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Items where Author is "Gray-Owen, S. D."

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Number of items: 8.

Article

Muenzner, P. and Dehio, C. and Fujiwara, T. and Achtman, M. and Meyer, T. F. and Gray-Owen, S. D.. (2000) Carcinoembryonic antigen family receptor specificity of Neisseria meningitidis Opa variants influences adherence to and invasion of proinflammatory cytokine-activated endothelial cells. Infection and immunity, Vol. 68, H. 6. pp. 3601-3607.

Dehio, C. and Gray-Owen, S. D. and Meyer, T. F.. (2000) Host cell invasion by pathogenic Neisseriae. Subcellular biochemistry, Vol. 33. pp. 61-96.

Popp, A. and Dehio, C. and Grunert, F. and Meyer, T. F. and Gray-Owen, S. D.. (1999) Molecular analysis of neisserial Opa protein interactions with the CEA family of receptors : identification of determinants contributing to the differential specificities of binding. Cellular Microbiology, Vol. 1, H. 2. pp. 169-181.

Wang, J. and Gray-Owen, S. D. and Knorre, A. and Meyer, T. F. and Dehio, C.. (1998) Opa binding to cellular CD66 receptors mediates the transcellular traversal of Neisseria gonorrhoeae across polarized T84 epithelial cell monolayers. Molecular microbiology, Vol. 30, H. 3. pp. 657-671.

Dehio, C. and Gray-Owen, S. D. and Meyer, T. F.. (1998) The role of neisserial Opa proteins in interactions with host cells. Trends in microbiology, Vol. 6, H. 12. pp. 489-495.

Gray-Owen, S. D. and Dehio, C. and Haude, A. and Grunert, F. and Meyer, T. F.. (1997) CD66 carcinoembryonic antigens mediate interactions between Opa-expressing Neisseria gonorrhoeae and human polymorphonuclear phagocytes. The EMBO journal, Vol. 16, H. 12. pp. 3435-3445.

Gray-Owen, S. D. and Lorenzen, D. R. and Haude, A. and Meyer, T. F. and Dehio, C.. (1997) Differential Opa specificities for CD66 receptors influence tissue interactions and cellular response to Neisseria gonorrhoeae. Molecular microbiology, Vol. 26, H. 5. pp. 971-980.

Book Section

Gray-Owen, S. D. and Dehio, C. and Naumann, M. and Rudel, T. and Meyer, T. F.. (2000) Neisseria. In: Principles of bacterial pathogenesis. San Diego, Calif. ; London.

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