Measuring secretion in chromaffin cells using electrophysiological and electrochemical methods
暂无分享,去创建一个
K. Gillis | R Borges | M Camacho | K D Gillis | R. Borges | M. Camacho | Ricardo Borges | K. D. Gillis
[1] A. Neiman,et al. Phospholipase D1 Production of Phosphatidic Acid at the Plasma Membrane Promotes Exocytosis of Large Dense-core Granules at a Late Stage* , 2007, Journal of Biological Chemistry.
[2] Antonio G. García,et al. L-type calcium channels are preferentially coupled to endocytosis in bovine chromaffin cells. , 2007, Biochemical and biophysical research communications.
[3] R. Wykes,et al. Differential Regulation of Endogenous N- and P/Q-Type Ca2+ Channel Inactivation by Ca2+/Calmodulin Impacts on Their Ability to Support Exocytosis in Chromaffin Cells , 2007, The Journal of Neuroscience.
[4] K. Gillis,et al. Phosphomimetic Mutation of Ser-187 of SNAP-25 Increases both Syntaxin Binding and Highly Ca2+-sensitive Exocytosis , 2007, The Journal of general physiology.
[5] T. Moser,et al. Measurements of membrane patch capacitance using a software-based lock-in system , 2007, Pflügers Archiv - European Journal of Physiology.
[6] A. Teschemacher,et al. Potentiation of Exocytosis by Phospholipase C-Coupled G-Protein-Coupled Receptors Requires the Priming Protein Munc13-1 , 2007, The Journal of Neuroscience.
[7] L. Polo-Parada,et al. An activity-dependent increased role for L-type calcium channels in exocytosis is regulated by adrenergic signaling in chromaffin cells , 2006, Neuroscience.
[8] Corey Smith,et al. Physiological stimulation regulates the exocytic mode through calcium activation of protein kinase C in mouse chromaffin cells. , 2006, The Biochemical journal.
[9] Yong Chen,et al. Coupling of electrochemistry and fluorescence microscopy at indium tin oxide microelectrodes for the analysis of single exocytotic events. , 2006, Angewandte Chemie.
[10] F. Azizi,et al. Two mechanistically distinct forms of endocytosis in adrenal chromaffin cells: Differential effects of SH3 domains and amphiphysin antagonism , 2006, FEBS letters.
[11] A. Elhamdani,et al. Double Patch Clamp Reveals That Transient Fusion (Kiss-and-Run) Is a Major Mechanism of Secretion in Calf Adrenal Chromaffin Cells: High Calcium Shifts the Mechanism from Kiss-and-Run to Complete Fusion , 2006, The Journal of Neuroscience.
[12] K. Gillis,et al. On-chip amperometric measurement of quantal catecholamine release using transparent indium tin oxide electrodes. , 2006, Analytical chemistry.
[13] T. Südhof,et al. Different Effects on Fast Exocytosis Induced by Synaptotagmin 1 and 2 Isoforms and Abundance But Not by Phosphorylation , 2006, The Journal of Neuroscience.
[14] M. Criado,et al. Intragranular pH rapidly modulates exocytosis in adrenal chromaffin cells , 2006, Journal of neurochemistry.
[15] Jianhua Xu,et al. Maintenance of quantal size and immediately releasable granules in rat chromaffin cells by glucocorticoid. , 2005, American journal of physiology. Cell physiology.
[16] Khajak Berberian,et al. Electrochemical imaging of fusion pore openings by electrochemical detector arrays. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[17] D. Sulzer,et al. Analysis of exocytotic events recorded by amperometry , 2005, Nature Methods.
[18] Manfred Lindau,et al. Patch amperometry: high-resolution measurements of single-vesicle fusion and release , 2005, Nature Methods.
[19] Thomas Voets,et al. CAPS1 Regulates Catecholamine Loading of Large Dense-Core Vesicles , 2005, Neuron.
[20] Tim J. Craig,et al. Regulation of the Fusion Pore Conductance during Exocytosis by Cyclin-dependent Kinase 5* , 2004, Journal of Biological Chemistry.
[21] Andrew D. Powell,et al. Identification of the P2Y12 Receptor in Nucleotide Inhibition of Exocytosis from Bovine Chromaffin Cells , 2004, Molecular Pharmacology.
[22] A. Henkel,et al. Staurosporine restores GTPγS induced block of rapid endocytosis in chromaffin cells , 2004, FEBS letters.
[23] J. Barclay,et al. Syntaxin/Munc18 Interactions in the Late Events during Vesicle Fusion and Release in Exocytosis*[boxs] , 2004, Journal of Biological Chemistry.
[24] J. Santos-Sacchi. Determination of Cell Capacitance Using the Exact Empirical Solution of ∂Y/∂Cm and Its Phase Angle , 2004 .
[25] A. Villarroel,et al. New Roles of Myosin II during Vesicle Transport and Fusion in Chromaffin Cells* , 2004, Journal of Biological Chemistry.
[26] Ling-gang Wu,et al. Capacitance measurements at the calyx of Held in the medial nucleus of the trapezoid body , 2004, Journal of Neuroscience Methods.
[27] J. B. Sørensen. Formation, stabilisation and fusion of the readily releasable pool of secretory vesicles , 2004, Pflügers Archiv.
[28] O. Yizhar,et al. Tomosyn inhibits priming of large dense-core vesicles in a calcium-dependent manner. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[29] Shyue-An Chan,et al. Low Frequency Stimulation of Mouse Adrenal Slices Reveals a Clathrin‐Independent, Protein Kinase C‐Mediated Endocytic Mechanism , 2003, The Journal of physiology.
[30] T. Südhof,et al. Examining Synaptotagmin 1 Function in Dense Core Vesicle Exocytosis under Direct Control of Ca2+ , 2003, The Journal of general physiology.
[31] M. Lindau,et al. Secretory Vesicles Membrane Area Is Regulated in Tandem with Quantal Size in Chromaffin Cells , 2003, The Journal of Neuroscience.
[32] G. Nagy,et al. Differential control of adrenal and sympathetic catecholamine release by alpha 2-adrenoceptor subtypes. , 2003, Molecular endocrinology.
[33] E. Carbone,et al. Distinct potentiation of L-type currents and secretion by cAMP in rat chromaffin cells. , 2003, Biophysical journal.
[34] D. Sulzer,et al. Intracellular Patch Electrochemistry: Regulation of Cytosolic Catecholamines in Chromaffin Cells , 2003, The Journal of Neuroscience.
[35] P. Jonas,et al. A large pool of releasable vesicles in a cortical glutamatergic synapse , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[36] Manfred Lindau,et al. Exocytosis of single chromaffin granules in cell-free inside-out membrane patches , 2003, Nature Cell Biology.
[37] J. Castracane,et al. Amperometric detection of quantal catecholamine secretion from individual cells on micromachined silicon chips. , 2003, Analytical chemistry.
[38] Peng Chen,et al. A highly Ca2+-sensitive pool of vesicles is regulated by protein kinase C in adrenal chromaffin cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[39] M. A. Brioso,et al. Hydralazine Reduces the Quantal Size of Secretory Events by Displacement of Catecholamines From Adrenomedullary Chromaffin Secretory Vesicles , 2002, Circulation research.
[40] E. Neher,et al. Protein Kinase C-Dependent Phosphorylation of Synaptosome-Associated Protein of 25 kDa at Ser187 Potentiates Vesicle Recruitment , 2002, The Journal of Neuroscience.
[41] Ricardo Borges,et al. New Approaches for Analysis of Amperometrical Recordings , 2002, Annals of the New York Academy of Sciences.
[42] Hee-Sup Shin,et al. A perforated patch‐clamp study of calcium currents and exocytosis in chromaffin cells of wild‐type and α1A knockout mice , 2002, Journal of neurochemistry.
[43] C. James,et al. An electrochemical detector array to study cell biology on the nanoscale. , 2002 .
[44] R. Burgoyne,et al. Complexin Regulates the Closure of the Fusion Pore during Regulated Vesicle Exocytosis* , 2002, The Journal of Biological Chemistry.
[45] H. McMahon,et al. Dynamin-dependent and dynamin-independent processes contribute to the regulation of single vesicle release kinetics and quantal size , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[46] A. Morales,et al. Nongenomic regulation of the kinetics of exocytosis by estrogens. , 2002, The Journal of pharmacology and experimental therapeutics.
[47] J. Roder,et al. Alterations in Exocytosis Induced by Neuronal Ca2+Sensor-1 in Bovine Chromaffin Cells , 2002, The Journal of Neuroscience.
[48] E. Neher,et al. The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[49] G. Ellis‐Davies,et al. Differential Regulation of Exocytosis by α- and β-SNAPs , 2002, The Journal of Neuroscience.
[50] J. Kornhuber,et al. A common molecular machinery for exocytosis and the 'kiss-and-run' mechanism in chromaffin cells is controlled by phosphorylation. , 2001, Journal of cell science.
[51] P. Washbourne,et al. SNAP-25 with mutations in the zero layer supports normal membrane fusion kinetics. , 2001, Journal of cell science.
[52] S A Chan,et al. Physiological stimuli evoke two forms of endocytosis in bovine chromaffin cells , 2001, The Journal of physiology.
[53] M. Lindau,et al. Exocytosis of Catecholamine (CA)-containing and CA-free Granules in Chromaffin Cells* , 2001, The Journal of Biological Chemistry.
[54] H. Horstmann,et al. Direct observation of membrane retrieval in chromaffin cells by capacitance measurements , 2001, FEBS letters.
[55] T. Südhof,et al. Intracellular calcium dependence of large dense-core vesicle exocytosis in the absence of synaptotagmin I , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[56] H. Palfrey,et al. Quantal Size Is Dependent on Stimulation Frequency and Calcium Entry in Calf Chromaffin Cells , 2001, Neuron.
[57] Thomas C. Südhof,et al. Munc18-1 Promotes Large Dense-Core Vesicle Docking , 2001, Neuron.
[58] W. Webb,et al. Robust, high-resolution, whole cell patch-clamp capacitance measurements using square wave stimulation. , 2001, Biophysical journal.
[59] Peng Chen,et al. The Relationship between Camp, Ca2+, and Transport of Cftr to the Plasma Membrane , 2001, The Journal of general physiology.
[60] A. Fox,et al. Activation of purinergic receptors by ATP inhibits secretion in bovine adrenal chromaffin cells , 2000, Brain Research.
[61] M. A. Brioso,et al. Automatic analysis for amperometrical recordings of exocytosis , 2000, Journal of Neuroscience Methods.
[62] E. Neher,et al. R-Type Ca2+ Channels Are Coupled to the Rapid Component of Secretion in Mouse Adrenal Slice Chromaffin Cells , 2000, The Journal of Neuroscience.
[63] T. Voets. Dissection of Three Ca2+-Dependent Steps Leading to Secretion in Chromaffin Cells from Mouse Adrenal Slices , 2000, Neuron.
[64] J. Haycock,et al. Synaptic Vesicle Transporter Expression Regulates Vesicle Phenotype and Quantal Size , 2000, The Journal of Neuroscience.
[65] A. Ewing,et al. VMAT-Mediated Changes in Quantal Size and Vesicular Volume , 2000, The Journal of Neuroscience.
[66] A. Teschemacher,et al. Bidirectional Modulation of Exocytosis by Angiotensin II Involves Multiple G-Protein-Regulated Transduction Pathways in Chromaffin Cells , 2000, The Journal of Neuroscience.
[67] R. Wightman,et al. Adrenaline Release by Chromaffin Cells: Constrained Swelling of the Vesicle Matrix Leads to Full Fusion , 2000 .
[68] M. Lindau,et al. Resolution of patch capacitance recordings and of fusion pore conductances in small vesicles. , 2000, Biophysical journal.
[69] R. J. Fisher,et al. Measurement of exocytosis by amperometry in adrenal chromaffin cells: effects of clostridial neurotoxins and activation of protein kinase C on fusion pore kinetics. , 2000, Biochimie.
[70] R. Wightman,et al. Vesicular Ca2+ Participates in the Catalysis of Exocytosis* , 2000, The Journal of Biological Chemistry.
[71] E. Neher,et al. Exocytotic mechanism studied by truncated and zero layer mutants of the C‐terminus of SNAP‐25 , 2000, The EMBO journal.
[72] K. Gillis,et al. Admittance-based measurement of membrane capacitance using the EPC-9 patch-clamp amplifier , 2000, Pflügers Archiv.
[73] R. Burgoyne,et al. Comparison of Cysteine String Protein (Csp) and Mutant α-SNAP Overexpression Reveals a Role for Csp in Late Steps of Membrane Fusion in Dense-Core Granule Exocytosis in Adrenal Chromaffin Cells , 2000, The Journal of Neuroscience.
[74] A. Teschemacher,et al. P2Y Purinoceptors Inhibit Exocytosis in Adrenal Chromaffin Cells via Modulation of Voltage-Operated Calcium Channels , 2000, The Journal of Neuroscience.
[75] H. Horstmann,et al. Rhythmic opening and closing of vesicles during constitutive exo‐ and endocytosis in chromaffin cells , 2000, The EMBO journal.
[76] R. Wightman,et al. Amine Weak Bases Disrupt Vesicular Storage and Promote Exocytosis in Chromaffin Cells , 1999, Journal of neurochemistry.
[77] T. Martin,et al. Ca2+-Dependent Activator Protein for Secretion Is Critical for the Fusion of Dense-Core Vesicles with the Membrane in Calf Adrenal Chromaffin Cells , 1999, The Journal of Neuroscience.
[78] E. Neher,et al. Different types of calcium channels and secretion from bovine chromaffin cells , 1999, The European journal of neuroscience.
[79] M. Criado,et al. A single amino acid near the C terminus of the synaptosomeassociated protein of 25 kDa (SNAP-25) is essential for exocytosis in chromaffin cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[80] E. Neher,et al. Early requirement for α‐SNAP and NSF in the secretory cascade in chromaffin cells , 1999 .
[81] M. Nowycky,et al. A Current Activated on Depletion of Intracellular Ca2+ Stores Can Regulate Exocytosis in Adrenal Chromaffin Cells , 1999, The Journal of Neuroscience.
[82] V. Valero,et al. High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism , 1999, Nature Cell Biology.
[83] Corey A. Smith. A Persistent Activity-Dependent Facilitation in Chromaffin Cells Is Caused by Ca2+ Activation of Protein Kinase C , 1999, The Journal of Neuroscience.
[84] P. Chameau,et al. Regulation of the Ca2+ Sensitivity of Exocytosis by Rab3a , 1998, Journal of neurochemistry.
[85] S. Misler,et al. α-Latrotoxin Alters Spontaneous and Depolarization-Evoked Quantal Release from Rat Adrenal Chromaffin Cells: Evidence for Multiple Modes of Action , 1998, The Journal of Neuroscience.
[86] Zhuan Zhou,et al. Timing of Dense-Core Vesicle Exocytosis Depends on the Facilitation L-Type Ca Channel in Adrenal Chromaffin Cells , 1998, The Journal of Neuroscience.
[87] E. Pothos,et al. D2-Like Dopamine Autoreceptor Activation Reduces Quantal Size in PC12 Cells , 1998, The Journal of Neuroscience.
[88] A. Gil,et al. Preferential localization of exocytotic active zones in the terminals of neurite-emitting chromaffin cells. , 1998, European journal of cell biology.
[89] Tao Xu,et al. Multiple kinetic components of exocytosis distinguished by neurotoxin sensitivity , 1998, Nature Neuroscience.
[90] E. Neher,et al. Cytosolic Ca2+ Acts by Two Separate Pathways to Modulate the Supply of Release-Competent Vesicles in Chromaffin Cells , 1998, Neuron.
[91] M. Nowycky,et al. Compensatory and excess retrieval: two types of endocytosis following single step depolarizations in bovine adrenal chromaffin cells , 1998, The Journal of physiology.
[92] M. Nowycky,et al. Short-Term Changes in the Ca2+-Exocytosis Relationship during Repetitive Pulse Protocols in Bovine Adrenal Chromaffin Cells , 1997, The Journal of Neuroscience.
[93] S. Kim,et al. Ca2+-channel-dependent and -independent inhibition of exocytosis by extracellular ATP in voltage-clamped rat adrenal chromaffin cells , 1997, Pflügers Archiv.
[94] E. Neher,et al. Multiple Forms of Endocytosis In Bovine Adrenal Chromaffin Cells , 1997, The Journal of cell biology.
[95] G. Alvarez de Toledo,et al. The exocytotic event in chromaffin cells revealed by patch amperometry , 1997, Nature.
[96] E Neher,et al. Estimation of mean exocytic vesicle capacitance in mouse adrenal chromaffin cells. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[97] D. Barnett,et al. An optimized approach to membrane capacitance estimation using dual-frequency excitation. , 1997, Biophysical journal.
[98] R. Wightman,et al. Effects of External Osmotic Pressure on Vesicular Secretion from Bovine Adrenal Medullary Cells* , 1997, The Journal of Biological Chemistry.
[99] A. Shigematsu,et al. Inhibition by protamine of catecholamine secretion and ion influxes in bovine adrenal medullary cells in culture. , 1996, Journal of Pharmacology and Experimental Therapeutics.
[100] R. J. Barnard,et al. Patch-clamp capacitance analysis of the effects of alpha-SNAP on exocytosis in adrenal chromaffin cells. , 1996, Journal of cell science.
[101] A. Oberhauser,et al. Simultaneous capacitance and amperometric measurements of exocytosis: a comparison. , 1996, Biophysical journal.
[102] W. Almers,et al. Ca2+ triggers massive exocytosis in Chinese hamster ovary cells. , 1996, The EMBO journal.
[103] E. Neher,et al. Protein Kinase C Enhances Exocytosis from Chromaffin Cells by Increasing the Size of the Readily Releasable Pool of Secretory Granules , 1996, Neuron.
[104] R. Chow,et al. Rapid fluctuations in transmitter release from single vesicles in bovine adrenal chromaffin cells. , 1996, Biophysical journal.
[105] K. Engisch,et al. Calcium dependence of large dense-cored vesicle exocytosis evoked by calcium influx in bovine adrenal chromaffin cells , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[106] Robert S Zucker,et al. Mechanisms Determining the Time Course of Secretion in Neuroendocrine Cells , 1996, Neuron.
[107] H. Palfrey,et al. Calmodulin Is the Divalent Cation Receptor for Rapid Endocytosis, but Not Exocytosis, in Adrenal Chromaffin Cells , 1996, Neuron.
[108] M. McNiven,et al. Rapid endocytosis coupled to exocytosis in adrenal chromaffin cells involves Ca2+, GTP, and dynamin but not clathrin. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[109] R. Wightman,et al. Simultaneous amperometric measurement of ascorbate and catecholamine secretion from individual bovine adrenal medullary cells. , 1995, Analytical chemistry.
[110] R. Wightman,et al. Colocalization of calcium entry and exocytotic release sites in adrenal chromaffin cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[111] E Neher,et al. Time course of Ca2+ concentration triggering exocytosis in neuroendocrine cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[112] R S Zucker,et al. Kinetics of the secretory response in bovine chromaffin cells following flash photolysis of caged Ca2+. , 1994, Biophysical journal.
[113] Richard J. Bookman,et al. Releasable pools and the kinetics of exocytosis in adrenal chromaffin cells , 1994, Neuron.
[114] J. A. Jankowski,et al. Extracellular Ionic Composition Alters Kinetics of Vesicular Release of Catecholamines and Quantal Size During Exocytosis at Adrenal Medullary Cells , 1994, Journal of neurochemistry.
[115] R. M. Wightman,et al. Rapid and Selective Cyclic Voltammetric Measurements of Epinephrine and Norepinephrine as a Method To Measure Secretion from Single Bovine Adrenal Medullary Cells , 1994 .
[116] V. Rohlíček,et al. Dual-frequency method for synchronous measurement of cell capacitance, membrane conductance and access resistance on single cells , 1994, Pflügers Archiv.
[117] J. A. Jankowski,et al. Zones of exocytotic release on bovine adrenal medullary cells in culture. , 1994, The Journal of biological chemistry.
[118] J. Vincent,et al. The GTPase Rab3a negatively controls calcium‐dependent exocytosis in neuroendocrine cells. , 1994, The EMBO journal.
[119] D. Donnelly. A novel method for rapid measurement of membrane resistance, capacitance, and access resistance. , 1994, Biophysical journal.
[120] H. V. Gersdorff,et al. Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals , 1994, Nature.
[121] M. Adams,et al. Three types of Ca2+ channel trigger secretion with different efficacies in chromaffin cells , 1994, Nature.
[122] E. Neher,et al. A Ca-dependent early step in the release of catecholamines from adrenal chromaffin cells. , 1993, Science.
[123] J. M. Fernández,et al. Release of secretory products during transient vesicle fusion , 1993, Nature.
[124] R. Zucker,et al. Multiple calcium-dependent processes related to secretion in bovine chromaffin cells , 1993, Neuron.
[125] J. A. Jankowski,et al. Analysis of diffusional broadening of vesicular packets of catecholamines released from biological cells during exocytosis. , 1992, Analytical chemistry.
[126] Y. Okada,et al. Exocytosis upon osmotic swelling in human epithelial cells. , 1992, Biochimica et biophysica acta.
[127] E Neher,et al. Calcium requirements for secretion in bovine chromaffin cells. , 1992, The Journal of physiology.
[128] J. A. Jankowski,et al. Direct observation of epinephrine and norepinephrine cosecretion from individual adrenal medullary chromaffin cells , 1992 .
[129] Robert H. Chow,et al. Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells , 1992, Nature.
[130] J. A. Jankowski,et al. Nicotinic receptor-mediated catecholamine secretion from individual chromaffin cells. Chemical evidence for exocytosis. , 1990, The Journal of biological chemistry.
[131] J. M. Fernández,et al. Phase tracking: an improved phase detection technique for cell membrane capacitance measurements. , 1989, Biophysical journal.
[132] Manfred Lindau,et al. Patch-clamp techniques for time-resolved capacitance measurements in single cells , 1988, Pflügers Archiv.
[133] E. Neher,et al. Rates of diffusional exchange between small cells and a measuring patch pipette , 1988, Pflügers Archiv.
[134] J. Zimmerberg,et al. Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[135] E. Neher,et al. Intracellularly injected tetanus toxin inhibits exocytosis in bovine adrenal chromaffin cells , 1986, Nature.
[136] E Neher,et al. Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[137] J F Pujol,et al. Normal pulse polarography with carbon fiber electrodes for in vitro and in vivo determination of catecholamines. , 1979, Analytical chemistry.
[138] R M Riggin,et al. Electrochemical detection of selected organic components in the eluate from high-performance liquid-chromatography. , 1974, Clinical chemistry.
[139] K. Cole. ELECTRIC IMPEDANCE OF HIPPONOË EGGS , 1935, The Journal of general physiology.
[140] David J Machado,et al. Good practices in single-cell amperometry. , 2008, Methods in molecular biology.
[141] Arto Heiskanen,et al. On-Chip Determination of Dopamine Exocytosis Using Mercaptopropionic Acid Modified Microelectrodes , 2007 .
[142] Andrew D. Powell,et al. Identification of the P2Y(12) receptor in nucleotide inhibition of exocytosis from bovine chromaffin cells. , 2004, Molecular pharmacology.
[143] J. Santos-Sacchi. Determination of cell capacitance using the exact empirical solution of partial differential Y/partial differential Cm and its phase angle. , 2004, Biophysical journal.
[144] G. Ellis‐Davies,et al. Differential regulation of exocytosis by alpha- and beta-SNAPs. , 2002, Journal of Neuroscience.
[145] T. Martin,et al. Ca(2+)-dependent activator protein for secretion is critical for the fusion of dense-core vesicles with the membrane in calf adrenal chromaffin cells. , 1999, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[146] E. Neher,et al. Early requirement for alpha-SNAP and NSF in the secretory cascade in chromaffin cells. , 1999, The EMBO journal.
[147] K. Gillis. Techniques for Membrane Capacitance Measurements , 1995 .
[148] H. Thoenen,et al. Inhibition of exocytosis by intracellularly applied antibodies against a chromaffin granule-binding protein , 1989, Nature.
[149] W. Almers,et al. Currents through the fusion pore that forms during exocytosis of a secretory vesicle , 1987, Nature.