117 results on '"Reid, Kenneth B. M."'
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2. The class A macrophage scavenger receptor type I (SR-AI) recognizes complement iC3b and mediates NF-κB activation
3. Surfactant protein A (SP-A) binds to phosphatidylserine and competes with annexin V binding on late apoptotic cells
4. The Classical and Regulatory Functions of C1q in Immunity and Autoimmunity
5. Role of Ca(super 2+) in the electrostatic stability and the functional activity of the globular domain of human Clq
6. Impaired Recognition of Apoptotic Neutrophils by the C1q/Calreticulin and CD91 Pathway in Systemic Lupus Erythematosus
7. Mammalian lectins in activation and clearance mechanisms involving the complement system
8. A Recombinant Fragment of Human Surfactant Protein D Reduces Alveolar Macrophage Apoptosis and Pro-Inflammatory Cytokines in Mice Developing Pulmonary Emphysema
9. The roles of surfactant proteins A and D in innate immunity
10. Pulmonary alveolar proteinosis: clinical aspects and current concepts on pathogenesis
11. Genomic Organization of the Mouse Gene for Lung Surfactant Protein D
12. Deficient Hydrophilic Lung Surfactant Proteins A and D with Normal Surfactant Phospholipid Molecular Species in Cystic Fibrosis
13. Inhibitory Effect of Pulmonary Surfactant Proteins A and D on Allergen-induced Lymphocyte Proliferation and Histamine Release in Children with Asthma
14. A second serine protease associated with mannan-binding lectin that activates complement
15. Measurement of pulmonary status and surfactant protein levels during dexamethasone treatment of neonatal respiratory distress syndrome
16. Localization of the gene cluster encoding the A, B, and C chains of human C1q to 1p34.1–1p36.3
17. HUMAN LUNG SURFACTANT PROTEINS (SP-A AND SP-D) CAN INHIBIT THE BINDING OF ALLERGEN -SPECIFIC IGE TO DUST MITE (DER.P)
18. Frequency of Mannose-Binding Protein Deficiency in Patients with Systemic Lupus Erythematosus
19. Identification of a gC1q-binding Protein (gC1q-R) on the Surface of Human Neutrophils: Subcellular Localization and Binding Properties in Comparison with the cC1q-R
20. Carrier Detection in Families With Properdin Deficiency by Microsatellite Haplotyping
21. Structural and functional studies on C4b-binding protein, a regulatory component of the human complement system
22. A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual
23. Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein.
24. Collectins and innate immunity in the lung
25. CL-46, a Novel Collectin Highly Expressed in Bovine Tthymus and Liver
26. Protein engineering of human properdin
27. Collectins and Pentraxins.
28. Interaction of Human Clq with IgG and 1gM: Revisited.
29. Helicobacter Infection in the Surfactant Protein D-Deficient Mouse.
30. Existence of Different but Overlapping IgG- and IgM-Binding Sites on the Globular Domain of Human Clq.
31. Surfactant protein D is proatherogenic in mice.
32. Interaction of C1q with IgG1, C-reactive Protein and Pentraxin 3: Mutational Studies Using Recombinant Globular Head Modules of Human C1q A, B, and C Chains.
33. Role of Ca2+ in the Electrostatic Stability and the Functional Activity of the Globular Domain of Human C1q.
34. A Recombinant Fragment of Human Surfactant Protein D Reduces Alveolar Macrophage Apoptosis and Pro-Inflammatory Cytokines in Mice Developing Pulmonary Emphysema.
35. Altered airway surfactant phospholipid composition and reduced lung function in asthma.
36. A novel PCR-based technique using expressed sequence tags and gene homology for murine genetic mapping: localization of the complement genes.
37. The A-domain of integrin α2 binds specifically to a range of collagens but is not a general receptor for the collagenous motif.
38. Isolation, sequence analysis and characterization of cDNA clones coding for the C chain of mouse C1q.
39. Molecular cloning of the cDNA coding for properdin, a positive regulator of the alternative pathway of human complement.
40. Expression of properdin in human monocytes.
41. Structural similarity between lung surfactant protein D and conglutinin.
42. Genetic Deficiencies of the Complement System and Association with Disease-Early Components.
43. Structure and activity of factor D̄ of the alternative pathway of human complement
44. The Biomedical Revolution at 40 Years.
45. Collectins and innate immunity in the lung : therapeutic potential of a recombinant fragment of surfactant protein D in lung disease
46. Protein engineering of human properdin
47. The molecular genetics of the human complement component C4
48. Molecular Interactions between MASP-2, C4, and C2 and Their Activation Fragments Leading to Complement Activation via the Lectin Pathway.
49. Nucleic Acid Is a Novel Ligand for Innate, Immune Pattern Recognition Collectins Surfactant Proteins A and D and Mannose-binding Lectin.
50. High-resolution Structural Insights into Ligand binding and Immune Cell Recognition by Human Lung Surfactant Protein D
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