MARTEGANI, ENZO
 Distribuzione geografica
Continente #
NA - Nord America 22.394
EU - Europa 10.153
AS - Asia 8.952
SA - Sud America 1.157
Continente sconosciuto - Info sul continente non disponibili 583
AF - Africa 205
OC - Oceania 16
Totale 43.460
Nazione #
US - Stati Uniti d'America 21.182
SG - Singapore 3.066
CN - Cina 2.231
IT - Italia 1.850
DE - Germania 1.573
SE - Svezia 1.191
VN - Vietnam 1.125
HK - Hong Kong 1.083
CA - Canada 1.065
PL - Polonia 1.043
RU - Federazione Russa 990
BR - Brasile 871
IE - Irlanda 777
UA - Ucraina 719
FR - Francia 587
GB - Regno Unito 469
IN - India 333
DK - Danimarca 309
FI - Finlandia 218
BD - Bangladesh 169
TR - Turchia 167
KR - Corea 141
NL - Olanda 100
JP - Giappone 98
AR - Argentina 93
IQ - Iraq 93
MX - Messico 79
AT - Austria 76
ZA - Sudafrica 76
ID - Indonesia 69
PK - Pakistan 67
ES - Italia 60
BE - Belgio 59
PH - Filippine 51
EC - Ecuador 47
CO - Colombia 44
SA - Arabia Saudita 37
VE - Venezuela 31
RO - Romania 29
UZ - Uzbekistan 29
KE - Kenya 28
LT - Lituania 28
MY - Malesia 24
CL - Cile 22
MA - Marocco 19
CZ - Repubblica Ceca 16
JM - Giamaica 16
JO - Giordania 16
TN - Tunisia 16
AE - Emirati Arabi Uniti 15
ET - Etiopia 15
EU - Europa 15
PE - Perù 15
EG - Egitto 14
IL - Israele 14
OM - Oman 14
CR - Costa Rica 13
IR - Iran 13
PY - Paraguay 13
AZ - Azerbaigian 12
CH - Svizzera 12
NP - Nepal 12
TH - Thailandia 12
UY - Uruguay 11
KZ - Kazakistan 10
BO - Bolivia 8
DZ - Algeria 8
LB - Libano 8
NI - Nicaragua 8
NZ - Nuova Zelanda 8
AU - Australia 7
HN - Honduras 7
SI - Slovenia 7
PS - Palestinian Territory 6
PT - Portogallo 6
SN - Senegal 6
GT - Guatemala 5
QA - Qatar 5
SY - Repubblica araba siriana 5
TW - Taiwan 5
AL - Albania 4
DO - Repubblica Dominicana 4
EE - Estonia 4
GR - Grecia 4
PA - Panama 4
BG - Bulgaria 3
BT - Bhutan 3
CI - Costa d'Avorio 3
GD - Grenada 3
GE - Georgia 3
KG - Kirghizistan 3
LU - Lussemburgo 3
LV - Lettonia 3
ME - Montenegro 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BB - Barbados 2
BH - Bahrain 2
BW - Botswana 2
CY - Cipro 2
GA - Gabon 2
Totale 42.850
Città #
Ann Arbor 4.104
Ashburn 2.107
Singapore 1.689
Woodbridge 1.564
Hong Kong 1.064
Fairfield 1.020
Frankfurt am Main 1.004
Kraków 974
Houston 951
Chandler 927
San Jose 846
Jacksonville 758
Dublin 757
Milan 757
Toronto 705
Wilmington 650
Dearborn 428
Seattle 400
New York 374
Santa Clara 368
Cambridge 324
Council Bluffs 315
Beijing 311
Princeton 278
Los Angeles 268
Dallas 237
Ho Chi Minh City 236
Chicago 222
Nanjing 210
Hanoi 198
The Dalles 197
Dong Ket 179
Shanghai 168
Hefei 166
Altamura 132
Lauterbourg 127
Lachine 126
Lawrence 122
Rome 121
Boardman 114
Seoul 114
Hangzhou 106
Buffalo 103
São Paulo 89
Guangzhou 77
Helsinki 77
Moscow 76
Orem 72
Nanchang 71
Ottawa 69
San Diego 66
Columbus 65
Vienna 61
Phoenix 57
Shenyang 56
Warsaw 55
Tokyo 53
Andover 52
North Kansas City 50
Denver 48
Montreal 48
Tianjin 48
Brooklyn 47
Brussels 47
Changsha 47
Washington 43
Atlanta 40
Da Nang 39
Fremont 39
Jinan 39
Johannesburg 39
Hebei 38
Montréal 38
Kunming 37
Zhengzhou 37
Chennai 36
Manchester 33
London 32
Baghdad 31
Boston 31
Haiphong 31
Jakarta 30
Kocaeli 30
Falls Church 28
Mountain View 28
Salt Lake City 28
Norwalk 27
Jiaxing 26
Tashkent 26
Munich 25
New Delhi 25
Nuremberg 24
Philadelphia 24
San Francisco 24
Rio de Janeiro 23
Stockholm 23
Amsterdam 22
Auburn Hills 22
Dhaka 22
Elk Grove Village 22
Totale 28.214
Nome #
Selective cytotoxicity of a bicyclic Ras inhibitor in cancer cells expressing K-RasG13D 785
RalGPS2 is involved in tunneling nanotubes formation in 5637 bladder cancer cells 710
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 692
Glucose-derived Ras pathway inhibitors: evidence of Ras-ligand binding and Ras-GEF (Cdc25) interaction inhibition 662
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 613
Detection of cAMP and of PKA activity in Saccharomyces cerevisiae single cells using Fluorescence Resonance Energy Transfer (FRET) probes 570
Hypotonic stress-induced calcium signaling in Saccharomyces cerevisiae involves TRP-like transporters on the endoplasmic reticulum membrane 568
Involvement of Aif1 in apoptosis triggered by lack of Hxk2 in the yeast Saccharomyces cerevisiae 567
The deubiquitinating enzyme UBPy/USP8 interacts with TrkA and inhibits neuronal differentiation in PC12 cells 556
Antagonism between salicylate and the cAMP signal controls yeast cell survival and growth recovery from quiescence 551
Dynamic of VE-cadherin-mediated spermatid–Sertoli cell contacts in the mouse seminiferous epithelium 549
Sugar-derived Ras inhibitors: Group epitope mapping by NMR spectroscopy and biological evaluation 546
Design and characterisation of a new class of inhibitors of Ras activation 546
Design, Synthesis and Biological Evaluation of Levoglucosenone-derived Ras Activation Inhibitors 537
Design, synthesis and biological evaluation of sugar-derived Ras inhibitors 519
Live-cell imaging of endogenous Ras-GTP shows predominant Ras activation at the plasma membrane and in the nucleus in Saccharomyces cerevisiae 499
Multi-level approach for the identification of structure-function relationships in neurofibromin type I protein 486
Studies on the mechanism of action of a new class of inhibitors of Ras activation 477
The transcription factor Swi4 is target for PKA regulation of cell size at the G1 to S transition in Saccharomyces cerevisiae 456
Guidelines and recommendations on yeast cell death nomenclature 437
Functional analysis of RalgPS2, a murine guanine nucleotide exchange factor for RalA GTPase 434
The budding yeast RasGEF Cdc25 reveals an unexpected nuclear localization 429
Lack of SNF1 induces localization of active Ras in mitochondria and triggers apoptosis in the yeast Saccharomyces cerevisiae 425
Functional coupling of the mammalian EGF receptor to the Ras/cAMP pathway in the yeast Saccharomyces cerevisiae 414
RalGPS2 interacts with AKT and PDK1 promoting tunneling nanotubes formation in bladder cancer and kidney cells microenvironment 397
Glucose-induced calcium influx in budding yeast involves a novel calcium transport system and can activate calcineurin 395
In S. cerevisiae hydroxycitric acid antagonizes chronological aging and apoptosis regardless of citrate lyase 394
Localization of Ras signaling complex in budding yeast 393
Peptide-nanoparticle ligation mediated by cutinase fusion for the development of cancer cell-targeted nanoconjugates 393
The role of feedback control mechanisms on the establishment of oscillatory regimes in the Ras/cAMP/PKA pathway in S. cerevisiae 392
The PH-PxxP domain of RalGPS2 promotes PC12 cells differentiation acting as a dominant negative for RalA GTPase activation 390
Role of RalGPS2, a new possible oncogene, in tunneling nanotubes formation 388
Methods to study the Ras2 protein activation state and the subcellular localization of Ras-GTP in saccharomyces cerevisiae 382
The overexpression of the 3' terminal region of the CDC25 gene of Saccharomyces cerevisiae causes growth inhibition and alteration of purine nucleotides pools 381
The N-terminal region of the Saccharomyces cerevisiae RasGEF Cdc25 is required for nutrient-dependent cell-size regulation 377
Nuclear Ras2-GTP Controls Invasive Growth in Saccharomyces cerevisiae 372
Lack of HXK2 induces localization of active Ras in mitochondria and triggers apoptosis in the yeast Saccharomyces cerevisiae 353
PKA-dependent regulation of Cdc25 RasGEF localization in budding yeast 350
Activation of amyloid precursor protein processing by growth factors is dependent on Ras GTPase activity 346
Functional studies on Ira proteins, the neurofibromin homologs in yeast 336
Recombinant human nerve growth factor with a marked activity in vitro and in vivo 334
Flow-cytometry and cell-cycle kinetics in continuous and fed-batch fermentations of budding yeast 329
Overexpression of the CDC25 gene, an upstream element of the RAS/adenylyl cyclase pathway in Saccharomyces cerevisiae, allows immunological identification and characterization of its gene product 328
Novel role for known and unknown calcium transport involved proteins in Saccharomyces cerevisiae 327
Simulation of the Ras/cAMP/PKA pathway in budding yeast highlights the establishment of stable oscillatory states 322
Characterization and properties of dominant-negative mutants of the ras specific guanine nucleotide exchange factor CDC25Mm 317
3-Nitrocoumarin is an efficient inhibitor of budding yeast phospholipase-C 317
Characterization of the role of RalGPS2, a RalA GEF, in transformed and cancer cells 315
Active Ras2 in mitochondria promotes regulated cell death in a cAMP/PKA pathway-dependent manner in budding yeast 312
Role of RalGPS2, a new possible oncogene, in trasformed and cancer cells 311
Evidence for inositol triphosphate as a second messenger for glucose-induced calcium signalling in budding yeast 308
Identification of different daughter and parent subpopulations in an asynchronously growing Saccharomyces cerevisiae population 300
Yeast as a model for Ras signalling 295
A new nerve growth factor-mimetic peptide active on neuropathic pain in rats 294
Modeling and stochastic simulation of the Ras/cAMP/PKA pathway in the yeast Saccharomyces cerevisiae evidences a key regulatory function for intracellular guanine nucleotides pools 292
Chromosome separation and exit from mitosis in budding yeast: Dependence on growth revealed by cAMP-mediated inhibition 291
Analysis of the gene expression profile of mouse male meiotic germ cells 290
Measurement of calcium uptake in yeast using 45Ca 290
Monitoring yeast intracellular ca2+ levels using an in vivo bioluminescence assay 288
Macromolecular syntheses in the cell cycle mutant cdc25 of budding yeast 287
Involvement of CDC25Mm/Ras-GRF1-dependent signaling in the control of neuronal excitability 286
Cloning and characterization of mouse UBPy, a deubiquitinating enzyme that interacts with the Ras guanine nucleotide exchange factor CDC25(Mm)/Ras-GRF1 286
Fast detection of PKA activity in Saccharomyces cerevisiae cell population using AKAR fluorescence resonance energy transfer probes 286
The PLC1 encoded phospholipase C in the yeast Saccharomyces cerevisiae is essential for glucose-induced phosphatidylinositol turnover and activation of plasma membrane H+-ATPase 284
The overexpression of the CDC25 gene of Saccharomyces cerevisiae causes a derepression of GAL system and an increase of GAL4 transcription 283
Whi2p links nutritional sensing to actin dependent Ras/cAMP/PKA regulation and apoptosis in yeast 282
Lack of HXK2 Induces Localization of Active Ras in Mitochondria and Triggers Apoptosis in the Yeast Saccharomyces cerevisiae 280
The minimal active domain of the mouse Ras exchange factor CDC25Mm 279
The Ras Guanine Nucleotide Exchange Factor CDC25Mm Is Present at the Synaptic Junction 278
Ptdlns(4,5)P2 and phospholipase C-independent lns(1,4,5)P3 signals induced by a nitrogen source in nitrogen-starved yeast cells 277
Ubiquitin Specific Peptidase 8 277
The maize (Zea mays) b-32 protein shows RIP activity in yeast cells 276
Calcium signaling and sugar-induced activation of plasma membrane H+-ATPase in Saccharomyces cerevisiae cells 275
The involvement of calcium carriers and of the vacuole in the glucose-induced calcium signaling and activation of the plasma membrane H+-ATPase in Saccharomyces cerevisiae cells 274
Molecular cloning of a gene involved in glucose sensing in the yeast Saccharomyces cerevisiae 273
Activation state of the Ras2 protein and glucose-induced signalling in Saccharomyces cerevisiae 271
Analysis of the secondary structure of the catalytic domain of mouse Ras exchange factor CDC25(Mm) 266
LACTOSE WHEY UTILIZATION AND ETHANOL-PRODUCTION BY TRANSFORMED SACCHAROMYCES-CEREVISIAE CELLS 264
INVOLVEMENT OF A CELL-SIZE CONTROL MECHANISM IN THE INDUCTION AND MAINTENANCE OF OSCILLATIONS IN CONTINUOUS CULTURES OF BUDDING YEAST 264
Monitoring Ca2+ Signaling in Yeast 262
Role of guanine nucleotides in the regulation of the Ras/cAMP pathway in Saccharomyces cerevisiae 259
ENHANCED EXPRESSION OF HETEROLOGOUS PROTEINS BY THE USE OF A SUPERINDUCIBLE VECTOR IN BUDDING YEAST 259
The large N-terminal domain of Cdc25 protein of the yeast S. cerevisiae is required for glucose-induced Ras2 activation. 258
Production of lactic acid from engineered Saccharomyces cerevisiae cells 257
Cloning by functional complementation of a mouse cDNA encoding a homologue of CDC25, a Saccharomyces cerevisiae RAS activator 256
Total cellular Ca2+ measurements in yeast using flame photometry 255
Monitoring cyclic-AMP changes in a single yeast cell 254
Cell cycle analysis in a human cell line (EUE cells) 252
Efficient production of recombinant DNA proteins in Saccharomyces cerevisiae by controlled high‐cell‐density fermentation 250
DEVELOPMENT OF A PH-CONTROLLED FED-BATCH SYSTEM FOR BUDDING YEAST 249
PH-PxxP domain of RalGPS2 is a dominant negative for the RalA activation in PC12 cells 247
Towards a yeast cell cycle hybrid model: A new experimental model to study the link between PKA activity and cello cycle in budding yeast 246
Saccharomyces cerevisiae Cdc25: a still puzzling GEF 245
Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H(+)-ATPase in the yeast Saccharomyces cerevisiae. 243
Expression of high levels of human tissue plasminogen activator in yeast under the control of an inducible GAL promoter 241
Flow‐Cytometric Determination of the Respiratory Activity in Growing Saccharomyces cerevisiae Populations 239
Heterologous gene expression in continuous cultures of budding yeast 239
Protein and cell volume distributions during the production of beta-galactosidase in batch cultures of Kluyveromyces lactis 239
Glucose regulation of calcium signalling in S. cerevisiae 239
Evidence for adenylate cyclase as a scaffold protein for Ras2-Ira interaction in Saccharomyces cerevisie 236
Totale 35.700
Categoria #
all - tutte 125.930
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 125.930


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.969 0 0 0 284 154 222 220 145 171 199 215 359
2022/20233.983 552 1.223 399 345 324 531 57 182 225 35 70 40
2023/20242.306 67 88 107 130 302 543 489 89 182 35 50 224
2024/20254.500 317 480 347 180 384 136 209 166 395 612 459 815
2025/202611.806 1.160 606 894 1.349 1.381 566 1.571 554 1.048 949 869 859
2026/20272.585 219 437 1.261 668 0 0 0 0 0 0 0 0
Totale 43.460