A. Daga

发表

Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon

P. Kuzmin, V. Frolov, P. Bashkirov, 2019, Nature Communications.

Dynamic constriction and fission of ER membranes by reticulon

P. Kuzmin, V. Frolov, S. Bova, 2018, bioRxiv.

Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

F. Boaretto, A. Martinuzzi, M. Mostacciuolo, 2003, Neurology.

Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain

J. McNew, Avani Verma, A. Daga, 2011, Proceedings of the National Academy of Sciences.

The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function.

N. Bresolin, E. Clementi, A. Martinuzzi, 2006, Brain : a journal of neurology.

Balancing ER dynamics: shaping, bending, severing, and mending membranes.

J. McNew, D. Pendin, A. Daga, 2011, Current opinion in cell biology.

Fusing a lasting relationship between ER tubules.

J. McNew, A. Daga, Tyler J. Moss, 2011, Trends in cell biology.

Defhc1.1, a homologue of the juvenile myoclonic gene EFHC1, modulates architecture and basal activity of the neuromuscular junction in Drosophila.

A. Delgado-Escueta, Vimlesh Kumar, A. Megighian, 2011, Human molecular genetics.

GTP-dependent packing of a three-helix bundle is required for atlastin-mediated fusion

S. Moro, J. McNew, D. Pendin, 2011, Proceedings of the National Academy of Sciences.

In vivo Analysis of CRISPR/Cas9 Induced Atlastin Pathological Mutations in Drosophila

D. Pendin, A. Montagna, A. Daga, 2020, Frontiers in Neuroscience.

Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum

N. Bresolin, F. Boaretto, A. Martinuzzi, 2009, Journal of Medical Genetics.

Spastin Binds to Lipid Droplets and Affects Lipid Metabolism

E. Rugarli, G. Mancuso, A. Schauss, 2015, PLoS genetics.

M. Feany, A. Martinuzzi, E. Sartori, 2005, The Journal of clinical investigation.

The Hereditary Spastic Paraplegia Gene, spastin, Regulates Microtubule Stability to Modulate Synaptic Structure and Function

K. Broadie, A. Daga, G. Orso, 2004, Current Biology.

The effects of ER morphology on synaptic structure and function in Drosophila melanogaster

M. Stern, Ethan Fan, J. McNew, 2016, Journal of Cell Science.

EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

M. T. Medina, Viet-Huong V. Nguyen, K. Yamakawa, 2016, Genetics in Medicine.

Natural Selection Favors a Newly Derived timeless Allele in Drosophila melanogaster

C. Kyriacou, M. Pegoraro, E. Tauber, 2007, Science.

Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin

A. Martinuzzi, J. McNew, M. Micaroni, 2009, Nature.

ER Morphology in the Pathogenesis of Hereditary Spastic Paraplegia

D. Pendin, A. Daga, Sonia Sonda, 2021, Cells.

Proteasome dysfunction induces excessive proteome instability and loss of mitostasis that can be mitigated by enhancing mitochondrial fusion or autophagy

L. Scorrano, G. Juhász, V. Gorgoulis, 2019, Autophagy.

Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca2+ Handling

P. Pizzo, Nelly Redolfi, D. Pendin, 2019, Front. Physiol..

Transgenic fruit-flies expressing a FRET-based sensor for in vivo imaging of cAMP dynamics.

M. Zaccolo, A. Fiala, K. Erbguth, 2007, Cellular signalling.

Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.

N. Bresolin, G. Comi, A. Trabacca, 2006, Archives of neurology.

Myoclonin1/EFHC1 in cell division, neuroblast migration, synapse/dendrite formation in juvenile myoclonic epilepsy

Antonio V. Delgado-Escueta, Thierry Grisar, A. Delgado-Escueta, 2012 .

Myoclonin 1 / EFHC 1 in cell division , neuroblast migration , synapse / dendrite formation in juvenile myoclonic epilepsy

A. Delgado-Escueta, T. Grisar, J. Loturco, 2012 .

Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion

L. Scorrano, D. Pendin, A. Daga, 2014, The Journal of cell biology.

Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution.

A. Ghelli, S. Bova, D. Pendin, 2018, Cell reports.

Interactions of Drosophila Cbl with epidermal growth factor receptors and role of Cbl in R7 photoreceptor cell development

U. Banerjee, A. Chawla, M. Czech, 1997, Molecular and cellular biology.

MyoD is required for myogenic stem cell function in adult skeletal muscle.

P. Silver, M. Rudnicki, U. Banerjee, 1996, Genes & development.

Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin

A. Martinuzzi, J. McNew, M. Micaroni, 2010, Nature.

Molecular characterization of the transcription termination factor from human mitochondria.

R. Aebersold, D. Hess, V. Micol, 1993, The Journal of biological chemistry.

EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

M. T. Medina, Viet-Huong V. Nguyen, K. Yamakawa, 2016, Genetics in Medicine.