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1 tion analysis showed that baseline values of surfactant protein D (46.6 ng/mL vs 34.6 ng/mL, p=0.0018
3 iagnosis and compare these results to plasma surfactant protein-D, a marker of pure alveolar epitheli
5 monstrate that reduced pulmonary edema fluid surfactant protein D and elevated plasma surfactant prot
6 olar lavage and various serum markers (e.g., surfactant protein D and KL-6) each may provide useful i
7 and blood concentrations of pneumoproteins (surfactant protein-D and club cell secretory protein), a
8 In a subset, we compared plasma levels of surfactant protein-D and von Willebrand factor antigen b
9 on molecules in the collectin family, namely surfactant proteins D and A (Sp-D and Sp-A, respectively
10 ptor for advanced glycation end products and surfactant protein D) and endothelial injury (angiopoiet
13 r inhibitor-1 (PAI-1), surfactant protein-A, surfactant protein-D, and intracellular adhesion molecul
14 n molecule-1, von Willebrand factor antigen, surfactant protein-D, and soluble tumor necrosis factor
15 eceptor for advanced glycation end products, surfactant protein D, angiopoietin-2, interleukin-6, int
16 soluble multitrimers of BAFF and APRIL using surfactant protein D as a scaffold, and we vaccinated mi
18 a levels of fibrinogen, chemokine ligand 18, surfactant protein D, C-reactive protein, Clara cell sec
19 surfactant protein A-deficient (SP-A-/-) or surfactant protein D-deficient (SP-D-/-) BALF, or a mixt
21 in, which evolved through duplication of the surfactant protein D gene in ruminants, prefers mannose
22 oluble tumor necrosis factor receptor-1, and surfactant protein-D) had nearly equivalent prognostic v
23 ding of three innate immune lectins, namely, surfactant protein D, human galectin-8, and Siglec-14, t
24 actor receptor 1, angiopoietin 2 (ANG2), and surfactant protein D increased in nonsurvivors, while DA
25 nt of peritoneal Mos with the lung collectin surfactant protein D inhibited AC uptake, and fluticason
28 e equivalent Arg-343 in the homologous human surfactant protein D, is sufficiently small to allow con
29 ated proteins such as endogenous eotaxin and surfactant protein D levels, which were both increased f
31 alysis, we identified four serum biomarkers (surfactant protein D, matrix metalloproteinase 7, CA19-9
32 ptor for advanced glycation end products and surfactant protein-D measurements within 24 hours (day 1
33 + carbohydrate recognition domains of human surfactant protein D (NCRD) with CL-43 (RCL-43-NCRD) and
34 re generally not inhibited by the collectins surfactant protein D or mannose binding lectin because o
35 ct of leukoreduced blood on plasma levels of surfactant protein-D or von Willebrand factor antigen wa
40 es, including von Willebrand factor antigen, surfactant protein D, protein C, plasminogen activator i
41 RATIONALE: Recombinant fragment of human surfactant protein D (rfhSP-D) has been shown to suppres
45 nary and activation-regulated chemokine, and surfactant protein D significantly increased the areas u
46 nary and activation-regulated chemokine, and surfactant protein D significantly strengthens this asso
49 tudies reveal that substantial quantities of surfactant protein D (SP-D) accumulate in the airspaces
55 collectins mannose-binding lectin (MBL) and surfactant protein D (SP-D) are regulated by tissue fibr
57 ins such as mannose-binding lectin (MBL) and surfactant protein D (SP-D) become temporarily deposited
64 m mannose-binding lectin (MBL) and pulmonary surfactant protein D (SP-D) have distinctive monosacchar
76 he recognition of influenza A virus (IAV) by surfactant protein D (SP-D) is mediated by interactions
92 previous studies documenting that pulmonary surfactant protein D (SP-D) protects C. neoformans cells
93 recognition domains (CRDs) of lung collectin surfactant protein D (SP-D) recognize sugar patterns on
102 ins, Clara cell secretory protein (CC16) and surfactant protein D (SP-D), and five systemic inflammat
104 emonstrated direct interactions of HNPs with surfactant protein D (SP-D), another important effector
105 f a collagenous C-type lectin, rat pulmonary surfactant protein D (SP-D), are sufficient to drive the
121 d, a tripartite fusion protein was made from surfactant protein D (SPD), HIV-1 Gag as a test antigen,
122 luid and in mice instilled with MAA-adducted surfactant protein D (SPD-MAA) were studied herein.
123 e was no detectable compensatory increase in surfactant protein D, the other known pulmonary collecti
124 infection, and, when combined with pulmonary surfactant protein D, their antiviral effects were addit
126 e 2-trimer form, and fusion with the body of surfactant protein D was used to produce the 4-trimer fo
130 ombinant homotrimeric fragment of human lung surfactant protein D with a series of bound ligands have