Results 191 to 200 of about 899,641 (334)

Association of Synovial Innate Immune Exhaustion With Worse Pain in Knee Osteoarthritis

open access: yesArthritis &Rheumatology, EarlyView.
Objective Uncontrolled pain remains a major clinical challenge in the management of knee osteoarthritis (OA), the most common disabling joint disease. Worse pain is associated with synovial innate immune cell infiltration (synovitis), but the role of innate immune‐regulatory cells in pain is unknown. Our objective was to identify synovial innate immune
Holly T. Philpott   +14 more
wiley   +1 more source

Double gene mutations of LRSAM1 and REEP1 and a new REEP1 mutation site found in a patient with amyotrophic lateral sclerosis with subjective paresthesia: A case report

open access: yesIbrain, EarlyView., 2023
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by selective degeneration of upper and lower motor neurons. Leucine‐rich repeats and sterility α mutations in motif 1 (LRSAM1) has been proven to be involved in the pathogenesis of ALS.
Ji‐Yao Qin   +6 more
wiley   +1 more source

Short-Range Guidance of Olfactory Bulb Axons Is Independent of Repulsive Factor Slit [PDF]

open access: bronze, 2001
Tatsumi Hirata   +3 more
openalex   +1 more source

Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants

open access: yesAutism Research, EarlyView.
Abstract This preliminary study sought to assess biomarkers of attention using electroencephalography (EEG) and eye tracking in two ultra‐rare monogenic populations associated with autism spectrum disorder (ASD). Relative to idiopathic ASD (n = 12) and neurotypical comparison (n = 49) groups, divergent attention profiles were observed for the monogenic
Caitlin M. Hudac   +12 more
wiley   +1 more source

Efferocytosis is restricted by axon guidance molecule EphA4 via ERK/Stat6/MERTK signaling following brain injury. [PDF]

open access: yesJ Neuroinflammation, 2023
Soliman E   +12 more
europepmc   +1 more source

m6A‐mRNA Reader YTHDF2 Identified as a Potential Risk Gene in Autism With Disproportionate Megalencephaly

open access: yesAutism Research, EarlyView.
ABSTRACT Among autistic individuals, a subphenotype of disproportionate megalencephaly (ASD‐DM) seen at three years of age is associated with co‐occurring intellectual disability and poorer prognoses later in life. However, many of the genes contributing to ASD‐DM have yet to be delineated. In this study, we identified additional ASD‐DM candidate genes
Sierra S. Nishizaki   +10 more
wiley   +1 more source

Axon Guidance Molecules in the Islets of Langerhans. [PDF]

open access: yesFront Endocrinol (Lausanne), 2022
Waters BJ, Blum B.
europepmc   +1 more source

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