THE SYNAPTIC VESICLE CYCLE

Short-Term Synaptic Plasticity

Zucker, R. S., & Regehr, W. G. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.092501.114547 · Cited by 5,068

SNAP receptors implicated in vesicle targeting and fusion

Söllner, T. H., Whiteheart, S. W., Brunner, M., Erdjument‐Bromage, H., Geromanos, S. J., Tempst, P., & Rothman, J. E. (1993) · Nature · doi:10.1038/362318a0 · Cited by 3,239

EVIDENCE FOR RECYCLING OF SYNAPTIC VESICLE MEMBRANE DURING TRANSMITTER RELEASE AT THE FROG NEUROMUSCULAR JUNCTION

Heuser, J. E., & Reese, T. S. (1973) · The Journal of Cell Biology · doi:10.1083/jcb.57.2.315 · Cited by 2,147

The synaptic vesicle cycle: a cascade of protein–protein interactions

Südhof, T. C. (1995) · Nature · doi:10.1038/375645a0 · Cited by 1,991

Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse

Geppert, M., Goda, Y., Hammer, R. E., Li, C., Rosahl, T. W., Stevens, C. F., & Südhof, T. C. (1994) · Cell · doi:10.1016/0092-8674(94)90556-8 · Cited by 1,483

Synaptic assembly of the brain in the absence of neurotransmitter secretion.

Verhage, M., Maia, A., Plomp, J., Brussaard, A., Heeroma, J., Vermeer, H., Toonen, R., Hammer, R., van den Berg, T. K., Missler, M., et al. (2000) · Science · doi:10.1126/science.287.5454.864 · Cited by 1,387

Membrane Fusion

Jahn, R., Lang, T., & Südhof, T. C. (2003) · Cell · doi:10.1016/s0092-8674(03)00112-0 · Cited by 1,364

Syntaxin: A Synaptic Protein Implicated in Docking of Synaptic Vesicles at Presynaptic Active Zones

Bennett, M. K., Calakos, N., & Scheller, R. H. (1992) · Science · doi:10.1126/science.1321498 · Cited by 1,263

SNARE-mediated membrane fusion

Chen, Y. A., & Scheller, R. H. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35052017 · Cited by 1,133

Definition of the readily releasable pool of vesicles at hippocampal synapses.

Rosenmund, C., & Stevens, C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80146-4 · Cited by 1,084

Neurotransmitter Release Machinery: Components of the Neuronal SNARE Complex and Their Function

Atasoy, D., & Kavalali, E. T. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_4 · Cited by 1

Low-frequency Neuromuscular Depression Is a Consequence of a Reduction in Nerve Terminal Ca2+ Currents at Mammalian Motor Nerve Endings

Silinsky, E. M. (2013) · Anesthesiology · doi:10.1097/aln.0b013e31829083d8 · Cited by 1

Neural Mechanisms of Fine-Grained Temporal Processing in Audition

Sakai, M. (2012) · otolaryngology · doi:10.4172/2161-119x.s3-001 · Cited by 1

Scientific Advances on Consciousness

Zhang, Y. (2017) · Lecture notes in computer science · doi:10.1007/978-3-319-70772-3_26 · Cited by 1

Studying the Effects of Inositol Pyrophosphates in an In Vitro Vesicle–Vesicle Fusion Assay

Sung, M. S., & Yoon, T. (2019) · Methods in molecular biology · doi:10.1007/978-1-0716-0167-9_13 · Cited by 1

Synaptische Übertragung

Feigenspan, A. (2017) · Springer eBooks · doi:10.1007/978-3-662-54117-3_11 · Cited by 1

Chapter 6 Structure and Function of Biomembranes and Membrane Phospholipids of Rat Salivary Glands

Kameyama, Y. (2009) · Elsevier eBooks · doi:10.1016/s1554-4516(09)10006-6 · Cited by 1

Structure and Function of Vertebrate and Invertebrate Active Zones

Garner, C. C., & Shen, K. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_3 · Cited by 1

Synapse Formation in the Mammalian Central Nervous System

Yasuda, M., & Umemori, H. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_4 · Cited by 1

Nerve and Muscle: Basic Concepts

Andrade, F. H. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6567-6_2 · Cited by 1

Nanoscale Components of Neurons: From Biomolecules to Nanodevices

Woolf, N. J., Priel, A., & Tuszyński, J. A. (2009) · Biological and medical physics series · doi:10.1007/978-3-642-03584-5_2 · Cited by 1

Initiation and Regulation of Synaptic Transmission by Presynaptic Calcium Channel Signaling Complexes

Sheng, Z., Lee, A., & Catterall, W. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_6 · Cited by 1

HTDP-2, a New Synthetic Compound, Inhibits Glutamate Release through Reduction of Voltage-Dependent Ca2+ Influx in Rat Cerebral Cortex Nerve Terminals

Lin, T., Lü, C.-W., Huang, S.-K., Chou, S. P., Kuo, Y., Chou, S.-H., Tzeng, W.-F., Leu, C.-Y., Huang, R.-F. S., Liew, Y., et al. (2011) · Pharmacology · doi:10.1159/000328774 · Cited by 1

Vesicle Priming in a SNAP

Müller, M., & Davis, G. W. (2010) · Neuron · doi:10.1016/j.neuron.2010.10.022 · Cited by 1

Regulation and functions of the lipid kinase PIP5K γ661 at synapses

Kanaho, Y., & Unoki, T. (2011) · Advances in Biological Regulation · doi:10.1016/j.advenzreg.2011.09.014 · Cited by 1

Y-27632 induces calcium-independent glutamate release in rat brain synaptosomes by a mechanism distinct from exocytosis

Lemeshchenko, V. V., Pekun, T. G., Waseem, T. V., & Fedorovich, S. V. (2012) · BIOPHYSICS · doi:10.1134/s0006350912030116 · Cited by 1

Spontaneous Neurotransmitter Release Depends on Intracellular Rather than ER Calcium Stores in Cultured Xenopus NMJ*

Ge, S., Li, R., Qi, L., He, X., & Xie, Z. (2006) · Tsinghua Science & Technology · doi:10.1016/s1007-0214(06)70214-0 · Cited by 1

Chromosomal Abnormalities and Putative Susceptibility Genes in Autism Spectrum Disorders

Gilling, M. (2015) · Cited by 1

Effects of Insulin on synapse formation and function; A possible role for insulin resistance

Hariharan, M. (2015) · DalSpace (Dalhousie University) · Cited by 1

Rapid Analysis of Synaptic Vesicle Endocytosis in Synaptosomes

Daniel, J. A., & Robinson, P. J. (2013) · Neuromethods · doi:10.1007/978-1-62703-676-4_9 · Cited by 1

Neuroproteome Dynamics in Modeled Brain Injury: A Systems Neurobiology Perspective

Lizhnyak, P. N., Yohannes, H., & Ottens, A. K. (2015) · CRC Press/Taylor & Francis, Boca Raton (FL) eBooks · Cited by 1

Die synaptische Übertragung

Bear, M. F., Connors, B. W., & Paradiso, M. A. (2018) · Springer eBooks · doi:10.1007/978-3-662-57263-4_5 · Cited by 1

Carbon-Fiber Amperometry in the Study of Exocytosis

Duffield, M. D., Raghupathi, R., & Keating, D. J. (2013) · Neuromethods · doi:10.1007/978-1-62703-676-4_3 · Cited by 1

The CLC Family of Chloride Channels and Transporters

Stauber, T., Novarino, G., & Jentsch, T. J. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374373-2.00012-1 · Cited by 1

Modulation by Histamine H3 Receptors of Neurotransmitter Release in the Basal Ganglia

Márquez-Gómez, R., García-Gálvez, A.-M., Morales-Figueroa, G.-E., & Arias‐Montaño, J. (2016) · The Receptors · doi:10.1007/978-3-319-40308-3_11 · Cited by 1

Molecular Mechanisms of Synaptic Plasticity and Memory and Their Dysfunction in Alzheimer's Disease ☆

Stephens, G. S., You, J. C., Fu, C.-H., & Chin, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21126-7 · Cited by 1

Glutamate transport in rat cerebral hemisphere nerve terminals under conditions of deep and profound hypothermia

Pastukhov, A. O., Krisanova, N., & Borisova, Т. (2017) · The Animal Biology · doi:10.15407/animbiol19.04.050 · Cited by 1

Visualization of synaptic vesicle dynamics with fluorescence proteins

Li, W., Geng, C., & Liu, B. (2018) · Folia Neuropathologica · doi:10.5114/fn.2018.74656 · Cited by 1

Long-term memory stabilized by noise-induced rehearsal

Wei, Y., & Koulakov, A. A. (2013) · BMC Neuroscience · doi:10.1186/1471-2202-14-s1-p220 · Cited by 1

Modulation of cPKCγ on Synapsin-Ia/b–Specific Phosphorylation Sites in the Developing Visual Cortex of Mice

Fu, T., Wang, J., Ding, Y., Zhang, Y., Han, S., & Li, J. (2019) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.19-26675 · Cited by 1

Exosomes: Natural Nanoparticles with Therapeutic Potential

Ratushnyak, M. G., & Semochkina, Y. P. (2020) · Nanotechnologies in Russia · doi:10.1134/s1995078020040126 · Cited by 1

Measuring Membrane Lipid Turnover with the pH-sensitive Fluorescent Lipid Analog ND6

Alamgir, S., Pelletier, O. B., Thomas, D. M., Rubio, V., Stawikowski, M. J., & Zhang, Q. (2021) · Journal of Visualized Experiments · doi:10.3791/62717 · Cited by 1

Connected neurons in multiple neocortical areas, comprising parallel circuits, encode essential information for visual shape learning

Nagayach, A., Ghafari, M., Zhao, Y., Collins, G. S., Singh, A., & Geller, A. I. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.102024 · Cited by 1

Deficits of Neurotransmitter Systems and Altered Brain Connectivity in Major Depression: A Translational Neuroscience Perspective

Yun, J., & Kim, Y. (2022) · Neuromethods · doi:10.1007/978-1-0716-2083-0_14 · Cited by 1

The notion of computation is fundamental to an autonomous neuroscience

Neske, G. T. (2010) · Complexity · doi:10.1002/cplx.20319 · Cited by 1

Synaptosomal Preparation and Its Application in Preclinical Studies

Feligioni, M., Buccarello, L., Hassanzadeh, K., & Corbo, M. (2022) · Neuromethods · doi:10.1007/978-1-0716-2569-9_2 · Cited by 1

Voltage-Gated Calcium Channel Auxiliary β Subunits

Borowik, S., & Colecraft, H. M. (2022) · Springer eBooks · doi:10.1007/978-3-031-08881-0_4 · Cited by 1

High‐Precision Mapping of Membrane Proteins on Synaptic Vesicles using Spectrally Encoded Super‐Resolution Imaging

Jiang, Y., Zhang, J., Jung, S., Chen, H., Xu, S., & Chiu, D. T. (2022) · Angewandte Chemie · doi:10.1002/ange.202217889 · Cited by 1

Sphingomyelinases as modulators of synaptic transmission

Gafurova, C. R., & Petrov, A. M. (2023) · Genes and Cells · doi:10.23868/gc546062 · Cited by 1

Intracellular Mechanism of Gastric Acid Secretion: What is the True Switch?

Urushidani, T. (2023) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.23-00166 · Cited by 1

Aagab is required for zebrafish larval development by regulating neural activity

Ding, S., Aziz, T., Meng, A., & Jia, S. (2024) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2024.01.003 · Cited by 1

Neuronal exosomes as a new signaling system

Yakovlev, A. A. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523040024 · Cited by 1

AMINO-GRAFTED MESOPOROUS SILICA NANOPARTICLES: ASSESSMENT OF NEUROMODULATORY, MEMBRANOTROPIC AND ANTIOXIDANT PROPERTIES IN CORTEX NERVE TERMINALS

Sotnik, S. (2024) · Biotechnologia Acta · doi:10.15407/biotech17.06.005 · Cited by 1

Prion Protein Misfolding at the Synapse

Šišková, Z., Perry, V. H., & Asuni, A. A. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7061-9_15 · Cited by 1

Molecular Chaperones in the Mammalian Brain: Regional Distribution, Cellular Compartmentalization and Synaptic Interactions

Wyttenbach, A., Quraishe, S., Bailey, J., & O'Connor, V. M. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7061-9_7 · Cited by 1

Endocytosis: Kiss and Run

Kavalali, E. T. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01381-4 · Cited by 1

Regulated versus Constitutive Secretion – A Major Form of Intercellular Communication

Stöckli, J., Piper, R. C., & James, D. E. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20037-0 · Cited by 1

Munc18 function in large dense-core vesicle exocytosis

Gulyás-Kovács, A. (2005) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-622 · Cited by 1

The neural cell adhesion molecule NCAM promotes maturation of the presynaptic endocytic machinery by switching synaptic vesicle recycling from AP3- to AP2-dependent mechanism in mice (Mus musculus, strain C57Bl/6J).

Shetty, A. (2008) · Cited by 1

Cell interactions in the CNS and their consequences for neuronal apoptosis

Berglund, M. (2005) · Figshare · Cited by 1

Endocytosis and Presynaptic Scaffolds

Haucke, V., & Gundelfinger, E. D. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01782-4 · Cited by 1

Neuromuscular Junction Physiology and Pathophysiology

Ubogu, E. E., & Ruff, R. L. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-156-7_1 · Cited by 1

SNARE-mediated plant immune responses at the cell periphery

Pajonk, S. (2007) · Kölner Universitäts PublikationsServer (Universität zu Köln) · Cited by 1

Synaptic Ultrastructure and Regulation of Synaptic Transmission in Caenorhabditis elegans

Kittelmann, M. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3269 · Cited by 1

Molecular and Cellular Mechanisms Behind Juvenile Neuronal Ceroid Lipofuscinosis (JNCL, Batten disease)

Luiro, K. (2006) · Työväentutkimus Vuosikirja · Cited by 1

Dendritic Organelles for Postsynaptic Trafficking

Hanus, C., & Ehlers, M. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_8 · Cited by 1

Good Players Left on the Sidelines: Why Some Synaptic Vesicles Don't Get in the Game

Price, G. D., & Trussell, L. O. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.003 · Cited by 1

Modulation of synaptic transmission by the voltage-gated potassium channel Eag1

Mortensen, L. S. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3264 · Cited by 1

Information and long term memory in calcium signalsPreprint

la Fuente, I. M. D., Malaina, I., Pérez‐Samartín, A., Cortés, J. M., Erramuzpe, A., Boyano, M. D., Bringas, C., Fedetz, M., & Martínez, L. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1506.02321 · Cited by 1

A Single Vesicle Assay to Study the Electrochemical Gradient Regulation in Glutamatergic and GABAergic Synaptic Vesicles

Farsi, Z. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5523 · Cited by 1

The role of filopodia in the formation of spine synapses

Arstikaitis, P. (2011) · cIRcle (University of British Columbia) · doi:10.14288/1.0071638 · Cited by 1

Functions of Vti1a and Vti1b in the Development of the Mouse Nervous System: Evidence from Double Knockout Mice

Kunwar, A. J. (2009) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3634 · Cited by 1

Synergistic SNARE Modulators of Neurotransmission: Complexins and SNAP-29

Sivakumar, N. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5635 · Cited by 1

Development of Fluorescence Activated Synaptosome Sorting (FASS) and analysis of VGLUT1 synapses from mouse brain

Biesemann, C. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3185 · Cited by 1

Probing Septin Function Through Interaction Screens: Identification of Novel Septins and Possible Regulatory Mechanisms

Steels, J. D. (2008) · TSpace (University of Toronto) · Cited by 1

Electrophysiological Analysis of the Synaptic Vesicle Priming Process

Nestvogel, D. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6444 · Cited by 1

Synaptic vesicle recycling investigated by high-resolution microscopy in a conventional and a sensory synapse

Kamin, D. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3212 · Cited by 1

Genetic Screen to Characterize Shank Interactors at the Drosophila Neuromuscular Junction

Hogg, A. (2018) · TSpace (University of Toronto) · Cited by 1

Multicolour optogenetics for studying the roles of cAMP and cGMP in synaptic plasticity and memory

Valencia, M. (2018) · TSpace (University of Toronto) · Cited by 1

Cyclin-Dependent Kinase 5 and Insulin Secretion

Bark, C., Rupnik, M. S., Jevšek, M., Mandic, S. A., & Berggren, P. (2008) · Springer eBooks · doi:10.1007/978-0-387-78887-6_11 · Cited by 1

Correction: The Scaffolding Protein SYD-2/Liprin-α Regulates the Mobility and Polarized Distribution of Dense-Core Vesicles in C. elegans Motor Neurons

Goodwin, P. R., & Juo, P. (2013) · PLoS ONE · doi:10.1371/annotation/dbc0d5dd-ab9b-4ae8-b5cf-507158f0761f · Cited by 1

Studying Molecular Interactions under Flow with Fluorescence Fluctuation Spectroscopy

Perego, E. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8028 · Cited by 1

SNARE-mediated membrane fusion on pore-spanning membranes – several fusion pathways analyzed by single-vesicle content release

Mühlenbrock, P. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8395 · Cited by 1

A Comprehensive Identification of Synaptic Vesicle Proteins in Rat Brains by cRPLC/MS-MS and 2DE/MALDI-TOF-MS

Lee, W. (2007) · Bulletin of the Korean Chemical Society · doi:10.5012/bkcs.2007.28.9.1499 · Cited by 1

A novel membrane-binding probe for the morphological and molecular characterization of synaptic vesicle recycling pathways

Revelo, N. H. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5048 · Cited by 1

Isolation and characterisation of synaptic vesicles from mouse brain

Ahmed, S. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-485 · Cited by 1

NMR Spectroscopic studies of calmodulin plasticity in calcium signalling

Rodríguez-Castañeda, F. (2008) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3418 · Cited by 1

Synaptojanin

Chang-Ileto, B., & Paolo, G. D. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01376-0 · Cited by 1

Active Zone☆

Wong, M. Y., & Kaeser, P. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04486-x · Cited by 1

Neuronal Action Potentials and Ion Channel Allostery

Kotermanski, S. E., & Cascio, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00279-0 · Cited by 1

Quantum Approaches to Neural Entrainment Through Audio-Visual- Tactile Stimulation of Hippocampal Theta Rhythms: Expanding the Frontiers of Cognitive Enhancement, Optimizing Glutamatergic Signaling, and Understanding Synaptic Plasticity Underlying Learning and MemoryPreprint

Termanini, R. W. (2023) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/xyjgc · Cited by 1

Mitochondrial Dysfunction and Neuronal Anomalies in POLG Mutant Midbrain OrganoidsPreprint

Chen, A., Yangzom, T., Sullivan, G. J., & Liang, K. X. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.27.559684 · Cited by 1

The Mechanisms of Exocytosis Studied in Cells and Models with Amperometry

Mellander, L. J. (2013) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 1

Analysis of mice deficient in late endosomal SNARE proteins VAMP8/endobrevin and Vti1b

Kanwar, N. (2007) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3204 · Cited by 1

A novel selective cell-permeable peptide disrupts presynaptic JNK2-STX1a interaction, providing neuroprotection and preventing glutamate-mediated excitotoxicity

Marcelli, S. (2018) · IRIS Research product catalog (Sapienza University of Rome) · Cited by 1

Investigation of Neuronal Membrane Fusion Using Fluorescence Correlation Spectroscopy

Vennekate, W. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3360 · Cited by 1

Transport Mechanisms of the Vesicular Glutamate Transporter 1

Preobraschenski, J. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3832 · Cited by 1

Analysis of the RAB family of GTPases in C. elegans and their role in regulating neuronal membrane trafficking

Sasidharan, N. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3162 · Cited by 1

The neurochemical consequences of aromatic L-amino acid decarboxylase deficiency

Allen, G. F. G. (2011) · UCL Discovery (University College London) · Cited by 1

Synaptic Pathology in Depression

Vollmayr, B., Henn, F. A., & Zink, M. (2006) · Springer eBooks · doi:10.1007/978-0-387-32562-0_29

New approaches to the study of mitochondrial Ca2+ dynamic

Perez, S. D. L. F. (2014) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/4528

Controlling pH Responsive Polymersome Assembly

Pearson, R., Warren, N. J., Armes, S. P., Lewis, A. L., & Battaglia, G. (2011) · UCL Discovery (University College London)

Investigation of SNARE-mediated exocytosis controlled by synaptic regulatory proteins

Shin, J. (2014) · Iowa State University Digital Repository (Iowa State University) · doi:10.31274/etd-180810-434

Neuronal Action Potentials and Ion Channel Allostery

Kotermanski, S. E., & Cascio, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.10028-8

Neuroproteome Dynamics in Modeled Brain Injury

Lizhnyak, P. N., Yohannes, H., & Ottens, A. K. (2015)

THE ROLE OF MUCOLIPIN-1 IN PATHOGENESIS OF THE LYSOSOMAL STORAGE DISEASE MUCOLIPIDOSIS TYPE IV

Miedel, M. T. (2008) · D-Scholarship@Pitt (University of Pittsburgh)

Distinguishing between the molecular interactions of synaptotagmin with SNAREs and with lipid bilayer using atomic force microscopy in recognition imaging mode

Takahashi, H., Henderson, R. M., Edwardson, J. M., & Takeyasu, K. (2013) · Archivum histologicum japonicum · doi:10.1679/aohc.74.9

Signal Molecules and Calcium

Damann, N., D’hoedt, D., & Nilius, B. (2009) · Springer eBooks · doi:10.1007/978-0-387-30370-3_26

Regulation of Presynaptic Calcium Channels

Chan, A. W., & Stanley, E. F. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-481-0_5

Investigation of the process of SNARE mediated synaptic vesicle exocytosis

Lai, Y. (2013) · Iowa State University Digital Repository (Iowa State University)

Snares and Munc18 in synaptic vesicle fusion

Rizo, J., & Südhof, T. C. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn898 · Cited by 539

Molecular machines governing exocytosis of synaptic vesicles

Jahn, R., & Fasshauer, D. (2012) · Nature · doi:10.1038/nature11320 · Cited by 1,004

The molecular machinery of synaptic vesicle exocytosis

Li, L., & Chin, L. (2003) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-2240-7 · Cited by 129

Mechanism of neurotransmitter release coming into focus

Rizo, J. (2018) · Protein Science · doi:10.1002/pro.3445 · Cited by 210

3. Molecular analysis of neurotransmitter release

Schiavo, G., & Stenbeck, G. (2017) · Princeton University Press eBooks · doi:10.2307/j.ctv3hh4x0.8