Results 161 to 170 of about 1,204,232 (364)
Investigating the Temperature Sensitivity of UV Line Ratios in the 280 nm Region of Solar-like Stars
Stellar UV spectra are fundamental diagnostics of physical and magnetic properties of stars. For instance, lines like Mg ii at 280 nm serve as valuable indicators of stellar activity, providing insights into the activity levels of Sun-like stars and ...
Valentina Penza +9 more
doaj +1 more source
ABSTRACT Background Poststroke fatigue (PSF) and frailty share substantial overlap in their manifestations, yet previous research has yielded conflicting results due to the use of heterogeneous frailty assessment tools. Objective To evaluate the independent impact of frailty on PSF using a unified measurement system (Tilburg Frailty Indicator, TFI ...
Chuan‐Bang Chen +6 more
wiley +1 more source
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin +12 more
wiley +1 more source
Reliable estimation of stellar surface gravity (log g ) for a large sample is crucial for evaluating stellar evolution models and understanding galactic structure; however, it is not easy to accomplish due to the difficulty in gathering a large ...
Qiqian Zhang +18 more
doaj +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Application of Bradford's Law of Scattering to the Literature of Stellar Physics
Shweta B. Joshi +2 more
openalex +1 more source
Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
Nuclear physics aspects of neutron capture and β-decay rates in stellar environment
A. Mengoni
openalex +1 more source

