Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Simon M. Langenegger"'
Autor:
Giovanni Picca, Markus Probst, Simon M. Langenegger, Oleg Khorev, Peter Bütikofer, Anant K. Menon, Robert Häner
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 1732-1739 (2020)
The chemical synthesis of molecular probes to identify and study membrane proteins involved in the biological pathway of protein glycosylation is described. Two short-chain glycolipid analogs that mimic the naturally occurring substrate mannosyl phos
Externí odkaz:
https://doaj.org/article/2306c694d9ec4eeeb0e5144e53485e37
Publikováno v:
CHIMIA, Vol 71, Iss 12 (2017)
Externí odkaz:
https://doaj.org/article/99f07754735647b6b884f781cb9b42bf
Publikováno v:
CHIMIA, Vol 71, Iss 3 (2017)
Externí odkaz:
https://doaj.org/article/89155efbfdaf4796b95ad960e66f6db0
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1589-1595 (2014)
Aromatic π–π stacking interactions are ubiquitous in nature, medicinal chemistry and materials sciences. They play a crucial role in the stacking of nucleobases, thus stabilising the DNA double helix. The following paper describes a series of chi
Externí odkaz:
https://doaj.org/article/2ee3b8468107406195563f98e60a90b1
Publikováno v:
CHIMIA, Vol 70, Iss 12 (2016)
Externí odkaz:
https://doaj.org/article/2f67099a96e14f0285f3404e15f9d843
Autor:
Caroline D. Bösch, Markus Probst, Yuliia Vyborna, Mykhailo Vybornyi, Simon M. Langenegger, Robert Häner
Publikováno v:
CHIMIA, Vol 69, Iss 12 (2015)
Externí odkaz:
https://doaj.org/article/ca5570edb462457aaf75d7edfbe85339
Publikováno v:
CHIMIA, Vol 59, Iss 11 (2005)
Chemically modified nucleic acids find widespread use as tools in research, as diagnostic reagents and as pharmaceutical compounds. While the major efforts in the past concentrated on the generation of sugar-based nucleotide analogues, the potential
Externí odkaz:
https://doaj.org/article/89e0b98d5cd24347ba86b199af95a51a
Publikováno v:
Bioconjugate Chemistry. 34:70-77
The precise arrangement of structural subunits is a key factor for the proper shape and function of natural and artificial supramolecular assemblies. In DNA nanotechnology, the geometrically well-defined double-stranded DNA scaffold serves as an elem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c850f78db9c295d5f9235d936cf96020
https://doi.org/10.1021/acs.bioconjchem.2c00077
https://doi.org/10.1021/acs.bioconjchem.2c00077
Autor:
Simon Rothenbühler, Adrian Gonzalez, Ioan Iacovache, Simon M. Langenegger, Benoît Zuber, Robert Häner
Publikováno v:
Rothenbühler, Simon; Gonzalez, Adrian; Iacovache, Ioan; Langenegger, Simon M.; Zuber, Benoît; Häner, Robert (2022). Tetraphenylethylene–DNA conjugates: influence of sticky ends and DNA sequence length on the supramolecular assembly of AIE-active vesicles. Organic & biomolecular chemistry, 20(18), pp. 3703-3707. Royal Society of Chemistry 10.1039/D2OB00357K
The supramolecular assembly of DNA conjugates, functionalized with tetraphenylethylene (TPE) sticky ends, into vesicular structures is described. The aggregation-induced emission (AIE) active TPE units allow to monitor the assembly process by fluores
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cacaeb2fd63579c3fd7cafde3e1813b5
Autor:
Simon M. Langenegger, Robert Häner
Publikováno v:
ChemBioChem; May2005, Vol. 6 Issue 5, p848-851, 4p