IRIS
GALLIANO, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 2.684
EU - Europa 2.006
AS - Asia 1.316
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 3
Totale 6.015
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Nazione #
US - Stati Uniti d'America 2.674
CN - Cina 1.303
IE - Irlanda 620
UA - Ucraina 430
DE - Germania 270
FI - Finlandia 260
GB - Regno Unito 126
IT - Italia 122
SE - Svezia 77
FR - Francia 52
CZ - Repubblica Ceca 18
BE - Belgio 17
CA - Canada 9
IN - India 7
RU - Federazione Russa 7
NL - Olanda 6
EU - Europa 3
IR - Iran 3
MU - Mauritius 3
TR - Turchia 3
NZ - Nuova Zelanda 2
AU - Australia 1
PA - Panama 1
RO - Romania 1
Totale 6.015
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Città #
Chandler 662
Dublin 619
Jacksonville 532
Nanjing 397
Nanchang 152
Ashburn 135
Princeton 117
Lawrence 116
Beijing 115
Changsha 105
Hebei 105
Shenyang 105
Jiaxing 98
Wilmington 93
Dearborn 89
Medford 84
Boardman 74
Ann Arbor 72
Tianjin 60
Hangzhou 53
Helsinki 45
Milan 38
Woodbridge 36
Shanghai 33
Verona 30
Norwalk 22
Houston 19
Brno 18
Brussels 17
Kunming 16
New York 16
Falls Church 13
Munich 13
Fairfield 12
Seattle 12
Los Angeles 10
Nürnberg 9
Pavia 9
Des Moines 8
Jinan 8
Paris 8
Guangzhou 5
Ningbo 5
Auburn Hills 4
Hefei 4
Lanzhou 4
Toronto 4
Borås 3
Detroit 3
Fuzhou 3
Montréal 3
Novokuznetsk 3
Pune 3
Taizhou 3
Tappahannock 3
Zhengzhou 3
Las Vegas 2
Monza 2
Redwood City 2
Romainville 2
Saint-Fons 2
Vigevano 2
Washington 2
Andover 1
Auckland 1
Berlin 1
Blackpool 1
Böblingen 1
Changchun 1
Civitavecchia 1
Croom 1
Falkenstein 1
Gandhi Nagar 1
Groningen 1
Hastings 1
Irvine 1
Mumbai 1
North Bergen 1
Norwich 1
Orange 1
Panama City 1
Pozzuoli 1
Samara 1
San Francisco 1
San Jose 1
Shijiazhuang 1
Shiraz 1
Sondrio 1
Sydney 1
Winnipeg 1
Wuhan 1
Zanjan 1
Totale 4.271
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Nome #
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 94
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 88
A novel splicing mutation causes an undescribed type of analbuminemia. 83
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 80
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 79
Analysis of human serum albumin variants by mass spectrometric procedures. 78
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 77
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 77
BEL β-trefoil: a novel lectin with antineoplastic properties in king bolete (Boletus edulis) mushrooms. 76
PH AND IONIC STRENGHT DEPENDENCE OF PROTEIN (UN)FOLDING AND LIGAND BINDING TO BOVINE BETA-LACTOGLOBULINS A AND B 73
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 72
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 72
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 70
A novel splicing mutation causes analbuminemia in a Portuguese boy. 70
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 68
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 67
Genetic variants showing apparent hot-spots in the human serum albumin gene. 66
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 66
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 65
Analbuminemia produced by a novel splicing mutation 65
Albumin locust valley: a new case of analbuminemia. 65
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 65
Analysis of human serum albumin variants by mass spectrometric procedures. 64
Computational and experimental approaches assess the interactions between bovine beta-lactoglobulin and synthetic compounds of pharmacological interest 62
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 62
Enzymatic properties of human hemalbumin. 61
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 61
Analbuminemia Zonguldak: case report and mutational analysis. 61
Phosphoprotein analysis of amniotic fluid samples from individual patients by a miniaturized LC-MS system 61
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 61
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 61
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 60
Novel nonsense mutation causes analbuminemia in a Moroccan family. 60
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 60
Structural transitions of human serum albumin: an investigation using electrophoretic techniques. 60
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 59
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS: from pooled to individual patient samples 59
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 59
The amino acid substitution in albumin Roma: 321 Glu----Lys. 59
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 58
Structural characterization of a chain termination mutant of human serum albumin. 58
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 58
Applications of a trypsin immobilized bioreactor coupled with mass spectrometry 57
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 57
Nitrative stress causes nitration, oxidation, and subunit cross linking in human hemoglobin 57
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 57
Mechanistic Insight into the Peroxidase Catalyzed Nitration of Tyrosine Derivatives by Nitrite and Hydrogen Peroxide 57
(Phospho) proteome analysis of amniotic fluid by micro-LC/LC-MS/MS 56
Phosphoproteome analysis by LC-MS: different approaches for the characterization of amniotic fluid 55
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 55
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 55
Pilot studies to evaluate the effectiveness of high LET particle irradiation in damaging neurotoxic protein aggregates 55
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 54
Studying protein phosphorylation by LC-MS: application to amniotic fluid 53
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 53
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 53
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 52
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 52
A new bisalbuminemia: bisalbuminemia of Kenitra 52
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 51
Human plasma retinol-binding protein (RBP4) is also a fatty acid-binding protein. 51
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 50
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 50
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 49
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 49
Miniaturization of integrated systems for phosphoprotein analysis: from pooled to individual patient samples 49
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 49
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. 49
Trypsin-based monolithic bioreactor coupled on-line with LC/MS/MS system for protein digestion and variant identification in standard solution and serum samples 49
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 49
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 48
Wards in the keyway: amino acids with anomalouspkas in calycins 48
Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. 48
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 48
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 47
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 47
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 47
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 46
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 46
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 45
Bovine beta-lactoglobulin acts as an acid-resistant drug carrier by exploiting its diverse binding regions. 45
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 45
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 45
Electrostatics of folded and unfolded bovine β-lactoglobulin. 45
Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid 44
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 44
High resolution crystal structure data of human plasma retinol-binding protein (RBP4) bound to retinol and fatty acids 43
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 43
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. 42
Three-dimensional structure and ligand-binding site of carp fishelectin (FEL). 42
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 41
BLGA protein solutions at high ionic strenght: vanishing attractive interactions and 'frustrated' aggregation 41
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 40
Molecular Genetics of Analbuminemia 40
Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms. 40
PROBING PROTEIN AGGREGATION BY TIME-RESOLVED FLUORESCENCE DURING BETA-LACTOGLOBULIN CRYSTAL GROWTH 40
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 39
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 39
Computational and experimental approaches for assessing the interactions between the model calycin beta-lactoglobulin and two antibacterial fluoroquinolones. 38
Analbuminemia: three cases resulting from different point mutations in the albumin gene. 37
Totale 5.598
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Categoria #
all - tutte 19.631
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 19.631
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20199 0 0 0 0 0 0 0 0 0 0 2 7
2019/20201.674 458 626 18 82 11 120 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
2023/2024467 50 120 7 35 53 140 3 36 2 19 2 0
Totale 6.099