IRIS
MINCHIOTTI, LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 3.183
AS - Asia 2.576
EU - Europa 2.121
SA - Sud America 333
AF - Africa 119
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.337
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Nazione #
US - Stati Uniti d'America 3.112
CN - Cina 1.379
SG - Singapore 522
IE - Irlanda 478
UA - Ucraina 367
DE - Germania 288
BR - Brasile 248
HK - Hong Kong 232
FI - Finlandia 219
VN - Vietnam 199
RU - Federazione Russa 196
FR - Francia 140
GB - Regno Unito 118
IT - Italia 114
SE - Svezia 91
ZA - Sudafrica 89
IN - India 48
JP - Giappone 38
BD - Bangladesh 34
CA - Canada 31
MX - Messico 29
AR - Argentina 27
CZ - Repubblica Ceca 27
PL - Polonia 23
TR - Turchia 20
IQ - Iraq 16
CO - Colombia 15
BE - Belgio 13
EC - Ecuador 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
AT - Austria 5
JO - Giordania 5
BO - Bolivia 4
KE - Kenya 4
MU - Mauritius 4
SA - Arabia Saudita 4
TN - Tunisia 4
UZ - Uzbekistan 4
DZ - Algeria 3
IR - Iran 3
LT - Lituania 3
PA - Panama 3
PS - Palestinian Territory 3
PT - Portogallo 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
EG - Egitto 2
ET - Etiopia 2
HU - Ungheria 2
JM - Giamaica 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
SR - Suriname 2
SY - Repubblica araba siriana 2
AL - Albania 1
AO - Angola 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CH - Svizzera 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EU - Europa 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
KH - Cambogia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MD - Moldavia 1
ML - Mali 1
MM - Myanmar 1
MN - Mongolia 1
OM - Oman 1
PR - Porto Rico 1
PY - Paraguay 1
QA - Qatar 1
RS - Serbia 1
SI - Slovenia 1
Totale 8.335
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Città #
Dublin 477
Chandler 467
Jacksonville 439
Nanjing 308
Singapore 255
Beijing 247
San Jose 242
Ashburn 239
Hong Kong 226
Dallas 161
Boardman 145
Nanchang 104
Changsha 92
Princeton 92
Lawrence 89
Johannesburg 85
Hebei 83
Lauterbourg 82
Jiaxing 78
Shenyang 76
Los Angeles 71
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
New York 31
Milan 29
Redondo Beach 29
Woodbridge 28
Brno 26
Moscow 25
Orem 24
Piscataway 24
Verona 23
Norwalk 21
Warsaw 20
São Paulo 19
The Dalles 16
Houston 15
Chennai 14
Brussels 13
Kunming 13
Turku 13
Montreal 12
London 10
Rio de Janeiro 10
Boston 9
Denver 9
Frankfurt am Main 9
Nürnberg 9
Paris 9
Fairfield 8
Guangzhou 8
Poplar 8
San Francisco 8
Santa Clara 8
Stockholm 8
Toronto 8
Ankara 7
Baku 7
Chicago 7
Des Moines 7
Falls Church 7
Guayaquil 7
Seattle 7
Atlanta 6
Curitiba 6
Guarulhos 6
Mexico City 6
Amsterdam 5
Buenos Aires 5
Can Tho 5
Charlotte 5
Dhaka 5
Haiphong 5
Jinan 5
Lima 5
Ningbo 5
Querétaro 5
Secaucus 5
Amman 4
Auburn Hills 4
Biên Hòa 4
Bogotá 4
Brasília 4
Brooklyn 4
Da Nang 4
Falkenstein 4
Istanbul 4
Karachi 4
Lanzhou 4
Totale 5.385
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Nome #
A novel splicing mutation causes an undescribed type of analbuminemia. 152
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 148
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 146
Molecular Genetics of Analbuminemia 143
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 139
A novel splicing mutation causes analbuminemia in a Portuguese boy. 134
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 130
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 127
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 126
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 122
Analbuminemia produced by a novel splicing mutation 121
A new proalbumin variant: albumin Jaffna (-1Arg--->Leu) 120
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 120
The molecular defect of Albumin Tagliacozzo: 313Lys--->Asn. 119
A new bisalbuminemia: bisalbuminemia of Kenitra 119
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 116
Analysis of human serum albumin variants by mass spectrometric procedures. 116
Analysis of human serum albumin variants by mass spectrometric procedures. 115
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 115
A structural study of pig liver glyceraldehyde-3-phosphate dehydrogenase. 113
A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin. 112
Analbuminemia Zonguldak: case report and mutational analysis. 111
A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge. 111
An active site-tyrosine-containing heptapeptide from D-amino acid oxidase. 111
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 110
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin 109
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 108
Binding and relaxometric properties of heme complexes with cyanogen bromide fragments of human serum albumin 107
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 106
Novel nonsense mutation causes analbuminemia in a Moroccan family. 105
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 103
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 103
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 103
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 102
Structural characterization of a chain termination mutant of human serum albumin. 101
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 99
D-amino acid oxidase primary structure: cyanogen bromide fragments and sequences of the cysteynyl peptides 99
MODIFIED HIGH_AFFINITY BINDING OF NICKEL; CALCIUM AND ZINC TO NATURAL MUTANTS OF HUMAN SERUM ALBUMIN AND PROALBUMIN 97
Genetic variation in human serum albumin: a 313 Lys-->Asn mutation in albumin reading identified by PCR analysis. 96
STRUCTURAL CHARACTERIZATION OF TWO GENETIC VARIANTS OF HUMAN SERUM ALBUMIN 95
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 95
The amino acid substitution in albumin Roma: 321 Glu----Lys. 94
Genetic variants showing apparent hot-spots in the human serum albumin gene. 93
High-performance liquid chromatography of complex mixtures of cyanogen bromide-produced peptides from different proteins. 93
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy. 93
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 93
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 93
Enzymatic properties of human hemalbumin. 92
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 92
The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant. 91
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 91
Separation of cyanogen bromide fragments from normal and abnormal human serum albumin by reversed-phase high-performance liquid chromatography. 90
Isolation, characterization and partial sequence of cyanogen bromide fragments and thiol peptides from pig kidney D-amino-acid oxidase. 90
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 87
Amino acid sequence around the pyridoxal 5'-phosphate binding sites of 6-phosphogluconate dehydrogenase. 85
Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin. 85
structural characterization of the subunits of spinach chloroplast glyceraldehyde-3-phoshate dehydrogenase (NADP). 84
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin. 83
High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin. 83
MUTATIONS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN FOUND IN ITALY 83
MUTATIONS IN THE GENE OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL CONSEQUENCES AND THERAPEUTIC POSSIBILITIES 81
PROTEIN AND DNA SEQUENCE ANALYSIS OF A PRIVATE GENETIC VARIANT: ALBUMIN ORTONOVO (Glu 505--Lys) 81
TWO ALLOALBUMINS WITH IDENTICAL ELECTROPHORETIC MOBILITY ARE PRODUCED BYDIFFERENTLY CHARGED AMINO ACID SUBSTITUTIONS 80
Structural characterization and fatty acid binding properties of two French genetic variants of human serum albumin. 80
Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. 79
Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant. 75
The molecular defect of albumin Castel di Sangro: 536 Lys----Glu. 75
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 75
Hormone binding to natural mutants of human serum albumin. 73
Structural characterization of three genetic variants of human serum albumin modified in subdomains IIB and IIIA. 72
Human serum albumin isoforms: genetic and molecular aspects and functional consequences. 72
Reactivity of D-amino acid oxidase with 1,2-cyclohexanedione: evidence for one arginine in the substrate-binding site. 69
Molecular heterogeneity of ferredoxin-NADP+ reductase from spinach leaves. 69
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. 68
Proceedings: Pyridoxal-phosphate-binding sites of 6-phosphogluconate dehydrogenase. 67
Isolation and characterization of a new form of the porcine pancreatic secretory trypsin inhibitor. Biochemical studies and high-resolution 1H-NMR 66
High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. 65
GENETIC VARIANTS OF HUMAN SERUM ALBUMIN: MOLECULAR AND FUNCTIONAL ASPECTS AND THERAPEUTIC POSSIBILITIES 65
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene. 64
The primary structure of D-amino acid oxidase from pig kidney. II. Isolation and sequence of overlap peptides and the complete sequence. 64
Genetic variants of human serum albumin: molecular defects and biological stability. 62
Clinical, genetic, and protein structural aspects of familial dysalbuminemic hyperthyroxinemia and hypertriiodothyroninemia 61
Purification and characterization of yeast thioredoxin reductase 60
Radioimmunoassay and chemical properties of glucose 6-phosphate dehydrogenase and of a specific NADP(H)-binding protein (FX) from human erythrocytes. 60
The primary structure of D-amino acid oxidase from pig kidney. I. Isolation and sequence of the tryptic peptides. 59
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects. 58
ANALBUMINEMIA: MOLECULAR ASPECTS AND CLINICAL CONSEQUENCES 56
Separation of fragments from human serum albumin and its charged variants by reversed-phase and cation-exchange high-performance liquid chromatography. 56
Analbuminemia: three cases resulting from different point mutations in the albumin gene. 55
Totale 8.386
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Categoria #
all - tutte 33.228
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 33.228
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021180 0 0 0 0 0 0 0 0 0 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
2024/20251.075 31 107 30 37 19 33 23 69 272 20 161 273
2025/20262.570 191 241 305 315 364 136 501 149 217 151 0 0
Totale 8.386