about
Potential role of glutathione in evolution of thiol-based redox signaling sites in proteinsThe effect of leaving radical on the formation of tetrahydroselenophene by SHi ring closure: an experimental and computational study.Design of Redox/Radical Sensing Molecules via Nitrile Imine-Mediated Tetrazole-ene Cycloaddition (NITEC).Conformational changes in redox pairs of protein structures.Evaluating the stability of disulfide bridges in proteins: a torsional potential energy surface for diethyl disulfide.Disulfides as redox switches: from molecular mechanisms to functional significance.Thiol-based redox signalling: rust never sleeps.Modeling Flexible Molecules in Solution: A pKa Case Study.Electrostatic catalysis of a Diels-Alder reaction.Insulin in motion: The A6-A11 disulfide bond allosterically modulates structural transitions required for insulin activity.Mechanical Stretching-Induced Electron-Transfer Reactions and Conductance Switching in Single Molecules.Probing the correlation between insulin activity and structural stability through introduction of the rigid A6-A11 bondQuantitative Analysis of Step-Growth Polymers by Size Exclusion ChromatographyStructures and Thermochemistry of Calcium-Containing MoleculesHIGH TORSIONAL ENERGY DISULFIDES: RELATIONSHIP BETWEEN CROSS-STRAND DISULFIDES AND RIGHT-HANDED STAPLESA mild, efficient and catalyst-free thermoreversible ligation system based on dithiooxalatesDecoloration rates of a photomerocyanine dye as a visual probe into hydrogen bonding interactionsRole of Water in the Dynamic Disproportionation of Zn-Based TCNQ(F4) Coordination Polymers (TCNQ = Tetracyanoquinodimethane)Tuning electron transfer through p-phenyleneethynylene molecular wires
P50
Q28652594-46D22A69-FA00-4843-B1C5-E2B0964EA49CQ35537249-8A198989-3D27-4A19-AFB7-3A526E8B15FDQ35689553-1C20B5DA-6C9E-4D67-A01D-475DADDB5D0BQ37420197-B1EAB359-6E0E-4124-85B8-D1562ACEE206Q37551975-6123A3DF-5E4B-495B-955F-B79D0C318E0CQ37563475-4F8C12FF-A667-4E60-9B6B-19530C84D2D5Q37868081-BED0B640-91DD-4CEF-8093-7C5259BCF48FQ46342337-EFDD00BB-E6AD-439B-9541-65C7567480F6Q46586485-2E3E5158-1635-4885-B6E4-F8B7E67F9505Q47135854-A4818081-AA82-4C28-A5AE-C6E72FBC85B0Q48053144-39660B3E-6E18-4CB1-8718-C4E4037FC584Q57174414-AFF882D3-F00D-4EE6-802A-E8326B13B20FQ57776935-9C66274F-6912-4898-8515-D7E89F391900Q58738683-116B7CA0-5C0A-422F-B954-D35E4521FA9DQ59248646-F3BE9B3C-BB77-4841-9ECD-D12E9E78F2F9Q60030053-08884F05-EB81-4959-8E50-B5B53204FE17Q60030311-7E1FF374-2D49-4DCC-B08A-12F56531CAF6Q60313828-AC00F3E8-B7A8-4202-A6B8-6C9F4BB33AE3Q64017889-62A9BC95-B718-44A0-AAE6-4308ECBBC97D
P50
description
chemist (1977-2019)
@en
scheikundige uit Australiƫ (1977-2019)
@nl
name
Naomi L Haworth
@ast
Naomi L Haworth
@es
Naomi L Haworth
@ga
Naomi L Haworth
@sq
Naomi L. Haworth
@en
Naomi L. Haworth
@nl
type
label
Naomi L Haworth
@ast
Naomi L Haworth
@es
Naomi L Haworth
@ga
Naomi L Haworth
@sq
Naomi L. Haworth
@en
Naomi L. Haworth
@nl
altLabel
N. Haworth
@en
N. L. Haworth
@en
Naomi Haworth
@en
Naomi Louise Haworth
@en
prefLabel
Naomi L Haworth
@ast
Naomi L Haworth
@es
Naomi L Haworth
@ga
Naomi L Haworth
@sq
Naomi L. Haworth
@en
Naomi L. Haworth
@nl
P106
P140
P1960
ACnAOKQAAAAJ
P21
P27
P31
P496
0000-0002-3299-3137
P569
1977-04-24T00:00:00Z
P570
2019-08-14T00:00:00Z