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Neuron
|
August 11, 1998
Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles
P Kantheti, X Qiao, M E Diaz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 23, 2000
Impaired fast-spiking, suppressed cortical inhibition, and increased susceptibility to seizures in mice lacking Kv3.2 K+ channel proteins
D Lau, E C Vega-Saenz de Miera, D Contreras, et al.
Neurology
|
November 14, 2001
Future directions for epilepsy research
M P Jacobs, G D Fischbach, M R Davis, et al.
Epilepsia
|
October 3, 2001
Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome
H A Heilstedt, D L Burgess, A E Anderson, et al.
Nature Genetics
|
October 4, 2000
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, D L Burgess, et al.
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of 8
Search research articles
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Showing results (71-80 of 75) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 75 results.
Neuron
|
August 11, 1998
Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles
P Kantheti, X Qiao, M E Diaz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 23, 2000
Impaired fast-spiking, suppressed cortical inhibition, and increased susceptibility to seizures in mice lacking Kv3.2 K+ channel proteins
D Lau, E C Vega-Saenz de Miera, D Contreras, et al.
Neurology
|
November 14, 2001
Future directions for epilepsy research
M P Jacobs, G D Fischbach, M R Davis, et al.
Epilepsia
|
October 3, 2001
Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome
H A Heilstedt, D L Burgess, A E Anderson, et al.
Nature Genetics
|
October 4, 2000
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, D L Burgess, et al.
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of 8