CONA, Alessandra
 Distribuzione geografica
Continente #
NA - Nord America 8.408
EU - Europa 8.390
AS - Asia 5.879
SA - Sud America 609
Continente sconosciuto - Info sul continente non disponibili 582
AF - Africa 228
OC - Oceania 14
Totale 24.110
Nazione #
US - Stati Uniti d'America 8.275
CN - Cina 2.656
DK - Danimarca 1.949
SG - Singapore 1.888
GB - Regno Unito 1.589
RU - Federazione Russa 1.530
IT - Italia 964
DE - Germania 662
VN - Vietnam 539
SE - Svezia 489
BR - Brasile 436
FI - Finlandia 321
UA - Ucraina 310
IE - Irlanda 124
CI - Costa d'Avorio 120
BD - Bangladesh 117
IN - India 111
KR - Corea 109
AL - Albania 95
HK - Hong Kong 91
FR - Francia 74
TR - Turchia 74
CA - Canada 72
NL - Olanda 60
AR - Argentina 56
JP - Giappone 52
IQ - Iraq 37
ID - Indonesia 36
PL - Polonia 34
ES - Italia 33
CO - Colombia 31
MX - Messico 31
AT - Austria 29
BE - Belgio 29
EC - Ecuador 27
ZA - Sudafrica 25
PK - Pakistan 23
MY - Malesia 21
VE - Venezuela 21
CL - Cile 20
SN - Senegal 20
PH - Filippine 19
UZ - Uzbekistan 16
LT - Lituania 15
SA - Arabia Saudita 15
CZ - Repubblica Ceca 13
MA - Marocco 13
AU - Australia 12
HU - Ungheria 11
CH - Svizzera 10
GR - Grecia 10
TH - Thailandia 10
EG - Egitto 9
KE - Kenya 9
PY - Paraguay 9
TN - Tunisia 9
AE - Emirati Arabi Uniti 8
NP - Nepal 8
IL - Israele 7
LV - Lettonia 7
JM - Giamaica 6
ET - Etiopia 5
MT - Malta 5
PS - Palestinian Territory 5
PT - Portogallo 5
TW - Taiwan 5
AZ - Azerbaigian 4
BO - Bolivia 4
CR - Costa Rica 4
DZ - Algeria 4
HN - Honduras 4
JO - Giordania 4
PA - Panama 4
RO - Romania 4
SK - Slovacchia (Repubblica Slovacca) 4
BG - Bulgaria 3
CG - Congo 3
DO - Repubblica Dominicana 3
IR - Iran 3
NG - Nigeria 3
RS - Serbia 3
BW - Botswana 2
EE - Estonia 2
GE - Georgia 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
LY - Libia 2
NZ - Nuova Zelanda 2
OM - Oman 2
QA - Qatar 2
RE - Reunion 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AM - Armenia 1
BB - Barbados 1
BH - Bahrain 1
BZ - Belize 1
CU - Cuba 1
Totale 23.508
Città #
Southend 1.390
Singapore 957
Ashburn 828
Woodbridge 692
Fairfield 679
Rome 541
Ann Arbor 514
San Jose 493
Chandler 480
Wilmington 480
Houston 335
Nanjing 310
Beijing 297
Boardman 270
Dearborn 260
Seattle 260
Dallas 226
Cambridge 225
Jacksonville 222
Helsinki 204
Hefei 183
Princeton 177
Shenyang 159
Ho Chi Minh City 156
Jinan 151
Dublin 123
Bremen 114
Dong Ket 112
Plano 104
Hanoi 103
Nanchang 100
Changsha 97
Hebei 96
Munich 95
Los Angeles 86
Hong Kong 84
Moscow 79
Seoul 78
Tianjin 76
Redwood City 75
Shanghai 69
New York 66
Zhengzhou 66
Frankfurt am Main 65
Orem 59
Jiaxing 58
The Dalles 51
Tokyo 48
Hangzhou 47
Izmir 45
Guangzhou 44
São Paulo 44
Kunming 40
Taizhou 39
Ningbo 38
San Diego 36
Redmond 34
Haikou 33
Chennai 31
Milan 31
Orange 30
Council Bluffs 29
Santa Clara 29
Taiyuan 29
London 28
Montreal 28
Turku 28
Warsaw 28
Chicago 26
Brussels 24
Brooklyn 21
Columbus 21
Dakar 20
Stockholm 20
Alameda 18
Amsterdam 18
Boston 18
Lanzhou 18
Manchester 18
Mumbai 18
Altamura 16
Phoenix 16
Basingstoke 15
Denver 15
Fremont 15
Mexico City 15
Rio de Janeiro 15
San Paolo di Civitate 15
Vienna 15
Da Nang 14
Florence 14
Haiphong 14
Jakarta 14
Atlanta 13
Baghdad 13
Fuzhou 13
Johannesburg 13
San Francisco 13
Tashkent 13
Verona 13
Totale 13.608
Nome #
Barley polyamine oxidase isoforms 1 and 2, a peculiar case of gene duplication 354
Plant amine oxidases “on the move”: An update 351
Cellular re-distribution of flavin-containing polyamine oxidase in differentiating root and mesocotyl of Zea mays L. seedlings 339
A barley polyamine oxidase isoform with distinct structural features and subcellular localization 316
Wound healing response and xylem differentiation in tobacco plants over-expressing a fungal endopolygalacturonase is mediated by copper amine oxidase activity 306
Involvement of polyamine oxidase in wound healing 305
The apoplastic copper AMINE OXIDASE1 mediates jasmonic acid-induced protoxylem differentiation in Arabidopsis roots 301
Perturbation of polyamine catabolism can strongly affect root development and xylem differentiation 294
The Arabidopsis polyamine oxidase/dehydrogenase 5 interferes with cytokinin and auxin signaling pathways to control xylem differentiation 293
Inhibition of polyamine and spermine oxidases by polyamine analogues 290
Cell Wall Amine Oxidases: New Players in Root Xylem Differentiation under Stress Conditions 270
Caratterizzazione dei geni codificanti la poliamminossidasi in mais ed orzo 265
Wound healing in plants: Cooperation of copper amine oxidase and flavin-containing poliamine oxidase 259
AtCuAOδ participates in abscisic acid-induced stomatal closure in Arabidopsis. 259
POLYAMINE OXIDASE2 of Arabidopsis contributes to ABA mediated plant developmental processes. 253
Polyamine catabolism: target for antiproliferative therapies in animals and stress tolerance strategies in plants 250
An Arabidopsis copper amine oxidase is involved in jasmonate-induced root xylem differentiation 243
A new and sensitive method for plant amino oxidase determination by measuring the liberated hydrogen peroxide 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
Barley polyamine oxidase isoform 1 (BPAO1) expression analysis 240
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp 240
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase 238
Copper Amine Oxidases from Plants 235
Cytotoxic effect induced by maize polyamine oxidase in presence of spermine in human cancer cells. 231
The copper amine oxidase AtCuAOδ participates in abscisic acid-induced stomatal closure in arabidopsis 229
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
Synthesis and biological evaluation of guanidino compounds endowed with subnanomolar affinity as competitive inhibitors of maize polyamine oxidase 221
Molecular basis for the binding of competitive inhibitors of maize polyamine oxidase 219
Improving stress tolerance of tomato plants through modification of polyamine metabolism. 216
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper-amine oxidase gene family 216
Does polyamine catabolism influence root development and xylem differentiation under stress conditions? 213
Is D1 protein turnover involved in the resistance to herbicides in higher plants? 210
Determination of copper amine oxidase activity in plant tissues 209
Biochemical characterization and biotechnological applications of copper amine oxidases and flavin polyamine oxidases 209
Polyamine oxidase, a hydrogen peroxide-producing enzyme, is up-regulated by light and down-regulated by auxin in the outer tissues of the maize mesocotyl 208
Comparative analysis of the role of the different Arabidopsis polyamine oxidases in plant defense responses to environmental stresses. 208
Arabidopsis N-acetyltransferase activity 2 preferentially acetylates 1,3-diaminopropane and thialysine 203
Characterization of maize polyamine oxidase 202
Nitrogen flow into regulatory molecules: The case of Polyamines and Polyamine oxidases. 202
Flavin-containing polyamine oxidase is a hydrogen peroxide source in the oxidative response to the protein phosphatase inhibitor cantharidin in Zea mays L 201
D1 protein turnover and sensitivity of higher plants to photosystem II-directed herbicides 201
Maize polyamine oxidase in the presence of spermine/spermidine induces the apoptosis of LoVo human colon adenocarcinoma cells 201
Histaminase PEGylation: Preparation and characterization of a new bioconjugate for therapeutic application 200
Long-term drought stress symptom: structural and functional reorganization of phosystem II 198
The apoplastic copper amine oxidase AtCuAOβ plays a role in stomatal closure induced by wounding, jasmonate or Microbe Associated Molecular Patterns (MAMPS). 198
Photosystem II core phosphorylation heterogeneity and the regulation of electron transfer in higher plants: a review 197
Purification of polyamine oxidase from maize seedlings by immunoadsorbent column 196
A new player in jasmonate-mediated stomatal closure: The Arabidopsis Thaliana copper amine oxidase β 195
Regulation of photosystem II core phosphorylation heterogeneity and its significance for D1 turnover 193
Influence of ozone and ultraviolet (UV-C) radiation on in vivo and in vitro tobacco culture 193
Involvement of Arabidopsis thaliana Copper Amine Oxidase β in maturation of root protoxylem precursors induced by leaf wounding. 192
Polyamine oxidase bound to cell walls from Zea Mays seedlings 189
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
Involvement of Arabidopsis Copper Amine Oxidase β in MeJA/wounding-induced stomatal closure. 183
A new and sensitive method for the assay of amine oxidase by measurement of the liberated peroxide 183
Xanthophyll cycle components and capacity for non-radiative energy dissipations in sun and shade leaves of Ligustrum ovalifolium exposed to conditions limiting photosynthesis 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
Polyamine oxidase is regulated by light and auxin in the maize mesocotyl 180
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 179
H2O2 production in maize mesocotyl segments elicited by GTP-γ-S and cantharidin is inhibited by N-isoprenylagmatine, a powerful and specific polyamine oxidase inhibtor 177
Enzymatic method for the determination of polyamines and diamines 176
Evidence of a simultaneous induction of diamine oxidase and peroxidase after wounding 175
A polyamine oxidase controls water-use efficiency in Solanum lycopersicum 174
Hydrogen peroxide: the player of polyamine action in development and stress responses 174
Involvement of ACA8/ACA10 in wounding-induced stomatal closure in Arabidopsis 174
Phosphorylation of PSII core in relation to D1 turnover in higher plants 173
Maize polyamine oxidase: A H2O2 delivering system in wall differentiation and cell death 173
The Arabidopsis polyamine oxidase/dehydrogenase 5 contributes to the cytokinin/auxin interplay controlling xylem differentiation. 173
Effects of perturbing expression of the polyamine catabolic gene AtCuAO4 on senescence, and stress responses in Arabidopsis thaliana 172
Dynamics of photosystem II core phosphorilation heterogeneity 172
Developmental, hormone- and stress-modulated expression profiles of four members of the Arabidopsis copper amine oxidase gene family 172
D1 turnover as an adaptation signal for plants to recover from drought 169
Testing seed germination from herbaria: Application of seed quality enhancement techniques and implication for plant resurrection and conservation 168
Members of AtCuAO gene family exhibit different tissue-and organ-specific expression patterns during seedling development and distinct responses to hormone or stress treatments 168
Solution and solid-phase synthesis of aminoalkylguanidines inhibiting polyamine oxidase and nitric oxide synthase 167
Emerging role of polyamine oxidases in plant development 167
Ruolo dell'auxina nell'espressione del gene codificante la poliammino osidasi (PAO) in Zea Mays 166
Characterization of Arabidopsis insertional mutants for copper-containing amine oxidases 165
AtCuAOβ AND RBOHD DISTINCT ROLES IN MECHANICAL WOUNDING-INDUCED STOMATAL CLOSURE 164
Occurrence of a cell-wall bound PAO in maize seedlings 163
Effects of perturbing expression of the polyamine catabolic AtCuAO gene family on growth and development in Arabidopsis thaliana. 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
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 159
Plant-based biorepellents against large white butterfly caterpillars in Brassica oleracea. 158
The four FAD-dependent histone demethylases of arabidopsis are differently involved in the control of flowering time 158
Polyamine oxidase expression in defense response to wounding in maize mesocotyl 156
Variations of carbon isotope discrimination and leaf photosynthesis among populations of Castanea sativa Mill 155
Structure-function relationship of maize polyamine oxidase 155
D1 turnover as indicator and protector against stress 155
The amino aldehydes produced by spermine and spermidine oxidation with maize polyamine oxidase have anti-leishmanial effect 152
Wounding-induced long-distance communication signals copper amine oxidase β-mediated stomatal closure and root protoxylem plasticity in arabidopsis 152
Efficiency of photochemistry and non-radiative energy dissipation in leaves exposed to conditions limiting photosynthetic electron flow 151
Long-term drought stress induces structural and functional reorgazization of photosystem II 148
Polyamine oxidase involvement in light-induced production of hydrogen peroxide in Zea mays L. 147
Totale 20.546
Categoria #
all - tutte 75.649
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 75.649


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.113 0 151 120 37 202 29 152 54 110 23 60 175
2022/20231.786 204 311 138 291 117 330 10 123 166 8 57 31
2023/20241.125 36 55 100 39 73 110 79 287 55 34 78 179
2024/20253.370 63 174 377 67 88 167 1.008 590 269 112 230 225
2025/20265.927 519 509 406 780 688 334 787 151 629 765 166 193
2026/2027214 116 98 0 0 0 0 0 0 0 0 0 0
Totale 24.110