BRISCHIGLIARO, MICHELE
 Distribuzione geografica
Continente #
NA - Nord America 422
EU - Europa 119
AS - Asia 60
SA - Sud America 1
Totale 602
Nazione #
US - Stati Uniti d'America 420
IT - Italia 70
CN - Cina 56
FI - Finlandia 13
SE - Svezia 11
DE - Germania 9
GB - Regno Unito 7
UA - Ucraina 3
CA - Canada 2
FR - Francia 2
IE - Irlanda 2
IN - India 2
RO - Romania 2
TR - Turchia 2
BR - Brasile 1
Totale 602
Città #
Chandler 120
Ashburn 46
Fairfield 37
Beijing 29
Padova 24
Houston 23
Cambridge 17
San Diego 14
Helsinki 13
Medford 13
Princeton 13
Wilmington 13
Roxbury 11
Seattle 11
Ann Arbor 10
Woodbridge 10
Gavardo 7
Berlin 6
Des Moines 6
Jinan 5
Sommacampagna 5
Boardman 4
Haikou 3
Nanjing 3
Shenyang 3
Castegnero 2
Chiampo 2
Dublin 2
Erlangen 2
Glasgow 2
Istanbul 2
Lancenigo-Villorba 2
London 2
Los Angeles 2
New York 2
Pune 2
Quinto di Treviso 2
Rome 2
Schio 2
Venice 2
Arzignano 1
Brescia 1
Fontanelle 1
Hangzhou 1
Hebei 1
Jiaxing 1
Kharkiv 1
Kunming 1
Leeds 1
Ningbo 1
Norwalk 1
Ogden 1
Paris 1
Pescara 1
Pocapaglia 1
Quzhou 1
Redwood City 1
Shaoxing 1
Somma Lombardo 1
Stockholm 1
São Paulo 1
Taizhou 1
Toronto 1
Tortorici 1
Vicenza 1
Washington 1
Zhengzhou 1
Totale 503
Nome #
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction 81
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 73
Cytochrome c oxidase deficiency 63
Exploring the role of dMpv17 in mitochondrial function and metabolism 51
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 35
MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders towards potential therapeutic approaches in experimental models 34
Drosophila melanogaster as a model to study mitochondrial diseases: functional characterization of dMpv17 and dApopt1 34
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster 33
Drosophila melanogaster as a model to study mitochondrial DNA depletion syndromes: functional characterization of dMpv17 31
Modelling the human mitochondrial disease related to APOPT1 in D. melanogaster 29
Shedding light on APOPT1 role in mitochondrial physiology and pathophysiology through a Drosophila melanogaster model 28
Functional characterization of dMpv17 in Drosophila melanogaster 27
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch 21
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B 21
Modelling the human mitochondrial disease related to APOPT1 in Drosophila melanogaster 20
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples 15
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 13
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals 8
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 7
Totale 624
Categoria #
all - tutte 3.547
article - articoli 2.529
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.076


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202092 0 0 6 15 2 1 16 7 3 33 8 1
2020/202189 2 2 6 5 4 9 11 5 10 12 8 15
2021/2022120 0 16 13 1 9 13 6 13 6 0 7 36
2022/2023222 34 21 9 35 40 28 2 14 29 0 4 6
2023/2024101 8 12 14 11 12 27 8 3 2 4 0 0
Totale 624