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 y a microleakage-testing device and confocal laser scanning microscope.
2 examined under light microscope and confocal laser scanning microscope.
3 -combined CPNE7 was confirmed under confocal laser scanning microscope.
4          Tissue was examined with a confocal laser scanning microscope.
5 nyl compounds were detected using a confocal laser scanning microscope.
6 -labeled neurons was mapped using a confocal laser-scanning microscope.
7 sses from single-color images collected with laser scanning microscopes.
8 tion (MSM) levels and visualized by confocal laser scanning microscope before being characterized by
9 anding wave can be produced in a single-spot laser scanning microscope by placing a plane reflector c
10  tissue sections were examined on a confocal laser scanning microscope by using dual channel immunofl
11 ining fluorophores that can be imaged with a laser scanning microscope can be analyzed using RICS.
12           Here, we show that the multiphoton laser-scanning microscope can provide high three-dimensi
13   The technique is implemented in a confocal laser scanning microscope (CLSM), thus allowing not only
14 ation microscopy data acquired on a confocal laser scanning microscope (CLSM), which will enable user
15 ere stained and examined whole in a confocal laser scanning microscope (CLSM).
16 y after photobleaching (FRAP) using confocal laser scanning microscopes (confocal FRAP) has become a
17                       Images obtained with a laser-scanning microscope contain a time structure that
18     Membrane repair assays with a two-photon laser-scanning microscope demonstrated that wild-type mu
19                                 Multi-photon laser scanning microscopes have many advantages over sin
20 onsistent with the size observed in Confocal Laser Scanning Microscope images.
21 scence measurements obtained with a confocal laser scanning microscope in biofilms: 1) linear drift,
22  Layer V neurons were imaged on a two-photon laser scanning microscope in fixed tissue sections.
23                 Although the introduction of laser-scanning microscopes in principle could facilitate
24 rized including sequential registration with laser scanning microscopes, line imaging and global or w
25                                            A laser scanning microscope (LSM) with a supercontinuum la
26 ed with the software packaged with the Zeiss laser-scanning microscope (LSM AIM, version 3.2).
27 on of a plane mirror to an existing confocal laser scanning microscope, may well prove useful in stud
28                Compared to standard confocal laser scanning microscope, MUM offers a clear advantage
29  skin model with a near-infrared multiphoton laser-scanning microscope (NIR-MPLSM).
30 ld nanorods excited at 830 nm on a far-field laser-scanning microscope produced strong two-photon lum
31          Time-lapse analysis with a 2-photon laser scanning microscope revealed that the growth cones
32    Membrane repair assays using a two-photon laser-scanning microscope revealed that calpain 4-defici
33  giant unilamellar vesicles under a confocal laser scanning microscope show that a family of thermall
34       Optical sections taken with a confocal laser-scanning microscope showed that the Lewis antigen
35 nofluorescence localization under a confocal laser-scanning microscope, the BIS3 protein in the trans
36  imaging method can be applied to commercial laser scanning microscopes thereby making it accessible
37 ense illumination, such as at the focus of a laser-scanning microscope, these SHG nanocrystals conver
38 rom-thick plastic sections and with confocal laser scanning microscope, thus further supporting the f
39 ical modifications that need to be made to a laser-scanning microscope to enable the measurements.
40 s easily integrated into standard two-photon laser-scanning microscopes to generate an axially elonga
41 ges with an Olympus FluoView FV1000 confocal laser scanning microscope using Olympus FluoView softwar
42  approximately 8000 lines s-1), although the laser scanning microscope was limited to < 1000 lines s-
43                                   A confocal laser scanning microscope was used for detection.
44                                By adapting a laser scanning microscope with a titanium sapphire femto
45 an be easily implemented on a Leica confocal laser scanning microscope, with better photon efficiency
46                            The Olympus IV100 Laser Scanning Microscope, with ultra-narrow microscope