IRIS
ZURZOLO, CHIARA
 Distribuzione geografica
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Continente #
AS - Asia 4.442
NA - Nord America 3.752
EU - Europa 2.965
SA - Sud America 580
Continente sconosciuto - Info sul continente non disponibili 185
AF - Africa 96
OC - Oceania 4
Totale 12.024
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Nazione #
US - Stati Uniti d'America 3.610
SG - Singapore 2.095
RU - Federazione Russa 1.307
CN - Cina 855
VN - Vietnam 728
IT - Italia 568
BR - Brasile 469
HK - Hong Kong 387
UA - Ucraina 190
DE - Germania 155
FR - Francia 141
NL - Olanda 137
FI - Finlandia 118
GB - Regno Unito 101
IE - Irlanda 82
CA - Canada 74
IN - India 73
JP - Giappone 67
SE - Svezia 52
MX - Messico 38
BD - Bangladesh 36
AR - Argentina 33
PL - Polonia 27
IQ - Iraq 26
PH - Filippine 26
KR - Corea 24
EC - Ecuador 22
ES - Italia 22
CI - Costa d'Avorio 21
ZA - Sudafrica 21
TR - Turchia 20
AT - Austria 18
PY - Paraguay 16
MA - Marocco 15
ID - Indonesia 14
TH - Thailandia 12
PK - Pakistan 11
CL - Cile 10
CO - Colombia 10
KE - Kenya 10
TW - Taiwan 10
VE - Venezuela 9
JM - Giamaica 8
EG - Egitto 7
IR - Iran 7
JO - Giordania 7
LT - Lituania 7
PE - Perù 7
CR - Costa Rica 6
RS - Serbia 6
LB - Libano 5
AU - Australia 4
BO - Bolivia 4
CZ - Repubblica Ceca 4
GT - Guatemala 4
IL - Israele 4
OM - Oman 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
AZ - Azerbaigian 3
BA - Bosnia-Erzegovina 3
BE - Belgio 3
CH - Svizzera 3
CW - ???statistics.table.value.countryCode.CW??? 3
ET - Etiopia 3
MY - Malesia 3
PS - Palestinian Territory 3
SA - Arabia Saudita 3
BB - Barbados 2
BG - Bulgaria 2
DK - Danimarca 2
DZ - Algeria 2
EU - Europa 2
GE - Georgia 2
HR - Croazia 2
KZ - Kazakistan 2
MD - Moldavia 2
MM - Myanmar 2
MR - Mauritania 2
NO - Norvegia 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
YE - Yemen 2
AO - Angola 1
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CG - Congo 1
CY - Cipro 1
DJ - Gibuti 1
GH - Ghana 1
GP - Guadalupe 1
GR - Grecia 1
HN - Honduras 1
HU - Ungheria 1
IS - Islanda 1
LC - Santa Lucia 1
Totale 11.833
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Città #
Singapore 960
San Jose 488
Hong Kong 373
Moscow 343
Ashburn 275
Beijing 226
Jacksonville 210
Ho Chi Minh City 209
Santa Clara 177
Hanoi 169
Chandler 163
The Dalles 154
Naples 142
Millbury 131
Los Angeles 121
Lauterbourg 119
Amsterdam 103
Boston 100
Princeton 94
Hefei 71
Nanjing 67
Buffalo 64
Tokyo 62
New York 58
Woodbridge 55
Wilmington 47
São Paulo 44
Munich 38
Houston 35
Napoli 34
Redondo Beach 34
Rome 34
Haiphong 32
Nanchang 31
Ann Arbor 30
Council Bluffs 29
Da Nang 29
Des Moines 29
Lawrence 29
Orem 28
Warsaw 26
Cagliari 24
Mexico City 24
Dallas 23
Montreal 23
Denver 20
Chicago 19
Shenyang 19
Seattle 18
Tianjin 18
Milan 17
Ottawa 17
Poplar 17
Toronto 17
Atlanta 16
Brooklyn 16
Shanghai 16
Rio de Janeiro 15
Seoul 15
Changsha 14
Stockholm 14
Norwalk 13
Nuremberg 13
Dublin 12
Falls Church 12
Kronberg 12
Kunming 12
San Francisco 12
Chennai 11
Hebei 11
Jiaxing 11
London 11
Turku 11
Baghdad 10
Biên Hòa 10
Brasília 10
Salvador 10
Belo Horizonte 9
Fairfield 9
Guayaquil 9
Manchester 9
Mumbai 9
Phoenix 9
Thái Nguyên 9
Vienna 9
Bắc Ninh 8
Can Tho 8
Florence 8
Johannesburg 8
Porto Alegre 8
Quảng Ngãi 8
Amman 7
Bangkok 7
Bari 7
Boardman 7
Casablanca 7
Falkenstein 7
Frankfurt am Main 7
Hải Dương 7
Kingston 7
Totale 6.189
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Nome #
Analisi del meccanismo di smistamento di proteine GPI-ancorate in cellule epiteliali polarizzate 268
The 37/67kDa laminin receptor (LR) inhibitor, NSC47924, affects 37/67kDa LR cell surface localization and interaction with the cellular prion protein 170
Regulation of sub-compartmental targeting and folding properties of the Prion-like protein Shadoo 151
Oligomerization is a specific requirement for apical sorting of GPI-anchored proteins but not for non-raft associated apical proteins 148
Characterization of the properties and trafficking of an anchorless form of the prion protein. 147
Regulation of trafficking and folding of cellular prion protein PrPC and its shadow Shadoo 142
Synthesis of extracellular matrix glycoproteins by a differentiated thyroid epithelial cell line. 137
Lipid rafts and sorting of GPI-anchored proteins 135
PrP(C) association with lipid rafts in the early secretory pathway stabilizes its cellular conformation. 133
PrPC is sorted to the basolateral membrane of epithelial cells independently of its association with rafts. 131
Human CD8 alpha glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCK II clones. 130
Analysis of detergent-resistant membranes associated with apical and basolateral GPI-anchored proteins in polarized epithelial cells. 130
Mechanism of sorting of GPI-anchored proteins in polarized epithelial cells 130
Detergent-resistant membrane domains but not the proteasome are involved in the misfolding of a PrP mutant retained in the endoplasmic reticulum. 127
The polarized epithelial phenotype is dominant in hybrids between polarized and unpolarized rat thyroid cell lines. 125
Plasma membrane and lysosomal localization of CB1 cannabinoid receptor are dependent on lipid rafts and regulated by anandamide in human breast cancer cells 124
Detergent insoluble microdomains are not involved in transcytosis of Polymeric Ig Receptor in FRT and MDCK cells 124
Doppel and PrPC co-immunoprecipitate in detergent-resistant membrane domains of epithelial FRT cells. 122
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance. 121
Lipid Rafts in Trafficking and Processing of Prion Protein and Amyloid Precursor Protein 121
Glycosylphosphatidylinositol-anchored proteins are preferentially targeted to the basolateral surface in Fischer rat thyroid epithelial cells. 121
Analysis of mechanisms of sorting of GPI-anchored proteins in polarized epithelial cells: role of the GPI-anchor and ectodomain 121
The neuroendocrine protein VGF is sorted into dense-core granules and is secreted apically by polarized rat thyroid epithelial cells. 120
Modulation of transcytotic and direct targeting pathways in a polarized thyroid cell line. 120
Lipid rafts and clathrin cooperate in the internalization of PrP in epithelial FRT cells. 120
In vivo localization of GPI-anchored proteins in epithelial cells. 119
Analysis of TrkA and p75NTR cellular localization and signalling capability after NGF stimulation 119
Cell Biology of Prion Protein 118
alpha-Adducin mutations increase Na/K pump activity in renal cells by affecting constitutive endocytosis: implications for tubular Na reabsorption 117
Sorting of GPI-anchored proteins in living epithelial cells 117
Polarized secretion of plasminogen activators by epithelial cell monolayers. 116
Protein oligomerization modulates raft partitioning and apical sorting of GPI-anchored proteins. 113
Study of mechanisms of protein delivery in polarized epithelial cells by live microscopy. 113
Differential recognition of a tyrosine-dependent signal in the basolateral and endocytic pathways of thyroid epithelial cells. 110
Detergent-insoluble GPI anchored proteins are apically sorted in FRT cells, but interference with cholesterol or sphingolipids differentially affects detergent insolubility and apical sorting 110
Detergent-resistant membrane microdomains and apical sorting of GPI-anchored proteins in polarized epithelial cells. 109
Imaging techniques to study protein sorting in polarized epithelial cells 109
The Highways and Byways of Prion Protein Trafficking 108
Caveolin and caveolae are not directly involved in GPI-anchored proteins sorting 107
Morphological changes induced by prolonged TSH stimulation or starvation in the rat thyroid cell line FRTL. 105
Synthesis of extracellular matrix glycoproteins by a differentiated thyroid epithelial cell line 105
Calcium levels in the Golgi complex regulate clustering and apical sorting of GPI-APs in polarized epithelial cells 104
Sensitivity of polarized epithelial cells to the pore forming toxin aerolysin 102
N-Glycosylation instead of cholesterol mediates oligomerization and apical sorting of GPI-APs in FRT cells. 100
Correlative cryo-electron microscopy reveals the structure of TNTs in neuronal cells 99
Prions hijack tunnelling nanotubes for intercellular spread. 95
Opposite polarity of virus budding and of viral envelope glycoprotein distribution in epithelial cells derived from different tissues. 94
In vivo biosynthesis of clathrin and other coated vesicle proteins from rat liver 94
α-Synuclein transfer between neurons and astrocytes indicates that astrocytes play a role in degradation rather than in spreading 94
Human CD8 alpha glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCK II clones 93
N- and O- glycans are not directly involved in the oligomerization and apical sorting of GPI proteins. 92
Plasma membrane organization of GPI-anchored proteins 92
The polarized epithelial phenotype is dominant in hybrids between polarized and unpolarized rat thyroid cell lines 91
Mechanisms of apical protein sorting in polarized thyroid epithelial cells. 90
Morphological changes induced by prolonged TSH stimulation or starvation in the rat thyroid cell line FRTL. 90
Glycosylphosphatidylinositol-anchored proteins are preferentially targeted to the basolateral surface in Fischer rat thyroid epithelial cells 90
Golgi sorting regulates organization and activity of GPI proteins at apical membranes 90
Exploring Bioinorganic Pattern Formation in Diatoms: A Story of Polarized Trafficking 89
Detergent insoluble microdomains are not involved in transcytosis of polymeric Ig receptor in FRT and MDCK cells. 88
Pathogenetic mechanisms in neurodegenerative processes induced by prion proteins 87
Plasticity in epithelial cell phenotype: modulation by expression of different cadherin cell adhesion molecules 87
Permeabilization of MDCK cells with cholesterol binding agents: dependence on substratum and confluency 86
Modulation of transcytotic and direct targeting pathways in a polarized thyroid cell line 86
Lipids as Targeting Signals: Lipid Rafts and Intracellular Trafficking 82
Mechanisms of apical protein sorting in polarized thyroid epithelial cells 82
GPI-Anchored proteins are confined in subdiffraction clusters at the apical surface of polarized epithelial cells 82
Polarity signals in epithelial cells 81
Cell Surface Biotinylation and Other Techniques for Determination of Surface Polarity of Epithelial Monolayers 80
Characterization of the role of dendritic cells in prion transfer to primary neurons. 80
A requirement for caveolin-1 and associated kinase FYN in integrin signaling and anchorage-dependent cell growth 77
Prions: protein only or something more? Overview of potential prion cofactors 76
Human CD8 glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCKII clones. 75
Clustering in the Golgi apparatus governs sorting and function of GPI-APs in polarized epithelial cells 75
Tunnelling nanotube formation is driven by Eps8/IRSp53‐dependent linear actin polymerization 74
3D reconstruction of the cerebellar germinal layer reveals tunneling connections between developing granule cells 74
Polarized sorting of GPI proteins 74
Studio delle interazioni proteine-rame, proteine-proteine, proteine-acidi nucleici e proteine-lipidi a livello dei microdomini di mebrana. Rilevanza per la comprensione delle "patologie da microdomini di membrana" come le malattie da prioni, la malattia di Alzheimer e le alterazioni del metabolismo lipidico. 73
Detergent-resistant membrane microdomains and apical sorting of GPI-anchored proteins in polarized epithelial cells 71
Trafficking and Membrane Organization of GPI-Anchored Proteins in Health and Diseases 71
Distinct v-SNAREs regulate direct and indirect apical delivery in polarized epithelial cells. 70
The order of rafts 70
Different GPI-attachment signals affect the oligomerisation of GPI-anchored proteins and their apical sorting. 69
Lipid rafts and host cell-pathogen interactions 68
Detergent-insoluble GPI-anchored proteins are apically sorted in fischer rat thyroid cells, but interference with cholesterol or sphingolipids differentially affects detergent insolubility and apical sorting. 68
VIP21/Caveolin, glycosphingolipid clusters, and the sorting of glycosylphosphatidyl inositol-anchored proteins in epithelial cells 67
Actin Assembly around the Shigella-Containing Vacuole Promotes Successful Infection 67
Tunneling nanotubes spread fibrillar α-synuclein by intercellular trafficking of lysosomes 67
Fate and propagation of endogenously formed Tau aggregates in neuronal cells 66
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance. 66
Organization of GPI-anchored proteins at the cell surface and its physiopathological relevance 65
Differential recognition of a tyrosine-dependent signal in the basolateral and endocytic pathways of thyroid epithelial cells. 65
Prion aggregates transfer through tunneling nanotubes in endocytic vesicles 65
Delivery of Na,K-ATPase in polarized epithelial cells 64
The Shp-1 and Shp-2, tyrosine phosphatases, are recruited on cell membrane in two distinct molecular complexes including Ret oncogenes. 64
Caveolin transfection results in caveolae formation but not apical sorting of glycosylphosphatidylinositol (GPI)-anchored proteins in epithelial cells. 64
The Wnt/Ca2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes 64
Glycosylphosphatidylinositol-anchored proteins: Membrane organization and transport 63
Gene expression profile of quinacrine-cured prion-infected mouse neuronal cells. 62
Studio del meccanismo di oligomerizzazione di proteine smistate alla superficie apicale in cellule epiteliali polarizzate 62
Tunneling nanotubes: A possible highway in the spreading of tau and other prion-like proteins in neurodegenerative diseases 61
Totale 9.850
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Categoria #
all - tutte 41.283
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 41.283
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022597 5 4 1 9 8 33 5 23 85 55 74 295
2022/2023593 125 42 17 33 48 37 21 60 69 99 31 11
2023/2024538 15 68 107 33 33 38 17 59 10 13 110 35
2024/20253.099 162 289 7 22 65 178 420 187 210 298 1.036 225
2025/20265.773 687 425 610 555 989 236 604 427 707 325 92 116
2026/2027139 139 0 0 0 0 0 0 0 0 0 0 0
Totale 12.024