about
E-selectin ligand complexes adopt an extended high-affinity conformation.Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex DevelopmentUrinary Tract Infection: Which Conformation of the Bacterial Lectin FimH Is Therapeutically Relevant?Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated With 46,XY Disorders of Sex Development in Egyptian Patients.What contributes to an effective mannose recognition domain?LST-3TM12 is a member of the OATP1B family and a functional transporter.The price of flexibility - a case study on septanoses as pyranose mimetics.Homodimer Architecture of QTRT2, the Noncatalytic Subunit of the Eukaryotic tRNA-Guanine TransglycosylaseKinITC-One Method Supports both Thermodynamic and Kinetic SARs as Exemplified on FimH AntagonistsDrug Discovery Summit: 11thSwiss Course on Medicinal ChemistryImprovement of Aglycone π-Stacking Yields Nanomolar to Sub-nanomolar FimH AntagonistsHydroxyl Groups in Synthetic and Natural-Product-Derived Therapeutics: A Perspective on a Common Functional Group
P50
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P50
description
researcher ORCID ID = 0000-0002-1481-9514
@en
wetenschapper
@nl
name
Christoph P. Sager
@ast
Christoph P. Sager
@en
Christoph P. Sager
@nl
type
label
Christoph P. Sager
@ast
Christoph P. Sager
@en
Christoph P. Sager
@nl
prefLabel
Christoph P. Sager
@ast
Christoph P. Sager
@en
Christoph P. Sager
@nl
P106
P31
P496
0000-0002-1481-9514