Results 71 to 80 of about 2,106 (149)
Foxo/Atrogin induction in human and experimental myositis
Skeletal muscle atrophy can occur rapidly in various fasting, cancerous, systemic inflammatory, deranged metabolic or neurogenic states. The ubiquitin ligase Atrogin-1 (MAFbx) is induced in animal models of these conditions, causing excessive myoprotein ...
Han-Kyu Lee +6 more
doaj +1 more source
Use of Janus Kinase Inhibitors in the Treatment of Genodermatoses: A Systematic Review
Introduction Genodermatoses are rare inherited skin disorders with limited treatment options. Emerging evidence suggests Janus kinase (JAK) inhibitors may offer therapeutic benefits by modulating underlying immune and inflammatory pathways. This study aims to systematically review the efficacy and safety of JAK inhibitors in treating genodermatoses ...
Pin-Chun Chen +4 more
wiley +1 more source
The idiopathic inflammatory myopathies (IM) represent a heterogeneous group of autoimmune diseases, of which dermatomyositis (DM), polymyositis (PM), and sporadic inclusion body myositis (IBM) are the most common.
Boel De Paepe +2 more
doaj +1 more source
Background: The risk of osteoporosis is known in myopathies requiring long-term steroid treatment and Pompe disease, but not in other hereditary myopathies or sporadic inclusion body myositis (sIBM).
F. Danckworth +3 more
doaj +1 more source
Serum-Circulating microRNAs in Sporadic Inclusion Body Myositis. [PDF]
Lucchini M +5 more
europepmc +1 more source
Idiopathic inflammatory myopathies (IIM) are a group of rare autoimmune diseases characterized by muscle weakness. IIMs are characterized by heterogeneity of manifestations and include several variants, each of which has peculiarities related to ...
A. A. Kolomeychuk +4 more
doaj +1 more source
The muscle-fiber phenotype of sporadic inclusion-body myositis (s-IBM), the most common muscle disease associated with aging, shares several pathological abnormalities with Alzheimer disease (AD) brain, including accumulation of amyloid-β 42 (Aβ42) and ...
Anna Nogalska +3 more
doaj +1 more source
Th1 response and systemic treg deficiency in inclusion body myositis.
ObjectiveSporadic inclusion body myositis (sIBM), the most frequent myositis in elderly patients, is characterized by the presence muscle inflammation and degeneration.
Yves Allenbach +16 more
doaj +1 more source
Autophagy (self-eating) is a conserved cellular degradation process that plays important roles in maintaining homeostasis and preventing nutritional, metabolic, and infection-mediated stresses.
Rekha Khandia +10 more
doaj +1 more source
Morphological and molecular comparison of HIV-associated and sporadic inclusion body myositis. [PDF]
Vogt S +16 more
europepmc +1 more source

