The DOI matches its Crossref record; 728 of the 728 references it cites were found in a registry or an index.
Mammalian Transient Receptor Potential TRPA1 Channels: From Structure to Disease
Open accessAbstract
The transient receptor potential ankyrin (TRPA) channels are Ca 2+ -permeable nonselective cation channels remarkably conserved through the animal kingdom. Mammals have only one member, TRPA1, which is widely expressed in sensory neurons and in non-neuronal cells (such as epithelial cells and hair cells). TRPA1 owes its name to the presence of 14 ankyrin repeats located in the NH 2 terminus of the channel, an unusual structural feature that may be relevant to its interactions with intracellular components. TRPA1 is primarily involved in the detection of an extremely wide variety of exogenous stimuli that may produce cellular damage. This includes a plethora of electrophilic compounds that interact with nucleophilic amino acid residues in the channel and many other chemically unrelated compounds whose only common feature seems to be their ability to partition in the plasma membrane. TRPA1 has been reported to be activated by cold, heat, and mechanical stimuli, and its function is modulated by multiple factors, including Ca 2+ , trace metals, pH, and reactive oxygen, nitrogen, and carbonyl species. TRPA1 is involved in acute and chronic pain as well as inflammation, plays key roles in the pathophysiology of nearly all organ systems, and is an attractive target for the treatment of related diseases. Here we review the current knowledge about the mammalian TRPA1 channel, linking its unique structure, widely tuned sensory properties, and complex regulation to its roles in multiple pathophysiological conditions.
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Items 401–600 of 728
Ultraviolet light and photosensitising agents activate TRPA1 via generation of oxidative stress
Hill, K., & Schaefer, M. (2008) · Cell Calcium · doi:10.1016/j.ceca.2008.08.001 · Cited by 71
de Oliveira, C., Garami, A., Lehto, S. G., Pákai, E., Tékus, V., Pohóczky, K., Youngblood, B. D., Wang, W., Kort, M. E., Kym, P. R., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5387-13.2014 · Cited by 71
Transient receptor potential A1 mediates gastric distention-induced visceral pain in rats
Kondo, T., Obata, K., Miyoshi, K., Sakùrai, J., Tanaka, J., Miwa, H., & Noguchi, K. (2009) · Gut · doi:10.1136/gut.2008.175901 · Cited by 71
A Potent and Site-Selective Agonist of TRPA1
Takaya, J., Mio, K., Shiraishi, T., Kurokawa, T., Otsuka, S., Mori, Y., & Uesugi, M. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b10162 · Cited by 71
Mechanisms of pruritogen‐induced activation of itch nerves in isolated mouse skin
Ru, F., Sun, H., Jurcakova, D., Herbstsomer, R. A., Meixong, J., Dong, X., & Undem, B. J. (2017) · The Journal of Physiology · doi:10.1113/jp273795 · Cited by 71
Dietrich, A., Steinritz, D., & Gudermann, T. W. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.04.005 · Cited by 71
TRPA1–FGFR2 binding event is a regulatory oncogenic driver modulated by miRNA-142-3p
Berrout, J., Kyriakopoulou, E., Moparthi, L., Hogea, A. S., Berrout, L., Ivan, C., Lorger, M., Boyle, J. P., Peers, C., Muench, S. P., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00983-w · Cited by 71
Vermeulen, W., De Man Joris, G., Schepper, H. U. D., Bult, H., Moreels, T. G., Pelckmans, P. A., & Winter, B. Y. D. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.10.014 · Cited by 70
Role of TRPM8 and TRPA1 for cold allodynia in patients with cold injury
Namer, B., Kleggetveit, I. P., Handwerker, H. O., Schmelz, M., & Jørum, E. (2008) · Pain · doi:10.1016/j.pain.2008.03.007 · Cited by 70
Pozsgai, G., Hajna, Z., Bagoly, T., et al. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.05.053 · Cited by 69
Ji, G., Zhou, S., & Carlton, S. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.039 · Cited by 68
Role of reactive oxygen species and TRP channels in the cough reflex
Taylor‐Clark, T. E. (2016) · Cell Calcium · doi:10.1016/j.ceca.2016.03.007 · Cited by 68
Potential Future Pharmacological Treatment of Bladder Dysfunction
Andersson, K. (2016) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.12577 · Cited by 68
Balemans, D., Aguilera‐Lizarraga, J., Florens, M. V., Jain, P., Denadai‐Souza, A., Viola, M. F., Alpizar, Y. A., der Merwe, V., Berghe, P. V., Talavera, K., et al. (2019) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00116.2018 · Cited by 68
Self-citationKojima, R., Nozawa, K., Doihara, H., Keto, Y., Kaku, H., Yokoyama, T., & Itou, H. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.11.020 · Cited by 67
Kurogi, M., Miyashita, M., Emoto, Y., Kubo, Y., & Saitoh, O. (2011) · Chemical Senses · doi:10.1093/chemse/bjr087 · Cited by 67
Structural basis of TRPA1 inhibition by HC-030031 utilizing species-specific differences
Gupta, R., Saito, S., Mori, Y., Itoh, S., Okumura, H., & Tominaga, M. (2016) · Scientific Reports · doi:10.1038/srep37460 · Cited by 67
Evolutionary tuning of TRPA1 and TRPV1 thermal and chemical sensitivity in vertebrates
Saito, S., & Tominaga, M. (2017) · Temperature · doi:10.1080/23328940.2017.1315478 · Cited by 67
Mouse TRPA1 function and membrane localization are modulated by direct interactions with cholesterol
Startek, J. B., Boonen, B., López‐Requena, A., Talavera, A., Alpizar, Y. A., Ghosh, D., Ranst, N. V., Nilius, B., Voets, T., & Talavera, K. (2019) · eLife · doi:10.7554/elife.46084 · Cited by 67
Self-citationNummenmaa, E., Hämäläinen, M., Moilanen, L. J., Paukkeri, E.-L., Nieminen, R., Moilanen, T., Vuolteenaho, K., & Moilanen, E. (2016) · Arthritis Research & Therapy · doi:10.1186/s13075-016-1080-4 · Cited by 66
Inflammatory pain control by blocking oxidized phospholipid-mediated TRP channel activation
Oehler, B., Kistner, K., Martin, C., Schiller, J., Mayer, R., Mohammadi, M., Sauer, R., Filipović, M. R., Nieto, F. R., Kloka, J. A., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05348-3 · Cited by 66
Chen, Y., Huang, Y., Yan, C. H., Chiu, P., Wei, Q., Zhao, J., Guo, X., Leung, F. K. L., & Lu, W. W. (2017) · Bone Research · doi:10.1038/boneres.2017.34 · Cited by 66
TRPA1 channel contributes to myocardial ischemia-reperfusion injury
Conklin, D. J., Guo, Y., Nystoriak, M. A., Jagatheesan, G., Obal, D., Kilfoil, P. J., Hoetker, J. D., Guo, L., Bolli, R., & Bhatnagar, A. (2019) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00106.2018 · Cited by 66
Activation of transient receptor potential A1 by a non‐pungent capsaicin‐like compound, capsiate
Shintaku, K., Uchida, K., Suzuki, Y., Zhou, Y., Fushiki, T., Watanabe, T., Yazawa, S., & Tominaga, M. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01634.x · Cited by 65
Drosophila TRPA1 isoforms detect UV light via photochemical production of H 2 O 2
Guntur, A. R., Gu, P., Takle, K. A., Chen, J., Xiang, Y., & Yang, C.-H. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1514862112 · Cited by 65
Smith, T. P., Haymond, T., Smith, S. N., & Sweitzer, S. M. (2014) · Journal of Pain Research · doi:10.2147/jpr.s65923 · Cited by 65
Stimulation of GLP-1 Secretion Downstream of the Ligand-Gated Ion Channel TRPA1
Emery, E. C., Diakogiannaki, E., Gentry, C., Psichas, A., Habib, A. M., Bevan, S., Fischer, M. J. M., Reimann, F. M., & Gribble, F. M. (2014) · Diabetes · doi:10.2337/db14-0737 · Cited by 65
Ku, D. D., Abdel-Razek, T. T., Dai, J., Kim‐Park, S., Fallon, M. B., & Abrams, G. A. (2002) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2002.03596.x · Cited by 64
Demartini, C., Tassorelli, C., Zanaboni, A. M., Tonsi, G., Francesconi, O., Nativi, C., & Greco, R. (2017) · The Journal of Headache and Pain · doi:10.1186/s10194-017-0804-4 · Cited by 64
TRPA1 and TRPV1 are differentially involved in heat nociception of mice
Hoffmann, T., Kistner, K., Miermeister, F., et al. (2013) · European Journal of Pain · doi:10.1002/j.1532-2149.2013.00331.x · Cited by 63
Streptozotocin Stimulates the Ion Channel TRPA1 Directly
Andersson, D. A., Filipović, M. R., Gentry, C., Eberhardt, M. J., Vastani, N., Leffler, A., Reeh, P. W., & Bevan, S. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.644476 · Cited by 63
Kimball, E. S., Prouty, S., Pavlick, K. P., Wallace, N. H., Schneider, C. R., & Hornby, P. J. (2007) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2007.00939.x · Cited by 63
Eilers, H., Cattaruzza, F., Nassini, R., Materazzi, S., Andrè, E., Chu, C., Cottrell, G. S., Schumacher, M. A., Geppetti, P., & Bunnett, N. W. (2010) · Anesthesiology · doi:10.1097/aln.0b013e3181d94e00 · Cited by 63
Peripherally Increased Artemin is a Key Regulator of TRPA1/V1 Expression in Primary Afferent Neurons
Ikeda-Miyagawa, Y., Kobayashi, K., Yamanaka, H., Okubo, M., Wang, S., Dai, Y., Yagi, H., Hirose, M., & Noguchi, K. (2015) · Molecular Pain · doi:10.1186/s12990-015-0004-7 · Cited by 63
Bahia, P. K., Parks, T. A., Stanford, K. R., Mitchell, D. A., Varma, S., Stevens, S. M., & Taylor‐Clark, T. E. (2016) · The Journal of General Physiology · doi:10.1085/jgp.201611581 · Cited by 63
Sághy, É., Sipos, É., Ács, P., Bölcskei, K., Pohóczky, K., Kemény, Á., Zoltán, S., Szőke, É., Sétáló, G., Komoly, S., et al. (2016) · Glia · doi:10.1002/glia.23051 · Cited by 63
Differential Contribution of TRPA1, TRPV4 and TRPM8 to Colonic Nociception in Mice
Mueller–Tribbensee, S. M., Karna, M., Khalil, M., Neurath, M. F., Reeh, P. W., & Engel, M. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128242 · Cited by 62
Patil, M. J., Jeske, N. A., & Akopian, A. N. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.09.031 · Cited by 62
Weller, K., Reeh, P. W., & Sauer, S. K. (2011) · Neuropeptides · doi:10.1016/j.npep.2011.07.011 · Cited by 61
Sura, L., Zima, V., Maršáková, L., Kádková, A., Barvı́k, I., & Vlachová, V. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.341859 · Cited by 61
Modulation of TRP Channels by Resveratrol and other Stilbenoids
Yu, L., Wang, S., Kogure, Y., Yamamoto, S., Noguchi, K., & Dai, Y. (2013) · Molecular Pain · doi:10.1186/1744-8069-9-3 · Cited by 61
Cicerale, S., Breslin, P. A. S., Beauchamp, G. K., & Keast, R. S. J. (2009) · Chemical Senses · doi:10.1093/chemse/bjp006 · Cited by 61
Methylglyoxal causes pain and hyperalgesia in human through C-fiber activation
Düll, M. M., Riegel, K., Tappenbeck, J., Ries, V., Strupf, M., Fleming, T. H., Sauer, S. K., & Namer, B. (2019) · Pain · doi:10.1097/j.pain.0000000000001644 · Cited by 61
Dux, M., Will, C., Vogler, B., Filipović, M. R., & Meßlinger, K. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13164 · Cited by 60
Involvement of TRPA1 Activation in Acute Pain Induced by Cadmium in Mice
Miura, S., Takahashi, K., Imagawa, T., Uchida, K., Saito, S., Tominaga, M., & Ohta, T. (2013) · Molecular Pain · doi:10.1186/1744-8069-9-7 · Cited by 60
Zhou, H.-R., & Pestka, J. J. (2015) · Toxicological Sciences · doi:10.1093/toxsci/kfv061 · Cited by 60
Graepel, R., Fernandes, E. S., Aubdool, A. A., Andersson, D. A., Bevan, S., & Brain, S. D. (2011) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.110.172403 · Cited by 60
Zhao, J., Shyue, S., Kou, Y. R., Lu, T., & Lee, T. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.15229 · Cited by 60
Molecular Basis of TRPA1 Regulation in Nociceptive Neurons. A Review
Kádková, A., Synytsya, V., Krůšek, J., Zímová, L., & Vlachová, V. (2017) · Physiological Research · doi:10.33549/physiolres.933553 · Cited by 60
Mitrovic, M., Shahbazian, A., Bock, E., Pabst, M. A., & Holzer, P. D. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00794.x · Cited by 59
Albin, K. C., & Simons, C. T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009520 · Cited by 59
Methyl p ‐hydroxybenzoate causes pain sensation through activation of TRPA1 channels
Fujita, F., Moriyama, T., Higashi, T., Shima, A., & Tominaga, M. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707219 · Cited by 59
TRPA1 expression and its functional activation in rodent cortex
Kheradpezhouh, E., Choy, J. M. C., Daria, V. R., & Arabzadeh, E. (2017) · Open Biology · doi:10.1098/rsob.160314 · Cited by 59
TRPA1 agonists delay gastric emptying in rats through serotonergic pathways
Doihara, H., Nozawa, K., Kawabata-Shoda, E., Kojima, R., Yokoyama, T., & Ito, H. (2009) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-009-0435-7 · Cited by 58
Have we found the tip link, transduction channel, and gating spring of the hair cell?
Gillespie, P. G., Dumont, R. A., & Kachar, B. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.06.007 · Cited by 58
Drews, A., Mohr, F., Rizun, O., Wagner, T. F. J., Dembla, S., Rudolph, S., Lambert, S., Konrad, M., Philipp, S. E., Behrendt, M., et al. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12521 · Cited by 58
Biological Roles of Resolvins and Related Substances in the Resolution of Pain
Lim, J. Y., Park, C., & Hwang, S. W. (2015) · BioMed Research International · doi:10.1155/2015/830930 · Cited by 57
Activation of transient receptor potential ankyrin 1 by eugenol
Chung, G., Im, S. T., Kim, Y., Jung, S. J., Rhyu, M., & Oh, S. B. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.047 · Cited by 57
Kaimoto, T., Hatakeyama, Y., Takahashi, K., Imagawa, T., Tominaga, M., & Ohta, T. (2016) · European Journal of Pain · doi:10.1002/ejp.840 · Cited by 57
Role of TRPA1 in acute cardiopulmonary toxicity of inhaled acrolein
Conklin, D. J., Haberzettl, P., Jagatheesan, G., Kong, M., & Hoyle, G. W. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.08.028 · Cited by 57
Krohn, I. K., Callebaut, I., Alpizar, Y. A., Steelant, B., Gerven, L. V., Skov, P. S., Kasran, A., Talavera, K., Wouters, M. M., Ceuppens, J. L., et al. (2017) · Allergy · doi:10.1111/all.13349 · Cited by 57
Self-citationWang, H., Schupp, M., Zurborg, S., & Heppenstall, P. A. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.242842 · Cited by 56
Hesperetin Stimulates Cholecystokinin Secretion in Enteroendocrine STC-1 Cells
Kim, H. Y., Park, M. S., Kim, K., Lee, Y. M., & Rhyu, M. R. (2013) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2012.077 · Cited by 56
Doihara, H., Nozawa, K., Kawabata-Shoda, E., Kojima, R., Yokoyama, T., & Ito, H. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.06.038 · Cited by 56
Cold stress increases reactive oxygen species formation via TRPA1 activation in A549 cells
Sun, W., Wang, Z., Cao, J., Cui, H., & Ma, Z. (2015) · Cell Stress and Chaperones · doi:10.1007/s12192-015-0663-3 · Cited by 56
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Bassoli, A., Borgonovo, G., Caimi, S., Scaglioni, L., Morini, G., Moriello, A. S., Marzo, V. D., & PETROCELLIS, L. D. (2008) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2008.12.057 · Cited by 55
Activation of TRPA1 by luminal stimuli induces EP4-mediated anion secretion in human and rat colon
Kaji, I., Yasuoka, Y., Karaki, S.-I., & Kuwahara, A. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00289.2011 · Cited by 55
Kurhanewicz, N. A., McIntosh-Kastrinsky, R., Tong, H., Ledbetter, A. D., Walsh, L., Farraj, A. K., & Hazari, M. S. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.10.008 · Cited by 55
Andrei, S. R., Ghosh, M., Sinharoy, P., Dey, S., Bratz, I. N., & Damron, D. S. (2017) · Channels · doi:10.1080/19336950.2017.1365206 · Cited by 55
PETROCELLIS, L. D., Moriello, A. S., Imperatore, R., Cristino, L., Starowicz, K., & Marzo, V. D. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.02122.x · Cited by 54
Transient receptor potential ankyrin 1 mediates chronic pancreatitis pain in mice
Cattaruzza, F., Johnson, C. E., Leggit, A., Grady, E. F., Schenk, A. K., Cevikbas, F., Cedron, W. J., Bondada, S., Kirkwood, R., Malone, B. J., et al. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00005.2013 · Cited by 54
Sensitization of TRPA1 by Protein Kinase A
Meents, J., Fischer, M. J. M., & McNaughton, P. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170097 · Cited by 54
Oxidative Stress in the Amygdala Contributes to Neuropathic Pain
Sagalajev, B., Wei, H., Chen, Z., Albayrak, I., Koivisto, A., & Pertovaara, A. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.12.009 · Cited by 54
Lin, A., Liu, M.-H., Ko, H., Perng, D., Lee, T., & Kou, Y. R. (2015) · Mediators of Inflammation · doi:10.1155/2015/148367 · Cited by 53
Oxidized Phospholipid OxPAPC Activates TRPA1 and Contributes to Chronic Inflammatory Pain in Mice
Liu, B., Tai, Y., Caceres, A. I., Achanta, S., Balakrishna, S., Shao, X., Fang, J., & Jordt, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165200 · Cited by 53
Oi‐Kano, Y., Iwasaki, Y., Nakamura, T., Watanabe, T., Goto, T., Kawada, T., Watanabe, K., & Iwai, K. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.11.009 · Cited by 53
Effects of luminal thymol on epithelial transport in human and rat colon
Kaji, I., Karaki, S.-I., & Kuwahara, A. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00503.2010 · Cited by 52
Injured versus Uninjured Afferents: Who Is to Blame for Neuropathic Pain?
Ringkamp, M., & Meyer, R. A. (2005) · Anesthesiology · doi:10.1097/00000542-200508000-00002 · Cited by 52
Rutten, K., Vry, J. D., Robens, A., Tzschentke, T., & van der Kam, E. L. (2010) · European Journal of Pain · doi:10.1016/j.ejpain.2010.07.011 · Cited by 52
Identification of a putative binding site critical for general anesthetic activation of TRPA1
Ton, H. T., Phan, T. X., Abramyan, A. M., Shi, L., & Ahern, G. P. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618144114 · Cited by 52
Bölcskei, K., Kriszta, G., Sághy, É., Payrits, M., Sipos, É., Vranesics, A., Berente, Z., Ábrahám, H., Ács, P., Komoly, S., et al. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.03.020 · Cited by 52
Capasso, R., Aviello, G., Romano, B., Borrelli, F., PETROCELLIS, L. D., Marzo, V. D., & Izzo, A. A. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01703.x · Cited by 51
Distinct expression of cold receptors (TRPM8 and TRPA1) in the rat nodose–petrosal ganglion complex
Hondoh, A., Ishida, Y., Ugawa, S., Ueda, T., Shibata, Y., Yamada, T., Shikano, M., Murakami, S., & Shimada, S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.01.016 · Cited by 51
Alvarez‐Collazo, J., Alonso-Carbajo, L., Lopez-Medina, A. I., Alpizar, Y. A., Tajada, S., Nilius, B., Voets, T., López‐López, J. R., Talavera, K., Pérez-García, M. T., et al. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1472-8 · Cited by 51
Self-citationSculptoreanu, A., Kullmann, F. A., Artim, D. E., Bazley, F. A., Schopfer, F. J., Woodcock, S. R., Freeman, B. Α., & de Groat, W. C. (2010) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.163154 · Cited by 51
Stueber, T., Eberhardt, M. J., Hadamitzky, C., Jangra, A., Schenk, S., Dick, F., Stoetzer, C., Kistner, K., Reeh, P. W., Binshtok, A. M., et al. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001050 · Cited by 51
Chapter 11 Bv8/Prokineticins and their Receptors
Negri, L., Lattanzi, R., Giannini, E., Canestrelli, M., Nicotra, A., & Melchiorri, P. (2009) · International review of neurobiology · doi:10.1016/s0074-7742(09)85011-3 · Cited by 51
TRPA 1 gene polymorphisms and childhood asthma
Gallo, V., Dijk, F. N., Holloway, J. W., Ring, S. M., Koppelman, G. H., Postma, D. S., Strachan, D. P., Granell, R., de Jongste, J. C., Jaddoe, V. W. V., et al. (2016) · Pediatric Allergy and Immunology · doi:10.1111/pai.12673 · Cited by 51
Alvarenga, E. M., de Souza, L. K. M., Araújo, T. S. L., Nogueira, K. D. M., Sousa, F. B. M., de Araújo, A. R., Martins, C. S., Pacífico, D. M., Brito, G. A. D. C., de Souza, E. P., et al. (2016) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2016.11.009 · Cited by 51
Gerven, L. V., Alpizar, Y. A., Steelant, B., Callebaut, I., Krohn, I. K., Wouters, M. M., Vermeulen, F. L., Boeckxstaens, G. E., Talavera, K., & Hellings, P. W. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.03.014 · Cited by 51
Self-citationÁlvarez-Berdugo, D., Rofes, L., Arreola, V., Martín, A., Molina, L. M., & Clavé, P. (2017) · Neurogastroenterology & Motility · doi:10.1111/nmo.13185 · Cited by 51
G-protein coupled receptors regulating cough
Maher, S. A., Dubuis, E. D., & Belvisi, M. G. (2011) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2011.06.005 · Cited by 50
Numbing the Senses: Role of TRPA1 in Mechanical and Cold Sensation
Story, G. M., & Gereau, R. W. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.009 · Cited by 50
TRP Channels and Thermosensation
Voets, T. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-05161-1_1 · Cited by 50
Comprehensive thermal preference phenotyping in mice using a novel automated circular gradient assay
Touška, F., Winter, Z., Mueller, A., Vlachová, V., Larsen, J. D., & Zimmermann, K. (2016) · Temperature · doi:10.1080/23328940.2015.1135689 · Cited by 50
So, K., Tei, Y., Zhao, M., Miyake, T., Hiyama, H., Shirakawa, H., Imai, S., Mori, Y., Nakagawa, T., Matsubara, K., et al. (2016) · Scientific Reports · doi:10.1038/srep23261 · Cited by 50
TRP Channels as Therapeutic Targets in Diabetes and Obesity
Zsombok, A., & Derbenev, A. V. (2016) · Pharmaceuticals · doi:10.3390/ph9030050 · Cited by 50
Roles of Transient Receptor Potential Ankyrin 1 in Oxaliplatin-Induced Peripheral Neuropathy
Nakagawa, T., & Kaneko, S. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00243 · Cited by 50
A Human TRPA1-Specific Pain Model
Heber, S., Gold-Binder, M., Ciotu, C. I., Witek, M., Ninidze, N., Kress, H. G., & Fischer, M. J. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.3048-18.2019 · Cited by 50
Al‐Shamlan, F., & El‐Hashim, A. Z. (2019) · Respiratory Research · doi:10.1186/s12931-019-1060-8 · Cited by 50
Ceuleers, H., Hanning, N., Heirbaut, J., Van Remoortel, S., Joossens, J., Van Der Veken, P., Francque, S. M., De bruyn, M., Lambeir, A., De Man, J. G., et al. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14396 · Cited by 49
Oguri, G., Nakajima, T., Yamamoto, Y., Takano, N., Tanaka, T., Kikuchi, H., Morita, T., Nakamura, F., Yamasoba, T., & Komuro, I. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01021.2013 · Cited by 49
Tsubota‐Matsunami, M., Noguchi, Y., Okawa, Y., Sekiguchi, F., & Kawabata, A. (2012) · Journal of Pharmacological Sciences · doi:10.1254/jphs.12086sc · Cited by 49
Babeș, A., Fischer, M. J. M., Filipović, M. R., Engel, M. A., Flonta, M., & Reeh, P. W. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.02.018 · Cited by 49
Olsen, R. V., Andersen, H. H., Møller, H. G., Eskelund, P. W., & Arendt‐Nielsen, L. (2014) · European Journal of Pain · doi:10.1002/j.1532-2149.2014.494.x · Cited by 49
Resiniferatoxin Mediated Ablation of TRPV1+ Neurons Removes TRPA1 as Well
Pecze, L., Pelsőczi, P., Kecskés, M., Winter, Z., Papp, A., Kaszás, K., Letoha, T., Vízler, C., & Oláh, Z. (2009) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100006600 · Cited by 49
Effect of cigarette smoking on cough reflex induced by TRPV1 and TRPA1 stimulations
Kanezaki, M., Ebihara, S., Gui, P., Ebihara, T., & Kohzuki, M. (2011) · Respiratory Medicine · doi:10.1016/j.rmed.2011.12.007 · Cited by 48
Zielińska, M., Jarmuż, A., Wasilewski, A., Sałaga, M., & Fichna, J. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000234 · Cited by 48
Fernandes, E. S., Russell, F. A., Alawi, K. M., Sand, C. A., Liang, L., Salamon, R., Bodkin, J. V., Aubdool, A. A., Arno, M. J., Gentry, C., et al. (2016) · Arthritis Research & Therapy · doi:10.1186/s13075-015-0905-x · Cited by 48
Meotti, F. C., Forner, S., Lima-Garcia, J. F., et al. (2013) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2013.03.008 · Cited by 47
Role of transient receptor potential ankyrin subfamily member 1 in pruritus induced by endothelin-1
Liang, J., Ji, Q., & Ji, W. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.02.009 · Cited by 47
Mizushima, T., Obata, K., Katsura, H., Yamanaka, H., Kobayashi, K., Dai, Y., Fukuoka, T., Tokunaga, A., Mashimo, T., & Noguchi, K. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.03.024 · Cited by 47
Neuro-immune interactions in chemical-induced airway hyperreactivity
Devos, F. C., Boonen, B., Alpizar, Y. A., Maes, T., Hox, V., Seys, S., Pollaris, L., Liston, A., Nemery, B., Talavera, K., et al. (2016) · European Respiratory Journal · doi:10.1183/13993003.01778-2015 · Cited by 47
Self-citationLaursen, W. J., Bagriantsev, S. N., & Gracheva, E. O. (2014) · Current topics in membranes · doi:10.1016/b978-0-12-800181-3.00004-x · Cited by 47
The C-terminal basic residues contribute to the chemical- and voltage-dependent activation of TRPA1
Samad, A., Sura, L., Benedikt, J., Ettrich, R. H., Minofar, B., Teisinger, J., & Vlachová, V. (2010) · Biochemical Journal · doi:10.1042/bj20101256 · Cited by 46
Kojima, R., Doihara, H., Nozawa, K., Kawabata-Shoda, E., Yokoyama, T., & Ito, H. (2009) · Pharmacology · doi:10.1159/000236524 · Cited by 46
Guntur, A. R., Gou, B., Gu, P., He, R., Stern, U., Xiang, Y., & Yang, C.-H. (2016) · Genetics · doi:10.1534/genetics.116.195172 · Cited by 46
Bodkin, J. V., & Brain, S. D. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02203.x · Cited by 45
Ding, Z., Gómez, T., Werkheiser, J. L., Cowan, A., & Rawls, S. M. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.09.030 · Cited by 45
Transient receptor potential channels in bladder function
Avelino, A., Charrua, A., Frias, B., Cruz, C. D., Boudes, M., Ridder, D. J. M. K. D., & Cruz, F. (2012) · Acta Physiologica · doi:10.1111/apha.12021 · Cited by 45
Yu, Y., Yang, J., Zuo, X., Gao, L., Wang, P., & Li, Y. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0137-z · Cited by 45
Primary alcohols activate human TRPA1 channel in a carbon chain length-dependent manner
Komatsu, T., Uchida, K., Fujita, F., Zhou, Y., & Tominaga, M. (2012) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-011-1069-4 · Cited by 45
Differences in the Chemesthetic Subqualities of Capsaicin, Ibuprofen, and Olive Oil
Bennett, S. M., & Hayes, J. E. (2012) · Chemical Senses · doi:10.1093/chemse/bjr129 · Cited by 45
Beckers, A. B., Weerts, Z. Z. R. M., Helyes, Z., Masclee, A., & Keszthelyi, D. (2017) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.14294 · Cited by 45
Mirrasekhian, E., Nilsson, J. L. Å., Shionoya, K., Blomgren, A., Zygmunt, P. M., Engblom, D., Högestôtt, E. D., & Blomqvist, A. (2018) · The FASEB Journal · doi:10.1096/fj.201800272r · Cited by 44
Sensitization of the trigeminovascular system following environmental irritant exposure
Kunkler, P. E., Zhang, L., Pellman, J. J., Oxford, G. S., & Hurley, J. H. (2015) · Cephalalgia · doi:10.1177/0333102415574845 · Cited by 44
Pittman, S. K., Gracias, N. G., Vasko, M. R., & Fehrenbacher, J. C. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2013.12.011 · Cited by 44
Cannabinoid receptor antagonists AM251 and AM630 activate TRPA1 in sensory neurons
Patil, M. J., Patwardhan, A. M., Salas, M. M., Hargreaves, K., & Akopian, A. N. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.05.024 · Cited by 44
Kichko, T. I., Kobal, G., & Reeh, P. W. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00164.2015 · Cited by 44
Nucleophile sensitivity of Drosophila TRPA1 underlies light-induced feeding deterrence
Du, E. J., Ahn, T. J., Wen, X., Seo, D., Na, D. L., Kwon, J. Y., Choi, M., Kim, H., Cho, H., & Kang, K. (2016) · eLife · doi:10.7554/elife.18425 · Cited by 44
TRPA1 and TRPV1 Antagonists Do Not Inhibit Human Acidosis-Induced Pain
Schwarz, M. G., Namer, B., Reeh, P. W., & Fischer, M. J. M. (2017) · Journal of Pain · doi:10.1016/j.jpain.2016.12.011 · Cited by 44
The planarian TRPA1 homolog mediates extraocular behavioral responses to near ultraviolet light
Birkholz, T. R., & Beane, W. S. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.152298 · Cited by 44
Effects of curcumin and curcumin analogues on TRP channels
Nalli, M., Ortar, G., Moriello, A. S., Marzo, V. D., & PETROCELLIS, L. D. (2017) · Fitoterapia · doi:10.1016/j.fitote.2017.09.007 · Cited by 44
Kichko, T. I., Neuhuber, W., Kobal, G., & Reeh, P. W. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13799 · Cited by 44
The Use of Cystometry in Small Rodents: A Study of Bladder Chemosensation
Uvin, P., Everaerts, W., Pinto, S., Alpizar, Y. A., Boudes, M., Gevaert, T., Voets, T., Nilius, B., Talavera, K., & Ridder, D. J. M. K. D. (2012) · Journal of Visualized Experiments · doi:10.3791/3869 · Cited by 43
Self-citationA Human Surrogate Model of Itch Utilizing the TRPA1 Agonist Trans-cinnamaldehyde
Højland, C. R., Andersen, H. H., Poulsen, J., Arendt‐Nielsen, L., & Gazerani, P. (2014) · Acta Dermato Venereologica · doi:10.2340/00015555-2103 · Cited by 43
Raffai, G., Kim, B., Park, S., Khang, G., Lee, D., & Vanhoutte, P. M. (2014) · International Journal of Nanomedicine · doi:10.2147/ijn.s56578 · Cited by 43
Startek, J. B., Talavera, K., Voets, T., & Alpizar, Y. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-30534-2 · Cited by 43
Self-citationUmbellulone modulates TRP channels
Zhong, J., Minassi, A., Prenen, J., Taglialatela‐Scafati, O., Appendino, G., & Nilius, B. (2011) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-011-1043-1 · Cited by 42
Self-citationMethylglyoxal activates the human transient receptor potential ankyrin 1 channel
Ohkawara, S., Tanaka‐Kagawa, T., Furukawa, Y., & Jinno, H. (2012) · The Journal of Toxicological Sciences · doi:10.2131/jts.37.831 · Cited by 42
Annexin A2 Regulates TRPA1-Dependent Nociception
Avenali, L., Narayanan, P., Rouwette, T., Cervellini, I., Sereda, M. W., Gómez‐Varela, D., & Schmidt, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1801-14.2014 · Cited by 42
Wu, W., Zhou, H.-R., & Pestka, J. J. (2016) · Archives of Toxicology · doi:10.1007/s00204-016-1687-x · Cited by 42
Wada, N., Shimizu, T., Shimizu, N., de Groat, W. C., Kanai, A., Tyagi, P., Κakizaki, H., & Yoshimura, N. (2018) · Neurourology and Urodynamics · doi:10.1002/nau.23539 · Cited by 42
Mammalian cold TRP channels: impact on thermoregulation and energy homeostasis
Señarís, R. M., Ordás, P., Reimúndez, A., & Viana, F. (2018) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-018-2145-9 · Cited by 42
Steinritz, D., Stenger, B., Dietrich, A., Gudermann, T. W., & Popp, T. (2018) · Cells · doi:10.3390/cells7080098 · Cited by 42
Transient receptor potential channels as novel drug targets in respiratory diseases.
Nassini, R., Materazzi, S., Siena, G. D., et al. (2010) · PubMed · Cited by 41
TRPA1 mediates the effects of hypothermia on the monocyte inflammatory response
Billeter, A. T., Galbraith, N. J., Walker, S., Lawson, C., Gardner, S. A., Sarojini, H., Galandiuk, S., & Polk, H. C. (2015) · Surgery · doi:10.1016/j.surg.2015.03.065 · Cited by 41
Li, C., Zhu, Y., Shenoy, M. M., Pai, R. K., Liu, L., & Pasricha, P. J. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00012.2012 · Cited by 41
Bodkin, J. V., Thakore, P., Aubdool, A. A., Liang, L., Fernandes, E. S., Nandi, M., Spina, D., Clark, J., Aaronson, P. I., Shattock, M. J., et al. (2014) · Pharmacology Research & Perspectives · doi:10.1002/prp2.52 · Cited by 41
Yamaguchi, K., Ono, K., Hitomi, S., Sago-Ito, M., Nodai, T., Goto, T., Harano, N., Watanabe, S., Inoue, H., Miyano, K., et al. (2016) · Pain · doi:10.1097/j.pain.0000000000000498 · Cited by 41
Marics, B., Peitl, B., Varga, A., Pázmándi, K., Bácsi, A., Németh, J., Szilvássy, Z., Jancsó, G., & Dux, M. (2016) · Cephalalgia · doi:10.1177/0333102416654883 · Cited by 41
Utsumi, D., Matsumoto, K., Tsukahara, T., et al. (2018) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2017.12.012 · Cited by 41
trans-Anethole of Fennel Oil is a Selective and Nonelectrophilic Agonist of the TRPA1 Ion Channel
Memon, T. A., Yarishkin, O. V., Reilly, C. A., Križaj, D., Olivera, B. M., & Teichert, R. W. (2019) · Molecular Pharmacology · doi:10.1124/mol.118.114561 · Cited by 41
Logu, F. D., Puma, S. L., Landini, L., Tuccinardi, T., Poli, G., Preti, D., Siena, G. D., Patacchini, R., Tsagareli, M. G., Geppetti, P., et al. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.02.019 · Cited by 41
Lee, S.-M., Cho, Y., Kim, T., Jin, M.-U., Ahn, D., Noguchi, K., & Bae, Y. (2012) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.07.003 · Cited by 40
Regulation of the transient receptor potential channel TRPA1 by its N-terminal ankyrin repeat domain
Zayats, V., Samad, A., Minofar, B., Roelofs, K. E., Stockner, T., & Ettrich, R. H. (2012) · Journal of Molecular Modeling · doi:10.1007/s00894-012-1505-1 · Cited by 40
UV light activates a Gαq/11-coupled phototransduction pathway in human melanocytes
Bellono, N. W., Najera, J. A., & Oancea, E. (2014) · The Journal of General Physiology · doi:10.1085/jgp.201311094 · Cited by 40
Prandini, P., Logu, F. D., Fusi, C., Provezza, L., Nassini, R., Montagner, G., Materazzi, S., Munari, S., Gilioli, E., Bezzerri, V., et al. (2016) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2016-0089oc · Cited by 40
Recent Progress in the Discovery and Development of TRPA1 Modulators
Skerratt, S. E. (2017) · Progress in medicinal chemistry · doi:10.1016/bs.pmch.2016.11.003 · Cited by 40
Du, C., Kang, J. M., Yu, W., Chen, M., Li, B., Liu, H., & Wang, H. (2018) · Respirology · doi:10.1111/resp.13433 · Cited by 40
Forster, A. B., Reeh, P. W., Meßlinger, K., & Fischer, M. J. M. (2009) · Molecular Pain · doi:10.1186/1744-8069-5-17 · Cited by 39
Hydrogen Sulfide’s Involvement in Modulating Nociception
Smith, H. S. (2009) · Pain Physician · doi:10.36076/ppj.2009/12/901 · Cited by 39
Yang, H., & Li, S. (2016) · Medical Science Monitor · doi:10.12659/msm.896557 · Cited by 39
Tsuchiya, K., Kubota, K., Ohbuchi, K., Kaneko, A., Ohno, N., Mase, A., Matsushima, H., Yamamoto, M., Miyano, K., Uezono, Y., et al. (2016) · Neurogastroenterology & Motility · doi:10.1111/nmo.12877 · Cited by 38
Agonist‐induced sensitisation of the irritant receptor ion channel TRPA1
Meents, J., Fischer, M. J. M., & McNaughton, P. A. (2016) · The Journal of Physiology · doi:10.1113/jp272237 · Cited by 38
Kang, J. M., Ding, Y., Li, B., Liu, H., Yang, X., & Chen, M. (2017) · Scientific Reports · doi:10.1038/srep43586 · Cited by 38
BDNF overexpression in the bladder induces neuronal changes to mediate bladder overactivity
Kashyap, M. P., Pore, S. K., de Groat, W. C., Chermansky, C., Yoshimura, N., & Tyagi, P. (2017) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00386.2017 · Cited by 38
Yao, L., Chen, S., Tang, H., Huang, P., Wei, S., Liang, Z., Chen, X., Wang, H., Tao, A., Chen, R., et al. (2018) · Toxicological Sciences · doi:10.1093/toxsci/kfy285 · Cited by 38
Dall'Acqua, M. C., Bonet, I. J. M., Zampronio, A. R., Tambeli, C. H., Parada, C. A., & Fischer, L. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.02.031 · Cited by 37
Kichko, T. I., Lennerz, J. K., Eberhardt, M. J., Babeș, R.-M., Neuhuber, W., Kobal, G., & Reeh, P. W. (2013) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.113.205971 · Cited by 37
Apomorphine Is a Bimodal Modulator of TRPA1 Channels
Schulze, A., Oehler, B., Urban, N. D., Schaefer, M., & Hill, K. (2012) · Molecular Pharmacology · doi:10.1124/mol.112.081976 · Cited by 37
Lee, K.-I., Lin, H., Lee, H., Tsai, F.-C., & Lee, T. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9908-0 · Cited by 37
Analgesic effect of dimethyl trisulfide in mice is mediated by TRPA1 and sst 4 receptors
Pozsgai, G., Payrits, M., Sághy, É., Sebestyén-Bátai, R., Steen, E., Szőke, É., Zoltán, S., Solymár, M., Garami, A., Orvos, P., et al. (2017) · Nitric Oxide · doi:10.1016/j.niox.2017.01.012 · Cited by 37
The S4–S5 linker – gearbox of TRP channel gating
Hofmann, L., Wang, H., Zheng, W., Philipp, S. E., Hidalgo, P., Cavalié, A., Chen, X., Beck, A., & Flockerzi, V. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.04.002 · Cited by 37
Oehler, B., Mohammadi, M., Perpiñá-Viciano, C., Hackel, D., Hoffmann, C., Brack, A., & Rittner, H. L. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00242 · Cited by 37
Sadofsky, L. R., Sreekrishna, K., Lin, Y., et al. (2014) · Cells · doi:10.3390/cells3020616 · Cited by 36
Hajna, Z., Sághy, É., Payrits, M., Aubdool, A. A., Szőke, É., Pozsgai, G., Bátai, I. Z., Nagy, L., Filotás, D., Helyes, Z., et al. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0802-z · Cited by 36
TRPV1 and TRPA1 stimulation induces MUC5B secretion in the human nasal airway in vivo
Alenmyr, L., Herrmann, A., Högestätt, E. D., Greiff, L., & Zygmunt, P. M. (2011) · Clinical Physiology and Functional Imaging · doi:10.1111/j.1475-097x.2011.01039.x · Cited by 35
Nyman, E., Franzén, Nolting, Klement, Liu, Nilsson, Rosén, Bjork, Weigelt, Wollberg, et al. (2013) · Journal of Pain Research · doi:10.2147/jpr.s37567 · Cited by 35
Role of Transient Receptor Potential A1 in Gastric Nociception
Kondo, T., Oshima, T., Obata, K., Sakùrai, J., Knowles, C. H., Matsumoto, T., Noguchi, K., & Miwa, H. (2010) · Digestion · doi:10.1159/000310836 · Cited by 35
Methyl syringate, a TRPA1 agonist represses hypoxia-induced cyclooxygenase-2 in lung cancer cells
Park, J., Shim, M. K., Jin, M., Rhyu, M., & Lee, Y. (2016) · Phytomedicine · doi:10.1016/j.phymed.2016.01.009 · Cited by 35
Intracellular cavity of sensor domain controls allosteric gating of TRPA1 channel
Zímová, L., Sinica, V., Kádková, A., Vyklicka, L., Zima, V., Barvı́k, I., & Vlachová, V. (2018) · Science Signaling · doi:10.1126/scisignal.aan8621 · Cited by 35
Park, J., Lee, J., Kim, M. A., Back, S. K., Hong, S. K., & Na, H. S. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.10.046 · Cited by 34
Nie, Y., Huang, C., Zhong, S., Wortley, M. A., Luo, Y.-L., Luo, W., Xie, Y., Lai, K., & Zhong, N. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.07.028 · Cited by 34
Fothergill, L. J., Callaghan, B. P., Rivera, L. R., Lieu, T., Poole, D. P., Cho, H., Bravo, D., & Furness, J. B. (2016) · Nutrients · doi:10.3390/nu8100623 · Cited by 34
Memon, T. A., Chase, K., Leavitt, L. S., Olivera, B. M., & Teichert, R. W. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.001 · Cited by 34
Ohara, K., Fukuda, T., Ishida, Y., Takahashi, C., Ohya, R., Katayama, M., Uchida, K., Tominaga, M., & Nagai, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-16150-6 · Cited by 34
Methylglyoxal Requires AC1 and TRPA1 to Produce Pain and Spinal Neuron Activation
Griggs, R. B., Laird, D. E., Donahue, R. R., Fu, W., & Taylor, B. K. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00679 · Cited by 33
Nilius, B., & Appendino, G. (2011) · EMBO Reports · doi:10.1038/embor.2011.200 · Cited by 33
Self-citationHow the TRPA1 receptor transmits painful stimuli: Inner workings revealed by electron cryomicroscopy
Brewster, M. S. J., & Gaudet, R. (2015) · BioEssays · doi:10.1002/bies.201500085 · Cited by 33
Galangal Pungent Component, 1′-Acetoxychavicol Acetate, Activates TRPA1
Narukawa, M., Koizumi, K., Iwasaki, Y., Kubota, K., & Watanabe, T. (2010) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.100133 · Cited by 33
Liu, Z., Hu, Y., Yu, X., Xi, J., Fan, X., Tse, C., Myers, A. C., Pasricha, P. J., Li, X. D., & Yu, S. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00374.2014 · Cited by 33
Jaramillo, I. C., Sturrock, A., Ghiassi, H., Woller, D. J., Deering‐Rice, C. E., Lighty, J. S., Paine, R., Reilly, C. A., & Kelly, K. E. (2017) · Journal of Environmental Science and Health Part A · doi:10.1080/10934529.2017.1400793 · Cited by 33
Effects of ginger and its pungent constituents on transient receptor potential channels
Kim, Y., Hong, C., Lee, S. W., Nam, J., & Kim, B. J. (2016) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2016.2791 · Cited by 33
UV light phototransduction depolarizes human melanocytes
Bellono, N. W., & Oancea, E. (2013) · Channels · doi:10.4161/chan.25322 · Cited by 32
Mori, N., Kawabata, F., Matsumura, S., Hosokawa, H., Kobayashi, S., Inoue, K., & Fushiki, T. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00645.2009 · Cited by 32
Lehto, S. G., Weyer, A. D., Youngblood, B. D., Zhang, M., Yin, R., Wang, W., Teffera, Y., Cooke, M., Stucky, C. L., Schenkel, L. B., et al. (2016) · Molecular Pain · doi:10.1177/1744806916677761 · Cited by 32
Brackley, A. D., Gómez, R. S., Dietert, K., Akopian, A. N., Glucksman, M., Du, J., Carlton, S. M., & Jeske, N. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-01999-4 · Cited by 32
Lieder, B., Zaunschirm, M., Holik, A., Ley, J. P., Hans, J., Krammer, G. E., & Somoza, V. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00316 · Cited by 32
Hiyama, H., Yano, Y., So, K., Imai, S., Nagayasu, K., Shirakawa, H., Nakagawa, T., & Kaneko, S. (2018) · Molecular Pain · doi:10.1177/1744806918789812 · Cited by 32
Cited by
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TRPA1 rare variants in chronic neuropathic and nociplastic pain patients
Marchi, M., Salvi, E., Andelic, M., Mehmeti, E., D'Amato, I., Cazzato, D., Chiappori, F., Lombardi, R., Cartelli, D., Devigili, G., et al. (2023) · Pain · doi:10.1097/j.pain.0000000000002905 · Cited by 29
TRPA1 promotes melanosome phagocytosis in keratinocytes via PAR-2/CYLD axis
Wang, Y., Li, Z., Wu, W., Liu, Y., Xiao, Y., Qi, D., Zhao, G., Zhou, M., Wang, H., Liu, J., et al. (2022) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2022.05.005 · Cited by 12
Giacco, V., Flower, G., Artamonova, M., Hunter, J., Padilla Requerey, A., & Hamilton, N. B. (2023) · Glia · doi:10.1002/glia.24347 · Cited by 11
Metadata
- Authors
- Talavera, K., Startek, J. B., Alvarez-Collazo, J., Boonen, B., Alpizar, Y. A., Sanchez, A., Naert, R., & Nilius, B.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2020-04-01
- Volume
- 100
- Issue
- 2
- Pages
- 725-803
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2987691534
- Cited by
- 403
- References
- 728
- FWCI
- 6.62
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.