ADUCCI, PATRIZIA
 Distribuzione geografica
Continente #
NA - Nord America 26.335
EU - Europa 5.566
AS - Asia 1.878
SA - Sud America 350
AF - Africa 23
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 5
Totale 34.166
Nazione #
US - Stati Uniti d'America 26.267
IT - Italia 2.168
DE - Germania 1.447
SG - Singapore 900
CN - Cina 448
UA - Ucraina 422
RU - Federazione Russa 291
GB - Regno Unito 289
BR - Brasile 288
SE - Svezia 253
IE - Irlanda 231
HK - Hong Kong 217
FR - Francia 167
FI - Finlandia 93
KR - Corea 78
VN - Vietnam 65
NL - Olanda 59
IN - India 39
CA - Canada 38
ES - Italia 38
ID - Indonesia 27
JP - Giappone 26
EC - Ecuador 23
PL - Polonia 22
BD - Bangladesh 19
MX - Messico 19
BE - Belgio 18
AT - Austria 12
CH - Svizzera 11
AR - Argentina 9
RO - Romania 9
PE - Perù 8
PT - Portogallo 8
CO - Colombia 6
KZ - Kazakistan 6
MA - Marocco 6
TR - Turchia 6
UZ - Uzbekistan 6
VE - Venezuela 6
ZA - Sudafrica 6
BG - Bulgaria 5
CZ - Repubblica Ceca 5
EU - Europa 5
IL - Israele 5
PH - Filippine 5
AU - Australia 4
AZ - Azerbaigian 4
IQ - Iraq 4
UY - Uruguay 4
AL - Albania 3
CL - Cile 3
EG - Egitto 3
GR - Grecia 3
JO - Giordania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
GT - Guatemala 2
KE - Kenya 2
KW - Kuwait 2
LT - Lituania 2
NO - Norvegia 2
NP - Nepal 2
OM - Oman 2
PA - Panama 2
PK - Pakistan 2
SK - Slovacchia (Repubblica Slovacca) 2
SM - San Marino 2
TN - Tunisia 2
XK - ???statistics.table.value.countryCode.XK??? 2
AG - Antigua e Barbuda 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
CR - Costa Rica 1
DK - Danimarca 1
DM - Dominica 1
GE - Georgia 1
HN - Honduras 1
HU - Ungheria 1
IR - Iran 1
KG - Kirghizistan 1
KH - Cambogia 1
LB - Libano 1
LK - Sri Lanka 1
LY - Libia 1
MC - Monaco 1
ML - Mali 1
MY - Malesia 1
MZ - Mozambico 1
NZ - Nuova Zelanda 1
PY - Paraguay 1
SA - Arabia Saudita 1
SC - Seychelles 1
TM - Turkmenistan 1
TW - Taiwan 1
Totale 34.166
Città #
Woodbridge 8.270
Wilmington 7.150
Houston 5.758
Ann Arbor 629
Fairfield 609
Singapore 470
Ashburn 445
Chandler 373
Jacksonville 362
Rome 348
Seattle 281
Dublin 225
Hong Kong 215
Cambridge 213
Beijing 203
Medford 165
Dearborn 157
Milan 120
New York 100
Santa Clara 88
Lawrence 79
Los Angeles 78
Dallas 77
The Dalles 67
Mülheim 66
Bologna 50
Buffalo 50
Council Bluffs 43
Menlo Park 42
Zhengzhou 36
Boardman 35
Munich 30
Naples 30
Turin 29
Redwood City 26
Ho Chi Minh City 24
San Diego 24
Florence 23
San Mateo 23
Palermo 22
Verona 22
Moscow 21
Shanghai 20
Falls Church 19
Napoli 19
Tokyo 19
University Park 19
Guangzhou 18
Mountain View 18
São Paulo 18
Hanoi 17
Toronto 17
Bari 16
Groningen 16
Padova 16
Rio de Janeiro 16
Torino 15
Brussels 14
Hefei 14
Salerno 14
Norwalk 13
Jakarta 12
Kunming 12
London 12
Battipaglia 11
Cagliari 11
Helsinki 11
Perugia 11
Pescara 11
Redondo Beach 11
Stockholm 11
Atlanta 10
Catania 10
Quito 10
Belo Horizonte 9
Montreal 9
Nanjing 9
Parma 9
Warsaw 9
Campinas 8
Como 8
Foggia 8
Guayaquil 8
Leawood 8
Modena 8
Olot 8
Phoenix 8
Poplar 8
Colorado Springs 7
Columbus 7
Morcone 7
Nuremberg 7
Orem 7
Prato 7
Reggio Calabria 7
Saint Petersburg 7
Siena 7
Vicenza 7
Vienna 7
Almaty 6
Totale 27.739
Nome #
Botanica: fondamenti di biologia delle piante 2.199
Fotosintesi 758
Phospholipase A2 affects the activity of fusicoccin receptors 751
Cold stress affects H+-ATPase and phospholipase D activity in Arabidopsis 542
Anti-proliferative effect of Rosmarinus officinalis L. extract on human melanoma A375 cells 540
Fusicoccin: phytotoxin or molecular signal? 531
Tyrosine phosphorylation inhibits the interaction of 14-3-3 proteins with the plant plasma membrane H+-ATPase 497
The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins 483
The 30-kilodalton protein present in purified fusicoccin receptor preparations is a 14-3-3-like protein 476
Binding of phosphatidic acid to 14-3-3 proteins hampers their ability to activate the plant plasma membrane H(+) -ATPase 474
ZmMPK6, a novel maize MAP kinase that interacts with 14-3-3 proteins 472
Regulation of CU, ZNSOD by metals in S-Cereivisiae and Zea-Mays 470
Ophiobolin a induces autophagy and activates the mitochondrial pathway of apoptosis in human melanoma cells 470
Cercospora beticola toxin: a reassessment of some in vitro effects 466
Polyamines as physiological regulators of 14-3-3 interaction with the plant plasma membrane H+-ATPase 464
Purification and photoaffinity labeling of fusicoccin receptors from maize 455
The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins 453
An improved Scatchard analysis of fusicoccin binding to maize coleoptile membranes. 446
Incubation of corn coleoptiles with auxin enhances in-vitro fusicoccin binding 444
Phosphorylation-dependent interaction between plant plasma membrane H+- ATPase and 14-3-3 proteins 438
Inactivation of solubilised fusicoccin-binding sites by endogenous plant hydrolases 437
The plasma membrane H+-ATPase from maize roots is phosphorylated in the C-terminal domain by a calcium-dependent protein kinase 436
Fusicoccin and its receptors - Perception and signal transduction 435
Pseudomonas syringae pv. syringae phytotoxins reversibly inhibit the plasma membrane H+-ATPase and disrupt unilamellar liposomes 435
The Maize Root Plasma Membrane H+-ATPase is Regulated by a Sugar-induced Transduction Pathway 435
On the reported occurrence of a fusicoccin conjugate in maize cobs. 434
The phytotoxin fusicoccin promotes platelet aggregation via 14-3-3-glycoprotein Ib-IX-V interaction 434
Fusicoccin effect on the in vitro interaction between plant 14-3-3 proteins and plasma membrane H+-ATPase 433
The phytotoxin fusicoccin, a selective stabilizer of 14-3-3 interactions? 433
Mutational analysis of the interaction between 14-3-3 proteins and plant plasma membrane H+-ATPase 430
Fusicoccin: Phytotoxin or molecular signal? 430
Specificity of ε and non-ε isoforms of Arabidopsis 14-3-3 proteins towards the H+-ATPase and other targets. 429
Effect of polyamines on the interaction of 14-3-3 proteins with the H+-ATPase 428
Characterization, functional validation and gene expression patterns of two 14-3-3 isoforms from Vitis vinifera 428
Characterization of ribes nigrum and rosmarinus officinalis food supplements 427
Some properties of a functional reconstituted plasmalemma H+- ATPase activated by fusicoccin. 424
Adenosine 5 '-monophosphate inhibits the association of 14-3-3 proteins with the plant plasma membrane H+-ATPase 423
A new agglutinating activity from wheat flour inhibited by tryptophan 422
From cytosol to organelles: 14-3-3 proteins as multifunctional regulators of plant cell 422
A phosphopeptide corresponding to the cytosolic stretch connecting transmembrane segments 8 and 9 of the plasma membrane H+-ATPase binds 14-3-3 proteins and inhibits fusicoccin induced activation of the H+-ATPase 420
Binding of 14-3-3 protein to the plasma membrane H+-ATPase AHA2 involves the three C-terminal residues Tyr(946)-Thr-Val and requires phosphorylation of Thr(947) 416
Fungal phytotoxin fusicoccin for the treatmant and diagnosis of coagulation-correlated pathologies. 416
A fluorimetric study of the lanthanides binding to concanavalin A 414
Presence of spectrin in untreated Friend erythroleukemic cells. Its accumulation upon treatment of the cells with dimethyl sulfoxide 412
Properties of proteoliposomes containing fusicoccin receptors from maize 411
Role of the C-terminal domain of 14-3-3 proteins in the interaction with the H+-ATPase 410
14-3-3-mediated activation of plasma membrane H+-ATPase is regulated by a sugar-sensing pathway 406
OGM: per saperne di più 399
Role of 14-3-3 proteins in the interaction with the plasma membrane H+-ATPase. 391
A Radioimmunoassay for Fusicoccin 391
Purification and Characterization of Leu-Proteinase, the Leucine Specific Serine Proteinase from Spinach (Spinacia oleracea L.) Leaves 388
Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase 387
Interaction studies of the arabidopsis 14-3-3 isoforms GF14-omega and GF14-epsilon with the plasma membrane H+-atpase 377
The fungal phytotoxin fusicoccin for the treatment and diagnosis of coagulation-correlated pathologies 368
La fusicoccina: da fitotossina a farmaco 366
Binding of the recombinant proteinase inhibitor eglin c, of the soybean Bowman-Birk proteinase inhibitor and of its chymotrypsin and trypsin inhibiting fragments to Leu-proteinase, the leucine specific serine proteinase from spinach (Spinacia oleracea L.) leaves: thermodynamic study 366
Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase 359
From plant to human physiology: role of the phytotoxin fusicoccin in the platelet aggregation process 358
The phytotoxin fusicoccin differently regulates 14-3-3 proteins association to mode III targets. 350
Role of calcium in plant hormone action 349
Papain action at neutral and alkaline pH regions 345
Entrapment into liposomes of fusicoccin binding sites 342
Fusicoccin binding sites: an autoradiographic study 341
Fusicoccin receptors.Evidence for endogenous ligand. 338
Organismi Geneticamente Modificati 331
Interaction of neutral polysaccharides with phosphatidylcholine multilamellar liposomes. Phase transitions studied by the binding of fluorescein-conjugated dextrans 329
Perception and transduction of hormone signals in higher plants. 329
Spodoptera littoralis oral secretions inhibit the activity of Phaseolus lunatus plasma membrane H+-ATPase 327
Esterolytic properties of leucine-proteinase, the leucine-specific serine proteinase from spinach (Spinacia oleracea L.) 325
Energia e Metabolismo: Respirazione (Capitolo 11) 323
Leucyl endopeptidase 317
Molecular dissection of 14-3-3 proteins interaction with the plant plasma membrane H+-ATPase 314
Interaction of neutral polysaccharides with human erythrocyte membrane: involvement of phospholipid bilayer 305
Temperature dependence of intracellular pH in higher plant cells. 31P-Nuclear Magnetic Resonance study on maize root tips. 298
Leucyl endopeptidase 292
Overexpression of 14-3-3 proteins enhances cold tolerance and increases levels of stress-responsive proteins of Arabidopsis plants 276
14-3-3 Proteins in Plant Hormone Signaling: Doing Several Things at Once 260
From plant physiology to pharmacology: fusicoccin leaves the leaves 257
The Salt Tolerance Related Protein (STRP) Mediates Cold Stress Responses and Abscisic Acid Signalling in Arabidopsis thaliana 125
Characterization of Salt Tolerance-Related Protein (STRP) of Arabidopsis thaliana, a new player in cold stress responses. 63
Biochemical characterization of Salt Tolerance-Related Protein (STRP): a new protein involved in cold stress in A. thaliana 62
The Arabidopsis Salt Tolerant Related Protein (STRP) is involved Abscisic Acid signaling and biosynthesis 49
Specificity of ε and non-ε isoforms of Arabidopsis 14-3-3 proteins towards the H+-ATPase and other targets 49
Salt Tolerance-Related Protein: a new protein involved in response to cold stress in Arabidopsis thaliana. 44
Salt Tolerance-Related Protein (STRP): a new player involved in cold stress response in Arabidopsis thaliana 44
Salt Tolerance-Related Protein (STRP): a new player involved in cold stress response in Arabidopsis thaliana 42
Salt Tolerance-Related Protein: a new protein involved in plant adaptation to low temperatures. 39
Characterization of Protein Kinase Activities in Spinach Leaves 7
Immunoaffinity chromatography of fusicoccin 7
The H+-ATPase purified from maize root plasma membranes retains fusicoccin in vivo activation 6
The fungal H+-ATPase from Neurospora crassa reconstituted with fusicoccin receptors senses fusicoccin signal 4
Protein kinase activity in soluble preparations from spinach leaf microsomes 3
Totale 34.351
Categoria #
all - tutte 68.161
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 68.161


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.032 0 0 0 0 0 483 512 456 166 159 193 63
2021/20221.144 37 86 78 87 25 108 63 79 138 127 67 249
2022/20231.417 127 74 35 189 111 271 102 118 152 39 163 36
2023/2024633 57 24 34 42 72 134 38 53 33 27 41 78
2024/20252.052 89 443 235 126 51 165 170 120 259 136 164 94
2025/20261.478 293 165 367 362 229 62 0 0 0 0 0 0
Totale 34.351