about
[GdPCP2A(H(2)O)(2)](-): a paramagnetic contrast agent designed for improved applications in magnetic resonance imaging.NMR relaxometric study of new Gd(III) macrocyclic complexes and their interaction with human serum albumin.Magnetic resonance imaging detection of tumor cells by targeting low-density lipoprotein receptors with Gd-loaded low-density lipoprotein particlesSynthesis and NMR Studies of Three Pyridine-Containing Triaza Macrocyclic Triacetate Ligands and Their Complexes with Lanthanide Ions.MEMRI and tumors: a method for the evaluation of the contribution of Mn(II) ions in the extracellular compartment.A novel AMPK activator reduces glucose uptake and inhibits tumor progression in a mouse xenograft model of colorectal cancer.Synthesis and biological evaluation of 1,4-diaryl-2-azetidinones as specific anticancer agents: activation of adenosine monophosphate activated protein kinase and induction of apoptosis.Target visualization by MRI using the avidin/biotin amplification route: synthesis and testing of a biotin-Gd-DOTA monoamide trimer.Synthesis and biological evaluation of combretastatin analogs as cell cycle inhibitors of the G1 to S transition in Saccharomyces cerevisiae.pH-dependent modulation of relaxivity and luminescence in macrocyclic gadolinium and europium complexes based on reversible intramolecular sulfonamide ligation.Enantio-differentiating catalytic oxidation by a biomimetic trinuclear copper complex containing L-histidine residues.Models for biological trinuclear copper clusters. Characterization and enantioselective catalytic oxidation of catechols by the copper(II) complexes of a chiral ligand derived from (S)-(-)-1,1'-binaphthyl-2,2'-diamine.Inhibition of the catecholase activity of biomimetic dinuclear copper complexes by kojic acid.Snf1/AMPK promotes SBF and MBF-dependent transcription in budding yeast.A new chiral, poly-imidazole N8-ligand and the related di- and tri-copper(ii) complexes: synthesis, theoretical modelling, spectroscopic properties, and biomimetic stereoselective oxidationsTowards MRI contrast agents of improved efficacy. NMR relaxometric investigations of the binding interaction to HSA of a novel heptadentate macrocyclic triphosphonate Gd(III)-complexDesigning Novel Contrast Agents for Magnetic Resonance Imaging. Synthesis and Relaxometric Characterization of three Gadolinium(III) Complexes Based on Functionalized Pyridine-Containing Macrocyclic LigandsCAMPHOR-BASED CHIRAL AUXILIARY: FORMAL SYNTHESIS OF ENANTIOMERICALLY ENRICHED β-AMINOPHOSPHONIC ACIDS VIA PTC ALKYLATIONCamphor-based oxazaphospholanes as chiral templates for the enantioselective synthesis of α-chlorophosphonic acidsA straightforward entry into enantiomerically enriched β-amino-α-hydroxyphosphonic acid derivativesSynthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents.New insights for pursuing high relaxivity MRI agents from modelling the binding interaction of Gd(III) chelates to HSA
P50
Q30618746-4F0F43A2-940E-4E8A-A3A3-E6F170F55994Q30892910-A2CF48A6-0DC0-4964-8356-028311090005Q31140222-D9753350-5A10-4154-AF6B-7CF36039D19CQ32020113-C338A7B5-724D-4A59-B58A-6F9939C87176Q38853054-DE45CE60-3061-47F7-BE5D-0778FB31903FQ38964866-AF6B7F05-6611-4398-BC0F-E6AFFFA452AAQ39397358-EA46BCC5-6D01-45DD-A772-0F86B142C2FFQ43038487-02D7EE0A-4874-4EF0-BE00-6FA6EDAE58B6Q43110285-723BB099-6156-4043-8E9D-EC369AC42CBCQ43692813-77BD1D5A-6F72-4B53-AEE0-D543360E902CQ44587462-A31C64E8-C4E2-4807-BB60-8C730CC7B7B8Q44975409-3AE5F0F9-8EF1-48B2-B5BE-049DC8FD8D81Q52078537-03C81598-CE1C-4D55-8056-EE0D99209B71Q54405849-53E85D0B-9199-4556-B13E-EE2223992D4FQ58233404-97178946-B76B-4227-BCC0-D35C5DC71053Q58830319-40DA349A-76A4-43C6-B596-275D79991F7CQ60219577-BBD63C5E-3F06-4C0D-822C-F5B0299623D1Q60219586-188F8171-ACBF-41A6-9E19-85E6C87573F1Q60219594-400DEBD2-E724-4870-B18A-79DE90FC5572Q60219599-BA025C59-CE6B-4BF4-A32A-4BD9F7DD9B12Q64899658-81393E4E-987A-41B3-8C2D-4C4C1D6A697AQ81577177-DBD8144D-0EBA-4ABD-98D5-849E39F9B34B
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Roberto Pagliarin
@ast
Roberto Pagliarin
@en
Roberto Pagliarin
@es
Roberto Pagliarin
@nl
Roberto Pagliarin
@sl
type
label
Roberto Pagliarin
@ast
Roberto Pagliarin
@en
Roberto Pagliarin
@es
Roberto Pagliarin
@nl
Roberto Pagliarin
@sl
prefLabel
Roberto Pagliarin
@ast
Roberto Pagliarin
@en
Roberto Pagliarin
@es
Roberto Pagliarin
@nl
Roberto Pagliarin
@sl
P1053
Q-3491-2016
P106
P1153
35615109800
P21
P31
P3829
P496
0000-0003-0744-853X