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Human Molecular Genetics|June 30, 2009
Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNAAdriana Malena, Emanuele Loro, Miriam Di Re, 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.Electrophoresis|April 22, 2009
Development and characterization of polyspecific anti-mitochondrion antibodies for proteomics studies on in toto tissue homogenatesEmanuele Loro, Elisabetta Gianazza, Silvia Cazzola, et al.Journal of Tissue Engineering and Regenerative Medicine|May 10, 2014
In vitro development of engineered muscle using a scaffold based on the pressure-activated microsyringe (PAM) techniqueDaniele Cei, Adriana Malena, Carmelo de Maria, 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.Cancer Letters|May 3, 2006
Human papillomavirus type 77 E7 protein is a weak deregulator of cell cycleMariam Mansour, Majid Touka, Adriana Malena, 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.Human Molecular Genetics|January 15, 2017
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patientsDoriana Borgia, Adriana Malena, Marco Spinazzi, et al.Brain : a Journal of Neurology|July 13, 2007
Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidantsLodovica Vergani, Adriana Malena, Patrizia Sabatelli, et al.Acta Neuropathologica|May 7, 2013
Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophyAdriana Malena, Maria Pennuto, Caterina Tezze, et al.Pageof 2