The DOI matches its Crossref record; 530 of the 530 references it cites were found in a registry or an index.
Molecular Structure and Physiological Function of Chloride Channels
Abstract
Cl−channels reside both in the plasma membrane and in intracellular organelles. Their functions range from ion homeostasis to cell volume regulation, transepithelial transport, and regulation of electrical excitability. Their physiological roles are impressively illustrated by various inherited diseases and knock-out mouse models. Thus the loss of distinct Cl−channels leads to an impairment of transepithelial transport in cystic fibrosis and Bartter's syndrome, to increased muscle excitability in myotonia congenita, to reduced endosomal acidification and impaired endocytosis in Dent's disease, and to impaired extracellular acidification by osteoclasts and osteopetrosis. The disruption of several Cl−channels in mice results in blindness. Several classes of Cl−channels have not yet been identified at the molecular level. Three molecularly distinct Cl−channel families (CLC, CFTR, and ligand-gated GABA and glycine receptors) are well established. Mutagenesis and functional studies have yielded considerable insights into their structure and function. Recently, the detailed structure of bacterial CLC proteins was determined by X-ray analysis of three-dimensional crystals. Nonetheless, they are less well understood than cation channels and show remarkably different biophysical and structural properties. Other gene families (CLIC or CLCA) were also reported to encode Cl−channels but are less well characterized. This review focuses on molecularly identified Cl−channels and their physiological roles.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Items 401–530 of 530
Strange, K. B. (1998) · The Journal of General Physiology · doi:10.1085/jgp.111.5.617 · Cited by 88
Buyse, G., Voets, T., Tytgat, J., Greef, C. D., Droogmans, G., Nilius, B., & Eggermont, J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.6.3615 · Cited by 87
Poulter, M. O., Barker, J. L., O'Carroll, A.-M., et al. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90486-y · Cited by 86
Vandewalle, A., Cluzeaud, F., Peng, K., Bens, M., Lüchow, A., Gunther, W. C., & Jentsch, T. J. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.2.c373 · Cited by 86
Self-citationLocation of a High Affinity Zn2+ Binding Site in the Channel of α1β1 γ-Aminobutyric AcidA Receptors
Horenstein, J., & Akabas, M. H. (1998) · Molecular Pharmacology · doi:10.1016/s0026-895x(24)13253-1 · Cited by 86
Function of the R Domain in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
Ma, J., Zhao, J., Drumm, M. L., Xie, J., & Davis, P. B. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.28133 · Cited by 85
Strata, F., & Cherubini, E. (1994) · The Journal of Physiology · doi:10.1113/jphysiol.1994.sp020378 · Cited by 85
Pacaud, P., Loirand, G., Mironneau, C., & Mironneau, J. (1989) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1989.tb11934.x · Cited by 84
Deficiency in induction but not expression of LTP in hippocampal slices from young rats.Preprint
Liao, D., & Malinow, R. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.138 · Cited by 83
Blockage of chloride channels by HEPES buffer
Yamamoto, D., & Suzuki, N. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0011 · Cited by 83
Mall, M. A., Bleich, M., Kuehr, J., et al. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.277.3.g709 · Cited by 83
Swelling-activated anion conductance in skate hepatocytes: regulation by cell Cl- and ATP
Jackson, P., Churchwell, K., Ballatori, N., Boyer, J. L., & Strange, K. B. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.270.1.c57 · Cited by 83
Horenstein, J., & Akabas, M. H. (1998) · PubMed · Cited by 82
von Weikersthal, S. F., Barrand, M. A., & Hladky, S. B. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.075aa.x · Cited by 81
Harvey, R. J., Schmieden, V., von Holst, A., Laube, B., Rohrer, H., & Betz, H. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00993.x · Cited by 80
Rasola, A., Galietta, L. J. V., Gruenert, D. C., & Romeo, G. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)42276-9 · Cited by 79
Stable and functional expression of the CIC-3 chloride channel in somatic cell lines
Kawasaki, M., Suzuki, M., Uchida, S., Sasaki, S., & Marumo, F. (1995) · Neuron · doi:10.1016/0896-6273(95)90275-9 · Cited by 79
Adler, D. A., Rugarli, E. I., Lingenfelter, P. A., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.17.9244 · Cited by 79
Association of ClC-3 Channel with Cl − Transport by Human Nonpigmented Ciliary Epithelial Cells
Coca‐Prados, M., Sánchez-Torres, J., & Peterson–Yantorno, K. (1996) · The Journal of Membrane Biology · doi:10.1007/s002329900044 · Cited by 78
Solubilization of the glycine receptor from rat spinal cord
Pfeiffer, F., & Betz, H. (1981) · Brain Research · doi:10.1016/0006-8993(81)91099-4 · Cited by 78
Twyman, R. E., & Macdonald, R. L. (1991) · The Journal of Physiology · doi:10.1113/jphysiol.1991.sp018512 · Cited by 78
Giustetto, M., Kirsch, J., Fritschy, J., Cantino, D., & Sassoé‐Pognetto, M. (1998) · The Journal of Comparative Neurology · Cited by 78
Immunochemical Identification of the α1- And α3–Subuntis of the GabaA-Receptor in Rat Brain
Benke, D., Cicin-Sain, A., Mertens, S., & Möhler, H. (1991) · Journal of Receptor Research · doi:10.3109/10799899109066418 · Cited by 77
Chuang, J.-Z., Milner, T. A., Zhu, M., & Sung, C.-H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-08-02919.1999 · Cited by 76
Postsynaptic clustering of γ-aminobutyric acid type A receptors by the γ3 subunit in vivo
Baer, K., Essrich, C., Benson, J. A., Benke, D., Bluethmann, H., Fritschy, J., & Lüscher, B. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12860 · Cited by 76
PKA holoenzyme is functionally coupled to CFTR by AKAPs
Huang, P., Trotter, K. W., Boucher, R. C., Milgram, S. L., & Stutts, M. J. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.278.2.c417 · Cited by 76
Wooltorton, J. R. A., McDonald, B. J., Moss, S. J., & Smart, T. G. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.633ba.x · Cited by 75
Alternative splicing of CFTR Cl- channels in heart
Horowitz, B., Tsung, S. S., Hart, P., Levesque, P. C., & Hume, J. R. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.264.6.h2214 · Cited by 75
Redhead, C. R., Edelman, A., Brown, D., Landry, D. W., & Al‐Awqati, Q. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.9.3716 · Cited by 74
Evidence for extra-mitochondrial localization of the VDAC/porin channel in eucaryotic cells
THINNES, F. P. (1992) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf00769533 · Cited by 74
PKA and arachidonic acid activation of human recombinant ClC-2 chloride channels
Tewari, K. P., Malinowska, D. H., Sherry, A. M., et al. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.1.c40 · Cited by 74
Insights into the structure, distribution and function of the cardiac chloride channels
Sorota, S. (1999) · Cardiovascular Research · doi:10.1016/s0008-6363(99)00039-5 · Cited by 73
Formation of CLC-0 Chloride Channels from Separated Transmembrane and Cytoplasmic Domains
Maduke, M. C., Williams, C., & Miller, C. (1998) · Biochemistry · doi:10.1021/bi972418o · Cited by 72
ClC-2 Contributes to Native Chloride Secretion by a Human Intestinal Cell Line, Caco-2
Mohammad-Panah, R., Gyömörey, K., Rommens, J. M., Choudhury, M., Li, C., Wang, Y., & Bear, C. E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006764200 · Cited by 72
Swelling-activated chloride channels in multidrug-sensitive and -resistant cells.
Ehring, G. R., Osipchuk, Y. V., & Cahalan, M. D. (1994) · The Journal of General Physiology · doi:10.1085/jgp.104.6.1129 · Cited by 72
Chinet, T., Fullton, J. M., Yankaskas, J. R., et al. (1994) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1994.266.4.c1061 · Cited by 71
Acidification of rat liver lysosomes: quantitation and comparison with endosomes
Dyke, R. W. V. (1993) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1993.265.4.c901 · Cited by 71
Aspects of calcium-activated chloride currents: A neuronal perspective
Scott, R. H., Sutton, K. G., Griffin, A., Stapleton, S. R., & Currie, K. (1995) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(95)00018-c · Cited by 70
Genomic Structure of a Novel Chloride Channel Gene, CLIC2, in Xq28
Heiss, N. S., & Poustka, A. (1997) · Genomics · doi:10.1006/geno.1997.4922 · Cited by 70
GABA-gated Cl− Channels in the rat retina
Feigenspan, A., & Bormann, J. (1998) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(97)00008-6 · Cited by 70
Wollnik, B., Kubisch, C., Steinmeyer, K., & Pusch, M. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.5.805 · Cited by 70
Lambert, I. H. (1987) · The Journal of Membrane Biology · doi:10.1007/bf01871184 · Cited by 69
Novel muscle chloride channel mutations and their effects on heterozygous carriers.
Mailänder, V., Heine, R., Deymeer, F., et al. (1996) · PubMed · Cited by 68
Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic mice.
Gronemeier, M., Condie, A., Prosser, J., Steinmeyer, K., Jentsch, T. J., & Jockusch, H. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)37556-7 · Cited by 68
Self-citationMechanism of voltage-dependent gating in skeletal muscle chloride channels
Fahlke, C. M., Rosenbohm, A., Mitrović, N., George, A. L., & Rüdel, R. (1996) · Biophysical Journal · doi:10.1016/s0006-3495(96)79269-x · Cited by 68
Regulation of CI− channels by multifunctional CaM kinase
Nishimoto, I., Wagner, J. A., Schulman, H., & Gardner, P. I. (1991) · Neuron · doi:10.1016/0896-6273(91)90057-7 · Cited by 68
Regulation of a Human Chloride Channel
Ho, M. W. Y., Kaetzel, M. A., Armstrong, D. L., & Shears, S. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101128200 · Cited by 68
Pore stoichiometry of a voltage-gated chloride channel
Fahlke, C. M., Rhodes, T. H., Desai, R. R., & George, A. L. (1998) · Nature · doi:10.1038/29319 · Cited by 67
Voets, T., Buyse, G., Tytgat, J., Droogmans, G., Eggermont, J., & Nilius, B. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021605 · Cited by 67
Heine, R., George, A. L., Pika, U., et al. (1994) · Human Molecular Genetics · doi:10.1093/hmg/3.7.1123 · Cited by 67
Block by MOPS reveals a conformation change in the CFTR pore produced by ATP hydrolysis
Ishihara, H., & Welsh, M. J. (1997) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1997.273.4.c1278 · Cited by 67
Absence of the Skeletal Muscle Sarcolemma Chloride Channel ClC-1 in Myotonic Mice
Gurnett, C. A., Kahl, S. D., Anderson, R. D., et al. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.16.9035 · Cited by 66
Sziics, G., Heinke, S., DROOGMANS, G., & Nilius, B. (1996) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf02207289 · Cited by 66
CBS domains in CIC chloride channels implicated in myotonia and nephrolithiasis (kidney stones).
Ponting, C. P. (1997) · PubMed · Cited by 65
Properties of human brain glycine receptors expressed in Xenopus oocytes
Gundersen, C. B., Miledi, R., & Parker, I. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0032 · Cited by 65
Jiang, Q., Li, J., Dubroff, R., Ahn, Y. J., Foskett, J. K., Engelhardt, J. F., & Kleyman, T. R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.18.13266 · Cited by 63
Shimada, K., Li, X., Xu, G., Nowak, D. E., Showalter, L., & Weinman, S. A. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.2.g268 · Cited by 63
pH-regulated chloride secretion in fetal lung epithelia
Blaisdell, C. J., Edmonds, R. D., Wang, X.-T., Guggino, S. E., & Zeitlin, P. L. (2000) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2000.278.6.l1248 · Cited by 63
Chebib, M., Mewett, K. N., & Johnston, G. A. R. (1998) · European Journal of Pharmacology · doi:10.1016/s0014-2999(98)00552-4 · Cited by 62
Non‐specific activation of the epithelial sodium channel by the CFTR chloride channel
Nagel, G., Szellas, T., Riordan, J. R., Friedrich, T., & Hartung, K. (2001) · EMBO Reports · doi:10.1093/embo-reports/kve045 · Cited by 62
Harvey, V. L., Chinchetru, M. A., & Darlison, M. G. (1994) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1994.62010010.x · Cited by 61
Single-channel currents underlying glycinergic inhibitory postsynaptic responses in spinal neurons
Takahashi, T., & Momiyama, A. (1991) · Neuron · doi:10.1016/0896-6273(91)90341-v · Cited by 61
A Voltage-Dependent Chloride Current Linked to the Cell Cycle in Ascidian Embryos
Block, M. L., & Moody, W. J. (1990) · Science · doi:10.1126/science.2309122 · Cited by 60
pICln Binds to a Mammalian Homolog of a Yeast Protein Involved in Regulation of Cell Morphology
Krapivinsky, G. B., Pu, W. T., Wickman, K. D., Krapivinsky, L., & Clapham, D. E. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.18.10811 · Cited by 60
Twyman, R. E., Green, R. M., & Macdonald, R. L. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp018914 · Cited by 60
Probes of the conduction process of a voltage-gated Cl- channel from Torpedo electroplax.
White, M. M., & Miller, C. (1981) · The Journal of General Physiology · doi:10.1085/jgp.78.1.1 · Cited by 60
Modulation of Voltage-dependent Properties of a Swelling-activated Cl− Current
Voets, T., Droogmans, G., & Nilius, B. (1997) · The Journal of General Physiology · doi:10.1085/jgp.110.3.313 · Cited by 60
Ludewig, U., Jentsch, T. J., & Pusch, M. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp021893 · Cited by 60
Self-citationBiology of the Postsynaptic Glycine Receptor
Vannier, C., & Triller, A. (1997) · International review of cytology · doi:10.1016/s0074-7696(08)61611-3 · Cited by 59
Miles, R. (1999) · Nature · doi:10.1038/16604 · Cited by 59
Molecular cloning reveals the existence of a fourth γ subunit of the vertebrate brain GABAAreceptor
Harvey, V. L., Kim, H.-C., & Darlison, M. G. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80339-v · Cited by 59
Cloning and Identification of the Gene Gob-5, Which Is Expressed in Intestinal Goblet Cells in Mice
Komiya, T., Tanigawa, Y., & Hirohashi, S. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0168 · Cited by 59
Mechanism of Ion Permeation in Skeletal Muscle Chloride Channels
Fahlke, C. M., Dürr, C., & George, A. L. (1997) · The Journal of General Physiology · doi:10.1085/jgp.110.5.551 · Cited by 59
Expression of the Voltage-Gated Chloride Channel ClC-2 in Rod Bipolar Cells of the Rat Retina
Enz, R., Ross, B. J., & Cutting, G. R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09841.1999 · Cited by 58
Independent gating of single pores in CLC-0 chloride channels
Ludewig, U., Pusch, M., & Jentsch, T. J. (1997) · Biophysical Journal · doi:10.1016/s0006-3495(97)78111-6 · Cited by 57
Self-citationClC-2 chloride channels contribute to HTC cell volume homeostasis
Roman, R. M., Smith, R. L., Feranchak, A. P., Clayton, G. H., Doctor, R. B., & Fitz, J. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.3.g344 · Cited by 57
Ion channel properties of the reconstituted chloroplast triose phosphate/phosphate translocator.
Schwarz, M., Gross, A., Steinkamp, T., Flügge, U., & Wagner, R. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43905-1 · Cited by 56
CLC Chloride Channels in Caenorhabditis elegans
Schriever, A. M., Friedrich, T., Pusch, M., & Jentsch, T. J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.48.34238 · Cited by 56
Self-citationSchumann, M. A., Gardner, P. I., & Raffin, T. A. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)53972-7 · Cited by 54
Kajita, H., Omori, K., & Matsuda, H. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00313.x · Cited by 54
Membrane ionic conductances in normal and denervated skeletal muscle of the rat during development
Camerino, D. C., Luca, A. D., Mambrini, M., et al. (1989) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00594192 · Cited by 54
Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
Ludewig, U., Jentsch, T. J., & Pusch, M. (1997) · The Journal of General Physiology · doi:10.1085/jgp.110.2.165 · Cited by 54
Self-citationCapacitance measurements reveal different pathways for the activation of CFTR
Weber, W.-M., Cuppens, H., Cassiman, J. J., Clauss, W. G., & Driessche, W. V. (1999) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004249900086 · Cited by 53
Park, K., Arreola, J., & Melvin, J. E. (1998) · The Journal of Membrane Biology · doi:10.1007/s002329900373 · Cited by 52
Weinreich, F., Riordan, J. R., & Nagel, G. (1999) · The Journal of General Physiology · doi:10.1085/jgp.114.1.55 · Cited by 52
Self-citationSchlenker, T., & Fitz, J. (1996) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1996.271.2.g304 · Cited by 52
Jonas, E. A., Knox, R. J., & Kaczmarek, L. K. (1997) · Neuron · doi:10.1016/s0896-6273(00)80343-8 · Cited by 51
Boehm, S., Harvey, R. J., von Hoist, A., Rohrer, H., & Betz, H. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.683bd.x · Cited by 51
Molecular distribution of volume-regulated chloride channels (ClC-2 and ClC-3) in cardiac tissues
Britton, F. C., Hatton, W. J., Rossow, C. F., Duan, D. D., Hume, J. R., & Horowitz, B. (2000) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2000.279.5.h2225 · Cited by 51
Taurine permeation through swelling-activated anion conductance in rat IMCD cells in primary culture
Boese, S. H., Wehner, F., & Kinne, R. K. H. (1996) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1996.271.3.f498 · Cited by 50
Choi, M. S. K., & COOKE, B. A. (1990) · FEBS Letters · doi:10.1016/0014-5793(90)80602-f · Cited by 50
Tulk, B., & Edwards, J. C. (1998) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1998.274.6.f1140 · Cited by 49
Conductance states activated by glycine and GABA in rat cultured spinal neurones
Smith, S. M., Zorec, R., & McBurney, R. N. (1989) · The Journal of Membrane Biology · doi:10.1007/bf01870424 · Cited by 48
Szűcs, G., Heinke, S., Droogmans, G., & Nilius, B. (1996) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050023 · Cited by 48
Kunzelmann, K., Slotki, I. N., Klein, P., Koslowsky, T. C., Ausiello, D. A., Greger, R. F., & Cabantchik, Z. I. (1994) · Journal of Cellular Physiology · doi:10.1002/jcp.1041610302 · Cited by 47
Hartenstein, B., Schenkel, J., Kuhse, J., Besenbeck, B., Kling, C., Becker, C., Betz, H., & Weiher, H. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00469.x · Cited by 46
Nehrke, K. W., Begenisich, T. B., Pilato, J., & Melvin, J. E. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.6.c2052 · Cited by 46
Villaz, M., Cinniger, J. C., & Moody, W. J. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp021000 · Cited by 46
Patch clamp investigation into the phosphate carrier from Saccharomyces cerevisiae mitochondria
Herick, K., Krämer, R., & Lühring, H. (1997) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(97)00050-9 · Cited by 45
Fatima-Shad, K., & Barry, P. H. (1992) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1992.0136 · Cited by 45
Hackam, A. S., Wang, T., Guggino, W. B., & Cutting, G. R. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.70010040.x · Cited by 43
Identification of ClC-2-like chloride currents in pig pancreatic acinar cells
Carew, M. A., & Thorn, P. (1996) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050252 · Cited by 43
Spasmodic, a mutation on chromosome 11 in the mouse
Lane, P. W., Ganser, A. L., Kerner, A., et al. (1987) · Journal of Heredity · doi:10.1093/oxfordjournals.jhered.a110414 · Cited by 41
Nakazato, H., Hattori, S., Furuse, A., Kawano, T., Karashima, S., Tsuruta, M., Yoshimuta, J., Endo, F., & Matsuda, I. (1997) · Kidney International · doi:10.1038/ki.1997.410 · Cited by 41
Mechanism of Inverted Activation of ClC-1 Channels Caused by a Novel Myotonia Congenita Mutation
Zhang, J., Sanguinetti, M. C., Kwieciński, H., & Ptáček, L. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.4.2999 · Cited by 41
P‐glycoprotein is not a swelling‐activated Cl− channel; possible role as a Cl− channel regulator
Vanoye, C. G., Altenberg, G. A., & Reuss, L. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.249bk.x · Cited by 41
Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker).
Koch, M. C., Ricker, K., Otto, M. J., Wolf, F., Zoll, B., Lorenz, C., Steinmeyer, K., & Jentsch, T. J. (1993) · Journal of Medical Genetics · doi:10.1136/jmg.30.11.914 · Cited by 39
Self-citationCysteine Modification of a Putative Pore Residue in Clc-0
Lin, C.-W., & Chen, T. (2000) · The Journal of General Physiology · doi:10.1085/jgp.116.4.535 · Cited by 38
Li, C., Breton, S., Morrison, R., Cannon, C. L., Emma, F., Sánchez‐Olea, R., Bear, C. E., & Strange, K. B. (1998) · The Journal of General Physiology · doi:10.1085/jgp.112.6.727 · Cited by 38
ICln Is Essential for Cellular and Early Embryonic Viability
Pu, W. T., Wickman, K., & Clapham, D. E. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.17.12363 · Cited by 37
Rychkov, G. Y., Pusch, M., Roberts, M. L., & Bretag, A. H. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0379k.x · Cited by 36
Developmental expression of ClC-2 in the rat nervous system
Clayton, G. H., Staley, K. J., Wilcox, C. L., Owens, G. C., & Smith, R. L. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00045-5 · Cited by 35
Astill, D., Rychkov, G. Y., Clarke, J. D., Hughes, B. P., Roberts, M. L., & Bretag, A. H. (1996) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(95)00281-2 · Cited by 35
Residues Lining the Inner Pore Vestibule of Human Muscle Chloride Channels
Fahlke, C. M., Desai, R. R., Gillani, N. B., & George, A. L. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m007649200 · Cited by 34
Relevance of the D13 Region to the Function of the Skeletal Muscle Chloride Channel, ClC-1
Hryciw, D. H., Rychkov, G. Y., Hughes, B. P., & Bretag, A. H. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.8.4304 · Cited by 34
Kajita, H., Whitwell, C., & Brown, P. D. (2000) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240000387 · Cited by 34
Monoclonal antibody against conductive chloride transport in pig ileal apical membrane vesicles
Racette, K. J., Gabriel, S. E., Gaspar, K. J., et al. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.2.c478 · Cited by 32
Ca[2+] sensitivity of volume-regulatory K[+] and Cl[-] channels in cultured human epithelial cells
挾間, 章. (1989) · Cited by 31
Evidence against the acidification hypothesis in cystic fibrosis
Gibson, G. A., Hill, W. G., & Weisz, O. A. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.4.c1088 · Cited by 30
Identification and characterisation of a homologue of p64 in rat tissues
Howell, S. W., Duncan, R. R., & Ashley, R. H. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00676-x · Cited by 29
Molecular and functional distributions of chloride conductances in rabbit ventricle
Wong, K. R., Trezise, A. E. O., Bryant, S. M., et al. (1999) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1999.277.4.h1403 · Cited by 27
Greef, C. D., van der Heyden, S., Viana, F., Eggermont, J., de Bruijn, E. A., Raeymaekers, L., Droogmans, G., & Nilius, B. (1995) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374662 · Cited by 22
Caesium ions activate chloride channels in rat cultured spinal cord neurones.
Hughes, D., McBurney, R. N., Smith, S. M., & Zorec, R. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016778 · Cited by 21
Purdy, M. D., & Wiener, M. C. (2000) · FEBS Letters · doi:10.1016/s0014-5793(99)01740-8 · Cited by 19
Ion channels on synaptic vesicle membranes studied by planar lipid bilayer method
Sato, M., Inoue, K., & Kasai, M. (1992) · Biophysical Journal · doi:10.1016/s0006-3495(92)81731-9 · Cited by 18
Doroshenko, P. A. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.437ae.x · Cited by 15
Separate Domains for Desensitization of GABA ρ 1 and β 2 Subunits Expressed in Xenopus Oocytes
Lu, L., & Huang, Y. (1998) · The Journal of Membrane Biology · doi:10.1007/s002329900398 · Cited by 15
Quaternary Structure of the Chloride Channel ClC-2
Ramjeesingh, M., Li, C., Huan, L., Garami, E., Wang, Y., & Bear, C. E. (2000) · Biochemistry · doi:10.1021/bi001282i · Cited by 14
Expression of a ClC chloride channel in Caenorhabditis elegans gamma-aminobutyric acid-ergic neurons
Bianchi, L. K., Miller, D. M., & George, A. L. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01525-7 · Cited by 12
Nehrke, K. W., Begenisich, T. B., Pilato, J., & Melvin, J. E. (2000) · American Journal of Physiology-Legacy Content · Cited by 11
Cited by
Kettenmann, H., Hanisch, U.-K., Noda, M., & Verkhratsky, A. (2011) · Physiological Reviews · doi:10.1152/physrev.00011.2010 · Cited by 3,547
The Retinal Pigment Epithelium in Visual Function
Strauss, O. (2005) · Physiological Reviews · doi:10.1152/physrev.00021.2004 · Cited by 2,828
Aromatic Rings in Chemical and Biological Recognition: Energetics and Structures
Salonen, L. M., Ellermann, M., & Diederich, F. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201007560 · Cited by 1,539
Physiology of cell volume regulation in vertebrates
Hoffmann, E. K., Lambert, I. H., & Pedersen, S. F. (2009) · Physiological Reviews · doi:10.1152/physrev.00037.2007 · Cited by 1,441
Gating the Selectivity Filter in ClC Chloride Channels
Dutzler, R., Campbell, E. B., & MacKinnon, R. (2003) · Science · doi:10.1126/science.1082708 · Cited by 727
Metadata
- Authors
- Jentsch, T. J., Stein, V., Weinreich, F., & Zdebik, A. A.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2002-04-01
- Volume
- 82
- Issue
- 2
- Pages
- 503-568
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2135426025
- Cited by
- 1,256
- References
- 530
- FWCI
- 5.74
- Type
- journal article
- Language
- en
- Open access
- closed
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.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
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.