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Gomez, Christopher M.
One or more keywords matched the following items that are connected to
Gomez, Christopher M.
Item Type
Name
Concept
Muscle, Smooth
Concept
Muscles
Concept
Muscle Contraction
Concept
Oculomotor Muscles
Concept
Muscle, Skeletal
Concept
Muscle Fibers, Skeletal
Concept
Muscle Spasticity
Concept
Muscle Weakness
Academic Article
A transgenic mouse model of the slow-channel syndrome.
Academic Article
Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome.
Academic Article
Presynaptic congenital myasthenic syndrome due to quantal release deficiency.
Academic Article
Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome.
Academic Article
Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
Academic Article
Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model.
Academic Article
Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome.
Academic Article
Induction of the morphologic changes of both acute and chronic experimental myasthenia by monoclonal antibody directed against acetylcholine receptor.
Academic Article
Skeletal muscle IP3R1 receptors amplify physiological and pathological synaptic calcium signals.
Academic Article
Further evidence for the role of IP 3R 1 in regulating subsynaptic gene expression and neuromuscular transmission.
Academic Article
Skeletal muscle calpain acts through nitric oxide and neural miRNAs to regulate acetylcholine release in motor nerve terminals.
Academic Article
Selective inhibition of caspases in skeletal muscle reverses the apoptotic synaptic degeneration in slow-channel myasthenic syndrome.
Academic Article
A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome.
Academic Article
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
Academic Article
ARSACS goes global.
Academic Article
Novel beta subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation.
Academic Article
Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms.
Academic Article
Chronic experimental autoimmune myasthenia gravis induced by monoclonal antibody to acetylcholine receptor: biochemical and electrophysiologic criteria.
Academic Article
Inositol-1,4,5-triphosphate receptors mediate activity-induced synaptic Ca2+ signals in muscle fibers and Ca2+ overload in slow-channel syndrome.
Academic Article
Myasthenia induced by monoclonal anti-acetylcholine receptor antibodies: clinical and electrophysiological aspects.
Academic Article
Anti-acetylcholine receptor antibodies directed against the alpha-bungarotoxin binding site induce a unique form of experimental myasthenia.
Academic Article
Role of botulinum toxin-A in refractory idiopathic overactive bladder patients without detrusor overactivity.
Search Criteria
Muscles