SANITA' di TOPPI, LUIGI
 Distribuzione geografica
Continente #
NA - Nord America 7.519
EU - Europa 3.133
AS - Asia 1.484
AF - Africa 71
SA - Sud America 68
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 5
Totale 12.305
Nazione #
US - Stati Uniti d'America 7.290
IT - Italia 1.748
CN - Cina 807
BG - Bulgaria 565
VN - Vietnam 235
CA - Canada 204
FI - Finlandia 173
SE - Svezia 153
SG - Singapore 118
DE - Germania 113
GB - Regno Unito 92
FR - Francia 67
IN - India 67
HK - Hong Kong 59
JP - Giappone 46
RU - Federazione Russa 43
KR - Corea 34
BR - Brasile 32
CH - Svizzera 28
SN - Senegal 27
MX - Messico 25
TR - Turchia 24
AU - Australia 23
UA - Ucraina 22
BE - Belgio 21
TW - Taiwan 21
ES - Italia 20
IR - Iran 20
CI - Costa d'Avorio 18
PK - Pakistan 14
PL - Polonia 14
ID - Indonesia 12
CZ - Repubblica Ceca 11
NL - Olanda 11
AR - Argentina 10
DZ - Algeria 10
MY - Malesia 9
CL - Cile 8
PT - Portogallo 8
RO - Romania 8
RS - Serbia 8
TH - Thailandia 8
CO - Colombia 7
DK - Danimarca 7
EC - Ecuador 7
GR - Grecia 6
NG - Nigeria 6
AT - Austria 5
EU - Europa 5
IQ - Iraq 4
EG - Egitto 3
IL - Israele 3
ZA - Sudafrica 3
LT - Lituania 2
NZ - Nuova Zelanda 2
PE - Perù 2
TN - Tunisia 2
AE - Emirati Arabi Uniti 1
BO - Bolivia 1
EE - Estonia 1
FK - Isole Falkland (Malvinas) 1
HR - Croazia 1
HU - Ungheria 1
IE - Irlanda 1
IS - Islanda 1
KZ - Kazakistan 1
MC - Monaco 1
MT - Malta 1
SA - Arabia Saudita 1
SC - Seychelles 1
SI - Slovenia 1
SO - Somalia 1
Totale 12.305
Città #
Woodbridge 1.572
Ann Arbor 852
Houston 821
Fairfield 645
Sofia 563
Ashburn 338
Beijing 306
Serra 285
New York 277
Princeton 244
Cambridge 239
Boulder 223
Wilmington 220
Seattle 218
Lawrence 192
Chandler 191
Medford 187
Ottawa 186
Des Moines 150
Milan 113
Florence 109
Nanjing 94
Dong Ket 85
Rome 85
Redwood City 66
Hong Kong 53
Dearborn 49
Nanchang 47
Pisa 43
Changsha 41
Genova 39
Hefei 35
Shenyang 34
Busto Arsizio 30
Guangzhou 29
Hebei 28
San Diego 28
Dakar 27
Kunming 25
Dallas 24
Bologna 21
Jacksonville 21
Jiaxing 20
London 20
Marseille 20
Shanghai 20
Abidjan 18
Taipei 17
Zhengzhou 16
Parma 15
Turin 15
Bern 14
Brussels 14
Giussano 13
Madrid 13
San Michele All'adige 13
Stockholm 13
Catania 12
Seoul 12
Tianjin 12
Tokyo 12
Livorno 11
Singapore 11
Hangzhou 10
Modena 10
Council Bluffs 9
Frankfurt am Main 9
Izmir 9
Norwalk 9
Sydney 9
Umeå 9
Bangalore 8
Monteriggioni 8
Mumbai 8
Padova 8
Valkenburg 8
Brisbane 7
Guiyang 7
Hillsboro 7
Jesi 7
Jinan 7
Kish 7
Napoli 7
Newport 7
Chengdu 6
Gif-sur-yvette 6
Islamabad 6
Jakarta 6
La Jolla 6
Lagos 6
Milazzo 6
Molise 6
Philadelphia 6
Pittsburgh 6
San Francisco 6
Wenzhou 6
Wuhan 6
Xian 6
Athens 5
Bristol 5
Totale 9.410
Nome #
Interazioni Piante-Ambiente 410
Photosynthetic traits and biochemical responses in strawberry (Fragaria × ananassa duch.) leaves supplemented with led lights 242
Phytochelatin synthase 1 regulates iron homeostasis in Arabidopsis thaliana 207
Effects of phytochelatin synthase on the secondary metabolism of Arabidopsis thaliana plants 186
Air pollution still limits epiphytic recolonization: heavy metals and ecophysiological parameters in threatened forest macrolichens of central europe 173
Dispensa di biologia vegetale 172
Le difese delle piante dai metalli pesanti 157
Aluminum effects on embryo suspensor polytene chromosomes of Phaseolus coccineus L 155
Looking at the present to gain knowledge on the past: what might be the primeval function of the phytochelatin synthase enzyme? 149
An integrated approach to highlight biological responses of Pisum sativum root to nano-TiO2 exposure in a biosolid-amended agricultural soil 147
Cadmium tolerance in Brassica juncea roots and shoots is affected by antioxidant status and phytochelatin biosynthesis 142
The morphogenic responses and phytochelatin complexes induced by arsenic in Pteris vittata change in the presence of cadmium 142
Oxidative stress and phytochelatin characterisation in bread wheat exposed to cadmium excess 137
The symbiosis between Nicotiana tabacum and the endomycorrhizal fungus Funneliformis mosseae increases the plant glutathione level and decreases leaf cadmium and root arsenic contents 134
The Arabidopsis thaliana Knockout Mutant for Phytochelatin Synthase1 (cad1-3) Is Defective in Callose Deposition, Bacterial Pathogen Defense and Auxin Content, But Shows an Increased Stem Lignification 127
Occurrence of different inter-varietal and inter-organ defence strategies towards supra-optimal zinc concentrations in two cultivars of Triticum aestivum L 123
Overexpression of AtPCS1 in tobacco increases arsenic and arsenic plus cadmium accumulation and detoxification 120
Characterization and quantification of thiol-peptides in Arabidopsis thaliana using combined dilution and high sensitivity HPLC-ESI-MS-MS 120
AQUA1 is a mercury sensitive poplar aquaporin regulated at transcriptional and post-translational levels by Zn stress 118
Phosphorus and metal removal combined with lipid production by the green microalga Desmodesmus sp.: An integrated approach 113
Evolution and functional differentiation of recently diverged phytochelatin synthase genes from Arundo donax L. 111
The phytochelatin synthase from Nitella mucronata (Charophyta) plays a role in the homeostatic control of iron(II)/(III) 110
From cyanobacteria to land plants: is the phytochelatin synthase enzyme necessary for both detoxification and homeostasis of metals? 110
Antifungal activity of diketopiperazines extracted from Alternaria alternata against Plasmopara viticola: an ultrastructural study. 108
Ancestral function of the phytochelatin synthase C-terminal domain in inhibition of heavy metal-mediated enzyme overactivation 106
Arsenic accumulation and thiol status in lichens exposed to As(V) in controlled conditions 104
Elevated atmospheric CO2 decreases oxidative stress and increases essential oil yield in leaves of Thymus vulgaris grown in a mini-FACE system 104
Proteomic analysis in the lichen Physcia adscendens exposed to cadmium stress. 103
Abscisic acid determination in Olea europea by radioimmunoassay 99
Phytoplasmas associated with tomato Stolbur disease 99
Response to copper stress in aposymbiotically grown lichen mycobiont Cladonia cristatella: uptake, viability, ergosterol and production of non-protein thiols 98
Overexpression of Arabidopsis phytochelatin synthase in tobacco plants enhances Cd2+ tolerance and accumulation but not translocation to the shoot. 96
Water availability modifies tolerance to photo-oxidative pollutants in transplants of the lichen Flavoparmelia caperata 95
Beyond peptidase activity of cyanobacterial phytochelatin synthases: the case of Nostoc sp., Gleiterinema sp., Gloeobacter violaceous 95
Phytochelatins govern zinc/copper homeostasis and cadmium detoxification in Cuscuta campestris parasitizing Daucus carota 91
Phytoplasma infection in tomato is associated with re-organization of plasma membrane, ER stacks, and actin filaments in sieve elements 91
Different compensatory mechanisms in two metal-accumulating aquatic macrophytes exposed to acute cadmium stress in outdoor artificial lakes 89
Hydrogen peroxide localization and antioxidant status in the recovery of apricot plants from European Stone Fruit Yellows 88
A Cd/Fe/Zn-responsive phytochelatin synthase is constitutively present in the ancient liverwort Lunularia cruciata (L.) Dumort. 87
Inhibition of sporulation and ultrastructural alterations of grapevine downy mildew by the endophytic fungus Alternaria alternata 87
Antioxidant status in herbaceous plants growing under elevated CO2 in mini-FACE rings 85
Differential responses to Cr(VI)-induced oxidative stress between Cr-tolerant and wild-type strains of Scenedesmus acutus (Chlorophyceae) 85
Phytoplasmas associated with tomato stolbur disease 85
null 85
Increase in ascorbate-glutathione metabolism as local and precocious systemic responses induced by cadmium in durum wheat plants 84
Responses of Xanthoria parietina thalli to environmentally relevant concentrations of hexavalent chromium 82
A bifasic response to cadmium stress in carrot: early acclimatory mechanisms give way to root collapse further to prolonged metal exposure 81
Intracellular response to cadmium in the moss Leptodictyum riparium 81
Balance of callose metabolism in phytoplasma/plant interaction 80
Nitric Oxide is Involved in Cadmium-Induced Programmed Cell Death in Arabidopsis Suspension Cultures 80
What might be the early function of the phytochelatin synthase enzyme? 80
PHYTOPLASMAS ASSOCIATED WITH TOMATO STOLBUR DISEASE 79
First and second line mechanisms of cadmium detoxification in the lichen photobiont Trebouxia impressa (Chlorophyta) 78
First and second line mechanisms of cadmium detoxification in the lichen photobiont Trebouxia impressa (Chlorophyta) 76
The capability to synthesize phytochelatins and the presence of constitutive and functional phytochelatin synthases are ancestral (plesiomorphic) characters for basal land plants 75
Identification of in vivo nitrosylated phytochelatins in Arabidopsis thaliana cells by liquid chromatography-direct electrospray-linear ion trap-mass spectrometry 75
Oxidative stress and phytochelatin characterization in wheat (Triticuym aestivum L.) exposed to cadmium excess 74
Antioxidant status, metal distribution and ultrastructural damage in Xanthoria parietina thalli exposed to environmentally-relevant concentrations of hexavalent chromium 74
Cell wall immobilization and antioxidant status of Xanthoria parietina thalli exposed to cadmium 74
Response to cadmium in higher plants 73
Elevated CO2 reduces vessel diameter and lignin deposition in some legume plants grown in mini-FACE rings 72
Correlation between hormonal homeostasis and morphogenic responses in Arabidopsis thaliana seedlings growing in a Cd/Cu/Zn multi-pollution context 72
Retaining unlogged patches in Mediterranean oak forests may preserve threatened forest macrolichens 71
The moss Leptodictyum riparium counteracts severe cadmium stress by activation of glutathione transferase and phytochelatin synthase, but slightly by phytochelatins 70
Cadmium accumulation and effects in two important crop plants for human consumption (tobacco and carrot) 69
Response of lichens to heavy metal stress by phytochelatin production 69
Lichens respond to heavy metals by phytochelatin synthesis 69
Overexpression of AtPCS1 gene affects Cd tolerance in Arabidopsis thaliana: changes in intracellular cadmium and root system morphology 69
Metabolite production from in vitro cultures of “hairy roots”: the example of ribosome-inactivating proteins. 69
Biological responses to aridity in Mediterranean ecosystems: stress and adaptation in mosses and lichens 69
Eukaryotic and Prokaryotic Phytochelatin Synthases Differ Less in Functional Terms Than Previously Thought: A Comparative Analysis of Marchantia polymorpha and Geitlerinema sp. PCC 7407 69
Licheni del Parco Nazionale d'Abruzzo, Lazio e Molise. Stato dell'arte. 68
Proteomic analysis as a tool for investigating arsenic stress in Pteris vittata roots colonized or not by arbuscular mycorrhizal symbiosis 68
Abiotic stresses in plants 68
Phytochelatin synthase in the charophyte Nitella mucronata: a primogenial role in metal micronutrient homeostasis? 68
Novel Coronavirus: How atmospheric particulate affects our environment and health 68
Response of barley plants to Fe deficiency and Cd contamination as affected by S starvation 66
The recovery of grapevine from phytoplasmas: variation of antioxidant status in leaf tissues 66
Cadmium tolerance and phytochelatin content of Arabidopsis seedlings overexpressing the phytochelatin synthase gene AtPCS1 65
Genome-wide inventory of metal homeostasis-related gene products including a functional phytochelatin synthase in the hypogeous mycorrhizal fungus Tuber melanosporum 64
Metal chelating peptides and proteins in plants 64
Phytochelatins and Phytochelatin synthases in Bryophytes 64
Production of ribosome-inactivating protein from “hairy root” cultures of Luffa cylindrica (L.) Roem. 64
On the role of H2O2 in the recovery of grapevine (Vitis vinifera, cv. Prosecco) from Flavescence dorée disease. 63
Cadmium tolerance, cysteine and thiol peptide levels in wild type and chroium-tolerant strains of Scenedesmus acutus (Chlorophyceae) 63
The "Recovery" phenomenon in Grapevine (Vitis vinifera) cv. Chardonnay infected by "Bois Noir" phytoplasma: investigation of proteome modifications by 2DE and Western Blot analysis 63
Iron deficiency modulates uptake and redistribution of reduced sulphur pool in barley plants 63
Water holding capacity, thallus anatomy and photosynthetic performance in Lobaria pulmonaria from retained-forest patches and isolated-trees 61
Recovery in apple trees infected with the apple proliferation phytoplasma: an ultrastructural and biochemical study 60
Responses of Xanthoria parietina thalli to cadmium: antioxidant status and stress protein biosynthesis 59
Le fitochelatine nei licheni come biomarker dell’inquinamento dell’aria da metalli pesanti 59
Supplemental red LED light promotes plant productivity, “photomodulate” fruit quality and increases Botrytis cinerea tolerance in strawberry 58
Catharanthus roseus phytoplasmas (chapter 9) 58
Phytochelatin synthases from cyanobacteria and land plants are less functionally different than previously thought. 58
Response to cadmium in carrot in vitro plants and cell cultures 57
Physiological and ultrastructural study of leaf tissues of apricots recovered from European Stone Fruit Yellows phytoplasma infection 56
CADMIUM, COPPER AND ZINC INDUCE THIOL-PEPTIDE PRODUCTION BUT DO NOT AFFECT GENE EXPRESSION INVOLVED IN THEIR SYNTHESIS IN ARABIDOPSIS THALIANA SEEDLINGS 56
Phytochelatin synthase manages iron homeostasis in the charophyte Nitella mucronata 55
Analisi proteomica nella diagnosi precoce di fitoplasmosi in Vitis vinifera 54
Ethylene biosynthesis and phytochelatin production in in vitro plants of Arabidopsis thaliana and Daucus carota 53
Totale 9.388
Categoria #
all - tutte 29.743
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 29.743


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019429 0 0 0 0 0 0 0 0 0 0 222 207
2019/20202.184 419 254 166 160 179 181 190 143 197 134 110 51
2020/20211.263 172 57 69 100 110 65 74 45 127 61 90 293
2021/20222.073 39 192 44 88 416 246 68 116 108 66 61 629
2022/20231.010 214 112 53 58 81 102 23 44 148 4 141 30
2023/20241.252 152 88 137 120 192 306 130 100 17 10 0 0
Totale 12.827