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 Here, we use
cytochemical,
microscopic, and transgenic assays in D. m
31 Moreover, using
cytochemical procedures, it was also shown that megalin
32 rature appear to be caused by differences in
cytochemical protocols, rather than the biological reaso
33 areas, despite the extensive structural and
cytochemical reorganization of the peripheral endings of
34 We conclude that past
cytochemical reports of blood-brain barrier (BBB) Na+, K
35 y expression of types II and IX collagen and
cytochemical staining for Alcian blue.
36 Cytochemical staining of cellular DNA with 4,6-diamidino
37 BMCMC in SCF exhibited
cytochemical staining properties, protease and histamine
38 hich on the basis of electron microscopy and
cytochemical staining seem to be lysosomal in origin.
39 e, thus eliminating the need for antibody or
cytochemical staining to detect its expression.
40 Using
cytochemical staining to detect vAc64z infected cells, w
41 ssayed for enzyme activity either by in situ
cytochemical staining with a post-azo-coupling method us
42 for erythroid and myeloid progenitor cells),
cytochemical staining, and mixed leucocyte reactions to
43 Cytochemical stains (Fontana-Masson, Prussian blue) and
44 Cytochemical studies confirmed that the distribution of
45 Cytochemical studies demonstrated that the distribution
46 Past basic and clinical
cytochemical studies of BBB Na+, K+-ATPase should be vie
47 Biochemical and
cytochemical studies reveal that cyclodextrin specifical
48 t there have been contrary reports from some
cytochemical studies.
49 their ligands appear likely to provide the '
cytochemical tags' that Sperry speculated enable axons p
50 Immunogold
cytochemical techniques were applied to ultrathin cryose
51 bieneusi by PCR, in situ hybridization, and
cytochemical techniques.
52 Cytochemical visualization of catalase using diaminobenz