Publications by authors named "Anna Maria Ghelli"

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Impaired plasma membrane calcium ATPase activity and mitochondrial dysfunction contribute to calcium dysregulation in Fabry disease-related painful neuropathy.
Francesco Formaggio, Asia Pizzi, Cecilia Delprete, Davide Pasqualini, Isabella Mataloni, Anna Maria Ghelli

Neurobiol Dis· September 2025

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Formation of I+III supercomplex rescues respiratory chain defects.
Chao Liang, Abhilash Padavannil, Shan Zhang, Sheryl Beh, David R L Robinson, Anna Maria Ghelli

Cell Metab· February 2025

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Mitochondrial chaperonin DNAJC15 promotes vulnerability to ferroptosis of chemoresistant ovarian cancer cells.
Stefano Miglietta, Manuela Sollazzo, Iacopo Gherardi, Sara Milioni, Beatrice Cavina, Anna Maria Ghelli

Open Biol· January 2025

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Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome () Gene.
Concetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, Luisa Iommarini, Gaia Tioli, Anna Maria Ghelli

Int J Mol Sci· January 2025

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A computational study to assess the pathogenicity of single or combinations of missense variants on respiratory complex I.
Laura Rigobello, Francesca Lugli, Leonardo Caporali, Alessio Bartocci, Jacopo Fadanni, Anna Maria Ghelli

Int J Biol Macromol· July 2024

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Use of bacterial photosynthetic vesicles to evaluate the effect of ionic liquids on the permeability of biological membranes.
Tancredi Bin, Giovanni Venturoli, Anna Maria Ghelli, Francesco Francia

Biochim Biophys Acta Biomembr· March 2024

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Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Serena Jasmine Aleo, Valentina Del Dotto, Martina Romagnoli, Claudio Fiorini, Giada Capirossi, Anna Maria Ghelli

Cell Rep Med· February 2024

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New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/ Mutation Associated with Leber's Hereditary Optic Neuropathy.
Francesco Musiani, Laura Rigobello, Luisa Iommarini, Valerio Carelli, Mauro Degli Esposti, Anna Maria Ghelli

Molecules· February 2022

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Organization of the Respiratory Supercomplexes in Cells with Defective Complex III: Structural Features and Metabolic Consequences.
Michela Rugolo, Claudia Zanna, Anna Maria Ghelli

Life (Basel)· April 2021

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Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects.
Elena Perli, Annalinda Pisano, Maria Gemma Pignataro, Antonio Francesco Campese, Maria Pelullo, Anna Maria Ghelli

FASEB J· June 2020

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Metabolomics hallmarks OPA1 variants correlating with their in vitro phenotype and predicting clinical severity.
Juan Manuel Chao de la Barca, Mario Fogazza, Michela Rugolo, Stéphanie Chupin, Valentina Del Dotto, Anna Maria Ghelli

Hum Mol Genet· May 2020

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Corrigendum to: "Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III." [Biochim. Biophys. Acta 2018;1859(3):182-190.].
Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, Leonardo Caporali, Fevzi Daldal, Anna Maria Ghelli

Biochim Biophys Acta Bioenerg· December 2018

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Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution.
Tatiana Trevisan, Diana Pendin, Aldo Montagna, Sergio Bova, Anna Maria Ghelli

Cell Rep· May 2018

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Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III.
Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, Leonardo Caporali, Fevzi Daldal, Anna Maria Ghelli

Biochim Biophys Acta Bioenerg· March 2018

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Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions.
Leonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, Alessandra Maresca, Maria Lucia Valentino

Biochim Biophys Acta· March 2013

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