LOTTI, MARINA
 Distribuzione geografica
Continente #
NA - Nord America 11.368
EU - Europa 6.423
AS - Asia 5.763
SA - Sud America 731
AF - Africa 96
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 24.396
Nazione #
US - Stati Uniti d'America 10.948
SG - Singapore 1.792
CN - Cina 1.568
IT - Italia 1.568
DE - Germania 929
VN - Vietnam 861
HK - Hong Kong 851
RU - Federazione Russa 815
SE - Svezia 750
BR - Brasile 589
IE - Irlanda 532
GB - Regno Unito 396
UA - Ucraina 387
CA - Canada 323
PL - Polonia 293
FI - Finlandia 176
IN - India 170
FR - Francia 165
KR - Corea 106
DK - Danimarca 88
TR - Turchia 74
MX - Messico 70
ID - Indonesia 69
NL - Olanda 67
AT - Austria 58
ES - Italia 56
AR - Argentina 46
JP - Giappone 43
BD - Bangladesh 42
GR - Grecia 38
ZA - Sudafrica 38
BE - Belgio 31
PK - Pakistan 31
IQ - Iraq 26
EC - Ecuador 24
RO - Romania 20
IR - Iran 18
PY - Paraguay 15
SA - Arabia Saudita 15
TW - Taiwan 14
CL - Cile 13
CO - Colombia 11
IL - Israele 11
MA - Marocco 11
PE - Perù 11
AU - Australia 10
KZ - Kazakistan 10
LT - Lituania 10
MY - Malesia 10
TN - Tunisia 10
CH - Svizzera 9
VE - Venezuela 9
CZ - Repubblica Ceca 8
UY - Uruguay 8
EG - Egitto 6
NO - Norvegia 6
AM - Armenia 5
DO - Repubblica Dominicana 5
HN - Honduras 5
HU - Ungheria 5
MU - Mauritius 5
NP - Nepal 5
TH - Thailandia 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
BO - Bolivia 4
DZ - Algeria 4
ET - Etiopia 4
JM - Giamaica 4
KE - Kenya 4
OM - Oman 4
PA - Panama 4
PH - Filippine 4
SC - Seychelles 4
AL - Albania 3
AZ - Azerbaigian 3
BG - Bulgaria 3
CR - Costa Rica 3
JO - Giordania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BN - Brunei Darussalam 2
BW - Botswana 2
EE - Estonia 2
LB - Libano 2
LK - Sri Lanka 2
NG - Nigeria 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
TT - Trinidad e Tobago 2
ZW - Zimbabwe 2
BH - Bahrain 1
BT - Bhutan 1
GG - Guernsey 1
GH - Ghana 1
GT - Guatemala 1
HR - Croazia 1
IS - Islanda 1
KG - Kirghizistan 1
KH - Cambogia 1
KI - Kiribati 1
Totale 24.382
Città #
Ann Arbor 2.005
Singapore 1.126
Ashburn 968
Woodbridge 912
Hong Kong 841
Fairfield 757
Milan 624
Chandler 587
Frankfurt am Main 580
Houston 555
Dublin 516
Wilmington 450
Jacksonville 404
Seattle 351
Cambridge 269
New York 259
Kraków 252
Beijing 246
Santa Clara 242
Dearborn 221
Hefei 212
Ho Chi Minh City 210
Princeton 190
Dallas 184
Los Angeles 179
Hanoi 141
Nanjing 135
Seoul 101
Shanghai 100
Helsinki 97
The Dalles 94
Dong Ket 90
Lawrence 87
Altamura 80
Chicago 79
Moscow 77
Toronto 71
Council Bluffs 69
Lachine 65
Montréal 65
San Diego 60
São Paulo 60
Buffalo 58
Ottawa 55
Jakarta 54
Vienna 51
Rome 50
Nanchang 48
Guangzhou 47
Andover 38
Boardman 34
London 32
Munich 32
Shenyang 31
Warsaw 30
Changsha 29
Hebei 29
Kent 29
Naples 29
Brussels 28
Jinan 28
Denver 27
Tianjin 27
Zhengzhou 27
Rio de Janeiro 26
Fremont 25
Brooklyn 23
Desio 23
Jiaxing 23
Manchester 23
Chennai 22
Norwalk 22
Poplar 22
Salt Lake City 21
Heraklion 20
Napoli 20
Ningbo 20
Falls Church 19
Johannesburg 19
Kunming 19
Romola 19
Tokyo 19
Montreal 18
Philadelphia 18
Quận Bình Thạnh 18
Haiphong 17
Kocaeli 17
Nuremberg 17
Phoenix 17
Campinas 16
Hangzhou 16
Huizen 16
Mexico City 16
Biên Hòa 15
Como 15
Mountain View 15
Sacramento 15
Taizhou 15
Edmonton 14
Auburn Hills 13
Totale 16.097
Nome #
Oxidative degradation of polyethylene by two novel laccase-like multicopper oxidases from Rhodococcus opacus R7 606
The "cold revolution". Present and future applications of cold-active enzymes and ice-binding proteins 454
The co-existence of cold activity and thermal stability in an Antarctic GH42 β-galactosidase relies on its hexameric quaternary arrangement 445
Structure of a bacterial ice binding protein with two faces of interaction with ice 419
Cryo-protective effect of an ice-binding protein derived from Antarctic bacteria 411
Diverse effects of aqueous polar co-solvents on Candida antarctica lipase B 385
Aggregation properties of a disordered protein are tunable by pH and depend on its net charge per residue 373
Education for a biobased economy: integrating life and social sciences in flexible short courses accessible from different backgrounds 371
Plasma-induced graft-polymerization of polyethylene glycol acrylate on polypropylene films: Chemical characterization and evaluation of the protein adsorption 367
Saturn-Shaped Ice Burst Pattern and Fast Basal Binding of an Ice-Binding Protein from an Antarctic Bacterial Consortium 362
The importance of fermentative conditions for the biotechnological production of lignin modifying enzymes from white-rot fungi 347
Enzymatic Production of Biodiesel: Strategies to Overcome Methanol Inactivation 346
Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes 345
Conversion of sugar beet residues into lipids by Lipomyces starkeyi for biodiesel production 326
Short-chain alcohols inactivate an immobilized industrial lipase through two different mechanisms 320
Structural and dynamics analysis of intrinsically disordered proteins by high-speed atomic force microscopy 315
Electrospray-ionization mass spectrometry as a tool for fast screening of protein structural properties 310
Effects of methanol on lipases: Molecular, kinetic and process issues in the production of biodiesel 294
Cold-Active β-Galactosidases: Insight into Cold Adaptation Mechanisms and Biotechnological Exploitation 285
Activity and Enantioselectivity of Wildtype and Lid Mutated Candida rugosa Lipase Isoform 1 in Organic Solvents 281
Order propensity of an intrinsically disordered protein, the cyclin-dependent-kinase inhibitor Sic1 281
Relevance of metal ions for lipase stability: Structural rearrangements induced in the Burkholderia glumae lipase by calcium depletion 275
Burkholderia cepacia lipase is a promising biocatalyst for biofuel production 274
The activity and stability of a cold-active acylaminoacyl peptidase rely on its dimerization by domain swapping 274
Amplification of cup1 gene is associated with evolution of copper tolerance in Saccharomyces cerevisiae 273
The lid is a structural and functional determinant of lipase activity and selectivity 269
Mechanism of non-phenolic substrate oxidation by the fungal laccase Type 1 copper site from Trametes versicolor: the case of benzo[a]pyrene and anthracene 261
Compaction Properties of an Intrinsically Disordered Protein: Sic1 and Its Kinase-Inhibitor Domain 261
Sustainable production of a biotechnologically relevant β-galactosidase in Escherichia coli cells using crude glycerol and cheese whey permeate 253
Cheese-whey permeate improves the fitness of Escherichia coli cells during recombinant protein production 250
Secondary structure, conformational stability and glycosylation of a recombinant Candida rugosa lipase studied by Fourier-transform infrared spectroscopy 249
Reciprocal influence of protein domains in the cold-adapted acyl aminoacyl peptidase from Sporosarcina psychrophila 249
Kinetics of inclusion body formation studied in intact cells by FT-IR spectroscopy 247
Application of site-directed lipase mutants on regioselective acylation of monosaccharides 247
Monitoring the transport of recombinant Candida rugosa lipase by a green fluorescent protein-lipase fusion 247
Extreme marine and coastal environments as a source of glycoside hydrolases involved in the degradation of oligosaccharides and polysaccharides 244
Sequence of the lid affects activity and specificity of Candida rugosa lipase isoenzymes 243
Structural and kinetic stability of the burkholderia glumae lipase 242
Laboratory evolution of copper tolerant yeast strains 241
Comparative analysis of Polyethylene-Degrading Laccases: Redox Properties and Enzyme-Polyethylene Interaction Mechanism. 237
Effects of methanol on a methanol-tolerant bacterial lipase 236
The cold-active lipase of Pseudomonas fragi: Heterologous expression, biochemical characterization and molecular modeling 234
A bacterial acyl aminoacyl peptidase couples flexibility and stability as a result of cold adaptation 232
Defining Structural Domains of an Intrinsically Disordered Protein: Sic1, the Cyclin-Dependent Kinase Inhibitor of Saccharomyces cerevisiae 230
Evolution of Stability in a Cold-Active Enzyme Elicits Specificity Relaxation and Highlights Substrate-Related Effects on Temperature Adaptation 225
In vivo aggregation of bovine beta-lactoglobulin is affected by Cys121 224
Structural determinants of cold activity and glucose tolerance of a family 1 glycoside hydrolase (GH1) from Antarctic Marinomonas sp. ef1 216
Concepts and tools to exploit the potential of bacterial inclusion bodies in protein science and biotechnology 214
Expression of cloned Saccharomyces diastaticus glucoamylase under natural and inducible promoters 214
Heterologous expression of bovine and porcine beta-lactoglobulins in Pichia pastoris: towards a comparative functional characterisation 210
A cold-active esterase enhances mesophilic properties through Mn2+ binding 207
Why and how protein aggregation has to be studied in vivo 207
Editorial: Protein stabilization - crossroad for protein-based processes and products 205
Unscrambling thermal stability and temperature adaptation in evolved variants of a cold-active lipase 205
Iron bioleaching and polymers accumulation by an extreme acidophilic bacterium 204
Fourier transform infrared spectroscopy analysis of the conformational quality of recombinant proteins within inclusion bodies 204
ENHANCED EXPRESSION OF HETEROLOGOUS PROTEINS BY THE USE OF A SUPERINDUCIBLE VECTOR IN BUDDING YEAST 201
Recombinant proteins and host cell physiology 200
A novel laccase from Trametes polyzona with high performance in the decolorization of textile dyes 198
Mn2+ binding affects the thermal properties of an Antarctic esterase 197
Molecular mechanism of deactivation of C. antarctica lipase B by methanol 196
Effects of recombinant protein misfolding and aggregation on bacterial membranes 192
Evaluation of the Conformational Stability of Recombinant Desulfurizing Enzymes from a Newly Isolated Rhodococcus sp. 191
Acyl transfer strategy for the biocatalytical characterisation of Candida rugosa lipases in organic solvents 190
Heterologous production of a novel Coriolopsis polyzona laccase in Saccharomyces cerevisiae 189
From urban trash to city cash: Technologies for sustainable development of cities through the valorisation of urban organic waste in Europe 189
Recombinant lipase from Candida rugosa for regioselective hydrolysis of peracetylated nucleosides. A comparison with commercial non recombinant lipases 188
Effect of the leader sequence on the expression of recombinant C-rugosa lipase by S-cerevisiae cells 188
Lipases: Molecular structure and function 187
Cloning and nucleotide sequences of two lipase genes from Candida cylindracea 187
Evolutionary history and activity towards oligosaccharides and polysaccharides of GH3 glycosidases from an Antarctic marine bacterium 186
Mutations in the lid region affect chain length specificity and thermostability of a Pseudomonas fragi lipase 185
Comparison of bovine and porcine β-lactoglobulin: A mass spectrometric analysis 185
The effect of thermodynamic properties of solvent mixtures explains the difference between methanol and ethanol in C.antarctica lipase B catalyzed alcoholysis 182
Directed evolution of a cold-active lipolytic enzyme 178
Promiscuity, stability and cold-adaptation of a newly isolated acylaminoacyl peptidase 178
Functional overexpression of a 1647 bp synthetic gene coding for C. rugosa lipase LIP1, a major industrial lipase 177
How disorder influences order and viceversa: mutual effects in fusion proteins containing an intrinsically disordered and a globular protein 177
Characterization of the Candida rugosa lipase system and overexpression of the lipl isoenzyme in a non-conventional yeast 176
Physiological and genetic modulation of inducible expression of Escherichia coli β-galactosidase in Saccharomyces cerevisiae 176
Endolysins from Antarctic Pseudomonas Display Lysozyme Activity at Low Temperature 173
Components of the E coli envelope are affected by and can react to protein over-production in the cytoplasm 170
High lipase production by Candida rugosa is associated with G1 cells. A flow cytometry study 169
Bacterial inclusion bodies as active and dynamic protein ensembles 169
Protein Aggregation in Bacteria: Functional and Structural Properties of Inclusion Bodies in Bacterial Cells 167
Sulfated and sulfonated polymers are able to solubilize efficiently the protein aggregates of different nature 165
Expression of heterologous gene in S. cerevisiae cells: production form pg/L to grams/liter 161
Mutants provide evidence of the importance of glycosydic chains in the activation of lipase 1 from Candida rugosa 158
Deactivation and unfolding are uncoupled in a bacterial lipase exposed to heat, low pH and organic solvents 155
Physiological and genetic modulation of the expression of heterologous proteins in budding yeast. 152
Organic chemistry and biological systems. Biochemistry 151
Localization of lipase genes on Candida rugosa chromosomes 151
Mutual effects of disorder and order in fusion proteins between intrinsically disordered domains and fluorescent proteins 149
Cloning and analysis of Candida cylindracea lipase sequences 145
Influence of upstream activating sequences on the expression of heterologous proteins in budding yeast 144
The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19 142
Protein Engineering in basic and applied biotechnology: a review 142
Variability within the Candida rugosa upases family 142
Polysaccharide degradation in an Antarctic bacterium: Discovery of glycoside hydrolases from remote regions of the sequence space 142
Location of protein S4 on the small ribosomal subunit of E. coli and B. stearothermophilus with protein- and hapten-specific antibodies 140
Totale 23.526
Categoria #
all - tutte 81.302
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 81.302


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.697 0 0 0 0 0 227 206 177 192 318 166 411
2021/20221.677 119 186 250 134 99 145 122 52 103 97 128 242
2022/20232.686 284 864 237 210 189 359 26 129 165 55 116 52
2023/20241.751 70 55 61 85 211 371 346 129 151 48 41 183
2024/20254.572 292 456 337 215 322 207 250 258 440 612 419 764
2025/20265.215 1.305 710 708 1.096 1.078 318 0 0 0 0 0 0
Totale 25.038