Results 111 to 120 of about 37,729 (256)
Temporal Bayesian classifiers for modelling muscular dystrophy expression data [PDF]
The analysis of microarray data from time-series experiments requires specialised algorithms, which take the temporal ordering of the data into account. In this paper we explore a new architecture of Bayesian classifier that can be used to understand how
Hoen, PAC't +3 more
core
Polygala cyparissias is a plant widespread in Southern Latin America. Recently, we demonstrated the gastroprotective activity of the extract, as well as for one of the isolated metabolites-1,7-dihydroxy-2,3-methylenedioxyxanthone (MDX).
Luiz Carlos Klein-Júnior +3 more
doaj +1 more source
Altered nuclear dynamics in MDX myofibers
Duchenne muscular dystrophy (DMD) is a genetic disorder in which the absence of dystrophin leads to progressive muscle degeneration and weakness. Although the genetic basis is known, the pathophysiology of dystrophic skeletal muscle remains unclear.
Shama R. Iyer +7 more
openaire +3 more sources
3D Topological Inorganic Electrides: Screening, Properties, and Applications
In inorganic electrides, zero‐, one‐, and two‐dimensional (0D, 1D, and 2D) interstitial anionic electrons interconnect within lattice cavities, collectively forming a three‐dimensional (3D) network, further coupling magnetism and topological features, leading to the emergence of 3D topological inorganic electrides.
Zhenzhou Guo +8 more
wiley +1 more source
Hybrid Passive Control Strategies for Reducing the Displacements at the Base of Seismic Isolated Structures [PDF]
In this paper, the use of hybrid passive control strategies to mitigate the seismic response of a base-isolated structure is examined. The control performance of three different types of devices used for reducing base displacements of isolated buildings ...
Di Matteo A., Masnata C., Pirrotta A.
core +1 more source
Sildenafil Ameliorates Cardiomyopathy in mdx Mice
Duchenne muscular dystrophy (DMD) is the most prevalent type of muscular dystrophy and is the result of an X‐linked mutation in the dystrophin gene. The progression of skeletal muscle damage is rapid in DMD patients and cardiomyopathy soon follows. We have investigated whether or not sildenafil citrate, a phosphodiesterase 5 (PDE5) inhibitor, can be ...
Heidi Gray +5 more
openaire +2 more sources
MyomiRs Expression in Limb Girdle Muscular Dystrophy
ABSTRACT This manuscript is a comprehensive review focused on the role of microRNAs (miRs)—short RNA molecules—in Limb Girdle Muscular Dystrophy (LGMD). LGMD encompasses various and heterogeneous rare genetic neuromuscular diseases, characterized by the progressive wasting and deterioration of muscle fibers, predominantly affecting the pelvic and ...
G. Breveglieri +7 more
wiley +1 more source
High energy‐conversion efficiency (ZT) of thermoelectric materials has been achieved in heavy metal chalcogenides, but the use of toxic Pb or Te is an obstacle for wide applications of thermoelectricity.
Xinyi He +9 more
doaj +1 more source
Decrease in Prosaposin in the Dystrophic mdx Mouse Brain
Duchenne muscular dystrophy caused by a mutation in the X-linked dystrophin gene induces metabolic and structural disorders in the brain. A lack of dystrophin in brain structures is involved in impaired cognitive function. Prosaposin (PS), a neurotrophic factor, is abundant in the choroid plexus and various brain regions.
Hui Ling Gao +8 more
openaire +5 more sources
ABSTRACT Background Hydrogen sulphide (H2S), a gasotransmitter synthesized by cystathionine‐γ‐lyase (CSE), exhibits antioxidant properties and may mimic exercise‐induced muscle protection. However, its mechanistic role in muscle atrophy and exercise intervention remains unclear.
Xiuru Li +5 more
wiley +1 more source

