ライフサイエンスコーパス: cytochemistry

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1 was investigated by means of ultrastructural cytochemistry.

2 ar architecture was examined by fluorescence cytochemistry.

3 -94 years) were cut for cytochrome c oxidase cytochemistry.

4 ar architecture was examined by fluorescence cytochemistry.

5 ssue samples were prepared for histology and cytochemistry.

6 the melanocyte nucleus by immunofluorescence cytochemistry.

7 ared to local CO activity, as revealed by CO cytochemistry.

8 a cells during subcellular fractionation and cytochemistry.

9 eoxyuridine (BrdU) was administered for BrdU cytochemistry and histology 1 hr later.

10 We employed RT-PCR, and immunohisto/cytochemistry and immunoelectron microscopy using beta-E

11 ase chain reaction, and immunohistochemistry/cytochemistry and immunoelectron microscopy using beta-e

12 Fluorescent analog cytochemistry and immunofluorescence localization of F-a

13 rocessing, we carried out immunofluorescence cytochemistry and inhibitor studies on human fetal lung

14 H(+)-ATPase were quantified using immunogold cytochemistry and morphometric analysis.

15 lasma membrane was examined using immunogold cytochemistry and showed this calcium pumping enzyme to

16 aluated by electroretinography (ERG), lectin cytochemistry, and correlative Western blot analysis of

17 analytical tool in medical diagnostics, RNA cytochemistry, and RNA aptamer development.

18 This 'fluorescent RNA cytochemistry' approach has resolved intranuclear sites

19 riking differences between rat and mouse PVN cytochemistry, but careful exploration of PVN ERbeta neu

20 ing cells or by chemical fixation and immuno-cytochemistry, but tend to increase actin bundling.

21 Ultrastructural examination using immunogold cytochemistry confirmed that activated caspase-3-positiv

22 By using immunofluorescence cytochemistry confocal microscopy of live or fixed cells

23 Immunohistochemistry and cytochemistry demonstrated active eNOS before and throug

24 Electron microscopy and immunogold cytochemistry demonstrated three distinct populations of

25 Ion capture cytochemistry detected the loss of the epidermal Ca(2+)

26 We have employed immunofluorescence, cytochemistry, fluorescent vital stains, and fluid-phase

27 Dual cytochemistry for cytochrome c oxidase and succinate deh

28 Cytochemistry for tyrosine-phosphorylated proteins was p

29 ptor mosaics visualized by anti-opsin immuno-cytochemistry in retinal wholemounts from a variety of m

30 over, results obtained from acid phosphatase cytochemistry indicated that vesicles accumulating kanam

31 This new field of 'fluorescent RNA cytochemistry' is summarized in this article, with empha

32 Quantitative cytochemistry of cytochrome oxidase (C.O.) was implement

33 mmunogold labeling of gp91(phox) and CeCl(3) cytochemistry showed the presence of gp91(phox) and oxid

34 Colony replating, immunophenotyping, and cytochemistry suggest that any perturbation of cellular

35 By immunoperoxidase electron microscopic cytochemistry, the antigen was localized to the limiting

36 th immunohistochemistry and acid phosphatase cytochemistry to better define the bacterium-host interp

37 Here we have used electron microscope cytochemistry to determine structural and functional dom

38 olytic cleavage, as well as acid phosphatase cytochemistry to identify which endocytic compartments a

39 Retrograde labeling was combined with cytochemistry to investigate phenotypic differences in p

40 Western blotting and cytochemistry used Siglec-F-Fc as a probe for directed p

41 Immunogold cytochemistry was performed on Lowicryl sections using a

42 L/Homer 1c (V-1L) immunoreactivity and TUNEL cytochemistry were used to quantify neuroprotective effe

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