IRIS
MINCHIOTTI, LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 3.682
AS - Asia 2.587
EU - Europa 2.139
SA - Sud America 343
AF - Africa 120
Continente sconosciuto - Info sul continente non disponibili 50
OC - Oceania 4
Totale 8.925
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Nazione #
US - Stati Uniti d'America 3.601
CN - Cina 1.384
SG - Singapore 526
IE - Irlanda 478
UA - Ucraina 367
DE - Germania 289
BR - Brasile 250
HK - Hong Kong 232
FI - Finlandia 219
VN - Vietnam 199
RU - Federazione Russa 196
FR - Francia 141
IT - Italia 123
GB - Regno Unito 119
SE - Svezia 91
ZA - Sudafrica 89
IN - India 48
JP - Giappone 38
BD - Bangladesh 36
CA - Canada 34
MX - Messico 29
AR - Argentina 28
CZ - Repubblica Ceca 27
PL - Polonia 23
TR - Turchia 20
CO - Colombia 18
EC - Ecuador 16
IQ - Iraq 16
BE - Belgio 13
NL - Olanda 13
PK - Pakistan 12
ES - Italia 11
PH - Filippine 9
AZ - Azerbaigian 8
CL - Cile 8
ID - Indonesia 8
VE - Venezuela 8
MA - Marocco 6
MY - Malesia 6
PE - Perù 6
PT - Portogallo 6
AT - Austria 5
JO - Giordania 5
BO - Bolivia 4
JM - Giamaica 4
KE - Kenya 4
MU - Mauritius 4
SA - Arabia Saudita 4
TN - Tunisia 4
UZ - Uzbekistan 4
DK - Danimarca 3
DZ - Algeria 3
IR - Iran 3
LT - Lituania 3
PA - Panama 3
PS - Palestinian Territory 3
AE - Emirati Arabi Uniti 2
AO - Angola 2
AU - Australia 2
CR - Costa Rica 2
EG - Egitto 2
ET - Etiopia 2
GT - Guatemala 2
HN - Honduras 2
HU - Ungheria 2
KG - Kirghizistan 2
KR - Corea 2
KZ - Kazakistan 2
LB - Libano 2
LV - Lettonia 2
NG - Nigeria 2
NP - Nepal 2
NZ - Nuova Zelanda 2
PY - Paraguay 2
SR - Suriname 2
SY - Repubblica araba siriana 2
AL - Albania 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CH - Svizzera 1
DO - Repubblica Dominicana 1
EU - Europa 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
KH - Cambogia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MD - Moldavia 1
ML - Mali 1
MM - Myanmar 1
MN - Mongolia 1
OM - Oman 1
PR - Porto Rico 1
QA - Qatar 1
RS - Serbia 1
Totale 8.871
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Città #
Dublin 477
Chandler 467
Jacksonville 439
San Jose 371
Nanjing 308
Ashburn 264
Singapore 257
Beijing 248
Hong Kong 226
Dallas 165
Boardman 145
Nanchang 104
Council Bluffs 95
Princeton 93
Changsha 92
Lawrence 89
Johannesburg 85
Hebei 83
Lauterbourg 82
Jiaxing 78
Shenyang 76
Los Angeles 73
Wilmington 66
Medford 62
Ann Arbor 61
Ho Chi Minh City 61
Munich 53
Dearborn 51
Hanoi 45
Shanghai 45
Tianjin 45
Hangzhou 44
Tokyo 37
Helsinki 35
Buffalo 34
Milan 32
New York 32
Redondo Beach 29
Woodbridge 28
Brno 26
Moscow 25
Orem 24
Piscataway 24
Verona 23
Norwalk 21
Warsaw 20
Houston 19
Santa Clara 19
São Paulo 19
The Dalles 16
Chennai 14
Brussels 13
Kunming 13
Turku 13
Atlanta 12
Montreal 12
Boston 11
London 10
Rio de Janeiro 10
San Francisco 10
Chicago 9
Denver 9
Frankfurt am Main 9
Nürnberg 9
Paris 9
Toronto 9
Des Moines 8
Fairfield 8
Guangzhou 8
Guayaquil 8
Poplar 8
Stockholm 8
Ankara 7
Baku 7
Falls Church 7
Seattle 7
Bogotá 6
Curitiba 6
Guarulhos 6
Mexico City 6
Amsterdam 5
Brooklyn 5
Buenos Aires 5
Can Tho 5
Charlotte 5
Dhaka 5
Haiphong 5
Jinan 5
Las Vegas 5
Lima 5
Ningbo 5
Phoenix 5
Querétaro 5
Secaucus 5
Amman 4
Auburn Hills 4
Biên Hòa 4
Bologna 4
Brasília 4
Columbus 4
Totale 5.679
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Nome #
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 250
A novel splicing mutation causes an undescribed type of analbuminemia. 155
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 154
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
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
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 126
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
A new bisalbuminemia: bisalbuminemia of Kenitra 121
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
A structural study of pig liver glyceraldehyde-3-phosphate dehydrogenase. 119
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
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
Novel nonsense mutation causes analbuminemia in a Moroccan family. 109
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 107
D-amino acid oxidase primary structure: cyanogen bromide fragments and sequences of the cysteynyl peptides 106
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. 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
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
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
Isolation, characterization and partial sequence of cyanogen bromide fragments and thiol peptides from pig kidney D-amino-acid oxidase. 94
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 94
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). 89
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 89
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 88
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 88
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 87
Amino acid sequence around the pyridoxal 5'-phosphate binding sites of 6-phosphogluconate dehydrogenase. 87
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
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
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 82
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 81
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 80
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
Hormone binding to natural mutants of human serum albumin. 76
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
Proceedings: Pyridoxal-phosphate-binding sites of 6-phosphogluconate dehydrogenase. 74
Isolation and characterization of a new form of the porcine pancreatic secretory trypsin inhibitor. Biochemical studies and high-resolution 1H-NMR 72
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. 69
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 68
Genetic variants of human serum albumin: molecular defects and biological stability. 67
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 66
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene. 66
The primary structure of D-amino acid oxidase from pig kidney. II. Isolation and sequence of overlap peptides and the complete sequence. 66
Purification and characterization of yeast thioredoxin reductase 63
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects. 63
The primary structure of D-amino acid oxidase from pig kidney. I. Isolation and sequence of the tryptic peptides. 63
Radioimmunoassay and chemical properties of glucose 6-phosphate dehydrogenase and of a specific NADP(H)-binding protein (FX) from human erythrocytes. 61
Separation of fragments from human serum albumin and its charged variants by reversed-phase and cation-exchange high-performance liquid chromatography. 61
Analbuminemia: three cases resulting from different point mutations in the albumin gene. 60
ANALBUMINEMIA: MOLECULAR ASPECTS AND CLINICAL CONSEQUENCES 59
Totale 8.925
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Categoria #
all - tutte 37.077
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 37.077
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022338 0 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
2024/20251.075 31 107 30 37 19 33 23 69 272 20 161 273
2025/20262.802 191 241 305 315 364 136 501 149 217 194 78 111
2026/2027307 44 263 0 0 0 0 0 0 0 0 0 0
Totale 8.925