戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  of representative cross-sections of a large number of specimens.
2 ative analysis of gene expression on a large number of specimens.
3 ive impact on both species diversity and the number of specimens.
4 ractical for use for the processing of large numbers of specimens.
5 used on very short notice to process a large number of specimens (3,936 swabs) in order to report pre
6                              Despite a large number of specimens and distinct anatomy, various analys
7 ns of tandem repeats within this locus for a number of specimens and isolates.
8 suming, especially when applied to the large number of specimens and taxa commonly included in ecolog
9 skin disinfection, collection of an adequate number of specimens and volume of blood, and prompt proc
10 have imposed constraints on the size, shape, number of specimens, and compatibility with various clea
11 tion, approach path, pleural puncture count, number of specimens, and presence of emphysema along the
12 nt drawback for laboratories receiving large numbers of specimens, as only a single sample can be pro
13  among resampling methods are reduced as the number of specimens available increase.
14  trapping can result in the capture of large numbers of specimens awaiting identification.
15 being performed, the methods being used, the number of specimens being processed, and the times to co
16                                          The number of specimens during the evaluation period ranged
17 though anelloviruses were present in a large number of specimens from both febrile and afebrile patie
18 ons as infected or uninfected, a substantial number of specimens from infected persons may be referen
19                                  The greater number of specimens generated by the increased emphasis
20             This approach breaks down as the number of specimens grows and fails to reliably characte
21 bspecific classification, but only a limited number of specimens have been available for examination,
22 od, patients have become older, and a higher number of specimens have been submitted from female pati
23 ; however, only a few studies with a limited number of specimens have focused on primary melanomas.
24 assay throughput to allow testing of a large number of specimens in a single run.
25 unt of time that it took to analyze the same number of specimens in tubes with PVA-formalin.
26 dent sequencing, significantly more than the number of specimens in which bacteria were detected (37
27 ery (59.4 versus 56.4 years, P < 0.0001) The number of specimens increased with patient age from the
28 around time for laboratories analyzing small numbers of specimens (&lt; 10 per batch) submitted for IgM
29 s varied between the states with the largest number of specimens, New Jersey, Florida, and Texas.
30              Diagnostic yield increased with number of specimens obtained and with longer specimen le
31                                   The median number of specimens obtained per lesion was 12 (mean, 14
32 iopsy needle gauge, image guidance modality, number of specimens obtained, and specimen length (< 5,
33 re reviewed and correlated with lesion size, number of specimens obtained, and type of SVAB probe use
34  summary, this study, performed on a limited number of specimens of this protected species, indicated
35   Finally, IRF-4 is expressed in significant numbers of specimens of primary central nervous system (
36  of variables for problems involving a large number of specimens or complex shapes.
37 82) of microcalcifications (P <.001); and by number of specimens per lesion, 17.5% (88 of 502) with 1
38                                          The number of specimens positive only by PCR among specimens
39 ends on factors such as costs related to the number of specimens processed rather than on the minimal
40 ractices, thus reducing the overall cost and number of specimens processed.
41 were restricted to 1 province and the annual number of specimens ranged from 91 to 534.
42                                  The minimum number of specimens required to obtain a diagnosis was d
43            During six decades, the growth in number of specimens sent to our national referral center
44                         Because of the small numbers of specimens tested, we were unable to draw any
45 n be rapidly identified while minimizing the number of specimens that must be tested.
46                         Applied to the total numbers of specimens, this yielded an estimated 240 000
47                               Increasing the number of specimens to five or more, per current recomme
48 e rabbit cornea, and the size of the defect, number of specimens with complete re-epithelialization,
49                  The size of the defect, the number of specimens with complete reepithelialization, a
50 acid extraction system that can handle small numbers of specimens with a short test turnaround time a