Results 121 to 130 of about 3,773 (193)

Development of High throughput Electrophysiology Assays of Recombinant Nav1.9 Channels [PDF]

Biophysical Journal, 2018
Matthew D. Fuller, Chris Mathes, Zhixin Lin, Mark L. Chapman, Nina Brinkwirth, Claudia Haarmann, Michael George, Niels Fertig, Andrea Brüggemann   +8 more
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

A triciklusos antidepresszívumok helye a fejfájások kezelésében [PDF]

, 2016
The two most important representatives of the primary headaches are migraine and tension-type headache. More than 10% of the population suffer from migraine and even a greater part, approximately 30-40% from tension-type headache.
Bereczki, Dániel, Bozsik, György, Csépány, Éva, Ertsey, Csaba, Gyüre, Tamás, Magyar, Máté   +5 more
core  

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

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

Editors' Pick: What a pain.., or not! [PDF]

, 2014
Kayser, M.H. (Manfred)
core   +2 more sources

Piezo1-mediated neuroexcitation via collaboration with KCa1.1 and Nav1.9 currents in myelinated Ah-type of trigeminal ganglion neurons in rats: Mechanistic insights with sex-specific effects. [PDF]

Mol Pain
Liu Y, Song Y, Ren X, Li M, Liu S, Li Z, Ding D, Lu X.   +7 more
europepmc   +1 more source

Familial episodic limb pain in kindreds with novel Nav1.9 mutations

Familial episodic limb pain in kindreds with novel Nav1.9 mutations
We previously performed genetic analysis in six unrelated families with infantile limb pain episodes, characterized by cold-induced deterioration and mitigation in adolescence, and reported two new mutations p.R222H/S in SCN11A responsible for these episodes.
openaire   +1 more source

A robust expression system reveals distinct gating mechanisms and calmodulin regulation of Na_V1.9 channels. [PDF]

Sci Adv
Theys M, De Waele J, Garud S, Willegems K, Van Petegem F, Bosmans F.   +5 more
europepmc   +1 more source

SDF1–CXCR4 signaling contributes to persistent pain and hypersensitivity via regulating excitability of primary nociceptive neurons: involvement of ERK-dependent Nav1.8 up-regulation [PDF]

, 2015

core   +1 more source

Proteomic analysis of isolated nerve terminals from NaV1.9 knockout mice reveals pathways relevant for pain perception. [PDF]

Pain
Rawat A, Vu DT, Erbacher C, Stigloher C, Üçeyler N, Metousis A, Mann M, Briese M, Sendtner M.   +8 more
europepmc   +1 more source