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Cells|November 27, 2021
ER Morphology in the Pathogenesis of Hereditary Spastic ParaplegiaSonia Sonda, Diana Pendin, Andrea DagaCurrent Opinion in Cell Biology|June 7, 2011
Balancing ER dynamics: shaping, bending, severing, and mending membranesDiana Pendin, James A McNew, Andrea DagaFrontiers in Neuroscience|November 12, 2020
<i>In vivo</i> Analysis of CRISPR/Cas9 Induced Atlastin Pathological Mutations in <i>Drosophila</i>Aldo Montagna, Nicola Vajente, Diana Pendin, et al.Trends in Cell Biology|May 10, 2011
Fusing a lasting relationship between ER tubulesTyler J Moss, Andrea Daga, James A McNewThe Journal of Cell Biology|January 29, 2014
Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletionValentina Debattisti, Diana Pendin, Elena Ziviani, et al.Current Biology : CB|July 10, 2004
The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and functionNick Trotta, Genny Orso, Maria Giovanna Rossetto, et al.Frontiers in Physiology|January 11, 2020
Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca<sup>2+</sup> HandlingNicola Vajente, Rosa Norante, Nelly Redolfi, et al.Proceedings of the National Academy of Sciences of the United States of America|June 22, 2011
Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domainTyler J Moss, Camilla Andreazza, Avani Verma, et al.Cell Reports|May 10, 2018
Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria DistributionTatiana Trevisan, Diana Pendin, Aldo Montagna, et al.The Journal of Clinical Investigation|November 9, 2005
Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastineGenny Orso, Andrea Martinuzzi, Maria Giovanna Rossetto, et al.Pageof 3