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Towards further harmonization of a glossary for exposure science-an ISES Europe statement.
J Expo Sci Environ Epidemiol. 2022 Jul;32(4):526-529. doi: 10.1038/s41370-021-00390-w. Epub 2021 Nov 2.
J Expo Sci Environ Epidemiol. 2022.
PMID: 34728760
Free PMC article.
Validity of Tier 1 Modelling Tools and Impacts on Exposure Assessments within REACH Registrations-ETEAM Project, Validation Studies and Consequences.
Schlueter U, Tischer M.
Schlueter U, et al.
Int J Environ Res Public Health. 2020 Jun 26;17(12):4589. doi: 10.3390/ijerph17124589.
Int J Environ Res Public Health. 2020.
PMID: 32604711
Free PMC article.
Review.
Item in Clipboard
Synthesis of a malaria candidate glycosylphosphatidylinositol (GPI) structure: a strategy for fully inositol acylated and phosphorylated GPIs.
Lu J, Jayaprakash KN, Schlueter U, Fraser-Reid B.
Lu J, et al. Among authors: schlueter u.
J Am Chem Soc. 2004 Jun 23;126(24):7540-7. doi: 10.1021/ja038807p.
J Am Chem Soc. 2004.
PMID: 15198601
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Orthoesters versus 2-O-acyl glycosides as glycosyl donors: theorectical and experimental studies.
Fraser-Reid B, Grimme S, Piacenza M, Mach M, Schlueter U.
Fraser-Reid B, et al. Among authors: schlueter u.
Chemistry. 2003 Oct 6;9(19):4687-92. doi: 10.1002/chem.200304856.
Chemistry. 2003.
PMID: 14566874
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Synthetic approaches to heavily lipidated phosphoglyceroinositides.
Schlueter U, Lu J, Fraser-Reid B.
Schlueter U, et al.
Org Lett. 2003 Feb 6;5(3):255-7. doi: 10.1021/ol0202161.
Org Lett. 2003.
PMID: 12556165
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Unexpected role of O-2 "protecting" groups of glycosyl donors in mediating regioselective glycosidation.
Fraser-Reid B, Lopez JC, Radhakrishnan KV, Mach M, Schlueter U, Gomez AM, Uriel C.
Fraser-Reid B, et al. Among authors: schlueter u.
J Am Chem Soc. 2002 Apr 3;124(13):3198-9. doi: 10.1021/ja012383m.
J Am Chem Soc. 2002.
PMID: 11916390
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