Results 51 to 60 of about 741,119 (226)

Metallic–Dissolution Triggered Defective NiCoAl‐CuO Electrocatalyst for Enhanced Ethanol Oxidation Reaction With Precisely Tuned Reaction Pathway

open access: yesCarbon Energy, EarlyView.
Metallic dissolution triggers Al/O vacancies in NiCoAl–CuO, steering C2‐selective ethanol oxidation to acetate. Hybrid electrolysis co‐produces hydrogen and acetate with high efficiency and reduced cell voltage. ABSTRACT Replacing the sluggish anodic oxygen evolution reaction (OER) with value‐added processes like the ethanol oxidation reaction (EOR ...
Ashish Gaur   +8 more
wiley   +1 more source

The vibration characteristics of badminton racket by modal analysis [PDF]

open access: yes, 2008
Badminton is very popular sports. However, the badminton racket has not been optimized yet as a sports tool, compared to that for tennis racket. This study is an attempt to investigate the effect of shuttle cock on the vibration characteristics of ...
長松 昭男   +3 more
core  

GRIA2 Variant Associated With Paradoxical Response to Perampanel Expanding the Spectrum of GRIA2‐Related Epileptic Encephalopathy: Case Report and Literature Review

open access: yesAnnals of the Child Neurology Society, EarlyView.
ABSTRACT Introduction GRIA2 encodes the GluA2 ionotropic α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptor subunit. Pathogenic GRIA2 variants cause epilepsy, developmental delay, and neurobehavioral disorders. Characterizations of clinical features, including seizure types and their treatments, in patients with GRIA2‐related ...
Sai Srihitha Dommata   +9 more
wiley   +1 more source

Editorial

open access: yesInternational Journal of Racket Sports Science, 2019
Racket Sports have been widely studied in science for the last years. The purpose of this Journal is to aggregate the most important advances and researches to affect the development and directions of racket sports science from now on.
David Cabello Manrique
doaj  

Functional profiling of STXBP1 missense variants using a novel dual‐readout fluorometric assay

open access: yesEpilepsia, EarlyView.
Abstract Objective STXBP1‐related disorders (STXBP1‐RD) are among the most common genetic neurodevelopmental disorders, marked by early onset epilepsy, global developmental delay, and motor impairments. Many missense variants remain uncharacterized, limiting accurate variant interpretation and hindering development of precision therapies.
Elisa A. Waxman   +11 more
wiley   +1 more source

THE EFFECT OF TENNIS RACKET STRING VIBRATION ABSORBER PLACEMENT ON TENNIS RACKET VIBRATIONS [PDF]

open access: yes, 2008
The purpose of this research was to analyze the vibration effect of tennis racket caused by impact on different locative vibration absorber and locations. In this experiment, The tennis racket was fixed and kept the face horizontalized to the ground with
Lin, Yuh-Yih   +3 more
core   +1 more source

Reversal of refractory epilepsy in an adult with GAMT deficiency: A case report and comparative literature review

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Guanidinoacetate methyltransferase (GAMT) deficiency is a rare autosomal recessive creatine biosynthesis disorder. Reports specifically focusing on adult patients remain scarce. Methods We report a 52‐year‐old female (the oldest documented case of GAMT deficiency to date) presenting with severe intellectual disability, refractory ...
Wei‐Hung Sung   +3 more
wiley   +1 more source

Impact of the integration of some teaching methods on the level of performance of some offensive strikes for beginners in table tennis [PDF]

open access: yesAssiut Journal of Sport Science and Arts, 2014
The kinetic tasks technique aims at motivating the learner to depend on himself and establish the kinetic skills as these tasks are provided for the learner without any intervention or participation on the part of the teacher.
Habib Reda Habib Ebrahim
doaj   +1 more source

MLH1 p.His112Arg Variant Is Associated With Increased Cancer Susceptibility

open access: yesInternational Journal of Cancer, EarlyView.
ABSTRACT Lynch syndrome, a prevalent hereditary cancer predisposition, is frequently caused by pathogenic variants in the MutL homolog 1 (MLH1) mismatch repair gene. However, a significant proportion of MLH1 missense variants remain classified as variants of uncertain significance (VUS), creating clinical ambiguity.
Amal Elfatih   +10 more
wiley   +1 more source

Sprint performance and force application of tennis players during manual wheelchair propulsion with and without holding a tennis racket.

open access: yesPLoS ONE, 2022
The objective of this exploratory research is to study the impact of holding a tennis racket while propelling a wheelchair on kinetic and temporal parameters in a field-based environment. 13 experienced wheelchair tennis players with disabilities (36.1 ±
Ilona Alberca   +6 more
doaj   +1 more source

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