コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 following exposure to surfactant lipids and surfactant protein A.
2 l infection, and as the SP-R210 receptor for surfactant protein A.
3 ells differentiate and exhibit expression of surfactant protein A, a constituent of the surfactant la
5 on of vascular endothelial growth factor and surfactant protein A and B, but this effect was countera
6 cs were analyzed using a combination of anti-surfactant protein A and BrdU immunohistochemistry and c
7 es even though several rare proteinopathies, surfactant protein A and C deficiencies, cause severe pu
9 es specific to the pulmonary epithelium, the surfactant protein A and Clara cell secretory protein ge
10 e role in production of parturition signals, surfactant protein A and platelet-activating factor, by
12 type II pneumocyte lineage markers MUC1 and surfactant protein-A and the Clara cell lineage marker C
13 ein (endothelial permeability) and preserved surfactant proteins A and B concentrations as compared w
19 vels of expression of mRNA for antimicrobial surfactant proteins A and D and sheep beta-defensin 1 we
20 r acute lung injury, lower concentrations of surfactant proteins A and D in the pulmonary edema fluid
25 ines (e.g., transforming growth factor-beta, surfactant protein A, and angiotensin II) and a specific
26 hromatography with noncovalently immobilized surfactant protein A, and was purified from rat lung by
29 explants, immunostaining of lung tissue for surfactant protein A, B, and C, and electron microscopic
31 hosphatidylcholine expanded 54-fold, and the surfactant proteins A, B, and C expanded 144-, 4-, and 1
32 itative lipidomic analysis of lipids and the surfactant proteins A, B, and C in lavage fluids from pa
33 uding lamellar body formation, expression of surfactant proteins A, B, and C, alpha-1-antitrypsin, an
35 eolar wall thickness, cell infiltration, and surfactant protein A concentration in bronchoalveolar la
36 2 +/- 2 n/field; p < 0.0001), and normalized surfactant protein A concentration was higher with flow-
37 uid surfactant protein D and elevated plasma surfactant protein A concentrations at the onset of acut
38 B. dermatitidis without or with normal BALF, surfactant protein A-deficient (SP-A-/-) or surfactant p
45 n = 8), whereas incubation of bacteria with surfactant protein A leads to significantly increased ad
47 onary surfactant isolated from gene-targeted surfactant protein A null mice (SP-A(-/-)) is deficient
49 neumonia and viral pneumonitis had decreased surfactant protein A/protein concentration (p < .001).
50 sphingomyelin ratio (r2 = .11, p < .001) and surfactant protein A/protein concentration (r2 = .03, p
52 o M. tuberculosis and indicate that SP-D and surfactant protein A serve different roles in the innate
53 ar macrophages (AM) from female mice lacking surfactant protein A (SP-A knockouts; KO) after "rescue"
54 munosuppressed Swiss Black mice deficient in surfactant protein A (SP-A(-/-)) and wild-type control m
56 binding capability of surfactant-associated surfactant protein A (SP-A) and surfactant protein D (SP
67 nserted in the protein-coding region for the surfactant protein A (SP-A) gene, which is highly expres
68 , tandem mutagenesis of Glu195 and Arg197 of surfactant protein A (SP-A) has implicated both residues
69 We previously reported that mice lacking surfactant protein A (SP-A) have increased airway hyperr
71 The current study investigated the role of surfactant protein A (SP-A) in opsonization and clearanc
72 hypothesize a central role for the collectin surfactant protein A (SP-A) in regulating the developmen
73 onal importance of the N-terminal domains of surfactant protein A (SP-A) including the N-terminal seg
74 onization of F. novicida with lung collectin surfactant protein A (SP-A) increased bacterial associat
84 The carbohydrate recognition domain (CRD) of surfactant protein A (SP-A) is critical for the modulati
100 Mass spectrometric characterization of the surfactant protein A (SP-A) receptor 210 (SP-R210) led t
102 report we have characterized the binding of surfactant protein A (SP-A) to bone marrow-derived macro
114 KGF is known to stimulate the expression of surfactant protein A (SP-A), an oxidant-sensitive T cell
118 retion of the major lung surfactant protein, surfactant protein A (SP-A), was first detected in amnio
119 ctin family of proteins, including pulmonary surfactant protein A (SP-A), we hypothesized that SP-A m
124 roteins B and C (SP-B/C); with SP-B/C and 5% surfactant protein A (SP-A); and with SP-B/C, SP-A, and
125 ctivators 1 and 2 (SRC-1 and SRC-2) regulate surfactant protein-A (SP-A) and platelet-activating fact
126 L-1alpha caused a dose-dependent increase in surfactant protein-A (SP-A) and SP-B mRNAs (maximally, f
133 One component of this defense mechanism, surfactant protein-A (SP-A), exerts multifunctional role
134 eptor (VDR); soluble C-type lectins, such as surfactant protein-A (SP-A), SP-D, and mannose-binding l
142 ophil elastase (NE) dependent degradation of surfactant proteins A (SP-A) and D (SP-D) in lungs of mi
144 e N-terminal domains of the lung collectins, surfactant proteins A (SP-A) and D (SP-D), are critical
149 mannose-binding lectin (MBL), and pulmonary surfactant protein A (SPA) are structurally similar mole
150 mannose-binding lectin (MBL), and pulmonary surfactant protein A (SPA) interact with human monocytes
153 , plasminogen activator inhibitor-1 (PAI-1), surfactant protein-A, surfactant protein-D, and intracel
154 ry edema fluid surfactant protein D, but not surfactant protein A, was lower in patients with worse o
155 acheal aspirate surfactant phospholipids and surfactant protein A were noted in children with bacteri