about
Discovery of N-[(2S)-5-(6-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide, a novel clinical AMPA receptor positive modulator1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK35-Aryl-4-carboxamide-1,3-oxazoles: potent and selective GSK-3 inhibitorsCrystallizing Membrane Proteins in the Lipidic Mesophase. Experience with Human Prostaglandin E2 Synthase 1 and an Evolving StrategyNovel hydroxyl tricyclics (e.g., GSK966587) as potent inhibitors of bacterial type IIA topoisomerasesNovel tricyclics (e.g., GSK945237) as potent inhibitors of bacterial type IIA topoisomerasesCrystallization and preliminary X-ray diffraction studies on ADP-ribosylation factor 1Thiophene antibacterials that allosterically stabilize DNA-cleavage complexes with DNA gyraseChallenges for and current status of research into positive modulators of AMPA receptors.Inhibition of PAD4 activity is sufficient to disrupt mouse and human NET formation.Protein arginine deiminase 2 binds calcium in an ordered fashion: implications for inhibitor design.Getting the chemistry right: protonation, tautomers and the importance of H atoms in biological chemistry.Structural basis of DNA gyrase inhibition by antibacterial QPT-1, anticancer drug etoposide and moxifloxacin.Crystallization and initial crystallographic analysis of covalent DNA-cleavage complexes of Staphyloccocus aureus DNA gyrase with QPT-1, moxifloxacin and etoposide.The structure of MSK1 reveals a novel autoinhibitory conformation for a dual kinase protein.Nerve growth factor alpha subunit: effect of site-directed mutations on catalytic activity and 7S NGF complex formation.Common themes and surprising differences in small G-proteins.ADP ribosylation factor 1 mutants identify a phospholipase D effector region and reveal that phospholipase D participates in lysosomal secretion but is not sufficient for recruitment of coatomer I.From PIM1 to PI3Kδ via GSK3β: Target Hopping through the Kinome.Frog lens beta A1-crystallin: the nucleotide sequence of the cloned cDNA and computer graphics modelling of the three-dimensional structure.Coupling the core of the anticancer drug etoposide to an oligonucleotide induces topoisomerase II-mediated cleavage at specific DNA sequences.A new class of antibacterials, the imidazopyrazinones, reveal structural transitions involved in DNA gyrase poisoning and mechanisms of resistance.Mechanism of Action of Mycobacterium tuberculosis Gyrase Inhibitors: A Novel Class of Gyrase PoisonsMechanistic and Structural Basis for the Actions of the Antibacterial Gepotidacin against Staphylococcus aureus GyraseHigh resolution structure of an oligomeric eye lens beta-crystallin. Loops, arches, linkers and interfaces in beta B2 dimer compared to a monomeric gamma-crystallinStructure of oligomeric beta B2-crystallin: an application of the T2 translation function to an asymmetric unit containing two dimersCrystallization of a new form of the eye lens protein beta B2-crystallinStructural aspects of the functional modules in human protein kinase-C alpha deduced from comparative analyses
P50
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P50
description
Forscher
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B Bax
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B Bax
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Ben Bax
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Ben Bax
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B Bax
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B Bax
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Ben Bax
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Ben Bax
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B Bax
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B Bax
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Ben Bax
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Ben Bax
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P108
P31
P496
0000-0003-1940-3785