ライフサイエンスコーパス: cytochemical

1 and mMCP-6 in both populations of cells, and cytochemical analysis confirmed the presence of chymotry

2 Cytochemical analysis demonstrates that high-mannose-con

3 eus, a finding that was further supported by cytochemical analysis.

4 Using both cytochemical and biochemical analyses, we find that the

5 Cytochemical and flow cytometric analysis confirmed that

6 Characterization (cytochemical and immunofluorescence) of the reticular/fi

7 Cytochemical and in vitro whole-cell patch clamp techniq

8 Together, these morphological, cytochemical, and physiological data suggest that the di

9 sitive assay systems, possibly formatted for cytochemical applications.

10 ntration with high temporal resolution and a cytochemical approach to determine glycogen stores in si

11 d 0.27 nm) were inactive in both the in situ cytochemical assay (IC(50) > 1 micrometer) and the osteo

12 hibitor was further studied using an in situ cytochemical assay for bafilomycin-sensitive V-H(+)-ATPa

13 r level, which can be assessed with standard cytochemical biomarkers and polarized light microscopy f

14 ed incorporating histological assessment and cytochemical biomarkers of toxic effects and early warni

15 hese findings provide the first quantitative cytochemical data of C.O. activity in humans.

16 s were examined in vitro for biophysical and cytochemical evidence of cardiogenic differentiation.

17 This cytochemical evidence strongly suggests that resting ast

18 Fluorescence and immuno-cytochemical experiments show that high-iron-grown organ

19 cardiovascular tissue is thought to involve cytochemical, extracellular matrix and systemic signals;

20 ve inhibitor was potently active in both the cytochemical (IC(50) = 63 nm) and resorption (IC(50) = 7

21 ophysiological characterization, rather than cytochemical identification.

22 cytokine cocktails as shown by morphologic, cytochemical, immunophenotypical, clonogenic, and gene e

23 therefore, uses topographic, structural, and cytochemical information from the rat to recognize corre

24 Unilateral electrolytic or cytochemical lesions placed in the thalamic ventrobasal

25 on of cells that had nonspecific esterase, a cytochemical marker for macrophages.

26 Specific antibodies and cytochemical markers combined with several imaging and m

27 cific vasculitic disorder and the underlying cytochemical mechanism of pathogenesis.

28 s as a result of the retrograde transport of cytochemical mediators released during the inflammatory

29 Three different cytochemical methods were used to detect acetylcholine i

30 Moreover, using cytochemical procedures, it was also shown that megalin

31 rature appear to be caused by differences in cytochemical protocols, rather than the biological reaso

32 areas, despite the extensive structural and cytochemical reorganization of the peripheral endings of

33 We conclude that past cytochemical reports of blood-brain barrier (BBB) Na+, K

34 y expression of types II and IX collagen and cytochemical staining for Alcian blue.

35 Cytochemical staining of cellular DNA with 4,6-diamidino

36 BMCMC in SCF exhibited cytochemical staining properties, protease and histamine

37 hich on the basis of electron microscopy and cytochemical staining seem to be lysosomal in origin.

38 e, thus eliminating the need for antibody or cytochemical staining to detect its expression.

39 Using cytochemical staining to detect vAc64z infected cells, w

40 ssayed for enzyme activity either by in situ cytochemical staining with a post-azo-coupling method us

41 for erythroid and myeloid progenitor cells), cytochemical staining, and mixed leucocyte reactions to

42 Cytochemical stains (Fontana-Masson, Prussian blue) and

43 Cytochemical studies confirmed that the distribution of

44 Cytochemical studies demonstrated that the distribution

45 Past basic and clinical cytochemical studies of BBB Na+, K+-ATPase should be vie

46 Biochemical and cytochemical studies reveal that cyclodextrin specifical

47 t there have been contrary reports from some cytochemical studies.

48 their ligands appear likely to provide the 'cytochemical tags' that Sperry speculated enable axons p

49 Immunogold cytochemical techniques were applied to ultrathin cryose

50 bieneusi by PCR, in situ hybridization, and cytochemical techniques.

51 Cytochemical visualization of catalase using diaminobenz