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Marcello Ziosi

Showing results (11-20 of 23) with videos related to

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Plos Genetics|October 2, 2010
dMyc functions downstream of Yorkie to promote the supercompetitive behavior of hippo pathway mutant cellsMarcello Ziosi, Luis Alberto Baena-López, Daniela Grifoni, et al.
BMC Biology|April 9, 2010
The lethal giant larvae tumour suppressor mutation requires dMyc oncoprotein to promote clonal malignancyFrancesca Froldi, Marcello Ziosi, Flavio Garoia, et al.
Antioxidants (Basel, Switzerland)|February 25, 2023
COVID-19 Causes Ferroptosis and Oxidative Stress in Human Endothelial CellsStanislovas S Jankauskas, Urna Kansakar, Celestino Sardu, et al.
Plos Genetics|July 27, 2021
An autoimmune disease risk variant: A trans master regulatory effect mediated by IRF1 under immune stimulation?Margot Brandt, Sarah Kim-Hellmuth, Marcello Ziosi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
CoQ<sub>10</sub> supplementation rescues nephrotic syndrome through normalization of H<sub>2</sub>S oxidation pathwayGiulio Kleiner, Emanuele Barca, Marcello Ziosi, et al.
Human Molecular Genetics|September 25, 2020
Coenzyme Q10 modulates sulfide metabolism and links the mitochondrial respiratory chain to pathways associated to one carbon metabolismPilar González-García, Agustín Hidalgo-Gutiérrez, Cristina Mascaraque, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2016
Decreased Coenzyme Q10 Levels in Multiple System Atrophy CerebellumEmanuele Barca, Giulio Kleiner, Guomei Tang, et al.
Science (New York, N.Y.)|May 4, 2023
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screensJohn A Morris, Christina Caragine, Zharko Daniloski, et al.
EMBO Molecular Medicine|November 19, 2016
Coenzyme Q deficiency causes impairment of the sulfide oxidation pathwayMarcello Ziosi, Ivano Di Meo, Giulio Kleiner, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 13, 2018
Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPKJuliana Harumi Arita, Mário H Barros, Felipe Gustavo Ravagnani, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Plos Genetics|October 2, 2010
dMyc functions downstream of Yorkie to promote the supercompetitive behavior of hippo pathway mutant cellsMarcello Ziosi, Luis Alberto Baena-López, Daniela Grifoni, et al.
BMC Biology|April 9, 2010
The lethal giant larvae tumour suppressor mutation requires dMyc oncoprotein to promote clonal malignancyFrancesca Froldi, Marcello Ziosi, Flavio Garoia, et al.
Antioxidants (Basel, Switzerland)|February 25, 2023
COVID-19 Causes Ferroptosis and Oxidative Stress in Human Endothelial CellsStanislovas S Jankauskas, Urna Kansakar, Celestino Sardu, et al.
Plos Genetics|July 27, 2021
An autoimmune disease risk variant: A trans master regulatory effect mediated by IRF1 under immune stimulation?Margot Brandt, Sarah Kim-Hellmuth, Marcello Ziosi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
CoQ<sub>10</sub> supplementation rescues nephrotic syndrome through normalization of H<sub>2</sub>S oxidation pathwayGiulio Kleiner, Emanuele Barca, Marcello Ziosi, et al.
Human Molecular Genetics|September 25, 2020
Coenzyme Q10 modulates sulfide metabolism and links the mitochondrial respiratory chain to pathways associated to one carbon metabolismPilar González-García, Agustín Hidalgo-Gutiérrez, Cristina Mascaraque, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2016
Decreased Coenzyme Q10 Levels in Multiple System Atrophy CerebellumEmanuele Barca, Giulio Kleiner, Guomei Tang, et al.
Science (New York, N.Y.)|May 4, 2023
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screensJohn A Morris, Christina Caragine, Zharko Daniloski, et al.
EMBO Molecular Medicine|November 19, 2016
Coenzyme Q deficiency causes impairment of the sulfide oxidation pathwayMarcello Ziosi, Ivano Di Meo, Giulio Kleiner, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 13, 2018
Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPKJuliana Harumi Arita, Mário H Barros, Felipe Gustavo Ravagnani, et al.
Pageof 3