679 results on '"Perkins, Stephen J."'
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52. Functional and structural characterisation of human colostrum free secretory component
53. Hydrodynamic Studies of a Complex Between the Fc Fragment of Human IgE and a Soluble Fragment of the FcεRI α Chain
54. Positive Selection during the Evolution of the Blood Coagulation Factors in the Context of Their Disease-Causing Mutations
55. Solution structure of deglycosylated human IgG1 shows the role of CH2 glycans in its conformation
56. Association of a Factor H Mutation With Hemolytic Uremic Syndrome Following a Diarrheal Illness
57. Identification of diverse lipid‐binding modes in the groove of zinc α2 glycoprotein reveals its functional versatility.
58. A Dimerization Site at SCR-17/18 in Factor H Clarifies a New Mechanism for Complement Regulatory Control
59. The EAHAD Coagulation Factor Variant Databases: important resources for haemostasis clinicians and researchers
60. The solution structure of the complement deregulator FHR5 reveals a compact dimer and provides new insights into CFHR5 nephropathy
61. The Oxford Handbook of Organizational Theory: Meta-Theoretical Perspectives
62. His-384 Allotypic Variant of Factor H Associated with Age-related Macular Degeneration Has Different Heparin Binding Properties from the Non-disease-associated Form
63. X‐Ray and Neutron Scattering Data and Their Constrained Molecular Modeling
64. Structural studies in solution of the recombinant N-terminal pair of short consensus/complement repeat domains of complement receptor type 2 (CR2/CD21) and interactions with it ligand C3dg
65. The EAHAD blood coagulation factor VII variant database
66. The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers
67. Atomistic Modeling of Scattering Curves for Human IgG1/4 Reveals New Structure-Function Insights
68. Crystal structure of zinc-α2-glycoprotein in complex with a fatty acid reveals multiple different modes of protein-lipid binding
69. Molecular basis of C-reactive protein binding and modulation of complement activation by factor H-related protein 4
70. Non-linearity of the collagen triple helix in solution and implications for collagen function
71. Investigation of the self-association and hetero-association interactions of H-NS and StpA from Enterobacteria
72. Flexibility in Mannan-Binding Lectin-Associated Serine Proteases-1 and -2 Provides Insight on Lectin Pathway Activation
73. Complement and Immunoglobulin Protein Structures by X-Ray and Neutron Solution Scattering and Analytical Ultracentrifugation
74. Degradation of C1-Inhibitor by Plasmin: Implications for the Control of Inflammatory Processes
75. Possible arrangement of the five domains in human complement factor I as determined by a combination of X-ray and neutron scattering and homology modeling
76. Atomistic modelling of scattering data in the Collaborative Computational Project for Small Angle Scattering (CCP-SAS)1
77. CoagMDB: A Database Analysis of Missense Mutations Within Four Conserved Domains in Five Vitamin K-Dependent Coagulation Serine Proteases Using a Text-Mining Tool
78. The Interactive Factor H-Atypical Hemolytic Uremic Syndrome Mutation Database and Website: Update and Integration of Membrane Cofactor Protein and Factor I Mutations With Structural Models
79. The solution structure of human coagulation factor VIIa in its complex with tissue factor is similar to free factor VIIa: a study of a heterodimeric receptor-ligand complex by x-ray and neutron scattering and computational modeling
80. Segmenting international assignments: organizational justice
81. A Userʼs Guide to the Interactive Web Database of Factor H-Associated Hemolytic Uremic Syndrome
82. An Interactive Web Database of Factor H-Associated Hemolytic Uremic Syndrome Mutations: Insights Into the Structural Consequences of Disease-Associated Mutations
83. Oligomerization of the amide sensor protein amiC by X-ray and neutron scattering and molecular modeling
84. Factor XI Deficiency Database: An Interactive Web Database of Mutations, Phenotypes, and Structural Analysis Tools
85. Bent domain structure of recombinant human IgE-Fc in solution by X-ray and neutron scattering in conjunction with an automated curve fitting procedure
86. Hydrodynamic studies of a complex between the Fc fragment of human IgE and a soluble fragment of the Fc-epsilon-RI alpha chain
87. Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency
88. Sociological Paradigms and Human Resources: An African Context
89. Molecular modeling of the domain structure of C9 of human complement by neutron and X-ray solution scattering
90. The solution structure of the human IgG2 subclass is distinct from those for human IgG1 and IgG4 providing an explanation for their discrete functions
91. An Expanded Conformation of an Antibody Fab Region by X-Ray Scattering, Molecular Dynamics, and smFRET Identifies an Aggregation Mechanism
92. Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces
93. Analogy and solution scattering modelling: new structural strategies for the multidomain proteins of complement, cartilage and the immunoglobulin superfamily
94. SCT: a suite of programs for comparing atomistic models with small-angle scattering data
95. Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15–base pair insertion in the F7 gene
96. X-Ray and neutron scattering analyses of hydration shells: a molecular interpretation based on sequence predictions and modelling fits
97. The Fab Conformations in the Solution Structure of Human Immunoglobulin G4 (IgG4) Restrict Access to Its Fc Region
98. Structural models for carcinoembryonic antigen and its complex with the single-chain Fv antibody molecule MFE23
99. Crystal structure of zinc-α2-glycoprotein in complex with a fatty acid reveals multiple different modes of protein-lipid binding.
100. Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
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