Results 101 to 110 of about 1,941 (169)

Inflammatory Mediators Increase Nav1.9 Current and Excitability in Nociceptors through a Coincident Detection Mechanism [PDF]

, 2008
Altered function of Na+ channels is responsible for increased hyperexcitability of primary afferent neurons that may underlie pathological pain states.
Clerc, Nadine, Coste, Bertrand, Crest, Marcel, Delmas, Patrick, Korogod, Sergiy M., Maingret, François, Padilla, Françoise   +6 more
core   +4 more sources

Characterization of persistent TTX-R Na+ currents in physiological concentration of sodium in rat visceral afferents

International Journal of Biological Sciences, 2009
Persistent tetrodotoxin-resistant (TTX-R) Na+ (Nav1.9/SCN11A) currents are not normally recorded in vagal afferent neurons (VANs) with 50 mM of extracellular Na+ although the functional expression of this current was observed in the presence of PGE2 or ...
Guo-Fen Qiao, Bai-Yan Li, Yu-Hong Zhou, Yan-Jie Lu, John H. Schild
doaj  

Yield of peripheral sodium channels gene screening in pure small fibre neuropathy

Journal of Neurology Neurosurgery & Psychiatry, 2018
Background Neuropathic pain is common in peripheral neuropathy. Recent genetic studies have linked pathogenic voltage-gated sodium channel (VGSC) variants to human pain disorders.
Ivo Eijkenboom, M. Sopacua, J. Hoeijmakers, B. D. de Greef, P. Lindsey, R. Almomani, M. Marchi, J. Vanoevelen, H. Smeets, S. Waxman, G. Lauria, I. Merkies, C. Faber, M. Gerrits   +13 more
semanticscholar   +1 more source

Biodegradable nanoparticles targeting circulating immune cells reduce central and peripheral sensitization to alleviate neuropathic pain following spinal cord injury. [PDF]

Neuropathic pain is a critical source of comorbidity following spinal cord injury (SCI) that can be exacerbated by immune-mediated pathologies in the central and peripheral nervous systems. In this article, we investigate whether drug-free, biodegradable,
Anderson, Aileen, Cummings, Brian, Griffin, Kate, Kalashnikova, Irina, Kolpek, Daniel, Park, Jonghyuck, Saito, Eiji, Saunders, Michael, Shea, Lonnie, Smith, Dominique   +9 more
core   +1 more source

The voltage-gated sodium channel Na(V)1.9 in visceral pain [PDF]

, 2015
Bulmer, DC, Hockley, JRF, Winchester, WJ
core   +1 more source

Sodium channels. [PDF]

, 2018
In 2000, with the completion of the human genome project, nine related channels were found to comprise the complete voltage-gated sodium gene family and they were renamed NaV1.1-NaV1.9.
Iseppon, F, Wood, JN
core  

Nav1.9 (SCN11A) [PDF]

Science-Business eXchange, 2013
openaire   +1 more source

Neurological perspectives on voltage-gated sodium channels [PDF]

, 2016
Abrahamsen, Akopian, Akopian, Alabi, Alzheimer, Amaya, Aurlien, Baker, Baker, Bennett, Beyreuther, Beyreuther, Beyreuther, Binshtok, Binshtok, Biton, Black, Black, Black, Black, Bohle, Bosmans, Brackenbury, Brittain, Bromley, Burge, Calabresi, Campbell, Cannon, Cardenas, Carrithers, Carter, Cattaneo, Catterall, Catterall, Cestele, Chambers, Chen, Cheung, Chioni, Choi, Chong, Clare, Conway, Corry, Cossette, Cox, Cox, Cummins, Cummins, Devor, Dib-Hajj, Dib-Hajj, Dib-Hajj, Dib-Hajj, Dib-Hajj, Dib-Hajj, Dichgans, Diss, Doty, Drizin, Durham, Ebell, Escayg, Estacion, F. Rugiero, Fang, Fertleman, Fink, Fischer, Fischer, Fraser, Fraser, French, Ganjehei, Garrido, Gasser, Giardina, Goldberg, Graff-Radford, Grieco, Haimovich, Hains, Hains, Hakim, Harmer, Hasegawa, Hedstrom, Herfst, Hernandez-Plata, Heron, Hewitt, Hille, Hiyama, Holland, Hollmann, Hoyt, Hsueh, Huth, Iqbal, Isom, Isom, J. E. Linley, J. N. Wood, Jang, Jarecki, Jiang, Jiang, Joshi, Jurkat-Rott, Kalra, Kalume, Kapoor, Kapoor, Kapplinger, Kearney, Kerr, Khasar, Khoromi, Kort, Kudrow, Kuhnert, Kyndt, Lai, Lamas, Lampl, Leo, Leterrier, Liao, Lim, Lin, Lindia, Liu, London, Lopez-Santiago, Lopez-Santiago, M. D. Baker, M. S. Minett, Mackenzie, Maitre, Mantegazza, Mao, Marini, McGowan, Meisler, Meisler, Minett, Misra, Mohammadi, Muth-Selbach, N. Eijkelkamp, Nalamachu, Nassar, Nassar, Nattel, Naylor, Nuyens, O'Malley, O'Roak, O'Roak, Okuse, Onkalp, Ou, Oyama, Padilla, Patino, Patino, Patino, Patlak, Payandeh, Payandeh, Pertin, Perucca, Pittenger, Planells-Cases, Poolos, Poon, Priest, Pt  cek, R. Cregg, R. Werdehausen, Ragsdale, Ragsdale, Ragsdale, Rajakulendran, Raman, Rauck, Renganathan, Rivera-Acevedo, Roberson, Robinson, Rogart, Rogawski, Ruetsch, Rugiero, Rusconi, Saenen, Sanders, Schwarz, Schwindt, Shank, Shao, Shao, Sijben, Smith, Sokolov, Song, Spampanato, Starmer, Stefani, Stevens, Stummann, Stys, St  hmer, St  hr, Sugawara, Tan, Taverna, Toledo-Aral, Uebachs, Vahedi, Vassilev, Vassilev, Veeramah, Veneroni, Volkers, von Gunten, Wang, Wang, Wang, Watanabe, Watanabe, Waxman, Waxman, Weiser, Weiss, Weiss, Weiss, West, Westenbroek, Whitaker, Wimmer, Wood, Yang, Yu, Yu, Zimmer, Zimmermann   +247 more
core   +1 more source

Blockade of voltage-gated sodium channels inhibits invasion of endocrine resistant breast cancer cells [PDF]

, 2016
Al Saleh, Al Saleh, Azuma, Azuma, Besson, Biki, Brackenbury, Brackenbury, Brackenbury, Brackenbury, Brackenbury, Brackenbury, Brackenbury, Brisson, Brisson, Carrithers, Chioni, Clare, Crill, Dib-Hajj, Ding, Diss, Djamgoz, FATIMA H. MOHAMMED, Fraser, Gao, Gialeli, Gillet, Gillet, Goldin, Goldin, Hagen, Hernández-Plata, Hernández-Plata, Hille, House, House, Isom, Ju, Kawakubo, Khajah, Kunzelmann, Laniado, Luqmani, MAITHAM A. KHAJAH, Maness, Mantegazza, Mao, MING YANG, Nelson, Nelson, Onkal, Potier, Roger, Sekton, Turnbull, WILLIAM J. BRACKENBURY, Yang, Yang, Yildirim, Yip, YUNUS A. LUQMANI, Zucker   +62 more
core   +1 more source

Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9. [PDF]

Pain, 2022
Ma T, Li L, Chen R, Yang L, Sun H, Du S, Xu X, Cao Z, Zhang X, Zhang L, Shi X, Liu JY.   +11 more
europepmc   +1 more source