Results 51 to 60 of about 97,622 (334)
Whole-mount Staining of Mouse Diaphragm Neuromuscular Junctions
The neuromuscular junction (NMJ) is a specialized synapse that connects the terminal end of a motor neuron and a skeletal muscle fiber. Defects in NMJ cause abnormalities of neuromuscular transmission, leading to NMJ disorders.
Rula Sha +5 more
doaj +1 more source
A Drosophila Mutant with a Temperature-Sensitive Block in Nerve Conduction [PDF]
A mutant, napts (no action potential, temperature-sensitive), is described in which axonal conduction fails at high temperature. Synaptic transmission at the larval neuromuscular junction is unimpaired.
Benzer, Seymour +4 more
core
Neurotoxicity refers to the direct or indirect effect of chemicals that disrupt the nervous system of humans or animals. Numerous chemicals can produce neurotoxic diseases in humans, and many more are used as experimental tools to disturb or damage the ...
Brust +15 more
core +2 more sources
Decreased Serum 5‐HT: Clinical Correlates and Regulatory Role in NMJ of MG
ABSTRACT Objective Although 5‐Hydroxytryptamine (5‐HT) indirectly stimulates muscle contraction and participates in regulating Acetylcholine receptor (AChR) cluster homeostasis in cellular, animal, and clinical studies, evidence regarding its potential to modulate muscle contraction in myasthenia gravis (MG) remains limited.
Xinru Shen +18 more
wiley +1 more source
Clinical assessment of neuromuscular transmission [PDF]
The concept of neuromuscular transmission as a separate physiological entity was introduced by Claude Bernard in 1851 when he demonstrated by means of curare that the junction between nerve endings and muscle fibres possessed unique properties. The logic and simplicity of Bernard’s experiments have not been surpassed by more modern methods and they ...
J P, Payne, R, Hughes
openaire +2 more sources
Insights Into the Antigenic Repertoire of Unclassified Synaptic Antibodies
ABSTRACT Objective We sought to characterize the sixth most common finding in our neuroimmunological laboratory practice (tissue assay‐observed unclassified neural antibodies [UNAs]), combining protein microarray and phage immunoprecipitation sequencing (PhIP‐Seq). Methods Patient specimens (258; 133 serums; 125 CSF) meeting UNA criteria were profiled;
Michael Gilligan +22 more
wiley +1 more source
Neuromuscular transmission in SCA6
Contains fulltext : 58763.pdf (Publisher’s version ) (Open Access)
Schelhaas, H.J. +3 more
openaire +4 more sources
Activity-dependent plasticity of transmitter release from nerve terminals in rat fast and slow muscles [PDF]
Available under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported license.Peer reviewedPublisher ...
Bewick, Guy Smith +4 more
core +1 more source
ABSTRACT Objective This study aimed to systematically observe the clinical manifestations, immune cell subsets, and dynamic changes in serological indicators in patients with myasthenia gravis (MG) before and after efgartigimod (EFG) treatment. Methods We analyzed the baseline data, laboratory parameters, and lymphocyte subset proportions in MG ...
Tiancheng Luo +9 more
wiley +1 more source
Molecular characterisation of congenital myasthenic syndromes in Southern Brazil [PDF]
Objective To perform genetic testing of patients with congenital myasthenic syndromes (CMS) from the Southern Brazilian state of Parana. Patients and methods Twenty-five CMS patients from 18 independent families were included in the study.
Abicht, A. +12 more
core +2 more sources

