Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Nichole L. Dudek"'
Publikováno v:
Brain Pathology. 20:176-189
Huntington's disease (HD) is a neurodegenerative disease caused by mutant huntingtin protein containing an expanded polyglutamine tract, which may cause abnormal protein-protein interactions such as increased association with calmodulin (CaM). We pre
Publikováno v:
The Journal of Neuroscience. 29:11550-11559
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a polyglutamine expansion in the huntingtin protein (htt). Increasing evidence suggests that transglutaminase (TGase) plays a critical role in the pathophysiolog
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 326:153-162
Transglutaminase (TGase)-induced activation of small G proteins via 5-hydroxytryptamine (HT)(2A) receptor signaling leads to platelet aggregation (Cell 115:851-862, 2003). We hypothesize that stimulation of 5-HT(2A) receptors in neurons activates TGa
Publikováno v:
The FASEB Journal. 29
Publikováno v:
American journal of physiology. Heart and circulatory physiology. 309(2)
The role of serotonin in the hemodynamic response to blood loss remains controversial. Caudal raphe serotonin neurons are activated during hypotensive hemorrhage, and their destruction attenuates sympathetic increases following blood loss in unanesth
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 64:58-65
The most prominent neuropathologic hallmarks of Huntington disease (HD) are cortical and striatal perinuclear cytoplasmic aggregates and intranuclear inclusions of mutant huntingtin. Our laboratory previously demonstrated that huntingtin protein colo
Publikováno v:
The FASEB Journal. 26
Publikováno v:
The FASEB Journal. 24
Publikováno v:
Psychopharmacology. 213(2-3)
Serotonin and especially serotonin 2A (5-HT(2A)) receptor signaling are important in the etiology and treatment of schizophrenia and affective disorders. We previously reported a novel 5-HT(2A) receptor effector, increased transglutaminase (TGase)-ca
Publikováno v:
Brain Pathology (Zurich, Switzerland)
Huntington's disease (HD) is a neurodegenerative disease caused by mutant huntingtin protein containing an expanded polyglutamine tract, which may cause abnormal protein-protein interactions such as increased association with calmodulin (CaM). We pre