BOSSI, FLEUR
 Distribuzione geografica
Continente #
NA - Nord America 8.281
EU - Europa 4.997
AS - Asia 3.013
SA - Sud America 347
Continente sconosciuto - Info sul continente non disponibili 341
AF - Africa 88
OC - Oceania 10
Totale 17.077
Nazione #
US - Stati Uniti d'America 8.155
PL - Polonia 1.602
SG - Singapore 1.132
SE - Svezia 619
CN - Cina 616
IT - Italia 543
DE - Germania 520
UA - Ucraina 407
RU - Federazione Russa 309
VN - Vietnam 302
HK - Hong Kong 289
BR - Brasile 266
FR - Francia 210
GB - Regno Unito 186
FI - Finlandia 156
KR - Corea 150
NL - Olanda 127
TR - Turchia 115
BD - Bangladesh 95
IE - Irlanda 78
BG - Bulgaria 77
CA - Canada 56
TW - Taiwan 56
IN - India 55
JP - Giappone 40
MX - Messico 39
BE - Belgio 36
ID - Indonesia 27
AR - Argentina 25
MA - Marocco 25
CH - Svizzera 20
ES - Italia 20
AT - Austria 19
CZ - Repubblica Ceca 18
ZA - Sudafrica 18
PK - Pakistan 15
PH - Filippine 14
IQ - Iraq 13
SN - Senegal 13
TH - Thailandia 13
CL - Cile 12
SA - Arabia Saudita 12
CO - Colombia 11
IR - Iran 10
VE - Venezuela 10
AE - Emirati Arabi Uniti 8
PT - Portogallo 8
UZ - Uzbekistan 8
AU - Australia 7
EC - Ecuador 7
MD - Moldavia 7
EE - Estonia 6
EU - Europa 6
IL - Israele 6
PE - Perù 6
DZ - Algeria 5
EG - Egitto 5
GE - Georgia 5
JO - Giordania 5
RO - Romania 5
BO - Bolivia 4
CR - Costa Rica 4
GR - Grecia 4
HN - Honduras 4
KE - Kenya 4
LB - Libano 4
MY - Malesia 4
NG - Nigeria 4
PA - Panama 4
PY - Paraguay 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
AZ - Azerbaigian 3
BB - Barbados 3
GT - Guatemala 3
HR - Croazia 3
LU - Lussemburgo 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
RS - Serbia 3
AM - Armenia 2
DM - Dominica 2
KH - Cambogia 2
LT - Lituania 2
NI - Nicaragua 2
NP - Nepal 2
SK - Slovacchia (Repubblica Slovacca) 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
UG - Uganda 2
AL - Albania 1
AN - Antille olandesi 1
AO - Angola 1
BW - Botswana 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
JM - Giamaica 1
Totale 16.727
Città #
Warsaw 1.537
Fairfield 850
Ashburn 805
Woodbridge 716
Ann Arbor 701
Singapore 688
Houston 526
Chandler 432
San Jose 353
Wilmington 352
Seattle 334
Jacksonville 316
Hong Kong 277
Cambridge 270
Dallas 243
Beijing 164
Trieste 154
Seoul 144
Princeton 136
Santa Clara 129
Boardman 116
Los Angeles 111
Izmir 95
Hefei 93
Ho Chi Minh City 92
Chicago 87
Council Bluffs 77
Sofia 77
Columbus 76
Moscow 75
New York 75
Dublin 74
Lauterbourg 61
Zgierz 58
Dearborn 57
Hanoi 53
Taipei 53
Munich 44
Frankfurt am Main 42
Helsinki 42
Milan 42
San Diego 40
Buffalo 39
São Paulo 37
Tokyo 33
The Dalles 32
Brussels 30
Düsseldorf 29
Saint Petersburg 26
Boston 25
Shanghai 25
Dong Ket 24
Falls Church 24
London 24
Atlanta 23
Amsterdam 21
Orem 21
Washington 21
Casablanca 20
Phoenix 19
Des Moines 18
Memphis 18
Kyiv 17
Nanjing 17
Miano 16
Stockholm 16
Miami 15
Montreal 15
Sacile 15
Buon Ma Thuot 14
Redmond 14
Redondo Beach 14
San Francisco 14
Dakar 13
Denver 13
North Bergen 13
Toronto 13
Vienna 13
Bern 12
Brooklyn 12
Da Nang 12
Jakarta 12
Turku 12
Haiphong 11
Jinan 11
Kunming 11
Paris 11
Redwood City 11
Venice 11
Brno 10
Mexico City 10
Rome 10
Belo Horizonte 9
Guangzhou 9
Mestre 9
Norwalk 9
Verona 9
Chennai 8
Johannesburg 8
Torino 8
Totale 11.633
Nome #
The complement component C3 is expressed by the endometrial ectopic tissue and is involved in the endometriotic lesion formation 862
RelB activation in anti-inflammatory decidual endothelial cells: a master plan to avoid pregnancy failure? 491
Aldosterone effects on glomerular structure and function 485
TRAIL Modulates the Immune System and Protects against the Development of Diabetes 429
Roles and Clinical Applications of OPG and TRAIL as Biomarkers in Cardiovascular Disease 425
Association between thyroid hormones and TRAIL 422
Circulating osteoprotegerin is associated with chronic kidney disease in hypertensive patients 418
Treponema pallidum (syphilis) antigen TpF1 induces angiogenesis through the activation of the IL-8 pathway 385
HMGA1 promotes breast cancer angiogenesis supporting the stability, nuclear localization and transcriptional activity of FOXM1 373
C1q as a novel player in angiogenesis with therapeutic implication in wound healing 369
C1q is involved in human trophoblast invasion 326
Pre-eclampsia affects procalcitonin production in placental tissue 317
Angiotensin 1-7 significantly reduces diabetes-induced leukocyte recruitment both in vivo and in vitro 309
C1q is associated with a reduced inflammatory response of decidual endothelial cells 305
Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion 305
C1q is responsible of the anti-inflammatory behavior of decidual endothelial cells 294
Pre-eclampsia is associated with defective production of C1q by invasive trophoblast 293
C1q: A novel angiogenic factor? 290
null 263
Osteoprotegerin increases leukocyte adhesion to endothelial cells both in vitro and in vivo. 255
ACE2 deficiency shifts energy metabolism towards glucose utilization 253
Bilirubin inhibits the TNFα-related induction of three endothelial adhesion molecules 243
Dyslipidemia and Diabetes Increase the OPG/TRAIL Ratio in the Cardiovascular System 243
Placental trophoblast and endothelial cells as target of maternal immune response. 237
In vivo targeting of human neutralizing antibodies against CD55 and CD59 to lymphoma cells increases the antitumor activity of rituximab. 229
CD38/CD31, the CCL3 and CCL4 chemokines, and CD49d/vascular cell adhesion molecule-1 are interchained by sequential events sustaining chronic lymphocytic leukemia cell survival. 228
Complement C1q and C8beta deficiency in an individual with recurrent bacterial meningitis and adult-onset systemic lupus erythematosus-like illness. 224
The seventh complement component is expressed on endothelial cells membrane and exerts an anti-inflammatory action 216
Bilirubin inhibits the TNFalpha-related induction of three endothelial adhesion molecules. 211
TRAIL reduces impaired glucose tolerance and NAFLD in the high-fat diet-fed mouse 210
The neutrophil-activating protein of Helicobacter pylori crosses endothelia to promote neutrophil adhesion in vivo. 195
Emerging Roles of the Complement System at Foeto-maternal Interface 193
The terminal complement complex induces vascular leakage: in vitro and in vivo evidence 193
MBL interferes with endovascular trophoblast invasion in pre-eclampsia. 192
Analysis of the molecular mechanisms of C1-inhibitor deficiency induced angioedema 192
C7 is expressed on endothelial cells as a trap for the assembling terminal complement complex and may exert anti-inflammatory function. 188
Mannose binding lectin and C3 act as recognition molecules for infectious agents in the vagina 187
Thrombus formation induced by antibodies to beta2-glycoprotein I is complement dependent and requires a priming factor. 187
Mutant p53 induces Golgi tubulo-vesiculation driving a prometastatic secretome 181
Orchestration of inflammation and adaptive immunity in Borrelia burgdorferi-induced arthritis by neutrophil-activating protein A. 176
Platelet-activating factor and kinin-dependent vascular leakage as a novel functional activity of the soluble terminal complement complex. 174
The Complement System at the Embryo Implantation Site: Friend or Foe? 173
Ischemic wound revascularization by the stromal vascular fraction relies on host-donor hybrid vessels 172
C1q induces in vivo angiogenesis and promotes wound healing 171
The soluble terminal complement complex (SC5b-9) up-regulates osteoprotegerin expression and release by endothelial cells: implications in rheumatoid arthritis. 167
Cross-talk between the complement and the kinin system in vascular permeability 167
Tanshinone VI inhibits the expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1. 167
Complement Activation and Thrombin Generation by MBL Bound to β2-Glycoprotein I 167
The C7 component of the complement system localizes to vascular smooth muscle cells and endothelium in human first trimester decidua 160
An alternative role of C1q in cell migration and tissue remodeling: contribution to trophoblast invasion and placental development. 159
VE-cadherin is a critical molecule for trophoblast-endothelial cell interaction in decidual spiral arteries. 159
Novel pathogenic mechanism and therapeutic approaches to angioedema associated with C1 inhibitor deficiency. 158
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Role of the B1 Bradykinin Receptor and gC1qR/p33 in Angioedema 153
Protective and regenerative effects of a novel medical device against esophageal mucosal damage using in vitro and ex vivo models 153
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Feto-maternal immune interaction at the placental level 151
Mast cells are critically involved in serum-mediated vascular leakage in chronic urticaria beyond high-affinity IgE receptor stimulation 147
Complement production by trophoblast cells at the feto-maternal interface. 145
Uterine immunity and microbiota: A shifting paradigm 145
New topics in bradykinin research 138
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The C2 fragment from Neisseria meningitidis antigen NHBA increases endothelial permeability by destabilizing adherens junctions 120
Decidual endothelial cells express surface-bound C1q as a molecular bridge between endovascular trophoblast and decidual endothelium. 119
Inhibitory effects of fenofibrate on apoptosis and cell proliferation in human endothelial cells in high glucose 115
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Endothelial cells are a target of both complement and kinin system. 92
Transcriptomics and immunological analyses reveal a pro-angiogenic and anti-inflammatory phenotype for decidual endothelial cells 86
Inflammation, complément et implantation 86
From the molecular mechanisms of C1-inhibitor deficiency induced angioedema to therapeutic choices 83
EMILIN1 represents a major stromal element determining human trophoblast invasion of the uterine wall. 76
Recruitment of circulating NK cells through decidual tissues: a possible mechanism controlling NK cell accumulation in the uterus during early pregnancy. 71
Phenotype characterization of the anti-inflammatory behavior of decidual endothelial cells 67
Totale 17.077
Categoria #
all - tutte 44.134
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 44.134


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.091 0 52 87 93 43 95 51 76 165 114 67 248
2022/20231.373 146 190 114 189 117 235 12 124 157 12 57 20
2023/2024803 47 62 71 20 81 110 125 135 25 19 62 46
2024/20251.531 31 30 147 134 135 141 118 95 230 178 142 150
2025/20264.005 393 210 320 318 405 349 577 97 447 548 222 119
2026/2027407 328 79 0 0 0 0 0 0 0 0 0 0
Totale 17.077