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2. The neoepitope of the complement C5b-9 Membrane Attack Complex is formed by proximity of adjacent ancillary regions of C9

3. Helical ultrastructure of the metalloprotease meprin α in complex with a small molecule inhibitor

4. Structure of the metastatic factor P-Rex1 reveals a two-layered autoinhibitory mechanism

6. Characterization of the pathoimmunology of necrotizing enterocolitis reveals novel therapeutic opportunities

7. The cryo-EM structure of the acid activatable pore-forming immune effector Macrophage-expressed gene 1

9. The first transmembrane region of complement component-9 acts as a brake on its self-assembly

11. Perforin proteostasis is regulated through its C2 domain: supra-physiological cell death mediated by T431D-perforin

12. Real-time visualization of perforin nanopore assembly

13. Smoothing a rugged protein folding landscape by sequence-based redesign

14. Correction: Corrigendum: N-terminal domain of Bothrops asper Myotoxin II Enhances the Activity of Endothelin Converting Enzyme-1 and Neprilysin

16. N-terminal domain of Bothrops asper Myotoxin II Enhances the Activity of Endothelin Converting Enzyme-1 and Neprilysin

17. Structure of the poly-C9 component of the complement membrane attack complex

20. IL-37 requires the receptors IL-18Rα and IL-1R8 (SIGIRR) to carry out its multifaceted anti-inflammatory program upon innate signal transduction

23. Maspin is not required for embryonic development or tumour suppression

26. The structural basis for membrane binding and pore formation by lymphocyte perforin

28. GABA production by glutamic acid decarboxylase is regulated by a dynamic catalytic loop

30. T cell receptor recognition of a 'super-bulged' major histocompatibility complex class I–bound peptide

31. The matrix refolded

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