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Virchows Archiv : an International Journal of Pathology|December 11, 2008
The monoclonal anti-BCL10 antibody (clone 331.1) is a sensitive and specific marker of pancreatic acinar cell carcinoma and pancreatic metaplasiaStefano La Rosa, Francesca Franzi, Silvia Marchet, et al.
Cell Metabolism|June 4, 2015
Opa1 overexpression ameliorates the phenotype of two mitochondrial disease mouse modelsGabriele Civiletto, Tatiana Varanita, Raffaele Cerutti, et al.
International Journal of Molecular Sciences|August 26, 2023
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) SubjectsMirko Baglivo, Alessia Nasca, Eleonora Lamantea, et al.
Human Mutation|July 12, 2020
Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletionsSilvia Marchet, Andrea Legati, Alessia Nasca, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 20, 2013
AAV-mediated liver-specific MPV17 expression restores mtDNA levels and prevents diet-induced liver failureEmanuela Bottani, Carla Giordano, Gabriele Civiletto, et al.
Brain : a Journal of Neurology|December 10, 2013
Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse modelDario Brunetti, Sabrina Dusi, Carla Giordano, et al.
Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 geneAlice Zanolini, Ana Potic, Franco Carrara, et al.
Frontiers in Pharmacology|August 28, 2020
Targeting Multiple Mitochondrial Processes by a Metabolic Modulator Prevents Sarcopenia and Cognitive Decline in SAMP8 MiceDario Brunetti, Emanuela Bottani, Agnese Segala, et al.
Mitochondrion|April 16, 2019
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB geneSilvia Marchet, Federica Invernizzi, Flavia Blasevich, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
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