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1 ave been shown to be visible as particles by freeze fracture.
2 a cells exposed to the sample surface during freeze fracture.
3 e possible sections of cells obtained during freeze fracture.
4 1- and RyR3-rescued junctions is revealed by freeze fracture.
5 s, and replicas of tetrad arrays obtained by freeze-fracture.
6 junctional areas per inferface determined by freeze-fracture.
8 ombined confocal microscopy and "grid-mapped freeze fracture," 36 mixed synapses containing 88 "micro
11 Borrelia burgdorferi have been visualized by freeze-fracture analysis but, until recently, not furthe
14 mbrane of Borrelia hermsii has been shown by freeze-fracture analysis to contain a low density of mem
18 ssment of subendothelial lipid deposition by freeze-fracture and deep-etch electron microscopy indica
19 rganization of the surface of protozoa using freeze-fracture and deep-etching; b) the cytoskeleton of
20 We report x-ray scattering, rheological, and freeze-fracture and polarizing microscopy studies of a l
21 ion imaging provides a morphological view of freeze-fractured cells after TOF-SIMS analysis is comple
22 al coupling hypotheses, we used "grid-mapped freeze fracture," conventional thin-section electron mic
23 were observed with the mutant proteins, and freeze fracture data showed that neither mutant protein
24 c omega-shaped images (and their equivalent, freeze fracture dimples) observed at the active zone adj
32 on pores identified earlier in mast cells by freeze-fracture electron microscopy and by electrophysio
36 t scattering, solute retention, 31P NMR, and freeze-fracture electron microscopy measurements, confir
38 of vesicles incubated with annexin B12 using freeze-fracture electron microscopy methods showed class
41 oscopy of GLUT1/lipid/detergent micelles and freeze-fracture electron microscopy of GLUT1 proteolipos
51 in specific light-harvesting proteins, using freeze-fracture electron microscopy to probe the organiz
53 n N-terminus mutants of AQP4, as measured by freeze-fracture electron microscopy versus live-cell ima
56 poplexes, the lipid membranes as observed in freeze-fracture electron microscopy were deformed into h
57 le particle analysis), negative staining and freeze-fracture electron microscopy, as well as previous
60 profound proteinuria, and with deep-etching freeze-fracture electron microscopy, we resolved the ult
61 ys of particles (OAPs) have been observed by freeze-fracture electron microscopy, we tested the hypot
78 to identify a typical surface layer, whereas freeze-fracture EM revealed that the T. denticola outer
79 aquaporin-1 (AQP1) tetramer showed that the freeze-fracture envelope accounted for the conserved tra
80 resistant membranes at a 1:100 ratio, where freeze-fracture experiments show that AQP-0 oligomerizes
84 finitive method for detecting gap junctions, freeze fracture, has not been used to examine the intera
86 were studied morphologically by quantitative freeze-fracture immunolabeling (FRIL); functionally by L
87 in high release probability boutons, whereas freeze-fracture immunolocalization demonstrated only a 1
89 tein complexes, we examined cryoimmobilized, freeze-fractured leaf tissues using (cryo)scanning elect
90 d receptor fields at ultrahigh-resolution at freeze-fractured membranes, tracked surface and internal
91 g receptor fields at ultrahigh-resolution at freeze-fractured membranes, tracking surface and interna
93 AQP4 is concentrated in glial square arrays, freeze-fracture methods may now provide biophysical insi
94 plexity of tight junction strands visible by freeze-fracture microscopy without affecting the levels
96 iated, endogenous syndapin I at membranes of freeze-fractured neurons revealed that membrane-bound sy
99 ermined from the density of a distinct 10-nm freeze-fracture particle, which appeared in the protopla
100 We show that the cross-sectional area of the freeze-fracture particles corresponds to the area of the
103 idylcholine lipid signal from water with the freeze-fracture preparation techniques described herein
108 ng light microscopic immunocytochemistry and freeze-fracture replica immunogold labeling of adult rat
112 mission electron microscopy, and grid-mapped freeze-fracture replica immunogold labeling, 10 close ap
113 for visualizing PI(4,5)P(2) by SDS-digested freeze-fracture replica labeling (SDS-FRL) to investigat
117 s in biological EM images obtained from both freeze-fracture replicas and plastic sections prepared w
118 e employed immunogold labeling of SDS-washed freeze-fracture replicas and stereoscopic confirmation o
119 microscopic analysis of immunogold-labelled freeze-fracture replicas confirms that GABA(B)Rs are hig
121 imeric intramembrane particle arrays seen in freeze-fracture replicas of tubular M21 membranes; the p
122 anes in IL-1beta-treated astrocytes, whereas freeze-fracture replicas showed strand-like arrays of in
123 ed which are seen in electron micrographs of freeze-fracture replicas with periodicities of 16 and 12
125 as electron microscopy of thin sections and freeze-fracture replicas, has shown that gap junctions a
130 s to be located in the complex ice matrix of freeze-fractured samples, a task that has not been routi
132 in the knobs, visualized by high-resolution freeze-fracture scanning EM, is distinct from that in th
139 ere, we apply a combined approach of TEM and freeze fracture to determine if gap junctions are presen
140 confirmed using polarized light microscopy, freeze fracture transmission electron microscopy, and X-