CASTAGNOLI, LUISA
 Distribuzione geografica
Continente #
NA - Nord America 22.372
AS - Asia 2.952
EU - Europa 2.645
SA - Sud America 389
AF - Africa 59
OC - Oceania 32
Continente sconosciuto - Info sul continente non disponibili 7
Totale 28.456
Nazione #
US - Stati Uniti d'America 22.286
SG - Singapore 1.246
CN - Cina 729
IT - Italia 499
DE - Germania 346
BR - Brasile 336
UA - Ucraina 312
RU - Federazione Russa 305
HK - Hong Kong 286
VN - Vietnam 267
IE - Irlanda 225
FR - Francia 189
GB - Regno Unito 168
FI - Finlandia 160
SE - Svezia 145
JP - Giappone 91
KR - Corea 83
PL - Polonia 77
IN - India 72
CA - Canada 54
NL - Olanda 53
CZ - Repubblica Ceca 42
AU - Australia 30
BD - Bangladesh 29
ID - Indonesia 26
AT - Austria 24
ZA - Sudafrica 24
BE - Belgio 23
IQ - Iraq 23
MX - Messico 21
EE - Estonia 17
ES - Italia 16
AR - Argentina 15
TR - Turchia 13
PK - Pakistan 12
SA - Arabia Saudita 11
LT - Lituania 10
EC - Ecuador 9
MY - Malesia 9
UZ - Uzbekistan 9
VE - Venezuela 9
EG - Egitto 8
CH - Svizzera 7
IL - Israele 7
MA - Marocco 7
CO - Colombia 6
EU - Europa 6
CL - Cile 5
DZ - Algeria 5
PT - Portogallo 5
PY - Paraguay 5
JO - Giordania 4
KE - Kenya 4
PH - Filippine 4
AE - Emirati Arabi Uniti 3
CR - Costa Rica 3
HR - Croazia 3
IR - Iran 3
LK - Sri Lanka 3
QA - Qatar 3
UY - Uruguay 3
AZ - Azerbaigian 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
DK - Danimarca 2
GE - Georgia 2
HU - Ungheria 2
KZ - Kazakistan 2
LU - Lussemburgo 2
MK - Macedonia 2
MU - Mauritius 2
PA - Panama 2
PW - Palau 2
RO - Romania 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TH - Thailandia 2
TW - Taiwan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BS - Bahamas 1
BW - Botswana 1
CG - Congo 1
CY - Cipro 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GR - Grecia 1
GT - Guatemala 1
HN - Honduras 1
KG - Kirghizistan 1
KW - Kuwait 1
LB - Libano 1
LV - Lettonia 1
NG - Nigeria 1
NI - Nicaragua 1
NO - Norvegia 1
NP - Nepal 1
Totale 28.451
Città #
Wilmington 5.801
Woodbridge 5.657
Houston 4.821
Fairfield 841
Singapore 670
Ashburn 581
Chandler 546
Ann Arbor 426
Seattle 345
Beijing 326
Cambridge 280
Hong Kong 272
San Jose 264
Jacksonville 238
Dublin 205
Rome 169
New York 163
The Dalles 162
Medford 158
Council Bluffs 127
Dearborn 117
Los Angeles 97
Helsinki 95
Munich 85
Ho Chi Minh City 76
Lawrence 76
Santa Clara 76
Hangzhou 66
Tokyo 65
Hanoi 64
Kraków 58
Fuzhou 50
Lauterbourg 50
San Diego 49
Buffalo 38
Milan 38
Orem 36
Moscow 35
São Paulo 34
Menlo Park 33
Brno 31
Mülheim 31
Falls Church 30
Dallas 28
London 28
Boardman 23
Brussels 23
Phoenix 22
Redwood City 22
Jakarta 20
Montreal 20
Nuremberg 20
Chennai 19
Johannesburg 19
Dong Ket 17
North Bergen 17
Da Nang 16
Norwalk 16
Amsterdam 15
Brooklyn 15
Hefei 15
Warsaw 15
Tartu 14
Turku 14
University Park 14
Boston 13
Chicago 13
Guangzhou 13
Rio de Janeiro 13
Stockholm 13
Columbus 12
San Mateo 12
Seoul 12
Zhengzhou 12
Redondo Beach 11
Toronto 11
Denver 10
Frankfurt am Main 10
Haiphong 10
Kendall Park 10
Melbourne 10
Shanghai 10
Antrodoco 9
Atlanta 9
Manchester 9
Nanjing 9
Paris 9
San Francisco 9
Verona 9
Brasília 8
Creede 8
Chiswick 7
Mountain View 7
Nanchang 7
Quito 7
Vienna 7
Cairo 6
Curitiba 6
Kuala Lumpur 6
New Delhi 6
Totale 24.127
Nome #
Protein interaction networks by proteome peptide scanning 645
Bayesian modeling of the yeast SH3 domain interactome predicts spatiotemporal dynamics of endocytosis proteins 555
Binding to DPF-motif by the POB1 EH domain is responsible for POB1-Eps15 interaction 533
MINT, the molecular interaction database: 2012 update 531
A two-hybrid system based on chimeric operator recognition for studying protein homo/heterodimerization in Escherichia coli 525
RNF11 is a GGA protein cargo and acts as a molecular adaptor for GGA3 ubiquitination mediated by Itch 516
A novel approach to protein-protein interaction: Complex formation between the p53 tumor suppressor and the HIV Tat proteins 514
HuPho: the human phosphatase portal 514
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes 512
The SH2 domain interaction landscape 511
Multiple modification and protein interaction signals drive the Ring finger protein 11 (RNF11) E3 ligase to the endosomal compartment 500
Combining affinity proteomics and network context to identify new phosphatase substrates and adapters in growth pathways 499
Control of ColE1 plasmid replication by antisense RNA 493
Benchmarking of the 2010 BioCreative Challenge III text-mining competition by the BioGRID and MINT interaction databases 492
Selectivity and promiscuity in the interaction network mediated by protein recognition modules 484
MINT and IntAct contribute to the second BioCreative challenge: serving the text-mining community with high quality molecular interaction data 477
Both Intrinsic Substrate Preference and Network Context Contribute to Substrate Selection of Classical Tyrosine Phosphatases. 476
The 4G10, pY20 and p-TYR-100 antibody specificity: profiling by peptide microarrays 475
Can we infer peptide recognition specificity mediated by SH3 domains? 473
Combining peptide recognition specificity and context information for the prediction of the 14-3-3-mediated interactome in S. cerevisiae and H. sapiens 470
The protein interaction network mediated by human SH3 domains 470
Tumor suppressor density-enhanced phosphatase-1 (DEP-1) inhibits the RAS pathway by direct dephosphorylation of ERK1/2 kinases 469
Construction, exploitation and evolution of a new peptide library displayed at high density by fusion to the major coat protein of filamentous phage 459
The central proline rich region of POB1/REPS2 plays a regulatory role in epidermal growth factor receptor endocytosis by binding to 14-3-3 and SH3 domain-containing proteins 458
PTPRJ (protein tyrosine phosphatase, receptor type, J) 447
Methods to reveal domain networks 445
MINT, the molecular interaction database: 2009 update 443
Counteracting effects operating on Src homology 2 domain-containing protein-tyrosine phosphatase 2 (SHP2) function drive selection of the recurrent Y62D and Y63C substitutions in Noonan syndrome 440
Alterations in the phosphoproteomic profile of cells expressing a non-functional form of the SHP2 phosphatase 440
Increasing the immunogenicity of protein antigens through the genetic insertion of VQGEESNDK sequence of human IL-1 beta into their sequence 439
MINT: the Molecular INTeraction database 438
DOMINO: a database of domain-peptide interactions 435
The adapter protein CD2AP binds to p53 protein in the cytoplasm and can discriminate its polymorphic variants P72R 434
The Protein-Protein Interaction tasks of BioCreative III: classification/ranking of articles and linking bio-ontology concepts to full text 433
Mapping the human phosphatome on growth pathways 431
The 4G10, pY20 and p-TYR-100 antibody specificity: profiling by peptide microarrays 425
Identification of new substrates of the protein-tyrosine phosphatase PTP1B by Bayesian integration of proteome evidence 421
The human phosphatase interactome: An intricate family portrait 420
VirusMINT: a viral protein interaction database 417
Reactive oxygen species and epidermal growth factor are antagonistic cues controlling SHP-2 dimerization 416
A combined experimental and computational strategy to define protein interaction networks for peptide recognition modules 415
Unusual binding properties of the SH3 domain of the yeast actin-binding protein Abp1: structural and functional analysis 414
Role of 14-3-3 proteins in the regulation of neutral trehalase in the yeast Saccharomyces cerevisiae 408
Enriching the viral-host interactomes with interactions mediated by SH3 domains 402
Signaling by EGFR 400
The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug. 398
Metformin Protects Skeletal Muscle from Cardiotoxin Induced Degeneration 389
Mapping protein-protein interactions with phage-displayed combinatorial peptide libraries 372
mentha: a resource for browsing integrated protein-interaction networks 363
CUBAN, a Case Study of Selective Binding: Structural Details of the Discrimination between Ubiquitin and NEDD8 298
Microfluidic-enhanced 3D bioprinting of aligned myoblast-laden hydrogels leads to functionally organized myofibers in vitro and in vivo 295
Fibro-adipogenic progenitors of dystrophic mice are insensitive to NOTCH regulation of adipogenesis 261
Myo-REG: A portal for signaling interactions in muscle regeneration 258
Metformin induces apoptosis and downregulates pyruvate kinase M2 in breast cancer cells only when grown in nutrient-poor conditions 257
A subset of RAB proteins modulates PP2A phosphatase activity 256
Metformin delays satellite cell activation and maintains quiescence 255
Deep Proteomics of Breast Cancer Cells Reveals that Metformin Rewires Signaling Networks Away from a Pro-growth State 239
CancerGeneNet: linking driver genes to cancer hallmarks 238
SIGNOR 2.0, the SIGnaling Network Open Resource 2.0: 2019 update 233
Regulation of myoblast differentiation by metabolic perturbations induced by metformin 231
Characterization by mass cytometry of different methods for the preparation of muscle mononuclear cells 230
DISNOR: A disease network open resource 229
Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration 228
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen 227
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 221
Ring Finger Protein 11 acts on ligand-activated EGFR via the direct interaction with the UIM region of ANKRD13 protein family 208
Group I Paks support muscle regeneration and counteract cancer-associated muscle atrophy 202
Adipogenesis of skeletal muscle fibro/adipogenic progenitors is affected by the WNT5a/GSK3/β-catenin axis 200
The immunosuppressant drug azathioprine restrains adipogenesis of muscle Fibro/Adipogenic Progenitors from dystrophic mice by affecting AKT signaling 189
Osteogenic differentiation of skeletal muscle progenitor cells is activated by the DNA damage response 176
SIGNOR: a database of causal relationships between biological entities 158
Biofabricating murine and human myo-substitutes for rapid volumetric muscle loss restoration 148
SIGNOR 3.0, the SIGnaling network open resource 3.0: 2022 update 129
A Resource to Infer Molecular Paths Linking Cancer Mutations to Perturbation of Cell Metabolism 110
Integrating Patient-Specific Information into Logic Models of Complex Diseases: Application to Acute Myeloid Leukemia 108
A Resource for the Network Representation of Cell Perturbations Caused by SARS-CoV-2 Infection 101
Characterization of the skeletal muscle secretome reveals a role for extracellular vesicles and il1α/il1β in restricting fibro/adipogenic progenitor adipogenesis 91
SCA-1 micro-heterogeneity in the fate decision of dystrophic fibro/adipogenic progenitors 89
Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders 85
High-Dimensional Single-Cell Quantitative Profiling of Skeletal Muscle Cell Population Dynamics during Regeneration 84
Transcription Factor Activation Profiles (TFAP) identify compounds promoting differentiation of Acute Myeloid Leukemia cell lines 81
Skeletal muscle subpopulation rearrangements upon rhabdomyosarcoma development through single-cell mass cytometry 51
Correction: Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders 10
Totale 28.712
Categoria #
all - tutte 67.577
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 67.577


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021229 0 0 0 0 0 0 0 0 0 0 145 84
2021/2022973 56 130 39 44 45 51 92 29 82 82 54 269
2022/20231.286 123 106 34 197 117 246 108 92 130 15 68 50
2023/2024519 60 15 36 19 58 159 11 34 5 16 2 104
2024/20252.130 77 288 174 135 96 202 150 116 225 199 248 220
2025/20263.387 319 182 354 327 307 143 573 425 401 348 8 0
Totale 28.712