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Biochemical and Biophysical Research Communications|November 14, 2012
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 geneChiara Fiorillo, Giacomo Brisca, Denise Cassandrini, et al.The Journal of Biological Chemistry|January 13, 2006
Notch 1 overexpression inhibits osteoblastogenesis by suppressing Wnt/beta-catenin but not bone morphogenetic protein signalingValerie Deregowski, Elisabetta Gazzerro, Leah Priest, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 28, 2006
Role of the RAM domain and ankyrin repeats on notch signaling and activity in cells of osteoblastic lineageValerie Deregowski, Elisabetta Gazzerro, Leah Priest, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.Endocrinology|September 10, 2003
Notch 1 impairs osteoblastic cell differentiationMaria Sciaudone, Elisabetta Gazzerro, Leah Priest, et al.American Journal of Physiology. Endocrinology and Metabolism|December 11, 2003
Potentiating role of IGFBP-2 on IGF-II-stimulated alkaline phosphatase activity in differentiating osteoblastsClaudia Palermo, Paola Manduca, Elisabetta Gazzerro, et al.The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.International Journal of Molecular Medicine|May 13, 2004
Alpha-actin gene mutations and polymorphisms in Italian patients with nemaline myopathyClaudio Graziano, Enrico Bertini, Carlo Minetti, et al.Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.Pageof 20