FANELLI, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 16.799
EU - Europa 6.034
AS - Asia 2.262
SA - Sud America 29
AF - Africa 8
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 6
Totale 25.145
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Nazione #
US - Stati Uniti d'America 16.761
GB - Regno Unito 2.603
SG - Singapore 863
SE - Svezia 806
IT - Italia 756
CN - Cina 720
DE - Germania 629
UA - Ucraina 428
FI - Finlandia 331
TR - Turchia 276
HK - Hong Kong 269
BG - Bulgaria 164
FR - Francia 106
RU - Federazione Russa 59
CA - Canada 35
BE - Belgio 31
ID - Indonesia 31
IN - India 30
LT - Lituania 28
IE - Irlanda 21
IR - Iran 21
NL - Olanda 20
BR - Brasile 14
MY - Malesia 11
JP - Giappone 10
CL - Cile 9
ES - Italia 9
CH - Svizzera 7
CZ - Repubblica Ceca 7
KR - Corea 7
RO - Romania 7
VN - Vietnam 7
PL - Polonia 5
A2 - ???statistics.table.value.countryCode.A2??? 4
AU - Australia 4
KZ - Kazakistan 4
DK - Danimarca 3
EU - Europa 3
NO - Norvegia 3
AR - Argentina 2
AT - Austria 2
BD - Bangladesh 2
CO - Colombia 2
EC - Ecuador 2
EG - Egitto 2
HU - Ungheria 2
MK - Macedonia 2
MX - Messico 2
NZ - Nuova Zelanda 2
SA - Arabia Saudita 2
TN - Tunisia 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
AO - Angola 1
CY - Cipro 1
GH - Ghana 1
GR - Grecia 1
HR - Croazia 1
IL - Israele 1
IQ - Iraq 1
JM - Giamaica 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 25.145
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Città #
Fairfield 2.608
Southend 2.240
Woodbridge 1.715
Ashburn 1.318
Houston 1.238
Santa Clara 1.122
Seattle 1.019
Chandler 941
Jacksonville 922
Ann Arbor 876
Wilmington 874
Cambridge 803
Singapore 718
Dearborn 643
Nyköping 427
Modena 279
Hong Kong 265
Beijing 234
San Diego 221
Helsinki 190
Des Moines 176
Princeton 170
Sofia 163
Eugene 150
Izmir 142
Bremen 128
New York 82
London 68
Redwood City 60
Grafing 57
Falls Church 52
Milan 43
Shanghai 39
San Mateo 38
Boardman 36
Chicago 36
Jakarta 30
Verona 30
Norwalk 29
Brussels 27
Leawood 24
Guangzhou 22
Kunming 22
Augusta 21
Dublin 21
Hefei 21
Saint Petersburg 21
Munich 19
Nanjing 18
Kilburn 17
Ottawa 17
Parma 16
Monmouth Junction 15
Toronto 15
Bologna 14
Indiana 14
Hounslow 13
San Giuliano Milanese 13
Abbiategrasso 12
Ardabil 12
Auburn Hills 12
Chiswick 12
Acton 11
Jinan 11
Menlo Park 11
San Francisco 11
Los Angeles 10
Naples 10
Frankfurt am Main 9
Mountain View 9
Napoli 9
Phoenix 9
Reggio Emilia 9
Paris 8
Rome 8
Sassuolo 8
Brno 7
Chengdu 7
Fremont 7
Wuhan 7
Cesena 6
Dongguan 6
Hanover 6
Pune 6
Reggio Nell'emilia 6
São Paulo 6
Amsterdam 5
Fuzhou 5
Hangzhou 5
Islington 5
Jinhua 5
Nanchang 5
Prescot 5
Shenyang 5
Zhengzhou 5
Astana 4
Carpi 4
Crosia 4
Dong Ket 4
Ferrara 4
Totale 20.842
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Nome #
A Small Chaperone Improves Folding and Routing of Rhodopsin Mutants Linked to Inherited Blindness 248
WebPSN: a web server for high-throughput investigation of structural communication in biomacromolecules 235
Small-Molecule Protein-Protein Interaction Inhibitor of Oncogenic Rho Signaling 232
Single Molecule Analysis of Functionally Asymmetric G Protein-coupled Receptor (GPCR) Oligomers Reveals Diverse Spatial and Structural Assemblies 225
Mutagenesis and modelling of the alpha(1b)-adrenergic receptor highlight the role of the helix 3/helix 6 interface in receptor activation 214
Network and atomistic simulations unveil the structural determinants of mutations linked to retinal diseases 214
Computational modeling approaches to Structure-Function Analysis of G Protein-Coupled Receptors 208
A model for constitutive lutropin receptor activation based on molecular simulation and engineered mutations in transmembrane helices 6 and 7 207
Wordom 207
Dark and photoactivated rhodopsin share common binding modes to transducin 202
The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition 201
Monomeric dark rhodopsin holds the molecular determinants for transducin recognition: insights from computational analysis 199
Superactive mutants of thromboxane prostanoid receptor: functional and computational analysis of an active form alternative to constitutively active mutants 199
Molecular dynamics simulations of the ligand-induced chemical information transfer in the 5-HT1A receptor 198
Network analysis to uncover the structural communication in GPCRs 197
Computational simulations of stem-cell factor c-Kit receptor interaction 197
Conserved amino acids participate in the structure networks deputed to intramolecular communication in the lutropin receptor 197
Quaternary structure predictions and structural communication features of GPCR dimers 196
Class A GPCR: Di/Oligomerization of Glycoprotein Hormone Receptors 196
Computational modeling of intramolecular and intermolecular communication in GPCRs 195
Theoretical study on the electrostatically driven step of receptor-G protein recognition 193
A functional transmembrane complex: The luteinizing hormone receptor with bound ligand and G protein 193
In silico screening of mutational effects on enzyme-proteic inhibitor affinity: A docking-based approach 192
Catching Functional Modes and Structural Communication in Dbl Family Rho Guanine Nucleotide Exchange Factors 192
Theoretical study on receptor-G protein recognition: new insights into the mechanism of the α1b-adrenergic receptor activation 192
Rhodopsin activation follows precoupling with transducin: Inferences from computational analysis 192
Nucleotide binding switches the information flow in ras GTPases 192
Computational Screening of Rhodopsin Mutations Associated with Retinitis Pigmentosa 191
Wordom: A user-friendly program for the analysis of molecular structures, trajectories, and free energy surfaces 191
Theoretical investigation of IL-6 multiprotein receptor assembly 190
Molecular basis of ligand binding and receptor activation in the oxytocin and vasopressin receptor family 190
Target Flexibility: An Emerging Consideration in Drug Discovery and Design 190
Auto-regulation of Secretory Flux by Sensing and Responding to the Folded Cargo Protein Load in the Endoplasmic Reticulum 189
Comparative molecular dynamics study of the seven-helix bundle arrangement of G-protein coupled receptors 188
Three dimensional molecular modeling of the α1a-adrenoceptor. Direct 3D-QSAR modeling of selective antagonists 188
Structural features of the inactive and active states of the melanin-concentrating hormone receptors: Insights from molecular simulations 188
Deciphering the deformation modes associated with function retention and specialization in members of the Ras superfamily 188
Update 1 of: Computational Modeling Approaches to Structure-Function Analysis of G Protein-Coupled Receptors 187
Dissecting intrinsic and ligand-induced structural communication in the β3 headpiece of integrins 187
Molecular dynamics simulations of m3-muscarinic receptor activation and QSAR analysis 187
Modulation of thermal noise and spectral sensitivity in Lake Baikal cottoid fish rhodopsins 187
Structure network analysis to gain insights into GPCR function 186
Computational modeling approaches to quantitative structure–binding kinetics relationships in drug discovery 185
Light on the structural communication in Ras GTPases 185
Structure-function relationships of the alpha(1b)-adrenergic receptor 183
Prototropic molecular forms and theoretical descriptors in QSAR analysis 183
Quaternary structure predictions and estimation of mutational effects on the free energy of dimerization of the OMPLA protein 183
Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in brazilian boys: a novel constitutively activating mutation in the first transmembrane helix 182
Nucleotide binding affects intrinsic dynamics and structural communication in Ras GTPases 181
The ad hoc supermolecule approach to receptor ligand design 180
Structure-activity relationships in 1,4-benzodioxan-related compounds. 10. Novel α1-adrenoreceptor antagonists related to openphendioxan: synthesis, biological evaluation, and α1d computational study 180
Computational quantum chemistry and adaptive ligand modeling in mechanistic QSAR 180
Theoretical quantitative structure-activity analysis of quinuclidine-based muscarinic cholinergic receptor ligands 179
Activation mechanism of human oxytocin receptor: A combined study of experimental and computer-simulated mutagenesis 179
Lutropin receptor function: Insights from natural, engineered, and computer-simulated mutations 179
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 3 179
Prediction of MEF2A-DNA interface by rigid body docking: A tool for fast estimation of protein mutational effects on DNA binding 179
Sequential unfolding of individual helices of bacterioopsin observed in molecular dynamics simulations of extraction from the purple membrane 178
Theoretical quantitative structure-activity analysis and pharmacophore modelling of selective non congeneric α1a-adrenergic antagonists 178
The DRY motif as a molecular switch of the human oxytocin receptor 178
Network-level analysis of light adaptation in rod cells under normal and altered conditions 178
Structural Determinants of Constitutive Activation of Gα Proteins: Transducin as a Paradigm 178
Dimerization and ligand binding affect the structure network of A(2A) adenosine receptor 178
Epilepsy and intellectual disability linked protein Shrm4 interaction with GABA B Rs shapes inhibitory neurotransmission 178
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 176
Multiscale quantum chemical approaches to QSAR modeling and drug design 175
Theoretical quantitative structure-activity relationship analysis of congeneric and non-congeneric α1-adrenoceptor antagonists: a chemometric study 175
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 173
Ligand-Receptor Communication and Drug Design 172
Amino acids of the α1B-adrenergic receptor involved in agonist binding: further differences in docking catecholamines to receptor subtypes 171
Light on the structure of thromboxane A2 receptor heterodimers 170
Modeling the structural communication in supramolecular complexes involving GPCRs 169
Structure-Function Relationships of the Luteinizing Hormone Receptor 168
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 167
Insight into mutation-induced activation of the luteinizing hormone receptor: Molecular simulations predict the functional behavior of engineered mutants at M398 167
Structural Aspects of the Luteinizing Hormone Receptor: Information from Molecular Modeling and Mutagenesis 164
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 163
Theoretical Quantitative Structure-Activity Relationship Analysis on Three Dimensional Models of Ligand-m1 Muscarinic Receptor Complexes 162
Constitutively active G protein-coupled receptor mutants: implications on receptor function and drug action 162
Enantiomeric resolution of sulfoxides on a DACH‐DNB chiral stationary phase: A quantitative structure–enantioselective retention relationship (QSERR) study 162
Inactive and active states and supramolecular organization of GPCRs: insights from computational modeling 162
FIPD 162
Probing fragment complementation by rigid-body docking: In silico reconstitution of calbindin D9k 162
Contributions of Intracellular Loops 2 and 3 of the Lutropin Receptor in Gs Coupling 162
Dimerization of the lutropin receptor: Insights from computational modeling 161
The catalytic site structural gate of adenosine deaminase allosterically modulates ligand binding to adenosine receptors 161
Mutational and computational analysis of the alpha-1b adrenergic receptor.Involvement of basic and hydrophobic residues in receptor activation and G protein coupling 160
Structural determinants involved in the activation and regulation of G protein-coupled receptors: lessons from the alpha1-adrenegic receptor subtypes 160
Homodimerization of neurotensin 1 receptor involves helices 1, 2, and 4: Insights from quaternary structure predictions and dimerization free energy estimations 160
The luteinizing hormone receptor: insights into structure-function relationships and hormone-receptor-mediated changes in gene expression in ovarian cancer cells 160
Conformational analysis, molecular modeling and quantitative structure-activity relationships studies of 2,4-diamino-6,7-dimethoxy-2-substituted quinazoline α1-adrenergic antagonists 160
In silico screening of mutational effects on transmembrane helix dimerization: insights from rigid-body docking and molecular dynamics simulations 157
Conformational analysis and theoretical quantitative size and shape-affinity relationships of N-4-protonated N-1-arylpiperazine 5-HT1A serotoninergic ligands 156
The α1a and α1b-adrenergic receptor subtypes: molecular mechanisms of receptor activation and of drug action 155
Ab initio modeling and molecular dynamics simulation of the alpha 1b-adrenergic receptor activation 154
Adenosine A(2A) Receptor-Antagonist/Dopamine D(2) Receptor-Agonist Bivalent Ligands as Pharmacological Tools to Detect A(2A)-D(2) Receptor Heteromers 154
Theoretical quantitative size and shape activity and selectivity analyses of 5-HT1A serotonin and α1-adrenergic receptor ligands 153
Mechanisms of inter- and intramolecular communication in GPCRs and G proteins 153
Membrane Estrogen Receptor (GPER) and Follicle-Stimulating Hormone Receptor (FSHR) Heteromeric Complexes Promote Human Ovarian Follicle Survival 153
Theoretical investigation of substrate specificity for cytochromes p450 IA2, p450 IID6 and p450 IIIA4 151
Totale 18.155
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Categoria #
all - tutte 106.682
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 106.682
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.828 0 0 0 0 0 839 955 706 605 217 270 236
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
2022/20232.743 274 304 200 211 413 487 37 263 330 26 117 81
2023/20241.753 64 110 260 111 357 163 121 176 60 49 87 195
2024/20252.228 396 86 114 462 1.155 15 0 0 0 0 0 0
Totale 25.352