IRIS
COCEANI, Flavio
 Distribuzione geografica
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Continente #
NA - Nord America 7.160
EU - Europa 4.341
AS - Asia 2.661
SA - Sud America 634
AF - Africa 80
Continente sconosciuto - Info sul continente non disponibili 18
OC - Oceania 3
Totale 14.897
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Nazione #
US - Stati Uniti d'America 6.983
GB - Regno Unito 1.230
RU - Federazione Russa 1.173
SG - Singapore 1.090
CN - Cina 723
UA - Ucraina 530
BR - Brasile 525
DE - Germania 487
VN - Vietnam 449
IT - Italia 342
HK - Hong Kong 176
SE - Svezia 134
CA - Canada 130
PL - Polonia 119
FI - Finlandia 108
IE - Irlanda 100
IN - India 50
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
UZ - Uzbekistan 7
VE - Venezuela 7
CO - Colombia 6
EE - Estonia 6
KE - Kenya 5
KR - Corea 5
RO - Romania 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
MA - Marocco 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
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 14.897
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Città #
Dallas 1.046
Southend 987
Ann Arbor 744
Woodbridge 661
Singapore 609
Chandler 514
Houston 509
Beijing 380
San Mateo 349
Ashburn 274
Jacksonville 255
Fairfield 253
Moscow 190
Falls Church 172
Hong Kong 170
Cambridge 145
Wilmington 119
Dong Ket 117
Warsaw 117
Pisa 103
Seattle 98
Dublin 95
Ho Chi Minh City 91
Stevenage 89
Portsmouth 88
Hefei 85
Los Angeles 82
The Dalles 82
Lawrence 79
Boardman 78
Dearborn 76
Ottawa 62
Hanoi 57
São Paulo 49
Redwood City 48
New York 43
Brooklyn 37
Santa Clara 33
Buffalo 32
Foggia 28
Helsinki 23
Tokyo 23
Munich 22
Old Bridge 22
Rio de Janeiro 22
Montreal 21
Denver 19
Chennai 18
Poplar 18
Fremont 17
Atlanta 16
Beauharnois 16
San Diego 16
Stockholm 16
Orem 15
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
Da Nang 8
Secaucus 8
Amsterdam 7
Augusta 7
Baku 7
Chicago 7
Dongguan 7
Hải Dương 7
Mumbai 7
San Francisco 7
Shanghai 7
Asunción 6
Caxias do Sul 6
Central District 6
Hortolândia 6
Kingston 6
Montréal 6
Ninh Bình 6
Pittsburgh 6
Poggibonsi 6
Ribeirão Preto 6
Thái Bình 6
Chatsworth 5
Guangzhou 5
Ha Long 5
Lahore 5
Totale 9.692
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Nome #
CYTOCHROME P450 3A13 AND ENDOTHELIN JOINTLY MEDIATE DUCTUS ARTERIOSUS CONSTRICTION TO OXYGEN IN MICE 286
Differential proteome profile in ischemic heart disease: Prognostic value in chronic angina versus myocardial infarction. A proof of concept. 283
Selective perfusion of coronary vasculature in preterm sheep: A methodological innovation undermined by unfavourable operation of the foramen ovale 269
Antenatal corrective cardiac surgery: an emerging area for technological innovation 252
Mouse aortic muscle cells respond to oxygen following cytochrome P450 3A13 gene transfer 249
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. 241
Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function 238
Gene profiling in ductus arteriosus and aorta: a question of consistency. 236
Cytochrome P450 during ontogenic development: occurrence in the ductus arteriosus and other tissues. 229
EDHF function in the ductus arteriosus: evidence against involvement of epoxyeicosatrienoic acids (EETs) and 12S-hydroxyeicosatetraenoic acid (12S-HETE) 227
Indomethacin promotes nitric oxide function in the ductus arteriosus in the mouse 225
Ductus arteriosus: gene profile for fetal maturation versus postnatal closure. 223
Gene expression in ductus arteriosus and aorta: comparison of birth and oxygen effects. 221
Cyclooxygenase-2/microsomal prostaglandin E synthase-1 complex in the preoptic-anterior hypothalamus of the mouse: involvement through fever to intravenous lipopolysaccharide 221
ATP-gated potassium channel activity of pulmonary resistance vessels in the lamb 220
Arachidonic acid epoxygenase and 12(S)-lipoxygenase: evidence of their concerted involvement in ductus arteriosus constriction to oxygen 214
CD36 deficiency leads to choroidal involution via COX2 down-regulation in rodents. 211
Carbon monoxide formation in the ductus arteriosus in the lamb: implications for the regulation of muscle tone 209
Cyclooxygenase (cox) function in the ductus arteriosus: another look 209
Carbon monoxide in vasoregulation: the promise and the challenge 207
Cyclooxygenase in the lamb ductus arteriosus: developmental changes and upregulation 207
Interactions between NO, CO and an endothelium-derived hyperpolarizing factor (EDHF) in maintaining patency of the ductus arteriosus in the mouse 206
Cyclooxygenase isoenzymes and patency of ductus arteriosus 206
Role of microsomal prostaglandin E synthase-1 (mPGES1)-derived PGE2 in patency of the ductus arteriosus in the mouse 202
Cyclooxygenase-1 and cyclooxygenase-2 in the mouse ductus arteriosus: individual activity and functional coupling with nitric oxide synthase. 198
Control mechanisms for the ductus arteriosus and the perinatal pulmonary circulation 196
Cyclooxygenase (COX) function in the ductus arteriosus: another look 196
Control of the ductus arteriosus - A new function for cytochrome P450, endothelin and nitric oxide 194
Occurrence of endothelium-derived relaxing factor/nitric oxide in the lamb ductus arteriosus. 189
Contractile and relaxing mechanisms in pulmonary resistance arteries of the preterm fetal lamb 187
Cardiopulmonary bypass in ewe's fetus: advances and setbacks in our learning curve. 186
Carbon monoxide and dilation of blood vessels 184
Carbon monoxide-induced relaxation of the ductus arteriosus in the lamb: evidence against the prime role of guanylyl cyclase. 184
Pyrogen-prostaglandin coupling in the pathogenesis of fever: evidence against a role for nitric oxide 177
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 172
Ductus arteriosus: involvement of a sarcolemmal cytochrome P-450 in O2 constriction? 169
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
Endothelin-1 release from lamb ductus arteriosus: relevance to postnatal closure of the vessel 165
Prostaglandin formation in feline cerebral microvessels: effect of endotoxin and interleukin-1. 165
Evidence against the involvement of a cytochrome P-450 mechanism in pulmonary hemodynamics in the newborn pig 164
Formation of interleukin-6 in the brain of the febrile cat: relationship to interleukin-1 163
Differential effects of endotoxin and cytokines on prostaglandin E2 formation in cerebral microvessels and brain parenchyma: implications for the pathogenesis of fever 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
The endothelin A receptor antagonists, PD 156707 (CI-1020) and PD 180988 (CI-1034), reverse the hypoxic pulmonary vasoconstriction in the perinatal lamb. 158
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
Function of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the ductus arteriosus from foetal lamb: differential development and change by oxygen and endotoxin. 157
The control of the ductus venosus: an update 156
Perinatal changes in choroidal 15-hydroxyprostaglandin dehydrogenase: implications for prostaglandin removal from brain. 156
Prostaglandin uptake and catabolism by the choroid plexus during development in sheep 154
Endothelin in the perinatal circulation 154
Further evidence implicating a cytochrome P-450-mediated reaction in the contractile tension of the lamb ductus arteriosus. 154
Evidence for an effector role of endothelin in closure of the ductus arteriosus at birth. 154
Cytochrome P450 in the contractile tone of the ductus arteriosus: regulatory and effector mechanisms 152
Effect of ciliary neurotrophic factor on body temperature and cerebrospinal fluid prostanoids in the cat 152
Leukotrienes in brain: natural occurrence and induced changes 151
Prostaglandin E2 in the pathogenesis of fever: an update 151
PGE2 in the perinatal brain: local synthesis and transfer across the blood-brain barrier 151
Response of newborn and adult sheep to pyrogens: relation between fever and brain eicosanoid changes 148
Isolated pulmonary resistance vessels from fetal lamb: contractile behaviour and response to endothelin-1. 148
Paradoxical coronary microcirculatory constriction during ischemia: a synergic function for nitric oxide and endothelin 148
The ETA receptor antagonist PD180988 (CI-1034) selectively reverses the pulmonary vasoconstrictor response to hypoxia in the lamb 147
Endothelin-1 release from the ductus arteriosus: are carbon monoxide and nitric oxide regulatory agents? 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
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. 139
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 14.915
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Categoria #
all - tutte 77.533
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 77.533
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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
2025/20263.936 349 1.075 716 839 763 194 0 0 0 0 0 0
Totale 14.915