CERVONE, Felice
 Distribuzione geografica
Continente #
NA - Nord America 8.336
EU - Europa 3.502
AS - Asia 1.694
SA - Sud America 157
AF - Africa 20
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 1
Totale 13.716
Nazione #
US - Stati Uniti d'America 8.220
IT - Italia 931
SG - Singapore 712
UA - Ucraina 515
IN - India 485
DE - Germania 476
CN - Cina 457
SE - Svezia 406
IE - Irlanda 381
FI - Finlandia 345
GB - Regno Unito 146
AR - Argentina 115
CA - Canada 102
BG - Bulgaria 99
BE - Belgio 41
BR - Brasile 31
FR - Francia 29
NL - Olanda 25
AT - Austria 22
CH - Svizzera 17
RO - Romania 14
ID - Indonesia 13
ES - Italia 12
MX - Messico 12
LT - Lituania 10
RU - Federazione Russa 10
CL - Cile 8
HK - Hong Kong 7
TG - Togo 7
DK - Danimarca 6
PL - Polonia 6
KR - Corea 5
NZ - Nuova Zelanda 5
ZA - Sudafrica 5
TR - Turchia 4
CZ - Repubblica Ceca 3
EE - Estonia 3
NG - Nigeria 3
PK - Pakistan 3
SA - Arabia Saudita 3
CO - Colombia 2
EG - Egitto 2
HU - Ungheria 2
IR - Iran 2
JP - Giappone 2
NO - Norvegia 2
PA - Panama 2
AU - Australia 1
DZ - Algeria 1
EU - Europa 1
IL - Israele 1
LU - Lussemburgo 1
MA - Marocco 1
SC - Seychelles 1
VE - Venezuela 1
Totale 13.716
Città #
Chandler 999
Fairfield 966
Ashburn 514
Woodbridge 476
Singapore 427
Houston 422
Ann Arbor 392
Dublin 381
Seattle 364
Cambridge 361
Wilmington 337
Beijing 319
Rome 293
Princeton 268
Plano 256
Jacksonville 206
Santa Clara 179
Dearborn 150
Grafing 145
Boston 138
Bremen 134
Millbury 122
Federal 115
Sofia 99
Boardman 95
Helsinki 92
San Paolo di Civitate 88
San Diego 82
Lawrence 73
Des Moines 63
Andover 59
Ottawa 52
Toronto 47
New York 45
Norwalk 45
Brussels 38
L’Aquila 33
Bühl 31
Falls Church 31
Fremont 28
Milan 27
Dallas 25
London 24
Vienna 22
Hefei 16
Frankfurt am Main 15
Ladispoli 15
Los Angeles 15
Nanjing 14
Brasília 13
Jakarta 13
Kunming 13
Washington 13
Cologne 12
Guangzhou 12
Bern 11
Parma 11
San Mateo 11
Auburn Hills 10
Pune 10
Falkenstein 9
Mannheim 9
Padova 9
Mexico City 8
Redmond 8
Redwood City 8
Stockholm 8
Jinan 7
Lomé 7
Phoenix 7
Buffalo 6
Catania 6
Laurel 6
Mazzano Romano 6
Moncalieri 6
Tavarnelle Val di Pesa 6
Zhengzhou 6
Bonn 5
Duncan 5
Indiana 5
Nanchang 5
Santiago 5
Southend 5
Auckland 4
Bari 4
Bologna 4
Florence 4
Hebei 4
Hong Kong 4
Lavras 4
Magenta 4
Montebelluna 4
Poznan 4
Provo 4
San Francisco 4
Seoul 4
Shanghai 4
Shenyang 4
Springfield 4
Torino 4
Totale 9.487
Nome #
Inibitore della pectina metilesterasi nella preparazione dei succhi di frutta e derivati 342
Homeostasis of cell wall-derived DAMPs is regulated through oxidation by Berberine-Bridge like proteins 121
An EFR-Cf-9 chimera confers enhanced resistance to bacterial pathogens by SOBIR1- and BAK1-dependent recognition of elf18 115
Combination of Pretreatment with White Rot Fungi and Modification of Primary and Secondary Cell Walls Improves Saccharification 111
Cell wall traits that influence plant development, immunity, and bioconversion 110
The Arabidopsis thaliana Class III Peroxidase AtPRX71 Negatively Regulates Growth under Physiological Conditions and in Response to Cell Wall Damage 108
Plant immunity triggered by engineered in vivo release of oligogalacturonides, damage-associated molecular patterns. 106
An Arabidopsis berberine‐bridge enzyme‐like protein specifically oxidizes cellulose oligomers and plays a role in immunity 105
A lower content of de-methylesterified homogalacturonan improves enzymatic cell separation and isolation of mesophyll protoplasts in Arabidopsis 99
Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification 99
Transgenic expression of pectin methylesterase inhibitors limits tobamovirus spread in tobacco and Arabidopsis 98
A functional pectin methylesterase inhibitor protein (SolyPMEI) is expressed during tomato fruit ripening and interacts with PME-1 96
Extracellular DAMPs in plants and mammals: immunity, tissue damage and repair 96
Engineering the cell wall by reducing de-methyl-esterified homogalacturonan improves saccharification of plant tissues for bioconversion 95
Transgenic Expression of a Fungal Endo-Polygalacturonase Increases Plant Resistance to Pathogens and Reduces Auxin Sensitivity 94
Controlled expression of pectic enzymes in Arabidopsis thaliana enhances biomass conversion without adverse effects on growth 93
GRP-3 and KAPP, encoding interactors of WAK1, negatively affect defense responses induced by oligogalacturonides and local response to wounding 89
How do pectin methylesterases and their inhibitors affect the spreading of tobamovirus? 86
Crystallization and preliminary X-ray diffraction study of the endopolygalacturonase from Fusarium moniliforme 85
Alteration of pectin integrity by expression of a fungal polygalacturonase enhances pathogen resistance. 85
Dampening the DAMPs: how plants maintain the homeostasis of cell wall molecular patterns and avoid hyper-immunity 84
A Single Amino-Acid Substitution Allows Endo-Polygalacturonase of Fusarium verticillioides to Acquire Recognition by PGIP2 from Phaseolus vulgaris 83
Overexpression of pectin methylesterase inhibitors in Arabidopsis restricts fungal infection by Botrytis cinerea 83
Deconstruction by microbial cell wall degrading enzymes to convert plant biomass into 2nd generation biofuels 82
Methyl esterification of pectin plays a role during plant-pathogen interactions and affects plant resistance to diseases 82
Analysis of the interaction between PGIP from Phaseolus vulgaris L. and fungal endopolygalacturonases using biosensor technology 81
The Arabidopsis NUCLEUS- AND PHRAGMOPLAST-LOCALIZED KINASE1-Related Protein Kinases Are Required for Elicitor-Induced Oxidative Burst and Immunity 81
A domain swap approach reveals a role of the plant wall-associated kinase 1 (WAK1) as a receptor of oligogalacturonides 81
Studi strutturali e molecolari dell'interazione fra poligalatturonasi fungine e PGIP.11° Incontro su "Aspetti Molecolari e fisiologici delle interazioni pianta-patogeno" 81
Reduced content of homogalacturonan does not alter the ion-mediated increase in xylem hydraulic conductivity in tobacco 80
Polygalacturonase-inhibiting proteins: players in plant innate immunity? 80
Pectin Methylesterase Is Induced in Arabidopsis upon Infection and Is Necessary for a Successful Colonization by Necrotrophic Pathogens 80
Bacterial endopectate lyase: evidence that plant cell wall pH prevents tissue maceration and increases the half-life of elicitor active oligogalacturonides 79
Structural Resolution of the Complex between a Fungal Polygalacturonase and a Plant Polygalacturonase-Inhibiting Protein by Small-Angle X-Ray Scattering 79
Purification and properties of two polygalacturonases from Trichoderma koningii 78
Four Arabidopsis berberine-bridge enzyme-like proteins are specific oxidases that inactivate the elicitor-active oligogalacturonides 78
Extracellular H2O2 induced by oligogalacturonides is not involved in the inhibition of the auxin-regulated rolB gene expression in tobacco leaf explants 78
EFFECTS OF OLIGOGALACTURONIDES ON TOBACCO LEAF EXPLANTS CULTURED ON ROOT-INDUCING MEDIUM 77
Oligosaccharins involved in plant growth and host/pathogen interactions 77
Oligogalacturonide oxidases (OGOXs) play a role in plant immunity and development 76
Loss of the arabidopsis protein kinases ANPs affects root cell wall composition, and triggers the cell wall damage syndrome 76
The esterification status and the length of acidic stretches of homogalacturonan is critical for plant biomass processing. 75
Antisense expression of the Arabidopsis thaliana AtPGIP1 gene reduces polygalacturonase-inhibiting protein accumulation and enhances susceptibility to Botrytis cinerea 75
Crystal structure of the endopolygalacturonase from the phytopathogenic fungus Colletotrichum lupini and its interaction with polygalacturonase-inhibiting proteins. 75
Endopolygalacturonase is not required for pathogenicity of cochliobolus carbonum on maize 74
Dansyl chloride binding to proteins. Quantitative estimation of N-terminal, lysyl and tyrosyl residues by the radioactive reagent 74
Integration of evolutionary and desolvation energy analysis identifies functional sites in a plant immunity protein 74
Molecular signalling and recognition in plant defense mechanisms 74
Recognition and signalling in the cell wall: the case of endopolygalacturonase, PGIP and oligogalacturonides 74
PECTIN MODIFICATION IMPROVES UTILIZATION OF PLANT BIOMASSES TO BIOFUEL CONVERSION 74
Simple procedures for the separation and identification of bovine milk whey proteins 72
Accumulation of PGIP, a leucine-rich receptor-like protein, correlates with the hypersensitive response in race-cultivar interactions 72
Polygalacturonase from Rhizoctonia fragariae: further characterization of two isoenzymes and their action towards strawberry tissue 71
A polygalacturonase-inhibiting protein in the flowers of Phaseolus vulgaris L. 71
Engineering plant resistance by constructing chimeric receptors that recognize damage-associated molecular patterns (DAMPs) 71
Cloning and characterization of the gene encoding the endopolygalacturonase of Fusarium moniliforme 71
Structure-function and molecular studies on fungal polygalacturonases and their inhibitors PGIPs 70
Isolation and characterization of pectin-inducible cDNA clones from the phytopathogenic fungus Fusarium moniliforme 70
Sensitive detection and measurement of oligogalacturonides in Arabidopsis 70
Multiple forms of polygalacturonase in two strains of Rhizoctonia solani 68
Crystal structure of the complex between pectin methylesterase and pectin methylesterase inhibitor 68
Pectin methylesterase inhibitors affect plant growth and defence against pathogens 68
Targeted pectin modification to improve cell wall saccharification for biofuel production 68
Enhancing immunity by engineering DAMPs 67
Pectinolytic activity in some ericoid mycorrhyzal fungi 66
Exploring the pectin network to identify determinants of plant resistance to pathogens 66
The crystal structure of polygalacturonase-inhibiting protein (PGIP), a leucine-rich repeat protein involved in plant defense 66
Oligogalacturonides inhibit the formation of roots on tobacco explants 65
Expression of endopolygalacturonase and other fungal genes induced by pectin 64
Characterization of a membrane-associated apoplastic lipoxygenase in Phaseolus vulgaris L. 64
Plant cell wall dynamics and wall-related susceptibility in plant-pathogen interactions 64
Oligogalacturonide signalling: sensing a breach in the wall 64
A polygalacturonase-inhibiting protein from alfalfa callus cultures 64
A class of cell wall-derived damage-associated molecular patterns affects plant-aphid interactions 64
Oligogalacturonides prevent rhizogenesis in rolB-transformed tobacco explants by inhibiting auxin-induced expression of the rolB gene 64
Structural basis for the interaction between pectin methylesterase and a specific inhibitor protein 63
Pectin modification to improve plant biomass utilization 63
The polygalacturonase-inhibiting protein PGIP2 of Phaseolus vulgaris has evolved a mixed mode of inhibition of endopolygalacturonase PG1 of Botrytis cinerea 62
Competitive inhibition of the auxin-induced elongation by α-D-oligogalacturonides in pea stem segments 62
Oligogalacturonides: plant damage-associated molecular patterns and regulators of growth and development 62
Targeted modification of homogalacturonan by transgenic expression of a fungal polygalacturonase alters plant growth 61
THE STRUCTURE OF HOMOGALACTURONAN IS CRITICAL FOR PLANT BIOMASS PROCESSING 61
Pectic enzymes as phytotoxins: absorption of polygalacturonase from Colletotrichum lindemuthianum to French bean protoplasts 60
Isolation of novel Arabidopsis mutants with altered defensin expression. 60
Fusarium moniliforme secretes four endopolygalacturonases derived from a single gene product 60
Phytotoxic effects and Phytoalexin-elicitor activity of microbial pectic enzymes 60
Polygalacturonase-inhibiting protein (PGIP) in plant defence: a structural view 60
Oligogalacturonide-induced changes in the nuclear proteome of Arabidopsis thaliana 59
Comparison of immunological reactivity of polygalacturonases from different fungi 58
Polygalacturonase, PGIP and oligogalacturonides in cell-cell communication 58
The interaction between fungal endopolygalacturonase and plant cell wall PGIP (Polygalacturonase-Inhibiting Protein) 58
Pectin modification to improve cell wall saccharification for biofuel production 58
Release of phytoalexin elicitor-active oligogalacturonides by microbial pectic enzymes 57
Mutagenesis studies to improve the polygalacturonase inhibiting protein (PGIP) 57
Structure-function and molecular studies on fungal polygalacturonases and their inhibitors PGIPs 57
Plant neurobiology: no brain, no gain? 57
Fungal invasion enzymes and their inhibition. 56
Expression and localization of polygalacturonase during the outgrowth of lateral roots in Allium porrum L. 56
Wounding in the plant tissue: the defense of a dangerous passage 56
null 56
Totale 7.743
Categoria #
all - tutte 40.402
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 1.669
selected - selezionate 0
volume - volumi 0
Totale 42.071


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.630 0 0 0 0 0 318 313 277 220 270 184 48
2020/20211.174 146 105 47 92 25 88 45 84 219 205 96 22
2021/20222.708 20 149 273 55 322 43 40 242 228 218 553 565
2022/20233.180 479 369 129 509 431 439 19 379 241 36 109 40
2023/20241.470 94 223 71 86 167 207 77 140 18 173 88 126
2024/2025971 176 122 123 187 233 130 0 0 0 0 0 0
Totale 14.050