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1 ochemical staining (Alizarin Red, Oil Red O, Toluidine Blue).
2 application of PDT using a 638-nm laser and toluidine blue.
3 and the result of vital staining with 0.05% Toluidine Blue.
4 sin, and semithin sections were stained with toluidine blue.
5 sections stained with Masson's trichrome and toluidine blue.
6 cut into 2-microM sections, and stained with toluidine blue.
7 reactive for tryptase and metachromatic with toluidine blue.
9 gy among patients with conjunctival lesions, toluidine blue 0.05% vital staining is a good screening
10 was followed by using three markers: acidic toluidine blue, alcian blue/safranin, and an antiserum t
12 7]uril, and two colorimetric assays based on toluidine blue and nickel complexation by pyrocatechol v
14 s were stained with hematoxylin and eosin or toluidine blue and scored for inflammation, cartilage da
17 emithin sections were prepared, stained with toluidine blue, and examined by light microscopy (LM).
18 ter extraction, teeth were stained with 0.5% toluidine blue, and subgingival debridement efficacy was
19 e EMF + CIA, cultured for 4 to 7 wks, formed toluidine-blue- and alizarin-red-stainable nodules, indi
21 macrophages/monocytes (CD14(+)), mast cells (toluidine blue(+)), dendritic cells (CD209(+)), T cells
22 application of PDT (using a 638-nm laser and toluidine blue) did not provide any additional benefit t
24 t were taken on PALM slides and stained with Toluidine Blue for laser microdissection with PALM micro
27 n of CD13 and low-level FcinRIalpha, uniform toluidine blue metachromasia, and uniform immunoreactivi
28 ode modified with a reagent layer containing toluidine blue O (TBO mediator), beta-hydroxybutyrate de
29 NMB), 1,9-Dimethyl Methylene Blue (DMMB) and Toluidine Blue O (TBO) on N. caninum, using in vitro and
30 eta-amino esters (PBAEs) in combination with toluidine blue O (TBO) to shorten aPDT exposure time.
31 related compounds new methylene blue (NMB), toluidine blue O (TBO), and dimethylmethylene blue (DMMB
33 e set that propelled the aqueous solution of toluidine blue O dye into a porous media (melamine foam)
36 or made by the electropolymerization of poly(toluidine blue O) (PTB) and glucose oxidase (GOx) with a
37 vity relationship analysis demonstrated that toluidine blue O, an MB derivative with similar bioenerg
38 rocedures for staining plastic sections with toluidine blue or hematoxylin and eosin, and show how to
39 ween 1 and 15 years of age were stained with toluidine blue or immunolabeled with a variety of glia-
40 ctions of rat Achilles tendons, stained with toluidine blue or Masson's trichrome, were examined in a
41 contrast in the image, aqueous solutions of toluidine blue or methylene blue were topically applied
42 tation was unable to grow in the presence of toluidine blue or on glycerol minimal media in the prese
45 articular cartilage matrix (by retention of toluidine blue stain) were determined in histology secti
47 ell distribution and number were assessed by toluidine blue staining and analyzed by Student's t-test
52 infiltration and MC markers were detected by toluidine blue staining and real-time PCR in human biops
53 ne immunocytochemistry on thin sections, and toluidine blue staining of adjacent sections, we establi
58 by articular cartilage structure and loss of toluidine blue staining scores) also was significantly a
61 rier for the immobilization of electroactive toluidine blue (Tb), hemin/G-quadruplex formed by interc
62 el-free electrochemical immunosensor using a toluidine blue (TB)/porous organic polymer (POP)/two-dim
65 bodies of DUM interneurons were stained with Toluidine blue, whereas only three male DUM interneurons