Benvenuti nell'Anagrafe della Ricerca d'Ateneo

TAVLADORAKI, Paraskevi
 Distribuzione geografica
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Continente #
NA - Nord America 7.498
EU - Europa 6.439
AS - Asia 4.622
SA - Sud America 366
AF - Africa 162
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 6
Totale 19.108
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Nazione #
US - Stati Uniti d'America 7.405
CN - Cina 2.117
SG - Singapore 1.460
DK - Danimarca 1.290
GB - Regno Unito 1.273
RU - Federazione Russa 1.236
IT - Italia 729
DE - Germania 530
SE - Svezia 517
VN - Vietnam 405
BR - Brasile 252
FI - Finlandia 216
UA - Ucraina 202
HK - Hong Kong 129
IN - India 103
CI - Costa d'Avorio 96
IE - Irlanda 95
AL - Albania 71
TR - Turchia 71
BD - Bangladesh 67
KR - Corea 63
FR - Francia 61
CA - Canada 45
JP - Giappone 45
AR - Argentina 43
NL - Olanda 38
ES - Italia 32
IQ - Iraq 28
BE - Belgio 27
ID - Indonesia 26
MX - Messico 25
PL - Polonia 25
CZ - Repubblica Ceca 19
CL - Cile 18
ZA - Sudafrica 18
PK - Pakistan 17
EC - Ecuador 15
SN - Senegal 15
CO - Colombia 14
LT - Lituania 14
VE - Venezuela 13
AU - Australia 12
AT - Austria 11
GR - Grecia 11
HU - Ungheria 9
MA - Marocco 8
MY - Malesia 8
NP - Nepal 8
PH - Filippine 8
SA - Arabia Saudita 8
TH - Thailandia 8
UZ - Uzbekistan 8
AE - Emirati Arabi Uniti 7
CH - Svizzera 7
IL - Israele 7
JM - Giamaica 7
EG - Egitto 5
PT - Portogallo 5
MT - Malta 4
PS - Palestinian Territory 4
BO - Bolivia 3
CG - Congo 3
CR - Costa Rica 3
HR - Croazia 3
NZ - Nuova Zelanda 3
PA - Panama 3
PE - Perù 3
PY - Paraguay 3
RO - Romania 3
RS - Serbia 3
TW - Taiwan 3
AM - Armenia 2
DZ - Algeria 2
EE - Estonia 2
ET - Etiopia 2
EU - Europa 2
IR - Iran 2
JO - Giordania 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NG - Nigeria 2
PR - Porto Rico 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
BW - Botswana 1
BZ - Belize 1
CU - Cuba 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
Totale 19.087
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Città #
Southend 1.086
Singapore 746
Woodbridge 716
Ashburn 712
Fairfield 666
Ann Arbor 491
Chandler 490
Wilmington 445
San Jose 420
Rome 414
Houston 344
Beijing 261
Nanjing 259
Seattle 253
Cambridge 223
Dearborn 218
Boardman 217
Dallas 166
Jacksonville 153
Princeton 131
Helsinki 130
Jinan 125
Shenyang 125
Hefei 123
Hong Kong 119
Dong Ket 100
Ho Chi Minh City 99
Dublin 95
Nanchang 87
Hebei 78
Los Angeles 75
Hanoi 74
Plano 74
Redwood City 71
Changsha 70
Moscow 70
Bremen 66
Munich 63
Orem 63
Seoul 55
Tianjin 55
Shanghai 54
Frankfurt am Main 51
The Dalles 51
Izmir 48
New York 47
Jiaxing 41
Kunming 41
Ningbo 41
Tokyo 40
Hangzhou 39
Zhengzhou 39
San Diego 34
Chennai 33
Council Bluffs 32
Guangzhou 32
London 28
Haikou 27
Redmond 26
São Paulo 26
Lanzhou 25
Santa Clara 25
Brussels 24
Columbus 24
Taiyuan 24
Taizhou 24
Orange 23
Montreal 22
Warsaw 22
Milan 20
Brooklyn 19
Mumbai 17
San Mateo 17
Turku 17
Basingstoke 16
Stockholm 16
Altamura 15
Dakar 15
Falls Church 15
Fremont 15
Chicago 14
Fuzhou 14
Jakarta 14
Haiphong 13
Alameda 12
Amsterdam 12
Falkenstein 12
Johannesburg 12
Baghdad 11
Brno 11
Manchester 11
Santiago 11
Verona 11
Yubileyny 11
Buffalo 10
Denver 10
Hillsboro 10
Pune 10
San Francisco 10
Atlanta 9
Totale 11.581
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Nome #
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 351
Plant amine oxidases “on the move”: An update 347
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 338
The members of Arabidopsis thaliana PAO gene family exhibit distinct tissue- and organ-specific expression pattern during seedling growth and flower development 310
The apoplastic copper AMINE OXIDASE1 mediates jasmonic acid-induced protoxylem differentiation in Arabidopsis roots 300
The Arabidopsis polyamine oxidase/dehydrogenase 5 interferes with cytokinin and auxin signaling pathways to control xylem differentiation 293
Cell wall amine oxidases: new players in root xylem differentiation under stress conditions 290
Functional diversity inside the Arabidopsis polyamine oxidase gene family 274
Cell Wall Amine Oxidases: New Players in Root Xylem Differentiation under Stress Conditions 270
The structure of maize polyamine oxidase K300M mutant in complex with the natural substrates provides a snapshot of the catalytic mechanism of polyamine oxidation 263
Caratterizzazione dei geni codificanti la poliamminossidasi in mais ed orzo 260
AtCuAOδ participates in abscisic acid-induced stomatal closure in Arabidopsis. 258
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana 257
Polyamine catabolism: target for antiproliferative therapies in animals and stress tolerance strategies in plants 250
An Arabidopsis polyamine oxidase undergoing proteasomal regulation 250
A single-chain antibody fragment is functionally expressed in the cytoplasm of both Escherichia coli and transgenic plants 249
POLYAMINE OXIDASE2 of Arabidopsis contributes to ABA mediated plant developmental processes. 248
An Arabidopsis copper amine oxidase is involved in jasmonate-induced root xylem differentiation 243
Ectopic expression of maize polyamine oxidase and pea copper amine oxidase in the cell wall of tobacco plants 241
The polyamines and their catabolic products are significant players in the turnover of nitrogenous molecules in plants 241
The MeJA-inducible copper amine oxidase AtAO1 is expressed in xylem tissue and guard cells 240
Isolation and characterization of three polyamine oxidase genes from Zea mays 236
Cytotoxic effect induced by maize polyamine oxidase in presence of spermine in human cancer cells. 229
The four lysine-specific histone demethylases of Arabidopsis differentially contribute to the control of flowering time and defence responses. 228
Transgenic plants expressing a functional "Single Chain Fv" antibody are specifically protected from virus attack 228
The copper amine oxidase AtCuAOδ participates in abscisic acid-induced stomatal closure in arabidopsis 226
Copper-containing amine oxidases and FAD-dependent polyamine oxidases are key players in plant tissue differentiation and organ development 224
Innovative processes and treatments to improve the shelf-life, safety and nutritional value of ready-to-eat vegetables. 222
Probing mammalian spermine oxidase enzyme-substrate complex through molecular modeling, site-directed mutagenesis and biochemical characterization 221
Functions of amine oxidases in plant development and defence 220
Isolation and characterization of three polyamine oxidase genes from Zea mays 217
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper-amine oxidase gene family 215
Improving stress tolerance of tomato plants through modification of polyamine metabolism. 214
Age- and Phytochrome- induced changes at the level of the translatable mRNA coding for the LHC-II apoprotein of Phaseolus vulgaris leaves. 213
THE FOUR LYSINE-SPECIFIC HISTONE DEMETHYLASES OF ARABIDOPSIS DIFFERENTIALLY CONTRIBUTE TO THE CONTROL OF FLOWERING TIME AND DEFENCE RESPONSES. 213
Determination of copper amine oxidase activity in plant tissues 209
Biochemical characterization and biotechnological applications of copper amine oxidases and flavin polyamine oxidases 209
Immunotherapy of plant viral diseases 208
FAD-containing polyamine oxidases: a timely challenge for researchers in biochemistry and physiology of plants 207
Inducible expression of maize polyamine oxidase in the nucleus of MCF-7 human breast cancer cells confers sensitivity to etoposide 205
Comparative analysis of the role of the different Arabidopsis polyamine oxidases in plant defense responses to environmental stresses. 205
Maize polyamine oxidase: primary structure from protein and cDNA sequencing 202
Arabidopsis N-acetyltransferase activity 2 preferentially acetylates 1,3-diaminopropane and thialysine 202
Caratterizzazione dei geni codificanti la Poliammino Ossidasi in mais ed orzo 201
Nitrogen flow into regulatory molecules: The case of Polyamines and Polyamine oxidases. 200
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 198
The apoplastic copper amine oxidase AtCuAOβ plays a role in stomatal closure induced by wounding, jasmonate or Microbe Associated Molecular Patterns (MAMPS). 198
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion RID A-4573-2009 193
A new player in jasmonate-mediated stomatal closure: The Arabidopsis Thaliana copper amine oxidase β 193
Involvement of Arabidopsis thaliana Copper Amine Oxidase β in maturation of root protoxylem precursors induced by leaf wounding. 192
Characterization of genes coding for polyamine oxidase from maize and barley 188
Leaf-wounding long-distance signaling targets AtCuAOβ leading to root phenotypic plasticity 188
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana RID A-4573-2009 184
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase 183
Involvement of Arabidopsis Copper Amine Oxidase β in MeJA/wounding-induced stomatal closure. 183
Distinct role of AtCuAOβ- and RBOHD-driven H2O2 production in wound-induced local and systemic leaf-to-leaf and root-to-leaf stomatal closure 182
Isolation of nuclei from plant tissues 182
Plantibodies: Immunomodulation and Immunotherapeutic potential 182
A polyamine oxidase of Solanum lycopersicum controls plant growth, xylem differentiation and drought stress tolerance 180
Functions of amine oxidases in plant development and defence 178
Hydrogen peroxide: the player of polyamine action in development and stress responses 174
Involvement of ACA8/ACA10 in wounding-induced stomatal closure in Arabidopsis 173
A polyamine oxidase controls water-use efficiency in Solanum lycopersicum 172
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion 171
The Arabidopsis polyamine oxidase/dehydrogenase 5 contributes to the cytokinin/auxin interplay controlling xylem differentiation. 171
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper amine oxidase gene family 171
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase RID A-4573-2009 170
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 168
Emerging role of polyamine oxidases in plant development 166
Characterization of Arabidopsis insertional mutants for copper-containing amine oxidases 163
Stress-triggered long-distance communication leads to phenotypic plasticity: The case of the early root protoxylem maturation induced by leaf wounding in arabidopsis 163
Enzyme activity inhibition of the ABA-inducible copper amine oxidase AtCuAOδ reverses most of the ABA-mediated stomatal closure in Arabidopsis 163
Unraveling the regulatory pathway of lysine-specific histone demethylases in plants 162
Characterization of genes coding for Polyamine Oxidase from maize and barley 160
Ectopic expression of maize polyamine oxidase and pea copper amine oxidase in tobacco plants provides evidence for the limiting amount of polyamines in the extracellular space. 158
The four FAD-dependent histone demethylases of arabidopsis are differently involved in the control of flowering time 158
A Solanum lycopersicum polyamine oxidase contributes to the control of plant growth, xylem differentiation, and drought stress tolerance 157
Caratterizzazione genotipica e fenotipica di mutanti inserzionali di Arabidopsis: movimenti stomatici 157
The expression of "Single chain" antibodies in transgenic plants 156
Stabilizing peptides, polypeptides and antibodies which include them 152
Wounding-induced long-distance communication signals copper amine oxidase β-mediated stomatal closure and root protoxylem plasticity in arabidopsis 151
Phytochrome control and circadian rhythm in LHC-I gene expression 150
De-etiolation causes a phytochrome-medieted increase of polyamine oxidase expression in outer tissues of the maize mesocotyl: a role in the photomodulation of growth and cell wall differentiation 145
Piante transgeniche in grado di esprimere amino ossidasi esogene e loro uso 144
Role of CuAOβ and RBOHD-derived hydrogen peroxide in wound-induced local and systemic signal propagation leading to stomatal closure in Arabidopsis thaliana. 133
Involvement of ACA8, ACA10 and CuAOβ in wounding-induced stomatal closure in Arabidopsis. Abstract #P17 130
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase RID B-9852-2011 RID A-4573-2009 130
CRISPR/Cas9-mediated mutagenesis of a polyamine oxidase gene increases tomato plant tolerance to drought stress. 128
null 125
Distinct roles of AtCuAOβ and RBOHD in wound-induced local and systemic leaf-to-leaf and root-to-leaf stomatal closure in Arabidopsis 122
Plant as a whole: rapid long-distance signaling mediated by Ca2+-ATPases and glutamate receptor-like channels triggers wound-induced stomatal closure. 120
Solanum lycopersicum CRISPR/Cas9 mutants for a polyamine oxidase gene exhibit improved drought stress tolerance and water-use efficiency. 117
Role of Arabidopsis ACA8 and ACA10 in stomatal modulation upon root wounding or MeJA treatment 112
Caratterizzazione genotipica di mutanti di genome editing in specie vegetali. 111
The tree of life of polyamine oxidases 110
null 109
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Maize polyamine oxidase: primary structure from protein and cDNA sequencing 75
Circadian rhythm in the expression of the mRNA coding for the apoprotein of the Light-Harvesting Complex of photosystem II: Phytochrome control and persistent far red reversibility 75
Isolation and characterization of three polyamino oxidase genes from Zea mays 68
Totale 19.353
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Categoria #
all - tutte 59.342
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 59.342
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.009 63 115 100 24 173 41 121 37 99 27 53 156
2022/20231.663 165 293 141 251 107 316 14 150 131 11 55 29
2023/2024892 45 48 83 28 61 91 61 219 33 25 62 136
2024/20252.707 41 141 308 52 71 135 838 501 201 110 172 137
2025/20264.408 432 401 247 516 513 293 595 117 457 597 97 143
2026/202751 51 0 0 0 0 0 0 0 0 0 0 0
Totale 19.511