IRIS
GALLIANO, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 4.274
AS - Asia 3.346
EU - Europa 2.679
SA - Sud America 375
AF - Africa 160
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 10.841
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Nazione #
US - Stati Uniti d'America 4.183
CN - Cina 1.761
SG - Singapore 691
IE - Irlanda 622
UA - Ucraina 438
DE - Germania 346
HK - Hong Kong 310
FI - Finlandia 285
BR - Brasile 277
VN - Vietnam 269
RU - Federazione Russa 261
GB - Regno Unito 175
FR - Francia 167
IT - Italia 154
ZA - Sudafrica 122
SE - Svezia 90
IN - India 67
BD - Bangladesh 42
JP - Giappone 42
CA - Canada 37
MX - Messico 35
AR - Argentina 32
IQ - Iraq 28
CZ - Repubblica Ceca 27
PL - Polonia 26
TR - Turchia 24
ES - Italia 20
BE - Belgio 18
PK - Pakistan 18
CO - Colombia 16
NL - Olanda 15
EC - Ecuador 14
ID - Indonesia 12
CL - Cile 11
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
KE - Kenya 6
LT - Lituania 6
PE - Perù 6
UZ - Uzbekistan 6
MU - Mauritius 5
MY - Malesia 5
PS - Palestinian Territory 5
TN - Tunisia 5
BO - Bolivia 4
IR - Iran 4
AE - Emirati Arabi Uniti 3
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
NP - Nepal 3
PT - Portogallo 3
PY - Paraguay 3
SY - Repubblica araba siriana 3
AL - Albania 2
AU - Australia 2
BG - Bulgaria 2
BH - Bahrain 2
CH - Svizzera 2
CR - Costa Rica 2
ET - Etiopia 2
GT - Guatemala 2
HU - Ungheria 2
JM - Giamaica 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
SV - El Salvador 2
TH - Thailandia 2
AO - Angola 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 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
MN - Mongolia 1
Totale 10.836
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Città #
Chandler 662
Dublin 621
Jacksonville 532
Nanjing 397
Singapore 350
Ashburn 314
San Jose 314
Hong Kong 303
Beijing 284
Dallas 218
Boardman 191
Nanchang 153
Princeton 117
Lawrence 116
Johannesburg 115
Changsha 111
Hebei 105
Shenyang 105
Lauterbourg 101
Los Angeles 99
Jiaxing 98
Wilmington 93
Dearborn 89
Ho Chi Minh City 86
Medford 84
Ann Arbor 72
Tianjin 62
Munich 61
Hanoi 60
Shanghai 57
Hangzhou 54
New York 53
Helsinki 52
Buffalo 43
Milan 41
Tokyo 41
Redondo Beach 40
Moscow 36
Orem 36
Woodbridge 36
Verona 30
Brno 26
Piscataway 26
Houston 23
Warsaw 23
Norwalk 22
São Paulo 21
Brussels 18
Chennai 18
The Dalles 18
Turku 18
Frankfurt am Main 16
Kunming 16
Santa Clara 16
Montreal 15
Seattle 15
Rio de Janeiro 14
Falls Church 13
London 13
Boston 12
Denver 12
Fairfield 12
San Francisco 12
Stockholm 12
Chicago 11
Des Moines 11
Atlanta 10
Baghdad 10
Guangzhou 10
Poplar 10
Brooklyn 9
Mexico City 9
Nürnberg 9
Paris 9
Pavia 9
Toronto 9
Baku 8
Charlotte 8
Haiphong 8
Jinan 8
New Delhi 8
Amsterdam 7
Ankara 7
Da Nang 7
Guayaquil 7
Secaucus 7
Amman 6
Buenos Aires 6
Can Tho 6
Manchester 6
Ningbo 6
Panama City 6
Santiago 6
Zhengzhou 6
Biên Hòa 5
Bogotá 5
Bắc Ninh 5
Curitiba 5
Dhaka 5
Hefei 5
Totale 7.092
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Nome #
A novel splicing mutation causes an undescribed type of analbuminemia. 152
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 148
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 146
Molecular Genetics of Analbuminemia 143
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 139
A novel splicing mutation causes analbuminemia in a Portuguese boy. 134
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 130
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 127
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 126
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS: from pooled to individual patient samples 126
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 123
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 122
Albumin locust valley: a new case of analbuminemia. 122
Analbuminemia produced by a novel splicing mutation 121
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 120
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 120
BEL β-trefoil: a novel lectin with antineoplastic properties in king bolete (Boletus edulis) mushrooms. 120
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 119
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 119
A new bisalbuminemia: bisalbuminemia of Kenitra 119
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 116
Analysis of human serum albumin variants by mass spectrometric procedures. 116
Analysis of human serum albumin variants by mass spectrometric procedures. 115
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 115
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS 114
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 112
Analbuminemia Zonguldak: case report and mutational analysis. 111
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 111
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 111
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 110
Pilot studies to evaluate the effectiveness of high LET particle irradiation in damaging neurotoxic protein aggregates 110
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 109
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 108
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 107
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 106
Novel nonsense mutation causes analbuminemia in a Moroccan family. 105
Mechanistic Insight into the Peroxidase Catalyzed Nitration of Tyrosine Derivatives by Nitrite and Hydrogen Peroxide 105
Trypsin-based monolithic bioreactor coupled on-line with LC/MS/MS system for protein digestion and variant identification in standard solution and serum samples 104
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 103
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 103
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 103
Applications of a trypsin immobilized bioreactor coupled with mass spectrometry 102
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 102
Structural characterization of a chain termination mutant of human serum albumin. 101
Human plasma retinol-binding protein (RBP4) is also a fatty acid-binding protein. 101
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 99
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. 98
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 97
Structural transitions of human serum albumin: an investigation using electrophoretic techniques. 97
High resolution crystal structure data of human plasma retinol-binding protein (RBP4) bound to retinol and fatty acids 97
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 96
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 95
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 95
PH AND IONIC STRENGHT DEPENDENCE OF PROTEIN (UN)FOLDING AND LIGAND BINDING TO BOVINE BETA-LACTOGLOBULINS A AND B 95
The amino acid substitution in albumin Roma: 321 Glu----Lys. 94
Genetic variants showing apparent hot-spots in the human serum albumin gene. 93
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 93
Phosphoprotein analysis of amniotic fluid samples from individual patients by a miniaturized LC-MS system 93
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 93
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 93
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 93
Enzymatic properties of human hemalbumin. 92
Phosphoproteome analysis by LC-MS: different approaches for the characterization of amniotic fluid 92
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 92
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 91
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 91
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 90
Computational and experimental approaches assess the interactions between bovine beta-lactoglobulin and synthetic compounds of pharmacological interest 89
Nitrative stress causes nitration, oxidation, and subunit cross linking in human hemoglobin 89
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 87
Wards in the keyway: amino acids with anomalouspkas in calycins 87
Studying protein phosphorylation by LC-MS: application to amniotic fluid 86
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 85
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 84
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 83
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 83
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 83
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 81
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 81
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 80
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 80
Neuronal proteins as targets of 3-hydroxykynurenine: Implications in neurodegenerative diseases 80
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 79
Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. 79
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 79
Three-dimensional structure and ligand-binding site of carp fishelectin (FEL). 79
BLGA protein solutions at high ionic strenght: vanishing attractive interactions and 'frustrated' aggregation 77
Electrostatics of folded and unfolded bovine β-lactoglobulin. 77
Bovine beta-lactoglobulin acts as an acid-resistant drug carrier by exploiting its diverse binding regions. 76
Miniaturization of integrated systems for phosphoprotein analysis: from pooled to individual patient samples 76
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 75
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 75
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 75
Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms. 73
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 72
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 72
PROBING PROTEIN AGGREGATION BY TIME-RESOLVED FLUORESCENCE DURING BETA-LACTOGLOBULIN CRYSTAL GROWTH 72
The extraordinary ligand binding properties of human serum albumin 70
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 69
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 69
Totale 9.947
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Categoria #
all - tutte 43.396
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 43.396
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021222 0 0 0 0 0 0 0 0 0 109 97 16
2021/2022466 8 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
2025/20263.344 265 300 386 393 485 170 669 196 268 212 0 0
Totale 10.925