IRIS
COCEANI, Flavio
 Distribuzione geografica
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Continente #
NA - Nord America 7.143
EU - Europa 4.298
AS - Asia 2.636
SA - Sud America 632
AF - Africa 79
Continente sconosciuto - Info sul continente non disponibili 18
OC - Oceania 3
Totale 14.809
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Nazione #
US - Stati Uniti d'America 6.967
GB - Regno Unito 1.228
RU - Federazione Russa 1.134
SG - Singapore 1.076
CN - Cina 720
UA - Ucraina 530
BR - Brasile 523
DE - Germania 487
VN - Vietnam 446
IT - Italia 342
HK - Hong Kong 176
SE - Svezia 133
CA - Canada 129
PL - Polonia 118
FI - Finlandia 108
IE - Irlanda 100
IN - India 47
AR - Argentina 43
DK - Danimarca 39
MX - Messico 35
ID - Indonesia 32
ZA - Sudafrica 32
JP - Giappone 25
BD - Bangladesh 24
EC - Ecuador 19
EU - Europa 18
ES - Italia 15
PK - Pakistan 14
PY - Paraguay 14
TR - Turchia 14
IQ - Iraq 13
NL - Olanda 13
FR - Francia 12
LT - Lituania 9
PE - Perù 8
AT - Austria 7
AZ - Azerbaigian 7
CI - Costa d'Avorio 7
CL - Cile 7
EG - Egitto 7
TN - Tunisia 7
VE - Venezuela 7
CO - Colombia 6
EE - Estonia 6
KE - Kenya 5
KR - Corea 5
RO - Romania 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
DZ - Algeria 4
ML - Mali 4
MY - Malesia 4
SA - Arabia Saudita 4
SN - Senegal 4
UY - Uruguay 4
GE - Georgia 3
IL - Israele 3
KZ - Kazakistan 3
PT - Portogallo 3
TT - Trinidad e Tobago 3
AL - Albania 2
AU - Australia 2
CG - Congo 2
CR - Costa Rica 2
ET - Etiopia 2
GA - Gabon 2
JM - Giamaica 2
KG - Kirghizistan 2
MA - Marocco 2
PA - Panama 2
PH - Filippine 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
GD - Grenada 1
IS - Islanda 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
NP - Nepal 1
NR - Nauru 1
OM - Oman 1
PS - Palestinian Territory 1
SI - Slovenia 1
SR - Suriname 1
SV - El Salvador 1
TH - Thailandia 1
TW - Taiwan 1
Totale 14.809
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Città #
Dallas 1.046
Southend 987
Ann Arbor 744
Woodbridge 661
Singapore 595
Chandler 514
Houston 508
Beijing 380
San Mateo 349
Ashburn 267
Jacksonville 255
Fairfield 253
Falls Church 172
Moscow 171
Hong Kong 170
Cambridge 145
Wilmington 119
Dong Ket 117
Warsaw 116
Pisa 103
Seattle 97
Dublin 95
Ho Chi Minh City 90
Stevenage 89
Portsmouth 88
Hefei 85
Los Angeles 82
The Dalles 82
Lawrence 79
Boardman 78
Dearborn 76
Ottawa 62
Hanoi 56
Redwood City 48
São Paulo 47
New York 43
Brooklyn 37
Buffalo 32
Santa Clara 32
Foggia 28
Helsinki 23
Tokyo 23
Munich 22
Old Bridge 22
Rio de Janeiro 22
Montreal 21
Denver 19
Fremont 17
Beauharnois 16
Chennai 16
Poplar 16
San Diego 16
Stockholm 15
Atlanta 14
Orem 14
Boston 13
Haiphong 13
Mexico City 13
Biên Hòa 12
Johannesburg 12
Norwalk 12
Phoenix 12
London 11
Porto Alegre 11
Belo Horizonte 10
Florence 10
Milan 10
Querétaro 9
Rome 9
Ankara 8
Brasília 8
Cape Town 8
Charlotte 8
Curitiba 8
Secaucus 8
Amsterdam 7
Augusta 7
Baku 7
Chicago 7
Da Nang 7
Dongguan 7
Hải Dương 7
San Francisco 7
Shanghai 7
Asunción 6
Caxias do Sul 6
Central District 6
Hortolândia 6
Kingston 6
Montréal 6
Mumbai 6
Ninh Bình 6
Pittsburgh 6
Poggibonsi 6
Ribeirão Preto 6
Thái Bình 6
Chatsworth 5
Guangzhou 5
Ha Long 5
Lahore 5
Totale 9.634
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Nome #
CYTOCHROME P450 3A13 AND ENDOTHELIN JOINTLY MEDIATE DUCTUS ARTERIOSUS CONSTRICTION TO OXYGEN IN MICE 284
Differential proteome profile in ischemic heart disease: Prognostic value in chronic angina versus myocardial infarction. A proof of concept. 281
Selective perfusion of coronary vasculature in preterm sheep: A methodological innovation undermined by unfavourable operation of the foramen ovale 267
Antenatal corrective cardiac surgery: an emerging area for technological innovation 249
Mouse aortic muscle cells respond to oxygen following cytochrome P450 3A13 gene transfer 247
Dual, constrictor-to-dilator, response of the mouse ductus arteriosus to the microsomal prostaglandin E synthase-1 inhibitor, 2-(6-chloro-1H-phenanthro[9,10d]imidazol-2-yl)isophthalonitrile. 237
Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function 237
Gene profiling in ductus arteriosus and aorta: a question of consistency. 234
Cytochrome P450 during ontogenic development: occurrence in the ductus arteriosus and other tissues. 227
EDHF function in the ductus arteriosus: evidence against involvement of epoxyeicosatrienoic acids (EETs) and 12S-hydroxyeicosatetraenoic acid (12S-HETE) 224
Indomethacin promotes nitric oxide function in the ductus arteriosus in the mouse 224
Gene expression in ductus arteriosus and aorta: comparison of birth and oxygen effects. 220
Ductus arteriosus: gene profile for fetal maturation versus postnatal closure. 220
ATP-gated potassium channel activity of pulmonary resistance vessels in the lamb 218
Cyclooxygenase-2/microsomal prostaglandin E synthase-1 complex in the preoptic-anterior hypothalamus of the mouse: involvement through fever to intravenous lipopolysaccharide 218
Arachidonic acid epoxygenase and 12(S)-lipoxygenase: evidence of their concerted involvement in ductus arteriosus constriction to oxygen 213
CD36 deficiency leads to choroidal involution via COX2 down-regulation in rodents. 209
Cyclooxygenase (cox) function in the ductus arteriosus: another look 207
Carbon monoxide formation in the ductus arteriosus in the lamb: implications for the regulation of muscle tone 205
Interactions between NO, CO and an endothelium-derived hyperpolarizing factor (EDHF) in maintaining patency of the ductus arteriosus in the mouse 205
Carbon monoxide in vasoregulation: the promise and the challenge 204
Cyclooxygenase in the lamb ductus arteriosus: developmental changes and upregulation 204
Cyclooxygenase isoenzymes and patency of ductus arteriosus 203
Role of microsomal prostaglandin E synthase-1 (mPGES1)-derived PGE2 in patency of the ductus arteriosus in the mouse 200
Cyclooxygenase-1 and cyclooxygenase-2 in the mouse ductus arteriosus: individual activity and functional coupling with nitric oxide synthase. 198
Control of the ductus arteriosus - A new function for cytochrome P450, endothelin and nitric oxide 193
Control mechanisms for the ductus arteriosus and the perinatal pulmonary circulation 193
Cyclooxygenase (COX) function in the ductus arteriosus: another look 193
Occurrence of endothelium-derived relaxing factor/nitric oxide in the lamb ductus arteriosus. 188
Cardiopulmonary bypass in ewe's fetus: advances and setbacks in our learning curve. 185
Contractile and relaxing mechanisms in pulmonary resistance arteries of the preterm fetal lamb 185
Carbon monoxide-induced relaxation of the ductus arteriosus in the lamb: evidence against the prime role of guanylyl cyclase. 183
Carbon monoxide and dilation of blood vessels 182
Pyrogen-prostaglandin coupling in the pathogenesis of fever: evidence against a role for nitric oxide 176
Design and serendipity in the path to prostaglandins. 174
Cytochrome P450 expression and catalytic activity in coronary arteries and liver of cattle. 172
Interleukin-1 receptor antagonist: effectiveness against interleukin-1 fever 171
Ductus arteriosus: involvement of a sarcolemmal cytochrome P-450 in O2 constriction? 168
Effect of endothelium removal on prostaglandin and nitric oxide function in pulmonary resistance arteries in the lamb. 168
Interleukin-6 as an endogenous pyrogen: induction of prostaglandin E2 in brain but not in peripheral blood mononuclear cells 166
Prostaglandin formation in feline cerebral microvessels: effect of endotoxin and interleukin-1. 165
Endothelin-1 release from lamb ductus arteriosus: relevance to postnatal closure of the vessel 163
Evidence against the involvement of a cytochrome P-450 mechanism in pulmonary hemodynamics in the newborn pig 163
Differential effects of endotoxin and cytokines on prostaglandin E2 formation in cerebral microvessels and brain parenchyma: implications for the pathogenesis of fever 162
Formation of interleukin-6 in the brain of the febrile cat: relationship to interleukin-1 162
Leukotrienes in cerebrospinal fluid of the conscious cat: effect of platelet-activating factor and pyrogens 159
Eicosanoid formation in the rat cerebral cortex: contribution of neurons and glia 159
Endothelium-denuded pulmonary resistance arteries from the fetal lamb: preparation and response to vasoactive agents. 158
Fever: a paradigm for eicosanoid function in brain 157
The endothelin A receptor antagonists, PD 156707 (CI-1020) and PD 180988 (CI-1034), reverse the hypoxic pulmonary vasoconstriction in the perinatal lamb. 157
Perinatal changes in choroidal 15-hydroxyprostaglandin dehydrogenase: implications for prostaglandin removal from brain. 156
Function of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the ductus arteriosus from foetal lamb: differential development and change by oxygen and endotoxin. 156
The control of the ductus venosus: an update 155
Prostaglandin uptake and catabolism by the choroid plexus during development in sheep 154
Endothelin in the perinatal circulation 153
Further evidence implicating a cytochrome P-450-mediated reaction in the contractile tension of the lamb ductus arteriosus. 153
Cytochrome P450 in the contractile tone of the ductus arteriosus: regulatory and effector mechanisms 152
Evidence for an effector role of endothelin in closure of the ductus arteriosus at birth. 152
Leukotrienes in brain: natural occurrence and induced changes 151
Prostaglandin E2 in the pathogenesis of fever: an update 151
Effect of ciliary neurotrophic factor on body temperature and cerebrospinal fluid prostanoids in the cat 151
PGE2 in the perinatal brain: local synthesis and transfer across the blood-brain barrier 151
Isolated pulmonary resistance vessels from fetal lamb: contractile behaviour and response to endothelin-1. 148
Response of newborn and adult sheep to pyrogens: relation between fever and brain eicosanoid changes 147
Paradoxical coronary microcirculatory constriction during ischemia: a synergic function for nitric oxide and endothelin 147
The ETA receptor antagonist PD180988 (CI-1034) selectively reverses the pulmonary vasoconstrictor response to hypoxia in the lamb 146
Does endothelin-1 reduce superior mesenteric artery blood flow velocity in preterm neonates? 146
Involvement of endothelin-1 in the hypoxic pulmonary vasoconstriction in the lamb. 146
Endothelin-1 release from the ductus arteriosus: are carbon monoxide and nitric oxide regulatory agents? 145
Eicosanoids in third ventricular cerebrospinal fluid of the fetal and newborn sheep. 145
Prostaglandins and fever: facts and controversies 144
Interleukin-6 and tumor necrosis factor in cerebrospinal fluid: changes during pyrogen fever 143
Lamb ductus venosus: evidence of a cytochrome P-450 mechanism in its contractile tension. 142
Endothelin-induced constriction of the ductus venosus in fetal sheep: developmental aspects and possible interaction with vasodilatory prostaglandin. 141
Differential uptake and catabolism of prostaglandin (PG)E(2) versus PGF2(alpha) in the sheep choroid plexus during development. 140
Oxygen-related prostaglandin synthesis in ductus arteriosus and other vascular cells. 138
Deletion of the ETA receptor suppresses oxygen-induced constriction but not postnatal closure of the ductus arteriosus 136
Prostaglandin E2: a pathogenetic link for fever 134
Prostaglandin E2 in cerebrospinal fluid of fetal and newborn sheep: central versus peripheral source 131
The response of the lamb ductus arteriosus to endothelin: developmental changes and influence of light 130
Endothelium-derived relaxing factor in pulmonary resistance vessels from fetal lamb: stimulation by oxygen and bradykinin. 129
Identification of specific prostaglandin E receptors on cardiac sarcolemmal membranes. 127
Inhibition of the contraction of the ductus arteriosus to oxygen by 1-aminobenzotriazole, a mechanism-based inactivator of cytochrome P450. 127
Endothelin-A receptor is necessary for oxygen constriction but not closure of the ductus arteriosus 123
Totale 14.827
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Categoria #
all - tutte 77.330
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 77.330
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.080 0 0 0 0 0 262 113 85 107 89 157 267
2021/20221.110 26 279 30 87 8 3 144 251 55 123 12 92
2022/20231.204 86 56 31 244 134 231 20 94 211 17 53 27
2023/2024325 56 20 53 17 19 90 20 10 0 9 2 29
2024/20252.516 13 7 159 59 48 187 441 814 172 76 382 158
2025/20263.848 349 1.075 716 839 763 106 0 0 0 0 0 0
Totale 14.827