MASULLO, DARIO
 Distribuzione geografica
Continente #
NA - Nord America 413
EU - Europa 169
AS - Asia 83
OC - Oceania 1
Totale 666
Nazione #
US - Stati Uniti d'America 401
IT - Italia 104
CN - Cina 64
IE - Irlanda 18
FI - Finlandia 16
IN - India 15
CA - Canada 11
UA - Ucraina 10
SE - Svezia 9
GB - Regno Unito 5
VN - Vietnam 4
BE - Belgio 2
DE - Germania 2
NL - Olanda 2
ES - Italia 1
NZ - Nuova Zelanda 1
PA - Panama 1
Totale 666
Città #
Chandler 99
Ashburn 37
Beijing 32
Millbury 28
Napoli 20
Nanjing 18
Princeton 17
Pune 15
Salerno 15
Des Moines 14
Ottawa 11
Wilmington 11
Boston 10
Jacksonville 10
Naples 10
Seattle 7
Angri 5
Rende 5
Dong Ket 4
Lawrence 4
Hebei 3
Sesto Fiorentino 3
Shenyang 3
Amsterdam 2
Boardman 2
Castellammare Di Stabia 2
Frattamaggiore 2
Houston 2
Jiaxing 2
Nanchang 2
Nutley 2
Rome 2
Tianjin 2
Washington 2
Woodbridge 2
Auckland 1
Brussels 1
Changsha 1
Fano 1
Indiana 1
Lonigo 1
Milan 1
Mugnano Di Napoli 1
Panama City 1
San Francisco 1
Schaarbeek 1
Venta De Baños 1
Vercelli 1
Watford 1
Totale 419
Nome #
Hyodeoxycholic acid derivatives as liver X receptor α and G-protein-coupled bile acid receptor agonists 58
Bile acids derivatives in the selective modulation of FXR and GP-BAR1 48
Insights on FXR selective modulation. Speculation on bile acid chemical space in the discovery of potent and selective agonists 47
Modification on Ursodeoxycholic Acid (UDCA) Scaffold. Discovery of Bile Acid Derivatives As Selective Agonists of Cell-Surface G-Protein Coupled Bile Acid Receptor 1 (GP-BAR1) 46
Synthesis of a new class of isoxazole derivatives with a dual FXR agonistic and COX-2 inhibitory activity. 40
Inspection on bile acid scaffold in the discovery of the first example of LXRa/GPBAR1 dual agonists 39
Bile acids derivatives in the selective modulation of FXR and GPBAR1 38
Investigation on bile acid receptor regulators. Discovery of cholanoic acid derivatives with dual G-protein coupled bile acid receptor 1 (GPBAR1) antagonistic and farnesoid X receptor (FXR) modulatory activity 34
Navigation in bile acid chemical space: discovery of novel FXR and GPBAR1 ligands 34
Synthesis of new bile acids derivatives as selective FXR/GPBAR1 ligands 33
Discovery of cholanoic acid derivatives as new modulators of bile acid receptors 31
Epoxide functionalization on cholane side chains in the identification of G-protein coupled bile acid receptor (GPBAR1) selective agonists 31
Inspection on bile acid scaffold in the discovery of the first example of LXR/GPBAR1 dual agonists 30
Towards FXR selectivity: manipulation of 6-ethylcholane scaffold 29
Synthesis of a new class of isoxazole derivatives with a dual FXR agonistic and COX-2 inhibitory activity 29
null 27
Speculation on 6-ethylcholane scaffold in the discovery of novel FXR and GPBAR1 ligands. 25
Navigation in bile acid chemical space: discovery of novel FXR and GPBAR1 modulators 24
Decoding the role of the nuclear receptor SHP in regulating hepatic stellate cells and liver fibrogenesis 23
Towards FXR selectivity: manipulation of 6-ethylcholane scaffold 21
Synthesis of new isoxazole derivatives as SHP agonists 19
Modification on bile acid scaffold in the identification of FXR and GP-BAR1 modulation 16
Totale 722
Categoria #
all - tutte 2.175
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.175


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20195 0 0 0 0 0 0 0 0 1 3 0 1
2019/202094 25 0 2 0 4 0 6 12 0 15 23 7
2020/202172 4 15 3 2 9 14 7 3 7 1 3 4
2021/2022144 3 3 7 0 4 5 9 8 19 1 33 52
2022/2023188 21 11 5 13 39 27 0 20 39 3 5 5
2023/2024115 8 27 7 2 6 37 9 10 9 0 0 0
Totale 722