Results 51 to 60 of about 25,234 (258)
Protocol for quantifying miRNA trafficking across the endosomal membrane
An in vitro protocol measures miRNA uptake into endosomes isolated from mammalian cell extracts, which are free of subcellular contaminants. Performed at 37 °C in the presence of ATP, it ensures the import of single‐stranded miRNA into the endosomal lumen.
Syamantak Ghosh +2 more
wiley +1 more source
SWSDesigner: The Graphical Interface of ODESWS [PDF]
ODESWS is a development environment to design Semantic Web Services (SWS) at the knowledge level. ODESWS describe the service following a problem-solving approach in which the SWS are modelled using tasks, to represent the SWS functional features, and ...
González-Cabero, R. +2 more
core
Accurate prediction of future surface wind speed (SWS) changes is the basis of scientific planning for wind turbines. Most studies have projected SWS changes in the 21st century over China on the basis of the multi-model ensemble (MME) of the 6th Coupled
Zheng-Tai Zhang, Chang-Ai Xu
doaj +1 more source
Mutations in Drosophila Swiss cheese (SWS) or its vertebrate orthologue neuropathy target esterase (NTE), respectively, cause progressive neuronal degeneration in Drosophila and mice and a complex syndrome in humans that includes mental retardation ...
Sudeshna Dutta +4 more
doaj +1 more source
ABSTRACT Objective To assess the association and discriminative performance of serum biomarkers with clinical disease progression and survival in patients with amyotrophic lateral sclerosis (ALS). Methods This retrospective study, conducted at Houston Methodist Hospital, Houston, TX, used longitudinal serum samples collected between January 2018 and ...
David R. Beers +7 more
wiley +1 more source
Patients with RTT have significantly lower SWS percent compared to control group. Significance is driven in the age group 2–5 year old. The significance in SWS percent is lost in 6–9 years ago. Comparison of SWS percent reveals an increasing tread in SWS
Siddharth S. Gupta (804370) +9 more
core +1 more source
Ocular Manifestations of the Sturge–Weber Syndrome
Sturge–Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a non-inherited congenital disorder characterized by neurologic, skin, and ocular abnormalities. A somatic activating mutation (R183Q) in the GNAQ gene during early embryogenesis has been
Kiana Hassanpour +4 more
doaj +1 more source
The Multiple Sclerosis Severity Allele rs10191329A and Cognitive Function: A UK Biobank Study
ABSTRACT The genome‐wide association study of Multiple Sclerosis severity linked the genetic variant rs10191329A to long‐term disability and implicated brain resilience as a determinant of outcome. We hypothesised that rs10191329A might influence cognition in other neurological diseases and healthy controls.
Ioanna Zimianiti +5 more
wiley +1 more source
Objective This study aimed to examine the association between slow-wave sleep ([SWS] N3 stage) and the risk of hypertension in patients with obstructive sleep apnea (OSA) or primary snorers.
Jing Zhang +8 more
doaj +1 more source
Heightened Delta Power during Slow-Wave-Sleep in Patients with Rett Syndrome Associated with Poor Sleep Efficiency. [PDF]
Sleep problems are commonly reported in Rett syndrome (RTT); however the electroencephalographic (EEG) biomarkers underlying sleep dysfunction are poorly understood.
Simon Ammanuel +9 more
doaj +1 more source

