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1 directly observed by electron microscopy of ultrathin sections.
2 nal fibers were closely studied in series of ultrathin sections.
3 me FP-labeled sieve elements in semithin and ultrathin sections.
4 nization (NALDI) targets without blotting or ultrathin sections.
6 tina was studied by reconstruction of serial ultrathin sections and compared with ON parasol cells st
7 eactivity occurred at sites which, in single ultrathin sections, appeared to be nonjunctional sites o
8 ls on motoneurones were identified on serial ultrathin sections at electron-microscopic level using a
10 total Glut4 immunogold reactivity in muscle ultrathin sections by up to 1.8-fold and dramatically in
11 microscopy, negatively stained whole cells, ultrathin-sectioned cells, and freeze-etched and frozen
12 ere, we used improved staining and automated ultrathin sectioning electron microscopy methods to anal
13 icroscopy, or electron micrographs of single ultrathin sections imaged by transmission electron micro
15 graphy, a microscopy technique that combines ultrathin sectioning of tissue with immunofluorescence a
16 array tomography, a technique that combines ultrathin sectioning of tissue with immunofluorescence,
17 ers of inflammatory cells were determined in ultrathin sections of endobronchial biopsies obtained fr
18 rations as well as 3D electron microscopy of ultrathin sections of high-pressure frozen and freeze-su
20 munogold staining for GLUT1 was performed on ultrathin sections of retinal specimens obtained from 1-
22 shape and apposition to collagen fibrils in ultrathin sections of the same tissues examined by trans
24 mined by transmission electron microscopy of ultrathin sections, of freeze-etched replicas, and of wh
25 on microscopy (EM) of negatively stained and ultrathin-sectioned organisms failed to identify a typic
26 cryo-electron tomography, and tomography of ultrathin sections reveals that the magnetite crystals a
27 more, we show through immunogold labeling of ultrathin sections that P64 is a component of virogenic
28 mbedding Glu immunocytochemistry on the same ultrathin sections, the simultaneous distribution of the
30 bedding GABA immunocytochemistry on the same ultrathin sections, was used to reveal simultaneously th
31 hree-dimensional reconstructions from serial ultrathin sections, we found that SV size did not correl
32 ssues were freeze-plunge embedded and serial ultrathin sections were collected on slot grids for immu
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