List of works - Andrea Daga

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

scientific article published on August 1, 2011

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

scientific article

Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastine

scientific article published on November 2005

Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon

scientific article published on 22 November 2019

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

scientific article

Fusing a lasting relationship between ER tubules ⬇️

scientific article published on May 6, 2011

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

scientific article

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

scientific article

Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

scientific article (publication date: 26 August 2003)

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

scientific article

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

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

scientific article

Natural selection favors a newly derived timeless allele in Drosophila melanogaster

scientific article published in June 2007

Patterning of cells in the Drosophila eye by Lozenge, which shares homologous domains with AML1.

scientific article published in May 1996

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

scientific article

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

scientific article published on 19 April 2019

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

scientific article published on 27 January 2014

Spastin binds to lipid droplets and affects lipid metabolism

scientific article

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

scientific article published on 23 February 2016

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

scientific article

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

scientific article published in July 2004

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

scientific article published on 12 July 2007

List of works by Andrea Daga

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

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

Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastine

Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon

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

Fusing a lasting relationship between ER tubules ⬇️

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

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

Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

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

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

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

Natural selection favors a newly derived timeless allele in Drosophila melanogaster

Patterning of cells in the Drosophila eye by Lozenge, which shares homologous domains with AML1.

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

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

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

Spastin binds to lipid droplets and affects lipid metabolism

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

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

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

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