
Two adult men presented with the rare Hoffmann′s syndrome (HS). Case 1: A 35-year-old male patient had progressive stiffness of lower limbs of 13 years and generalized muscle hypertrophy and myalgia of 3 years duration.
Atchayaram Nalini   +3 more
doaj   +1 more source

Rag GTPases are cardioprotective by regulating lysosomal function. [PDF]

open access: yes, 2014
The Rag family proteins are Ras-like small GTPases that have a critical role in amino-acid-stimulated mTORC1 activation by recruiting mTORC1 to lysosome.
Guan, Kun-Liang   +8 more
core   +2 more sources

Bone Geometry Is Altered by Follistatin‐Induced Muscle Growth in Young Adult Male Mice

open access: yesJBMR Plus, 2021
The development of the musculoskeletal system and its maintenance depends on the reciprocal relationship between muscle and bone. The size of skeletal muscles and the forces generated during muscle contraction are potent sources of mechanical stress on ...
Audrey S M Chan   +8 more
doaj   +1 more source

Progression of myopathology in Kearns-Sayre syndrome [PDF]

open access: yes, 1992
We report on the progression of myopathology by comparing two biopsies from a patient with a Kearns-Sayre-Syndrome. The first biopsy was taken in 1979 and showed 10% ragged-red fibers.
B. Meurers   +11 more
core   +1 more source

Unusual Case of Masseter Muscle Hypertrophy in Adolescence—Case Report and Literature Overview

open access: yesDiagnostics, 2022
Unilateral hypertrophy of the masseter muscle is a very rare pathological entity in children. Its etiology is uncertain and it requires a high degree of suspicion, as it must be differentiated from other conditions of the masseter area.
Elena Ţarcă   +8 more
doaj   +1 more source

Muscle hypertrophy in myotonia congenita [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 2003
A 28 year old male presented to our neurology service with stiffness of a few years’ duration in all muscles. The stiffness was maximum at the onset of exercise and his muscles loosened up after some time. He had no difficulty in releasing his grip after holding an object. He had very well developed muscles in spite …
B, Varkey, L, Varkey
openaire   +2 more sources

Roles played by protein metabolism and myogenic progenitor cells in exercise-induced muscle hypertrophy and their relation to resistance training regimens

open access: yesJournal of Physical Fitness and Sports Medicine, 2012
To learn the mechanisms underlying resistance exercise-induced muscle hypertrophy, recent studies on muscle protein metabolism and myogenic progenitor cells were reviewed. Numerous studies have suggested that activation of the translation process plays a
Naokata Ishii   +3 more
doaj   +1 more source

miRNA transcriptome and myofiber characteristics of lamb skeletal muscle during hypertrophic growth1

open access: yesFrontiers in Genetics, 2022
Postnatal muscle growth is achieved through hypertrophy of the muscle fibers and is impacted by the activity of satellite cells, the quiescent muscle stem cell.
M. A. Greene   +5 more
doaj   +1 more source

INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano   +27 more
wiley   +1 more source

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