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Molecular Biology of the Cell|January 1, 1997
Subcellular analysis of Ca2+ homeostasis in primary cultures of skeletal muscle myotubesM Brini, F De Giorgi, M Murgia, et al.
The Journal of Biological Chemistry|November 15, 1988
Multiple divergent mRNAs code for a single human calmodulinR Fischer, M Koller, M Flura, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 1996
Subcellular imaging of intramitochondrial Ca2+ with recombinant targeted aequorin: significance for the regulation of pyruvate dehydrogenase activityG A Rutter, P Burnett, R Rizzuto, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 16, 1998
Double-stranded DNA can be translocated across a planar membrane containing purified mitochondrial porinI Szabò, G Bàthori, F Tombola, et al.
Biochemistry|September 24, 1999
NMR solution structure of a complex of calmodulin with a binding peptide of the Ca2+ pumpB Elshorst, M Hennig, H Försterling, et al.
Cell Calcium|September 1, 1994
Cytosolic free calcium concentration in the mitogenic stimulation of T lymphocytes by anti-CD3 monoclonal antibodiesM Murgia, M Mion, L Veronese, et al.
Cell Death and Differentiation|July 25, 2015
Reduced mitochondrial Ca(2+) transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenaseV Granatiero, V Giorgio, T Calì, et al.
Cell Death and Differentiation|July 11, 2002
Cleavage of plasma membrane calcium pumps by caspases: a link between apoptosis and necrosisB L Schwab, D Guerini, C Didszun, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 10, 2004
An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 geneD Guidetti, B Casali, R L Mazzei, et al.
European Journal of Biochemistry|September 1, 1994
Processing of the pre-beta-amyloid protein by cathepsin D is enhanced by a familial Alzheimer's disease mutationR N Dreyer, K M Bausch, P Fracasso, et al.
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