IRIS
SALAMINO, FRANCA
 Distribuzione geografica
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Continente #
EU - Europa 17.953
AS - Asia 1.499
NA - Nord America 1.240
SA - Sud America 120
Continente sconosciuto - Info sul continente non disponibili 77
AF - Africa 22
OC - Oceania 16
Totale 20.927
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Nazione #
IT - Italia 17.671
US - Stati Uniti d'America 1.155
SG - Singapore 669
CN - Cina 409
VN - Vietnam 240
FR - Francia 144
BR - Brasile 69
BD - Bangladesh 46
HK - Hong Kong 40
CA - Canada 36
DE - Germania 29
AR - Argentina 21
JP - Giappone 20
GB - Regno Unito 19
FI - Finlandia 17
AU - Australia 16
IN - India 13
MX - Messico 13
NL - Olanda 13
JM - Giamaica 12
CO - Colombia 11
CH - Svizzera 9
ID - Indonesia 9
ES - Italia 8
IQ - Iraq 7
AE - Emirati Arabi Uniti 6
CR - Costa Rica 6
IE - Irlanda 5
RO - Romania 5
SA - Arabia Saudita 5
EC - Ecuador 4
PH - Filippine 4
PL - Polonia 4
TR - Turchia 4
UA - Ucraina 4
UZ - Uzbekistan 4
ZA - Sudafrica 4
BO - Bolivia 3
DZ - Algeria 3
GT - Guatemala 3
KR - Corea 3
KZ - Kazakistan 3
MA - Marocco 3
NI - Nicaragua 3
PE - Perù 3
PK - Pakistan 3
RU - Federazione Russa 3
SK - Slovacchia (Repubblica Slovacca) 3
TT - Trinidad e Tobago 3
VE - Venezuela 3
BE - Belgio 2
CL - Cile 2
CY - Cipro 2
DO - Repubblica Dominicana 2
ET - Etiopia 2
JO - Giordania 2
KE - Kenya 2
LT - Lituania 2
MT - Malta 2
MY - Malesia 2
NO - Norvegia 2
PA - Panama 2
PR - Porto Rico 2
PY - Paraguay 2
RS - Serbia 2
SE - Svezia 2
SN - Senegal 2
TH - Thailandia 2
TW - Taiwan 2
UY - Uruguay 2
AL - Albania 1
AW - Aruba 1
BG - Bulgaria 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
EE - Estonia 1
EG - Egitto 1
HN - Honduras 1
HU - Ungheria 1
IR - Iran 1
LB - Libano 1
LK - Sri Lanka 1
MK - Macedonia 1
MQ - Martinica 1
OM - Oman 1
TG - Togo 1
TN - Tunisia 1
Totale 20.850
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Città #
Genova 11.565
Genoa 3.592
Rapallo 1.344
Vado Ligure 1.080
San Jose 403
Singapore 311
Lauterbourg 129
Ashburn 81
Ho Chi Minh City 64
New York 55
Beijing 49
Hanoi 44
Hong Kong 37
Santa Clara 33
Frankfurt am Main 26
Tokyo 18
Council Bluffs 17
Helsinki 17
Da Nang 14
Los Angeles 13
Haiphong 12
Amsterdam 11
Bordighera 11
Chicago 11
Phoenix 11
Montreal 10
São Paulo 10
Jacksonville 9
Rome 9
Zurich 9
Mexico City 8
Tianjin 8
Washington 8
Brooklyn 7
Buffalo 7
Kingston 7
Naples 7
Toronto 7
Dallas 6
Des Moines 6
Houston 6
San Francisco 6
Atlanta 5
Dublin 5
Hải Dương 5
Madrid 5
Milan 5
Orem 5
San José 5
Durham 4
Huntsville 4
Iowa City 4
Jeddah 4
Las Vegas 4
London 4
Marseille 4
Nha Trang 4
Ninh Bình 4
Paris 4
Queens 4
The Bronx 4
Warsaw 4
Abu Dhabi 3
Acalanes Ridge 3
Baghdad 3
Bari 3
Biên Hòa 3
Bogotá 3
Buenos Aires 3
Cagliari 3
Cardiff 3
Charlotte 3
City of London 3
Cleveland 3
Curtea de Argeş 3
Edmonton 3
Fort Lauderdale 3
Greensboro 3
Guangzhou 3
Guatemala City 3
Istanbul 3
Johannesburg 3
Lahore 3
Managua 3
Memphis 3
Mumbai 3
New Orleans 3
Palermo 3
Philadelphia 3
Rio de Janeiro 3
Seattle 3
Silver Spring 3
Sumter 3
Sydney 3
Tashkent 3
Turin 3
Wilmington 3
Abingdon 2
Addis Ababa 2
Algiers 2
Totale 19.276
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Nome #
Activation of calpain 1 and protein kinase C alpha promotes a constitutive expression and release of matrix metalloproteinase 9 in peripheral blood mononuclear cells from cystic fibrosis patients 321
"Intracellular calpastatin proteolysis: a salvage mechanism or a prelude to cell damage?" 267
Abnormal activation of calpain and protein kinase Cα promotes a constitutive release of matrix metalloproteinase 9 in peripheral blood mononuclear cells from cystic fibrosis patients 249
Calpain digestion and HSP90-based chaperone protection modulate the level of plasma membrane F508del-CFTR. 248
Evidence for alteration of calpain/calpastatin system in PBMC of cystic fibrosis patients 231
Role of the calpain-calpastatin system in the density-dependent growth arrest 215
A vincristine-resistant murine erythroleukemia cell line secretes a differentiation enhancing factor. 213
Acyl-CoA-binding protein is a potent m-calpain activator 210
Calpain inhibition promotes the rescue of F(508)del-CFTR in PBMC from cystic fibrosis patients. 201
Autolysis of human erythrocytes calpain produces two active enzyme forms with different cell localization 200
Modulation of the calpain autoproteolysis by calpastatin and phospholipids 198
Characterization of a new p94-like calpain form in human lymphocytes 198
Characterization of the calpain/calpastatin system in human hemopoietic cell lines 197
Effect of extremely low frequency magnetic fields on calpain activation 193
Activation of neutrophil calpain following its translocation to the plasma membrane induced by phorbol ester or fMet-Leu-Phe.. 191
Physiological Roles of Calpain 1 Associated to Multiprotein NMDA Receptor Complex. 190
Differential regulation of the calpain-calpastatin complex by the L-domain of calpastatin 189
Binding to erythrocyte membrane is the physiological mechanism for activation of Ca2+-dependent neutral proteinase. 188
Degradation of CFTR-generated protein clusters by calpain: A physiological or a pathological role? 181
The calpain-calpastatin system in mammalian cells: properties and possible functions 178
Activation of NADPH oxidase and phosphorylation of membrane proteins in human neutrophils: coordinate inhibition by a surface antigen-directed monoclonal antibody. 176
Changes during fasting in the activity of a specific lysosomal proteinase, fructose-1,6-bisphosphatase converting enzyme. 174
Characterization of the defective calpain-endogenous calpain inhibitor system in erythrocytes from Milan hypertensive rats. 173
Changes in rabbit-liver lysosomes and fructose 1,6-bisphosphatase induced by cold and fasting. 172
Characterization of the calpastatin defect in erythrocytes from patients with essential hypertension. 171
Changes in calpastatin localization and expression during calpain activation: a new mechanism for the regulation of intracellular Ca(2+)-dependent proteolysis. 171
Regulation of calpain activity in rat brain with altered Ca2+ homeostasis 171
Binding of protein kinase C to neutrophil membranes in the presence of Ca2+ and its activation by a Ca2+-requiring proteinase. 171
Glucose 6-phosphate dehydrogenase activity in membranes of erythrocytes from normal individuals and subjects with Mediterranean G6PD deficiency. 171
Characterization of the inactive form of fructose-1,6-bisphosphate aldolase isolated from livers of fasted rabbits. 171
Properties and intracellular localization of calpain activator protein 171
Cathepsin M: a lysosomal proteinase with aldolase-inactivating activity 170
Changes in intracellular localization of calpastatin during calpain activation 168
Binding of Zn2+ to rabbit muscle fructose 1,6-bisphosphatase and its effect on the catalytic properties. 167
Interactions of Zn2+ and Mg2+ with rabbit liver fructose 1,6 bisphosphatase. 167
On the mechanism of inhibition of fructose 1,6-bisphosphatase by fructose 2,6-bisphosphate. 166
Potentiation of NMDA Receptor-Dependent Cell Responses by Extracellular High Mobility Group Box 1 Protein. 165
The role of calpain in the selective increased phosphorylation of the anion-transport protein in red cell of hypertensive subjects. 164
"Association of calpastatin with inactive calpain: a novel mechanism to control the activation of the protease?" 164
Interaction between Calpain-1 and HSP90: New Insights into the Regulation of Localization and Activity of the Protease. 162
Cytosolic calcium dependent proteinase of human erythrocytes: formation of an enzyme-natural inhibitor complex induced by Ca2+ ions. 161
Changes in intracellular calpastatin localization are mediated by reversible phosphorylation 161
Proteolytic degradation of nitric oxide synthase isoforms by calpain is modulated by the expression levels of HSP90. 159
Binding of monoclonal antibody to cathepsin M located on the external surface of rabbit lysosomes. 159
Comparative patterns of 'in vitro' oxidative hemolysis of normal and glucose 6-phosphate dehydrogenase (G6PD)-deficient erythrocytes. 159
Age-dependent degradation of calpastatin in kidney of hypertensive rats 159
“In vivo degradation of Nitric-Oxide Synthase isozymes by Calpain is regulated by HSP90” 159
Biochemical responses in activated human neutrophils mediated by protein kinase C and a Ca2+-requiring proteinase. 157
Inactivation of fructose 1,6-bisphosphatase by a lysosomal proteinase is reversed by cystamine. 156
Inactivation of liver aldolase in fasting rabbits: evidence for the accumulation of two different immunoreactive forms. 156
Changes in activity of fructose-1,6-bisphosphate aldolase in livers of fasted rabbits and accumulation of crossreacting immune material. 156
Involvement of erythrocyte calpain in glycine- and carnitine-treated isovaleric acidemia. 155
Decreased level of calpain inhibitor activity in kidney from Milan hypertensive rats. 154
Adaptive modifications in the calpain/calpastatin system in brain cells after persistent alteration in Ca2+ homeostasis 154
Cytosolic levels of calpastatin are regulated by limited proteolysis 153
"Cytosolic levels of calpastatin are regulated by limited proteolysis" 153
Role of calpain in the regulation of CFTR (cystic fibrosis transmembrane conductance regulator) turnover 153
The plasma membrane calcium pump is the preferred calpain substrate within the erythrocyte 152
Phosphorylation and proteolytic modification of specific cytoskeletal proteins in human neutrophils stimulated by phorbol 12-myristate 13-acetate. 152
ATP induces the release of a neutral serine proteinase and enhances the production of superoxide anion in membranes from phorbol ester-activated neutrophils. 151
Isolation and characterization of calpain activator protein from bovine brain. 150
The calpastatin defect in hypertension is possibly due to a specific degradation by calpain. 150
Two cytosolic, Ca2+-dependent, neutral proteinases from rabbit liver: purification and properties of the proenzymes. 149
Role of calpain-1 in the early phase of experimental ALS 149
Endogenous inhibitors of lysosomal proteinases 148
“Susceptibility of NOS isoforms to calpain digestion is modulated by the expression levels of HSP90” 145
Calpain-mediated activation of NO synthase in human neuroblastoma SK-N-BE cells 144
An endogenous activator of the Ca2+-dependent proteinase of human neutrophils that increases its affinity for Ca2+. 144
In vitro correction of erythrocyte glucose 6-phosphate dehydrogenase (G6PD) deficiency. 144
Different susceptibility of red cell membrane proteins to calpain degradation. 143
Origin of tryptophan in fructose 1,6-bisphosphatase purified from livers of fed rabbits. 140
Biotechnological traps for the reduction of inflammation due to cardiopulmonary bypass. 140
Role of phospholipids in the activation of the Ca2+-dependent neutral proteinase of human erythrocytes. 139
Limited proteolysis of liver aldolase and fructose 1,6-bisphosphatase by lysosomal proteinases: effect on complex formation. 139
Association of calpastatin with inactive calpain: a novel mechanism to control the activation of the protease? 139
Characterization of the single peptide generated from the amino-terminus end of alpha- and beta-hemoglobin chains by the Ca2+-dependent neutral proteinase. 138
Proteolysis of human reticulocyte membrane proteins: evidence for a physiological role of the acid endopeptidases. 138
Localization of two lysosomal proteinases on the external surface of the lysosomal membrane. 137
Mechanism of action of a new component of the ca2+dependent proteolytic system in rat brain:the calpain activator 136
Regulation of the Ca2+-dependent neutral proteinases from rabbit liver by an endogenous inhibitor. 136
Is the Expression of [-G93A(+)] human SOD1 a model to study neurodegenerations? 136
Interaction of rabbit liver cathepsin M and fructose 1,6-bisphosphatase converting enzyme with their endogenous inhibitors. 135
In vivo degradation of nitric oxide synthase (NOS) and heat shock protein 90 (HSP90) by calpain is modulated by the formation of a NOS-HSP90 heterocomplex 133
Decay of proteinase and peptidase activities of human and rabbit erythrocytes during cellular aging. 131
Characterization of three rabbit liver lysosomal proteinases with fructose 1,6-bisphosphatase converting enzyme activity. 130
Identification of two calpastatin forms in rat skeletal muscle and their susceptibility to digestion by homologous calpains. 130
Cytolytic effects of neutrophils: role for a membrane-bound neutral proteinase. 129
Differences and similarities among three acidic endopeptidases associated with human erythrocyte membranes. Molecular and functional studies. 129
Calcium binding properties of human erythrocytes calpain 128
Phosphorylation of rat brain calpastatins by protein kinase C. 128
Phosphorylation of proteins in human neutrophils activated with phorbol myristate acetate or with chemotactic factor. 128
Modulation of inhibitory efficiency of rat skeletal muscle calpastatin by phosphorylation. 128
Evidence for an interaction between fructose 1,6-bisphosphatase and fructose 1,6-bisphosphate aldolase. 127
Decreased level of calpain inhibitor activity in red blood cells from Milan hypertensive rats. 126
Cytosolic Ca2+-dependent neutral proteinases from rabbit liver: activation of the proenzymes by Ca2+ and substrate. 126
Cytosolic calcium dependent neutral proteinase of human erythrocytes: the role of calcium ions on the molecular and catalytic properties of the enzyme. 124
Following association to the membrane, human erythrocyte procalpain is converted and released as fully active calpain. 124
Properties of calpastatin forms in rat brain 123
Identification of proteolytic activities in the cytosolic compartment of mature human erythrocytes. 123
“Involvement of the Calpain/Calpastatin System in Familial Amyotrophic Lateral Sclerosis” 123
Totale 16.171
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Categoria #
all - tutte 58.866
article - articoli 51.466
book - libri 0
conference - conferenze 6.408
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 992
Totale 117.732
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.633 42 98 88 202 68 127 144 307 66 173 70 248
2022/20231.597 145 84 16 216 244 316 0 103 297 12 150 14
2023/2024762 40 95 8 77 115 174 17 29 49 18 40 100
2024/20252.764 173 192 65 149 390 304 259 403 143 93 260 333
2025/20263.729 479 71 181 249 481 407 694 151 343 350 104 219
2026/2027434 434 0 0 0 0 0 0 0 0 0 0 0
Totale 20.927