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The Journal of Biological Chemistry|May 9, 2015
A Novel Mutation in Isoform 3 of the Plasma Membrane Ca2+ Pump Impairs Cellular Ca2+ Homeostasis in a Patient with Cerebellar Ataxia and Laminin Subunit 1α MutationsTito Calì, Raffaele Lopreiato, Joshua Shimony, et al.
The EMBO Journal|July 29, 2006
Yeast homolog of a cancer-testis antigen defines a new transcription complexElena Kisseleva-Romanova, Raffaele Lopreiato, Agnès Baudin-Baillieu, et al.
International Journal of Molecular Sciences|December 23, 2023
Structural Integrity of Nucleolin Is Required to Suppress TDP-43-Mediated Cytotoxicity in Yeast and Human Cell ModelsCaterina Peggion, Maria Lina Massimino, Daniel Pereira, et al.
Frontiers in Cellular Neuroscience|April 29, 2021
Nucleolin Rescues TDP-43 Toxicity in Yeast and Human Cell ModelsCaterina Peggion, Maria Lina Massimino, Roberto Stella, et al.
EMBO Molecular Medicine|November 12, 2010
Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuliVeronica Costa, Marta Giacomello, Roman Hudec, et al.
Scientific Reports|July 28, 2017
Generation and validation of novel adeno-associated viral vectors for the analysis of Ca2+ homeostasis in motor neuronsRosa Pia Norante, Maria Lina Massimino, Paolo Lorenzon, et al.
Pediatric Neurology|September 18, 2023
Electroclinical Features in Two Novel STRADA Patients and a Functional Yeast Assay for the Validation of Missense STRADA MutationsCaterina Ancora, Marco Marchi, Claudia Maria Bonardi, et al.
Food Microbiology|March 3, 2021
Large-scale sequencing and comparative analysis of oenological Saccharomyces cerevisiae strains supported by nanopore refinement of key genomesArianna Basile, Fabio De Pascale, Federico Bianca, et al.
Disease Models & Mechanisms|March 26, 2016
Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxiaKarla P Figueroa, Sharan Paul, Tito Calì, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 16, 2017
A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defectMattia Vicario, Tito Calì, Domenico Cieri, et al.
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