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1 ape of a ring of cells that stained red with Safranin.
2                           We have found that safranin also inhibits hGR in a noncompetitive fashion,
3  markers: acidic toluidine blue, alcian blue/safranin, and an antiserum to gonadotropin-releasing hor
4 pared hybrid system of GC/MWCNTs-NH2/Den/GDH/Safranin as anode in a membraneless enzyme-based glucose
5                                 We report on safranin-based stain that uniformly stains oocysts of Cy
6 -phenazinium chloride (safranin) showed that safranin bound at this same site.
7 es in young animals to mixed alcian blue and safranin granules in older animals, and an increase in G
8  of 200 kDa) were colored with two red dyes, Safranin O and Pararosanilin, selected to block the exci
9                          Cartilage damage on safranin O histologic slides was quantified with Osteoar
10 s of cartilage proteoglycan (aggrecan) using Safranin O staining and antibodies to neoepitopes genera
11 stochemistry revealed a dramatic decrease in Safranin O staining and reduced anti-aggrecan staining (
12 lied to demonstrate morphologic changes, and Safranin O staining was performed to analyze the relatio
13 radation, and loss of glycosaminoglycans (by Safranin O staining).
14 dimethylmethylene blue assay, histology with Safranin O staining, and immunohistochemistry with anti-
15 an content was determined by alcian blue and Safranin O staining, CD44 protein expression by immunohi
16 , samples underwent histologic analysis with safranin O staining.
17 cans and profoundly reduced the intensity of Safranin O staining.
18      Only repetitive loading induced loss of Safranin O staining.
19 nt of glucose dehydrogenase (GDH) enzyme and safranin O to amine-derivative multiwalled carbon nanotu
20 by ATP in permeabilized cells as measured by safranin O uptake.
21 plasma membrane permeable to succinate, ADP, safranin O, and other small molecules.
22 endochondral ossification as demonstrated by Safranin O, Picrosirius red, and aniline blue staining.
23 genic histological analysis was performed by Safranin O, Picrosirius red, and aniline blue staining.
24      Histologic analysis was performed using Safranin O-fast green staining, and articular cartilage
25 ted surface layer of variable thickness with Safranin O-positive formations sometimes present, a roug
26                                     However, Safranin O-stained sections from the Jnk2(-/-) mice exhi
27                      The loss of aggrecan in Safranin O-stained sections was quantified by morphometr
28                                              Safranin O-staining revealed that cellular constructs de
29 ubricin-specific monoclonal antibody 9G3 and Safranin O.
30                                              Safranin-O staining shows that tissue-engineered cartila
31 -2,8-dimethyl-5-phenyl-phenazinium chloride (safranin) showed that safranin bound at this same site.
32 d full fluorescence, modified acid-fast- and safranin-stained smears of Cryptosporidium and Cyclospor
33 (ii) in modified acid-fast-, trichrome-, and safranin-stained smears, and (iii) with two commercial t
34 ocedures, such as the modified acid-fast and safranin stains, are generally employed.
35 hromotrope, Gram-chromotrope, acid-fast, and safranin stains.

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