Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins
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Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderIdentification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling.Translational potential of astrocytes in brain disorders.Hsc70 chaperone activity is required for the cytosolic slow axonal transport of synapsin.New treatment perspectives in autism spectrum disorders.Autism and Epilepsy: Exploring the Relationship Using Experimental Models.Altered synaptobrevin-II trafficking in neurons expressing a synaptophysin mutation associated with a severe neurodevelopmental disorder.Selective lowering of synapsins induced by oligomeric α-synuclein exacerbates memory deficits.
P2860
Q30840162-C1F89724-BFA4-4ADD-BC9F-398816AF37F3Q35408613-92501051-03B1-4065-97B4-5DCCA98C3CD3Q38589482-A59ADE53-AC5A-4B83-9ED6-AF4911C3A0F6Q38755587-CC104C0E-026C-48B9-B179-4D62089EC8B0Q41906721-14851B98-ABBE-494A-A109-9487AD4A38FCQ41933122-E5233129-505F-4F4C-AF88-278DCB5452DCQ45826766-2EFDA119-1913-47F3-A117-4EDF03F0B885Q46362244-1EC1876F-301A-44FC-92D6-8460E217791B
P2860
Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins
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name
Involvement of synaptic genes ...... sorders: the case of synapsins
@en
type
label
Involvement of synaptic genes ...... sorders: the case of synapsins
@en
prefLabel
Involvement of synaptic genes ...... sorders: the case of synapsins
@en
P2093
P2860
P921
P356
P1476
Involvement of synaptic genes ...... sorders: the case of synapsins
@en
P2093
Anna Corradi
Fabio Benfenati
Silvia Giovedí
P2860
P356
10.3389/FPED.2014.00094
P50
P577
2014-09-04T00:00:00Z