IRIS
GALLIANO, MONICA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.794
AS - Asia 3.388
EU - Europa 2.798
SA - Sud America 396
AF - Africa 168
Continente sconosciuto - Info sul continente non disponibili 99
OC - Oceania 4
Totale 12.647
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.588
CN - Cina 1.775
SG - Singapore 698
IE - Irlanda 622
UA - Ucraina 440
DE - Germania 353
HK - Hong Kong 312
BR - Brasile 286
FI - Finlandia 285
RU - Federazione Russa 282
VN - Vietnam 270
IT - Italia 213
GB - Regno Unito 185
FR - Francia 172
ZA - Sudafrica 122
SE - Svezia 91
CA - Canada 76
IN - India 67
BD - Bangladesh 45
JP - Giappone 42
MX - Messico 36
AR - Argentina 33
IQ - Iraq 28
CZ - Repubblica Ceca 27
PL - Polonia 27
TR - Turchia 24
ES - Italia 22
CO - Colombia 20
PK - Pakistan 19
BE - Belgio 18
EC - Ecuador 18
NL - Olanda 16
CR - Costa Rica 15
HN - Honduras 14
CL - Cile 12
CW - ???statistics.table.value.countryCode.CW??? 12
ID - Indonesia 12
IL - Israele 11
JM - Giamaica 10
PH - Filippine 10
AZ - Azerbaigian 9
PR - Porto Rico 9
SV - El Salvador 9
TT - Trinidad e Tobago 9
VE - Venezuela 9
AT - Austria 8
SA - Arabia Saudita 8
JO - Giordania 7
MA - Marocco 7
NI - Nicaragua 7
PA - Panama 7
PE - Perù 7
SC - Seychelles 7
KE - Kenya 6
LT - Lituania 6
MY - Malesia 6
PT - Portogallo 6
UZ - Uzbekistan 6
DK - Danimarca 5
GT - Guatemala 5
MU - Mauritius 5
PS - Palestinian Territory 5
TN - Tunisia 5
BO - Bolivia 4
GP - Guadalupe 4
IR - Iran 4
PY - Paraguay 4
AE - Emirati Arabi Uniti 3
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
NP - Nepal 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
AL - Albania 2
AO - Angola 2
AU - Australia 2
BG - Bulgaria 2
BH - Bahrain 2
CH - Svizzera 2
EE - Estonia 2
ET - Etiopia 2
GR - Grecia 2
HU - Ungheria 2
KZ - Kazakistan 2
LB - Libano 2
LK - Sri Lanka 2
LV - Lettonia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
RS - Serbia 2
SN - Senegal 2
SR - Suriname 2
BB - Barbados 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GE - Georgia 1
Totale 12.548
Salva come PNG Salva come JPEG
Città #
Chandler 662
Dublin 621
San Jose 543
Jacksonville 536
Ashburn 417
Nanjing 397
Singapore 353
Hong Kong 305
Beijing 285
Council Bluffs 280
Dallas 224
Boardman 191
Nanchang 153
Princeton 118
Lawrence 116
Johannesburg 115
Changsha 111
Los Angeles 111
Hebei 105
Shenyang 105
Lauterbourg 101
Jiaxing 98
Wilmington 94
Dearborn 89
Ho Chi Minh City 87
Medford 84
Ann Arbor 72
New York 67
Tianjin 62
Munich 61
Hanoi 60
Shanghai 58
Hangzhou 54
Helsinki 52
Milan 49
Buffalo 47
Santa Clara 42
Tokyo 41
Redondo Beach 40
Orem 37
Moscow 36
Woodbridge 36
Verona 30
Houston 29
Brno 26
Piscataway 26
São Paulo 24
Montreal 23
Warsaw 23
Norwalk 22
Atlanta 21
San Francisco 20
Brussels 18
Chennai 18
Frankfurt am Main 18
The Dalles 18
Turku 18
Chicago 17
Brooklyn 16
Denver 16
Kunming 16
Seattle 16
Boston 15
London 14
Rio de Janeiro 14
Toronto 14
Falls Church 13
Naples 13
Des Moines 12
Fairfield 12
North Bergen 12
Stockholm 12
Willemstad 12
Phoenix 11
San José 11
Baghdad 10
Charlotte 10
Guangzhou 10
Pavia 10
Poplar 10
San Pedro Sula 10
Las Vegas 9
Mexico City 9
Nürnberg 9
Paris 9
Rome 9
Baku 8
Detroit 8
Guayaquil 8
Haiphong 8
Jinan 8
New Delhi 8
San Salvador 8
Amsterdam 7
Ankara 7
Columbus 7
Da Nang 7
Managua 7
Miami 7
Santiago 7
Totale 7.905
Salva come PNG Salva come JPEG
Nome #
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 264
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 162
A novel splicing mutation causes an undescribed type of analbuminemia. 162
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 160
Molecular Genetics of Analbuminemia 158
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 148
A novel splicing mutation causes analbuminemia in a Portuguese boy. 144
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS: from pooled to individual patient samples 140
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 139
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 139
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 138
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 138
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 136
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 135
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 135
Analbuminemia produced by a novel splicing mutation 134
BEL β-trefoil: a novel lectin with antineoplastic properties in king bolete (Boletus edulis) mushrooms. 132
Albumin locust valley: a new case of analbuminemia. 131
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 130
Pilot studies to evaluate the effectiveness of high LET particle irradiation in damaging neurotoxic protein aggregates 130
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 129
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 129
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 129
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 128
Applications of a trypsin immobilized bioreactor coupled with mass spectrometry 127
Analysis of human serum albumin variants by mass spectrometric procedures. 127
A new bisalbuminemia: bisalbuminemia of Kenitra 127
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS 126
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 126
Analysis of human serum albumin variants by mass spectrometric procedures. 125
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 125
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 125
Phosphoprotein analysis of amniotic fluid samples from individual patients by a miniaturized LC-MS system 124
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 123
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 123
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 121
Trypsin-based monolithic bioreactor coupled on-line with LC/MS/MS system for protein digestion and variant identification in standard solution and serum samples 121
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 121
Analbuminemia Zonguldak: case report and mutational analysis. 120
Mechanistic Insight into the Peroxidase Catalyzed Nitration of Tyrosine Derivatives by Nitrite and Hydrogen Peroxide 119
Human plasma retinol-binding protein (RBP4) is also a fatty acid-binding protein. 119
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 118
Novel nonsense mutation causes analbuminemia in a Moroccan family. 117
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 117
Studying protein phosphorylation by LC-MS: application to amniotic fluid 116
Structural characterization of a chain termination mutant of human serum albumin. 115
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 114
Phosphoproteome analysis by LC-MS: different approaches for the characterization of amniotic fluid 113
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 113
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 111
The amino acid substitution in albumin Roma: 321 Glu----Lys. 111
Genetic variants showing apparent hot-spots in the human serum albumin gene. 110
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 110
High resolution crystal structure data of human plasma retinol-binding protein (RBP4) bound to retinol and fatty acids 110
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. 109
Computational and experimental approaches assess the interactions between bovine beta-lactoglobulin and synthetic compounds of pharmacological interest 108
PH AND IONIC STRENGHT DEPENDENCE OF PROTEIN (UN)FOLDING AND LIGAND BINDING TO BOVINE BETA-LACTOGLOBULINS A AND B 108
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 107
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 106
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 106
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 106
Enzymatic properties of human hemalbumin. 105
Structural transitions of human serum albumin: an investigation using electrophoretic techniques. 105
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 104
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 104
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 104
Nitrative stress causes nitration, oxidation, and subunit cross linking in human hemoglobin 104
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 104
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 103
Wards in the keyway: amino acids with anomalouspkas in calycins 102
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 102
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 102
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 101
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 101
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 98
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 97
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 97
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 97
Electrostatics of folded and unfolded bovine β-lactoglobulin. 97
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 94
Three-dimensional structure and ligand-binding site of carp fishelectin (FEL). 94
Neuronal proteins as targets of 3-hydroxykynurenine: Implications in neurodegenerative diseases 94
Bovine beta-lactoglobulin acts as an acid-resistant drug carrier by exploiting its diverse binding regions. 93
Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. 93
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 92
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 92
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 92
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 90
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 89
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 89
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 88
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 88
Clinical, genetic, and protein structural aspects of familial dysalbuminemic hyperthyroxinemia and hypertriiodothyroninemia 88
BLGA protein solutions at high ionic strenght: vanishing attractive interactions and 'frustrated' aggregation 87
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 86
Miniaturization of integrated systems for phosphoprotein analysis: from pooled to individual patient samples 86
Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms. 86
Mutants and molecular dockings reveal that the primary L-thyroxine binding site in human serum albumin is not the one which can cause familial dysalbuminemic hyperthyroxinemia 86
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 85
PROBING PROTEIN AGGREGATION BY TIME-RESOLVED FLUORESCENCE DURING BETA-LACTOGLOBULIN CRYSTAL GROWTH 83
Totale 11.496
Salva come PNG Salva come JPEG
Categoria #
all - tutte 52.501
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 52.501
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022433 0 0 0 0 9 10 14 37 24 13 75 251
2022/20231.820 167 127 15 162 220 170 0 114 762 9 43 31
2023/2024533 50 120 7 35 53 140 3 36 2 19 40 28
2024/20251.416 31 142 49 61 35 43 25 93 357 24 215 341
2025/20263.637 265 300 386 393 485 170 669 196 268 266 84 155
2026/20271.429 67 352 317 473 220 0 0 0 0 0 0 0
Totale 12.647