Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rhian M. Evans"'
Publikováno v:
Academic Forensic Pathology. 1:82-91
Shaken baby syndrome (SBS) is routinely diagnosed on the basis of a classic triad of autopsy findings, namely retinal hemorrhage, subdural hemorrhage, and anoxic encephalopathy. However, ongoing controversy exists regarding the specificity and potent
Autor:
Christophe Altier, Haitao You, Rhian M. Evans, Emmanuel Bourinet, Gerald W. Zamponi, Shahid Hameed, Alexandre Mezghrani
Publikováno v:
Journal of Biological Chemistry. 285:1032-1040
We have investigated the heterodimerization of ORL1 receptors and classical members of the opioid receptor family. All three classes of opioid receptors could be co-immunoprecipitated with ORL1 receptors from both transfected tsA-201 cell lysate and
Autor:
Kevin Chapman, Christophe Altier, Nathalie Vergnolle, Anthony H. Dickenson, Elizabeth A. Matthews, Camila Squarzoni Dale, Andrew J. Castiglioni, Gerald W. Zamponi, Alexandra E. Kisilevsky, Rhian M. Evans, Diane Lipscombe
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 27(24)
N-type calcium channels are essential mediators of spinal nociceptive transmission. The core subunit of the N-type channel is encoded by a single gene, and multiple N-type channel isoforms can be generated by alternate splicing. In particular, cell-s
Autor:
Gerald W. Zamponi, Rhian M. Evans
Publikováno v:
Trends in neurosciences. 29(11)
Calcium influx into presynaptic nerve terminals via voltage-gated Ca2+ channels is an essential step in neurotransmitter release. The predominant Ca2+ channel species in synaptic nerve terminals are P/Q-type and N-type channels, with their relative l
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