TISI, RENATA ANITA
 Distribuzione geografica
Continente #
NA - Nord America 8.107
EU - Europa 5.332
AS - Asia 3.602
SA - Sud America 545
AF - Africa 65
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 2
Totale 17.665
Nazione #
US - Stati Uniti d'America 7.891
IT - Italia 1.378
SG - Singapore 1.145
CN - Cina 1.050
DE - Germania 898
SE - Svezia 518
RU - Federazione Russa 512
HK - Hong Kong 487
BR - Brasile 438
PL - Polonia 438
IE - Irlanda 329
VN - Vietnam 292
GB - Regno Unito 260
FR - Francia 211
UA - Ucraina 201
DK - Danimarca 160
CA - Canada 153
IN - India 135
FI - Finlandia 110
AT - Austria 89
JP - Giappone 86
ID - Indonesia 81
TR - Turchia 69
NL - Olanda 64
MX - Messico 55
KR - Corea 51
AR - Argentina 40
BE - Belgio 40
BD - Bangladesh 39
ES - Italia 39
ZA - Sudafrica 39
TW - Taiwan 33
LT - Lituania 25
EC - Ecuador 23
IQ - Iraq 22
PK - Pakistan 20
CZ - Repubblica Ceca 15
CO - Colombia 14
CL - Cile 11
AU - Australia 10
SA - Arabia Saudita 10
TH - Thailandia 10
JO - Giordania 9
PH - Filippine 9
UZ - Uzbekistan 9
HU - Ungheria 8
CH - Svizzera 7
IR - Iran 7
PE - Perù 7
RO - Romania 7
GR - Grecia 5
IL - Israele 5
KE - Kenya 5
MA - Marocco 5
PY - Paraguay 5
VE - Venezuela 5
AZ - Azerbaigian 4
BG - Bulgaria 4
DZ - Algeria 4
OM - Oman 4
AE - Emirati Arabi Uniti 3
AF - Afghanistan, Repubblica islamica di 3
DO - Repubblica Dominicana 3
EG - Egitto 3
MY - Malesia 3
PT - Portogallo 3
TN - Tunisia 3
AM - Armenia 2
BY - Bielorussia 2
ET - Etiopia 2
EU - Europa 2
HN - Honduras 2
LV - Lettonia 2
MO - Macao, regione amministrativa speciale della Cina 2
NO - Norvegia 2
NP - Nepal 2
PA - Panama 2
PS - Palestinian Territory 2
QA - Qatar 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
UY - Uruguay 2
BH - Bahrain 1
BN - Brunei Darussalam 1
GE - Georgia 1
GT - Guatemala 1
KG - Kirghizistan 1
KH - Cambogia 1
KI - Kiribati 1
KZ - Kazakistan 1
MD - Moldavia 1
MK - Macedonia 1
MT - Malta 1
NZ - Nuova Zelanda 1
RE - Reunion 1
SC - Seychelles 1
Totale 17.665
Città #
Ann Arbor 2.248
Ashburn 708
Singapore 656
Frankfurt am Main 600
Milan 506
Hong Kong 462
Chandler 450
Woodbridge 406
Kraków 390
Wilmington 378
Fairfield 370
Houston 315
Dublin 313
Jacksonville 195
New York 178
Seattle 168
Beijing 167
Santa Clara 142
Dearborn 139
Los Angeles 131
Cambridge 110
Princeton 105
Dallas 103
Nanjing 90
Hefei 86
Dong Ket 83
Shanghai 82
Vienna 78
Jakarta 68
Ho Chi Minh City 67
Rome 62
Altamura 57
Moscow 56
São Paulo 55
Helsinki 51
Tokyo 46
Warsaw 45
Buffalo 44
Lawrence 44
Council Bluffs 41
Munich 41
Brussels 39
Seoul 39
Guangzhou 38
The Dalles 36
Hangzhou 35
Denver 34
Toronto 33
Chicago 32
Hanoi 30
Lachine 29
Andover 28
Montreal 28
Ottawa 27
Boardman 25
Brooklyn 25
Nanchang 25
Fremont 23
Shenyang 23
Tianjin 23
Atlanta 22
San Diego 22
Orem 21
Mexico City 20
Taipei 20
Zhengzhou 20
Columbus 19
Johannesburg 19
Stockholm 18
Changsha 17
London 17
Poplar 17
Chennai 16
Falls Church 16
Hebei 16
Kent 16
Kunming 16
Florence 15
Boston 14
Jinan 14
Mountain View 14
Rio de Janeiro 14
Brescia 13
Desio 13
Huizen 13
Norwalk 13
Nuremberg 13
Phoenix 13
Dhaka 12
Lappeenranta 12
Manchester 12
New Delhi 12
Washington 12
Capralba 11
Edmonton 11
New Taipei City 11
Olomouc 11
Ankara 10
Bergamo 10
Genoa 10
Totale 11.503
Nome #
Calcium homeostasis and signaling in fungi and their relevance for pathogenicity of yeasts and filamentous fungi 696
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 601
The Multi-Level Mechanism of Action of a Pan-Ras Inhibitor Explains its Antiproliferative Activity on Cetuximab-Resistant Cancer Cells 596
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 555
Natural compounds in cancer prevention: effects of coffee extracts and their main polyphenolic component 5-CQA on oncogenic Ras proteins 550
Structure–function relationships of the Mre11 protein in the control of DNA end bridging and processing 526
DNA binding modes influence Rap1 activity in the regulation of telomere length and MRX functions at DNA ends 493
Design and characterisation of a new class of inhibitors of Ras activation 489
The MRX complex regulates Exo1 resection activity by altering DNA end structure 475
The ATP-bound conformation of the Mre11-Rad50 complex is essential for Tel1/ATM activation 460
Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human cancer, affect ROS, calcium homeostasis and mitochondrial permeability transition in yeast 455
Studies on the mechanism of action of a new class of inhibitors of Ras activation 442
Structurally distinct Mre11 domains mediate MRX functions in resection, end-tethering and DNA damage resistance 423
Synthesis, Molecular Modeling and Biological Evaluation of Metabolically Stable Analogues of the Endogenous Fatty Acid Amide Palmitoylethanolamide 414
Hypotonic stress-induced calcium signaling in Saccharomyces cerevisiae involves TRP-like transporters on the endoplasmic reticulum membrane 413
Multi-level approach for the identification of structure-function relationships in neurofibromin type I protein 400
Cannabidiol Antiproliferative Effect in Triple-Negative Breast Cancer MDA-MB-231 Cells Is Modulated by Its Physical State and by IGF-1 398
Functional analysis of RalgPS2, a murine guanine nucleotide exchange factor for RalA GTPase 350
Localization of Ras signaling complex in budding yeast 334
The budding yeast RasGEF Cdc25 reveals an unexpected nuclear localization 333
Glucose-induced calcium influx in budding yeast involves a novel calcium transport system and can activate calcineurin 319
The N-terminal region of the Saccharomyces cerevisiae RasGEF Cdc25 is required for nutrient-dependent cell-size regulation 302
On the propagation of the OH radical produced by Cu-amyloid beta peptide model complexes. Insight from molecular modelling 301
Functional and structural insights into the MRX/MRN complex, a key player in recognition and repair of DNA double-strand breaks 300
AMPK Phosphorylation Is Controlled by Glucose Transport Rate in a PKA-Independent Manner 292
PKA-dependent regulation of Cdc25 RasGEF localization in budding yeast 287
Novel roles for ion transporters in cell death pathways in budding yeast 283
Natural products attenuating biosynthesis, processing, and activity of ras oncoproteins: State of the art and future perspectives 282
Rif2 interaction with Rad50 counteracts Tel1 functions in checkpoint signalling and DNA tethering by releasing Tel1 from MRX binding 276
Functional studies on Ira proteins, the neurofibromin homologs in yeast 258
3-Nitrocoumarin is an efficient inhibitor of budding yeast phospholipase-C 257
Evidence for inositol triphosphate as a second messenger for glucose-induced calcium signalling in budding yeast 248
Modeling Calcium Signaling in S. cerevisiae Highlights the Role and Regulation of the Calmodulin-Calcineurin Pathway in Response to Hypotonic Shock 248
Measurement of calcium uptake in yeast using 45Ca 244
Yeast as a model for Ras signalling 239
Novel role for known and unknown calcium transport involved proteins in Saccharomyces cerevisiae 237
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 234
Sae2 and Rif2 regulate MRX endonuclease activity at DNA double-strand breaks in opposite manners 231
The Ku complex promotes DNA end-bridging and this function is antagonized by Tel1/ATM kinase 230
Functional and molecular insights into the role of Sae2 C-terminus in the activation of MRX endonuclease 225
Ptdlns(4,5)P2 and phospholipase C-independent lns(1,4,5)P3 signals induced by a nitrogen source in nitrogen-starved yeast cells 223
Monitoring yeast intracellular ca2+ levels using an in vivo bioluminescence assay 221
Calcium signaling and sugar-induced activation of plasma membrane H+-ATPase in Saccharomyces cerevisiae cells 220
Total cellular Ca2+ measurements in yeast using flame photometry 212
Monitoring Ca2+ Signaling in Yeast 209
The PLC1 encoded phospholipase C in the yeast Saccharomyces cerevisiae is essential for glucose-induced phosphatidylinositol turnover and activation of plasma membrane H+-ATPase 207
PH-PxxP domain of RalGPS2 is a dominant negative for the RalA activation in PC12 cells 206
Two cancer cancer-related mutations in ATP synthase mitochondrial ATP6 gene impact the ATP synthase dimers formation during permeability transition 202
Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H(+)-ATPase in the yeast Saccharomyces cerevisiae. 194
Saccharomyces cerevisiae Cdc25: a still puzzling GEF 194
The large N-terminal domain of Cdc25 protein of the yeast S. cerevisiae is required for glucose-induced Ras2 activation. 190
Molecular Dynamics Simulations Reveal Structural Interconnections within Sec14-PH Bipartite Domain from Human Neurofibromin 189
Glucose regulation of calcium signalling in S. cerevisiae 188
Dynamic Properties of the DNA Damage Response Mre11/Rad50 Complex 147
Mutations in mitochondrial ATP6 gene encoding subunit of ATP synthase and their impact on cell physiology in yeast S. cerevisiae 141
The Ycx1 protein encoded by the yeast YDL206W gene plays a role in calcium and calcineurin signaling 141
Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA RNP complex formation and telomerase activity 140
Checkpoint activation and recovery: regulation of the 9–1–1 axis by the PP2A phosphatase 130
Stn1 supports Mec1 function in protecting stalled replication forks from degradation 82
Phospholipase C is required for glucose-induced calcium influx in budding yeast 41
Surface functionalization with short PAS-sequence affects H-ferritin nanocage stability 17
Totale 18.190
Categoria #
all - tutte 51.310
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 51.310


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.399 0 0 0 0 0 196 190 168 199 248 151 247
2021/20221.554 150 170 172 169 90 139 92 70 78 111 113 200
2022/20232.082 276 520 229 237 160 282 30 84 131 58 44 31
2023/20241.446 61 52 70 108 145 317 265 104 102 41 49 132
2024/20252.700 167 224 173 149 206 158 202 118 272 404 220 407
2025/20263.746 736 355 479 975 889 312 0 0 0 0 0 0
Totale 18.190