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Autophagy|October 29, 2010
Autophagy in Gaucher disease due to saposin C deficiencyMassimo Tatti, Marialetizia Motta, Rosa Salvioli
Autophagy|October 31, 2012
Cathepsin-mediated regulation of autophagy in saposin C deficiencyMassimo Tatti, Marialetizia Motta, Sabrina Di Bartolomeo, et al.
International Journal of Molecular Sciences|May 14, 2025
Molecular Dynamics Simulations of the SPRED2Leu100Pro EVH-1 Domain Complexed with the GAP-Related Domain of NeurofibrominMartina Terrusa, Elisa Sangiovanni, Marialetizia Motta, et al.
Human Molecular Genetics|September 6, 2012
Reduced cathepsins B and D cause impaired autophagic degradation that can be almost completely restored by overexpression of these two proteases in Sap C-deficient fibroblastsMassimo Tatti, Marialetizia Motta, Sabrina Di Bartolomeo, et al.
Human Molecular Genetics|May 1, 2015
BCM-95 and (2-hydroxypropyl)-β-cyclodextrin reverse autophagy dysfunction and deplete stored lipids in Sap C-deficient fibroblastsMassimo Tatti, Marialetizia Motta, Susanna Scarpa, et al.
Human Molecular Genetics|June 14, 2014
Gaucher disease due to saposin C deficiency is an inherited lysosomal disease caused by rapidly degraded mutant proteinsMarialetizia Motta, Serena Camerini, Massimo Tatti, et al.
Protein Expression and Purification|April 6, 2011
Efficient one-step chromatographic purification and functional characterization of recombinant human Saposin CMarialetizia Motta, Massimo Tatti, Simone Martinelli, et al.
Human Molecular Genetics|May 21, 2010
Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sortingAnna M Vaccaro, Marialetizia Motta, Massimo Tatti, et al.
Human Molecular Genetics|July 29, 2016
SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signallingMarialetizia Motta, Giovanni Chillemi, Valentina Fodale, et al.
Human Molecular Genetics|November 28, 2018
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signalingMarialetizia Motta, Miray Fidan, Emanuele Bellacchio, et al.
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