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Caterina Garone

Professoressa associata

Dipartimento di Scienze Mediche e Chirurgiche

Settore scientifico disciplinare: MED/03 GENETICA MEDICA

Pubblicazioni

Pettenuzzo, Ilaria; Carli, Sara; Sánchez-Cuesta, Ana; Isidori, Federica; Montanari, Francesca; Grippa, Mina; Lanzoni, Giulia; Ambrosetti, Irene; Di Pisa, Veronica; Cordelli, Duccio Maria; Mondardini, Maria Cristina; Pippucci, Tommaso; Ragni, Luca; Cenacchi, Giovanna; Costa, Roberta; Lima, Mario; Capristo, Maria Antonietta; Tropeano, Concetta Valentina; Caporali, Leonardo; Carelli, Valerio; Brunelli, Elena; Maffei, Monica; Ahmed Sheikhmaye, Hodman; Fetta, Anna; Brea-Calvo, Gloria; Garone, Caterina, COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2024, 1, pp. 1 - 9 [articolo]

Garone, C; De Giorgio, F; Carli, S, Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases, «JOURNAL OF TRANSLATIONAL MEDICINE», 2024, 22, Article number: 238, pp. 238 - 255 [articolo]Open Access

Pietra, Andrea; Palombo, Flavia; Giannotta, Melania; Maffei, Monica; Fiorini, Claudio; Costa, Roberta; Cenacchi, Giovanna; Carelli, Valerio; Cordelli, Duccio Maria; Pini, Antonella; Garone, Caterina, Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder, «NEUROLOGY. GENETICS», 2023, 9, pp. 1 - 5 [articolo]Open Access

Rebelo-Guiomar, Pedro; Pellegrino, Simone; Dent, Kyle C; Sas-Chen, Aldema; Miller-Fleming, Leonor; Garone, Caterina; Van Haute, Lindsey; Rogan, Jack F; Dinan, Adam; Firth, Andrew E; Andrews, Byron; Whitworth, Alexander J; Schwartz, Schraga; Warren, Alan J; Minczuk, Michal, A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit, «NATURE COMMUNICATIONS», 2022, 13, Article number: 929, pp. 1 - 14 [articolo]Open Access

Garone C.; Pietra A.; Nesci S., From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases, «LIFE», 2022, 12, Article number: 401, pp. 401 - 420 [articolo]Open Access

Boschetti E.; D'Angelo R.; Tardio M.L.; Costa R.; Giordano C.; Accarino A.; Malagelada C.; Clavenzani P.; Tugnoli V.; Caio G.; Righi V.; Garone C.; D'Errico A.; Cenacchi G.; Dotti M.T.; Stanghellini V.; Sternini C.; Pironi L.; Rinaldi R.; Carelli V.; De Giorgio R., Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy, «AMERICAN JOURNAL OF PHYSIOLOGY: GASTROINTESTINAL AND LIVER PHYSIOLOGY», 2021, 320, pp. G768 - G779 [articolo]

Mancuso M.; La Morgia C.; Valentino M.L.; Ardissone A.; Lamperti C.; Procopio E.; Garone C.; Siciliano G.; Musumeci O.; Toscano A.; Primiano G.; Servidei S.; Carelli V., SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy, «MITOCHONDRION», 2021, 58, pp. 243 - 245 [articolo]

Mercatelli D.; Balboni N.; De Giorgio F.; Aleo E.; Garone C.; Giorgi F.M., The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis Workflow, «METHODS AND PROTOCOLS», 2021, 4, Article number: 28, pp. 1 - 16 [articolo]Open Access

Quadalti C.; Garone C., mtDNA maintenance: Disease and therapy, in: The Human Mitochondrial Genome: From Basic Biology to Disease, Bologna, Giuseppe Gasparre, Anna Maria Porcelli, 2020, pp. 411 - 442 [capitolo di libro]

Protasoni M.; Bruno C.; Donati M.A.; Mohamoud K.; Severino M.; Allegri A.; Robinson A.J.; Reyes A.; Zeviani M.; Garone C., Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement, «MOLECULAR GENETICS AND METABOLISM», 2020, 129, pp. 26 - 34 [articolo]Open Access

Dominguez-Gonzalez C.; Madruga-Garrido M.; Mavillard F.; Garone C.; Aguirre-Rodriguez F.J.; Donati M.A.; Kleinsteuber K.; Marti I.; Martin-Hernandez E.; Morealejo-Aycinena J.P.; Munell F.; Nascimento A.; Kalko S.G.; Sardina M.D.; Alvarez del Vayo C.; Serrano O.; Long Y.; Tu Y.; Levin B.; Thompson J.L.P.; Engelstad K.; Uddin J.; Torres-Torronteras J.; Jimenez-Mallebrera C.; Marti R.; Paradas C.; Hirano M., Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy, «ANNALS OF NEUROLOGY», 2019, 86, pp. 293 - 303 [articolo]Open Access

Lindsey Van Haute, Song-Yi Lee, Beverly J. McCann, Christopher A. Powell, Dhiru Bansal, Lina Vasiliauskaitė, Caterina Garone, Sanghee Shin, Jong-Seo Kim, Michaela Frye, Joseph G. Gleeson, Eric A. Miska, Hyun-Woo Rhee, Michal Minczuk, NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs, «NUCLEIC ACIDS RESEARCH», 2019, 47, pp. 8720 - 8733 [articolo]Open Access

Manoli I.; Sysol J.R.; Epping M.W.; Li L.; Wang C.; Sloan J.L.; Pass A.; Gagne J.; Ktena Y.P.; Li L.; Trivedi N.S.; Ouattara B.; Zerfas P.M.; Hoffmann V.; Abu-Asab M.; Tsokos M.G.; Kleiner D.E.; Garone C.; Cusmano-Ozog K.; Enns G.M.; Vernon H.J.; Andersson H.C.; Grunewald S.; Elkahloun A.G.; Girard C.L.; Schnermann J.; DiMauro S.; Andres-Mateos E.; Vandenberghe L.H.; Chandler R.J.; Venditti C.P., FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia, «JCI INSIGHT», 2018, 3, pp. 1 - 16 [articolo]

Kullar P.J.; Gomez-Duran A.; Gammage P.A.; Garone C.; Minczuk M.; Golder Z.; Wilson J.; Montoya J.; Hakli S.; Karppa M.; Horvath R.; Majamaa K.; Chinnery P.F., Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family, «BRAIN», 2018, 141, pp. 55 - 62 [articolo]

Pacitti, Dario; Levene, Michelle; Garone, Caterina; Nirmalananthan, Niranjanan; Bax, Bridget E, Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far, «FRONTIERS IN GENETICS», 2018, 9, Article number: 669, pp. 1 - 22 [articolo]

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