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1 h transmission electron microscopy on serial ultrathin sections.
2  directly observed by electron microscopy of ultrathin sections.
3 nal fibers were closely studied in series of ultrathin sections.
4 me FP-labeled sieve elements in semithin and ultrathin sections.
5 nization (NALDI) targets without blotting or ultrathin sections.
6                                       Serial ultrathin section analysis and 3D reconstructions reveal
7 tina was studied by reconstruction of serial ultrathin sections and compared with ON parasol cells st
8 eactivity occurred at sites which, in single ultrathin sections, appeared to be nonjunctional sites o
9 ls on motoneurones were identified on serial ultrathin sections at electron-microscopic level using a
10 in, and their axons were analyzed in serial, ultrathin sections by electron microscopy.
11  total Glut4 immunogold reactivity in muscle ultrathin sections by up to 1.8-fold and dramatically in
12  microscopy, negatively stained whole cells, ultrathin-sectioned cells, and freeze-etched and frozen
13 ere, we used improved staining and automated ultrathin sectioning electron microscopy methods to anal
14 icroscopy, or electron micrographs of single ultrathin sections imaged by transmission electron micro
15                                       IEM of ultrathin-sectioned, intact treponemes also demonstrated
16 graphy, a microscopy technique that combines ultrathin sectioning of tissue with immunofluorescence a
17  array tomography, a technique that combines ultrathin sectioning of tissue with immunofluorescence,
18 We analyzed microglia in a volume of serial, ultrathin sections of central macaque retina in which ma
19 ers of inflammatory cells were determined in ultrathin sections of endobronchial biopsies obtained fr
20 rations as well as 3D electron microscopy of ultrathin sections of high-pressure frozen and freeze-su
21 opy and gold labeling electron microscopy on ultrathin sections of PM sheets.
22 munogold staining for GLUT1 was performed on ultrathin sections of retinal specimens obtained from 1-
23 n 10 samples, each containing 32 consecutive ultrathin sections of the entire neuroepithelium.
24  shape and apposition to collagen fibrils in ultrathin sections of the same tissues examined by trans
25 ruses by transmission electron microscopy of ultrathin sections of tissues or infected tissue culture
26 ic antibodies, which reacted with virions in ultrathin sections of VZV-infected cells.
27 mined by transmission electron microscopy of ultrathin sections, of freeze-etched replicas, and of wh
28            The non-destructive collection of ultrathin sections on silicon wafers for post-embedding
29 on microscopy (EM) of negatively stained and ultrathin-sectioned organisms failed to identify a typic
30  cryo-electron tomography, and tomography of ultrathin sections reveals that the magnetite crystals a
31                                              Ultrathin sections scanned with super-resolution STED mi
32 s were reconstructed from a volume of serial ultrathin sections taken 2 mm temporal to the centre of
33      Here, we show by immunogold labeling of ultrathin sections that enzymes involved in autotrophic
34 more, we show through immunogold labeling of ultrathin sections that P64 is a component of virogenic
35 mbedding Glu immunocytochemistry on the same ultrathin sections, the simultaneous distribution of the
36 r synaptic inputs, three sets of horizontal, ultrathin sections through central macaque retina were c
37           We imaged the tagged proteins from ultrathin sections using stimulated emission depletion (
38 bedding GABA immunocytochemistry on the same ultrathin sections, was used to reveal simultaneously th
39 hree-dimensional reconstructions from serial ultrathin sections, we found that SV size did not correl
40 ssues were freeze-plunge embedded and serial ultrathin sections were collected on slot grids for immu
41                                              Ultrathin sections were reacted with antibodies for the