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Activation of a TRPC3-Dependent Cation Current through the Neurotrophin BDNF
Open accessAbstract
Nonvoltage-gated cation currents, which are activated following stimulation of phospholipase C (PLC), appear to be major modes for Ca2+ and Na+ entry in mammalian cells. The TRPC channels may mediate some of these conductances since their expression in vitro leads to PLC-dependent cation influx. We found that the TRPC3 protein was highly enriched in neurons of the central nervous system (CNS). The temporal and spatial distribution of TRPC3 paralleled that of the neurotrophin receptor TrkB. Activation of TrkB by brain-derived nerve growth factor (BDNF) led to production of a PLC-dependent, nonselective cation conductance in pontine neurons. Evidence is provided that TRPC3 contributes to this current in vivo. Thus, activation of TrkB and PLC leads to a TRPC3-dependent cation influx in CNS neurons.
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“Bath application of a low concentration (20 ng/ ml) of BDNF did not by itself induce spine-head enlargement (n = 30) (Fig. 4A) or inward currents (0.5 ± 1.2 pA, n = 5) (Fig. 4B) (19, 20).”
From Protein synthesis and neurotrophin-dependent structural plasticity of single dendritic spines (2008) · cites this paper as [20]
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“Bath application of a low concentration (20 ng/ ml) of BDNF did not by itself induce spine-head enlargement (n = 30) (Fig. 4A) or inward currents (0.5 ± 1.2 pA, n = 5) (Fig. 4B) (19, 20).”
From Protein synthesis and neurotrophin-dependent structural plasticity of single dendritic spines (2008) · cites this paper as [20]
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Cites
Berridge, M. J. (1998) · Neuron · doi:10.1016/s0896-6273(00)80510-3 · Cited by 2,200
Neurotrophins and Neuronal Plasticity
Thoenen, H. (1995) · Science · doi:10.1126/science.270.5236.593 · Cited by 1,927
Ca2+ Influx Regulates BDNF Transcription by a CREB Family Transcription Factor-Dependent Mechanism
Tao, X., Finkbeiner, S., Arnold, D. B., Shaywitz, A. J., & Greenberg, M. E. (1998) · Neuron · doi:10.1016/s0896-6273(00)81010-7 · Cited by 1,561
Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol
Hofmann, T., Obukhov, A. G., Schaefer, M., Harteneck, C., Gudermann, T. W., & Schultz, G. (1999) · Nature · doi:10.1038/16711 · Cited by 1,511
Store depletion and calcium influx
Parekh, A. B., & Penner, R. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.4.901 · Cited by 1,398
Montell, C., & Rubin, G. M. (1989) · Neuron · doi:10.1016/0896-6273(89)90069-x · Cited by 1,151
Self-citationBerridge, M. J. (1995) · Biochemical Journal · doi:10.1042/bj3120001 · Cited by 1,095
Intracellular Signaling Pathways Activated by Neuropathic Factors
Segal, R. A., & Greenberg, M. E. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.002335 · Cited by 955
SK&F 96365, a novel inhibitor of receptor-mediated calcium entry
Merritt, J. E., Armstrong, W. P., Benham, C. D., Hallam, T. J., Jacob, R., Jaxa‐Chamiec, A. A., Leigh, B. K., McCarthy, S., Moores, K., & RINK, T. J. (1990) · Biochemical Journal · doi:10.1042/bj2710515 · Cited by 768
The trp gene is essential for a light-activated Ca2+ channel in Drosophila photoreceptors
Hardie, R., & Minke, B. (1992) · Neuron · doi:10.1016/0896-6273(92)90086-s · Cited by 742
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TRPC Channels: Prominent Candidates of Underlying Mechanism in Neuropsychiatric Diseases
Zeng, C., Tian, F., & Xiao, B. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9004-2 · Cited by 38
Heterogeneous distribution of TRPC proteins in the embryonic cortex
Boisseau, S., Kunert‐Keil, C., Lucke, S., & Bouron, A. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0532-6 · Cited by 36
Stepping Out of the Shade: Control of Neuronal Activity by the Scaffold Protein Kidins220/ARMS
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TRP_2, a Lipid/Trafficking Domain That Mediates Diacylglycerol-induced Vesicle Fusion
van Rossum, D. B., Oberdick, D., Rbaibi, Y., Bhardwaj, G., Barrow, R. K., Nikolaidis, N., Snyder, S. H., Kiselyov, K. I., & Patterson, R. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804707200 · Cited by 34
Kalwa, H., Storch, U., Demleitner, J., Fiedler, S., Mayer, T., Kannler, M., Fahlbusch, M., Barth, H., Smrcka, A. V., Hildebrandt, F., et al. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24883 · Cited by 33
Hartmann, J., & Konnerth, A. (2008) · Acta Physiologica · doi:10.1111/j.1748-1716.2008.01923.x · Cited by 32
The potential neuroprotective effects of stingless bee honey
Zulkifli, N. A., Hassan, Z., Mustafa, M. Z., Azman, W. N. W., Hadie, S. N. H., Ghani, N., & Zin, A. A. M. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1048028 · Cited by 38
Hayat, S., Wigley, C. B., & Robbins, J. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00051-4 · Cited by 32
Song, T., Hao, Q., Zheng, Y., Liu, Q., & Wang, Y.-X. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00148.2015 · Cited by 32
Kleiman, R. J., Tian, N., Križaj, D., Hwang, T. N., Copenhagen, D. R., & Reichardt, L. F. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.472 · Cited by 32
Inhibition of TRPC3 channels by a novel pyrazole compound confers antiseizure effects
Nagib, M. M., Zhang, S., Yasmen, N., Li, L., Hou, R., Yu, Y. H., Boda, V. K., Wu, Z., Li, W., & Jiang, J. (2022) · Epilepsia · doi:10.1111/epi.17190 · Cited by 31
Becker, B., Tian, C., Zucker, I. H., & Wang, H. (2016) · The Journal of Physiology · doi:10.1113/jp272318 · Cited by 30
Compartmentalization of calcium entry pathways in mouse rods
Križaj, D. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04469.x · Cited by 30
Berninger, B., & Poo, M. (1999) · Nature · doi:10.1038/44727 · Cited by 29
Ene, F. A., Kalmbach, A., & Kandler, K. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00686.2006 · Cited by 28
Sawamura, S., Hatano, M., Takada, Y., Hino, K., Kawamura, T., Tanikawa, J., Nakagawa, H., Hase, H., Nakao, A., Hirano, M., et al. (2016) · Molecular Pharmacology · doi:10.1124/mol.115.102863 · Cited by 28
Wang, Y., Teng, H., Gao, Y., Zhang, F., Ding, Y., & Huang, Z.-H. (2016) · Glia · doi:10.1002/glia.23049 · Cited by 27
Feetham, C. H., O’Brien, F., & Barrett‐Jolley, R. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00760 · Cited by 27
Extracellular molecular signals shaping dendrite architecture during brain development
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Pinto, M. C. X., Tonelli, F. M. P., Vieira, A. L. G., Kihara, A. H., Ulrich, H., & Resende, R. R. (2015) · Integrative Biology · doi:10.1039/c5ib00285k · Cited by 25
Interplay Between Intra- and Extracellular Calcium Ions
Lee, E. H., Kim, D. H., & Allen, P. D. (2006) · Molecules and Cells · doi:10.1016/s1016-8478(23)12859-7 · Cited by 27
Functional food development: Insights from TRP channels
Zhang, Z.-M., Wu, X., Zhang, G., Ma, X., & He, D. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.03.023 · Cited by 25
Woo, J. S., Cho, C., Kim, D. H., & Lee, E. H. (2010) · Experimental & Molecular Medicine · doi:10.3858/emm.2010.42.9.061 · Cited by 25
Developmental regulation of TRPC3 ion channel expression in the mouse cochlea
Phan, P. A. B., Tadros, S. F., Kim, Y., Birnbaumer, L., & Housley, G. D. (2010) · Histochemistry and Cell Biology · doi:10.1007/s00418-010-0686-x · Cited by 25
TRPC3 ion channel subunit immunolocalization in the cochlea
Tadros, S. F., Kim, Y. S., Phan, P. A. B., Birnbaumer, L., & Housley, G. D. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-009-0653-6 · Cited by 25
Substance P Evokes Cation Currents Through TRP Channels in HEK293 Cells
Eun-Souk, O. H., Gover, T. D., Cordoba-Rodriguez, R., & Weinreich, D. M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00026.2003 · Cited by 25
II. Genetic approaches to pain therapy
Wood, J. N. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.278.4.g507 · Cited by 25
Zhou, F., & Roper, S. N. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00607.2013 · Cited by 24
The puzzling role of TRPC3 channels in motor coordination
Trebak, M. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0740-5 · Cited by 24
Neurokinin-neurotrophin interactions in airway smooth muscle
Meuchel, L. W., Stewart, A. L., Smelter, D. F., Abcejo, A. J., Thompson, M. A., Zaidi, S. I. A., Martin, R. J., & Prakash, Y. S. (2011) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00320.2010 · Cited by 25
Photopharmacology and opto-chemogenetics of TRPC channels-some therapeutic visions
Ćurčić, S., Tiapko, O., & Groschner, K. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.04.003 · Cited by 23
TRPC channels as emerging targets for seizure disorders
Yu, Y., Li, W., & Jiang, J. (2022) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2022.06.007 · Cited by 23
Takeda, M., Takahashi, M., & Matsumoto, S. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.048 · Cited by 23
Zhang, S., Romero, L. O., Deng, S., Wang, J., Li, Y., Yang, L., Hamilton, D. J., Miller, D. D., Liao, F., Cordero-Morales, J. F., et al. (2021) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.0c00571 · Cited by 22
Schaich, C. L., Wellman, T. L., Koi, B., & Erdös, B. (2016) · Autonomic Neuroscience · doi:10.1016/j.autneu.2016.02.011 · Cited by 22
TRPC Channels and Parkinson’s Disease
Sukumaran, P., Sun, Y., Schaar, A., Selvaraj, S., & Singh, B. B. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-94-024-1088-4_8 · Cited by 24
Nedungadi, T. P., & Cunningham, J. T. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00388.2013 · Cited by 20
- Activation of TRP Channels in Mammalian Systems
Zhu, M. X. (2016) · CRC Press eBooks · doi:10.1201/b10896-8 · Cited by 19
McGurk, J., Shim, S., Kim, J. Y., Wen, Z., Song, H., & Ming, G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3599-11.2011 · Cited by 20
Muscle Contractions Guide Rohon–Beard Peripheral Sensory Axons
Paulus, J. D., Willer, G. B., Willer, J. R., Gregg, R. G., & Halloran, M. C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2179-09.2009 · Cited by 20
Scott, A. L. M., Zhang, M., & Nurse, C. A. (2015) · The Journal of Physiology · doi:10.1113/jp270725 · Cited by 20
Gees, M., Owsianik, G., Nilius, B., & Voets, T. (2012) · Comprehensive physiology · doi:10.1002/j.2040-4603.2012.tb00410.x · Cited by 19
Expression of TRPC6 in Renal Cortex and Hippocampus of Mouse during Postnatal Development
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TRP Channels Regulation of Rho GTPases in Brain Context and Diseases
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Sun, D., Ma, H., Ma, J., Wang, J., Deng, X., Hu, C., & Deng, X. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0586-5 · Cited by 18
Vascular and non‐vascular contributors to memory reduction during traumatic brain injury
Charkviani, M., Muradashvili, N., & Lominadze, D. G. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14390 · Cited by 17
TRPC3 protein is expressed across the lifespan in human prefrontal cortex and cerebellum
Roedding, A. S., Gao, A. F., Wu, A. M. L., Li, P. P., Kish, S. J., & Warsh, J. J. (2009) · Brain Research · doi:10.1016/j.brainres.2008.12.069 · Cited by 18
The Role of TRP Ion Channels in Testicular Function
Kumar, P. G., & Shoeb, M. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-0265-3_46 · Cited by 18
Schilling, W. P. (2001) · Circulation Research · doi:10.1161/01.res.88.3.256 · Cited by 18
Multiple acute effects on the membrane potential of PC12 cells produced by nerve growth factor (NGF)
Shimazu, K., Takeda, K., Yu, Z., Jiang, H., Liu, X., Nelson, P. G., & Guroff, G. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20309 · Cited by 17
Amphetamines abuse and depression: Focus on TRPC channels
Fu, Y.-P., & Wang, Y. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114391 · Cited by 17
Louhivuori, L. M., Jansson, L. C., Turunen, P. M., Jäntti, M. H., Nordström, T., Louhivuori, V., & Åkerman, K. E. O. (2014) · Stem Cells and Development · doi:10.1089/scd.2014.0209 · Cited by 16
Schaich, C. L., Wellman, T. L., Einwag, Z., Dutko, R. A., & Erdös, B. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00459.2017 · Cited by 20
Kann, O., Taubenberger, N., Huchzermeyer, C., Papageorgiou, I. E., Benninger, F., Heinemann, U., & Kovács, R. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.10.004 · Cited by 17
Regulation of radial glial process growth by glutamate via mGluR5/TRPC3 and neuregulin/ErbB4
Louhivuori, L. M., Turunen, P. M., Louhivuori, V., Yellapragada, V., Nordström, T., Uhlén, P., & Åkerman, K. E. O. (2017) · Glia · doi:10.1002/glia.23230 · Cited by 17
Hong, D. K., Kho, A. R., Lee, S. H., Kang, B. S., Park, M. K., Choi, B. Y., & Suh, S. W. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076665 · Cited by 15
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Tai, Y., & Jia, Y. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-94-024-1088-4_9 · Cited by 15
Black, E. A. E., Smith, P., McIsaac, W., & Ferguson, A. V. (2018) · Physiological Reports · doi:10.14814/phy2.13704 · Cited by 17
Ortiz‐Romero, P., González-Simón, A., Egea, G., Jurado, L. A. P., & Campuzano, V. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.670785 · Cited by 15
Regulation of GABAergic neurotransmission by purinergic receptors in brain physiology and disease
Juvenal, G. D. A., Higa, G. S. V., Marques, L. B., Zampieri, T. T., Viana, F. J. C., Britto, L. R. G., Tang, Y. C., Illés, P., Virgilio, F. D., Ulrich, H., et al. (2024) · Purinergic Signalling · doi:10.1007/s11302-024-10034-x · Cited by 16
TRP Channels in the Brain: What Are They There For?
(2017) · Frontiers in neuroscience · doi:10.1201/9781315152837-17 · Cited by 14
Cesca, F., Satapathy, A., Ferrea, E., Nieus, T. R., Benfenati, F., & Scholz‐Starke, J. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.654699 · Cited by 14
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Wetzel, A., Jablonka, S., & Blum, R. (2013) · Channels · doi:10.4161/chan.23153 · Cited by 14
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Boda, V. K., Yasmen, N., Jiang, J., & Li, W. (2024) · Medicinal Research Reviews · doi:10.1002/med.22048 · Cited by 13
Blair, N. T., Carvacho, I., Chaudhuri, D., Clapham, D. E., DeCaen, P. G., Delling, M., Doerner, J. F., Fan, L., Ha, K., Jordt, S. E., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f78/2019.4 · Cited by 13
TRPC1 is required for survival and proliferation of cochlear spiral ganglion stem/progenitor cells
Chen, H., Wang, C., Shih, C., Chueh, S., Liu, S.-F., Chen, H.-K., & Lin, Y. (2015) · International Journal of Pediatric Otorhinolaryngology · doi:10.1016/j.ijporl.2015.10.027 · Cited by 11
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Barde, Y. (2002) · Nature · doi:10.1038/419683a · Cited by 11
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Zhou, F.-M. (2010) · Reviews in the Neurosciences · doi:10.1515/revneuro.2010.21.2.95 · Cited by 10
Turunen, P. M., Louhivuori, L. M., Louhivuori, V., Kukkonen, J. P., & Åkerman, K. E. O. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.02.005 · Cited by 10
BDNF rapidly induces aspartate release from cultured CNS neurons
Numakawa, T., Takei, N., & Hatanaka, H. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(00)00103-6 · Cited by 10
Zhang, C., Xu, C., Ma, C., Zhang, Q., Bu, S., Zhang, D., Yu, L., & Wang, H. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.915409 · Cited by 9
Exploring phospholipase C-coupled Ca 2+ signalling networks using boolean modelling
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Li, S., Gosling, M., & Poll, C. T. (2005) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-005-1465-8 · Cited by 9
Teng, S.-W., Chen, X.-L., & Chen, Z.-Y. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03552-0 · Cited by 9
Diacylglycerol‐mediated regulation of Aplysia bag cell neuron excitability requires protein kinase C
Sturgeon, R. M., & Magoski, N. S. (2016) · The Journal of Physiology · doi:10.1113/jp272152 · Cited by 8
Phelan, K. D., Shwe, U. T., Wu, H., & Zheng, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116260 · Cited by 8
The odyssey of the TR(i)P journey to the cellular membrane
Rivera, B. I., Orellana‐Serradell, O., Servili, E., Santos, R., Brauchi, S. E., & Cerda, O. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1414935 · Cited by 8
Verlinden, S. M. D., Norton, T., Larsen, M. L. V., Schroyen, M., Youssef, A., & Everaert, N. (2022) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2022.111199 · Cited by 8
6.5 Mechanosensory Transduction
Martinac, B., & Kloda, A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374920-8.00618-4 · Cited by 8
Transient receptor potential canonical channels in angiogenesis and axon guidance
Yu, P., & Du, J. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0755-x · Cited by 9
Montell, C. (2010) · Cell · doi:10.1016/j.cell.2010.03.043 · Cited by 8
Self-citationXie, W., Song, Y., Li, D., Pan, L., Wu, Q.-J., & Tian, X. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12620 · Cited by 8
TRP Channels and Axon Pathfinding
Yuan, X., & Cui, K. (2006) · Frontiers in neuroscience · doi:10.1201/9781420005844.ch4 · Cited by 8
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Joshi, A., Giorgi, F. M., & Sanna, P. P. (2024) · eNeuro · doi:10.1523/eneuro.0118-24.2024 · Cited by 6
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Expression of TRPC3 in cortical lesions from patients with focal cortical dysplasia
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Signaling Through the Neurotrophin Receptors
Ng, Y. P., Lo, K. Y., Cheung, Z. H., & Ip, N. Y. (2006) · Springer eBooks · doi:10.1007/0-387-30395-2_2 · Cited by 5
Deng, G., Liu, D., Zhong, Y., Wang, M., Su, B., Jiang, H., Zhai, Y., Peng, H., Zhang, C., & Feng, J. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1687359 · Cited by 4
Amores-Bonet, L., KLEENE, R. B., Theis, T., & Schachner, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231710027 · Cited by 4
Silva-Cardoso, G. K., Boda, V. K., Li, W., & N’Gouemo, P. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176722 · Cited by 4
Molecules that specify modality: Mechanisms of nociception
Wood, J. N., & Heath, M. J. S. (2000) · Journal of Pain · doi:10.1054/jpai.2000.9807a · Cited by 4
Haley, E., Choi, W.-Y., Fan, C., Sun, W., Du, J., & Lü, W. (2019) · Journal of Visualized Experiments · doi:10.3791/58754 · Cited by 4
Transient Receptor Potential channels (TRP) in GtoPdb v.2023.3
Blair, N. T., Caceres, A. I., Carvacho, I., Chaudhuri, D., Clapham, D. E., Clercq, K. D., Delling, M., Doerner, J. F., Fan, L., Grimm, C. M., et al. (2023) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f78/2023.3 · Cited by 4
Metadata
- Authors
- Li, H.-S., Xu, X.-Z. S., & Montell, C.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Montell, Craig
- ORCID
- Montell, Craig
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1999-09
- Volume
- 24
- Issue
- 1
- Pages
- 261-273
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W1968399538
- Cited by
- 345
- References
- 55
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 9 · 2023: 9 · 2022: 11 · 2021: 5 · 2020: 6 · 2019: 6 · 2018: 10 · 2017: 11 · 2016: 10 · 2015: 11 · 2014: 11 · 2013: 12 · 2012: 18
- FWCI
- 7.03
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuron (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (EY10852)
- Topics
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- TRPC3, TRPC channels, brain-derived neurotrophic factor, TrkB receptor, neurotrophin signaling, phospholipase C, calcium influx, sodium influx, pontine neurons, central nervous system neurons, cation conductance
- MeSH terms
- Animals, Cations, Cell Line, Cerebral Cortex, Electric Conductivity, Humans, Ion Channels, Neurons, Type C Phospholipases, Pons, Tissue Distribution, Transfection, Brain-Derived Neurotrophic Factor, Receptor, trkB, TRPC Cation Channels, Rats
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