Zobrazeno 1 - 10
of 314
pro vyhledávání: '"Elaine, Sanders-Bush"'
Autor:
Uade B Olaghere Da Silva, Michael V Morabito, Clinton E Canal, David C Airey, Ronald B Emeson, Elaine Sanders-Bush
Publikováno v:
Frontiers in Neuroscience, Vol 4 (2010)
Transcripts encoding 5-HT2C receptors are modified posttranscriptionally by RNA editing, generating up to 24 protein isoforms. In recombinant cells, the fully edited isoform, 5-HT2C-VGV, exhibits blunted G-protein coupling and reduced constitutive ac
Externí odkaz:
https://doaj.org/article/ba24d819bba5466da6eb2677ee25a476
Autor:
Elaine Sanders-Bush, David C. Airey, Ana Carneiro, Jing Wang, Lu Lu, Ran Ye, Bing Zhang, Randy D. Blakely, Robert W. Williams
Publikováno v:
Genes, Brain and Behavior. 13:247-260
The biogenic amine serotonin (5-HT, 5-hydroxytryptamine) exerts powerful, modulatory control over multiple physiological functions in the brain and periphery, ranging from mood and appetite to vasoconstriction and gastrointestinal motility. In order
Autor:
Ana Carneiro, Elaine Sanders-Bush, Charisma R. Shah, W. Anthony Owens, Brent J. Thompson, Hideki Iwamoto, Ran Ye, Jennifer E. Sauer, Padmanabhan Mannangatti, Douglas G. McMahon, James S. Sutcliffe, Jordan Cohen, Lynette C. Daws, Randy D. Blakely, Jacqueline N. Crawley, Christopher L. Muller, Travis M. Kerr, Sammanda Ramamoorthy, Jeremy Veenstra-VanderWeele, Tammy Jessen
Publikováno v:
Proceedings of the National Academy of Sciences. 109:5469-5474
Fifty years ago, increased whole-blood serotonin levels, or hyperserotonemia, first linked disrupted 5-HT homeostasis to Autism Spectrum Disorders (ASDs). The 5-HT transporter (SERT) gene ( SLC6A4 ) has been associated with whole blood 5-HT levels an
Publikováno v:
Neuroscience
Previous human postmortem brain tissue research has implicated abnormalities of 5-HT receptor availability in depression and suicide. Although altered abundance of 5-HT 1A, 5-HT 2A, and 5-HT 2C receptors (5-HT(1A), 5-HT(2A), and 5-HT(2C)) has been re
Autor:
David C. Airey, Elaine Sanders-Bush
Publikováno v:
Molecular Interventions. 8:200-203
Publikováno v:
Neuropharmacology. 52:1671-1677
Extensive evidence suggests that 5-HT2 receptors may play a role in mental disorders including schizophrenia. In addition, several studies indicate that G(q)-coupled 5-HT(2A) receptors are likely targets for the initiation of events leading to the ha
Autor:
Douglas E. Vaughan, Elaine Sanders-Bush, Nancy J. Brown, Corrie A. Painter, James A.S. Muldowney
Publikováno v:
Thrombosis and Haemostasis. 97:263-271
SummaryThe acute physiologic release of tissue-type plasminogen activator (t-PA) from the endothelium is critical for vascular homeostasis. This process is prostacyclin- and nitric oxide (NO)-independent in humans. It has been suggested that calcium
Autor:
Elaine Sanders-Bush, Ian D. Tomlinson, Sandra J. Rosenthal, David M. Hercules, Anthony P. Gies, Paul J. Gresch, Joel Dillard, Rebecca L. Orndorff
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:6262-6266
Biologically active small molecule derivatives that can be conjugated to quantum dots have the promise of revolutionizing fluorescent imaging in biology. In order to achieve this several technical hurdles have to be surmounted, one of which is non-sp
Autor:
Elizabeth A. Hackler, Elaine Sanders-Bush, Paul J. Gresch, Saikat Sengupta, John C. Gore, Greg H. Turner, Ariel Y. Deutch, Malcolm J. Avison
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 320:1023-1029
Activation of 5-hydroxytryptamine2C (5-HT(2C)) receptors by the 5-HT(2) receptor agonist m-chlorophenylpiperazine (m-CPP) elicits anxiety in humans and anxiety-like behavior in animals. We compared the effects of m-CPP with the anxiogenic GABA(A) rec
Autor:
David C. Airey, Monsheel S. Sodhi, Caitlin C. Shannon, Elaine Sanders-Bush, Elizabeth A. Hackler
Publikováno v:
Neuroscience Research. 55:96-104
Post-transcriptional RNA editing of the G-protein coupled 5-hydroxytryptamine-2C (5-HT 2C ) receptor predicts an array of 24 receptor isoforms, some of which are characterized by reduced constitutive activity and potency to initiate intracellular sig