MARTEGANI, ENZO
 Distribuzione geografica
Continente #
NA - Nord America 20.502
EU - Europa 10.074
AS - Asia 8.939
SA - Sud America 1.132
Continente sconosciuto - Info sul continente non disponibili 582
AF - Africa 205
OC - Oceania 15
Totale 41.449
Nazione #
US - Stati Uniti d'America 19.336
SG - Singapore 3.065
CN - Cina 2.229
IT - Italia 1.803
DE - Germania 1.570
SE - Svezia 1.191
VN - Vietnam 1.125
HK - Hong Kong 1.083
PL - Polonia 1.042
CA - Canada 1.040
RU - Federazione Russa 990
BR - Brasile 858
IE - Irlanda 777
UA - Ucraina 719
FR - Francia 585
GB - Regno Unito 446
IN - India 333
DK - Danimarca 309
FI - Finlandia 218
BD - Bangladesh 168
TR - Turchia 167
KR - Corea 141
NL - Olanda 100
JP - Giappone 98
IQ - Iraq 93
AR - Argentina 87
MX - Messico 79
AT - Austria 76
ZA - Sudafrica 76
ID - Indonesia 67
PK - Pakistan 67
BE - Belgio 59
ES - Italia 59
PH - Filippine 49
EC - Ecuador 44
CO - Colombia 42
SA - Arabia Saudita 36
VE - Venezuela 31
RO - Romania 29
KE - Kenya 28
LT - Lituania 28
UZ - Uzbekistan 28
CL - Cile 22
MY - Malesia 21
MA - Marocco 19
CZ - Repubblica Ceca 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
IR - Iran 13
PY - Paraguay 13
AZ - Azerbaigian 12
CH - Svizzera 12
JM - Giamaica 12
NP - Nepal 12
TH - Thailandia 12
UY - Uruguay 11
KZ - Kazakistan 10
DZ - Algeria 8
LB - Libano 8
NZ - Nuova Zelanda 8
BO - Bolivia 7
CR - Costa Rica 7
SI - Slovenia 7
AU - Australia 6
HN - Honduras 6
PS - Palestinian Territory 6
PT - Portogallo 6
SN - Senegal 6
NI - Nicaragua 5
QA - Qatar 5
SY - Repubblica araba siriana 5
TW - Taiwan 5
AL - Albania 4
DO - Repubblica Dominicana 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
BH - Bahrain 2
BW - Botswana 2
CY - Cipro 2
EE - Estonia 2
GA - Gabon 2
GT - Guatemala 2
HR - Croazia 2
Totale 40.844
Città #
Ann Arbor 4.104
Ashburn 1.718
Singapore 1.689
Woodbridge 1.564
Hong Kong 1.064
Fairfield 1.020
Frankfurt am Main 1.004
Kraków 974
Houston 950
Chandler 927
Dublin 757
Jacksonville 756
Milan 749
San Jose 716
Toronto 699
Wilmington 649
Dearborn 428
Seattle 395
New York 364
Santa Clara 347
Cambridge 324
Beijing 310
Princeton 276
Los Angeles 252
Council Bluffs 247
Ho Chi Minh City 236
Dallas 224
Chicago 212
Nanjing 210
Hanoi 198
The Dalles 196
Dong Ket 179
Shanghai 168
Hefei 166
Altamura 132
Lauterbourg 127
Lachine 126
Lawrence 121
Rome 118
Seoul 114
Boardman 113
Hangzhou 106
Buffalo 102
São Paulo 82
Guangzhou 77
Helsinki 77
Moscow 76
Orem 72
Nanchang 71
Ottawa 69
Columbus 63
San Diego 63
Vienna 61
Shenyang 56
Warsaw 54
Tokyo 53
Andover 52
North Kansas City 50
Tianjin 48
Brussels 47
Changsha 47
Montreal 42
Brooklyn 41
Denver 41
Da Nang 39
Jinan 39
Johannesburg 39
Fremont 38
Hebei 38
Montréal 38
Phoenix 38
Kunming 37
Zhengzhou 37
Chennai 36
Manchester 32
Baghdad 31
Haiphong 31
London 31
Jakarta 30
Kocaeli 30
Washington 30
Boston 29
Falls Church 28
Mountain View 28
Atlanta 27
Norwalk 27
Jiaxing 26
New Delhi 25
Salt Lake City 25
Tashkent 25
Munich 24
Nuremberg 24
Rio de Janeiro 23
Stockholm 23
Amsterdam 22
Auburn Hills 22
Dhaka 22
Elk Grove Village 22
Nairobi 22
San Francisco 22
Totale 27.433
Nome #
Selective cytotoxicity of a bicyclic Ras inhibitor in cancer cells expressing K-RasG13D 759
RalGPS2 is involved in tunneling nanotubes formation in 5637 bladder cancer cells 699
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 666
Glucose-derived Ras pathway inhibitors: evidence of Ras-ligand binding and Ras-GEF (Cdc25) interaction inhibition 647
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 602
Detection of cAMP and of PKA activity in Saccharomyces cerevisiae single cells using Fluorescence Resonance Energy Transfer (FRET) probes 554
Involvement of Aif1 in apoptosis triggered by lack of Hxk2 in the yeast Saccharomyces cerevisiae 547
Hypotonic stress-induced calcium signaling in Saccharomyces cerevisiae involves TRP-like transporters on the endoplasmic reticulum membrane 539
Sugar-derived Ras inhibitors: Group epitope mapping by NMR spectroscopy and biological evaluation 538
Design and characterisation of a new class of inhibitors of Ras activation 536
Antagonism between salicylate and the cAMP signal controls yeast cell survival and growth recovery from quiescence 534
Dynamic of VE-cadherin-mediated spermatid–Sertoli cell contacts in the mouse seminiferous epithelium 530
The deubiquitinating enzyme UBPy/USP8 interacts with TrkA and inhibits neuronal differentiation in PC12 cells 526
Design, Synthesis and Biological Evaluation of Levoglucosenone-derived Ras Activation Inhibitors 522
Design, synthesis and biological evaluation of sugar-derived Ras inhibitors 507
Live-cell imaging of endogenous Ras-GTP shows predominant Ras activation at the plasma membrane and in the nucleus in Saccharomyces cerevisiae 483
Studies on the mechanism of action of a new class of inhibitors of Ras activation 471
Multi-level approach for the identification of structure-function relationships in neurofibromin type I protein 470
The transcription factor Swi4 is target for PKA regulation of cell size at the G1 to S transition in Saccharomyces cerevisiae 434
Guidelines and recommendations on yeast cell death nomenclature 422
Functional analysis of RalgPS2, a murine guanine nucleotide exchange factor for RalA GTPase 417
Lack of SNF1 induces localization of active Ras in mitochondria and triggers apoptosis in the yeast Saccharomyces cerevisiae 413
The budding yeast RasGEF Cdc25 reveals an unexpected nuclear localization 410
Functional coupling of the mammalian EGF receptor to the Ras/cAMP pathway in the yeast Saccharomyces cerevisiae 390
Glucose-induced calcium influx in budding yeast involves a novel calcium transport system and can activate calcineurin 380
The role of feedback control mechanisms on the establishment of oscillatory regimes in the Ras/cAMP/PKA pathway in S. cerevisiae 378
The PH-PxxP domain of RalGPS2 promotes PC12 cells differentiation acting as a dominant negative for RalA GTPase activation 376
Localization of Ras signaling complex in budding yeast 376
In S. cerevisiae hydroxycitric acid antagonizes chronological aging and apoptosis regardless of citrate lyase 376
RalGPS2 interacts with AKT and PDK1 promoting tunneling nanotubes formation in bladder cancer and kidney cells microenvironment 376
Methods to study the Ras2 protein activation state and the subcellular localization of Ras-GTP in saccharomyces cerevisiae 372
Peptide-nanoparticle ligation mediated by cutinase fusion for the development of cancer cell-targeted nanoconjugates 372
Role of RalGPS2, a new possible oncogene, in tunneling nanotubes formation 365
The N-terminal region of the Saccharomyces cerevisiae RasGEF Cdc25 is required for nutrient-dependent cell-size regulation 361
Nuclear Ras2-GTP Controls Invasive Growth in Saccharomyces cerevisiae 358
The overexpression of the 3' terminal region of the CDC25 gene of Saccharomyces cerevisiae causes growth inhibition and alteration of purine nucleotides pools 353
Lack of HXK2 induces localization of active Ras in mitochondria and triggers apoptosis in the yeast Saccharomyces cerevisiae 338
PKA-dependent regulation of Cdc25 RasGEF localization in budding yeast 326
Activation of amyloid precursor protein processing by growth factors is dependent on Ras GTPase activity 325
Recombinant human nerve growth factor with a marked activity in vitro and in vivo 322
Flow-cytometry and cell-cycle kinetics in continuous and fed-batch fermentations of budding yeast 315
Functional studies on Ira proteins, the neurofibromin homologs in yeast 312
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 311
Characterization and properties of dominant-negative mutants of the ras specific guanine nucleotide exchange factor CDC25Mm 306
3-Nitrocoumarin is an efficient inhibitor of budding yeast phospholipase-C 306
Simulation of the Ras/cAMP/PKA pathway in budding yeast highlights the establishment of stable oscillatory states 298
Characterization of the role of RalGPS2, a RalA GEF, in transformed and cancer cells 298
Evidence for inositol triphosphate as a second messenger for glucose-induced calcium signalling in budding yeast 297
Role of RalGPS2, a new possible oncogene, in trasformed and cancer cells 297
Active Ras2 in mitochondria promotes regulated cell death in a cAMP/PKA pathway-dependent manner in budding yeast 294
Novel role for known and unknown calcium transport involved proteins in Saccharomyces cerevisiae 293
Identification of different daughter and parent subpopulations in an asynchronously growing Saccharomyces cerevisiae population 289
Yeast as a model for Ras signalling 285
Measurement of calcium uptake in yeast using 45Ca 284
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 279
A new nerve growth factor-mimetic peptide active on neuropathic pain in rats 279
Involvement of CDC25Mm/Ras-GRF1-dependent signaling in the control of neuronal excitability 277
Analysis of the gene expression profile of mouse male meiotic germ cells 276
Cloning and characterization of mouse UBPy, a deubiquitinating enzyme that interacts with the Ras guanine nucleotide exchange factor CDC25(Mm)/Ras-GRF1 276
Chromosome separation and exit from mitosis in budding yeast: Dependence on growth revealed by cAMP-mediated inhibition 275
Monitoring yeast intracellular ca2+ levels using an in vivo bioluminescence assay 273
Whi2p links nutritional sensing to actin dependent Ras/cAMP/PKA regulation and apoptosis in yeast 271
Ubiquitin Specific Peptidase 8 271
The overexpression of the CDC25 gene of Saccharomyces cerevisiae causes a derepression of GAL system and an increase of GAL4 transcription 269
The minimal active domain of the mouse Ras exchange factor CDC25Mm 267
Macromolecular syntheses in the cell cycle mutant cdc25 of budding yeast 267
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 266
Ptdlns(4,5)P2 and phospholipase C-independent lns(1,4,5)P3 signals induced by a nitrogen source in nitrogen-starved yeast cells 265
Lack of HXK2 Induces Localization of Active Ras in Mitochondria and Triggers Apoptosis in the Yeast Saccharomyces cerevisiae 264
The Ras Guanine Nucleotide Exchange Factor CDC25Mm Is Present at the Synaptic Junction 263
Calcium signaling and sugar-induced activation of plasma membrane H+-ATPase in Saccharomyces cerevisiae cells 263
Fast detection of PKA activity in Saccharomyces cerevisiae cell population using AKAR fluorescence resonance energy transfer probes 263
The PLC1 encoded phospholipase C in the yeast Saccharomyces cerevisiae is essential for glucose-induced phosphatidylinositol turnover and activation of plasma membrane H+-ATPase 260
Analysis of the secondary structure of the catalytic domain of mouse Ras exchange factor CDC25(Mm) 258
Molecular cloning of a gene involved in glucose sensing in the yeast Saccharomyces cerevisiae 257
Activation state of the Ras2 protein and glucose-induced signalling in Saccharomyces cerevisiae 255
Monitoring Ca2+ Signaling in Yeast 251
The maize (Zea mays) b-32 protein shows RIP activity in yeast cells 251
Role of guanine nucleotides in the regulation of the Ras/cAMP pathway in Saccharomyces cerevisiae 248
Cloning by functional complementation of a mouse cDNA encoding a homologue of CDC25, a Saccharomyces cerevisiae RAS activator 247
LACTOSE WHEY UTILIZATION AND ETHANOL-PRODUCTION BY TRANSFORMED SACCHAROMYCES-CEREVISIAE CELLS 247
INVOLVEMENT OF A CELL-SIZE CONTROL MECHANISM IN THE INDUCTION AND MAINTENANCE OF OSCILLATIONS IN CONTINUOUS CULTURES OF BUDDING YEAST 247
The large N-terminal domain of Cdc25 protein of the yeast S. cerevisiae is required for glucose-induced Ras2 activation. 246
ENHANCED EXPRESSION OF HETEROLOGOUS PROTEINS BY THE USE OF A SUPERINDUCIBLE VECTOR IN BUDDING YEAST 246
Production of lactic acid from engineered Saccharomyces cerevisiae cells 242
DEVELOPMENT OF A PH-CONTROLLED FED-BATCH SYSTEM FOR BUDDING YEAST 242
Total cellular Ca2+ measurements in yeast using flame photometry 242
Efficient production of recombinant DNA proteins in Saccharomyces cerevisiae by controlled high‐cell‐density fermentation 240
PH-PxxP domain of RalGPS2 is a dominant negative for the RalA activation in PC12 cells 236
Cell cycle analysis in a human cell line (EUE cells) 235
Expression of high levels of human tissue plasminogen activator in yeast under the control of an inducible GAL promoter 233
Saccharomyces cerevisiae Cdc25: a still puzzling GEF 232
Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H(+)-ATPase in the yeast Saccharomyces cerevisiae. 231
Monitoring cyclic-AMP changes in a single yeast cell 231
Flow‐Cytometric Determination of the Respiratory Activity in Growing Saccharomyces cerevisiae Populations 230
Heterologous gene expression in continuous cultures of budding yeast 228
Towards a yeast cell cycle hybrid model: A new experimental model to study the link between PKA activity and cello cycle in budding yeast 227
Protein and cell volume distributions during the production of beta-galactosidase in batch cultures of Kluyveromyces lactis 223
Glucose regulation of calcium signalling in S. cerevisiae 221
Failure of acrosomogenesis in germ cells of the wobbler mutant reflects impaired vesicle trafficking 221
Totale 34.146
Categoria #
all - tutte 121.139
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 121.139


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.572 0 282 321 284 154 222 220 145 171 199 215 359
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
2026/2027574 219 355 0 0 0 0 0 0 0 0 0 0
Totale 41.449