Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lily Y. J. Zhang"'
Autor:
Amy I. Smith-Dijak, Wissam B. Nassrallah, Lily Y. J. Zhang, Michal Geva, Michael R. Hayden, Lynn A. Raymond
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Huntington disease (HD) is an inherited neurodegenerative disorder caused by a mutation in the huntingtin gene. The onset of symptoms is preceded by synaptic dysfunction. Homeostatic synaptic plasticity (HSP) refers to processes that maintain the sta
Externí odkaz:
https://doaj.org/article/e96ca48365e947b3aff8e9ccdb535974
Autor:
Jing Fan, Edward H. Y. Li, Clare M. Gladding, Liang Wang, Lily Y. J. Zhang, Paul J. Lombroso, Jian Xu, Lynn A. Raymond
Publikováno v:
Journal of Neurochemistry. 130:145-159
Striatal neurodegeneration and synaptic dysfunction in Huntington's disease are mediated by the mutant huntingtin (mHtt) protein. MHtt disrupts calcium homeostasis and facilitates excitotoxicity, in part by altering NMDA receptor (NMDAR) trafficking
Autor:
Ainsley Coquinco, Max S. Cynader, Marja D. Sepers, Lynn A. Raymond, Liang Wang, Clare M. Gladding, Lily Y. J. Zhang, Jing Fan, Alexandra M. Kaufman, Austen J. Milnerwood, Hwan Lee, Joy Yi Qiao, Yu Tian Wang
Publikováno v:
Neurobiology of Disease, Vol 48, Iss 1, Pp 40-51 (2012)
We recently reported evidence for disturbed synaptic versus extrasynaptic NMDAR transmission in the early pathogenesis of Huntington's disease (HD), a late-onset neurodegenerative disorder caused by CAG repeat expansion in the gene encoding huntingti
Autor:
Austen J. Milnerwood, Clare M. Gladding, Jian Xu, Lily Y. J. Zhang, Paul J. Lombroso, Marja D. Sepers, Lynn A. Raymond
Publikováno v:
Human Molecular Genetics. 21:3739-3752
In Huntington's disease (HD), the mutant huntingtin (mhtt) protein is associated with striatal dysfunction and degeneration. Excitotoxicity and early synaptic defects are attributed, in part, to altered NMDA receptor (NMDAR) trafficking and function.
Autor:
Lynn A. Raymond, Liang Wang, Alexandra M. Kaufman, Lily Y. J. Zhang, Jing Fan, Clare M. Gladding, Austen J. Milnerwood
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 3, Pp 999-1009 (2012)
Huntington disease (HD) is a dominantly inherited neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the protein huntingtin (htt). Previous studies have shown enhanced N-methyl-d-aspartate (NMDA)-induced excitotoxicity in neuron
Autor:
Lily Y. J. Zhang, Ashley A. George, Liang Wang, Jing Fan, Lynn A. Raymond, Oana Cristina Vasuta
Publikováno v:
Journal of Neurochemistry. 115:1045-1056
NMDA receptors (NMDARs) mediate excitatory synaptic transmission during repetitive or prolonged glutamate release, playing a critical role in synaptic plasticity or cell death, respectively. Evidence indicates that a major pathway of NMDAR signaling
Publikováno v:
The Journal of Neuroscience. 29:10928-10938
Evidence suggests that NMDA-type glutamate receptors contribute to degeneration of striatal medium-sized spiny neurons (MSNs) in Huntington's disease (HD). Previously, we demonstrated that NMDA receptor (NMDAR)-mediated current and/or toxicity is inc
Autor:
Alaa El-Husseini, Oana Cristina Vasuta, Bo Li, Christine Sutton, Lynn A. Raymond, Lily Y. J. Zhang, Lavan Sornarajah
Publikováno v:
Journal of Neurophysiology. 99:3052-3062
Regulation of N-methyl-d-aspartate receptor (NMDAR) activity by desensitization is important in physiological and pathological states; NMDAR desensitization contributes in shaping synaptic responses and may be protective by limiting calcium influx du
Autor:
Jing, Fan, Oana Cristina, Vasuta, Lily Y J, Zhang, Liang, Wang, Ashley, George, Lynn A, Raymond
Publikováno v:
Journal of neurochemistry. 115(4)
NMDA receptors (NMDARs) mediate excitatory synaptic transmission during repetitive or prolonged glutamate release, playing a critical role in synaptic plasticity or cell death, respectively. Evidence indicates that a major pathway of NMDAR signaling
Autor:
Mannie M Y Fan, Lily Y. J. Zhang, Lynn A. Raymond, Catherine M. Cowan, Michael R. Hayden, Jacqueline Shehadeh, Rona K. Graham, Jing Fan
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 28(48)
Huntington disease (HD), caused by CAG expansion in the ubiquitously expressed huntingtin gene, is characterized by early dysfunction and death of striatal medium-sized spiny neurons (MSNs). Previous work has shown MSN-specific alterations in NMDA re