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1 small neuronal subsets provided a Golgi-like vital stain.
2 asure by using triphenyltetrazolium chloride vital staining.
3 k-up time, Schirmer test, and ocular surface vital staining.
4              Heart tissue was evaluated with vital staining and histologic examination.
5 regions were fully contractile and viable by vital staining and microscopy but demonstrated 25% reduc
6                     We have used a series of vital stains and other cytological methods to analyze sp
7         Corneas were stained with Richardson vital stain, and the wound area was recorded.
8 munofluorescence, cytochemistry, fluorescent vital stains, and fluid-phase markers in conjunction wit
9                                          The vital stain approach used in the present study will perm
10                                              Vital staining assays demonstrated that low concentratio
11                                    Using the vital stain FM 4-64 to label the plasma membrane of livi
12      Evans blue (EB) dye was injected as the vital stain for cardiomyocyte injury.
13 }-6-aminocaproyl-d-erythro-sphingos ine as a vital stain for chlamydiae proved to be a sensitive meth
14         The fluorescent C(6)-NBD-ceramide, a vital stain for the Golgi apparatus, did not stain these
15 n, or beta-COP (a specific golgi protein) or vital stains for endoplasmic reticulum (ER) and golgi.
16 orofluorescein diacetate (a vacuolar luminal vital stain), had a pronounced shift in red/green fluore
17                                              Vital staining indicates that the side of the embryo tha
18 h conjunctival lesions, toluidine blue 0.05% vital staining is a good screening tool.
19  escape, we followed acidification using the vital stain LysoTracker red and acquisition of the proto
20                                              Vital staining of clustered embryos demonstrates that th
21  endplates (pi-junctions) were identified by vital staining of lateral plantar nerve (LPN) and sural
22 with high synaptic density as ascertained by vital staining of recycling synaptic vesicles, and were
23                               Intraoperative vital staining of retinal breaks is possible in an anima
24 , peeling of the internal limiting membrane, vital staining of the internal limiting membrane with in
25                In the present study, we show vital staining of transgene expression in living cardiac
26      Class II AMPs cause rapid influx of the vital stain SYTOX and an increase in intracellular Ca2+,
27      The primary aim of this work was to use vital stain techniques for real-time detection of develo
28 This approach makes use of a lineage-tracing vital stain that is retained through cell generations an
29 expressed with Bax, little cell death and no vital staining were observed.
30                                              Vital staining with 0.05% Toluidine blue dye did not dis
31  to conjunctival papilloma and the result of vital staining with 0.05% Toluidine Blue.
32  nature of this compartment was confirmed by vital staining with a pH sensitive dye, LysoSensor yello
33                                              Vital staining with Evans blue dye revealed loss of sarc
34                                              Vital staining with Evans blue dye revealed that muscle
35 ata on new techniques and technology such as vital staining with methylene blue and protoporphyrin fl
36 ia compressa zygotes were investigated using vital staining with rhodamine phalloidin (RP).
37 try, scanning electron microscopy (SEM), and vital staining with tetracycline-HCl.
38                                              Vital staining with toluidine blue 0.05% aqueous solutio
39 duces muscle membrane damage, as revealed by vital staining (with Evans blue dye) of the diaphragm an