Results 281 to 290 of about 9,917,456 (366)
Connected Edge Monophonic Domination Number of a Graph
P. Arul +2 more
openalex +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
Perspectives of health, and human and social sciences professionals on student transformation regarding racial discrimination in healthcare. [PDF]
Lambert M +4 more
europepmc +1 more source
Extremal hypergraphs for matching number and domination number
Erfang Shan +3 more
openalex +2 more sources
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
Molecular Characteristics of Epidemiologically Successful <i>Salmonella</i> Enteritidis in Poland. [PDF]
Kamińska E +6 more
europepmc +1 more source
ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich +10 more
wiley +1 more source
Domination and power domination in a one-pentagonal carbon nanocone structure. [PDF]
Pandian S, N M.
europepmc +1 more source
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source
On Religious Influence in Bioethics: The Limits of Pluriversalism. [PDF]
Spitale G +14 more
europepmc +1 more source

