Benvenuti nell'Anagrafe della Ricerca d'Ateneo

TAVLADORAKI, Paraskevi
 Distribuzione geografica
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Continente #
NA - Nord America 7.185
EU - Europa 6.396
AS - Asia 4.578
SA - Sud America 355
AF - Africa 162
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 6
Totale 18.697
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Nazione #
US - Stati Uniti d'America 7.108
CN - Cina 2.108
SG - Singapore 1.457
DK - Danimarca 1.290
GB - Regno Unito 1.272
RU - Federazione Russa 1.236
IT - Italia 695
DE - Germania 530
SE - Svezia 517
VN - Vietnam 405
BR - Brasile 243
FI - Finlandia 216
UA - Ucraina 202
HK - Hong Kong 128
IN - India 102
CI - Costa d'Avorio 96
IE - Irlanda 94
AL - Albania 71
TR - Turchia 71
KR - Corea 63
FR - Francia 58
JP - Giappone 45
AR - Argentina 42
NL - Olanda 38
BD - Bangladesh 37
CA - Canada 37
ES - Italia 31
IQ - Iraq 28
BE - Belgio 27
ID - Indonesia 26
PL - Polonia 25
MX - Messico 24
CZ - Repubblica Ceca 19
CL - Cile 18
ZA - Sudafrica 18
PK - Pakistan 17
SN - Senegal 15
CO - Colombia 14
EC - Ecuador 14
LT - Lituania 14
VE - Venezuela 13
AU - Australia 12
AT - Austria 11
GR - Grecia 9
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
EG - Egitto 5
JM - Giamaica 5
PT - Portogallo 5
MT - Malta 4
PS - Palestinian Territory 4
BO - Bolivia 3
CG - Congo 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
CR - Costa Rica 2
DZ - Algeria 2
EE - Estonia 2
ET - Etiopia 2
EU - Europa 2
HR - Croazia 2
IR - Iran 2
JO - Giordania 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NG - Nigeria 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 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
HN - Honduras 1
IM - Isola di Man 1
KE - Kenya 1
KW - Kuwait 1
LK - Sri Lanka 1
Totale 18.678
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Città #
Southend 1.086
Singapore 744
Woodbridge 715
Ashburn 674
Fairfield 666
Ann Arbor 491
Chandler 490
Wilmington 445
Rome 404
Houston 343
San Jose 320
Nanjing 259
Beijing 256
Seattle 252
Cambridge 223
Dearborn 218
Boardman 217
Dallas 162
Jacksonville 152
Princeton 131
Helsinki 130
Jinan 125
Shenyang 125
Hefei 123
Hong Kong 118
Dong Ket 100
Ho Chi Minh City 99
Dublin 94
Nanchang 87
Hebei 78
Hanoi 74
Plano 74
Redwood City 71
Changsha 70
Moscow 70
Los Angeles 69
Bremen 66
Munich 63
Orem 63
Seoul 55
Tianjin 55
Shanghai 54
Frankfurt am Main 51
The Dalles 51
Izmir 48
Jiaxing 41
Kunming 41
Ningbo 41
New York 40
Tokyo 40
Hangzhou 39
Zhengzhou 39
San Diego 34
Chennai 33
Council Bluffs 32
Guangzhou 32
London 28
Haikou 27
Redmond 26
Lanzhou 25
Brussels 24
São Paulo 24
Taiyuan 24
Taizhou 24
Columbus 23
Orange 23
Warsaw 22
Montreal 21
Milan 19
Santa Clara 19
Brooklyn 18
Mumbai 17
San Mateo 17
Turku 17
Basingstoke 16
Stockholm 16
Altamura 15
Dakar 15
Falls Church 15
Fremont 15
Fuzhou 14
Jakarta 14
Chicago 13
Haiphong 13
Alameda 12
Amsterdam 12
Falkenstein 12
Johannesburg 12
Baghdad 11
Brno 11
Manchester 11
Santiago 11
Yubileyny 11
Hillsboro 10
Pune 10
San Francisco 10
Verona 10
Boston 9
Denver 9
Mexico City 9
Totale 11.387
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Nome #
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 349
Plant amine oxidases “on the move”: An update 337
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 336
The members of Arabidopsis thaliana PAO gene family exhibit distinct tissue- and organ-specific expression pattern during seedling growth and flower development 308
The Arabidopsis polyamine oxidase/dehydrogenase 5 interferes with cytokinin and auxin signaling pathways to control xylem differentiation 290
Cell wall amine oxidases: new players in root xylem differentiation under stress conditions 288
Functional diversity inside the Arabidopsis polyamine oxidase gene family 272
The apoplastic copper AMINE OXIDASE1 mediates jasmonic acid-induced protoxylem differentiation in Arabidopsis roots 268
Cell Wall Amine Oxidases: New Players in Root Xylem Differentiation under Stress Conditions 266
The structure of maize polyamine oxidase K300M mutant in complex with the natural substrates provides a snapshot of the catalytic mechanism of polyamine oxidation 262
AtCuAOδ participates in abscisic acid-induced stomatal closure in Arabidopsis. 255
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana 252
Caratterizzazione dei geni codificanti la poliamminossidasi in mais ed orzo 247
An Arabidopsis polyamine oxidase undergoing proteasomal regulation 247
POLYAMINE OXIDASE2 of Arabidopsis contributes to ABA mediated plant developmental processes. 247
Polyamine catabolism: target for antiproliferative therapies in animals and stress tolerance strategies in plants 246
A single-chain antibody fragment is functionally expressed in the cytoplasm of both Escherichia coli and transgenic plants 245
An Arabidopsis copper amine oxidase is involved in jasmonate-induced root xylem differentiation 241
The polyamines and their catabolic products are significant players in the turnover of nitrogenous molecules in plants 239
Ectopic expression of maize polyamine oxidase and pea copper amine oxidase in the cell wall of tobacco plants 238
The MeJA-inducible copper amine oxidase AtAO1 is expressed in xylem tissue and guard cells 237
Isolation and characterization of three polyamine oxidase genes from Zea mays 233
Cytotoxic effect induced by maize polyamine oxidase in presence of spermine in human cancer cells. 226
Transgenic plants expressing a functional "Single Chain Fv" antibody are specifically protected from virus attack 226
Copper-containing amine oxidases and FAD-dependent polyamine oxidases are key players in plant tissue differentiation and organ development 222
Innovative processes and treatments to improve the shelf-life, safety and nutritional value of ready-to-eat vegetables. 220
The copper amine oxidase AtCuAOδ participates in abscisic acid-induced stomatal closure in arabidopsis 219
Probing mammalian spermine oxidase enzyme-substrate complex through molecular modeling, site-directed mutagenesis and biochemical characterization 218
Functions of amine oxidases in plant development and defence 214
Isolation and characterization of three polyamine oxidase genes from Zea mays 214
Age- and Phytochrome- induced changes at the level of the translatable mRNA coding for the LHC-II apoprotein of Phaseolus vulgaris leaves. 212
THE FOUR LYSINE-SPECIFIC HISTONE DEMETHYLASES OF ARABIDOPSIS DIFFERENTIALLY CONTRIBUTE TO THE CONTROL OF FLOWERING TIME AND DEFENCE RESPONSES. 210
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper-amine oxidase gene family 210
Improving stress tolerance of tomato plants through modification of polyamine metabolism. 209
Immunotherapy of plant viral diseases 207
Determination of copper amine oxidase activity in plant tissues 205
Biochemical characterization and biotechnological applications of copper amine oxidases and flavin polyamine oxidases 205
FAD-containing polyamine oxidases: a timely challenge for researchers in biochemistry and physiology of plants 204
Inducible expression of maize polyamine oxidase in the nucleus of MCF-7 human breast cancer cells confers sensitivity to etoposide 203
Comparative analysis of the role of the different Arabidopsis polyamine oxidases in plant defense responses to environmental stresses. 202
Caratterizzazione dei geni codificanti la Poliammino Ossidasi in mais ed orzo 199
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 197
Maize polyamine oxidase: primary structure from protein and cDNA sequencing 197
The apoplastic copper amine oxidase AtCuAOβ plays a role in stomatal closure induced by wounding, jasmonate or Microbe Associated Molecular Patterns (MAMPS). 196
Nitrogen flow into regulatory molecules: The case of Polyamines and Polyamine oxidases. 195
Arabidopsis N-acetyltransferase activity 2 preferentially acetylates 1,3-diaminopropane and thialysine 192
The four lysine-specific histone demethylases of Arabidopsis differentially contribute to the control of flowering time and defence responses. 190
A new player in jasmonate-mediated stomatal closure: The Arabidopsis Thaliana copper amine oxidase β 190
Involvement of Arabidopsis thaliana Copper Amine Oxidase β in maturation of root protoxylem precursors induced by leaf wounding. 187
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion RID A-4573-2009 186
Characterization of genes coding for polyamine oxidase from maize and barley 183
Leaf-wounding long-distance signaling targets AtCuAOβ leading to root phenotypic plasticity 182
Distinct role of AtCuAOβ- and RBOHD-driven H2O2 production in wound-induced local and systemic leaf-to-leaf and root-to-leaf stomatal closure 180
Isolation of nuclei from plant tissues 180
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase 180
Involvement of Arabidopsis Copper Amine Oxidase β in MeJA/wounding-induced stomatal closure. 180
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana RID A-4573-2009 179
Plantibodies: Immunomodulation and Immunotherapeutic potential 179
A polyamine oxidase of Solanum lycopersicum controls plant growth, xylem differentiation and drought stress tolerance 177
Functions of amine oxidases in plant development and defence 176
Hydrogen peroxide: the player of polyamine action in development and stress responses 172
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion 170
The Arabidopsis polyamine oxidase/dehydrogenase 5 contributes to the cytokinin/auxin interplay controlling xylem differentiation. 170
Involvement of ACA8/ACA10 in wounding-induced stomatal closure in Arabidopsis 169
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase RID A-4573-2009 168
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper amine oxidase gene family 168
Emerging role of polyamine oxidases in plant development 165
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 163
Characterization of Arabidopsis insertional mutants for copper-containing amine oxidases 162
Unraveling the regulatory pathway of lysine-specific histone demethylases in plants 161
Stress-triggered long-distance communication leads to phenotypic plasticity: The case of the early root protoxylem maturation induced by leaf wounding in arabidopsis 161
Enzyme activity inhibition of the ABA-inducible copper amine oxidase AtCuAOδ reverses most of the ABA-mediated stomatal closure in Arabidopsis 160
Characterization of genes coding for Polyamine Oxidase from maize and barley 157
The four FAD-dependent histone demethylases of arabidopsis are differently involved in the control of flowering time 156
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. 155
The expression of "Single chain" antibodies in transgenic plants 153
A polyamine oxidase controls water-use efficiency in Solanum lycopersicum 152
Caratterizzazione genotipica e fenotipica di mutanti inserzionali di Arabidopsis: movimenti stomatici 152
A Solanum lycopersicum polyamine oxidase contributes to the control of plant growth, xylem differentiation, and drought stress tolerance 151
Stabilizing peptides, polypeptides and antibodies which include them 149
Phytochrome control and circadian rhythm in LHC-I gene expression 149
Wounding-induced long-distance communication signals copper amine oxidase β-mediated stomatal closure and root protoxylem plasticity in arabidopsis 146
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 144
Piante transgeniche in grado di esprimere amino ossidasi esogene e loro uso 142
Role of CuAOβ and RBOHD-derived hydrogen peroxide in wound-induced local and systemic signal propagation leading to stomatal closure in Arabidopsis thaliana. 130
Involvement of ACA8, ACA10 and CuAOβ in wounding-induced stomatal closure in Arabidopsis. Abstract #P17 128
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase RID B-9852-2011 RID A-4573-2009 125
null 125
CRISPR/Cas9-mediated mutagenesis of a polyamine oxidase gene increases tomato plant tolerance to drought stress. 124
Distinct roles of AtCuAOβ and RBOHD in wound-induced local and systemic leaf-to-leaf and root-to-leaf stomatal closure in Arabidopsis 119
Plant as a whole: rapid long-distance signaling mediated by Ca2+-ATPases and glutamate receptor-like channels triggers wound-induced stomatal closure. 117
Solanum lycopersicum CRISPR/Cas9 mutants for a polyamine oxidase gene exhibit improved drought stress tolerance and water-use efficiency. 115
null 109
Role of Arabidopsis ACA8 and ACA10 in stomatal modulation upon root wounding or MeJA treatment 108
Caratterizzazione genotipica di mutanti di genome editing in specie vegetali. 107
The tree of life of polyamine oxidases 106
null 82
Maize polyamine oxidase: primary structure from protein and cDNA sequencing 73
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 71
Isolation and characterization of three polyamino oxidase genes from Zea mays 68
Totale 18.956
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Categoria #
all - tutte 56.050
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 56.050
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021321 0 0 0 0 0 0 0 0 0 109 63 149
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
2025/20264.048 432 401 247 516 513 293 595 117 457 477 0 0
Totale 19.100