ライフサイエンスコーパス: FTA

1 FTA loaded HNPs were prepared, characterized and evaluat

2 rength cutoffs correlating with at least 95% FTA-ABS reactivity.

3 fluorescent treponemal antibody absorption (FTA Abs) assays.

4 fluorescent treponemal antibody absorption (FTA-ABS) IgG assay were evaluated by the CAPTIA EIA.

5 fluorescent treponemal antibody absorption (FTA-ABS) tests.

6 fluorescent treponemal antibody-absorption (FTA-ABS) test.

7 fluorescent treponemal antibody absorption [FTA-ABS] test, and Inno-LIA line immunoassay).

8 umor efficacy of farnesylthiosalicylic acid (FTA) loaded (lipid-cationic) lipid-PEG-PLGA hybrid nanop

9 encing protocols for poliovirus isolates and FTA cards using next-generation sequencing (NGS), aiming

10 other discrepant sample (CAPTIA negative and FTA-ABS positive [at an intensity of 3+], unblinded) was

11 icated that one patient (CAPTIA negative and FTA-ABS positive [minimally reactive], blinded) had poss

12 lieu of confirmatory testing with TP-PA and FTA-ABS.

13 s (1) with active syphilis (reactive RPR and FTA-ABS) and (2) without current syphilis (nonreactive R

14 We found evidence of CIA, TPPA, and FTA Abs seroreversion.

15 cules, CA], fluorescent treponemal antibody [FTA] assay [Zeus Scientific, Raritan, NJ], Treponema pal

16 ssay [TPHA]/fluorescent treponemal antibody [FTA] positive) and low-titer (n=249; RPR titer <1:8 and

17 fter a treatment period of 5days, IN applied FTA loaded HNPs achieved a significant decrease of 55.7%

18 of 55.7% in tumor area, equal to IV applied FTA loaded HNPs.

19 ort of PFASs at a former fire training area (FTA) on Cape Cod, Massachusetts, where PFAS-containing a

20 15) but lower than for sera reactive on both FTA Abs and TPPA assays (12.37; P < .001) or for sera re

21 amples that were persistently nonreactive by FTA-ABS test.

22 %) converted from nonreactive to reactive by FTA-ABS test; 4 (3.6%) were reactive by FTA-ABS tests bu

23 e by FTA-ABS test; 4 (3.6%) were reactive by FTA-ABS tests but later became nonreactive.

24 ent treponemal antibody absorption test (CSF-FTA-ABS) and a reactive CSF-TPPA did not differ signific

25 A sera and sera that were reactive on either FTA Abs or TPPA assays (2.19 vs 2.32; P = .15) but lower

26 eement ranged from 86.1% (83.7 to 88.2%) for FTA-ABS to 99.7% (99.0 to 99.9%) for Advia-Centaur CIA;

27 , the ability to obtain full PV genomes from FTA cards will aid in facilitating global poliovirus sur

28 AtGGT-IA/FTA and AtGGT-IB were co-expressed in baculovirus-infect

29 ly available nonsolvable cellulose material (FTA DMPK-C card).

30 d the potential utility of IN application of FTA loaded HNPs as a non-invasive approach in glioblasto

31 NA in whole blood collected on filter paper (FTA Card) was evaluated.

32 5 repeated doses of 500muM freshly prepared FTA loaded HNPs via IN or intravenous (IV) application.

33 es between results were resolved by repeated FTA-ABS testing (technologists were blinded to previous

34 uggest that some BFP reactions may represent FTA-negative syphilis.

35 ycopersicon esculentum) FTase alpha-subunit (FTA) as bait.

36 The FTA-ABS IgG procedure was performed by technologists unb

37 sults indicate that unsaturated zones at the FTA and at hydraulically downgradient former domestic wa

38 S composition near the water table below the FTA and wastewater-infiltration beds.

39 ted (unblinded) as minimally reactive by the FTA method were subsequently interpreted (blinded) as no

40 require subjective interpretation, like the FTA-ABS test, may be biased by RPR test results.

41 g downgradient transect originating near the FTA and analyzed for PFAS content.

42 Compared to the FTA assay as the gold standard, the evaluated treponemal

43 Compared to the FTA-ABS assay, the CAPTIA EIA had a sensitivity and spec

44 R test reactive at a dilution >1:8 while the FTA-ABS test remained nonreactive.

45 nd low-titer (n=249; RPR titer <1:8 and TPHA/FTA positive) active syphilis and 950 uninfected women.

46 tive [at an intensity of 3+], unblinded) was FTA negative with repeated testing (blinded).

47 coveries than the procedure used for Whatman FTA DMPK-A, but the time needed for sample preparation w

48 uccal swab samples were collected on Whatman FTA cards and mailed by post for analysis.

49 uccal swab samples were collected on Whatman FTA cards and were mailed by post for analysis.

50 ) and blood (23 horses) spotted onto Whatman FTA cards.

51 commercial cards was also performed (Whatman FTA DMPK and Agilent Bond Elut DMS) using elution proced

52 pyrosequencing was combined with the Whatman FTA paper technology for the rapid extraction of fungal