IRIS
MINCHIOTTI, LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 2.133
EU - Europa 1.641
AS - Asia 1.123
OC - Oceania 3
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.903
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Nazione #
US - Stati Uniti d'America 2.125
CN - Cina 1.021
IE - Irlanda 476
UA - Ucraina 360
DE - Germania 238
FI - Finlandia 204
IT - Italia 97
GB - Regno Unito 83
SE - Svezia 82
SG - Singapore 73
FR - Francia 45
CZ - Repubblica Ceca 26
JP - Giappone 17
BE - Belgio 13
RU - Federazione Russa 9
IN - India 8
CA - Canada 7
NL - Olanda 6
IR - Iran 3
MU - Mauritius 2
NZ - Nuova Zelanda 2
AU - Australia 1
EU - Europa 1
LT - Lituania 1
PA - Panama 1
PT - Portogallo 1
TR - Turchia 1
Totale 4.903
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Città #
Dublin 475
Chandler 467
Jacksonville 439
Nanjing 308
Boardman 145
Ashburn 114
Nanchang 104
Beijing 98
Princeton 92
Lawrence 89
Changsha 86
Hebei 83
Jiaxing 78
Shenyang 76
Wilmington 66
Medford 62
Ann Arbor 61
Dearborn 51
Hangzhou 44
Tianjin 43
Singapore 41
Shanghai 38
Helsinki 33
Woodbridge 28
Brno 26
Milan 26
Piscataway 24
Verona 23
Norwalk 21
Munich 20
Tokyo 17
Brussels 13
Kunming 13
Houston 11
Nürnberg 9
Fairfield 8
Los Angeles 8
Paris 8
Falls Church 7
Des Moines 6
New York 6
Jinan 5
Seattle 5
Auburn Hills 4
Lanzhou 4
Ningbo 4
Borås 3
Detroit 3
Guangzhou 3
Montréal 3
Moscow 3
Naples 3
Taizhou 3
Toronto 3
Antwerp 2
Chicago 2
Hefei 2
Las Vegas 2
Novokuznetsk 2
Pavia 2
Pune 2
Romainville 2
Rome 2
Saint-Fons 2
Tappahannock 2
Vigevano 2
Zhengzhou 2
Andover 1
Auckland 1
Bangalore 1
Benxi 1
Blackpool 1
Changchun 1
Civitavecchia 1
Croom 1
Falkenstein 1
Gandhi Nagar 1
Groningen 1
Hastings 1
Irvine 1
Lincoln 1
Mumbai 1
Newark 1
North Bergen 1
Norwich 1
Orange 1
Panama City 1
Pozzuoli 1
San Jose 1
Shijiazhuang 1
Shiraz 1
Sondrio 1
Sydney 1
Washington 1
Winnipeg 1
Wuhan 1
Zanjan 1
Totale 3.469
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Nome #
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 99
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 92
A novel splicing mutation causes an undescribed type of analbuminemia. 86
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 85
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 83
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
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. 76
A novel splicing mutation causes analbuminemia in a Portuguese boy. 75
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 72
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 72
Analbuminemia produced by a novel splicing mutation 71
Genetic variants showing apparent hot-spots in the human serum albumin gene. 69
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 69
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 68
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 68
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 68
Analbuminemia Zonguldak: case report and mutational analysis. 67
Enzymatic properties of human hemalbumin. 66
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 66
Analysis of human serum albumin variants by mass spectrometric procedures. 65
Novel nonsense mutation causes analbuminemia in a Moroccan family. 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
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 63
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 63
A structural study of pig liver glyceraldehyde-3-phosphate dehydrogenase. 63
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 63
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 62
Structural characterization of a chain termination mutant of human serum albumin. 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
D-amino acid oxidase primary structure: cyanogen bromide fragments and sequences of the cysteynyl peptides 61
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 61
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 61
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 60
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 57
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 57
Isolation, characterization and partial sequence of cyanogen bromide fragments and thiol peptides from pig kidney D-amino-acid oxidase. 57
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant 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
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 56
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 55
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 55
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 54
A new bisalbuminemia: bisalbuminemia of Kenitra 54
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
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 52
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 51
Hormone binding to natural mutants of human serum albumin. 51
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 51
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
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 49
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 49
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 49
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 48
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 48
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 47
Amino acid sequence around the pyridoxal 5'-phosphate binding sites of 6-phosphogluconate dehydrogenase. 47
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 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
Isolation and characterization of a new form of the porcine pancreatic secretory trypsin inhibitor. Biochemical studies and high-resolution 1H-NMR 44
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 44
Proceedings: Pyridoxal-phosphate-binding sites of 6-phosphogluconate dehydrogenase. 44
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 43
Molecular Genetics of Analbuminemia 42
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 41
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 40
Purification and characterization of yeast thioredoxin reductase 39
Analbuminemia: three cases resulting from different point mutations in the albumin gene. 38
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 37
The primary structure of D-amino acid oxidase from pig kidney. II. Isolation and sequence of overlap peptides and the complete sequence. 37
Genetic variants of human serum albumin: molecular defects and biological stability. 36
Radioimmunoassay and chemical properties of glucose 6-phosphate dehydrogenase and of a specific NADP(H)-binding protein (FX) from human erythrocytes. 36
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects. 35
ANALBUMINEMIA: MOLECULAR ASPECTS AND CLINICAL CONSEQUENCES 34
The primary structure of D-amino acid oxidase from pig kidney. I. Isolation and sequence of the tryptic peptides. 31
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 28
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 28
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene. 28
Separation of fragments from human serum albumin and its charged variants by reversed-phase and cation-exchange high-performance liquid chromatography. 27
Clinical, genetic, and protein structural aspects of familial dysalbuminemic hyperthyroxinemia and hypertriiodothyroninemia 27
Totale 4.952
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Categoria #
all - tutte 19.661
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 19.661
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020390 0 0 0 0 7 89 24 95 8 124 42 1
2020/2021587 76 62 12 67 2 79 4 93 12 88 80 12
2021/2022342 4 14 2 7 5 4 9 25 19 14 58 181
2022/20231.343 124 98 5 124 154 121 0 87 574 8 30 18
2023/2024420 39 91 5 27 37 117 3 27 2 16 35 21
2024/2025211 31 107 30 37 6 0 0 0 0 0 0 0
Totale 4.952