BRISCHIGLIARO, MICHELE
 Distribuzione geografica
Continente #
NA - Nord America 494
AS - Asia 152
EU - Europa 149
SA - Sud America 1
Totale 796
Nazione #
US - Stati Uniti d'America 492
IT - Italia 87
CN - Cina 77
SG - Singapore 69
FI - Finlandia 13
SE - Svezia 11
DE - Germania 9
FR - Francia 8
GB - Regno Unito 7
NL - Olanda 4
UA - Ucraina 3
CA - Canada 2
IE - Irlanda 2
IN - India 2
RO - Romania 2
RU - Federazione Russa 2
TR - Turchia 2
AZ - Azerbaigian 1
BR - Brasile 1
HR - Croazia 1
KR - Corea 1
Totale 796
Città #
Chandler 120
Singapore 56
Ashburn 51
Fairfield 37
Santa Clara 34
Padova 30
Beijing 29
Boardman 23
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
Haikou 3
Nanjing 3
New York 3
Shenyang 3
Castegnero 2
Cava de' Tirreni 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
Baku 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
Shanghai 1
Shaoxing 1
Somma Lombardo 1
Stockholm 1
São Paulo 1
Taizhou 1
Toronto 1
Tortorici 1
Vicenza 1
Washington 1
Zagreb 1
Zhengzhou 1
Totale 631
Nome #
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction 95
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 87
Cytochrome c oxidase deficiency 80
Exploring the role of dMpv17 in mitochondrial function and metabolism 59
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 49
MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders towards potential therapeutic approaches in experimental models 42
Drosophila melanogaster as a model to study mitochondrial diseases: functional characterization of dMpv17 and dApopt1 42
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster 42
Drosophila melanogaster as a model to study mitochondrial DNA depletion syndromes: functional characterization of dMpv17 40
Functional characterization of dMpv17 in Drosophila melanogaster 37
Modelling the human mitochondrial disease related to APOPT1 in D. melanogaster 35
Shedding light on APOPT1 role in mitochondrial physiology and pathophysiology through a Drosophila melanogaster model 34
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B 33
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch 30
Modelling the human mitochondrial disease related to APOPT1 in Drosophila melanogaster 29
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster 27
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples 26
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals 17
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features 14
Totale 818
Categoria #
all - tutte 4.939
article - articoli 3.445
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 8.384


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202069 0 0 0 0 0 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
2024/2025171 3 34 25 32 59 18 0 0 0 0 0 0
Totale 818