Pages that link to "Q30840162"
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The following pages link to Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder (Q30840162):
Displaying 18 items.
- A C1-C2 Module in Munc13 Inhibits Calcium-Dependent Neurotransmitter Release (Q42513230) (← links)
- Emerging Monogenic Complex Hyperkinetic Disorders. (Q44707117) (← links)
- Critical Role of Trp-588 of Presynaptic Munc13-1 for Ligand Binding and Membrane Translocation. (Q47290370) (← links)
- Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open Questions (Q47618500) (← links)
- Resveratrol inhibits phorbol ester-induced membrane translocation of presynaptic Munc13-1. (Q50888051) (← links)
- Presynaptic disorders: a clinical and pathophysiological approach focused on the synaptic vesicle (Q57175515) (← links)
- SYT1-associated neurodevelopmental disorder: a case series (Q58194861) (← links)
- Autaptic cultures of human induced neurons as a versatile platform for studying synaptic function and neuronal morphology (Q64072801) (← links)
- Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release (Q64083815) (← links)
- Heterodimerization of UNC-13/RIM regulates synaptic vesicle release probability but not priming in (Q64104459) (← links)
- Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms (Q89285568) (← links)
- Stxbp1/Munc18-1 haploinsufficiency impairs inhibition and mediates key neurological features of STXBP1 encephalopathy (Q89775482) (← links)
- Defects in Axonal Transport in Inherited Neuropathies (Q90333426) (← links)
- Spinal TNF-α impedes Fbxo45-dependent Munc13-1 ubiquitination to mediate neuropathic allodynia in rats (Q90452898) (← links)
- Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission (Q92118567) (← links)
- Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment (Q92725689) (← links)
- Munc13 Is a Molecular Target of Bryostatin 1 (Q93057430) (← links)
- Open syntaxin overcomes exocytosis defects of diverse mutants in C. elegans (Q101165782) (← links)