Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Gloria J. Klapstein"'
Publikováno v:
Inflammopharmacology. 20:109-126
It has become increasingly clear that inflammatory processes play a significant role in the pathophysiology of Alzheimer's disease (AD). Neuroinflammation is characterized by the activation of astrocytes and microglia and the release of proinflammato
Autor:
Oanh Kieu Nguyen, Gloria J. Klapstein, Nan Ping Wu, Véronique M. André, Harry V. Vinters, Susan Koh, Jorge Flores-Hernandez, Michael Levine, Carlos Cepeda, Snow T. Nguyen, Gary W. Mathern
Publikováno v:
Developmental Neuroscience. 27:59-76
Seizures in cortical dysplasia (CD) could be from cytomegalic neurons and balloon cells acting as epileptic ‘pacemakers’, or abnormal neurotransmission. This study examined these hypotheses using in vitro electrophysiological techniques to determ
Autor:
Oanh Kieu Nguyen, Jorge Flores-Hernandez, Carlos Cepeda, Gary W. Mathern, Emily L. Jocoy, Raymond S. Hurst, Michael Levine, Harry V. Vinters, Elizabeth Hernández-Echeagaray, Gloria J. Klapstein, M.K. Boylan, Christopher R. Calvert, Véronique M. André, Marjorie A. Ariano
Publikováno v:
Journal of Neuroscience Research. 72:472-486
The mechanisms responsible for seizure generation in cortical dysplasia (CD) are unknown, but morphologically abnormal cells could contribute. We examined the passive and active membrane properties of cells from pediatric CD in vitro. Normal- and abn
Autor:
E S Jokel, Kathryn Chase, Carlos Cepeda, Frederick M. Boyce, B A Cadigan, L Warzecki, Michael Levine, C McIntyre, Neil Aronin, Gloria J. Klapstein, M Campbell, Genevieve A. Laforet, P. H. Reddy, C R Calvert, Marian DiFiglia, D A Tagle, M. A. Ariano, E Sapp
Publikováno v:
The Journal of Neuroscience. 21:9112-9123
Neurons in Huntington's disease exhibit selective morphological and subcellular alterations in the striatum and cortex. The link between these neuronal changes and behavioral abnormalities is unclear. We investigated relationships between essential n
Autor:
Raymond S. Hurst, Scott Zeitlin, Hadi Shojaeian Zanjani, Carlos Cepeda, Michael Levine, Eve S. Jokel, Ellen M. Carpenter, Mauricio E. Vargas, Ahrin Koppel, Marie-Françoise Chesselet, Ehud Gruen, Argiris Efstratiadis, Gloria J. Klapstein
Publikováno v:
Journal of Neuroscience Research. 58:515-532
We used two mouse models of Huntington's disease (HD) to examine changes in glutamate receptor sensitivity and striatal electrophysiology. One model, a transgenic, consisted of mice expressing exon 1 of the human HD gene and carrying 141–157 CAG re
Publikováno v:
Neuropharmacology. 38:927-933
The ability of the selective Group III mGluR agonist L-serine-O-phosphate (L-SOP) to inhibit lateral perforant path (LPP) evoked responses in the dentate gyrus was tested in hippocampal slices from commissurally-kindled rats 1-2 days after the last s
Publikováno v:
Journal of Neurophysiology. 78:1651-1661
Klapstein, Gloria J. and William F. Colmers. Neuropeptide Y suppresses epileptiform activity in rat hippocampus in vitro. J. Neurophysiol. 78: 1651–1661, 1997. Neuropeptide Y (NPY) potently inhibits glutamate-mediated synaptic transmission in areas
Autor:
Jorge Flores-Hernandez, Marian DiFiglia, Christopher R. Calvert, Carlos Cepeda, Scott H. Chandler, Elizabeth Hernández-Echeagaray, Neil Aronin, Michael Levine, Gloria J. Klapstein, Marjorie A. Ariano
Publikováno v:
Journal of neurophysiology. 93(5)
Huntington's disease (HD) is a neurodegenerative disorder that mainly affects the projection neurons of the striatum and cerebral cortex. Genetic mouse models of HD have shown that neurons susceptible to the mutation exhibit morphological and electro
Autor:
Gloria J. Klapstein, Michael Levine
Publikováno v:
Journal of neurophysiology. 93(2)
We used the oxygen/glucose deprivation (OGD) model of ischemia in corticostriatal brain slices to test the hypothesis that metabolic deficiencies in R6/2 transgenic Huntington's disease (HD) mice will impair their recovery from an ischemic challenge.
Autor:
Nigel T. Maidment, Mahadevan Gajendiran, Marie-Françoise Chesselet, Jie Shen, Matthew S. Goldberg, Sheila M. Fleming, Anushree Bhatnagar, Larry C. Ackerson, Gloria J. Klapstein, Edward G. Meloni, Michael Levine, Carlos Cepeda, Bryan L. Roth, James Palacino, Nanping Wu, Hoa A. Lam
Publikováno v:
The Journal of biological chemistry. 278(44)
Loss-of-function mutations in parkin are the major cause of early-onset familial Parkinson's disease. To investigate the pathogenic mechanism by which loss of parkin function causes Parkinson's disease, we generated a mouse model bearing a germline d