IRIS
MINCHIOTTI, LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 4.224
AS - Asia 2.593
EU - Europa 2.191
SA - Sud America 343
AF - Africa 124
Continente sconosciuto - Info sul continente non disponibili 58
OC - Oceania 4
Totale 9.537
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Nazione #
US - Stati Uniti d'America 4.070
CN - Cina 1.384
SG - Singapore 526
IE - Irlanda 478
UA - Ucraina 369
DE - Germania 293
BR - Brasile 250
HK - Hong Kong 233
FI - Finlandia 219
RU - Federazione Russa 200
VN - Vietnam 199
IT - Italia 153
FR - Francia 145
GB - Regno Unito 124
SE - Svezia 91
ZA - Sudafrica 89
CA - Canada 58
IN - India 48
JP - Giappone 38
BD - Bangladesh 36
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
ES - Italia 12
PK - Pakistan 12
HN - Honduras 11
CR - Costa Rica 10
PH - Filippine 9
TT - Trinidad e Tobago 9
AZ - Azerbaigian 8
CL - Cile 8
CW - ???statistics.table.value.countryCode.CW??? 8
ID - Indonesia 8
JM - Giamaica 8
PR - Porto Rico 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
IL - Israele 4
KE - Kenya 4
MU - Mauritius 4
NI - Nicaragua 4
SA - Arabia Saudita 4
SC - Seychelles 4
SV - El Salvador 4
TN - Tunisia 4
UZ - Uzbekistan 4
DK - Danimarca 3
DZ - Algeria 3
GT - Guatemala 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
EG - Egitto 2
ET - Etiopia 2
GP - Guadalupe 2
GR - Grecia 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
AM - Armenia 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BS - Bahamas 1
CH - Svizzera 1
DO - Repubblica Dominicana 1
EE - Estonia 1
EU - Europa 1
GD - Grenada 1
GE - Georgia 1
GY - Guiana 1
KH - Cambogia 1
Totale 9.473
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Città #
Dublin 477
Chandler 467
Jacksonville 442
San Jose 417
Nanjing 308
Ashburn 274
Singapore 257
Beijing 248
Hong Kong 227
Council Bluffs 216
Dallas 166
Boardman 145
Nanchang 104
Princeton 93
Changsha 92
Lawrence 89
Johannesburg 85
Hebei 83
Lauterbourg 82
Los Angeles 80
Jiaxing 78
Shenyang 76
Wilmington 66
Medford 62
Ann Arbor 61
Ho Chi Minh City 61
Munich 53
Dearborn 51
Hanoi 45
Shanghai 45
Tianjin 45
Hangzhou 44
Buffalo 38
New York 37
Tokyo 37
Helsinki 35
Milan 33
Redondo Beach 29
Woodbridge 28
Santa Clara 27
Brno 26
Moscow 25
Orem 24
Piscataway 24
Verona 23
Norwalk 21
Houston 20
Warsaw 20
São Paulo 19
Montreal 18
Atlanta 16
The Dalles 16
Chennai 14
Brussels 13
Chicago 13
Kunming 13
Turku 13
Boston 12
Denver 12
San Francisco 12
Frankfurt am Main 11
London 11
Naples 10
Rio de Janeiro 10
Nürnberg 9
Paris 9
Phoenix 9
San José 9
Toronto 9
Des Moines 8
Fairfield 8
Guangzhou 8
Guayaquil 8
Poplar 8
San Pedro Sula 8
Seattle 8
Stockholm 8
Willemstad 8
Ankara 7
Baku 7
Brooklyn 7
Falls Church 7
Bogotá 6
Curitiba 6
Guarulhos 6
Mexico City 6
Amsterdam 5
Bologna 5
Buenos Aires 5
Can Tho 5
Chaguanas 5
Charlotte 5
Columbus 5
Detroit 5
Dhaka 5
Haiphong 5
Jinan 5
Las Vegas 5
Lima 5
Ningbo 5
Totale 5.938
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Nome #
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 261
A novel splicing mutation causes an undescribed type of analbuminemia. 161
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 160
Molecular Genetics of Analbuminemia 157
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 156
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 147
A novel splicing mutation causes analbuminemia in a Portuguese boy. 142
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 138
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 138
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 136
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 134
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 134
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 132
Analbuminemia produced by a novel splicing mutation 132
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 128
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 127
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 127
Analysis of human serum albumin variants by mass spectrometric procedures. 126
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 125
A new bisalbuminemia: bisalbuminemia of Kenitra 125
Analysis of human serum albumin variants by mass spectrometric procedures. 124
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 124
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 124
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 123
A structural study of pig liver glyceraldehyde-3-phosphate dehydrogenase. 123
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 122
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 122
Analbuminemia Zonguldak: case report and mutational analysis. 119
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 119
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 118
Novel nonsense mutation causes analbuminemia in a Moroccan family. 116
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 116
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 115
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 113
Structural characterization of a chain termination mutant of human serum albumin. 112
D-amino acid oxidase primary structure: cyanogen bromide fragments and sequences of the cysteynyl peptides 112
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 111
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 110
Genetic variants showing apparent hot-spots in the human serum albumin gene. 109
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 109
The amino acid substitution in albumin Roma: 321 Glu----Lys. 107
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 105
Enzymatic properties of human hemalbumin. 104
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 104
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 104
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 103
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 102
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 102
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 102
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 101
Isolation, characterization and partial sequence of cyanogen bromide fragments and thiol peptides from pig kidney D-amino-acid oxidase. 101
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 101
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 101
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 101
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 100
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 100
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 97
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 96
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 94
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 93
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 93
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 91
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 91
Amino acid sequence around the pyridoxal 5'-phosphate binding sites of 6-phosphogluconate dehydrogenase. 90
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 89
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 88
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 87
Clinical, genetic, and protein structural aspects of familial dysalbuminemic hyperthyroxinemia and hypertriiodothyroninemia 87
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 86
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 86
Isolation and characterization of a new form of the porcine pancreatic secretory trypsin inhibitor. Biochemical studies and high-resolution 1H-NMR 86
Hormone binding to natural mutants of human serum albumin. 86
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 85
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 85
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 84
Proceedings: Pyridoxal-phosphate-binding sites of 6-phosphogluconate dehydrogenase. 79
The primary structure of D-amino acid oxidase from pig kidney. II. Isolation and sequence of overlap peptides and the complete sequence. 76
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. 75
Genetic variants of human serum albumin: molecular defects and biological stability. 74
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 73
Radioimmunoassay and chemical properties of glucose 6-phosphate dehydrogenase and of a specific NADP(H)-binding protein (FX) from human erythrocytes. 70
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 69
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects. 69
Purification and characterization of yeast thioredoxin reductase 68
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene. 68
The primary structure of D-amino acid oxidase from pig kidney. I. Isolation and sequence of the tryptic peptides. 67
Analbuminemia: three cases resulting from different point mutations in the albumin gene. 66
ANALBUMINEMIA: MOLECULAR ASPECTS AND CLINICAL CONSEQUENCES 62
Separation of fragments from human serum albumin and its charged variants by reversed-phase and cation-exchange high-performance liquid chromatography. 62
Totale 9.537
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Categoria #
all - tutte 39.771
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 39.771
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022315 0 0 0 0 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
2026/2027919 44 304 231 317 23 0 0 0 0 0 0 0
Totale 9.537