Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Karine Descroix"'
Autor:
Olivier Berteau, Pierre-Alexandre Driguez, Jonathan E. Ulmer, Annie Malleron, Corine Sandström, Eric Morssing Vilén, Ramesh Babu Namburi, Alhosna Benjdia, Julie Beneteau, Karine Descroix, Christine Le Narvor, Lassalle Gilbert, Dorothe Spillmann, David Bonnaffé
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2014, 289 (35), pp.24289-24303. ⟨10.1074/jbc.M114.573303⟩
Journal of Biological Chemistry 35 (289), 24289-24303. (2014)
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2014, 289 (35), pp.24289-24303. ⟨10.1074/jbc.M114.573303⟩
Journal of Biological Chemistry 35 (289), 24289-24303. (2014)
Background: Sulfatases are emerging as key adaptive tools of commensal bacteria to their host. Results: The first bacterial endo-O-sulfatase and three exo-O-sulfatases from the human commensal Bacteroides thetaiotaomicron, specific for glycosaminogly
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 6:1341-1349
β-(1,3)-Glucans are widely distributed within microorganisms or seaweeds in which they act as membrane components or for energy storage, respectively. Since these glucans are not biosynthesized by mammals, they are likely to activate the immune syst
Autor:
Vincent Ferrières, Karine Descroix, Laurent Legentil, Caroline Nugier-Chauvin, Balla Sylla, Richard Daniellou
Publikováno v:
ChemInform. 45
The synthesis of β-(13)-glucans is at present has more than a chemical challenge. The discovery of their biological properties found development for new anti- cancer therapies, the efficient preparation of pure and structurally well-defined β-(1
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (39), pp.7728-7749. ⟨10.1039/c4ob01200c⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (39), pp.7728-7749. ⟨10.1039/c4ob01200c⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (39), pp.7728-7749. ⟨10.1039/c4ob01200c⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (39), pp.7728-7749. ⟨10.1039/c4ob01200c⟩
International audience; Shigella flexneri serotypes 1b and 1a are Gram-negative enteroinvasive bacteria causing shigellosis in humans. The O-antigen from S. flexneri 1b is a { → 2)-[3Ac/4Ac]-α-L-RHAP-(1 → 2)-α-L-Rhap-(1 → 3)-[2Ac]-α-L-Rhap-(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e1e17a729cc3f8238696489b55a6831
https://hal-pasteur.archives-ouvertes.fr/pasteur-02043357
https://hal-pasteur.archives-ouvertes.fr/pasteur-02043357
Autor:
Karine Descroix, Richard Daniellou, Laurent Legentil, Balla Sylla, Caroline Nugier-Chauvin, Vincent Ferrieres
Publikováno v:
Beta-Glucan, Structure, Chemistry and Specific Application
Vaclav Vetvicka and Miroslav Novak. Beta-Glucan, Structure, Chemistry and Specific Application, Bentham Science Publishers, pp.102-111, 2013, Biology and Chemistry of Beta Glucan, 978-1-60805-301-8. ⟨10.2174/9781608052608113020007⟩
Vaclav Vetvicka and Miroslav Novak. Beta-Glucan, Structure, Chemistry and Specific Application, Bentham Science Publishers, pp.102-111, 2013, Biology and Chemistry of Beta Glucan, 978-1-60805-301-8. ⟨10.2174/9781608052608113020007⟩
The lightning progress in the understanding of enzymatic mechanisms, democratization of molecular biology tools and their introduction in chemistry laboratories, the pressure of green chemistry notions leading to the need for alternative sustainable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d435243f5138f336c99ea7c3a5be788c
https://hal.science/hal-00961650
https://hal.science/hal-00961650
Autor:
Isabelle André, Claire Moulis, Sandrine Morel, Samuel Tranier, Thu Hoai Tran, Magali Remaud-Simeon, Karine Descroix, Lionel Mourey, Elise Champion, Frédéric Guérin, Sophie Barbe, Laurence A. Mulard, Pierre Monsan
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2012, 134 (45), pp.18677-18688. ⟨10.1021/ja306845b⟩
Journal of the American Chemical Society, 2012, 134 (45), pp.18677-18688. ⟨10.1021/ja306845b⟩
Journal of the American Chemical Society, American Chemical Society, 2012, 134 (45), pp.18677-18688. ⟨10.1021/ja306845b⟩
Journal of the American Chemical Society, 2012, 134 (45), pp.18677-18688. ⟨10.1021/ja306845b⟩
International audience; Iterative saturation mutagenesis and combinato-rial active site saturation focused on vicinal amino acids were used to alter the acceptor specificity of amylosucrase from Neisseria polysaccharea, a sucrose-utilizing α-transgl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f25d1bc62edcd0ec05d01fcd9a3e04c9
https://hal.archives-ouvertes.fr/hal-03003058/file/champion-jacs12.pdf
https://hal.archives-ouvertes.fr/hal-03003058/file/champion-jacs12.pdf
Autor:
Thomas Pesnot, Sebastian S. Gehrke, Karine Descroix, Yayoi Yoshimura, Warren W. Wakarchuk, Monica M. Palcic, Gerd K. Wagner
Galactosyltransferases (GalT) are important molecular targets in a range of therapeutic areas, including infection, inflammation, and cancer. GalT inhibitors are therefore sought after as potential lead compounds for drug discovery. We have recently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b2df8a59462b66d08986bb4c4bba1d3
https://doi.org/10.1021/jm201154p
https://doi.org/10.1021/jm201154p
Autor:
Vaclav Vetvicka, Vincent Ferrières, Sujata Saraswat-Ohri, Frank Jamois, Karine Descroix, Aruna Vashishta, Jean-Claude Yvin
Publikováno v:
Carbohydrate Research
Carbohydrate Research, Elsevier, 2011, 346 (14), pp.2213-21. ⟨10.1016/j.carres.2011.06.020⟩
Carbohydrate Research, 2011, 346 (14), pp.2213-21. ⟨10.1016/j.carres.2011.06.020⟩
Carbohydrate Research, Elsevier, 2011, 346 (14), pp.2213-21. ⟨10.1016/j.carres.2011.06.020⟩
Carbohydrate Research, 2011, 346 (14), pp.2213-21. ⟨10.1016/j.carres.2011.06.020⟩
International audience; (1→3)-β-D-Glucans are well-established natural biological immunomodulators. However, problems inherited with the natural origin of these polysaccharides bring about significant setbacks, including batch-to-batch heterogenei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c025f5fd2171c9442970ef2476f3fb
https://hal.archives-ouvertes.fr/hal-00753333
https://hal.archives-ouvertes.fr/hal-00753333
Autor:
Sujata Saraswat-Ohri, Aruna Vashishta, Frank Jamois, Vincent Ferrières, Vaclav Vetvicka, Jean-Claude Yvin, Karine Descroix
Publikováno v:
Journal of Medicinal Food
Journal of Medicinal Food, Mary Ann Liebert, 2011, 14 (4), pp.369-76. ⟨10.1089/jmf.2010.0081⟩
Journal of Medicinal Food, 2011, 14 (4), pp.369-76. ⟨10.1089/jmf.2010.0081⟩
Journal of Medicinal Food, Mary Ann Liebert, 2011, 14 (4), pp.369-76. ⟨10.1089/jmf.2010.0081⟩
Journal of Medicinal Food, 2011, 14 (4), pp.369-76. ⟨10.1089/jmf.2010.0081⟩
International audience; Despite the fact that β-glucans are well-established immunomodulators, the problems with batch-to-batch heterogeneity remains problematic. The aim of this study was to prepare and evaluate new type of synthetic oligosaccharid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a5b12acf1ea0077c1ac01c2cd8e888c
https://hal.archives-ouvertes.fr/hal-00753565
https://hal.archives-ouvertes.fr/hal-00753565
Double diastereoselection explains limitations in synthesizing mannose-containing beta-(1,3)-glucans
Autor:
Karine Descroix, Laurent Legentil, Balla Sylla, Richard Daniellou, Frank Jamois, Jean-Claude Yvin, Cedric Gervaise, Vincent Ferrières, Caroline Nugier-Chauvin, Christophe Pain
Publikováno v:
Carbohydrate Research
Carbohydrate Research, Elsevier, 2010, 345 (10), pp.1366-70. ⟨10.1016/j.carres.2010.04.018⟩
Carbohydrate Research, 2010, 345 (10), pp.1366-70. ⟨10.1016/j.carres.2010.04.018⟩
Carbohydrate Research, Elsevier, 2010, 345 (10), pp.1366-70. ⟨10.1016/j.carres.2010.04.018⟩
Carbohydrate Research, 2010, 345 (10), pp.1366-70. ⟨10.1016/j.carres.2010.04.018⟩
International audience; It is known that 3-O-glycosylation of glucosidic acceptors bearing acyl groups in the 4 and 6 positions instead of a 4,6-O-benzylidene ring mainly affords alpha-glycosides. Described here is an unexpected stereochemical outcom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6726e3e20fd5a02e1f20375f6c300634
https://hal.archives-ouvertes.fr/hal-00759103
https://hal.archives-ouvertes.fr/hal-00759103