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Unteers' lung found significant decreases in levels of SP-A [28]. Unfortunately, there was little overlap in the sets of identified proteins between our studies and therefore little basis for comparison. When the DEF and RED proteins are individually examined as subgroups of the identified proteins, the changes are similar to those noted for all proteins. In both of these groups of proteins, more
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Eduction in their synthesis remains to be determined. b) Strain differences at 24 hr after infection Extending the analysis to mice infected 24 hr earlier we gained some additional insight into the response pattern. Three gen-Ali et al. Proteome Science 2010, 8:34 http://www.proteomesci.com/content/8/1/Page 10 ofTable 2: Changes in protein expression between wild-type and SP-A-/- mice for control,
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(?- or -shaped response pattern) toward the levels seen under baseline conditions, suggesting a peak response at 4 hr(or at least earlier than 24 hr). 3) In a third set (n = 5), levels of some proteins at 24 hr were continuing to either increase or decrease from levels seen at 4 hr, suggesting slower and/or more sustained responses to infection. With respect to all identified proteins, the ratio
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(CC16) Ceruloplasmin isoforms Chain A, The Crystal structure of novel mammalian lectin Ym1-suggests a saccharide binding site Chain B, Chimeric human mouse carbonmonoxyhemoglobin (Human zeta, Mouse beta 2) Chia protein Coiled-coil domain containing 122 Contrapsin (Serine protease inhibitor A3K) Creatine kinase M-type (EC.2.7.3.2) (Creatine kinase M chain) (M-CK) (Similar to) Ferritin light chain 1
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Al 10 (Cytokeratin-10) (CK-10) (Keratin-10) Lysozyme 2 Peroxiredoxin 6 Pregnancy zone protein SEC14-like 3 Toll-like receptor 13 precursor Transferrin Accession No. P07724 Q3UCL0 P48036 Q58EV2 P60709 Q80XP1 P06684 P14152 P63260 Q60574 O88844 A2A513 P08905 Q6GT24 Q61838 Q5SQ27 Q6R5N8 Q921I1 WT -3.61 3.05 23.19 -166.30 11.33 5.47 12.19 2.02 0.67 1.80 10.70 24.80 4.36 4.30 5.37 8.92 -4.87 -12.29
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Infection, typically increases, in both strains of mice (Table 3). The first group of note includes betaactin, myosin IIB (a non-muscle myosin), creatine kinase M, and Rho GDP dissociation inhibitor-alpha. All of these are proteins that play a role in phagocytosis [36] and are increased in both strains. These increases could be related to the presence of increased numbers of phagocytic cells to co

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