Benvenuti nell'Anagrafe della Ricerca d'Ateneo

TAVLADORAKI, Paraskevi
 Distribuzione geografica
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Continente #
NA - Nord America 7.860
EU - Europa 6.466
AS - Asia 4.653
Continente sconosciuto - Info sul continente non disponibili 409
SA - Sud America 384
AF - Africa 163
OC - Oceania 16
Totale 19.951
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Nazione #
US - Stati Uniti d'America 7.741
CN - Cina 2.120
SG - Singapore 1.463
DK - Danimarca 1.290
GB - Regno Unito 1.274
RU - Federazione Russa 1.236
IT - Italia 751
DE - Germania 532
SE - Svezia 517
VN - Vietnam 409
BR - Brasile 259
FI - Finlandia 216
UA - Ucraina 202
HK - Hong Kong 132
IN - India 103
CI - Costa d'Avorio 96
IE - Irlanda 95
AL - Albania 72
BD - Bangladesh 72
TR - Turchia 71
CA - Canada 63
KR - Corea 63
FR - Francia 62
JP - Giappone 45
AR - Argentina 44
NL - Olanda 38
ES - Italia 32
ID - Indonesia 29
IQ - Iraq 28
BE - Belgio 27
MX - Messico 26
PL - Polonia 25
CO - Colombia 20
CZ - Repubblica Ceca 19
CL - Cile 18
EC - Ecuador 18
PK - Pakistan 18
ZA - Sudafrica 18
SN - Senegal 15
LT - Lituania 14
VE - Venezuela 14
AU - Australia 12
AT - Austria 11
GR - Grecia 11
MY - Malesia 11
PH - Filippine 10
HU - Ungheria 9
NP - Nepal 9
TH - Thailandia 9
AE - Emirati Arabi Uniti 8
MA - Marocco 8
SA - Arabia Saudita 8
UZ - Uzbekistan 8
CH - Svizzera 7
IL - Israele 7
JM - Giamaica 7
CR - Costa Rica 6
EG - Egitto 5
PT - Portogallo 5
MT - Malta 4
PA - Panama 4
PS - Palestinian Territory 4
BO - Bolivia 3
CG - Congo 3
HR - Croazia 3
JO - Giordania 3
NZ - Nuova Zelanda 3
PE - Perù 3
PY - Paraguay 3
RO - Romania 3
RS - Serbia 3
TW - Taiwan 3
AM - Armenia 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EE - Estonia 2
ET - Etiopia 2
EU - Europa 2
HN - Honduras 2
IR - Iran 2
KE - Kenya 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
GA - Gabon 1
GE - Georgia 1
Totale 19.525
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Città #
Southend 1.086
Ashburn 763
Singapore 748
Woodbridge 717
Fairfield 667
Ann Arbor 491
Chandler 490
San Jose 477
Wilmington 445
Rome 422
Houston 349
Beijing 263
Nanjing 259
Seattle 253
Cambridge 223
Dearborn 218
Boardman 217
Dallas 168
Jacksonville 153
Princeton 131
Helsinki 130
Jinan 125
Shenyang 125
Hefei 123
Hong Kong 122
Ho Chi Minh City 101
Dong Ket 100
Dublin 95
Nanchang 87
Los Angeles 85
Hebei 78
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
New York 51
The Dalles 51
Council Bluffs 50
Izmir 48
Jiaxing 41
Kunming 41
Ningbo 41
Tokyo 40
Hangzhou 39
Zhengzhou 39
San Diego 35
Chennai 33
Guangzhou 32
Santa Clara 30
London 29
Haikou 27
Redmond 26
São Paulo 26
Lanzhou 25
Montreal 25
Brussels 24
Columbus 24
Taiyuan 24
Taizhou 24
Orange 23
Brooklyn 22
Warsaw 22
Milan 21
Chicago 20
Mumbai 17
Phoenix 17
San Mateo 17
Turku 17
Basingstoke 16
Stockholm 16
Altamura 15
Dakar 15
Falls Church 15
Fremont 15
Fuzhou 14
Haiphong 14
Jakarta 14
San Francisco 13
Alameda 12
Amsterdam 12
Buffalo 12
Falkenstein 12
Johannesburg 12
Toronto 12
Baghdad 11
Brno 11
Denver 11
Manchester 11
Rio de Janeiro 11
Santiago 11
Verona 11
Yubileyny 11
Totale 11.785
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Nome #
Plant amine oxidases “on the move”: An update 362
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 357
A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. 341
The members of Arabidopsis thaliana PAO gene family exhibit distinct tissue- and organ-specific expression pattern during seedling growth and flower development 314
The apoplastic copper AMINE OXIDASE1 mediates jasmonic acid-induced protoxylem differentiation in Arabidopsis roots 310
Cell wall amine oxidases: new players in root xylem differentiation under stress conditions 294
The Arabidopsis polyamine oxidase/dehydrogenase 5 interferes with cytokinin and auxin signaling pathways to control xylem differentiation 294
Functional diversity inside the Arabidopsis polyamine oxidase gene family 274
Caratterizzazione dei geni codificanti la poliamminossidasi in mais ed orzo 272
Cell Wall Amine Oxidases: New Players in Root Xylem Differentiation under Stress Conditions 272
AtCuAOδ participates in abscisic acid-induced stomatal closure in Arabidopsis. 267
The structure of maize polyamine oxidase K300M mutant in complex with the natural substrates provides a snapshot of the catalytic mechanism of polyamine oxidation 264
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana 260
An Arabidopsis polyamine oxidase undergoing proteasomal regulation 255
A single-chain antibody fragment is functionally expressed in the cytoplasm of both Escherichia coli and transgenic plants 254
POLYAMINE OXIDASE2 of Arabidopsis contributes to ABA mediated plant developmental processes. 254
Polyamine catabolism: target for antiproliferative therapies in animals and stress tolerance strategies in plants 252
Ectopic expression of maize polyamine oxidase and pea copper amine oxidase in the cell wall of tobacco plants 246
An Arabidopsis copper amine oxidase is involved in jasmonate-induced root xylem differentiation 246
Isolation and characterization of three polyamine oxidase genes from Zea mays 242
The polyamines and their catabolic products are significant players in the turnover of nitrogenous molecules in plants 242
The MeJA-inducible copper amine oxidase AtAO1 is expressed in xylem tissue and guard cells 241
Cytotoxic effect induced by maize polyamine oxidase in presence of spermine in human cancer cells. 236
The copper amine oxidase AtCuAOδ participates in abscisic acid-induced stomatal closure in arabidopsis 235
The four lysine-specific histone demethylases of Arabidopsis differentially contribute to the control of flowering time and defence responses. 230
Copper-containing amine oxidases and FAD-dependent polyamine oxidases are key players in plant tissue differentiation and organ development 230
Transgenic plants expressing a functional "Single Chain Fv" antibody are specifically protected from virus attack 230
Functions of amine oxidases in plant development and defence 227
Innovative processes and treatments to improve the shelf-life, safety and nutritional value of ready-to-eat vegetables. 224
Isolation and characterization of three polyamine oxidase genes from Zea mays 223
Probing mammalian spermine oxidase enzyme-substrate complex through molecular modeling, site-directed mutagenesis and biochemical characterization 223
Improving stress tolerance of tomato plants through modification of polyamine metabolism. 218
Comparative analysis of the role of the different Arabidopsis polyamine oxidases in plant defense responses to environmental stresses. 218
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper-amine oxidase gene family 218
Age- and Phytochrome- induced changes at the level of the translatable mRNA coding for the LHC-II apoprotein of Phaseolus vulgaris leaves. 217
THE FOUR LYSINE-SPECIFIC HISTONE DEMETHYLASES OF ARABIDOPSIS DIFFERENTIALLY CONTRIBUTE TO THE CONTROL OF FLOWERING TIME AND DEFENCE RESPONSES. 216
Immunotherapy of plant viral diseases 213
Determination of copper amine oxidase activity in plant tissues 212
FAD-containing polyamine oxidases: a timely challenge for researchers in biochemistry and physiology of plants 212
Biochemical characterization and biotechnological applications of copper amine oxidases and flavin polyamine oxidases 211
Inducible expression of maize polyamine oxidase in the nucleus of MCF-7 human breast cancer cells confers sensitivity to etoposide 208
Caratterizzazione dei geni codificanti la Poliammino Ossidasi in mais ed orzo 207
Arabidopsis N-acetyltransferase activity 2 preferentially acetylates 1,3-diaminopropane and thialysine 207
Nitrogen flow into regulatory molecules: The case of Polyamines and Polyamine oxidases. 205
Maize polyamine oxidase: primary structure from protein and cDNA sequencing 204
The apoplastic copper amine oxidase AtCuAOβ plays a role in stomatal closure induced by wounding, jasmonate or Microbe Associated Molecular Patterns (MAMPS). 203
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 202
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion RID A-4573-2009 197
Involvement of Arabidopsis thaliana Copper Amine Oxidase β in maturation of root protoxylem precursors induced by leaf wounding. 197
A new player in jasmonate-mediated stomatal closure: The Arabidopsis Thaliana copper amine oxidase β 197
Characterization of genes coding for polyamine oxidase from maize and barley 193
Characterization of a lysine-specific histone demethylase from Arabidopsis thaliana RID A-4573-2009 191
Isolation of nuclei from plant tissues 191
Leaf-wounding long-distance signaling targets AtCuAOβ leading to root phenotypic plasticity 189
Involvement of Arabidopsis Copper Amine Oxidase β in MeJA/wounding-induced stomatal closure. 186
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase 185
A polyamine oxidase of Solanum lycopersicum controls plant growth, xylem differentiation and drought stress tolerance 185
Distinct role of AtCuAOβ- and RBOHD-driven H2O2 production in wound-induced local and systemic leaf-to-leaf and root-to-leaf stomatal closure 184
Plantibodies: Immunomodulation and Immunotherapeutic potential 183
Functions of amine oxidases in plant development and defence 181
A polyamine oxidase controls water-use efficiency in Solanum lycopersicum 178
Hydrogen peroxide: the player of polyamine action in development and stress responses 178
Involvement of ACA8/ACA10 in wounding-induced stomatal closure in Arabidopsis 178
The Arabidopsis polyamine oxidase/dehydrogenase 5 contributes to the cytokinin/auxin interplay controlling xylem differentiation. 175
POLYAMINE CATABOLISM IN ARABIDOPSIS THALIANA 175
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase RID A-4573-2009 174
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper amine oxidase gene family 174
Characterization of Arabidopsis insertional mutants for copper-containing amine oxidases 172
Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion 172
Unraveling the regulatory pathway of lysine-specific histone demethylases in plants 171
Emerging role of polyamine oxidases in plant development 170
Stress-triggered long-distance communication leads to phenotypic plasticity: The case of the early root protoxylem maturation induced by leaf wounding in arabidopsis 165
Enzyme activity inhibition of the ABA-inducible copper amine oxidase AtCuAOδ reverses most of the ABA-mediated stomatal closure in Arabidopsis 165
Characterization of genes coding for Polyamine Oxidase from maize and barley 164
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. 162
A Solanum lycopersicum polyamine oxidase contributes to the control of plant growth, xylem differentiation, and drought stress tolerance 161
Caratterizzazione genotipica e fenotipica di mutanti inserzionali di Arabidopsis: movimenti stomatici 161
Wounding-induced long-distance communication signals copper amine oxidase β-mediated stomatal closure and root protoxylem plasticity in arabidopsis 160
The four FAD-dependent histone demethylases of arabidopsis are differently involved in the control of flowering time 159
The expression of "Single chain" antibodies in transgenic plants 158
Stabilizing peptides, polypeptides and antibodies which include them 155
Phytochrome control and circadian rhythm in LHC-I gene expression 153
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 148
Piante transgeniche in grado di esprimere amino ossidasi esogene e loro uso 145
Role of CuAOβ and RBOHD-derived hydrogen peroxide in wound-induced local and systemic signal propagation leading to stomatal closure in Arabidopsis thaliana. 138
Involvement of ACA8, ACA10 and CuAOβ in wounding-induced stomatal closure in Arabidopsis. Abstract #P17 136
CRISPR/Cas9-mediated mutagenesis of a polyamine oxidase gene increases tomato plant tolerance to drought stress. 134
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase RID B-9852-2011 RID A-4573-2009 134
Plant as a whole: rapid long-distance signaling mediated by Ca2+-ATPases and glutamate receptor-like channels triggers wound-induced stomatal closure. 126
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 125
Solanum lycopersicum CRISPR/Cas9 mutants for a polyamine oxidase gene exhibit improved drought stress tolerance and water-use efficiency. 121
Role of Arabidopsis ACA8 and ACA10 in stomatal modulation upon root wounding or MeJA treatment 116
Caratterizzazione genotipica di mutanti di genome editing in specie vegetali. 116
The tree of life of polyamine oxidases 113
null 109
null 82
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 82
Maize polyamine oxidase: primary structure from protein and cDNA sequencing 80
Isolation and characterization of three polyamino oxidase genes from Zea mays 72
Totale 19.783
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Categoria #
all - tutte 61.809
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 61.809
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022831 0 0 100 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
2026/2027491 71 80 340 0 0 0 0 0 0 0 0 0
Totale 19.951