IRIS
GALLIANO, MONICA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.889
AS - Asia 3.368
EU - Europa 2.697
SA - Sud America 392
AF - Africa 161
Continente sconosciuto - Info sul continente non disponibili 87
OC - Oceania 4
Totale 11.598
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.786
CN - Cina 1.771
SG - Singapore 697
IE - Irlanda 622
UA - Ucraina 439
DE - Germania 347
HK - Hong Kong 311
FI - Finlandia 285
BR - Brasile 282
VN - Vietnam 270
RU - Federazione Russa 261
GB - Regno Unito 175
FR - Francia 169
IT - Italia 162
ZA - Sudafrica 122
SE - Svezia 90
IN - India 67
BD - Bangladesh 44
JP - Giappone 42
CA - Canada 40
MX - Messico 35
AR - Argentina 33
IQ - Iraq 28
CZ - Repubblica Ceca 27
PL - Polonia 26
TR - Turchia 24
ES - Italia 21
CO - Colombia 20
BE - Belgio 18
EC - Ecuador 18
PK - Pakistan 18
NL - Olanda 15
CL - Cile 12
ID - Indonesia 12
PH - Filippine 10
AZ - Azerbaigian 9
VE - Venezuela 9
AT - Austria 8
SA - Arabia Saudita 8
JO - Giordania 7
MA - Marocco 7
PA - Panama 7
PE - Perù 7
KE - Kenya 6
LT - Lituania 6
MY - Malesia 6
PT - Portogallo 6
UZ - Uzbekistan 6
MU - Mauritius 5
PS - Palestinian Territory 5
TN - Tunisia 5
BO - Bolivia 4
CR - Costa Rica 4
IR - Iran 4
JM - Giamaica 4
PY - Paraguay 4
AE - Emirati Arabi Uniti 3
DK - Danimarca 3
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
GT - Guatemala 3
NP - Nepal 3
SV - El Salvador 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
ET - Etiopia 2
HN - Honduras 2
HU - Ungheria 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
TT - Trinidad e Tobago 2
BN - Brunei Darussalam 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
KG - Kirghizistan 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MD - Moldavia 1
MG - Madagascar 1
ML - Mali 1
MM - Myanmar 1
Totale 11.508
Salva come PNG Salva come JPEG
Città #
Chandler 662
Dublin 621
Jacksonville 532
San Jose 482
Nanjing 397
Singapore 353
Ashburn 347
Hong Kong 304
Beijing 285
Dallas 221
Boardman 191
Nanchang 153
Council Bluffs 131
Princeton 118
Lawrence 116
Johannesburg 115
Changsha 111
Hebei 105
Shenyang 105
Lauterbourg 101
Los Angeles 101
Jiaxing 98
Wilmington 93
Dearborn 89
Ho Chi Minh City 87
Medford 84
Ann Arbor 72
Tianjin 62
Munich 61
Hanoi 60
New York 57
Shanghai 57
Hangzhou 54
Helsinki 52
Buffalo 43
Milan 42
Tokyo 41
Redondo Beach 40
Orem 37
Moscow 36
Woodbridge 36
Santa Clara 33
Verona 30
Houston 27
Brno 26
Piscataway 26
Warsaw 23
Norwalk 22
São Paulo 21
Brussels 18
Chennai 18
The Dalles 18
Turku 18
Atlanta 16
Frankfurt am Main 16
Kunming 16
Montreal 15
San Francisco 15
Seattle 15
Boston 14
Rio de Janeiro 14
Chicago 13
Falls Church 13
London 13
Denver 12
Des Moines 12
Fairfield 12
Stockholm 12
Baghdad 10
Guangzhou 10
Pavia 10
Poplar 10
Toronto 10
Brooklyn 9
Mexico City 9
Nürnberg 9
Paris 9
Baku 8
Charlotte 8
Guayaquil 8
Haiphong 8
Jinan 8
New Delhi 8
Amsterdam 7
Ankara 7
Da Nang 7
Phoenix 7
Santiago 7
Secaucus 7
Amman 6
Bogotá 6
Buenos Aires 6
Can Tho 6
Manchester 6
Ningbo 6
Panama City 6
Rome 6
Zhengzhou 6
Biên Hòa 5
Bắc Ninh 5
Totale 7.480
Salva come PNG Salva come JPEG
Nome #
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 250
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 155
A novel splicing mutation causes an undescribed type of analbuminemia. 155
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 149
Molecular Genetics of Analbuminemia 149
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 142
A novel splicing mutation causes analbuminemia in a Portuguese boy. 136
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 133
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 133
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS: from pooled to individual patient samples 130
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 130
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 127
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 127
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 126
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 126
Albumin locust valley: a new case of analbuminemia. 124
BEL β-trefoil: a novel lectin with antineoplastic properties in king bolete (Boletus edulis) mushrooms. 124
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 123
Analbuminemia produced by a novel splicing mutation 123
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 123
Analysis of human serum albumin variants by mass spectrometric procedures. 122
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 122
A new bisalbuminemia: bisalbuminemia of Kenitra 122
Analysis of human serum albumin variants by mass spectrometric procedures. 119
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 119
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS 117
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 117
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 117
Analbuminemia Zonguldak: case report and mutational analysis. 115
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 115
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 115
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 114
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 113
Pilot studies to evaluate the effectiveness of high LET particle irradiation in damaging neurotoxic protein aggregates 113
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 112
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 110
Mechanistic Insight into the Peroxidase Catalyzed Nitration of Tyrosine Derivatives by Nitrite and Hydrogen Peroxide 110
Novel nonsense mutation causes analbuminemia in a Moroccan family. 109
Applications of a trypsin immobilized bioreactor coupled with mass spectrometry 108
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 107
Human plasma retinol-binding protein (RBP4) is also a fatty acid-binding protein. 107
Trypsin-based monolithic bioreactor coupled on-line with LC/MS/MS system for protein digestion and variant identification in standard solution and serum samples 107
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 106
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 105
Structural characterization of a chain termination mutant of human serum albumin. 105
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 105
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 104
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 103
Genetic variants showing apparent hot-spots in the human serum albumin gene. 102
Structural transitions of human serum albumin: an investigation using electrophoretic techniques. 101
PH AND IONIC STRENGHT DEPENDENCE OF PROTEIN (UN)FOLDING AND LIGAND BINDING TO BOVINE BETA-LACTOGLOBULINS A AND B 101
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. 101
High resolution crystal structure data of human plasma retinol-binding protein (RBP4) bound to retinol and fatty acids 101
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 100
The amino acid substitution in albumin Roma: 321 Glu----Lys. 100
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 99
Computational and experimental approaches assess the interactions between bovine beta-lactoglobulin and synthetic compounds of pharmacological interest 98
Phosphoprotein analysis of amniotic fluid samples from individual patients by a miniaturized LC-MS system 97
Phosphoproteome analysis by LC-MS: different approaches for the characterization of amniotic fluid 97
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 97
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 96
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 96
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 96
Nitrative stress causes nitration, oxidation, and subunit cross linking in human hemoglobin 96
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 96
Enzymatic properties of human hemalbumin. 95
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 95
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 95
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 94
Wards in the keyway: amino acids with anomalouspkas in calycins 92
Studying protein phosphorylation by LC-MS: application to amniotic fluid 91
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 91
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 90
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 90
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 90
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 89
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 88
Three-dimensional structure and ligand-binding site of carp fishelectin (FEL). 88
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 86
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 86
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 85
Neuronal proteins as targets of 3-hydroxykynurenine: Implications in neurodegenerative diseases 85
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 84
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 83
Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. 83
Electrostatics of folded and unfolded bovine β-lactoglobulin. 83
Bovine beta-lactoglobulin acts as an acid-resistant drug carrier by exploiting its diverse binding regions. 82
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 82
BLGA protein solutions at high ionic strenght: vanishing attractive interactions and 'frustrated' aggregation 82
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 81
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 81
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 80
Miniaturization of integrated systems for phosphoprotein analysis: from pooled to individual patient samples 79
Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms. 78
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 77
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 77
PROBING PROTEIN AGGREGATION BY TIME-RESOLVED FLUORESCENCE DURING BETA-LACTOGLOBULIN CRYSTAL GROWTH 77
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 75
Clinical, genetic, and protein structural aspects of familial dysalbuminemic hyperthyroxinemia and hypertriiodothyroninemia 75
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 74
Totale 10.560
Salva come PNG Salva come JPEG
Categoria #
all - tutte 48.398
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 48.398
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022458 0 16 3 6 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
2026/2027380 67 313 0 0 0 0 0 0 0 0 0 0
Totale 11.598