about
A hyperpolarized equilibrium for magnetic resonanceToward biocompatible nuclear hyperpolarization using signal amplification by reversible exchange: quantitative in situ spectroscopy and high-field imaging.Delivering strong 1H nuclear hyperpolarization levels and long magnetic lifetimes through signal amplification by reversible exchange.Application of parahydrogen induced polarization techniques in NMR spectroscopy and imaging.Improving NMR and MRI sensitivity with parahydrogen.Improving the hyperpolarization of (31)P nuclei by synthetic design.Synthesis and hyperpolarisation of eNOS substrates for quantification of NO production by 1H NMR spectroscopyThe theory and practice of hyperpolarization in magnetic resonance using parahydrogen.Probing signal amplification by reversible exchange using an NMR flow systemCXCR4 chemokine receptor antagonists: nickel(II) complexes of configurationally restricted macrocycles.Aspartate-Based CXCR4 Chemokine Receptor Binding of Cross-Bridged Tetraazamacrocyclic Copper(II) and Zinc(II) Complexes.Iridium N-heterocyclic carbene complexes as efficient catalysts for magnetization transfer from para-hydrogen.Catalytic Transfer of Magnetism using a Neutral Iridium Phenoxide Complex.Iridium(III) hydrido N-heterocyclic carbene-phosphine complexes as catalysts in magnetization transfer reactions.Strategies for the hyperpolarization of acetonitrile and related ligands by SABRE.Utilization of SABRE-derived hyperpolarization to detect low-concentration analytes via 1D and 2D NMR methods.Correctionto Iridium(III) Hydrido N-Heterocyclic Carbene–Phosphine Complexes as Catalysts in Magnetization Transfer Reactions.Investigating pyridazine and phthalazine exchange in a series of iridium complexes in order to define their role in the catalytic transfer of magnetisation from para-hydrogen.Extending the Scope of 19F Hyperpolarization through Signal Amplification by Reversible Exchange in MRI and NMR Spectroscopy.Using 2 H labelling to improve the NMR detectability of pyridine and its derivatives by SABRE.Deactivation of signal amplification by reversible exchange catalysis, progress towards in vivo application.Engineering molecularly imprinted polymers (MIPs) for the selective extraction and quantification of the novel psychoactive substance (NPS) methoxphenidine and its regioisomers.Developments and advances concerning the hyperpolarisation technique SABRE.Using hyperpolarised NMR and DFT to rationalise the unexpected hydrogenation of quinazoline to 3,4-dihydroquinazolineRapid Identification of Novel Psychoactive and Other Controlled Substances Using Low-Field 1H NMR Spectroscopy.Synthesis and phototoxicity of polyethylene glycol (PEG) substituted metal-free and metallo-porphyrins: effect of PEG chain length, coordinated metal, and axial ligandQuick Test for Determination of N-Bombs (Phenethylamine Derivatives, NBOMe) Using High-Performance Liquid Chromatography: A Comparison between Photodiode Array and Amperometric DetectionHyperpolarization of Pyridyl Fentalogues by Signal Amplification By Reversible Exchange (SABRE)Benchtop NMR analysis of piperazine-based drugs hyperpolarised by SABREHitting the Jackpot - development of gas chromatography-mass spectrometry (GC-MS) and other rapid screening methods for the analysis of 18 fentanyl-derived synthetic opioids
P50
Q30714562-80F5B492-6B84-4F43-A894-DF416BF76D43Q30727427-6FDE479C-AA0B-4FFD-8986-46BE231277A3Q33594864-BAE05A05-7ABB-443F-BF84-F1421B163497Q34209315-FD8BD7D4-F062-4215-801B-EB14CC73530EQ34310687-7D752F7F-140A-4E20-93FA-7534DFE4C61CQ35595362-C1E191D1-C1E8-45F7-ADCC-F4CDF70C7D8BQ36330852-A9AE8BFC-F3F6-4823-A82E-80FEA8FA41A7Q38055787-461FC1DC-3536-469E-A5BF-B9F76F205AB3Q39197675-253BFB27-CAFA-4531-B955-4DFC75CF015AQ39297457-7387DD4D-21CE-4461-9D5B-D7A75CA6A772Q40599515-1061C6AA-DEAC-42D4-A2A5-C7B5348A12BEQ41817621-0AC7399A-FD6B-43CC-9F2A-80EA74BDD3ADQ42320346-4E2C1877-EFA4-4C0E-A5D1-441E467FD644Q42848067-D3BFDB42-EDEA-407E-9A4A-7DBD0EB56623Q43128769-330A8164-FC7D-4E19-BAB0-4EE03876561CQ43530203-C9EC73C7-CC51-461F-845B-3D5025FCA318Q45950113-CBE0BA76-15D3-4B86-9EEC-275A9C86FE83Q47134247-48523AEF-A0FC-4D04-98E3-006A36E33492Q47741815-B420C60D-F785-4762-A2FD-C11F1200FF5DQ48351689-DC42CAA1-EFD0-429D-BA3D-B2AB7372FA79Q50275989-FDE18D02-1C26-4814-BDEC-FCE71EB2FB5FQ52578570-4CE0637E-F6FA-490B-B40E-D9588E9140F3Q53584170-696080F6-F6F1-49F7-92AB-F79035798830Q58697625-FE5A9062-389A-4CBA-90F4-AC1859D13EEFQ64999605-80A7E98C-B0AC-4936-BB37-FC239843C7D1Q84939110-AEAD77FF-66F1-40C3-99F1-EF9AEF7A20A1Q90139030-0416CF1C-8E56-42B1-A867-8F3B9AA29862Q92028407-2C80F971-14E8-4468-A7EF-A9A5FC2A58DDQ92689816-5B2D4A04-18A5-47D8-8CE5-3178B6FB346DQ92988247-B3EA87CD-A3B1-41DF-9EF5-91F5D93DA3CE
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ryan E Mewis
@ast
Ryan E Mewis
@en
Ryan E Mewis
@es
Ryan E Mewis
@nl
Ryan E Mewis
@sl
type
label
Ryan E Mewis
@ast
Ryan E Mewis
@en
Ryan E Mewis
@es
Ryan E Mewis
@nl
Ryan E Mewis
@sl
altLabel
Ryan E. Mewis
@en
prefLabel
Ryan E Mewis
@ast
Ryan E Mewis
@en
Ryan E Mewis
@es
Ryan E Mewis
@nl
Ryan E Mewis
@sl
P106
P21
P31
P496
0000-0002-3756-6505