IRIS
CAMONI, LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 18.698
EU - Europa 3.259
AS - Asia 2.295
SA - Sud America 364
Continente sconosciuto - Info sul continente non disponibili 224
AF - Africa 54
OC - Oceania 6
Totale 24.900
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Nazione #
US - Stati Uniti d'America 18.559
IT - Italia 1.001
SG - Singapore 993
DE - Germania 759
CN - Cina 458
RU - Federazione Russa 349
BR - Brasile 278
HK - Hong Kong 230
UA - Ucraina 226
GB - Regno Unito 218
VN - Vietnam 181
IE - Irlanda 164
FR - Francia 133
SE - Svezia 115
JP - Giappone 100
BD - Bangladesh 83
FI - Finlandia 74
CA - Canada 67
IN - India 58
ES - Italia 57
KR - Corea 51
ID - Indonesia 34
NL - Olanda 33
PL - Polonia 28
CH - Svizzera 23
AR - Argentina 22
BE - Belgio 21
MX - Messico 21
ZA - Sudafrica 18
CO - Colombia 16
TR - Turchia 16
EC - Ecuador 14
CL - Cile 12
IQ - Iraq 12
JM - Giamaica 12
CZ - Repubblica Ceca 11
PK - Pakistan 11
AT - Austria 10
CR - Costa Rica 9
MA - Marocco 9
UZ - Uzbekistan 9
PH - Filippine 8
PT - Portogallo 8
VE - Venezuela 8
KE - Kenya 7
LT - Lituania 7
GR - Grecia 6
GT - Guatemala 6
IL - Israele 6
MY - Malesia 6
NP - Nepal 6
EU - Europa 5
HN - Honduras 5
UY - Uruguay 5
AU - Australia 4
DO - Repubblica Dominicana 4
JO - Giordania 4
PE - Perù 4
AZ - Azerbaigian 3
BB - Barbados 3
BO - Bolivia 3
DZ - Algeria 3
EG - Egitto 3
IR - Iran 3
NG - Nigeria 3
SA - Arabia Saudita 3
SC - Seychelles 3
SV - El Salvador 3
TN - Tunisia 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
CI - Costa d'Avorio 2
CY - Cipro 2
DK - Danimarca 2
EE - Estonia 2
GA - Gabon 2
KG - Kirghizistan 2
KH - Cambogia 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
PY - Paraguay 2
RO - Romania 2
RS - Serbia 2
SM - San Marino 2
TH - Thailandia 2
XK - ???statistics.table.value.countryCode.XK??? 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AG - Antigua e Barbuda 1
AL - Albania 1
BG - Bulgaria 1
GE - Georgia 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LK - Sri Lanka 1
MD - Moldavia 1
ML - Mali 1
Totale 24.677
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Città #
Woodbridge 4.815
Wilmington 4.176
Houston 4.062
Ashburn 613
Singapore 611
Fairfield 411
San Jose 390
Ann Arbor 375
Rome 268
Chandler 243
Hong Kong 228
Jacksonville 212
Seattle 179
Council Bluffs 165
Dublin 156
Beijing 154
New York 150
Dearborn 135
Cambridge 123
Medford 108
Los Angeles 99
Tokyo 89
Santa Clara 88
The Dalles 80
Dallas 66
Buffalo 53
Lawrence 52
Ho Chi Minh City 50
Hanoi 48
Milan 42
Moscow 42
Mülheim 42
North Bergen 35
São Paulo 29
Lauterbourg 28
Munich 25
Bologna 24
Menlo Park 24
Naples 23
Chicago 22
Warsaw 22
Boardman 21
Helsinki 20
London 20
San Diego 20
Orem 19
Atlanta 17
Denver 17
Guangzhou 17
Nuremberg 16
San Mateo 16
Shanghai 16
Zhengzhou 16
Chennai 15
Redwood City 15
Stockholm 15
Verona 15
Florence 14
Fribourg 14
Hefei 14
Jakarta 14
Turin 14
Brooklyn 13
Falls Church 13
Johannesburg 13
Manchester 13
Rio de Janeiro 13
Toronto 13
Montreal 12
Battipaglia 11
Brasília 11
Brussels 11
Delhi 11
Washington 11
Detroit 10
Frankfurt am Main 10
Mexico City 10
Mountain View 10
Perugia 10
Philadelphia 10
Poplar 10
University Park 10
Valencia 10
Changsha 9
Haiphong 9
Nanjing 9
Phoenix 9
San Pietro Viminario 9
Bari 8
Brno 8
Chengdu 8
Curitiba 8
Kunming 8
Las Vegas 8
Norwalk 8
Olot 8
Redondo Beach 8
Salt Lake City 8
Tashkent 8
Tübingen 8
Totale 19.278
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Nome #
Fotosintesi 816
Cold stress affects H+-ATPase and phospholipase D activity in Arabidopsis 590
Fusicoccin: phytotoxin or molecular signal? 563
Tyrosine phosphorylation inhibits the interaction of 14-3-3 proteins with the plant plasma membrane H+-ATPase 529
The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins 516
Binding of phosphatidic acid to 14-3-3 proteins hampers their ability to activate the plant plasma membrane H(+) -ATPase 512
14-3-3 proteins activate a plant calcium-dependent protein kinase (CDPK) 507
Ophiobolin a induces autophagy and activates the mitochondrial pathway of apoptosis in human melanoma cells 507
ZmMPK6, a novel maize MAP kinase that interacts with 14-3-3 proteins 506
Polyamines as physiological regulators of 14-3-3 interaction with the plant plasma membrane H+-ATPase 496
The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins 480
Phosphorylation-dependent interaction between plant plasma membrane H+- ATPase and 14-3-3 proteins 474
The plasma membrane H+-ATPase from maize roots is phosphorylated in the C-terminal domain by a calcium-dependent protein kinase 470
Pseudomonas syringae pv. syringae phytotoxins reversibly inhibit the plasma membrane H+-ATPase and disrupt unilamellar liposomes 465
Fusicoccin: Phytotoxin or molecular signal? 465
The phytotoxin fusicoccin promotes platelet aggregation via 14-3-3-glycoprotein Ib-IX-V interaction 464
Effect of polyamines on the interaction of 14-3-3 proteins with the H+-ATPase 463
The Maize Root Plasma Membrane H+-ATPase is Regulated by a Sugar-induced Transduction Pathway 462
From cytosol to organelles: 14-3-3 proteins as multifunctional regulators of plant cell 460
Corpeptins, new bioactive lipodepsipeptides from cultures of Pseudomonas corrugata 459
Adenosine 5 '-monophosphate inhibits the association of 14-3-3 proteins with the plant plasma membrane H+-ATPase 458
The phytotoxin fusicoccin, a selective stabilizer of 14-3-3 interactions? 456
Mutational analysis of the interaction between 14-3-3 proteins and plant plasma membrane H+-ATPase 455
14-3-3-mediated activation of plasma membrane H+-ATPase is regulated by a sugar-sensing pathway 453
Syringopeptins, Pseudomonas syringae pv. syringae phytotoxins, resemble syringomycin in closing stomata 449
Role of the C-terminal domain of 14-3-3 proteins in the interaction with the H+-ATPase 445
Fungal phytotoxin fusicoccin for the treatmant and diagnosis of coagulation-correlated pathologies. 440
Studies on the effect of syringomycin and syringopeptins on the functions of plant mitochondria 434
A new syringopeptin produced by a Pseudomonas syringae strain from laurel 430
Biological activities of pseudomycin A, a lipodepsinonapeptide from Pseudomonas syringae MSU 16H 419
Interaction studies of the arabidopsis 14-3-3 isoforms GF14-omega and GF14-epsilon with the plasma membrane H+-atpase 418
The fungal phytotoxin fusicoccin for the treatment and diagnosis of coagulation-correlated pathologies 418
Role of 14-3-3 proteins in the interaction with the plasma membrane H+-ATPase. 416
La fusicoccina: da fitotossina a farmaco 416
Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase 414
Toxins of Pseudomonas syringae pv. syringae affect H+-transport across the plasma membrane of maize 413
Effect of syringomycin-E and syringopeptins on isolated plant mitochondria 400
Structure of fuscopeptins, phytotoxic metabolites of Pseudomonas fuscovaginae 398
Lipodepsipeptides from Pseudomonas syringae pv. syringae 395
The phytotoxin fusicoccin differently regulates 14-3-3 proteins association to mode III targets. 389
From plant to human physiology: role of the phytotoxin fusicoccin in the platelet aggregation process 382
Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase 382
Spodoptera littoralis oral secretions inhibit the activity of Phaseolus lunatus plasma membrane H+-ATPase 353
Molecular dissection of 14-3-3 proteins interaction with the plant plasma membrane H+-ATPase 338
Overexpression of 14-3-3 proteins enhances cold tolerance and increases levels of stress-responsive proteins of Arabidopsis plants 314
14-3-3 Proteins in Plant Hormone Signaling: Doing Several Things at Once 310
From plant physiology to pharmacology: fusicoccin leaves the leaves 288
The Surprising Story of Fusicoccin: A Wilt-Inducing Phytotoxin, a Tool in Plant Physiology and a 14-3-3-Targeted Drug 250
A Biostimulant based on a brown alga (Ecklonia maxima) and yeast extract confers resistance toward Pseudomonas syringae pv. tomato DC3000 234
Phenotypical and biochemical characterization of tomato plants treated with triacontanol 185
MicroRNA expression profiles in Moringa oleifera Lam: seedlings at different growth conditions 181
The Salt Tolerance Related Protein (STRP) Mediates Cold Stress Responses and Abscisic Acid Signalling in Arabidopsis thaliana 174
Glucose availability dictates the fate of human melanoma cells treated with Ophiobolin A 172
Borate and phosphite treatments of potato plants (Solanum tuberosum L.) as a proof of concept to reinforce the cell wall structure and reduce starch digestibility 168
Phenotypical and biochemical characterization of tomato plants treated with triacontanol 159
Exposure to Moringa oleifera microRNAs induces proteomic changes linked to tumorigenesis and epithelial-mesenchymal transition in HeLa cells 157
Salt Tolerance-Related Protein (STRP): a new player involved in cold and salt stress responses in Arabidopsis thaliana. 127
14-3-3 proteins and cold stress: a possible novel mechanism involving 14-3-3 regulation of plasma membrane H+-ATPase and Phospholipase D 121
The Salt Tolerance-Related Protein (STRP) Is a Positive Regulator of the Response to Salt Stress in Arabidopsis thaliana 115
14-3-3 proteins and the plasma membrane H+-ATPase are involved in maize (Zea mays) magnetic induction 114
14-3-3ε acts as a negative regulator of the response of Arabidopsis thaliana to Pst DC3000 107
Role of Salt Tolerance-Related Protein (STRP) in salt stress responses in Arabidopsis thaliana 104
Biochemical characterization of Salt Tolerance-Related Protein (STRP): a new protein involved in cold stress in A. thaliana 99
Bridging model systems and crop improvement: expression of the Arabidopsis Salt ToleranceRelated Protein (STRP) enhances cold tolerance in tomato 98
A Biostimulant Based on Ecklonia maxima and Yeast Extract Increases the Resistance of Tomato Plants Toward Pseudomonas syringae pv. tomato DC3000 96
Characterization of Salt Tolerance-Related Protein (STRP) of Arabidopsis thaliana, a new player in cold stress responses. 93
14-3-3 proteins are involved in the plant response to plant pathogens 89
Specificity of ε and non-ε isoforms of Arabidopsis 14-3-3 proteins towards the H+-ATPase and other targets 86
The Arabidopsis Salt Tolerant Related Protein (STRP) is involved Abscisic Acid signaling and biosynthesis 83
Salt Tolerance-Related Protein (STRP): a new player involved in cold stress response in Arabidopsis thaliana 83
Salt Tolerance-Related Protein: a new protein involved in response to cold stress in Arabidopsis thaliana. 81
Salt Tolerance-Related Protein: a new protein involved in plant adaptation to low temperatures. 73
The Emerging Role of the Salt Tolerance-Related Protein in the Abiotic Stress Response of Arabidopsis thaliana 69
STRP, a novel Arabidopsis protein with a protective role against abiotic stresses 68
Salt Tolerance-Related Protein (STRP): a new player involved in cold stress response in Arabidopsis thaliana 67
Beyond abiotic stresses: the Salt Tolerance-Related Protein (STRP) confers enhanced protection against Pseudomonas syringae pv. tomato (Pst) DC3000 in Arabidopsis thaliana 67
Role of the Salt Tolerance-Related Protein (STRP) in the responses of Arabidopsis thaliana to infection by Pseudomonas syringae pv. tomato DC3000 65
Sex-Related Differences in Physiological and Biochemical Responses of Populus nigra to Bifunctionalized Silver Nanoparticles and Silver Ions Exposure In Vitro 61
Mechanism of action of pseudomycins 53
Flagellin recognition triggers zinc mobilization in Arabidopsis thaliana as a response to Salmonella Typhimurium invasion 52
Flagellin-driven zinc redistribution as a plant immune strategy against Salmonella Typhimurium 33
Graphene nanomaterials and copper co-exposure in Populus nigra L.: ultrastructural, biochemical, and nutritional impact under in vitro conditions 29
Totale 24.900
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Categoria #
all - tutte 59.324
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 59.324
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022504 0 0 0 0 29 69 31 28 76 74 38 159
2022/2023907 78 37 29 101 78 178 59 64 77 19 155 32
2023/2024563 39 22 31 25 55 150 15 39 29 17 47 94
2024/20251.529 86 312 164 100 42 113 141 69 130 116 122 134
2025/20263.402 309 135 301 410 291 148 468 317 342 319 190 172
2026/20271.444 270 193 587 381 13 0 0 0 0 0 0 0
Totale 24.900