X-linked intellectual disability-associated mutations in synaptophysin disrupt synaptobrevin II retrieval

Journal of Neuroscience

Volumn 33, Issue 34, 2013, Pages 13695-13700

  Gordon, Sarah L ^a   Cousin, Michael A ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

SYNAPTOBREVIN 2; SYNAPTOPHYSIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; EMBRYO; ENDOCYTOSIS; FLUORESCENCE IMAGING; GENE MUTATION; INTELLECTUAL IMPAIRMENT; MOUSE; NERVE ENDING; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; SYNAPSE; X CHROMOSOMAL INHERITANCE; X CHROMOSOME LINKED DISORDER;

ACTION POTENTIALS; ANIMALS; AXONS; CELLS, CULTURED; CEREBRAL CORTEX; EMBRYO, MAMMALIAN; FEMALE; GREEN FLUORESCENT PROTEINS; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NEURONS; PATCH-CLAMP TECHNIQUES; POINT MUTATION; SYNAPTOPHYSIN; TRANSFECTION; TRANSPORT VESICLES; VESICLE-ASSOCIATED MEMBRANE PROTEIN 2; VESICULAR GLUTAMATE TRANSPORT PROTEINS;

EID: 84882595827     PISSN: 02706474     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.0636-13.2013     Document Type: Article

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