Результаты поиска - Michael F. Jarvis
- Отображение 1 - 14 результаты of 14
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Adenosine kinase: A key regulator of purinergic physiology по Detlev Boison, Michael F. Jarvis
Опубликовано 2020Revisão -
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P2X Receptors as Drug Targets по R. Alan North, Michael F. Jarvis
Опубликовано 2012Revisão -
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Painful Purinergic Receptors по Diana L. Donnelly‐Roberts, Steve McGaraughty, Char‐Chang Shieh, Prisca Honoré, Michael F. Jarvis
Опубликовано 2007Revisão -
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Monosodium Iodoacetate-Induced Joint Pain is Associated with Increased Phosphorylation of Mitogen Activated Protein Kinases in the Rat Spinal Cord по Young-Lim Lee, Madhavi Pai, Jill‐Desiree Brederson, Denise Wilcox, Gin C. Hsieh, Michael F. Jarvis, Robert S. Bitner
Опубликовано 2011Artigo -
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Modulation of BzATP and formalin induced nociception: attenuation by the P2X receptor antagonist, TNP‐ATP and enhancement by the P2X<sub>3</sub> allosteric modulator, cibacron blue... по Michael F. Jarvis, Carol T. Wismer, Edmund Schweitzer, Haixia Yu, Tim van Biesen, Kevin J. Lynch, Edward C. Burgard, Elizabeth A. Kowaluk
Опубликовано 2001Artigo -
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Effects of A‐317491, a novel and selective P2X<sub>3</sub>/P2X<sub>2/3</sub> receptor antagonist, on neuropathic, inflammatory and chemogenic nociception following intrathecal and... по Steve McGaraughty, Carol T. Wismer, Chang Z. Zhu, Joseph P. Mikusa, Prisca Honoré, Katharine L. Chu, Chih‐Hung Lee, Connie R. Faltynek, Michael F. Jarvis
Опубликовано 2003Artigo -
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Update of P2X receptor properties and their pharmacology: IUPHAR Review 30 по Péter Illés, Christa E. Müller, Kenneth A. Jacobson, Thomas Grütter, Annette Nicke, Samuel J. Fountain, Charles Kennedy, Günther Schmalzing, Michael F. Jarvis, Stanko S. Stojilković, Brian F. King, Francesco Di Virgilio
Опубликовано 2020Revisão -
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A-317491, a novel potent and selective non-nucleotide antagonist of P2X <sub>3</sub> and P2X <sub>2/3</sub> receptors, reduces chronic inflammatory and neuropathic pain in the rat по Michael F. Jarvis, Edward C. Burgard, Steve McGaraughty, Prisca Honoré, Kevin J. Lynch, Timothy J. Brennan, Alberto Subieta, Tim van Biesen, Jayne Cartmell, Bruce R. Bianchi, Wende Niforatos, Karen Kage, Haixia Yu, Joe Mikusa, Carol T. Wismer, Chang Z. Zhu, Katharine L. Chu, Chih‐Hung Lee, Andrew O. Stewart, James S. Polakowski, Bryan F. Cox, Elizabeth A. Kowaluk, Michael Williams, James P. Sullivan, Connie R. Faltynek
Опубликовано 2002Artigo -
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A-803467, a potent and selective Na <sub>v</sub> 1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat по Michael F. Jarvis, Prisca Honoré, Char‐Chang Shieh, Mark L. Chapman, Shailen K. Joshi, Xu-Feng Zhang, Michael E. Kort, William Carroll, Brian E. Marron, Robert N. Atkinson, James B. Thomas, Dong Liu, Michael J. Krambis, Yi Liu, Steve McGaraughty, Katharine L. Chu, Rosemarie Roeloffs, Chengmin Zhong, Joseph P. Mikusa, Gricelda Hernandez, Donna M. Gauvin, Carrie L. Wade, Chang Zhu, Madhavi Pai, Marc J. C. Scanio, Lei Shi, Irene Drizin, Robert J. Gregg, Mark A. Matulenko, Ahmed H. Hakeem, Michael F. Gross, Matthew S. Johnson, Kennan C. Marsh, P. Kay Wagoner, James P. Sullivan, Connie R. Faltynek, Douglas S. Krafte
Опубликовано 2007Artigo
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Связанные темы
Receptor
Medicine
Pharmacology
Biology
Internal medicine
Chemistry
Biochemistry
Nociception
Agonist
Neuroscience
Allodynia
Hyperalgesia
Neuropathic pain
Antagonist
Cell biology
Immunology
P2 receptor
Anesthesia
Chronic pain
Gene
Inflammation
Receptor antagonist
Adenosine receptor
Allosteric modulator
Allosteric regulation
Anatomy
Dorsal root ganglion
Dorsum
Electrophysiology
Endocrinology