212 results on '"Law, Ruby H. P."'
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2. The role of NINJ1 protein in programmed cellular destruction
3. Proteoform-resolved profiling of plasminogen activation reveals novel abundant phosphorylation site and primary N-terminal cleavage site
4. A High-Throughput Small-Angle X-ray Scattering Assay to Determine the Conformational Change of Plasminogen
5. Perforin proteostasis is regulated through its C2 domain: supra-physiological cell death mediated by T431D-perforin
6. Front Cover: Synthesis and Structural Characterization of Macrocyclic Plasmin Inhibitors (ChemMedChem 6/2023)
7. Synthesis and Structural Characterization of Macrocyclic Plasmin Inhibitors
8. 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
10. Model for surface-dependent factor XII activation: the roles of factor XII heavy chain domains
11. A mechanism for hereditary angioedema caused by a lysine 311–to–glutamic acid substitution in plasminogen
12. X-ray crystal structure of the streptococcal specific phage lysin PlyC
13. Structure of Granzyme C Reveals an Unusual Mechanism of Protease Autoinhibition
14. A Common Fold Mediates Vertebrate Defense and Bacterial Attack
15. Molecular Biology and Assembly of Yeast Mitochondrial ATP Synthase
16. Subunit 8 of Yeast Mitochondrial ATP Synthase: Biochemical Genetics and Membrane Assembly
17. Innentitelbild: Application and Structural Analysis of Triazole‐Bridged Disulfide Mimetics in Cyclic Peptides (Angew. Chem. 28/2020)
18. Inside Cover: Application and Structural Analysis of Triazole‐Bridged Disulfide Mimetics in Cyclic Peptides (Angew. Chem. Int. Ed. 28/2020)
19. Application and Structural Analysis of Triazole‐Bridged Disulfide Mimetics in Cyclic Peptides
20. Effective targeting of intact and proteolysed CDCP1 for imaging and treatment of pancreatic ductal adenocarcinoma
21. Anti-CDCP1 immuno-conjugates for detection and inhibition of ovarian cancer
22. The structural basis for membrane binding and pore formation by lymphocyte perforin
23. Molecular genetic analysis of the central hydrophobic domain of subunit 8 of yeast mitochondrial ATP synthase
24. Structure and Function Characterization of the a1a2 Motifs of Streptococcus pyogenes M Protein in Human Plasminogen Binding
25. Tranexamic acid is an active site inhibitor of urokinase plasminogen activator
26. Highly Potent and Selective Plasmin Inhibitors Based on the Sunflower Trypsin Inhibitor-1 Scaffold Attenuate Fibrinolysis in Plasma
27. A cyclic peptide inhibitor of the iNOS–SPSB protein–protein interaction as a potential anti-infective agent
28. Characterising the Subsite Specificity of Urokinase‐Type Plasminogen Activator and Tissue‐Type Plasminogen Activator using a Sequence‐Defined Peptide Aldehyde Library
29. A Cyclic Peptide Inhibitor of the iNOS–SPSB Protein–Protein Interaction as a Potential Anti-Infective Agent
30. X-ray crystal structure of plasmin with tranexamic acid–derived active site inhibitors
31. Structural studies of plasmin inhibition.
32. Highly Potent and Selective Plasmin Inhibitors Based on the Sunflower Trypsin Inhibitor‑1 Scaffold Attenuate Fibrinolysis in Plasma.
33. Characterising the Subsite Specificity of Urokinase‐Type Plasminogen Activator and Tissue‐Type Plasminogen Activator using a Sequence‐Defined Peptide Aldehyde Library.
34. Structure of the poly-C9 component of the complement membrane attack complex
35. Preferential Acquisition and Activation of Plasminogen Glycoform II by PAM Positive Group A Streptococcal Isolates
36. Stability of the Octameric Structure Affects Plasminogen-Binding Capacity of Streptococcal Enolase
37. Conformational Changes during Pore Formation by the Perforin-Related Protein Pleurotolysin
38. Import into Isolated Yeast Mitochondria of Radiolabeled Proteins Synthesized In Vitro
39. Maspin is not required for embryonic development or tumour suppression
40. Defining the interaction of perforin with calcium and the phospholipid membrane
41. Perforin forms transient pores on the target cell plasma membrane to facilitate rapid access of granzymes during killer cell attack
42. Structural characterization of the mechanism through which human glutamic acid decarboxylase auto-activates
43. The Subtilisin-Like Protease AprV2 Is Required for Virulence and Uses a Novel Disulphide-Tethered Exosite to Bind Substrates
44. Characterisation of Peptide Microarrays for Studying Antibody-Antigen Binding Using Surface Plasmon Resonance Imagery
45. The X-Ray Crystal Structure of Escherichia coli Succinic Semialdehyde Dehydrogenase; Structural Insights into NADP+/Enzyme Interactions
46. Prodepth: Predict Residue Depth by Support Vector Regression Approach from Protein Sequences Only
47. The MACPF/CDC family of pore-forming toxins
48. X-ray crystal structure of the fibrinolysis inhibitor α2-antiplasmin
49. The N terminus of the serpin, tengpin, functions to trap the metastable native state
50. GABA production by glutamic acid decarboxylase is regulated by a dynamic catalytic loop
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