Results 91 to 100 of about 582,200 (259)

Heterotropic regulation and negative homotropic cooperativity

open access: yesFEBS Open Bio, EarlyView.
We identified a structural module common to some proteins that couple negative cooperativity with heterotropic regulation, two features that rarely coexist. These proteins are ring‐like and present an ordered asymmetry whereby noncontacting subunits are symmetric, and their tertiary structure differs from that of contacting subunits.
Veronica Morea   +5 more
wiley   +1 more source

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz   +3 more
wiley   +1 more source

Sex Representation in US Stroke Clinical Trials: A Decade of Trends and Challenges

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Stroke remains a major cause of disability and mortality in the US, with significant sex‐based disparities, and females remain underrepresented in stroke clinical trials. We aimed to examine sex representation in US‐based stroke clinical trials, identify trial characteristics associated with higher female enrollment (≥ 50%), and ...
Chaitali Dagli   +5 more
wiley   +1 more source

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

Response of soil erosion and non-point source pollution to different rainfall, vegetation and land preparation measures in Miyun reservoir area during 2010–2023

open access: yesInternational Soil and Water Conservation Research
Soil erosion and non-point source pollution are critical global environmental issues, with profound implications for ecosystems, agricultural productivity, and water quality.
Runze Yang   +10 more
doaj   +1 more source

Strongly Extreme Points and Middle Point Locally Uniformly Convex in Orlicz Spaces Equipped with s-Norm

open access: yesJournal of Function Spaces, 2019
As is well known, the extreme points and strongly extreme points play important roles in Banach spaces. In this paper, the criterion for strongly extreme points in Orlicz spaces equipped with s-norm is given.
Yunan Cui, Yujia Zhan
doaj   +1 more source

Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi   +8 more
wiley   +1 more source

Sufficient Statistics and Extreme Points

open access: yesThe Annals of Probability, 1978
A convex set $M$ is called a simplex if there exists a subset $M_e$ of $M$ such that every $P \in M$ is the barycentre of one and only one probability measure $\mu$ concentrated on $M_e$. Elements of $M_e$ are called extreme points of $M$. To prove that a set of functions or measures is a simplex, usually the Choquet theorem on extreme points of convex
openaire   +3 more sources

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

A Fitness Landscape-Based Method for Extreme Point Analysis of Part Surface Morphology

open access: yesMachines
Advancements in Industry 4.0 and smart manufacturing have increased the demand for precise and intricate part surface geometries, making the analysis of surface morphology essential for ensuring assembly precision and product quality. This study presents
Jinshan Sun, Wenbin Tang
doaj   +1 more source

Home - About - Disclaimer - Privacy