Differential Control of the Releasable Vesicle Pools by SNAP-25 Splice Variants and SNAP-23

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

Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution

Sutton, R. B., Fasshauer, D., Jahn, R., & Brunger, A. T. (1998) · Nature · doi:10.1038/26412 · Cited by 2,417

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

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Co‐operative action of calcium ions in transmitter release at the neuromuscular junction

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Membrane fusion and exocytosis.

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SNARE-mediated membrane fusion

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

Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells

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Structure and Conformational Changes in NSF and Its Membrane Receptor Complexes Visualized by Quick-Freeze/Deep-Etch Electron Microscopy

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SNARE Function Analyzed in Synaptobrevin/VAMP Knockout Mice

Schoch, S., Deák, F., Königstorfer, A., Mozhayeva, M. G., Sara, Y., Südhof, T. C., & Kavalali, E. T. (2001) · Science · doi:10.1126/science.1064335 · Cited by 664

Snares and Munc18 in synaptic vesicle fusion

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

Characterization of SNAP-25 gene from marine teleostean, Lateolabrax japonicus

Chen, K., Huang, X., Chai, Y., & Gaisano, H. Y. (2007) · Chinese Journal of Oceanology and Limnology · doi:10.1007/s00343-007-0378-0 · Cited by 1

SNARE complex assembly and disassembly dynamics in response to Ca2+ current activation in live cells

Fang, Q., Zhao, Y., An, D., & Lindau, M. (2025) · Biophysical Journal · doi:10.1016/j.bpj.2025.04.005 · Cited by 1

A SNAP25 PROMOTER VARIANT IS ASSOCIATED WITH SCHIZOPHRENIA AND A DISTURBED SNAP25B/SNAP25A EXPRESSION RATIO IN PATIENTS

Méary, A., Dumaine, A., Llorca, P., Lançon, C., Schürhoff, F., Szöke, A., Leboyer, M., & Jamain, S. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.02.835 · Cited by 1

Spatial and Temporal Aspects of Exocytosis Studied on the Isolated Plasma Membranes

Milošević, I. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-1044-2_21 · Cited by 1

Endophilin-A controls recruitment, priming and fusion of neurosecretory vesiclesPreprint

Gowrisankaran, S., Steubler, V., Houy, S., del Castillo, J. G. P., Gelker, M., Kroll, J., Pinheiro, P. S., Halbsgut, N., Raimundo, N., Sørensen, J. B., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/540864 · Cited by 1

Modelling, estimation and analysis of dynamic processes from image sequences using temporal random closed sets and point processes with application to the cell exocytosis and endocytosis

Fernández, E. D. (2010) · TDX (Tesis Doctorals en Xarxa)

Probing modes of vesicle docking in neurosecretory cells with evanescent wave microscopy

Kochubey, O. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3293

Protein Mediated Membrane Fusion

Jahn, R. (2006) · Wiley-VCH eBooks · doi:10.1002/3527600906.mcb.200500023

CAPS (Ca2+-dependent Activator Protein for Secretion) Promotes Maturation of Large Dense Core Vesicles in Adrenal Medulla

Liu, Y. (2010) · Publications of the UdS (Saarland University) · doi:10.22028/d291-21354

The role of RAB3A in the secretory vesicle cycle

van Weering, J. R. T. (2008) · Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam)

Presynaptic molecular mechanisms that control quantal neurotransmitter discharge

Castro, R. G. (2009) · Publications of the UdS (Saarland University) · doi:10.22028/d291-21248

Biophysikalische und thermodynamische Charakterisierung der neuronalen SNARE-Komplexbildung

Wiederhold, K. (2008) · doi:10.53846/goediss-270

The timing of the final assembly of the SNARE complex in exocytosis

Walter, A. M. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3650

Synaptotagmin is an environmentally sensitive calcium ion sensor.

Murphy, J. (2010) · University of Minnesota Digital Conservancy (University of Minnesota)

Trafficking in Neuroendocrine Cells

Martin, T. F. J. (2007) · Elsevier eBooks · doi:10.1016/b978-012369437-9/50021-9

Funktionelle Rolle von SNARE-Proteinen bei der Myelinisierung

Feldmann, A. (2009) · Gutenberg Open Science · doi:10.25358/openscience-4319

SNAP-25 and Cdk5 as exocytotic regulators : Consequences for synaptic function and insulin release

Johansson, J. U. (2007) · Figshare

Functional Studies of SNAP-25 using a knock-out and rescue approach

Delgado-Martínez, I. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3299

Real time course of transmitter release of SSVs and LDCVs; SNARE function analysed in synaptobrevin2 and cellubrevin knock out mice

Zhao, Y. (2003) · doi:10.53846/goediss-601

Components controlling vesicle trafficking and regulated exocytosis in pancreatic beta-cells

Mandic, S. A. (2009) · Figshare

Two closely related Arabidopsis thaliana SNAREs localized in different compartments of Nicotiana tabacum secretory pathway

Rossi, M. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)

FUSION PORE OF CALCIUM TRIGGERED EXOCYTOSIS

Han, X. (2004)

Characterization of VAMP-2 gene from marine teleostean, Lateolabrax japonicus

Chen, K., Huang, X., Bao, Z., & Gaisano, H. Y. (2006) · Science in China Series C Life Sciences · doi:10.1007/s11427-006-2035-9

CELLULAR FUNCTION OF THE IA-MOTONEURON CIRCUIT FOLLOWING PERIPHERAL NERVE REGENERATION

Bullinger, K. L. (2009) · Journal of Bioresource Management

Role of Munc13 Isoforms in Regulating Large Dense Core Vesicle Exocytosis in Chromaffin Cells

Man, K. N. M. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5351

Promotes Maturation of Large Dense Core Vesicles in Adrenal Medulla

Medizin, T. (2010)

Dissertation zur Erlangung des Doktorgrades der Mathematisch-Naturwissenschaftlichen Fakult¨ der Georg-August-Universitzu G¨

Wiederhold, K. (2008)

CAUSES AND CONSEQUENCES OF REDUCED EXPRESSION OF SNAP-25 IN NEURONAL NETWORKS

Astis, S. D. (2013) · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) · doi:10.13130/de-astis-silvia_phd2013-01-16

Role of secretory granule heterogeneity in calcium-triggered exocytosis

Rao, T. C. (2016) · Human Biology

Structure and Function Relationship of Syntaxin-1 in Neurotransmitter Release

Park, S. (2015) · TSpace (University of Toronto)

Satnav for cells: Destination membrane fusion

Holt, M. G. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.10.001

Roles of Sec5 in the Regulation of Dense-Core Vesicle Secretion in PC12 Cells

Jiang, T. (2011) · TSpace (University of Toronto)

Molecular mechanisms of synaptic vesicle recycling with a focus on Endophilin A and Rabconnectin-3a

Gowrisankaran, S. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7717

The Role of HuD in Alternative Splicing and Alternative Polyadenylation in the Brain

Sena, R. M. (2020) · UNM’s Digital Repository (University of New Mexico)

Klonieren und Charakterisieren von P/Q-Typ-Calciumkanälen für Mikroskopie an lebenden Zellen

Juha, M. T. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4030

Faculty Opinions recommendation of Sequential N- to C-terminal SNARE complex assembly drives priming and fusion of secretory vesicles.

Neher, E. (2006) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1031317.387753

Faculty Opinions recommendation of Open syntaxin docks synaptic vesicles.

Chapman, E. R. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1091993.549887

Faculty Opinions recommendation of Dissecting docking and tethering of secretory vesicles at the target membrane.

Rettig, J. (2006) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1040076.488993

Characterisation of the Early Endosomal SNARE Complex

Zwilling, D. (2005) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3218

Spatial and temporal aspects of PI(4,5)P2 and SNAREs in exocytosis studied using isolated membrane sheets and capacitance measurements

Milošević, I. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3296

Roles of α-neurexins in synapse stabilization and Ca2+-dependent endocrine secretion

Dudanova, I. (2007) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3222

Fluoreszenzmikroskopische Studien an Plasmamembranen zur Untersuchung der molekularen Mechanismen der neuronalen Exocytose

Zilly, F. E. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-660

Fluoreszenzmikroskopische Studien an Plasmamembranen zur Untersuchung der molekularen Mechanismen der neuronalen Exocytose

Zilly, F. E. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-152

Faculty Opinions recommendation of Endophilin-A coordinates priming and fusion of neurosecretory vesicles via intersectin.

Wu, L. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737514163.793581071

Prognostic significance of serum annexin A7 in severe traumatic brain injury: A prospective longitudinal cohort study

Zhao, Y., Xu, Y., Yang, K., & Wang, H. (2022) · Clinica Chimica Acta · doi:10.1016/j.cca.2022.08.010

Excitation-Secretion Coupling of Dense-Core Vesicle Release

Cirkovic, V. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10009

Isoswitching in human brain development and agingPreprint

Erdogdu, B., Ji, H. J., Rudnick, Z., Pertea, M., & Salzberg, S. L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.05.652255

Activity-dependent muscarinic signalling regulates presynaptic PKC pathway and neurotransmission machinery at the neuromuscular junction

Polishchuk, A., Just‐Borràs, L., Cilleros‐Mañé, V., Balanyà-Segura, M., Simón, C. S., Tomàs, M., Jami-ElHirchi, M., Díaz-Wallach, M., Hurtado, E., Tomàs, J. M., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02440-4

DYNAMIQUE DE L'ASSEMBLAGE MOLÉCULAIRE SYNAPTIQUE : ÉTUDE DE LA DIFFUSION LATÉRALE DE LA SYNTAXIN 1A

Ribrault, C. (2010) · OpenGrey (Institut de l'Information Scientifique et Technique)

Development of presynaptic calcium dynamics and short-term plasticity in the SC-Ca1 synapse

Scullin, C. S. (2010) · UNM’s Digital Repository (University of New Mexico)

Mecanismes moleculars implicats en la secreció de pèptids en cèl•lules glials del sistema nerviós central

Mercader, S. P. (2011) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya)

SNAP-25 is a component of a ubiquitous SNARE complex required for evoked neuroexocytosis in GABAergic neurons

Tafoya, L. C. R. (2011) · UNM’s Digital Repository (University of New Mexico)

Presynaptic Substrates Mediating Fos- and Jun-dependent Plasticity at the Drosophila Neuromuscular Junction

Kim, S. M. (2007) · UA Campus Repository (The University of Arizona)

Additional file 1 of Synaptic retrograde regulation of the PKA-induced SNAP-25 and Synapsin-1 phosphorylation

Polishchuk, A., Cilleros‐Mañé, V., Just‐Borràs, L., Balanyà-Segura, M., Vandellòs Pont, G., Silvera-Simón, C., Tomàs, M., García, N., Tomàs, J. M., & Lanuza, M. A. (2024) · Figshare · doi:10.6084/m9.figshare.26572696

Contribution à l'étude des facteurs génétiques et environnementaux de susceptibilité aux troubles bipolaires : études du trouble bipolaire à début précoce et des traumatismes affectifs de l’enfance

Étain, B. (2009) · theses.fr (ABES) · doi:10.70675/bd9df83dz576fz4899za6bbz17f5d6ef945d

Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses

Schorova, L. (2018) · theses.fr (ABES) · doi:10.70675/a30a505az5e81z4089za24azcf43d27e33ce

Synaptopathies auditives et vestibulaires : de la physiologie moléculaire à la thérapie génique

Calvet, C. (2020) · theses.fr (ABES) · doi:10.70675/8920e327zd8ffz457ez9711zcfc53af428dc

New regulators in oxytocin and vasopressin release : role of the endolysosomal two-pore channels

Martucci, L. L. (2021) · theses.fr (ABES) · doi:10.70675/027d1ae2zd2ebz4677za019ze6ccd94cafe9

Occurrence of neuronal dysfunction in mice with virus- or toxic-induced lesions in the central nervous system

Dembowski, M., Burigk, L., Baumgärtner, W., & Hansmann, F. (2026) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2026.104096

Identifying the importance of phosphorylation of SNAP-25 at Ser187 in protein kinase C-mediated enhancement of exocytosis

Shu, Y. (2007) · doi:10.32469/10355/4757

Studien zu den biochemischen und strukturellen Eigenschaften von Snapin und zu seiner Rolle in der neuronalen Exozytose

Vites, O. (2005) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-172

Large Dense Core Vesicle Exocytosis in Mouse Chromaffin Cells is Regulated by Munc13s and Baiap3

Shin, Y. J. (2008) · doi:10.53846/goediss-1341

Differential Abilities of SNAP-25 Homologs to Support Neuronal Function

Delgado-Martínez, I., Nehring, R. B., & Sørensen, J. B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5092-06.2007 · Cited by 140

SNAP‐25 and Gene‐targeted Mouse Mutants

Bark, C. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2008.04009.x · Cited by 10

The SNAP-25 Protein Family

Kádková, A., Radecke, J., & Sørensen, J. B. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.09.020 · Cited by 97

Synaptotagmin Interaction with SNAP-25 Governs Vesicle Docking, Priming, and Fusion Triggering

Mohrmann, R., de Wit, H., Connell, E., Pinheiro, P. S., Leese, C., Bruns, D., Davletov, B. A., Verhage, M., & Sørensen, J. B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1236-13.2013 · Cited by 83

The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis

Sørensen, J. B., Matti, U., Wei, S., Nehring, R. B., Voets, T., Ashery, U., Binz, T., Neher, E., & Rettig, J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.251673298 · Cited by 169