CINECA IRIS Institutional Research Information System

KEILING, BRIGITTE EVELIN
 Distribuzione geografica
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Continente #
NA - Nord America 2.679
EU - Europa 1.878
AS - Asia 698
AF - Africa 46
SA - Sud America 23
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
Totale 5.334
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Nazione #
US - Stati Uniti d'America 2.578
CN - Cina 447
IT - Italia 333
SE - Svezia 290
IE - Irlanda 277
UA - Ucraina 219
DE - Germania 167
FR - Francia 164
FI - Finlandia 131
CA - Canada 94
KR - Corea 88
AT - Austria 87
GB - Regno Unito 78
VN - Vietnam 51
IN - India 42
PL - Polonia 42
RU - Federazione Russa 26
JP - Giappone 23
BE - Belgio 22
BR - Brasile 17
KE - Kenya 11
ES - Italia 8
GR - Grecia 8
HK - Hong Kong 8
PT - Portogallo 7
TW - Taiwan 7
MU - Mauritius 6
NL - Olanda 6
SG - Singapore 6
ZA - Sudafrica 6
AU - Australia 5
CO - Colombia 5
GH - Ghana 5
ID - Indonesia 5
AE - Emirati Arabi Uniti 4
ET - Etiopia 4
MX - Messico 4
TH - Thailandia 4
CU - Cuba 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
EG - Egitto 3
EU - Europa 3
IR - Iran 3
PK - Pakistan 3
CM - Camerun 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
RO - Romania 2
SC - Seychelles 2
TR - Turchia 2
AZ - Azerbaigian 1
BG - Bulgaria 1
BJ - Benin 1
CG - Congo 1
HR - Croazia 1
IL - Israele 1
LT - Lituania 1
LY - Libia 1
ML - Mali 1
MW - Malawi 1
MY - Malesia 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
RS - Serbia 1
UZ - Uzbekistan 1
Totale 5.334
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Città #
Chandler 405
Beijing 326
Dublin 273
Torino 153
Ann Arbor 145
Nyköping 140
Fairfield 139
Houston 134
Ashburn 119
Villeurbanne 92
Wilmington 89
Medford 88
Vienna 87
Woodbridge 85
Jacksonville 82
Princeton 80
Dearborn 69
Seattle 69
Ottawa 63
Cambridge 56
Pisa 56
New York 47
Fremont 39
Warsaw 39
Dong Ket 38
Redwood City 26
Boston 25
Boardman 24
Washington 24
Milan 21
Turin 21
Brussels 17
Toronto 17
Nanjing 16
San Diego 16
Athens 12
Norwalk 12
Shanghai 12
Verona 12
Guangzhou 11
Lachine 11
Düsseldorf 10
Falls Church 9
Hefei 9
Fuzhou 8
Hyderabad 8
Kunming 8
Mountain View 8
Auburn Hills 7
Cleveland 7
Zhengzhou 7
Detroit 6
San Mateo 6
Xian 6
Cislago 5
Des Moines 5
Helsinki 5
Los Angeles 5
Munich 5
Nanchang 5
Abu Dhabi 4
Berlin 4
Central District 4
Hanover 4
Hebei 4
Leuven 4
Nairobi 4
Redmond 4
Silver Spring 4
São Paulo 4
Tokyo 4
Aarhus 3
Aguascalientes 3
Albuquerque 3
Collegno 3
Denver 3
Erlangen 3
Frankfurt am Main 3
Hangzhou 3
Jakarta 3
Menlo Park 3
Miaoli 3
New Haven 3
Paris 3
Perugia 3
Pune 3
Rio De Janeiro 3
Rome 3
Sabatier 3
Seoul 3
Singapore 3
Taipei 3
Upper Marlboro 3
Winston Salem 3
Abuja 2
Assiut 2
Bari 2
Bogotá 2
Borgaro Torinese 2
Brasília 2
Totale 3.444
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Nome #
Hemozoin and the human monocyte--a brief review of their interactions 365
Oxidative stress-mediated antimalarial activity of plakortin, a natural endoperoxide from the tropical sponge Plakortis simplex 181
Role of the Lipoperoxidation Product 4-Hydroxynonenal in the Pathogenesis of Severe Malaria Anemia and Malaria Immunodepression 145
Involvement of inflammatory chemokines in survival of human monocytes fed with malarial pigment 141
Preferential binding of 4-hydroxynonenal to lysine residues in specific parasite proteins in plakortin-treated Plasmodium falciparum-parasitized red blood cells 134
Unravelling the immune signature of Plasmodium falciparum transmission-reducing immunity 134
Induction of oxidative stress in human aqueous and vitreous humors by Nd:YAG laser posterior capsulotomy 123
Malarial pigment hemozoin impairs chemotactic motility and transendothelial migration of monocytes via 4-hydroxynonenal 116
Oxidative Stress, Lipid Peroxidation, and Loss of Hyaluronic Acid in the Human Vitreous Affected by Synchysis Scintillans 114
Inhibition of erythropoiesis in malaria anaemia: role of hemozoin and hemozoin-generated 4-hydroxynonenal 109
Band 3/complement-mediated recognition and removal of normally senescent and pathological human erythrocytes 107
Syk inhibitors interfere with erythrocyte membrane modification during P falciparum growth and suppress parasite egress 107
Plasma advanced oxidative protein products are associated with anti-oxidative stress pathway genes and malaria in a longitudinal cohort 101
Fibrinogen as bioactive signal molecule in the immune response to hemozoin 97
HNE produced by the malaria parasite Plasmodium falciparum generates HNE-protein adducts and decreases erythrocyte deformability 96
Early gene expression profiling through a macro-arrayapproach on non-apoptotic human monocytes fed withhemozoin (malarial pigment) 89
Enhanced Proinflammatory Response and Missing Apoptosis in Hemozoin-Fed Human Monocytes: a HSP-27-Mediated Anomaly in Falciparum Malaria 89
Phagocytosis of malarial pigment hemozoin inhibits NADPH-oxidase activity in human monocyte-derived macrophages. 88
Antimalarial NADPH-Consuming Redox-Cyclers as Superior G6PD Deficiency Copycats. 88
No red blood cell damage and no hemolysis in G6PD-deficient subjects after ingestion of low vicine/convicine Vicia faba seeds 88
Interactions between hemozoin and the human monocyte-Brief review 84
Clinical impact of the two ART resistance markers, K13 gene mutations and DPC3 in Vietnam 83
16alpha-bromoepiandrosterone, an antimalarial analogue of the hormone dehydroepiandrosterone, enhances phagocytosis of ring stage parasitized erythrocytes: a novel mechanism for antimalarial activity 82
Effect of diamide on polyphosphoinositide metabolism in red blood cells. 80
Effects of Hemozoin and Hemozoin-Generated Molecules on Immune and Non-Immune Host Cells 79
Inhibition of erythropoiesis in malaria anemia: role of hemozoin and hemozoin-generated 4-hydroxynonenal. 78
Host fibrinogen stably bound to hemozoin rapidly activates monocytes via TLR-4 and CD11b/CD18-integrin: a new paradigm of hemozoin action 76
Inhibition of erythropoiesis in malaria anaemia. Role of hemozoin and hemozoin-generated 4-hydroxynonenal 75
A luminescence method for the quantitative determination of phagocytosis of erythrocytes, of malaria-parasitized erythrocytes and of malarial pigment. 73
Role of 4-hydroxynonenal in the hemozoin-mediated inhibition of differentiation of human monocytes to dendritic cells induced by GM-CSF/IL-4 71
4-Hydroxynonenal in the Physiology and Pathology of Malaria 70
The hidden faces of hemozoin and its dangerous midwives. 70
Replication of Plasmodium in reticulocytes can occur without hemozoin formation, resulting in chloroquine resistance. 69
Hemozoin stability and dormant induction of heme oxygenase in hemozoin-fed human monocytes. 69
null 68
Malaria-derived hemozoin exerts early modulatory effects on the phenotype and maturation of human dendritic cells 63
15(S)-hydroxyeicosatetraenoic acid (15-HETE), a product of arachidonic acid peroxidation, is an active component of hemozoin toxicity to monocytes. 62
Transfer of 4-hydroxynonenal from parasitized to non-parasitized erythrocytes in rosettes. Proposed role in severe malaria anemia 59
Biophysical and biochemical properties of nanocrystal hemozoin produced by malaria parasite 59
Maturation dependence of the turnover of phosphatidylinositides in rabbit red blood cells. 58
Hemozoin (malarial pigment) inhibits differentiation and maturation of human monocyte-derived dendritic cells: a peroxisome proliferator-activated receptor-gamma-mediated effect 58
Impaired migration of hemozoin-fed human monocytes : impact of 4-hydroxynonenal 58
Hemozoin is a Prominent Inflammatory Virulence Factor in Malaria-Associated Acute Respiratory Distress Syndrome 57
Blood oxidative stress markers and Plasmodium falciparum malaria in non-immune African children 57
Phagocytosis of the malarial pigment, hemozoin, impairs expression of major histocompatibility complex class II antigen, CD54, and CD11c in human monocytes. 56
Impairment of macrophage functions after ingestion of Plasmodium falciparum-infected erythrocytes or isolated malarial pigment 56
Involvement of polyphosphoinositides in the ATP turnover of intact human erythrocytes and in the ATPase activity of purified membranes. 55
Metabolism of phosphatidylinositides in rabbit red blood cells. 55
Simultaneous determination of phagocytosis of Plasmodium falciparum-parasitized and non-parasitized red blood cells by flow cytometry 55
Hemozoin- and 4-hydroxynonenal-mediated inhibition of erythropoiesis. Possible role in malarial dyserythropoiesis and anemia 54
Malaria Pigment 52
Phagocytosis of P. falciparum malarial pigment hemozoin by human monocytes inactivates monocyte protein kinase C 51
Malaria-parasitized erythrocytes and hemozoin nonenzymatically generate large amounts of hydroxy fatty acids that inhibit monocyte functions. 49
Maturation of rabbit reticulocytes: strong decline of the turnover of polyphosphoinositides. 48
Inherited glutathione reductase deficiency and plasmodium falciparum malaria. A case report 48
Non-enzymatic generation of lipid mediators by heme catalysis: Interference with the immune defence in malaria 48
METABOLIC DISORDERS 47
Hemozoin Induces Lung Inflammation and Correlates with Malaria-Associated Acute Respiratory Distress Syndrome 47
Proteins and phospholipids of thrombocytes and erythrocytes in glucose-6-phosphate dehydrogenase deficient patients 47
The role of age and exposure to Plasmodium falciparum in the rate of acquisition of naturally acquired immunity: a randomized controlled trial. 46
Hemozoin Induces Hepatic Inflammation in Mice and Is Differentially Associated with Liver Pathology Depending on the Plasmodium Strain 46
Role of hemozoin and hemozoin-generated 4-hydroxynonenal in the pathogenesis of malaria diserythropoiesis 44
Malarial pigment (haemozoin): a very active 'inert' substance 43
Plasmodium Impairs Antibacterial Innate Immunity to Systemic Infections in Part Through Hemozoin-Bound Bioactive Molecules 43
Intérêt des variétés de féveroles (Vicia faba L.) à faibles teneurs en vicine et convicine en alimentation humaine. Les variétés à faibles teneurs en vicine et convicine réduisent le risque du favisme chez l’homme hemizygote porteur d’une mutation de forte déficience en glucose-6-phosphate déshydrogénase (G6PD) 41
Malaria pigment hemozoin impairs gm-csf receptor expression and function by 4-hydroxynonenal 40
Increased levels of 4-hydroxynonenal in human monocytes fed with malarial pigment hemozoin. A possible clue for hemozoin toxicity. 39
The involvement of hemozoin toxicity in depression of cellular immunity. 38
An Optimized Dihydrodibenzothiazepine Lead Compound (SBI-0797750) as a Potent and Selective Inhibitor of Plasmodium falciparum and P. vivax Glucose 6-Phosphate Dehydrogenase 6-Phosphogluconolactonase 36
Malarial pigment haemozoin, IFN-gamma,TNF-lpha, IL-1beta and LPS do not stilulate expression of inducibile nitric oxide synthase and production of nitric oxide in immuno-purified human monocytes 33
Biological activity of malarial nanocrystal hemozoin is due to host fibrinogen: a newly described mechanism of innate immune response to malaria 33
Immunopathological effects of malaria pigment or hemozoin and other crystals 30
Hemozoin is a Prominent Inflammatory Virulence Factor in Malaria-Associated Acute Respiratory Distress Syndrome. 29
Relaxometric studies of erythrocyte suspensions infected by Plasmodium falciparum: a tool for staging infection and testing anti-malarial drugs 28
Neutrophil extracellular traps drive inflammatory pathogenesis in malaria 18
Cytochrome CYP4F11 and 4-hydroxynonenal conjugation in malaria pigment hemozoin-fed monocytes inhibits ω-hydroxylation of OH-PUFAs 13
Role of hemozoin (HZ) and HZ-generated hydroxynonenal (HNE) in malaria dys-erythropoiesis 9
Phagocytosis of malarial pigmnet haemozoin by human monocytes. A confocal microscopy study 5
Posttranslational Modification of Human Cytochrome CYP4F11 by 4-Hydroxynonenal Impairs ω-Hydroxylation in Malaria Pigment Hemozoin-Fed Monocytes: The Role in Malaria Immunosuppression 4
Micromolar Dihydroartemisinin Concentrations Elicit Lipoperoxidation in Plasmodium falciparum-Infected Erythrocytes 3
Totale 5.559
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Categoria #
all - tutte 15.748
article - articoli 0
book - libri 0
conference - conferenze 3.134
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 18.882
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019130 0 0 0 0 0 0 0 0 0 0 96 34
2019/2020695 19 8 32 50 50 114 94 57 79 102 74 16
2020/2021782 115 72 84 34 69 70 53 31 68 69 41 76
2021/2022782 22 27 32 58 24 31 59 46 25 120 181 157
2022/20231.249 124 145 23 97 126 313 99 73 126 24 72 27
2023/2024398 63 88 38 19 24 104 8 26 3 25 0 0
Totale 5.559