IRIS
CASTAGNOLI, LUISA
 Distribuzione geografica
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Continente #
NA - Nord America 23.575
AS - Asia 3.048
EU - Europa 2.809
SA - Sud America 413
Continente sconosciuto - Info sul continente non disponibili 264
AF - Africa 61
OC - Oceania 32
Totale 30.202
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Nazione #
US - Stati Uniti d'America 23.430
SG - Singapore 1.253
CN - Cina 742
IT - Italia 623
DE - Germania 348
BR - Brasile 346
UA - Ucraina 312
RU - Federazione Russa 307
HK - Hong Kong 286
VN - Vietnam 268
IE - Irlanda 225
FR - Francia 192
GB - Regno Unito 182
FI - Finlandia 160
SE - Svezia 148
BD - Bangladesh 94
JP - Giappone 94
KR - Corea 83
CA - Canada 77
PL - Polonia 77
IN - India 74
NL - Olanda 56
CZ - Repubblica Ceca 42
AU - Australia 30
ID - Indonesia 27
AT - Austria 24
ZA - Sudafrica 24
BE - Belgio 23
IQ - Iraq 23
MX - Messico 22
AR - Argentina 18
EE - Estonia 18
LT - Lituania 18
ES - Italia 17
VE - Venezuela 14
CR - Costa Rica 13
PK - Pakistan 13
TR - Turchia 13
SA - Arabia Saudita 12
EC - Ecuador 11
CO - Colombia 10
EG - Egitto 9
MY - Malesia 9
UZ - Uzbekistan 9
IL - Israele 8
JM - Giamaica 8
CH - Svizzera 7
MA - Marocco 7
EU - Europa 6
PT - Portogallo 6
CL - Cile 5
DZ - Algeria 5
HN - Honduras 5
PH - Filippine 5
PY - Paraguay 5
JO - Giordania 4
KE - Kenya 4
AE - Emirati Arabi Uniti 3
BB - Barbados 3
DK - Danimarca 3
GT - Guatemala 3
HR - Croazia 3
IR - Iran 3
LK - Sri Lanka 3
NI - Nicaragua 3
PR - Porto Rico 3
QA - Qatar 3
UY - Uruguay 3
AZ - Azerbaigian 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
GE - Georgia 2
HU - Ungheria 2
KZ - Kazakistan 2
LU - Lussemburgo 2
MK - Macedonia 2
MQ - Martinica 2
MU - Mauritius 2
NG - Nigeria 2
PA - Panama 2
PW - Palau 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 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
BG - Bulgaria 1
BH - Bahrain 1
BS - Bahamas 1
BW - Botswana 1
CG - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GR - Grecia 1
KG - Kirghizistan 1
Totale 29.935
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Città #
Wilmington 5.802
Woodbridge 5.658
Houston 4.822
Fairfield 841
Ashburn 778
Singapore 675
Chandler 546
Ann Arbor 426
San Jose 349
Seattle 346
Beijing 328
Cambridge 280
Hong Kong 272
Jacksonville 238
Council Bluffs 213
Dublin 205
Rome 180
New York 175
The Dalles 170
Medford 158
Dearborn 117
Los Angeles 110
Santa Clara 97
Helsinki 95
Munich 85
Ho Chi Minh City 77
Lawrence 76
Tokyo 68
Hangzhou 66
Hanoi 64
Kraków 58
Fuzhou 50
Lauterbourg 50
Milan 50
San Diego 49
Buffalo 46
Dallas 39
Orem 37
São Paulo 36
Moscow 35
Menlo Park 33
Brno 31
Mülheim 31
Falls Church 30
North Bergen 30
London 29
Denver 27
Phoenix 26
Redwood City 24
Boardman 23
Brussels 23
Montreal 22
Brooklyn 21
Jakarta 20
Nuremberg 20
Chennai 19
Chicago 19
Johannesburg 19
Dong Ket 17
Toronto 17
Atlanta 16
Columbus 16
Da Nang 16
Norwalk 16
Amsterdam 15
Hefei 15
Warsaw 15
Boston 14
Rio de Janeiro 14
Stockholm 14
Tartu 14
Turku 14
University Park 14
Guangzhou 13
San Mateo 12
Seoul 12
Zhengzhou 12
Frankfurt am Main 11
Redondo Beach 11
Haiphong 10
Kendall Park 10
Melbourne 10
San Francisco 10
San José 10
Shanghai 10
Verona 10
Washington 10
Antrodoco 9
Manchester 9
Nanjing 9
Paris 9
Brasília 8
Creede 8
Miami 8
Turin 8
Vilnius 8
Cairo 7
Chiswick 7
Kingston 7
Mountain View 7
Totale 24.696
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Nome #
Protein interaction networks by proteome peptide scanning 658
Bayesian modeling of the yeast SH3 domain interactome predicts spatiotemporal dynamics of endocytosis proteins 569
MINT, the molecular interaction database: 2012 update 562
Binding to DPF-motif by the POB1 EH domain is responsible for POB1-Eps15 interaction 555
HuPho: the human phosphatase portal 549
RNF11 is a GGA protein cargo and acts as a molecular adaptor for GGA3 ubiquitination mediated by Itch 542
A two-hybrid system based on chimeric operator recognition for studying protein homo/heterodimerization in Escherichia coli 541
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes 540
A novel approach to protein-protein interaction: Complex formation between the p53 tumor suppressor and the HIV Tat proteins 533
The SH2 domain interaction landscape 531
Multiple modification and protein interaction signals drive the Ring finger protein 11 (RNF11) E3 ligase to the endosomal compartment 520
Combining affinity proteomics and network context to identify new phosphatase substrates and adapters in growth pathways 519
Control of ColE1 plasmid replication by antisense RNA 518
Benchmarking of the 2010 BioCreative Challenge III text-mining competition by the BioGRID and MINT interaction databases 502
Tumor suppressor density-enhanced phosphatase-1 (DEP-1) inhibits the RAS pathway by direct dephosphorylation of ERK1/2 kinases 495
Selectivity and promiscuity in the interaction network mediated by protein recognition modules 495
MINT and IntAct contribute to the second BioCreative challenge: serving the text-mining community with high quality molecular interaction data 491
The 4G10, pY20 and p-TYR-100 antibody specificity: profiling by peptide microarrays 491
Both Intrinsic Substrate Preference and Network Context Contribute to Substrate Selection of Classical Tyrosine Phosphatases. 487
Combining peptide recognition specificity and context information for the prediction of the 14-3-3-mediated interactome in S. cerevisiae and H. sapiens 485
The protein interaction network mediated by human SH3 domains 485
Can we infer peptide recognition specificity mediated by SH3 domains? 484
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 476
Construction, exploitation and evolution of a new peptide library displayed at high density by fusion to the major coat protein of filamentous phage 469
PTPRJ (protein tyrosine phosphatase, receptor type, J) 461
Methods to reveal domain networks 461
MINT: the Molecular INTeraction database 459
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 458
MINT, the molecular interaction database: 2009 update 457
DOMINO: a database of domain-peptide interactions 456
Increasing the immunogenicity of protein antigens through the genetic insertion of VQGEESNDK sequence of human IL-1 beta into their sequence 456
The adapter protein CD2AP binds to p53 protein in the cytoplasm and can discriminate its polymorphic variants P72R 455
Alterations in the phosphoproteomic profile of cells expressing a non-functional form of the SHP2 phosphatase 453
The Protein-Protein Interaction tasks of BioCreative III: classification/ranking of articles and linking bio-ontology concepts to full text 450
Mapping the human phosphatome on growth pathways 444
The human phosphatase interactome: An intricate family portrait 443
The 4G10, pY20 and p-TYR-100 antibody specificity: profiling by peptide microarrays 442
VirusMINT: a viral protein interaction database 436
Reactive oxygen species and epidermal growth factor are antagonistic cues controlling SHP-2 dimerization 430
Identification of new substrates of the protein-tyrosine phosphatase PTP1B by Bayesian integration of proteome evidence 429
Signaling by EGFR 428
Unusual binding properties of the SH3 domain of the yeast actin-binding protein Abp1: structural and functional analysis 427
A combined experimental and computational strategy to define protein interaction networks for peptide recognition modules 426
Role of 14-3-3 proteins in the regulation of neutral trehalase in the yeast Saccharomyces cerevisiae 424
The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug. 415
Enriching the viral-host interactomes with interactions mediated by SH3 domains 412
Metformin Protects Skeletal Muscle from Cardiotoxin Induced Degeneration 409
Mapping protein-protein interactions with phage-displayed combinatorial peptide libraries 378
mentha: a resource for browsing integrated protein-interaction networks 376
Microfluidic-enhanced 3D bioprinting of aligned myoblast-laden hydrogels leads to functionally organized myofibers in vitro and in vivo 318
CUBAN, a Case Study of Selective Binding: Structural Details of the Discrimination between Ubiquitin and NEDD8 313
Fibro-adipogenic progenitors of dystrophic mice are insensitive to NOTCH regulation of adipogenesis 294
Myo-REG: A portal for signaling interactions in muscle regeneration 282
A subset of RAB proteins modulates PP2A phosphatase activity 275
Metformin delays satellite cell activation and maintains quiescence 272
Metformin induces apoptosis and downregulates pyruvate kinase M2 in breast cancer cells only when grown in nutrient-poor conditions 271
CancerGeneNet: linking driver genes to cancer hallmarks 253
Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration 252
SIGNOR 2.0, the SIGnaling Network Open Resource 2.0: 2019 update 252
Deep Proteomics of Breast Cancer Cells Reveals that Metformin Rewires Signaling Networks Away from a Pro-growth State 249
Regulation of myoblast differentiation by metabolic perturbations induced by metformin 249
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen 247
DISNOR: A disease network open resource 244
Characterization by mass cytometry of different methods for the preparation of muscle mononuclear cells 242
Adipogenesis of skeletal muscle fibro/adipogenic progenitors is affected by the WNT5a/GSK3/β-catenin axis 237
Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8 233
Ring Finger Protein 11 acts on ligand-activated EGFR via the direct interaction with the UIM region of ANKRD13 protein family 220
The immunosuppressant drug azathioprine restrains adipogenesis of muscle Fibro/Adipogenic Progenitors from dystrophic mice by affecting AKT signaling 219
Group I Paks support muscle regeneration and counteract cancer-associated muscle atrophy 219
Osteogenic differentiation of skeletal muscle progenitor cells is activated by the DNA damage response 197
SIGNOR: a database of causal relationships between biological entities 186
Biofabricating murine and human myo-substitutes for rapid volumetric muscle loss restoration 172
SIGNOR 3.0, the SIGnaling network open resource 3.0: 2022 update 149
Integrating Patient-Specific Information into Logic Models of Complex Diseases: Application to Acute Myeloid Leukemia 129
A Resource to Infer Molecular Paths Linking Cancer Mutations to Perturbation of Cell Metabolism 123
A Resource for the Network Representation of Cell Perturbations Caused by SARS-CoV-2 Infection 118
Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders 108
Characterization of the skeletal muscle secretome reveals a role for extracellular vesicles and il1α/il1β in restricting fibro/adipogenic progenitor adipogenesis 108
SCA-1 micro-heterogeneity in the fate decision of dystrophic fibro/adipogenic progenitors 108
Transcription Factor Activation Profiles (TFAP) identify compounds promoting differentiation of Acute Myeloid Leukemia cell lines 99
High-Dimensional Single-Cell Quantitative Profiling of Skeletal Muscle Cell Population Dynamics during Regeneration 99
Skeletal muscle subpopulation rearrangements upon rhabdomyosarcoma development through single-cell mass cytometry 63
Correction: Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders 20
Totale 30.202
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Categoria #
all - tutte 75.166
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 75.166
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022748 0 0 0 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
2025/20263.669 319 182 354 327 307 143 573 425 401 348 167 123
2026/20271.208 128 168 632 280 0 0 0 0 0 0 0 0
Totale 30.202