SPLICS: a split green fluorescent protein-based contact site sensor for narrow and wide heterotypic organelle juxtaposition

Domenico Cieri, Mattia Vicario, Marta Giacomello, +8

Cell Death and Differentiation

TOM70 Sustains Cell Bioenergetics by Promoting IP3R3-Mediated ER to Mitochondria Ca2+ Transfer

Riccardo Filadi, Nuno Santos Leal, Bernadette Schreiner, +8

Current Biology

Reductive StressSignal TransductionMitochondrial FunctionMitochondria Ca2+ TransferNatural Sciences +12

Tau localises within mitochondrial sub-compartments and its caspase cleavage affects ER-mitochondria interactions and cellular Ca2+ handling

Domenico Cieri, Mattia Vicario, Francesca Vallese, +8

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

MitophagySignal TransductionMitochondrial FunctionNatural SciencesMolecular Biology +9

An expanded palette of improved SPLICS reporters detects multiple organelle contacts in vitro and in vivo

Francesca Vallese, Cristina Catoni, Domenico Cieri, +8

Nature Communications

Perturbations in cell signaling elicit early cardiac defects in mucopolysaccharidosis type II

Roberto Costa, Andrea Urbani, Marika Salvalaio, +8

Human Molecular Genetics

Cardiac MuscleHeart FailurePathologyMucopolysaccharidosis Type IiMorphogens Release +20

splitGFP Technology Reveals Dose-Dependent ER-Mitochondria Interface Modulation by α-Synuclein A53T and A30P Mutants

Tito Calí, Denis Ottolini, Mattia Vicario, +5

Cells

A split-GFP tool reveals differences in the sub-mitochondrial distribution of wt and mutant alpha-synuclein

Mattia Vicario, Domenico Cieri, Francesca Vallese, +7

Cell Death and Disease

Zebrafish Tg(hb9:MTS-Kaede): a new in vivo tool for studying the axonal movement of mitochondria

Giorgia Bergamin, Domenico Cieri, Giovanni Vazza, +2

Biochimica et Biophysica Acta (BBA) - General Subjects

Developmental BiologyMolecular NeuroscienceMitochondrial FunctionZebrafish TgOrganelle Dynamic +9

A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxia

Mattia Vicario, Ginevra Zanni, Francesca Vallese, +16

Neurobiology of Disease

Neurodegenerative DiseasesMolecular NeuroscienceNeuronal-enriched Isoform 2Degenerative DiseaseNeurology +8

A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect

Mattia Vicario, Tito Calí, Domenico Cieri, +13

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Novel Pmca3 MutationBiochemistryNatural SciencesPathologyMolecular Biology +2