Výsledky vyhledávání - Anna Ghelli
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Leber's Hereditary Optic Neuropathy (LHON) Pathogenic Mutations Induce Mitochondrial-dependent Apoptotic Death in Transmitochondrial Cells Incubated with Galactose Medium Autor Anna Ghelli, Claudia Zanna, Anna Maria Porcelli, Anthony H.V. Schapira, Andrea Martinuzzi, Valério Carelli, Michela Rugolo
Vydáno 2003Artigo -
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Respiratory Complex I Dysfunction Due to Mitochondrial DNA Mutations Shifts the Voltage Threshold for Opening of the Permeability Transition Pore toward Resting Levels Autor Anna Maria Porcelli, Alessia Angelin, Anna Ghelli, Elisa Mariani, Andrea Martinuzzi, Valério Carelli, Valeria Petronilli, Paolo Bernardi, Michela Rugolo
Vydáno 2008Artigo -
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The Background of Mitochondrial DNA Haplogroup J Increases the Sensitivity of Leber's Hereditary Optic Neuropathy Cells to 2,5-Hexanedione Toxicity Autor Anna Ghelli, Anna Maria Porcelli, Claudia Zanna, Sara Vidoni, Stefano Mattioli, Anna Barbieri, Luisa Iommarini, Maria Pala, Alessandro Achilli, Antonio Torroni, Michela Rugolo, Valério Carelli
Vydáno 2009Artigo -
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Defective Oxidative Phosphorylation in Thyroid Oncocytic Carcinoma Is Associated with Pathogenic Mitochondrial DNA Mutations Affecting Complexes I and III Autor Elena Bonora, Anna Maria Porcelli, Giuseppe Gasparre, A. Biondi, Anna Ghelli, Valério Carelli, Alessandra Baracca, Giovanni Tallini, Andrea Martinuzzi, Giorgio Lenaz, Michela Rugolo, G. Cara Romeo
Vydáno 2006Artigo -
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The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy Autor Maria Lucia Valentino, Piero Barboni, Anna Ghelli, Laura Bucchi, Chiara Rengo, Alessandro Achilli, Antonio Torroni, Alessandra Lugaresi, Raffaele Lodi, Bruno Barbiroli, M. T. Dotti, Antonio Federico, Agostino Baruzzi, Valério Carelli
Vydáno 2004Artigo -
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OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion Autor Claudia Zanna, Anna Ghelli, Anna Maria Porcelli, Mariusz Karbowski, Richard J. Youle, Simone Schimpf, Bernd Wissinger, Marcello Pinti, Andrea Cossarizza, Sara Vidoni, Maria Lucia Valentino, Michela Rugolo, Valério Carelli
Vydáno 2007Artigo -
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Oestrogens ameliorate mitochondrial dysfunction in Leber’s hereditary optic neuropathy Autor Carla Giordano, Monica Montopoli, Elena Perli, Maurizia Orlandi, Marianna Fantin, Fred N. Ross‐Cisneros, Laura Caparrotta, Andrea Martinuzzi, Eugenio Ragazzi, Anna Ghelli, Alfredo A. Sadun, Giulia d’Amati, Valério Carelli
Vydáno 2010Artigo -
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Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy Autor Annalinda Pisano, Carmela Preziuso, Luisa Iommarini, Elena Perli, Paola Grazioli, Antonio Francesco Campese, Alessandra Maresca, Monica Montopoli, Laura Masuelli, Alfredo A. Sadun, Giulia d’Amati, Valério Carelli, Anna Ghelli, Carla Giordano
Vydáno 2015Artigo -
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Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment Autor Luisa Iommarini, Ivana Kurelac, Mariantonietta Capristo, Maria Antonietta Calvaruso, Valentina Giorgio, Christian Bergamini, Anna Ghelli, Patrizia Nanni, Carla De Giovanni, Valério Carelli, Romana Fato, Pier‐Luigi Lollini, Michela Rugolo, Giuseppe Gasparre, Anna Maria Porcelli
Vydáno 2013Artigo -
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Mitochondrial chaperonin DNAJC15 promotes vulnerability to ferroptosis of chemoresistant ovarian cancer cells Autor Stefano Miglietta, Manuela Sollazzo, Iacopo Gherardi, Sara Milioni, Beatrice Cavina, Lorena Marchio, Monica De Luise, Camelia Alexandra Coadă, Marco Fiorillo, Anna Myriam Perrone, Ivana Kurelac, Giuseppe Gasparre, Luisa Iommarini, Anna Ghelli, Anna Maria Porcelli
Vydáno 2025Artigo -
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The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes Autor Anna Ghelli, Concetta Valentina Tropeano, Maria Antonietta Calvaruso, Alessandra Marchesini, Luisa Iommarini, Anna Maria Porcelli, Claudia Zanna, Vera De Nardo, Andrea Martinuzzi, Flemming Wibrand, John Vissing, Ivana Kurelac, Giuseppe Gasparre, Nur Selamoglu, Fevzi Daldal, Michela Rugolo
Vydáno 2013Artigo -
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Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors Autor Giuseppe Gasparre, Anna Maria Porcelli, Elena Bonora, Lucia Fiammetta Pennisi, Matteo Toller, Luisa Iommarini, Anna Ghelli, Massimo Moretti, Christine M. Betts, Giuseppe Martinelli, Alberto Rinaldi Ceroni, Francesco Curcio, Valério Carelli, Michela Rugolo, Giovanni Tallini, G. Cara Romeo
Vydáno 2007Artigo -
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A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene <i>MTND1</i>, an <i>Oncojanus</i> Function Autor Giuseppe Gasparre, Ivana Kurelac, Mariantonietta Capristo, Luisa Iommarini, Anna Ghelli, Claudio Ceccarelli, Giordano Nicoletti, Patrizia Nanni, Carla De Giovanni, Katia Scotlandi, Christine M. Betts, Valério Carelli, Pier‐Luigi Lollini, G. Cara Romeo, Michela Rugolo, Anna Maria Porcelli
Vydáno 2011Artigo
Vyhledávací nástroje:
Související témata
Biology
Mitochondrion
Gene
Genetics
Biochemistry
Mitochondrial DNA
Mutation
Cell biology
Respiratory chain
Chemistry
Oxidative phosphorylation
Enzyme
Leber's hereditary optic neuropathy
Apoptosis
Cancer research
Coenzyme Q – cytochrome c reductase
Cytochrome c
Medicine
Molecular biology
Optic nerve
Optic neuropathy
Phenotype
Programmed cell death
ATPase
Cancer
Cytochrome
Mitochondrial biogenesis
Mitochondrial respiratory chain
Oligomycin
Penetrance