FANELLI, Francesca
 Distribuzione geografica
Continente #
NA - Nord America 15.579
EU - Europa 5.942
AS - Asia 1.146
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 6
OC - Oceania 4
Totale 22.702
Nazione #
US - Stati Uniti d'America 15.545
GB - Regno Unito 2.658
SE - Svezia 801
IT - Italia 661
DE - Germania 597
CN - Cina 484
UA - Ucraina 428
FI - Finlandia 313
TR - Turchia 276
HK - Hong Kong 269
BG - Bulgaria 164
FR - Francia 100
BE - Belgio 80
RU - Federazione Russa 57
CA - Canada 32
IN - India 30
IE - Irlanda 25
IR - Iran 21
SG - Singapore 18
NL - Olanda 12
MY - Malesia 11
CL - Cile 9
ES - Italia 8
CH - Svizzera 7
JP - Giappone 7
KR - Corea 7
RO - Romania 7
VN - Vietnam 7
PL - Polonia 5
A2 - ???statistics.table.value.countryCode.A2??? 4
KZ - Kazakistan 4
AU - Australia 3
BR - Brasile 3
DK - Danimarca 3
EU - Europa 3
NO - Norvegia 3
AR - Argentina 2
AT - Austria 2
CO - Colombia 2
CZ - Repubblica Ceca 2
EC - Ecuador 2
HU - Ungheria 2
MK - Macedonia 2
MX - Messico 2
TN - Tunisia 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
BD - Bangladesh 1
CY - Cipro 1
EG - Egitto 1
GH - Ghana 1
GR - Grecia 1
HR - Croazia 1
ID - Indonesia 1
IL - Israele 1
IQ - Iraq 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
SA - Arabia Saudita 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 22.702
Città #
Fairfield 2.608
Southend 2.240
Woodbridge 1.715
Ashburn 1.311
Houston 1.238
Seattle 1.019
Chandler 941
Jacksonville 922
Ann Arbor 876
Wilmington 874
Cambridge 803
Dearborn 643
Nyköping 427
Hong Kong 265
Modena 257
San Diego 221
Beijing 192
Des Moines 176
Helsinki 172
Princeton 170
Sofia 163
Eugene 150
Izmir 142
Bremen 128
London 93
New York 82
Brussels 77
Redwood City 60
Grafing 57
Falls Church 52
San Mateo 38
Milan 37
Boardman 34
Verona 30
Norwalk 29
Dublin 25
Leawood 24
Kunming 22
Augusta 21
Hefei 21
Saint Petersburg 21
Shanghai 21
Chiswick 19
Hounslow 19
Nanjing 18
Kilburn 17
Monmouth Junction 15
Toronto 15
Guangzhou 14
Indiana 14
Ottawa 14
Parma 13
San Giuliano Milanese 13
Abbiategrasso 12
Acton 12
Ardabil 12
Auburn Hills 12
Jinan 11
Menlo Park 11
San Francisco 11
Los Angeles 10
Prescot 10
Bologna 9
Chicago 9
Islington 9
Mountain View 9
Napoli 9
Fremont 7
Rome 7
Cesena 6
Hanover 6
Naples 6
Paris 6
Pune 6
Reggio Nell'emilia 6
Chengdu 5
Dongguan 5
Hangzhou 5
Nanchang 5
Phoenix 5
Shenyang 5
Zhengzhou 5
Amsterdam 4
Astana 4
Carpi 4
Crosia 4
Dong Ket 4
Ferrara 4
Fuzhou 4
Isorella 4
Las Vegas 4
Mumbai 4
Reggiolo 4
Washington 4
Wuhan 4
Alexandria 3
Bedok 3
Changsha 3
Chongqing 3
Foggia 3
Totale 18.866
Nome #
A Small Chaperone Improves Folding and Routing of Rhodopsin Mutants Linked to Inherited Blindness 231
WebPSN: a web server for high-throughput investigation of structural communication in biomacromolecules 222
Small-Molecule Protein-Protein Interaction Inhibitor of Oncogenic Rho Signaling 213
Single Molecule Analysis of Functionally Asymmetric G Protein-coupled Receptor (GPCR) Oligomers Reveals Diverse Spatial and Structural Assemblies 213
Mutagenesis and modelling of the alpha(1b)-adrenergic receptor highlight the role of the helix 3/helix 6 interface in receptor activation 202
Network and atomistic simulations unveil the structural determinants of mutations linked to retinal diseases 197
Computational modeling approaches to Structure-Function Analysis of G Protein-Coupled Receptors 193
A model for constitutive lutropin receptor activation based on molecular simulation and engineered mutations in transmembrane helices 6 and 7 190
The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition 188
Dark and photoactivated rhodopsin share common binding modes to transducin 187
Conserved amino acids participate in the structure networks deputed to intramolecular communication in the lutropin receptor 185
Superactive mutants of thromboxane prostanoid receptor: functional and computational analysis of an active form alternative to constitutively active mutants 184
Monomeric dark rhodopsin holds the molecular determinants for transducin recognition: insights from computational analysis 182
Rhodopsin activation follows precoupling with transducin: Inferences from computational analysis 182
Wordom 182
Molecular dynamics simulations of the ligand-induced chemical information transfer in the 5-HT1A receptor 181
Computational modeling of intramolecular and intermolecular communication in GPCRs 181
Network analysis to uncover the structural communication in GPCRs 181
In silico screening of mutational effects on enzyme-proteic inhibitor affinity: A docking-based approach 180
Molecular basis of ligand binding and receptor activation in the oxytocin and vasopressin receptor family 180
Theoretical study on the electrostatically driven step of receptor-G protein recognition 179
A functional transmembrane complex: The luteinizing hormone receptor with bound ligand and G protein 179
Computational simulations of stem-cell factor c-Kit receptor interaction 179
Nucleotide binding switches the information flow in ras GTPases 178
Theoretical study on receptor-G protein recognition: new insights into the mechanism of the α1b-adrenergic receptor activation 177
Computational Screening of Rhodopsin Mutations Associated with Retinitis Pigmentosa 176
Update 1 of: Computational Modeling Approaches to Structure-Function Analysis of G Protein-Coupled Receptors 176
Catching Functional Modes and Structural Communication in Dbl Family Rho Guanine Nucleotide Exchange Factors 176
Wordom: A user-friendly program for the analysis of molecular structures, trajectories, and free energy surfaces 175
Quaternary structure predictions and structural communication features of GPCR dimers 175
Dissecting intrinsic and ligand-induced structural communication in the β3 headpiece of integrins 175
Class A GPCR: Di/Oligomerization of Glycoprotein Hormone Receptors 175
Three dimensional molecular modeling of the α1a-adrenoceptor. Direct 3D-QSAR modeling of selective antagonists 174
Comparative molecular dynamics study of the seven-helix bundle arrangement of G-protein coupled receptors 173
Theoretical investigation of IL-6 multiprotein receptor assembly 173
Deciphering the deformation modes associated with function retention and specialization in members of the Ras superfamily 173
Structural features of the inactive and active states of the melanin-concentrating hormone receptors: Insights from molecular simulations 172
Target Flexibility: An Emerging Consideration in Drug Discovery and Design 172
Structure-function relationships of the alpha(1b)-adrenergic receptor 171
Auto-regulation of Secretory Flux by Sensing and Responding to the Folded Cargo Protein Load in the Endoplasmic Reticulum 171
Light on the structural communication in Ras GTPases 170
Structure-activity relationships in 1,4-benzodioxan-related compounds. 10. Novel α1-adrenoreceptor antagonists related to openphendioxan: synthesis, biological evaluation, and α1d computational study 169
Computational quantum chemistry and adaptive ligand modeling in mechanistic QSAR 169
Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in brazilian boys: a novel constitutively activating mutation in the first transmembrane helix 169
Lutropin receptor function: Insights from natural, engineered, and computer-simulated mutations 168
Nucleotide binding affects intrinsic dynamics and structural communication in Ras GTPases 168
Quaternary structure predictions and estimation of mutational effects on the free energy of dimerization of the OMPLA protein 167
Prediction of MEF2A-DNA interface by rigid body docking: A tool for fast estimation of protein mutational effects on DNA binding 167
Structure network analysis to gain insights into GPCR function 167
Theoretical quantitative structure-activity analysis of quinuclidine-based muscarinic cholinergic receptor ligands 166
Prototropic molecular forms and theoretical descriptors in QSAR analysis 166
The ad hoc supermolecule approach to receptor ligand design 166
The DRY motif as a molecular switch of the human oxytocin receptor 166
Computational modeling approaches to quantitative structure–binding kinetics relationships in drug discovery 165
Modulation of thermal noise and spectral sensitivity in Lake Baikal cottoid fish rhodopsins 165
An intracellular loop (IL2) residue confers different basal constitutive activities to the human lutropin receptor and human thyrotropin receptor through structural communication between IL2 and helix 6, via helix 3 164
Network-level analysis of light adaptation in rod cells under normal and altered conditions 164
Structural Determinants of Constitutive Activation of Gα Proteins: Transducin as a Paradigm 164
Molecular dynamics simulations of m3-muscarinic receptor activation and QSAR analysis 164
Sequential unfolding of individual helices of bacterioopsin observed in molecular dynamics simulations of extraction from the purple membrane 161
Epilepsy and intellectual disability linked protein Shrm4 interaction with GABA B Rs shapes inhibitory neurotransmission 161
Light on the structure of thromboxane A2 receptor heterodimers 159
Multiscale quantum chemical approaches to QSAR modeling and drug design 159
A Mixed Protein Structure Network and Elastic Network Model Approach to Predict the Structural Communication in Biomolecular Systems: The PDZ2 Domain from Tyrosine Phosphatase 1E As a Case Study 159
Quantitative structure-affinity/selectivity relationship analysis on three-dimensional models of the complexes between the ETA and ETB receptors and C-terminal endothelin hexapeptide antagonists 158
Theoretical quantitative structure-activity analysis and pharmacophore modelling of selective non congeneric α1a-adrenergic antagonists 158
Structure-Function Relationships of the Luteinizing Hormone Receptor 158
Modeling the structural communication in supramolecular complexes involving GPCRs 158
Theoretical quantitative structure-activity relationship analysis of congeneric and non-congeneric α1-adrenoceptor antagonists: a chemometric study 158
Ligand-Receptor Communication and Drug Design 157
Activation mechanism of human oxytocin receptor: A combined study of experimental and computer-simulated mutagenesis 156
Insight into mutation-induced activation of the luteinizing hormone receptor: Molecular simulations predict the functional behavior of engineered mutants at M398 156
Pleiotropic effects of substitutions of a highly conserved leucine in transmembrane helix III of the human lutropin/choriogonadotropin receptor with respect to constitutive activation and hormone responsiveness 154
Amino acids of the α1B-adrenergic receptor involved in agonist binding: further differences in docking catecholamines to receptor subtypes 154
The formation of a salt bridge between helices 3 and 6 is responsible for the constitutive activity and lack of hormone responsiveness of the naturally occurring L457R mutation of the human lutropin receptor 152
The catalytic site structural gate of adenosine deaminase allosterically modulates ligand binding to adenosine receptors 151
Contributions of Intracellular Loops 2 and 3 of the Lutropin Receptor in Gs Coupling 151
Theoretical Quantitative Structure-Activity Relationship Analysis on Three Dimensional Models of Ligand-m1 Muscarinic Receptor Complexes 149
Structural Aspects of the Luteinizing Hormone Receptor: Information from Molecular Modeling and Mutagenesis 149
Dimerization of the lutropin receptor: Insights from computational modeling 148
Structural determinants involved in the activation and regulation of G protein-coupled receptors: lessons from the alpha1-adrenegic receptor subtypes 148
Constitutively active G protein-coupled receptor mutants: implications on receptor function and drug action 148
The luteinizing hormone receptor: insights into structure-function relationships and hormone-receptor-mediated changes in gene expression in ovarian cancer cells 148
Probing fragment complementation by rigid-body docking: In silico reconstitution of calbindin D9k 148
Homodimerization of neurotensin 1 receptor involves helices 1, 2, and 4: Insights from quaternary structure predictions and dimerization free energy estimations 147
Inactive and active states and supramolecular organization of GPCRs: insights from computational modeling 147
Mutational and computational analysis of the alpha-1b adrenergic receptor.Involvement of basic and hydrophobic residues in receptor activation and G protein coupling 146
Enantiomeric resolution of sulfoxides on a DACH‐DNB chiral stationary phase: A quantitative structure–enantioselective retention relationship (QSERR) study 146
Conformational analysis, molecular modeling and quantitative structure-activity relationships studies of 2,4-diamino-6,7-dimethoxy-2-substituted quinazoline α1-adrenergic antagonists 145
The α1a and α1b-adrenergic receptor subtypes: molecular mechanisms of receptor activation and of drug action 144
In silico screening of mutational effects on transmembrane helix dimerization: insights from rigid-body docking and molecular dynamics simulations 144
Conformational analysis and theoretical quantitative size and shape-affinity relationships of N-4-protonated N-1-arylpiperazine 5-HT1A serotoninergic ligands 142
FIPD 140
Mechanisms of inter- and intramolecular communication in GPCRs and G proteins 139
Adenosine A(2A) Receptor-Antagonist/Dopamine D(2) Receptor-Agonist Bivalent Ligands as Pharmacological Tools to Detect A(2A)-D(2) Receptor Heteromers 139
Dimerization and ligand binding affect the structure network of A(2A) adenosine receptor 139
Theoretical quantitative size and shape activity and selectivity analyses of 5-HT1A serotonin and α1-adrenergic receptor ligands 138
The alpha1a and alpha1b-adrenergic receptor subtypes: molecular mechanisms of receptor activation and of drug action 138
Phenylpiperazinylalkylamino substituted pyridazinones as potent alpha(1) adrenoceptor antagonists 136
IIsoxazolo-[3,4-d]-pyridazin-7-(6H)-ones and their corresponding 4,5-disubstituted-3-(2H)-pyridazinone analogues as new substrates for alpha1-adrenoceptor selective antagonists: synthesis, modeling, and binding studies 136
Totale 16.641
Categoria #
all - tutte 86.295
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 86.295


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191.909 0 0 0 0 0 0 0 0 216 373 767 553
2019/20206.036 462 199 245 545 757 839 955 706 605 217 270 236
2020/20214.249 442 190 356 417 394 218 372 501 179 579 387 214
2021/20223.254 188 491 423 168 80 154 282 154 276 259 510 269
2022/20232.806 274 304 200 211 413 487 43 275 341 28 137 93
2023/20241.472 70 122 273 116 381 163 121 176 50 0 0 0
Totale 22.906