BRISCHIGLIARO, MICHELE
 Distribuzione geografica
Continente #
NA - Nord America 423
EU - Europa 122
AS - Asia 82
SA - Sud America 1
Totale 628
Nazione #
US - Stati Uniti d'America 421
IT - Italia 73
CN - Cina 56
SG - Singapore 21
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
KR - Corea 1
Totale 628
Città #
Chandler 120
Ashburn 46
Fairfield 37
Beijing 29
Padova 25
Houston 23
Cambridge 17
San Diego 14
Helsinki 13
Medford 13
Princeton 13
Wilmington 13
Singapore 12
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
New York 3
Shenyang 3
Castegnero 2
Chiampo 2
Dublin 2
Erlangen 2
Glasgow 2
Istanbul 2
Lancenigo-Villorba 2
London 2
Los Angeles 2
Pune 2
Quinto di Treviso 2
Rome 2
Schio 2
Venice 2
Arzignano 1
Brescia 1
Fontanelle 1
Hangzhou 1
Hebei 1
Incheon 1
Jiaxing 1
Kharkiv 1
Kunming 1
Leeds 1
Ningbo 1
Norwalk 1
Ogden 1
Paese 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 519
Nome #
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction 83
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 75
Cytochrome c oxidase deficiency 67
Exploring the role of dMpv17 in mitochondrial function and metabolism 52
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 37
MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders towards potential therapeutic approaches in experimental models 35
Drosophila melanogaster as a model to study mitochondrial diseases: functional characterization of dMpv17 and dApopt1 35
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster 34
Drosophila melanogaster as a model to study mitochondrial DNA depletion syndromes: functional characterization of dMpv17 33
Modelling the human mitochondrial disease related to APOPT1 in D. melanogaster 30
Shedding light on APOPT1 role in mitochondrial physiology and pathophysiology through a Drosophila melanogaster model 29
Functional characterization of dMpv17 in Drosophila melanogaster 28
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch 22
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B 22
Modelling the human mitochondrial disease related to APOPT1 in Drosophila melanogaster 21
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples 16
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 14
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals 9
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 8
Totale 650
Categoria #
all - tutte 4.003
article - articoli 2.818
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.821


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
2023/2024124 8 12 14 11 12 27 8 3 2 4 17 6
2024/20253 3 0 0 0 0 0 0 0 0 0 0 0
Totale 650