Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Torben Leßmann"'
Autor:
Luis Alejandro Zúñiga, Torben Leßmann, Karan Uppal, Nicola Bisek, Enping Hong, Caroline E. Rasmussen, Jens-Jakob Karlsson, Joachim Zettler, Lars Holten-Andersen, Kathy Bang, Dhruv Thakar, Yu-Chi Lee, Salomon Martinez, Simran Singh Sabharwal, Sebastian Stark, Frank Faltinger, Oliver Kracker, Samuel Weisbrod, Robin Müller, Tobias Voigt, Kornelia Bigott, Mohammad Tabrizifard, Vibeke Miller Breinholt, Amer M. Mirza, David B. Rosen, Kennett Sprogøe, Juha Punnonen
Publikováno v:
Cancer Cell International, Vol 22, Iss 1, Pp 1-17 (2022)
Abstract Background Intratumoral (IT) delivery of toll-like receptor (TLR) agonists has shown encouraging anti-tumor benefit in preclinical and early clinical studies. However, IT delivery of TLR agonists may lead to rapid effusion from the tumor mic
Externí odkaz:
https://doaj.org/article/9c07ff8778c14891ac4c75977cba6fba
Autor:
Paola Grandi, Ed Hurt, Johannes Lechner, Jochen Baßler, Elisabeth Petfalski, Olivier Gadal, Torben Leßmann, David Tollervey
Publikováno v:
Molecular Cell. 8(3):517-529
A nuclear GTPase, Nug1p, was identified in a genetic screen for components linked to 60S ribosomal subunit export. Nug1p cosedimented with nuclear 60S preribosomes and was required for subunit export to the cytoplasm. Tagged Nug1p coprecipitated with
Publikováno v:
ChemInform. 39
Publikováno v:
Chemical Society reviews. 37(7)
The aim of this tutorial review is to introduce the reader to the concept, synthesis and application of natural product-inspired compound collections as an important field in chemical biology. This review will discuss how potentially interesting scaf
Autor:
Herbert Waldmann, Stefan Sommer, Jayant D. Umarye, Victor Mamane, Ana B. García, Torben Lessmann
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2007, 63 (26), pp.5754-5767. ⟨10.1016/j.tet.2007.01.041⟩
Tetrahedron, Elsevier, 2007, 63 (26), pp.5754-5767. ⟨10.1016/j.tet.2007.01.041⟩
A systematic study on the asymmetric allylation of aldehydes on solid support is reported. Different kinds of chiral allylboron reagents with complementary direction of stereoinduction were applied successfully in this reagent-controlled transformati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc6f1e6d521973a46f89d918c6544518
https://hal.archives-ouvertes.fr/hal-02266152
https://hal.archives-ouvertes.fr/hal-02266152
Autor:
Jayant D. Umarye, Victor Mamane, Herbert Waldmann, Stefan Sommer, Torben Leßmann, Ana B. García
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2007, 13 (12), pp.3305-3319. ⟨10.1002/chem.200601698⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2007, 13 (12), pp.3305-3319. ⟨10.1002/chem.200601698⟩
A strategy aiming at the introduction of stereocenters into polymer-bound natural-product-derived and -inspired compound collections is presented. Treatment of immobilized aldehydes with Brown's pinene-derived allylboranes results in the stereoselect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ade89b74336c06832f6f850c73acdc6
https://hal.archives-ouvertes.fr/hal-02266151
https://hal.archives-ouvertes.fr/hal-02266151
Autor:
Herbert Waldmann, Torben Lessmann
Publikováno v:
Chemical communications (Cambridge, England). (32)
Organic transformations on substrates which are immobilized on an insoluble, polymeric carrier have found broad application in compound collection synthesis. In contrast to other synthetic methodologies in solid-phase organic synthesis, reactions tha
Autor:
Herbert Waldmann, Stefan Sommer, Jayant D. Umarye, Victor Mamane, Torben Leßmann, Ana B. García
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2006, pp.3868-3870. ⟨10.1039/b607816h⟩
Chemical Communications, Royal Society of Chemistry, 2006, pp.3868-3870. ⟨10.1039/b607816h⟩
Enantiocomplementary allylation of solid phase-bound aldehydes gives rise to a natural product-derived compound collection, including all stereoisomers of cryptocarya diacetate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ef32e5fdf988dbac02aaeaa8fee59a
https://hal.archives-ouvertes.fr/hal-02266153
https://hal.archives-ouvertes.fr/hal-02266153
Autor:
Torben Leßmann, Herbert Waldmann
Publikováno v:
Chemical Communications; Aug2006, Vol. 2006 Issue 32, p3380-3389, 10p