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Sergio Papa

Showing results (71-80 of 103) with videos related to

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Neuromuscular Disorders : NMD|May 12, 2009
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegiaRoberto Negro, Stefano Zoccolella, Rosa Dell'aglio, et al.
The Journal of Vascular Access|June 8, 2026
An alternative to inside-out access for central venous catheter placement in thoracic central vein obstructionAnna Maria Ierardi, Pierpaolo Biondetti, Velio Ascenti, et al.
Biochimica Et Biophysica Acta|January 8, 2013
Epigallocatechin-3-gallate prevents oxidative phosphorylation deficit and promotes mitochondrial biogenesis in human cells from subjects with Down's syndromeDaniela Valenti, Domenico De Rasmo, Anna Signorile, et al.
FEBS Letters|September 26, 2006
Occurrence of A-kinase anchor protein and associated cAMP-dependent protein kinase in the inner compartment of mammalian mitochondriaAnna Maria Sardanelli, Anna Signorile, Rosanna Nuzzi, et al.
Diagnostics (Basel, Switzerland)|January 21, 2023
Chest X-ray in Emergency Radiology: What Artificial Intelligence Applications Are Available?Giovanni Irmici, Maurizio Cè, Elena Caloro, et al.
Biochemical and Biophysical Research Communications|November 9, 2019
Decreased amount of vimentin N-terminal truncated proteolytic products in parkin-mutant skin fibroblastsRosa Anna Siciliano, Maria Fiorella Mazzeo, Anna Ferretta, et al.
The Journal of Biological Chemistry|February 16, 2006
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex IArcangela Iuso, Salvatore Scacco, Claudia Piccoli, et al.
Cells|March 17, 2019
Increased Levels of cAMP by the Calcium-Dependent Activation of Soluble Adenylyl Cyclase in <i>Parkin</i>-Mutant FibroblastsPaola Tanzarella, Anna Ferretta, Simona Nicol Barile, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
The Journal of Biological Chemistry|August 29, 2003
Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complexSalvatore Scacco, Vittoria Petruzzella, Sandy Budde, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Neuromuscular Disorders : NMD|May 12, 2009
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegiaRoberto Negro, Stefano Zoccolella, Rosa Dell'aglio, et al.
The Journal of Vascular Access|June 8, 2026
An alternative to inside-out access for central venous catheter placement in thoracic central vein obstructionAnna Maria Ierardi, Pierpaolo Biondetti, Velio Ascenti, et al.
Biochimica Et Biophysica Acta|January 8, 2013
Epigallocatechin-3-gallate prevents oxidative phosphorylation deficit and promotes mitochondrial biogenesis in human cells from subjects with Down's syndromeDaniela Valenti, Domenico De Rasmo, Anna Signorile, et al.
FEBS Letters|September 26, 2006
Occurrence of A-kinase anchor protein and associated cAMP-dependent protein kinase in the inner compartment of mammalian mitochondriaAnna Maria Sardanelli, Anna Signorile, Rosanna Nuzzi, et al.
Diagnostics (Basel, Switzerland)|January 21, 2023
Chest X-ray in Emergency Radiology: What Artificial Intelligence Applications Are Available?Giovanni Irmici, Maurizio Cè, Elena Caloro, et al.
Biochemical and Biophysical Research Communications|November 9, 2019
Decreased amount of vimentin N-terminal truncated proteolytic products in parkin-mutant skin fibroblastsRosa Anna Siciliano, Maria Fiorella Mazzeo, Anna Ferretta, et al.
The Journal of Biological Chemistry|February 16, 2006
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex IArcangela Iuso, Salvatore Scacco, Claudia Piccoli, et al.
Cells|March 17, 2019
Increased Levels of cAMP by the Calcium-Dependent Activation of Soluble Adenylyl Cyclase in <i>Parkin</i>-Mutant FibroblastsPaola Tanzarella, Anna Ferretta, Simona Nicol Barile, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
The Journal of Biological Chemistry|August 29, 2003
Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complexSalvatore Scacco, Vittoria Petruzzella, Sandy Budde, et al.
Pageof 11