Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Jean B Peloquin"'
Autor:
Clinton J Doering, Renata Rehak, Stephan Bonfield, Jean B Peloquin, William K Stell, Silvina C Mema, Yves Sauvé, John E McRory
Publikováno v:
PLoS ONE, Vol 3, Iss 7, p e2538 (2008)
The Cacna1f(nob2) mouse is reported to be a naturally occurring null mutation for the Ca(v)1.4 calcium channel gene and the phenotype of this mouse is not identical to that of the targeted gene knockout model. We found two mRNA species in the Cacna1f
Externí odkaz:
https://doaj.org/article/56f5aa9b351f402baf3e9557557d3889
Publikováno v:
Channels. 1:4-11
Cav1.4 channels are the latest calcium channels to be described in the literature. Originally identified in 1997 from the human genome project, several reports have since been published describing mutations in the CACNA1F gene encoding Cav1.4 channel
Publikováno v:
Journal of Neurophysiology. 96:465-470
Direct interactions between the presynaptic N-type calcium channel and the β subunit of the heterotrimeric G-protein complex cause voltage-dependent inhibition of N-type channel activity, crucially influencing neurotransmitter release and contributi
Publikováno v:
Channels (Austin, Tex.). 1(1)
Ca(v)1.4 channels are the latest calcium channels to be described in the literature. Originally identified in 1997 from the human genome project, several reports have since been published describing mutations in the CACNA1F gene encoding Ca(v)1.4 cha
Publikováno v:
Neuroscience. 151(4)
The CACNA1F gene encodes the pore-forming subunit of the L-type Cav1.4 voltage-gated calcium channel (VGCC) and plays a central role in tonic vesicular release at photoreceptor ribbon synapses. The main objective of this study was to examine the effe
Publikováno v:
Neuroscience. 150(2)
Congenital stationary night blindess-2 (incomplete congenital stationary night blindness (iCSNB) or CSNB-2) is a nonprogressive, X-linked retinal disease which can lead to clinical symptoms such as myopia, hyperopia, nystagmus, strabismus, decreased
Publikováno v:
Voltage-Gated Calcium Channels ISBN: 9780306478406
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f013cf080c56be24a5a6e60e9a6ea8a7
https://doi.org/10.1007/0-387-27526-6_5
https://doi.org/10.1007/0-387-27526-6_5
Publikováno v:
Neuroscience. 143(3)
We have investigated the channel structural determinants that underlie the difference in gating properties of Cav3.1 and Cav3.3 T-type channels, by creating a series of chimeric channel constructs in which the major transmembrane domains were swapped
Autor:
Gregory T. Macleod, Gerald W. Zamponi, Jean B. Peloquin, Harold L. Atwood, S. Karunanithi, Lina Chen, John E. McRory, Milton P. Charlton
Publikováno v:
The European journal of neuroscience. 23(12)
Voltage-gated Ca 2+ channels in nerve terminals open in response to action potentials and admit Ca 2+ , the trigger for neurotransmitter release. The cacophony gene encodes the primary presynaptic voltage-gated Ca 2+ channel in Drosophila motor-nerve
Autor:
Jean B. Peloquin, Gerald W. Zamponi, Wendy Barr, Terrance P. Snutch, Janette Mezeyova, Rhian M. Evans, Chris Bladen, David Parker, Houman Khosravani, John E. McRory
Publikováno v:
Epilepsia. 47(3)
Summary: Purpose: Childhood absence epilepsy (CAE) is an idiopathic form of seizure disorder that is believed to have a genetic basis. Methods: We examined the biophysical consequences of seven mutations in the Cav3.2 T-type calcium channel gene link