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Valerio Carelli

Showing results (81-90 of 371) with videos related to

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Biochimica Et Biophysica Acta. Bioenergetics|June 18, 2018
Corrigendum to: "Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III." [Biochim. Biophys. Acta 2018;1859(3):182-190.]Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, et al.
DNA and Cell Biology|June 30, 2020
Interaction Between Mitochondrial DNA Variants and Mitochondria/Endoplasmic Reticulum Contact Sites: A Perspective ReviewCaterina Vianello, Veronica Cocetta, Federico Caicci, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2006
Optic nerve structure in healthy subjectsGiacomo Savini, Maurizio Zanini, Maurizio Zannini, et al.
The Journal of Biological Chemistry|November 26, 2002
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose mediumAnna Ghelli, Claudia Zanna, Anna Maria Porcelli, et al.
Frontiers in Neurology|June 25, 2021
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future PerspectivesCamille Peron, Alessandra Maresca, Andrea Cavaliere, et al.
Nature Communications|April 22, 2017
The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibilityChun-Shik Shin, Prashant Mishra, Jeramie D Watrous, et al.
Biochimica Et Biophysica Acta|March 10, 2009
Retinal ganglion cell neurodegeneration in mitochondrial inherited disordersValerio Carelli, Chiara La Morgia, Maria Lucia Valentino, et al.
Neurology. Genetics|May 24, 2019
First <i>TMEM126A</i> missense mutation in an Italian proband with optic atrophy and deafnessChiara La Morgia, Leonardo Caporali, Francesca Tagliavini, et al.
Molecular Genetics & Genomic Medicine|December 13, 2023
Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleepLaura Licchetta, Lucia Di Giorgi, Margherita Santucci, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 3, 2010
Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber's hereditary optic neuropathyPaula Yuri Sacai, Solange Rios Salomão, Valerio Carelli, et al.
Pageof 38

Showing results (81-90 of 371) with videos related to

Sort By:
Pageof 38
Biochimica Et Biophysica Acta. Bioenergetics|June 18, 2018
Corrigendum to: "Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III." [Biochim. Biophys. Acta 2018;1859(3):182-190.]Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, et al.
DNA and Cell Biology|June 30, 2020
Interaction Between Mitochondrial DNA Variants and Mitochondria/Endoplasmic Reticulum Contact Sites: A Perspective ReviewCaterina Vianello, Veronica Cocetta, Federico Caicci, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2006
Optic nerve structure in healthy subjectsGiacomo Savini, Maurizio Zanini, Maurizio Zannini, et al.
The Journal of Biological Chemistry|November 26, 2002
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose mediumAnna Ghelli, Claudia Zanna, Anna Maria Porcelli, et al.
Frontiers in Neurology|June 25, 2021
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future PerspectivesCamille Peron, Alessandra Maresca, Andrea Cavaliere, et al.
Nature Communications|April 22, 2017
The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibilityChun-Shik Shin, Prashant Mishra, Jeramie D Watrous, et al.
Biochimica Et Biophysica Acta|March 10, 2009
Retinal ganglion cell neurodegeneration in mitochondrial inherited disordersValerio Carelli, Chiara La Morgia, Maria Lucia Valentino, et al.
Neurology. Genetics|May 24, 2019
First <i>TMEM126A</i> missense mutation in an Italian proband with optic atrophy and deafnessChiara La Morgia, Leonardo Caporali, Francesca Tagliavini, et al.
Molecular Genetics & Genomic Medicine|December 13, 2023
Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleepLaura Licchetta, Lucia Di Giorgi, Margherita Santucci, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 3, 2010
Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber's hereditary optic neuropathyPaula Yuri Sacai, Solange Rios Salomão, Valerio Carelli, et al.
Pageof 38