Vittoria Petruzzella

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Top Venues

Human molecular genetics

Journal of personalized medicine

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Paola Zanfardino, Alessandro Amati, Stefano Doccini, Sharon N Cox, Apollonia Tullo, Giovanna Longo, Annamaria D'Erchia, Ernesto Picardi, Claudia Nesti, Filippo Maria Santorelli, Vittoria Petruzzella
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts. Human molecular genetics (2024)
Paola Zanfardino, Alessandro Amati, Stefano Doccini, Sharon N Cox, Apollonia Tullo, Giovanna Longo, Annamaria D'Erchia, Ernesto Picardi, Claudia Nesti, Filippo Maria Santorelli, Vittoria Petruzzella
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts. Human molecular genetics 33 (9) (2024)
Maria Teresa Rocchetti, Davide Bizzoca, Lorenzo Moretti, Enrico Ragni, Francesco Luca Moretti, Giovanni Vicenti, Giuseppe Solarino, Alessandro Rizzello, Vittoria Petruzzella, Luigi Leonardo Palese, Salvatore Scacco, Giuseppe Banfi, Biagio Moretti, Antonio Gnoni
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial. Journal of personalized medicine 13 (6) (2023)
Maria Teresa Rocchetti, Davide Bizzoca, Lorenzo Moretti, Enrico Ragni, Francesco Luca Moretti, Giovanni Vicenti, Giuseppe Solarino, Alessandro Rizzello, Vittoria Petruzzella, Luigi Leonardo Palese, Salvatore Scacco, Giuseppe Banfi, Biagio Moretti, Antonio Gnoni
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial. Journal of personalized medicine 13 (6) (2023)
Alessandra Amendolare, Flaviana Marzano, Vittoria Petruzzella, Rosa Anna Vacca, Luisa Guerrini, Graziano Pesole, Elisabetta Sbisà, Apollonia Tullo
The Underestimated Role of the p53 Pathway in Renal Cancer. Cancers 14 (23) (2022)
Paola Zanfardino, Giovanna Longo, Alessandro Amati, Federica Morani, Ernesto Picardi, Francesco Girolamo, Mariella Pafundi, Sharon N Cox, Caterina Manzari, Apollonia Tullo, Stefano Doccini, Filippo M Santorelli, Vittoria Petruzzella
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts. Human molecular genetics (2022)
Alessandra Amendolare, Flaviana Marzano, Vittoria Petruzzella, Rosa Anna Vacca, Luisa Guerrini, Graziano Pesole, Elisabetta Sbisà, Apollonia Tullo
The Underestimated Role of the p53 Pathway in Renal Cancer. Cancers 14 (23) (2022)
Alessandra Amendolare, Flaviana Marzano, Vittoria Petruzzella, Rosa Anna Vacca, Luisa Guerrini, Graziano Pesole, Elisabetta Sbisà, Apollonia Tullo
The Underestimated Role of the p53 Pathway in Renal Cancer. Cancers 14 (23) (2022)
Paola Zanfardino, Stefano Doccini, Filippo M Santorelli, Vittoria Petruzzella
Tackling Dysfunction of Mitochondrial Bioenergetics in the Brain. International journal of molecular sciences 22 (15) (2021)
Beatrice Berti, Giovanna Longo, Francesco Mari, Stefano Doccini, Ilaria Piccolo, Maria Alice Donati, Francesca Moro, Renzo Guerrini, Filippo Maria Santorelli, Vittoria Petruzzella
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction. BMC medical genomics 14 (1) (2021)
Aurelio Reyes, Paola Favia, Sara Vidoni, Vittoria Petruzzella, Massimo Zeviani
RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPases. PLoS genetics 16 (7) (2020)
Silvana Guerriero, Francesco D'Oria, Giacomo Rossetti, Rosa Anna Favale, Stefano Zoccolella, Giovanni Alessio, Vittoria Petruzzella
CMT2A Harboring Mitofusin 2 Mutation with Optic Nerve Atrophy and Normal Visual Acuity. International medical case reports journal 13 (2020)
Gianluca Fichi, Valentina Naef, Amilcare Barca, Giovanna Longo, Baldassare Fronte, Tiziano Verri, Filippo Maria Santorelli, Maria Marchese, Vittoria Petruzzella
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System. International journal of molecular sciences 20 (10) (2019)
Angelica Bianco, Luigi Bisceglia, Maria Fara De Caro, Valeria Galeandro, Patrizia De Bonis, Apollonia Tullo, Stefano Zoccolella, Silvana Guerriero, Vittoria Petruzzella
Leber's hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene - case report. BMC medical genetics 19 (1) (2018)
Angelica Bianco, Alessio Valletti, Giovanna Longo, Luigi Bisceglia, Julio Montoya, Sonia Emperador, Silvana Guerriero, Vittoria Petruzzella
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers. BMC research notes 11 (1) (2018)