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2009
2008
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2008. Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors.
Eur. Journ. Med. Chem.. 43(2):315-326. Abstract
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2008. Presentation of the functional receptor-binding domain of the bacterial adhesin F17a-G on bacteriophage M13.
Antonie Van Leeuwenhoek International Journal of General and Molecular Microbiology. 93(1-2):219-226.
2007
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2007. Chloroplasts assemble the major subunit FaeG of Escherichia coli F4 (K88) fimbriae to strand-swapped dimers.
Journal Molecular Biology. 368(3):791-799. Abstract
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2007. 1,2,3-Triazolylalkylribitol derivatives as nucleoside hydrolase inhibitors.
Bioorg. & Med. Chem. Lett.. 17(9):2523-2526. Abstract
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2007. A live Salmonella enterica serovar Enteritidis vaccine allows serological differentiation between vaccinated and infected animals.
75(5):2461-2468. Abstract
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2007. Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors.
Abstract
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2007. Purification and crystallization of Vibrio fischeri CcdB and its complexes with fragments of gyrase and CcdA.
63(Pt 4):356-360. Abstract
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2007. Combining sites of bacterial fimbriae.
Current opinion in structural biology. 17(5):506-512. Abstract
2006
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2006. Crystallization of ornithine acetyltransferase from yeast by counter-diffusion and preliminary X-ray study.
62(Pt 12):1294-1297. Abstract
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2006. N-terminal truncation enables crystallization of the receptor-binding domain of the FedF bacterial adhesin.
Acta Cryst. F. 62(Pt 12):1278-1282. Abstract
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2006. The affinity of the FimH fimbrial adhesin is receptor-driven and quasi-independent of Escherichia coli pathotypes.
Molecular Microbiology. 61(6):1556-1568. Abstract
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2006. Molecular basis for the preferential cleft recognition by dromedary heavy-chain antibodies.
103(12):4586-4591. Abstract
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2006. N-terminal truncation enables crystallization of the receptor-binding domain of the FedF bacterial adhesin.
Acta Crystallographica Section F-Structural Biology and Crystallization Communications. 62:1278-1282.
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2006. The affinity of the FimH fimbrial adhesin is receptor-driven and quasi-independent of Escherichia coli pathotypes.
Molecular Microbiology. 61(6):1556-1568.
2005
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2005. Crystallization of the C-terminal domain of the addiction antidote CcdA in complex with its toxin CcdB.
61(Pt 10):949-952. Abstract
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2005. Impact of natural variation in bacterial F17G adhesins on crystallization behaviour.
Acta Cryst. D. 61(Pt 8):1149-1159. Abstract
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2005. Crystallization and crystal manipulation of the Pterocarpus angolensis seed lectin.
Acta Crystallographica Section D. 61(Pt 6):685-689. Abstract
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2005. Molecular basis of gyrase poisoning by the addiction toxin CcdB.
348(5):1091-1102. Abstract
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2005. Strong in vivo maturation compensates for structurally restricted H3 loops in antibody repertoires.
280(14):14114-14121. Abstract
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2005. Crystallization of the FaeE chaperone of Escherichia coli F4 fimbriae.
Acta Crystallographica Section F. 61(Pt 4):427-431. Abstract
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2005. Isolation and structural characterization of epilancin 15X, a novel lantibiotic from a clinical strain of Staphylococcus epidermidis.
579(9):1917-1922. Abstract
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2005. Receptor binding studies disclose a novel class of high-affinity inhibitors of the Escherichia coli FimH adhesin.
Molecular Microbiology. 55(2):441-455. Abstract
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2005. Crystallization of the FaeE chaperone of Escherichia coli F4 fimbriae.
Acta Crystallographica Section F-Structural Biology and Crystallization Communications. 61:427-431.
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2005. Receptor binding studies disclose a novel class of high-affinity inhibitors of the Escherichia coli FimH adhesin.
Molecular Microbiology. 55(2):441-455.