BRISCHIGLIARO, MICHELE

BRISCHIGLIARO, MICHELE  

Dipartimento di Biologia - DiBio  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B 2022 Brischigliaro, MicheleSturlese, MattiaFrigo, ElenaFernandez-Vizarra, ErikaMoro, StefanoViscomi, CarloZeviani, Massimo + EMBO REPORTS - -
Cytochrome c oxidase deficiency 2020 Brischigliaro M.Zeviani M. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
Drosophila melanogaster as a model to study mitochondrial diseases: functional characterization of dMpv17 and dApopt1 2016 Samantha CorràMichele BrischigliaroCristiano De PittàRodolfo Costa - - Book of abstracts
Drosophila melanogaster as a model to study mitochondrial DNA depletion syndromes: functional characterization of dMpv17 2017 Samantha CorràMichele BrischigliaroVanessa ChecchettoIldikò SzabòMassimo ZevianiRodolfo CostaCristiano De Pittà + - - Book of abstracts
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction 2021 Peruzzo, RobertaCorrà, SamanthaCosta, RobertoBrischigliaro, MicheleVaranita, TatianaRampazzo, ChiaraLeanza, LuigiZeviani, MassimoDe Pittà, CristianoViscomi, CarloCosta, RodolfoSzabò, Ildikò + NATURE COMMUNICATIONS - -
Exploring the role of dMpv17 in mitochondrial function and metabolism 2019 Samantha CorràMichele BrischigliaroVanessa ChecchettoChiara RampazzoIldikò SzabòMassimo ZevianiRodolfo CostaCristiano De Pittà + - - Book of abstracts
Functional characterization of dMpv17 in Drosophila melanogaster 2018 Samantha CorràMichele BrischigliaroVanessa ChecchettoChiara RampazzoIldikò SzabòMassimo ZevianiRodolfo CostaCristiano De Pittà + - - Libro degli abstract
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 2019 Michele BrischigliaroSamantha CorràClaudia TregnagoMassimo ZevianiRodolfo CostaCristiano De Pittà + FRONTIERS IN PHYSIOLOGY - -
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 2019 Brischigliaro, MicheleTregnago, ClaudiaFernandez-Vizarra, ErikaZeviani, MassimoCosta, RodolfoDe Pittà, Cristiano + FRONTIERS IN PHYSIOLOGY - -
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples 2022 Brischigliaro, MicheleFrigo, ElenaFernandez-Vizarra, ErikaBernardi, PaoloViscomi, Carlo STAR PROTOCOLS - -
MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders towards potential therapeutic approaches in experimental models 2017 Martorano LauraCorrà SamanthaBrischigliaro MicheleDe Pittà CristianoArgenton FrancescoCosta RodolfoGhezzi Daniele + - - Book of abstracts
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals 2022 Brischigliaro, MicheleBadocco, DenisCosta, RodolfoViscomi, CarloZeviani, MassimoPastore, PaoloFernández-Vizarra, Erika FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY - -
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster 2021 Brischigliaro M.Frigo E.De Pitta C.Szabo I.Zeviani M.Costa R. + JOURNAL OF MOLECULAR MEDICINE - -
Modelling the human mitochondrial disease related to APOPT1 in D. melanogaster 2018 Michele BrischigliaroSamantha CorràMassimo ZevianiRodolfo CostaCristiano De Pittà + - - Book of abstracts
Modelling the human mitochondrial disease related to APOPT1 in Drosophila melanogaster 2019 Michele BrischigliaroSamantha CorràClaudia TregnagoMassimo ZevianiRodolfo CostaCristiano De Pittà + - - Book of abstracts
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 2021 Brischigliaro, MichelePrudent, JulienFernandez-Vizarra, ErikaWhitworth, Alexander JZeviani, Massimo + EJMG - -
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 2020 Brischigliaro M.Johnson M.Zeviani M. + JOURNAL OF MEDICAL GENETICS - -
Shedding light on APOPT1 role in mitochondrial physiology and pathophysiology through a Drosophila melanogaster model 2017 Samantha CorràMichele BrischigliaroMassimo ZevianiCristiano De PittàRodolfo Costa - - Book of abstracts
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch 2022 Fernández-Vizarra ErikaBrischigliaro MicheleZeviani Massimo + CELL METABOLISM - -