IRIS
CAMPAGNOLI, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 897
EU - Europa 691
AS - Asia 442
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.033
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Nazione #
US - Stati Uniti d'America 895
CN - Cina 428
IE - Irlanda 211
UA - Ucraina 142
DE - Germania 108
FI - Finlandia 80
GB - Regno Unito 41
IT - Italia 40
SE - Svezia 29
FR - Francia 14
BE - Belgio 11
JP - Giappone 11
CZ - Repubblica Ceca 9
RU - Federazione Russa 4
CA - Canada 2
IN - India 2
NL - Olanda 2
AU - Australia 1
EU - Europa 1
HK - Hong Kong 1
NZ - Nuova Zelanda 1
Totale 2.033
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Città #
Chandler 228
Dublin 210
Jacksonville 168
Nanjing 117
Beijing 60
Ann Arbor 55
Ashburn 54
Nanchang 42
Shanghai 34
Lawrence 32
Medford 32
Princeton 32
Jiaxing 30
Changsha 28
Hebei 27
Piscataway 27
Shenyang 27
Dearborn 26
Boardman 24
Wilmington 21
Helsinki 18
Hangzhou 16
Tianjin 15
Verona 14
Woodbridge 14
Brussels 11
Tokyo 11
Milan 10
Norwalk 10
Brno 9
Nürnberg 8
Los Angeles 4
Kunming 3
Auburn Hills 2
Des Moines 2
Fairfield 2
Florence 2
Houston 2
Jinan 2
Munich 2
New York 2
Seattle 2
Tappahannock 2
Toronto 2
Zhengzhou 2
Blackpool 1
Croom 1
Falkenstein 1
Fuzhou 1
Groningen 1
Guangzhou 1
Hastings 1
Lanzhou 1
Mumbai 1
Ningbo 1
Norwich 1
Novokuznetsk 1
Orange 1
Pavia 1
Sydney 1
Taizhou 1
Washington 1
Totale 1.458
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Nome #
Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis. 98
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. 90
A novel splicing mutation causes an undescribed type of analbuminemia. 84
A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman. 82
Structural analysis and fatty acid binding properties of two Croatian variants of human serum albumin. 79
Structural analysis, fatty acid and thyroxine binding properties of Vancouver and Naskapi variants of human serum albumin. 78
Mapping the 5-50-kDa fraction of human amniotic fluid proteins by 2-DE and ESI-MS 78
Structural caracterization of the oligosaccharide chains of human a1-microglobulin from urine and amniotic fluid. 73
A novel splicing mutation causes analbuminemia in a Portuguese boy. 72
A novel two bases deletion in the albumin gene causes analbuminaemia in a young turkish man. 70
Analbuminemia produced by a novel splicing mutation 68
Albumin locust valley: a new case of analbuminemia. 68
Genetic variants showing apparent hot-spots in the human serum albumin gene. 67
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 66
Analbuminemia Zonguldak: case report and mutational analysis. 64
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT) 64
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. 63
Novel nonsense mutation causes analbuminemia in a Moroccan family. 62
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy. 60
Human alpha-1-Microglobulin is Covalently Bound to Kynurenine Derived Chromophores 59
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. 59
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. 55
Albumin Benkovac (c.1175 A > G; p.Glu392Gly): a novel genetic variant of human serum albumin. 55
Structural and biochemical characterization of a new type of lectin isolated from carp eggs. 55
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene 52
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 49
Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene. 49
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 48
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 46
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family. 46
Molecular Genetics of Analbuminemia 41
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant 41
Could the Oxidation of α1-Antitrypsin Prevent the Binding of Human Neutrophil Elastase in COVID-19 Patients? 23
Totale 2.064
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Categoria #
all - tutte 6.860
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 6.860
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020527 131 170 10 31 2 42 13 32 4 64 27 1
2020/2021240 33 23 6 28 1 29 4 36 5 38 32 5
2021/2022134 4 1 1 3 2 0 6 10 6 3 20 78
2022/2023600 47 58 3 70 58 56 0 36 253 2 10 7
2023/2024231 16 40 1 12 22 46 4 20 1 14 35 20
2024/202511 11 0 0 0 0 0 0 0 0 0 0 0
Totale 2.064