IRIS
GALLIANO, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 2.867
EU - Europa 2.054
AS - Asia 1.510
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 3
Totale 6.440
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Nazione #
US - Stati Uniti d'America 2.857
CN - Cina 1.333
IE - Irlanda 620
UA - Ucraina 430
DE - Germania 283
FI - Finlandia 262
SG - Singapore 142
IT - Italia 136
GB - Regno Unito 127
SE - Svezia 77
FR - Francia 52
CZ - Repubblica Ceca 26
JP - Giappone 19
BE - Belgio 18
RU - Federazione Russa 10
CA - Canada 9
IN - India 7
NL - Olanda 6
EU - Europa 3
IR - Iran 3
MU - Mauritius 3
TR - Turchia 3
AZ - Azerbaigian 2
LT - Lituania 2
NZ - Nuova Zelanda 2
AT - Austria 1
AU - Australia 1
BG - Bulgaria 1
BY - Bielorussia 1
GE - Georgia 1
PA - Panama 1
PT - Portogallo 1
RO - Romania 1
Totale 6.440
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Città #
Chandler 662
Dublin 619
Jacksonville 532
Nanjing 397
Boardman 191
Nanchang 152
Ashburn 141
Princeton 117
Lawrence 116
Beijing 115
Changsha 105
Hebei 105
Shenyang 105
Jiaxing 98
Singapore 97
Wilmington 93
Dearborn 89
Medford 84
Ann Arbor 72
Tianjin 60
Hangzhou 53
Shanghai 49
Helsinki 47
Milan 38
Woodbridge 36
Verona 30
Brno 26
Piscataway 26
Munich 24
Norwalk 22
Houston 19
Tokyo 19
Brussels 18
Kunming 16
New York 16
Falls Church 13
Fairfield 12
Seattle 12
Los Angeles 11
Nürnberg 9
Pavia 9
Des Moines 8
Jinan 8
Paris 8
Guangzhou 6
Ningbo 5
Auburn Hills 4
Chicago 4
Hefei 4
Lanzhou 4
Toronto 4
Borås 3
Detroit 3
Fuzhou 3
Montréal 3
Moscow 3
Naples 3
Novokuznetsk 3
Pune 3
Taizhou 3
Tappahannock 3
Zhengzhou 3
Antwerp 2
Baku 2
Frankfurt am Main 2
Las Vegas 2
Monza 2
Redwood City 2
Romainville 2
Rome 2
Saint-Fons 2
Vigevano 2
Washington 2
Ambrolauri 1
Andover 1
Auckland 1
Baoding 1
Benxi 1
Berlin 1
Blackpool 1
Böblingen 1
Changchun 1
Civitavecchia 1
Croom 1
Falkenstein 1
Gandhi Nagar 1
Groningen 1
Handan 1
Hastings 1
Irvine 1
Langfang 1
Lincoln 1
London 1
Minsk 1
Mumbai 1
Newark 1
North Bergen 1
Norwich 1
Orange 1
Panama City 1
Totale 4.592
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Nome #
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 101
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 94
A novel splicing mutation causes an undescribed type of analbuminemia. 88
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 86
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 84
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 82
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 82
BEL β-trefoil: a novel lectin with antineoplastic properties in king bolete (Boletus edulis) mushrooms. 82
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 81
Analysis of human serum albumin variants by mass spectrometric procedures. 80
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 78
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 77
A novel splicing mutation causes analbuminemia in a Portuguese boy. 77
PH AND IONIC STRENGHT DEPENDENCE OF PROTEIN (UN)FOLDING AND LIGAND BINDING TO BOVINE BETA-LACTOGLOBULINS A AND B 76
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 74
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 73
Analbuminemia produced by a novel splicing mutation 72
Albumin locust valley: a new case of analbuminemia. 72
Genetic variants showing apparent hot-spots in the human serum albumin gene. 69
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 69
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 69
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 68
Analbuminemia Zonguldak: case report and mutational analysis. 68
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 68
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 67
Enzymatic properties of human hemalbumin. 66
Computational and experimental approaches assess the interactions between bovine beta-lactoglobulin and synthetic compounds of pharmacological interest 65
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS: from pooled to individual patient samples 65
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 65
Analysis of human serum albumin variants by mass spectrometric procedures. 65
Novel nonsense mutation causes analbuminemia in a Moroccan family. 64
Phosphoprotein analysis of amniotic fluid samples from individual patients by a miniaturized LC-MS system 64
The amino acid substitution in albumin Roma: 321 Glu----Lys. 64
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 64
Applications of a trypsin immobilized bioreactor coupled with mass spectrometry 63
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 63
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 63
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 63
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 63
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 63
Structural characterization of a chain termination mutant of human serum albumin. 62
Structural transitions of human serum albumin: an investigation using electrophoretic techniques. 62
Mechanistic Insight into the Peroxidase Catalyzed Nitration of Tyrosine Derivatives by Nitrite and Hydrogen Peroxide 62
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 61
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 61
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS 61
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 60
Nitrative stress causes nitration, oxidation, and subunit cross linking in human hemoglobin 60
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 59
Pilot studies to evaluate the effectiveness of high LET particle irradiation in damaging neurotoxic protein aggregates 59
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 58
Phosphoproteome analysis by LC-MS: different approaches for the characterization of amniotic fluid 58
Studying protein phosphorylation by LC-MS: application to amniotic fluid 58
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 57
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 57
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 57
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 56
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 56
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 56
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 56
A new bisalbuminemia: bisalbuminemia of Kenitra 56
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. 55
Human plasma retinol-binding protein (RBP4) is also a fatty acid-binding protein. 55
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 53
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 53
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 52
Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. 52
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 52
Miniaturization of integrated systems for phosphoprotein analysis: from pooled to individual patient samples 52
Trypsin-based monolithic bioreactor coupled on-line with LC/MS/MS system for protein digestion and variant identification in standard solution and serum samples 52
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 51
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 51
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 51
Electrostatics of folded and unfolded bovine β-lactoglobulin. 51
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 50
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 50
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 50
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 49
Wards in the keyway: amino acids with anomalouspkas in calycins 49
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 49
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 49
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 49
Bovine beta-lactoglobulin acts as an acid-resistant drug carrier by exploiting its diverse binding regions. 48
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 48
High resolution crystal structure data of human plasma retinol-binding protein (RBP4) bound to retinol and fatty acids 48
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 47
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 46
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 46
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. 45
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 45
Three-dimensional structure and ligand-binding site of carp fishelectin (FEL). 44
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 43
BLGA protein solutions at high ionic strenght: vanishing attractive interactions and 'frustrated' aggregation 43
Molecular Genetics of Analbuminemia 42
Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms. 42
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 41
PROBING PROTEIN AGGREGATION BY TIME-RESOLVED FLUORESCENCE DURING BETA-LACTOGLOBULIN CRYSTAL GROWTH 41
Computational and experimental approaches for assessing the interactions between the model calycin beta-lactoglobulin and two antibacterial fluoroquinolones. 41
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 40
The extraordinary ligand binding properties of human serum albumin 40
Totale 5.994
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Categoria #
all - tutte 26.438
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 26.438
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020479 0 0 0 0 0 120 38 120 11 147 42 1
2020/2021712 94 72 11 82 2 89 5 119 16 109 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
2024/2025359 31 142 49 61 35 41 0 0 0 0 0 0
Totale 6.524