about
Amino derivatives of indolone-N-oxide: preparation and antiplasmodial properties.Cold Atmospheric Plasma Induces a Predominantly Necrotic Cell Death via the Microenvironment.Antiplasmodial activity of New Caledonia and Vanuatu traditional medicines.Routine identification of medical fungi by the new Vitek MS matrix-assisted laser desorption ionization-time of flight system with a new time-effective strategyAn extraction method of positive blood cultures for direct identification of Candida species by Vitek MS matrix-assisted laser desorption ionization time of flight mass spectrometry.Discovery of new thienopyrimidinone derivatives displaying antimalarial properties toward both erythrocytic and hepatic stages of Plasmodium.Analysis of the type II-A CRISPR-Cas system of Streptococcus agalactiae reveals distinctive features according to genetic lineages.Structure-Activity Relationships of the Bioactive Thiazinoquinone Marine Natural Products Thiaplidiaquinones A and B.Biologically Active Acetylenic Amino Alcohol and N-Hydroxylated 1,2,3,4-Tetrahydro-β-carboline Constituents of the New Zealand Ascidian Pseudodistoma opacum.Biological activities of nitidine, a potential anti-malarial lead compoundWayanin and guaijaverin, two active metabolites found in a Psidium acutangulum Mart. ex DC (syn. P. persoonii McVaugh) (Myrtaceae) antimalarial decoction from the Wayana Amerindians.Discovery and preliminary structure-activity relationship studies on tecomaquinone I and tectol as novel farnesyltransferase and plasmodial inhibitors.Antiplasmodial activity of some phenolic compounds from Cameroonians Allanblackia.Chemical composition and anticancer, antiinflammatory, antioxidant and antimalarial activities of leaves essential oil of Cedrelopsis grevei.New findings on Simalikalactone D, an antimalarial compound from Quassia amara L. (Simaroubaceae).Antileishmanial pharmacomodulation in 8-nitroquinolin-2(1H)-one series.Synthesis, characterization, and antileishmanial activities of gold(I) complexes involving quinoline functionalized N-heterocyclic carbenes.Synthesis and biological evaluation of new bis-indolone-N-oxides.The C-type lectin receptors dectin-1, MR, and SIGNR3 contribute both positively and negatively to the macrophage response to Leishmania infantum.In vitro anthelmintic activity of the essential oils of Zanthoxylum zanthoxyloides and Newbouldia laevis against Strongyloides ratti.LRH-1 mediates anti-inflammatory and antifungal phenotype of IL-13-activated macrophages through the PPARγ ligand synthesisAdaptation and optimization of a fluorescence-based assay for in vivo antimalarial drug screening.Imported Plasmodium knowlesi malaria in a French tourist returning from Thailand.Schistosomiasis haematobium, Corsica, France.Disseminated Ochroconis gallopava infection in a heart transplant patient.Macrocyclic spermidine alkaloids from Androya decaryi L. Perrier.Contribution of molecular diagnosis to the management of cutaneous leishmaniasis in travellers.Synthesis, characterization, and antileishmanial activity of neutral N-heterocyclic carbenes gold(I) complexes.Novel 8-nitroquinolin-2(1 H )-ones as NTR-bioactivated antikinetoplastid molecules: Synthesis, electrochemical and SAR studyAlveolar and blood T lymphocyte profiles in Pneumocystis jirovecii-positive patients: effects of HIV statusSimultaneous cutaneous infection due to Paecilomyces lilacinus and Alternaria in a heart transplant patientConcomitant cases of disseminated Geotrichum clavatum infections in patients with acute myeloid leukemia2-Aryl-3H-indol-3-ones: synthesis, electrochemical behaviour and antiplasmodial activities
P50
Q30769989-5E2AEEC8-415C-4C14-8C02-6D5703169603Q33465829-1C006B73-2212-4969-A99E-5BCE9D914A07Q33809767-DAB3A6C7-6A68-456F-A9D5-5B64CFCA7C2AQ34229233-C55FF423-ED7E-4287-9C6B-8D01B86F381AQ34571811-47454DE7-7650-4306-B719-92F78ED2D673Q35581798-FCB6534D-5BBF-4094-8758-5991302125B8Q35739591-603A8FFA-A09D-41AA-82D0-D9D476DB1515Q35743501-4574EDEC-773D-4E30-8728-6AC3AF345A16Q35869357-F2BB73A2-C49E-4F4F-B554-343B94E9E7C3Q35885688-0D0C2CF3-FA6E-4786-8034-15CFF2B7BC71Q36004561-CA8058A0-2BC2-424A-AD0D-6F302C66526EQ36033986-641C1D7A-2E22-4A5E-89FF-BF27CA48D8CFQ36612797-9C07B0F6-F3EB-4E5F-89CB-6910E208DC7CQ38086388-0191D176-9553-40A2-B7D0-80001B1A1AA0Q38370265-64B52639-5D4D-4E72-BE28-0E0969D493A0Q38890538-713DC345-F76B-4FE5-992D-AD6B97B2343EQ38902731-8B5A71D2-A12D-4621-BAB8-0A82DF14CE0DQ39156911-97A3300B-1EBC-4450-B3A6-033E169019BEQ39301725-ED380AB4-10E7-4F4A-AEF1-1F72595CA769Q39465362-10D12796-8FFD-47DD-82E3-228DC7E5883CQ39977001-8D7EFF23-3E93-436B-BD0F-2614F52A1BB7Q40210891-651E5FCF-06FE-42F0-A8D8-06BA638D2C1FQ42072207-045F81BB-D795-4E9B-A129-217B2DED72B8Q42920057-6984A44B-845C-4C88-ABD7-4DE8CF0B3136Q44567529-585B1B90-8528-48EE-BB33-28CE7063A4A8Q45056048-D44AE3E3-CE74-4863-BD71-834FD51149E3Q46966925-C3C00ED7-DACC-49AB-B8CC-265B2364BAD5Q50044106-03530E21-1930-4718-87A7-24BC254DC850Q58842873-152E126A-A8A2-45C6-A0FA-4ECD9D1B9650Q84596488-F1C0E7C9-739B-43FE-BE9E-765487D188D4Q85211921-B193A484-27EE-4DB4-B108-7383BAA75AA4Q87049512-6FD0654E-9DD8-4625-9080-CD70AF8B62F8Q87569331-56957789-ABBA-45CD-8267-3A53A7D8C4A2
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Alexis Valentin
@ast
Alexis Valentin
@en
Alexis Valentin
@es
Alexis Valentin
@nl
type
label
Alexis Valentin
@ast
Alexis Valentin
@en
Alexis Valentin
@es
Alexis Valentin
@nl
prefLabel
Alexis Valentin
@ast
Alexis Valentin
@en
Alexis Valentin
@es
Alexis Valentin
@nl
P106
P31
P496
0000-0002-2133-112X