ライフサイエンスコーパス: Giemsa

1 Giemsa stain revealed that BI were aggregates of mesench

2 itivity of 54% and a specificity of 87%; and Giemsa stain (> 2% ICO) had a sensitivity of 46% and a s

3 tide composition, of different isochores and Giemsa light and Giemsa dark bands.

4 of different isochores and Giemsa light and Giemsa dark bands.

5 immunofluorescence, electron microscopy, and Giemsa staining.

6 is correlated with subtelomeric regions and Giemsa-light bands (R bands).

7 high-resolution molecular karyotype arrays, Giemsa banding (G-banding) and fluorescent in situ hybri

8 at a dosage of 10 mg/kg/day as determined by Giemsa-stained organ impression smears.

9 the cultures were monitored for infection by Giemsa staining and PCR.

10 osinophils, they were purified (>95% pure by Giemsa-stained cytospin preparations) from liver granulo

11 the Apis mellifera karyotype as revealed by Giemsa stain.

12 S technique is approximately 400 chromosomal Giemsa bands, the data presented here provide the first

13 PCR-HRM analysis of DNA extracts from Giemsa-stained thick blood smears or corresponding blood

14 Gram, Giemsa, calcofluor white, and acridine orange stains and

15 by flow cytometric analysis and May-Grunwald Giemsa staining.

16 films stained with Wright's or May-Grunwald-Giemsa, determination of blood counts, platelet size and

17 Biopsy-based tests (i.e., culture, histology Giemsa stain and rapid urease test) and non-invasive tes

18 s with atrophy, the sensitivity of histology Giemsa stain was 100%, 100%, 88%, and 66%, respectively,

19 e frequency of induced chromatid breakage in Giemsa-stained preparations was determined.

20 Morphology of the parasite was confirmed in Giemsa-reagent stained blood smears for the Type I sampl

21 aplasma-like inclusions were demonstrated in Giemsa-stained culture samples.

22 hin 2 weeks, infected cells were detected in Giemsa-stained culture samples, and the organisms subseq

23 icroscopic identification of the organism in Giemsa-stained thin blood smears, detection of babesial

24 ted 4 to 5 hours earlier than it was seen in Giemsa-stained preparations and 8 hours earlier than it

25 ed by six different procedures that included Giemsa, trichrome, chromotrope, Gram-chromotrope, acid-f

26 Standard malaria diagnosis is Giemsa stained peripheral blood smear but false negative

27 in regions of high GC, and in R and lightest Giemsa bands.

28 H&E staining for histology and modified Giemsa staining for the detection of H. pylori was condu

29 ted PCR assay and microscopic examination of Giemsa-stained blood films for detection and identificat

30 d objective supplement to the examination of Giemsa-stained blood smears and may replace microscopy f

31 nal method, i.e., microscopic examination of Giemsa-stained lesion scraping (46.7%), biopsy culture (

32 ts for duplicate microscopic examinations of Giemsa-stained blood smears as the reference diagnostic

33 roperties of cells, morphological studies of Giemsa-stained cells, annexin V binding, and DNA fragmen

34 was as sensitive and specific as the use of Giemsa-stained blood smears and inoculation of hamsters.

35 ency of infected red blood cells assessed on Giemsa-stained blood smears.

36 Parasitemia was monitored on Giemsa-stained blood smears or by flow cytometry.

37 now been coupled with the fluorescence-plus-Giemsa method of Perry and Wolff to produce harlequin en

38 se bands showed this more than the gene-poor Giemsa dark bands, and morphometric analyses demonstrate

39 sex-mismatched transplants using a two-step Giemsa/fluorescence in situ hybridization assay on isola

40 We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us t

41 s of blood from infected mice stained by the Giemsa or the indirect immunofluorescence method, numero

42 1 lie distally, near the lower border of the Giemsa band adjacent to the distal one-third of CFA9.

43 btained by reading 100 fields of traditional Giemsa-stained thick-smear blood films.

44 Microscopic diagnosis of malaria using Giemsa-stained blood smears is the standard of care in r

45 ure was monitored by staining the cells with Giemsa and quantifying the wound area with SigmaS can co

46 mated blood culture, malaria microscopy with Giemsa-stained blood films, and human immunodeficiency v

47 from three slides, two of them stained with Giemsa (on which Plasmodium parasites could still be see

48 id and in the pouch wall after staining with Giemsa or after enzymatic digestion followed by fluoresc

49 raphs of hematologically stained (eg, Wright-Giemsa) examples of mouse basophils exist in the literat

50 We observed, using Wright-Giemsa and 4',6-diamidine-2-phenylindole-dihydrochloride

51 cted STAT1(-/-) mice and stained with Wright-Giemsa had basophil characteristics.