Dott.ssa Camilla Ceccatelli Berti

Ricercatore a tempo determinato

Pubblicazioni selezionate

Boni, C, Rossi, M, Montali, I, Tiezzi, C, Vecchi, A, Penna, A, Doselli, S, Reverberi, V, Ceccatelli Berti, C, Montali, A, Schivazappa, S, Laccabue, D, Missale, G, & Fisicaro, P. (2023) What Is the Current Status of Hepatitis B Virus Viro-Immunology?, Clinics in Liver Disease, 27, 819-836.

Tiezzi, C, Rossi, M, Vecchi, A, Doselli, S, Penna, A, Fisicaro, P, Montali, I, Ceccatelli Berti, C, Reverberi, V, Montali, A, Missale, G, Ferrari, C, & Boni, C. (2023) FluoroSpot assay to analyze SARS-CoV-2-specific T cell responses, Star Protocols, 4.

Tiezzi, C, Vecchi, A, Rossi, M, Cavazzini, D, Bolchi, A, Laccabue, D, Doselli, S, Penna, A, Sacchelli, L, Brillo, F, Meschi, T, Ticinesi, A, Nouvenne, A, Donofrio, G, Zanelli, P. et al. (2023) Natural heteroclitic-like peptides are generated by SARS-CoV-2 mutations, Iscience, 26.

Montali, I, Ceccatelli Berti, C, Morselli, M, Acerbi, G, Barili, V, Pedrazzi, G, Montanini, B, Boni, C, Alfieri, A, Pesci, M, Loglio, A, Degasperi, E, Borghi, M, Perbellini, R, Penna, A. et al. (2023) Deregulated intracellular pathways define novel molecular targets for HBV-specific CD8 T cell reconstitution in chronic hepatitis B, Journal of Hepatology, 79, 50-60.

Ceccatelli Berti, C, Gihaz, S, Figuccia, S, Choi, J. Y, Pal Anasuya, C, Goffrini, P, & Ben Mamoun, C. (2023) Evidence for a Conserved Function of Eukaryotic Pantothenate Kinases in the Regulation of Mitochondrial Homeostasis and Oxidative Stress, International Journal of Molecular Sciences, 24, 435-448.

Magistrati, M, Gilea, A. I, Ceccatelli Berti, C, Baruffini, E, & Dallabona, C. (2023) Modopathies Caused by Mutations in Genes Encoding for Mitochondrial RNA Modifying Enzymes: Molecular Mechanisms and Yeast Disease Models, International Journal of Molecular Sciences, 24, 1-35.

Gilea, A. I, Ceccatelli Berti, C, Magistrati, M, Di Punzio, G, Goffrini, P, Baruffini, E, & Dallabona, C. (2021) Saccharomyces cerevisiae as a tool for studying mutations in nuclear genes involved in diseases caused by mitochondrial DNA instability, Genes, 12, 1-34.

Figuccia, S, Degiorgi, A, Ceccatelli Berti, C, Baruffini, E, Dallabona, C, & Goffrini, P. (2021) Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants, International Journal of Molecular Sciences, 22, 1-18.

Cappuccio, G, Ceccatelli Berti, C, Baruffini, E, Sullivan, J, Shashi, V, Jewett, T, Stamper, T, Maitz, S, Canonico, F, Revah-Politi, A, Kupchik, G. S, Anyane-Yeboa, K, Aggarwal, V, Benneche, A, Bratland, E. et al. (2021) Bi-allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease, Human Mutation, 42, 745-761.

Ceccatelli Berti, C, Di Punzio, G, Dallabona, C, Baruffini, E, Goffrini, P, Lodi, T, & Donnini, C. (2021) The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases, Genes, 12.

Ceccatelli Berti, C, Gilea, A. I, Armando De Gregorio, M, & Goffrini, P. (2020) Exploring Yeast as a Study Model of Pantothenate Kinase-Associated Neurodegeneration and for the Identification of Therapeutic Compounds, International Journal of Molecular Sciences, 22, 1-20.

Sharkia, R, Wierenga, K, Kessel, A, Azem, A, Bertini, E, Carrozzo, R, Torraco, A, Goffrini, P, Ceccatelli Berti, C, Mccormick, M, Plecko, B, Klein, A, Abela, L, Hengel, H, SchöLs, L. et al. (2019) Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome, Journal of Inherited Metabolic Disease, 42, 264-275.

OláHová, M, Ceccatelli Berti, C, Collier, J, Alston, C, Jameson, E, Jones, S, Edwards, N, He, L, Chinnery, P, Horvath, R, Goffrini, P, Taylor, R, & Sayer, J. (2019) Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease, Human Molecular Genetics Online, 28, 3766-3776.

Andrea, L, Aurelio, R, Ceccatelli Berti, C, Oliver, S, Silvia, M, Costanza, L, Ferrari, A, Robinson, A. J, Ulrich, M. H, Roland, L, Massimo, Z, Goffrini, P, & Daniele, G. (2017) A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy, Journal of Medical Genetics, 54, 815-824.

Alston, C. L, Ceccatelli Berti, C, Blakely, E. L, OláHová, M, Langping, H, Mcmahon, C. J, Olpin, S. E, Hargreaves, I. P, Nolli, C, Mcfarland, R, Goffrini, P, O'Sullivan, M. J, & Taylor, R. W. (2015) A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency, Human Genetics, 134, 869-879.

Ceccatelli Berti, C, Dallabona, C, Lazzaretti, M, Dusi, S, Tosi, E, Tiranti, V, & Goffrini, P. (2015) Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism, Microbial Cell, 2, 126-135.

Campusnet SCVSA   |   Versione Mobile
Non cliccare qui!