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Marta Maglione

Showing results (1-10 of 28) with videos related to

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Nature Neuroscience|June 27, 2013
Seeing the forest tree by tree: super-resolution light microscopy meets the neurosciencesMarta Maglione, Stephan J Sigrist
Methods in Molecular Biology (Clifton, N.J.)|April 12, 2025
Imaging Synapse Ultrastructure and Organization with STED MicroscopyMarta Maglione, Stephan J Sigrist
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2021
Rapid Ca<sup>2+</sup> channel accumulation contributes to cAMP-mediated increase in transmission at hippocampal mossy fiber synapsesRyota Fukaya, Marta Maglione, Stephan J Sigrist, et al.
Glia|May 15, 2010
Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32Marta Maglione, Oliver Tress, Brigitte Haas, et al.
Nature Communications|March 23, 2019
Autophagy within the mushroom body protects from synapse aging in a non-cell autonomous mannerAnuradha Bhukel, Christine Brigitte Beuschel, Marta Maglione, et al.
Journal of Neurogenetics|January 23, 2020
Interactions between amyloid precursor protein-like (APPL) and MAGUK scaffolding proteins contribute to appetitive long-term memory in <i>Drosophila melanogaster</i>Bryon Silva, Christian Niehage, Marta Maglione, et al.
Cell Stress|November 30, 2022
A pathological role of the Hsp40 protein Ydj1/DnaJA1 in models of Alzheimer's diseaseJelena Tadic, Julia Ring, Andrea Jerkovic, et al.
Plos Biology|June 21, 2021
Recruitment of release sites underlies chemical presynaptic potentiation at hippocampal mossy fiber boutonsMarta Orlando, Anton Dvorzhak, Felicitas Bruentgens, et al.
Nanoscale|April 5, 2023
Fluorinated dendritic amphiphiles, their stomatosome aggregates and application in enzyme encapsulationTiffany Guitton-Spassky, Florian Junge, Abhishek Kumar Singh, et al.
Plos Genetics|July 14, 2011
Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humansOliver Tress, Marta Maglione, Armin Zlomuzica, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Nature Neuroscience|June 27, 2013
Seeing the forest tree by tree: super-resolution light microscopy meets the neurosciencesMarta Maglione, Stephan J Sigrist
Methods in Molecular Biology (Clifton, N.J.)|April 12, 2025
Imaging Synapse Ultrastructure and Organization with STED MicroscopyMarta Maglione, Stephan J Sigrist
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2021
Rapid Ca<sup>2+</sup> channel accumulation contributes to cAMP-mediated increase in transmission at hippocampal mossy fiber synapsesRyota Fukaya, Marta Maglione, Stephan J Sigrist, et al.
Glia|May 15, 2010
Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32Marta Maglione, Oliver Tress, Brigitte Haas, et al.
Nature Communications|March 23, 2019
Autophagy within the mushroom body protects from synapse aging in a non-cell autonomous mannerAnuradha Bhukel, Christine Brigitte Beuschel, Marta Maglione, et al.
Journal of Neurogenetics|January 23, 2020
Interactions between amyloid precursor protein-like (APPL) and MAGUK scaffolding proteins contribute to appetitive long-term memory in <i>Drosophila melanogaster</i>Bryon Silva, Christian Niehage, Marta Maglione, et al.
Cell Stress|November 30, 2022
A pathological role of the Hsp40 protein Ydj1/DnaJA1 in models of Alzheimer's diseaseJelena Tadic, Julia Ring, Andrea Jerkovic, et al.
Plos Biology|June 21, 2021
Recruitment of release sites underlies chemical presynaptic potentiation at hippocampal mossy fiber boutonsMarta Orlando, Anton Dvorzhak, Felicitas Bruentgens, et al.
Nanoscale|April 5, 2023
Fluorinated dendritic amphiphiles, their stomatosome aggregates and application in enzyme encapsulationTiffany Guitton-Spassky, Florian Junge, Abhishek Kumar Singh, et al.
Plos Genetics|July 14, 2011
Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humansOliver Tress, Marta Maglione, Armin Zlomuzica, et al.
Pageof 3