Results 31 to 40 of about 6,995 (226)

AMPK Phosphorylation Impacts Apoptosis in Differentiating Myoblasts Isolated from Atrophied Rat Soleus Muscle

open access: yesCells, 2023
Regrowth of atrophied myofibers depends on muscle satellite cells (SCs) that exist outside the plasma membrane. Muscle atrophy appears to result in reduced number of SCs due to apoptosis.
Natalia A. Vilchinskaya   +4 more
doaj   +1 more source

Gross anatomy of the intrinsic muscles of the scapular and humeral joint regions in crab-eating fox (Cerdocyon thous, Linnaeus 1776)

open access: yesActa Scientiarum: Biological Sciences, 2018
  The crab-eating fox (Cerdocyon thous) is a wild canid with a wide distribution in South America that is susceptible to traumas due to road kills - an event in which some specimens can survive.
Juan Fernando Velez-Garcia   +2 more
doaj   +1 more source

Altered expression of fragile X mental retardation-1 (FMR1) in the thymus in autoimmune myasthenia gravis

open access: yesJournal of Neuroinflammation, 2021
Predisposition to autoimmunity and inflammatory disorders is observed in patients with fragile X-associated syndromes. These patients have increased numbers of CGG triplets in the 5’ UTR region of FMR1 (Fragile X Mental Retardation 1) gene, that affects ...
Scott Thomas   +8 more
doaj   +1 more source

Single-cell mass cytometry on peripheral cells in Myasthenia Gravis identifies dysregulation of innate immune cells

open access: yesFrontiers in Immunology, 2023
Myasthenia Gravis (MG) is a neurological autoimmune disease characterized by disabling muscle weaknesses due to anti-acetylcholine receptor (AChR) autoantibodies.
Julien Verdier   +12 more
doaj   +1 more source

On the Myology of tlic Edentata.

open access: yesProceedings of the Zoological Society of London, 1899
(Uploaded by Plazi from the Biodiversity Heritage Library) No abstract provided.
Windle, Bertram C. A. (Bertram Coghill Alan),   +1 more
openaire   +3 more sources

Abstract | 002 | Muscle and brain dysfunction associated with modern (digital) critical care. Mechanisms and interventions

open access: yesEuropean Journal of Translational Myology
ations, emphasizing muscle-specific outcomes and translational myology applications. In pediatric patients with primary or neurological dysphagia, NMES improves suprahyoid, facial, and tongue muscle activation, enhances swallowing efficiency and reduces
Lars Larssson
doaj   +1 more source

Anatomical differences in three wing muscles of the Grey heron (Ardea cinerea), the Common buzzard (Buteo buteo) and the Common kestrel (Falco tinnunculus): a possible functional interpretation

open access: yesRivista Italiana di Ornitologia - Research in Ornithology, 2015
In this paper, a description of the coracobrachialis caudalis, the scapulotriceps and the extensor carpi radialis muscles is presented in three different species (Common kestrel, Common buzzard and Grey heron) that exhibit notably differing flight styles.
Marco Canova   +5 more
doaj   +1 more source

Need for NAD+: Focus on Striated Muscle Laminopathies

open access: yesCells, 2020
Laminopathies are a heterogeneous group of rare diseases caused by genetic mutations in the LMNA gene, encoding A-type lamins. A-type lamins are nuclear envelope proteins which associate with B-type lamins to form the nuclear lamina, a meshwork ...
Déborah Cardoso, Antoine Muchir
doaj   +1 more source

2020 Padua Muscle Days: Thirty years of translational research in Mobility Medicine

open access: yesEuropean Journal of Translational Myology, 2020
More that half-century of skeletal muscle research is continuing at the Padua University (Italy) under the auspices of the Interdepartmental Research Centre of Myology (CIR-Myo), the European Journal of Translational Myology (EJTM) and recently also with
Ugo Carraro
doaj   +1 more source

Safety and Tolerability of Givinostat: Evidence From Real‐World and Clinical Practice

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aim of our study was to establish the prevalence of adverse events in a real‐world setting in boys living with Duchenne muscular dystrophy (DMD) treated with givinostat as part of an Expanded Access Program (EAP) in Italy. Methods The cohort included 90 ambulant boys, with age when treatment started between 6 and 23 years (mean ...
Marika Pane   +19 more
wiley   +1 more source

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