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ItalianoPORCELLI, ANNA MARIA
Pubblicazioni
Risultati 1 - 20 di 80 (tempo di esecuzione: 0.001 secondi).
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | |
|---|---|---|---|---|---|---|
| 1 | A cellular model for cancer progression: Role of mitochondrial mutations and metabolism | G. Romeo; G. Gasparre; A.M. Porcelli; M. Rugolo | 2010 | JOURNAL OF BIOTECHNOLOGY | 4.02 Riassunto (Abstract) | |
| 2 | A practical approach for the detection of DNA nanostructures in single live human cells by fluorescence microscopy | C. Bergamini;P. Angelini;K.J. Rhoden;A.M. Porcelli;R. Fato;G. Zuccheri | 2014 | METHODS | 1.01 Articolo in rivista | |
| 3 | AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations | A.M.Porcelli; C. Zanna; A. Montanaro; V.Carelli; A.Ghelli; M.Rugolo | 2004 | s.n | 4.02 Riassunto (Abstract) | |
| 4 | Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder | Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; Gasparre G.; Kurelac I.; De Nardo V.; Martinuzzi A.; Vissing J.; Selamoglu N.; Daldal F.; Rugolo M. | 2012 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 4.02 Riassunto (Abstract) | |
| 5 | Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I | Clara Musicco;Antonella Cormio;Maria Antonietta Calvaruso;Luisa Iommarini;Giuseppe Gasparre;Anna Maria Porcelli;Anna Maria Timperio;Lello Zolla;Maria Nicola Gadaleta | 2014 | MOLECULAR BIOSYSTEMS | 1.01 Articolo in rivista | |
| 6 | The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. | Porcelli A.M.; Ghelli A.; Iommarini L.; Mariani E.; Hoque M.; Zanna C.; Gasparre G.; Rugolo M. | 2008 | CELLULAR AND MOLECULAR LIFE SCIENCES | 1.01 Articolo in rivista | |
| 7 | Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance | A.M. PORCELLI; A. GHELLI; C. ZANNA; P. VALENTE; S. FERRONI; M. RUGOLO | 2004 | CELL DEATH AND DIFFERENTIATION | 1.01 Articolo in rivista | |
| 8 | ATP depletion and caspase independent death of cybrids bearing Leber's Hereditary Optic neuropathy MTDNA mutations incubated in galactose medium. A model for endonuclease G-mediated apoptosis | A. Ghelli; C. Zanna; A.M. Porcelli; V. Carelli; M. Rugolo | 2004 | Dipartimento Biologia Ev. SP. | 4.02 Riassunto (Abstract) | |
| 9 | The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. | Ghelli A.; Porcelli A.M.; Zanna C.; Vidoni S.; Mattioli S.; Barbieri A.; Iommarini L.; Pala M.; Achilli A.; Torroni A.; Rugolo M.; Carelli V. | 2009 | PLOS ONE | 1.01 Articolo in rivista | |
| 10 | Cancer cells contribute to distinct malignant traits depending on their MYC and pJNK relative levels | Manuela Sollazzo, Francesca Froldi, Simona Paglia, Anna Maria Porcelli, Daniela Grifoni | 2019 | 4.03 Poster | ||
| 11 | Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. | ZANNA C.; GHELLI A.; PORCELLI AM.; MARTINUZZI A.; Carelli V.; RUGOLO M. | 2005 | APOPTOSIS | 1.01 Articolo in rivista | |
| 12 | Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations | C.Zanna; A.M.Porcelli; A.Ghelli; V.Carelli; A.Martinuzzi; M.Rugolo | 2004 | s.n | 4.02 Riassunto (Abstract) | |
| 13 | Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes. | Iommarini L.; Calvaruso M.A.; Kurelac I.; Gasparre G.; Porcelli A.M. | 2013 | THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY | 1.01 Articolo in rivista | |
| 14 | A Comprehensive Characterization of Mitochondrial DNA Mutations in Glioblastoma Multiforme | Michele Vidone;Rosanna Clima;Mariangela Santorsola;Claudia Calabrese;Giulia Girolimetti;Ivana Kurelac;Laura Benedetta Amato;Luisa Iommarini;Elisa Trevisan;Marco Leone;Riccardo Soffietti;Isabella Morra;Giuliano Faccani;Marcella Attimonelli;Anna Maria Porcelli;Giuseppe Gasparre | 2015 | THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY | 1.01 Articolo in rivista | |
| 15 | Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. | Caporali L;Ghelli AM;Iommarini L;Maresca A;Valentino ML;La Morgia C;Liguori R;Zanna C;Barboni P;De Nardo V;Martinuzzi A;Rizzo G;Tonon C;Lodi R;Calvaruso MA;Cappelletti M;Porcelli AM;Achilli A;Pala M;Torroni A;Carelli V | 2013 | BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE | 1.01 Articolo in rivista | |
| 16 | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose | Alessandra Locatelli, Luisa Iommarini, Alessandra Graziadio, Alberto Leoni, Anna Maria Porcelli, Stefano Iotti, Emil Malucelli, Francesco Francia, Giovanni Venturoli, Giovanna Farruggia | 2019 | RSC ADVANCES | 1.01 Articolo in rivista | |
| 17 | Deep sequencing unearths Nuclear mitochondrial Sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants. | Petruzzella V.; Carrozzo R.; Calabrese C.; Dell'aglio R.; Trentadue R.; Piredda R.; Artuso L.; Rizza T.; Bianchi M.; Porcelli A.M.; Guerriero S.; Gasparre G.; Attimonelli M. | 2012 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | |
| 18 | Defective ciliogenesis in thyroid hürthle cell tumors is associated with increased autophagy | Lee, Junguee; Yi, Shinae; Kang, Yea Eun; Chang, Joon Young; Kim, Jung Tae; Sul, Hae Joung; Kim, Jong Ok; Kim, Jin Man; Kim, Joon; Porcelli, Anna Maria; Kim, Koon Soon; Shong, Minho | 2016 | ONCOTARGET | 1.01 Articolo in rivista | |
| 19 | Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III | BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G. | 2006 | CANCER RESEARCH | 1.01 Articolo in rivista | |
| 20 | Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation | C. Zanna; A. Ghelli; A. M.Porcelli; M. Karbowski; R.J. Youle; V. Carelli; M. Rugolo | 2006 | s. n. | 4.02 Riassunto (Abstract) |
Dettaglio
PORCELLI, ANNA MARIA
DIPARTIMENTO DI FARMACIA E BIOTECNOLOGIE
Docenti di ruolo di IIa fascia
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