Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zoljargal Baatarkhuu"'
Autor:
Jean-Luc Ferrer, Philippe Chaignon, Alain Wagner, Franck Borel, Zoljargal Baatarkhuu, Myriam Seemann
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports
Scientific Reports, 2018, 8 (1), pp.17892. ⟨10.1038/s41598-018-35586-y⟩
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.17892. ⟨10.1038/s41598-018-35586-y⟩
Scientific Reports
Scientific Reports, 2018, 8 (1), pp.17892. ⟨10.1038/s41598-018-35586-y⟩
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.17892. ⟨10.1038/s41598-018-35586-y⟩
As multidrug resistant pathogenic microorganisms are a serious health menace, it is crucial to continuously develop novel medicines in order to overcome the emerging resistance. The methylerythritol phosphate pathway (MEP) is an ideal target for anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::443ca381a1e8559840927d4eecb0babf
http://link.springer.com/article/10.1038/s41598-018-35586-y
http://link.springer.com/article/10.1038/s41598-018-35586-y
Autor:
Alain Van Dorsselaer, Sergii Kolodych, J.-Y. Bonnefoy, Sarah Cianférani, Alain Wagner, Jitka Eberova, Zoljargal Baatarkhuu, Johann Stojko, Oleksandr Koniev
Publikováno v:
Bioconjugate Chemistry. 26:1863-1867
Thiols are among the most frequently used functional groups in the field of bioconjugation. While there exists a variety of heterobifunctional reagents that allow for coupling thiols to other functions (e.g., amines, carboxylic acids), there is no sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc73a17fcf271588c7d4d556747f5b5
https://doi.org/10.1021/acs.bioconjchem.5b00440
https://doi.org/10.1021/acs.bioconjchem.5b00440
Autor:
Sergii Kolodych, François Debaene, Alain Wagner, Alain Van Dorsselaer, J.-Y. Bonnefoy, Oleksandr Koniev, Zoljargal Baatarkhuu, Sarah Cianférani
Publikováno v:
Bioconjugate chemistry. 26(2)
Amine-to-thiol coupling is the most common route for the preparation of antibody–drug conjugates (ADC). It is usually achieved by using heterobifunctional reagents possessing an activated ester at one end and a maleimide group at the other. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117b5cdb907ffd2f2d823978ef090de1
https://pubmed.ncbi.nlm.nih.gov/25614935
https://pubmed.ncbi.nlm.nih.gov/25614935
Autor:
Oleksandr Koniev, Sergii Kolodych, Zoljargal Baatarkhuu, Johann Stojko, Jitka Eberova, Jean-Yves Bonnefoy, Sarah Cianférani, Alain Van Dorsselaer, Alain Wagner
Publikováno v:
Bioconjugate Chemistry; Sep2015, Vol. 26 Issue 9, p1863-1867, 5p