IRIS
ZURZOLO, CHIARA
 Distribuzione geografica
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Continente #
AS - Asia 4.460
NA - Nord America 4.123
EU - Europa 2.997
SA - Sud America 587
Continente sconosciuto - Info sul continente non disponibili 185
AF - Africa 97
OC - Oceania 4
Totale 12.453
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Nazione #
US - Stati Uniti d'America 3.955
SG - Singapore 2.097
RU - Federazione Russa 1.308
CN - Cina 859
VN - Vietnam 730
IT - Italia 593
BR - Brasile 471
HK - Hong Kong 390
UA - Ucraina 190
DE - Germania 156
FR - Francia 141
NL - Olanda 137
FI - Finlandia 118
GB - Regno Unito 104
CA - Canada 87
IE - Irlanda 83
IN - India 73
JP - Giappone 67
SE - Svezia 52
MX - Messico 39
BD - Bangladesh 38
AR - Argentina 34
PL - Polonia 27
IQ - Iraq 26
PH - Filippine 26
KR - Corea 24
EC - Ecuador 22
ES - Italia 22
CI - Costa d'Avorio 21
TR - Turchia 21
ZA - Sudafrica 21
AT - Austria 18
PY - Paraguay 16
MA - Marocco 15
ID - Indonesia 14
TH - Thailandia 13
CO - Colombia 12
PK - Pakistan 11
CL - Cile 10
CR - Costa Rica 10
KE - Kenya 10
TW - Taiwan 10
VE - Venezuela 10
JM - Giamaica 9
EG - Egitto 7
IR - Iran 7
JO - Giordania 7
LT - Lituania 7
PE - Perù 7
RS - Serbia 6
LB - Libano 5
TT - Trinidad e Tobago 5
AU - Australia 4
BO - Bolivia 4
CZ - Repubblica Ceca 4
GT - Guatemala 4
IL - Israele 4
OM - Oman 4
SA - Arabia Saudita 4
TN - Tunisia 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
GE - Georgia 3
MD - Moldavia 3
MY - Malesia 3
PS - Palestinian Territory 3
VI - Stati Uniti Isole Vergini 3
BB - Barbados 2
BG - Bulgaria 2
CG - Congo 2
DK - Danimarca 2
DZ - Algeria 2
EU - Europa 2
HN - Honduras 2
HR - Croazia 2
KZ - Kazakistan 2
MM - Myanmar 2
MR - Mauritania 2
NO - Norvegia 2
PR - Porto Rico 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
YE - Yemen 2
AO - Angola 1
BF - Burkina Faso 1
BH - Bahrain 1
BM - Bermuda 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CY - Cipro 1
DJ - Gibuti 1
GH - Ghana 1
GP - Guadalupe 1
Totale 12.258
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Città #
Singapore 962
San Jose 592
Hong Kong 374
Moscow 343
Ashburn 305
Beijing 227
Jacksonville 210
Ho Chi Minh City 209
Santa Clara 183
Hanoi 170
Chandler 163
The Dalles 154
Naples 150
Millbury 131
Los Angeles 121
Lauterbourg 119
Council Bluffs 104
Amsterdam 103
Boston 100
Princeton 94
Hefei 71
Nanjing 67
Buffalo 65
New York 65
Tokyo 62
Woodbridge 55
Phoenix 54
Wilmington 47
São Paulo 44
Munich 38
Rome 36
Houston 35
Napoli 34
Redondo Beach 34
Haiphong 32
Nanchang 32
Lawrence 31
Ann Arbor 30
Da Nang 29
Des Moines 29
Orem 29
Warsaw 26
Cagliari 24
Dallas 24
Mexico City 24
Montreal 24
Denver 22
Chicago 20
Shenyang 19
Atlanta 18
Milan 18
Seattle 18
Tianjin 18
Ottawa 17
Poplar 17
Toronto 17
Brooklyn 16
Shanghai 16
Rio de Janeiro 15
Seoul 15
Changsha 14
Stockholm 14
Dublin 13
Norwalk 13
Nuremberg 13
San Francisco 13
Falls Church 12
Kronberg 12
Kunming 12
Brasília 11
Chennai 11
Hebei 11
Jiaxing 11
London 11
Turku 11
Baghdad 10
Biên Hòa 10
Salvador 10
Belo Horizonte 9
Fairfield 9
Guayaquil 9
Manchester 9
Mumbai 9
Thái Nguyên 9
Vienna 9
Bangkok 8
Bắc Ninh 8
Can Tho 8
Florence 8
Johannesburg 8
Porto Alegre 8
Quảng Ngãi 8
Amman 7
Bari 7
Boardman 7
Casablanca 7
Falkenstein 7
Frankfurt am Main 7
Hải Dương 7
Kingston 7
Totale 6.488
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Nome #
Analisi del meccanismo di smistamento di proteine GPI-ancorate in cellule epiteliali polarizzate 279
The 37/67kDa laminin receptor (LR) inhibitor, NSC47924, affects 37/67kDa LR cell surface localization and interaction with the cellular prion protein 174
Regulation of sub-compartmental targeting and folding properties of the Prion-like protein Shadoo 156
Oligomerization is a specific requirement for apical sorting of GPI-anchored proteins but not for non-raft associated apical proteins 153
Characterization of the properties and trafficking of an anchorless form of the prion protein. 149
Regulation of trafficking and folding of cellular prion protein PrPC and its shadow Shadoo 143
PrPC is sorted to the basolateral membrane of epithelial cells independently of its association with rafts. 142
Synthesis of extracellular matrix glycoproteins by a differentiated thyroid epithelial cell line. 140
PrP(C) association with lipid rafts in the early secretory pathway stabilizes its cellular conformation. 138
Lipid rafts and sorting of GPI-anchored proteins 137
Human CD8 alpha glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCK II clones. 136
Mechanism of sorting of GPI-anchored proteins in polarized epithelial cells 134
Analysis of detergent-resistant membranes associated with apical and basolateral GPI-anchored proteins in polarized epithelial cells. 132
Cell Biology of Prion Protein 131
Detergent-resistant membrane domains but not the proteasome are involved in the misfolding of a PrP mutant retained in the endoplasmic reticulum. 130
The polarized epithelial phenotype is dominant in hybrids between polarized and unpolarized rat thyroid cell lines. 129
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance. 126
Plasma membrane and lysosomal localization of CB1 cannabinoid receptor are dependent on lipid rafts and regulated by anandamide in human breast cancer cells 126
Detergent insoluble microdomains are not involved in transcytosis of Polymeric Ig Receptor in FRT and MDCK cells 126
Doppel and PrPC co-immunoprecipitate in detergent-resistant membrane domains of epithelial FRT cells. 126
Lipid Rafts in Trafficking and Processing of Prion Protein and Amyloid Precursor Protein 125
Analysis of mechanisms of sorting of GPI-anchored proteins in polarized epithelial cells: role of the GPI-anchor and ectodomain 125
Analysis of TrkA and p75NTR cellular localization and signalling capability after NGF stimulation 125
The neuroendocrine protein VGF is sorted into dense-core granules and is secreted apically by polarized rat thyroid epithelial cells. 123
Modulation of transcytotic and direct targeting pathways in a polarized thyroid cell line. 123
Glycosylphosphatidylinositol-anchored proteins are preferentially targeted to the basolateral surface in Fischer rat thyroid epithelial cells. 123
Lipid rafts and clathrin cooperate in the internalization of PrP in epithelial FRT cells. 123
alpha-Adducin mutations increase Na/K pump activity in renal cells by affecting constitutive endocytosis: implications for tubular Na reabsorption 122
Sorting of GPI-anchored proteins in living epithelial cells 122
In vivo localization of GPI-anchored proteins in epithelial cells. 121
Polarized secretion of plasminogen activators by epithelial cell monolayers. 119
Protein oligomerization modulates raft partitioning and apical sorting of GPI-anchored proteins. 116
Study of mechanisms of protein delivery in polarized epithelial cells by live microscopy. 115
Detergent-resistant membrane microdomains and apical sorting of GPI-anchored proteins in polarized epithelial cells. 114
Differential recognition of a tyrosine-dependent signal in the basolateral and endocytic pathways of thyroid epithelial cells. 113
Detergent-insoluble GPI anchored proteins are apically sorted in FRT cells, but interference with cholesterol or sphingolipids differentially affects detergent insolubility and apical sorting 112
Imaging techniques to study protein sorting in polarized epithelial cells 112
Caveolin and caveolae are not directly involved in GPI-anchored proteins sorting 112
The Highways and Byways of Prion Protein Trafficking 111
Morphological changes induced by prolonged TSH stimulation or starvation in the rat thyroid cell line FRTL. 107
Calcium levels in the Golgi complex regulate clustering and apical sorting of GPI-APs in polarized epithelial cells 107
Synthesis of extracellular matrix glycoproteins by a differentiated thyroid epithelial cell line 106
Sensitivity of polarized epithelial cells to the pore forming toxin aerolysin 103
N-Glycosylation instead of cholesterol mediates oligomerization and apical sorting of GPI-APs in FRT cells. 103
Correlative cryo-electron microscopy reveals the structure of TNTs in neuronal cells 102
Prions hijack tunnelling nanotubes for intercellular spread. 99
In vivo biosynthesis of clathrin and other coated vesicle proteins from rat liver 98
Opposite polarity of virus budding and of viral envelope glycoprotein distribution in epithelial cells derived from different tissues. 97
Human CD8 alpha glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCK II clones 96
α-Synuclein transfer between neurons and astrocytes indicates that astrocytes play a role in degradation rather than in spreading 96
N- and O- glycans are not directly involved in the oligomerization and apical sorting of GPI proteins. 95
The polarized epithelial phenotype is dominant in hybrids between polarized and unpolarized rat thyroid cell lines 95
Mechanisms of apical protein sorting in polarized thyroid epithelial cells. 94
Plasma membrane organization of GPI-anchored proteins 94
Glycosylphosphatidylinositol-anchored proteins are preferentially targeted to the basolateral surface in Fischer rat thyroid epithelial cells 94
Morphological changes induced by prolonged TSH stimulation or starvation in the rat thyroid cell line FRTL. 93
Golgi sorting regulates organization and activity of GPI proteins at apical membranes 93
Exploring Bioinorganic Pattern Formation in Diatoms: A Story of Polarized Trafficking 91
Pathogenetic mechanisms in neurodegenerative processes induced by prion proteins 91
Detergent insoluble microdomains are not involved in transcytosis of polymeric Ig receptor in FRT and MDCK cells. 89
Plasticity in epithelial cell phenotype: modulation by expression of different cadherin cell adhesion molecules 88
Permeabilization of MDCK cells with cholesterol binding agents: dependence on substratum and confluency 87
Modulation of transcytotic and direct targeting pathways in a polarized thyroid cell line 87
GPI-Anchored proteins are confined in subdiffraction clusters at the apical surface of polarized epithelial cells 85
Characterization of the role of dendritic cells in prion transfer to primary neurons. 84
Polarity signals in epithelial cells 84
Lipids as Targeting Signals: Lipid Rafts and Intracellular Trafficking 83
Tunnelling nanotube formation is driven by Eps8/IRSp53‐dependent linear actin polymerization 82
Mechanisms of apical protein sorting in polarized thyroid epithelial cells 82
A requirement for caveolin-1 and associated kinase FYN in integrin signaling and anchorage-dependent cell growth 80
Cell Surface Biotinylation and Other Techniques for Determination of Surface Polarity of Epithelial Monolayers 80
Clustering in the Golgi apparatus governs sorting and function of GPI-APs in polarized epithelial cells 80
Prions: protein only or something more? Overview of potential prion cofactors 78
Polarized sorting of GPI proteins 77
Human CD8 glycoprotein is expressed at the apical plasma membrane domain in permanently transformed MDCKII clones. 76
3D reconstruction of the cerebellar germinal layer reveals tunneling connections between developing granule cells 75
Tunneling nanotubes provide a route for SARS-CoV-2 spreading 74
Different GPI-attachment signals affect the oligomerisation of GPI-anchored proteins and their apical sorting. 74
Detergent-resistant membrane microdomains and apical sorting of GPI-anchored proteins in polarized epithelial cells 73
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
Trafficking and Membrane Organization of GPI-Anchored Proteins in Health and Diseases 73
Tunneling nanotubes spread fibrillar α-synuclein by intercellular trafficking of lysosomes 73
Distinct v-SNAREs regulate direct and indirect apical delivery in polarized epithelial cells. 71
The order of rafts 71
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. 71
Prion aggregates transfer through tunneling nanotubes in endocytic vesicles 70
The Wnt/Ca2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes 69
Fate and propagation of endogenously formed Tau aggregates in neuronal cells 68
VIP21/Caveolin, glycosphingolipid clusters, and the sorting of glycosylphosphatidyl inositol-anchored proteins in epithelial cells 68
Lipid rafts and host cell-pathogen interactions 68
Caveolin transfection results in caveolae formation but not apical sorting of glycosylphosphatidylinositol (GPI)-anchored proteins in epithelial cells. 68
Actin Assembly around the Shigella-Containing Vacuole Promotes Successful Infection 68
Delivery of Na,K-ATPase in polarized epithelial cells 67
Organization of GPI-anchored proteins at the cell surface and its physiopathological relevance 66
Differential recognition of a tyrosine-dependent signal in the basolateral and endocytic pathways of thyroid epithelial cells. 66
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance. 66
Glycosylphosphatidylinositol-anchored proteins: Membrane organization and transport 66
The Shp-1 and Shp-2, tyrosine phosphatases, are recruited on cell membrane in two distinct molecular complexes including Ret oncogenes. 65
Multifaceted roles of tunneling nanotubes in intercellular communication. 65
Proteomic landscape of tunneling nanotubes reveals CD9 and CD81 tetraspanins as key regulators 64
Totale 10.171
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Categoria #
all - tutte 43.934
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 43.934
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022588 0 0 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
2026/2027568 154 205 209 0 0 0 0 0 0 0 0 0
Totale 12.453