The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Ca2+ buffering and action potential-evoked Ca2+ signaling in dendrites of pyramidal neurons
Open accessAbstract
The effect of the fluorescent Ca2+ indicator dye Fura-2 on Ca2+ dynamics was studied in proximal apical dendrites of neocortical layer V and hippocampal CA1 pyramidal neurons in rat brain slices using somatic whole-cell recording and a charge-coupled device camera. A single action potential evoked a transient increase of intradendritic calcium concentration ([Ca2+]i) that was reduced in size and prolonged when the Fura-2 concentration was increased from 20 to 250 microM. Extrapolation to zero Fura-2 concentration suggests that "physiological" transients at 37 degrees C have large amplitudes (150-300 nM) and fast decays (time constant < 100 ms). Assuming a homogeneous compartment model for the dendrite, 0.5-1% of the total Ca2+ entering during an action potential was estimated to remain free. Washout of cytoplasmic Ca2+ buffers was not detectable, suggesting that they are relatively immobile. During trains of action potentials, [Ca2+]i increased and rapidly reached a steady state (time constant < 200 ms), fluctuating around a plateau level which depended linearly on the action potential frequency. Thus, the mean dendritic [Ca2+]i encodes the action potential frequency during physiological patterns of electrical activity and may regulate Ca(2+)-dependent dendritic functions in an activity-dependent way.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“relative to the resting level of intracellular Ca2+ (20–50 nM) (109–111)”
From Synaptic memory and CaMKII (2023) · cites this paper as [111]
Citations
Cites
A new generation of Ca2+ indicators with greatly improved fluorescence properties.
Grynkiewicz, G., Poenie, M., & Tsien, R. Y. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)83641-4 · Cited by 21,722
Calcium's Role in Mechanotransduction during Muscle Development
Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,552
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023
Lev, S., Moreno, H., Martinez, R., Canoll, P., Peles, E., Musacchio, J. M., Plowman, G. D., Rudy, B., & Schlessinger, J. (1995) · Nature · doi:10.1038/376737a0 · Cited by 1,382
Calcium-binding proteins in the nervous system
Baimbridge, K. G., Celio, M. R., & ROGERS, J. H. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90081-i · Cited by 1,329
Active propagation of somatic action potentials into neocortical pyramidal cell dendrites
Stuart, G. J., & Sakmann, B. (1994) · Nature · doi:10.1038/367069a0 · Cited by 1,289
Self-citationDendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950
Activity-Dependent Action Potential Invasion and Calcium Influx into Hippocampal CA1 Dendrites
Spruston, N., Schiller, Y., Stuart, G. J., & Sakmann, B. J. (1995) · Science · doi:10.1126/science.7716524 · Cited by 839
Self-citationStuart, G. J., Dodt, H., & Sakmann, B. J. (1993) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374949 · Cited by 800
Self-citation
Cited by
Sorted by citations
Items 101–200 of 558
Egger, V., Svoboda, K., & Mainen, Z. F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-20-07551.2003 · Cited by 170
Bistability in the Ca2+/Calmodulin-Dependent Protein Kinase-Phosphatase System
Zhabotinsky, A. M. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76469-1 · Cited by 161
Lee, S., Schwaller, B., & Neher, E. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-2-00419.x · Cited by 168
Schmidt, H., Stiefel, K. M., Račay, P., Schwaller, B., & Eilers, J. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.035824 · Cited by 168
Calcium entry induces mitochondrial oxidant stress in vagal neurons at risk in Parkinson's disease
Goldberg, J. A., Guzmán, J. N., Estep, C. M., Ilijić, E., Kondapalli, J., Sánchez-Padilla, J., & Surmeier, D. J. (2012) · Nature Neuroscience · doi:10.1038/nn.3209 · Cited by 167
NMDA Receptor-Mediated Na+Signals in Spines and Dendrites
Rose, C. R., & Konnerth, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-12-04207.2001 · Cited by 166
Calcium dysregulation in neuronal aging and Alzheimer's disease: history and new directions
Thibault, O., Porter, N. M., Chen, K.-C., Blalock, E. M., Kaminker, P. G., Clodfelter, G. V., Brewer, L. D., & Landfield, P. W. (1998) · Cell Calcium · doi:10.1016/s0143-4160(98)90064-1 · Cited by 166
Baylor, S. M., & Hollingworth, S. (1998) · The Journal of General Physiology · doi:10.1085/jgp.112.3.297 · Cited by 167
Fluorescence imaging of large-scale neural ensemble dynamics
Kim, T. H., & Schnitzer, M. J. (2022) · Cell · doi:10.1016/j.cell.2021.12.007 · Cited by 165
Characterization and Subcellular Targeting of GCaMP-Type Genetically-Encoded Calcium Indicators
Mao, T., O’Connor, D. H., Scheuß, V., Nakai, J., & Svoboda, K. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001796 · Cited by 164
Layer-specific integration of locomotion and sensory information in mouse barrel cortex
Ayaz, A., Stäuble, A., Hamada, M., Wulf, M.-A., Saleem, A. B., & Helmchen, F. (2019) · Nature Communications · doi:10.1038/s41467-019-10564-8 · Cited by 155
Self-citationTsubokawa, H., & Ross, W. N. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05782.1997 · Cited by 157
Intracellular calcium strongly potentiates agonist-activated TRPC5 channels
Blair, N. T., Kaczmarek, J. S., & Clapham, D. E. (2009) · The Journal of General Physiology · doi:10.1085/jgp.200810153 · Cited by 157
Putting a finishing touch on GECIs
Rose, T., Goltstein, P. M., Portugues, R., & Griesbeck, O. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00088 · Cited by 165
Hosoi, N., Sakaba, T., & Neher, E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4122-07.2007 · Cited by 154
Fast Calcium Signals inDrosophilaMotor Neuron Terminals
Macleod, G. T., Hegström-Wojtowicz, M., Charlton, M. P., & Atwood, H. L. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00515.2002 · Cited by 153
Closed-loop all-optical interrogation of neural circuits in vivo
Zhang, Z., Russell, L. E., Packer, A. M., Gauld, O. M., & Häusser, M. (2018) · Nature Methods · doi:10.1038/s41592-018-0183-z · Cited by 147
Nevian, T., & Sakmann, B. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3332-03.2004 · Cited by 155
Self-citationCellular Level Brain Imaging in Behaving Mammals: An Engineering Approach
Hamel, E. O., Grewe, B. F., Parker, J. G., & Schnitzer, M. J. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.055 · Cited by 150
Interpreting in vivo calcium signals from neuronal cell bodies, axons, and dendrites: a review
Ali, F., & Kwan, A. C. (2019) · Neurophotonics · doi:10.1117/1.nph.7.1.011402 · Cited by 149
Imaging the coordination of multiple signalling activities in living cells
Welch, C. M., Elliott, H. L., Danuser, G. M., & Hahn, K. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3212 · Cited by 132
STDP in a Bistable Synapse Model Based on CaMKII and Associated Signaling Pathways
Graupner, M., & Brunel, N. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030221 · Cited by 147
Monitoring activity in neural circuits with genetically encoded indicators
Broussard, G. J., Liang, R., & Tian, L. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00097 · Cited by 148
Adaptation and Temporal Decorrelation by Single Neurons in the Primary Visual Cortex
Wang, X., Liu, Y., Sanchez-Vives, M. V., & McCormick, D. A. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00242.2003 · Cited by 135
Reporting neural activity with genetically encoded calcium indicators
Hires, S. A., Tian, L., & Looger, L. L. (2008) · Journal of Neurocytology · doi:10.1007/s11068-008-9029-4 · Cited by 142
Imaging fictive locomotor patterns in larval Drosophila
Pulver, S. R., Bayley, T. G., Taylor, A. L., Berni, J., Bate, M., & Hedwig, B. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00731.2015 · Cited by 136
Physiology of intracellular calcium buffering
Eisner, D. A., Neher, E., Taschenberger, H., & Smith, G. L. (2023) · Physiological Reviews · doi:10.1152/physrev.00042.2022 · Cited by 162
Fast and Accurate Detection of Action Potentials From Somatic Calcium Fluctuations
Sasaki, T., Takahashi, N., Matsuki, N., & Ikegaya, Y. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00084.2008 · Cited by 136
Calcium dynamics and buffering in motoneurones of the mouse spinal cord
Paleček, J., Lips, M. B., & Keller, B. U. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00485.x · Cited by 136
Altered Neuronal Excitability in Cerebellar Granule Cells of Mice Lacking Calretinin
Gall, D., Roussel, C., Susa, I., D'Angelo, E. U., Rossi, P., Bearzatto, B., Galas, M., Blum, D. L., Schurmans, S., & Schiffmann, S. N. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-28-09320.2003 · Cited by 133
Simons, S. B., Escobedo, Y., Yasuda, R., & Dudek, S. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904775106 · Cited by 134
Calcium Dynamics in the Extracellular Space of Mammalian Neural Tissue
Egelman, D. M., & Montague, P. R. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)77345-5 · Cited by 133
Vanselow, B. K., & Keller, B. U. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00433.x · Cited by 132
Calcium Spikes in Basal Dendrites of Layer 5 Pyramidal Neurons during Action Potential Bursts
Kampa, B. M., & Stuart, G. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3062-05.2006 · Cited by 128
Low Mobility of the Ca2+ Buffers in Axons of Cultured Aplysia Neurons
Gabso, M., Neher, E., & Spira, M. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)81247-7 · Cited by 129
Interplay between Na+/Ca2+ Exchangers and Mitochondria in Ca2+ Clearance at the Calyx of Held
Kim, M., Korogod, N., Schneggenburger, R., Ho, W., & Lee, S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0454-05.2005 · Cited by 128
A DNA-based voltmeter for organelles
Saminathan, A., Devany, J. M., Veetil, A. T., Suresh, B., Pillai, K. S., Schwake, M., & Krishnan, Y. (2020) · Nature Nanotechnology · doi:10.1038/s41565-020-00784-1 · Cited by 131
Photon Shot Noise Limits on Optical Detection of Neuronal Spikes and Estimation of Spike Timing
Wilt, B. A., Fitzgerald, J. E., & Schnitzer, M. J. (2013) · Biophysical Journal · doi:10.1016/j.bpj.2012.07.058 · Cited by 127
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126
Calcium indicator loading of neurons using single-cell electroporation
Nevian, T., & Helmchen, F. (2007) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-007-0234-2 · Cited by 126
Self-citationSupralinear Ca2+ Signaling by Cooperative and Mobile Ca2+ Buffering in Purkinje Neurons
Maeda, H., Ellis‐Davies, G. C. R., Ito, K., Miyashita, Y., & Kasai, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)81045-4 · Cited by 124
SK channels and the varieties of slow after‐hyperpolarizations in neurons
Vogalis, F., Storm, J. F., & Lancaster, B. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03040.x · Cited by 122
Heterogeneous presynaptic release probabilities: functional relevance for short-term plasticity.
Trommershäuser, J., Schneggenburger, R., Zippelius, A., & Neher, E. (2003) · Biophysical Journal · doi:10.1016/s0006-3495(03)74967-4 · Cited by 124
Lee, S., Rosenmund, C., Schwaller, B., & Neher, E. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-3-00405.x · Cited by 124
Endogenous Calcium Buffering Capacity of Substantia Nigral Dopamine Neurons
Foehring, R. C., Zhang, X. F., Lee, J. C. F., & Callaway, J. C. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00038.2009 · Cited by 123
Calcium dynamics of spines depend on their dendritic location
Holthoff, K., Tsay, D., & Yuste, R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00576-7 · Cited by 117
Endogenous Ca 2+ Buffer Concentration and Ca 2+ Microdomains in Hippocampal Neurons
Müller, A., Kukley, M., Stausberg, P., Beck, H., Müller, W. S., & Dietrich, D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3799-04.2005 · Cited by 116
Synaptically Activated Ca2+ Waves in Layer 2/3 and Layer 5 Rat Neocortical Pyramidal Neurons
Larkum, M. E., Watanabe, S., Nakamura, T., Lasser‐Ross, N., & Ross, W. N. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.037614 · Cited by 112
Dendritic release of glutamate suppresses synaptic inhibition of pyramidal neurons in rat neocortex
Zilberter, Y. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00489.x · Cited by 114
Scheuß, V., Yasuda, R., Sobczyk, A., & Svoboda, K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1962-06.2006 · Cited by 111
Abel, H. J., Lee, J. C. F., Callaway, J. C., & Foehring, R. C. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00583.2003 · Cited by 110
Optical probing of neuronal circuits with calcium indicators
Peterlin, Z. A., Kozloski, J., Mao, B.-Q., Tsiola, A., & Yuste, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3619 · Cited by 108
Calcium microdomains in regulated exocytosis
Oheim, M., Kirchhoff, F., & Stühmer, W. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.08.007 · Cited by 108
Facilitation through Buffer Saturation: Constraints on Endogenous Buffering Properties
Matveev, V., Zucker, R. S., & Sherman, A. (2004) · Biophysical Journal · doi:10.1016/s0006-3495(04)74324-6 · Cited by 108
A Sodium-Pump-Mediated Afterhyperpolarization in Pyramidal Neurons
Gulledge, A. T., Dasari, S., Onoue, K., Stephens, E. K., Hasse, J. M., & Avesar, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0220-13.2013 · Cited by 105
A Bayesian approach for inferring neuronal connectivity from calcium fluorescent imaging data
Mishchenko, Y., Vogelstein, J. T., & Paninski, L. (2011) · The Annals of Applied Statistics · doi:10.1214/09-aoas303 · Cited by 104
The Properties and Implications of NMDA Spikes in Neocortical Pyramidal Cells
Rhodes, P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3791-05.2006 · Cited by 105
Widespread and Highly Correlated Somato-dendritic Activity in Cortical Layer 5 Neurons
Beaulieu-Laroche, L., Toloza, E. H. S., Brown, N. J., & Harnett, M. T. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.014 · Cited by 102
Opposing Effects of Neuronal Activity on Structural Plasticity
Fauth, M. J., & Tetzlaff, C. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00075 · Cited by 110
Sandler, V. M., & Barbara, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04325.1999 · Cited by 102
Endogenous calcium buffering in motoneurones of the nucleus hypoglossus from mouse
Lips, M. B., & Keller, B. U. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.105bi.x · Cited by 102
The calcium-activated slow AHP: cutting through the Gordian knot
Andrade, R., Foehring, R. C., & Tzingounis, A. V. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00047 · Cited by 106
Inference of neuronal network spike dynamics and topology from calcium imaging data
Lütcke, H., Gerhard, F., Zenke, F., Wulfram Gerstner, B., & Helmchen, F. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00201 · Cited by 101
Self-citationAn Inconvenient Truth: Calcium Sensors Are Calcium Buffers
McMahon, S. M., & Jackson, M. B. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.09.005 · Cited by 100
Role of the Neurogranin Concentrated in Spines in the Induction of Long-Term Potentiation
Zhabotinsky, A. M., Camp, R. N., Epstein, I. R., & Lisman, J. E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0729-06.2006 · Cited by 96
Calmodulin Activation by Calcium Transients in the Postsynaptic Density of Dendritic Spines
Keller, D. X., Franks, K. M., Bartol, T. M., & B, T. J. S. A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002045 · Cited by 97
Dineley, K. E., Malaiyandi, L. M., & Reynolds, I. J. (2002) · Molecular Pharmacology · doi:10.1124/mol.62.3.618 · Cited by 98
Mues, M., Bartholomäus, I., Thestrup, T., Griesbeck, O., Wekerle, H., Kawakami, N., & Krishnamoorthy, G. (2013) · Nature Medicine · doi:10.1038/nm.3180 · Cited by 100
Ohana, O., & Sakmann, B. J. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.135by.x · Cited by 93
Self-citationSimulation of Dendritic CaV1.3 Channels in Cat Lumbar Motoneurons: Spatial Distribution
Elbasiouny, S. M., Bennett, D. J., & Mushahwar, V. K. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00391.2005 · Cited by 92
Marshall, J. D., & Schnitzer, M. J. (2013) · ACS Nano · doi:10.1021/nn401410k · Cited by 91
Murayama, M., Pérez‐Garci, E., Lüscher, H., & Larkum, M. E. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00082.2007 · Cited by 91
Kaiser, K. M. M., Zilberter, Y., & Sakmann, B. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.t01-1-00017.x · Cited by 89
Self-citationKim, Y., Hsu, C.-L., Cembrowski, M. S., Mensh, B. D., & Spruston, N. (2015) · eLife · doi:10.7554/elife.06414 · Cited by 90
Cavazzini, M., Bliss, T., & Emptage, N. J. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.06.013 · Cited by 93
Dana, H., Novák, O., Guardado-Montesino, M., Fransen, J. W., Hu, A., Borghuis, B. G., Guo, C., Kim, D. S., & Svoboda, K. (2018) · PLoS ONE · doi:10.1371/journal.pone.0205444 · Cited by 87
Burst firing in identified rat geniculate interneurons
Zhu, J., Uhlrich, D. J., & Lytton, W. W. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00665-4 · Cited by 85
Associative Long-Term Depression in the Hippocampus Is Dependent on Postsynaptic N-Type Ca2+Channels
Normann, C., Peckys, D. B., Schulze, C. H., Walden, J., Jónás, P., & Bischofberger, J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08290.2000 · Cited by 85
Voltage imaging to understand connections and functions of neuronal circuits
Antic, S. D., Empson, R. M., & Knöpfel, T. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00226.2016 · Cited by 85
Dendritic Calcium Encodes Striatal Neuron Output during Up-States
Kerr, J. N. D., & Plenz, D. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01499.2002 · Cited by 83
Wanaverbecq, N., Marsh, S. J., AlQatari, M., & Brown, D. A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.035782 · Cited by 83
Voltage-activated intracellular calcium transients in thalamic relay cells and interneurons
Munsch, T., Budde, T., & Pape, H. (1997) · Neuroreport · doi:10.1097/00001756-199707280-00001 · Cited by 82
Competitive Calcium Binding: Implications for Dendritic Calcium Signaling
Markram, H., Roth, A., & Helmchen, F. (1998) · Journal of Computational Neuroscience · doi:10.1023/a:1008891229546 · Cited by 78
Self-citationAltered Calcium Metabolism in Aging CA1 Hippocampal Pyramidal Neurons
Oh, M. M., Oliveira, F. A., Waters, J., & Disterhoft, J. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5457-12.2013 · Cited by 81
Pivovarova, N. B., Pozzo‐Miller, L. D., Hongpaisan, J., & Andrews, S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10653.2002 · Cited by 81
Wide-field and two-photon imaging of brain activity with voltage- and calcium-sensitive dyes
Homma, R., Baker, B. J., Jin, L., Garaschuk, O., Konnerth, A., Cohen, L. B., & Zečević, D. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2009.0084 · Cited by 81
Efficient Ca2+ buffering in fast‐spiking basket cells of rat hippocampus
Aponte, Y., Bischofberger, J., & Jónás, P. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.147298 · Cited by 81
Neural anatomy and optical microscopy (NAOMi) simulation for evaluating calcium imaging methods
Song, A. K., Gauthier, J. L., Pillow, J. W., Tank, D. W., & Charles, A. S. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109173 · Cited by 78
Canepari, M., Djurisic, M. R., & Zečević, D. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.125005 · Cited by 78
Eilers, J., & Konnerth, A. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80067-0 · Cited by 77
Lee, S., Kim, M., Park, K. H., Earm, Y. E., & Ho, W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-06891.2002 · Cited by 76
NG2 glial cells integrate synaptic input in global and dendritic calcium signals
Sun, W., Matthews, E. A., Nicolas, V., Schoch, S., & Dietrich, D. (2016) · eLife · doi:10.7554/elife.16262 · Cited by 75
Müller, A., Kukley, M., Uebachs, M., Beck, H., & Dietrich, D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3816-06.2007 · Cited by 75
Action Potential Timing Determines Dendritic Calcium during Striatal Up-States
Kerr, J. N. D., & Plenz, D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4475-03.2004 · Cited by 74
Experience-Dependent Plasticity of Odor Representations in the Telencephalon of Zebrafish
Jacobson, G. A., Rupprecht, P., & Friedrich, R. W. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.007 · Cited by 74
Rózsa, B. J., Zelles, T., Vizi, E. S., & Lendvai, B. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3906-03.2004 · Cited by 72
Effects of cholinergic modulation on responses of neocortical neurons to fluctuating input
Tang, A. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.502 · Cited by 73
Murthy, V. N., Sejnowski, T. J., & Stevens, C. F. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.2.901 · Cited by 70
Lancaster, B., Hu, H., Ramakers, G. M. J., & Storm, J. F. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00809.x · Cited by 70
Imaging of Ca2+ transients induced in Paramecium cells by a polyamine secretagogue
Klauke, N., & Plattner, H. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.8.975 · Cited by 70
Metadata
- Authors
- Helmchen, F., Imoto, K., & Sakmann, B.
- Affiliations
- Max Planck Society (DE)
- Max Planck Institute for Medical Research (DE)
- ORCID
- Helmchen, F.
- Venue
- Biophysical Journal
- Publisher
- Elsevier BV
- Published
- 1996-02
- Volume
- 70
- Issue
- 2
- Pages
- 1069-1081
- ISSN
- 0006-3495 (ISSN-L)
- PMC
- PMC1225009
- OpenAlex
- W2006602134
- Cited by
- 559
- References
- 47
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 2 · 2023: 9 · 2022: 13 · 2021: 9 · 2020: 11 · 2019: 14 · 2018: 18 · 2017: 12 · 2016: 18 · 2015: 27 · 2014: 23 · 2013: 17 · 2012: 27
- FWCI
- 10.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biophysical Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- calcium buffering, dendritic calcium signaling, pyramidal neurons, hippocampal CA1, fura-2, calcium indicator dyes, action potential frequency
- MeSH terms
- Action Potentials, Animals, Biophysics, Buffers, Calcium, Cell Compartmentation, Dendrites, Fluorescent Dyes, Indicators and Reagents, Kinetics, Models, Neurological, Signal Transduction, Fura-2, Rats, Wistar, Pyramidal Cells, Rats, Biophysical Phenomena, In Vitro Techniques
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