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FEBS Letters|February 16, 2010
Signal transduction to the permeability transition poreAndrea Rasola, Marco Sciacovelli, Boris Pantic, et al.Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
Activation of mitochondrial ERK protects cancer cells from death through inhibition of the permeability transitionAndrea Rasola, Marco Sciacovelli, Federica Chiara, et al.Genes|April 8, 2014
Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cellsAnnalisa Botta, Adriana Malena, Emanuele Loro, et al.Autophagy|September 16, 2016
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNAAdriana Malena, Boris Pantic, Doriana Borgia, et al.Human Molecular Genetics|June 9, 2017
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cellsSara Vianello, Boris Pantic, Aurora Fusto, et al.Experimental Cell Research|February 25, 2016
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblastsBoris Pantic, Doriana Borgia, Silvia Giunco, et al.Neurology|September 28, 2018
The clinical spectrum of CASQ1-related myopathyClaudio Semplicini, Cinzia Bertolin, Luca Bello, et al.Nature Communications|December 7, 2021
2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNABoris Pantic, Daniel Ives, Mara Mennuni, et al.Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.Pageof 1