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Halogenated diarylacetylenes repress c-myc expression in cancer cells2',6'-Dihalostyrylanilines, pyridines, and pyrimidines for the inhibition of the catalytic subunit of methionine S-adenosyltransferase-2Arylquins target vimentin to trigger Par-4 secretion for tumor cell apoptosisTritium-labeled (E,E)-2,5-bis(4'-hydroxy-3'-carboxystyryl)benzene as a probe for β-amyloid fibrilsSynthesis and characterization of pseudocantharidins, novel phosphatase modulators that promote the inclusion of exon 7 into the SMN (survival of motoneuron) pre-mRNAFluorinated N,N-dialkylaminostilbenes for Wnt pathway inhibition and colon cancer repression.Development of 6H-Chromeno[3,4-c]pyrido[3',2':4,5]thieno[2,3-e]pyridazin-6-ones as Par-4 SecretagoguesN-Aryl benzenesulfonamide inhibitors of [3H]-thymidine incorporation and β-catenin signaling in human hepatocyte-derived Huh-7 carcinoma cells.Application of Mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents.Par-4 secretion: stoichiometry of 3-arylquinoline binding to vimentin.Synthesis of a norcantharidin-tethered guanosine: Protein phosphatase-1 inhibitors that change alternative splicing.Fluorinated N,N'-diarylureas as AMPK activators.Antineoplastic Isoflavonoids Derived from Intermediate ortho-Quinone Methides Generated from Mannich Bases.Quantification of trans-2,6-difluoro-4'-N,N-dimethylaminostilbene in rat plasma: application to a pharmacokinetic studyBis(N-amidinohydrazones) and N-(amidino)-N'-aryl-bishydrazones: New classes of antibacterial/antifungal agents.Synthesis and tautomerization of hydroxylated isoflavones bearing heterocyclic hemi-aminals.Analysis of trans-2,6-difluoro-4'-(N,N-dimethylamino)stilbene (DFS) in biological samples by liquid chromatography-tandem mass spectrometry: metabolite identification and pharmacokinetics.Developing antineoplastic agents that target peroxisomal enzymes: cytisine-linked isoflavonoids as inhibitors of hydroxysteroid 17-beta-dehydrogenase-4 (HSD17B4).Fluorinated N,N'-Diarylureas As Novel Therapeutic Agents Against Cancer Stem Cells.Phenylethynyl-substituted Heterocycles Inhibit Cyclin D1 and Induce the Expression of Cyclin-dependent Kinase Inhibitor p21Wif1/Cip1 in Colorectal Cancer Cells.Induction of AMPK activation by N,N'-diarylurea FND-4b decreases growth and increases apoptosis in triple negative and estrogen-receptor positive breast cancersSemisynthetic aurones inhibit tubulin polymerization at the colchicine-binding site and repress PC-3 tumor xenografts in nude mice and myc-induced T-ALL in zebrafishA crystal structure of coil 1B of vimentin in the filamentous form provides a model of a high-order assembly of a vimentin filamentAn Underlying Mechanism of Dual Wnt Inhibition and AMPK Activation: Mitochondrial Uncouplers Masquerading as Wnt InhibitorsOne-Pot Synthesis of B-Ring Ortho-Hydroxylated Sappanin-Type Homoisoflavonoids
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Vitaliy M Sviripa
@ast
Vitaliy M Sviripa
@en
Vitaliy M Sviripa
@es
Vitaliy M Sviripa
@nl
Vitaliy M Sviripa
@sl
type
label
Vitaliy M Sviripa
@ast
Vitaliy M Sviripa
@en
Vitaliy M Sviripa
@es
Vitaliy M Sviripa
@nl
Vitaliy M Sviripa
@sl
prefLabel
Vitaliy M Sviripa
@ast
Vitaliy M Sviripa
@en
Vitaliy M Sviripa
@es
Vitaliy M Sviripa
@nl
Vitaliy M Sviripa
@sl
P106
P31
P496
0000-0002-7272-373X