Camille Péron

Fondazione IRCCS Istituto Neurologico Carlo Besta

Italy

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Articles (14)

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2024

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2024

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2024

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2023

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2023

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2021

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (6)

Valeria Tiranti

Associate Professor

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Ejona Rusha

Head of Core Facility

Helmholtz Zentrum München

GERMANY

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Andrea Cavaliere

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Sonia Levi

Full Professor

Vita-Salute San Raffaele University

ITALY

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VALENTINA DEL DOTTO

Junior assistant professor

University of Bologna

ITALY

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Dario Brunetti

Assistant Professor of Applied Medical Sciences

University of Milan

ITALY

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Camille Péron

Research Interests

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Articles (14)

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzer

Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A

Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene <i>C19orf12</i>

Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12

Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.

The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs

TFG binds LC3C to regulate ULK1 localization and autophagosome formation.

Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome.

Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives

Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA

Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)

Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Collaborators (6)

Valeria Tiranti

Ejona Rusha

Andrea Cavaliere

Sonia Levi

VALENTINA DEL DOTTO

Dario Brunetti

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