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M Brini

Showing results (41-50 of 53) with videos related to

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Gene|January 1, 1996
Targeting aequorin and green fluorescent protein to intracellular organellesF De Giorgi, M Brini, C Bastianutto, et al.
The International Journal of Artificial Organs|May 1, 1990
Intradialytic variations in hemoglobin affinity for oxygen during bicarbonate dialysis and hemodiafiltrationF Soliani, T Lusenti, V Franco, et al.
The Journal of Rheumatology|May 17, 2000
Intercellular adhesion molecule 1 gene polymorphisms in polymyalgia rheumatica/giant cell arteritis: association with disease risk and severityC Salvarani, B Casali, L Boiardi, et al.
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.
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.
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.
Methods in Cell Biology|January 19, 1999
Targeting GFP to organellesF De Giorgi, Z Ahmed, C Bastianutto, 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.
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.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Gene|January 1, 1996
Targeting aequorin and green fluorescent protein to intracellular organellesF De Giorgi, M Brini, C Bastianutto, et al.
The International Journal of Artificial Organs|May 1, 1990
Intradialytic variations in hemoglobin affinity for oxygen during bicarbonate dialysis and hemodiafiltrationF Soliani, T Lusenti, V Franco, et al.
The Journal of Rheumatology|May 17, 2000
Intercellular adhesion molecule 1 gene polymorphisms in polymyalgia rheumatica/giant cell arteritis: association with disease risk and severityC Salvarani, B Casali, L Boiardi, et al.
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.
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.
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.
Methods in Cell Biology|January 19, 1999
Targeting GFP to organellesF De Giorgi, Z Ahmed, C Bastianutto, 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.
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.
Pageof 6