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1 ractical, for instance for samples held in a cryostat.
2 ins were rapidly frozen and sectioned with a cryostat.
3 rneas and six human corneas with a microtome-cryostat.
4 l mode of the device in-equilibrium with the cryostat.
5 ient conditions and in situ to a measurement cryostat.
6           DESIGN, SETTING, AND PARTICIPANTS: CRYOSTAT-2 was an interventional, randomized, open-label
7                               An N(2)-cooled cryostat allows for NMR isotherm measurements at both ro
8 ll increments of NO were introduced into the cryostat and the following reactions were monitored by t
9                                              Cryostat and vibratome vertical sections and wholemount
10 oad exceeding the available cooling power of cryostats at millikelvin temperatures.
11         The tissue is then sectioned using a cryostat before being dissected using an LM instrument.
12                                              Cryostat biopsy specimens from 27 long-term recipients b
13 of peroxo Delta 9D at 4.2 K in the Mossbauer cryostat caused the release of O(2) and the reappearance
14  digitally and thickness was determined from cryostat cross sections.
15                           Furthermore, using cryostat-cut sections of I. ricinus, we show that both a
16 perating in a deep-underground lead-shielded cryostat decreases the quasiparticle burst rate by a fac
17 mount fixed tissue onto the chuck inside the cryostat during cryosectioning.
18 e counted in 5-microm sections obtained with cryostat from each harvested heart.
19 o indicates that this technique could reduce cryostat heating for fast gates, a vital requirement for
20 e the total power consumption of most modern cryostats, including those that reach millikelvin temper
21 m specimens were quick frozen, then cut by a cryostat into 30-micron-thick sections.
22 pid movement of a large optically accessible cryostat is used in combination with nanosecond time-res
23 reated with H2O2 or aflatoxin B1 and then to cryostat liver sections of rats treated with aflatoxin B
24         Genomic DNA isolated from a panel of cryostat microdissected metastatic prostate adenocarcino
25                 Upon developing a compatible cryostat module for enabling cryogenic temperatures ([Fo
26 ermine the level of COX deficiency in serial cryostat muscle sections (mean age, 42.6 years; range, 3
27 lar associations of dystrophin with actin in cryostat muscle tissue sections by combining resonance e
28 sically retained by simple filtration in the cryostat of the DNP polarizer, and a pure hyperpolarized
29 ed stillborn to 85 years, were fresh frozen, cryostat sectioned, and prepared for indirect immunofluo
30 ge, 6 months to 67 years) were fresh frozen, cryostat sectioned, and prepared for indirect immunofluo
31                            Immunolabeling of cryostat-sectioned eyes harvested from Abca4(-/-) mice r
32                                              Cryostat-sectioned tissue revealed extensive GluR 5/6/7-
33 emoved and activity was measured, lungs were cryostat-sectioned to detect the presence of ICAM-1 by i
34         Immunocytochemistry was performed on cryostat sections (14 microm) of caudal brainstem, using
35 (-IR) axons in the female rat bladder, using cryostat sections and whole wall thickness preparations.
36  cortical neurites grew robustly on neonatal cryostat sections but only sparsely on sections from adu
37                                    Moreover, cryostat sections can also be subjected to various treat
38 mined br radioligand binding analysis and in cryostat sections derived from normal liver and hepatoma
39 ocytes and E-cadherin on epithelial cells in cryostat sections from 34 diagnostic biopsy specimens an
40 r cortex were plated onto various regions of cryostat sections from developing and adult hamster brai
41          Labeled MSCs were observed in 5-mum cryostat sections from each harvested heart.
42                                              Cryostat sections from monkey brain and spinal cord were
43                                Ten 30-microm cryostat sections from the macula (foveal and perifoveal
44 , we performed immunohistological studies on cryostat sections obtained from 26 breast cancer biopsie
45 njugated secondary antibody was performed on cryostat sections of 90 renal transplant biopsies, inclu
46 n both single AV nodal cells in vitro and in cryostat sections of AV nodal tissue in situ.
47                                              Cryostat sections of brains obtained from rats immediate
48 lls were examined by immunohistochemistry in cryostat sections of bronchial/nasal biopsies obtained f
49 uorescence (IF) for desmosomal components on cryostat sections of fresh epithelia was supported by im
50                                              Cryostat sections of fresh nonfixed corneas were obtaine
51                                              Cryostat sections of frontal cortex and subcortical whit
52 d IV activities were demonstrated in unfixed cryostat sections of gingival tissue from chronic period
53                                              Cryostat sections of heart and lung were prepared for in
54 l medium, neurons were cultured onto unfixed cryostat sections of mature rat CNS tissue.
55 and bind selectively to endothelial cells in cryostat sections of mouse tissues.
56                                              Cryostat sections of nasal/bronchial biopsies obtained f
57 rom degradation by exogenous gelatinase B in cryostat sections of nerve in vitro.
58 otein extracts in immunoblot analysis and to cryostat sections of ocular tissues in immunofluorescenc
59 focal microscopy of rat cardiac myocytes and cryostat sections of rat left ventricle papillary muscle
60  in wholemounts of urothelium or detrusor or cryostat sections of the bladder.
61                                              Cryostat sections of the developing brain provide a usef
62 ed using 125I-PP receptor autoradiography on cryostat sections of the entire brain cut in three plane
63 table polypeptides and their distribution in cryostat sections of the limbocorneal area were investig
64 stry were employed on paraformaldehyde-fixed cryostat sections of the pigeon eye and surrounding orbi
65                                              Cryostat sections of the rat hippocampus were used as ti
66 sing cells was established by immunostaining cryostat sections of the retina with antibodies against
67            Previous studies have depended on cryostat sections of tissues selected grossly.
68    Mice were injected with 125I-estrogen and cryostat sections thaw mounted onto emulsion-coated slid
69                              C4d staining of cryostat sections was done by a sensitive three-layer im
70 te outgrowth from cortical explants onto the cryostat sections was visualized with a fluorescent vita
71                                              Cryostat sections were analyzed by DHM to measure the sp
72 rain, spinal cord, and eyes were frozen, and cryostat sections were collected on slides, hybridized w
73                        Five-micrometer-thick cryostat sections were cut and in situ hybridization was
74                              Five-micrometer cryostat sections were cut, and in situ hybridization wa
75                             Serial 50 microm cryostat sections were obtained throughout the medulla,
76                             Serial 50 microm cryostat sections were obtained throughout the rostral h
77                                  Consecutive cryostat sections were prepared from eyes at different s
78                             Whole mounts and cryostat sections were prepared from the central nervous
79                                              Cryostat sections were probed with antibodies directed a
80                                              Cryostat sections were stained for interleukin (IL)-12 o
81 ival times ranging from 10 hours to 28 days, cryostat sections were stained for routine histology and
82                                              Cryostat sections were taken and labeled in vitro by one
83        Corneal thickness was determined from cryostat sections, and mRNA expression was measured by r
84  was used to detect class II MHC proteins on cryostat sections, followed by computer-assisted image a
85 ction of microRNA (miRNA) and they often use cryostat sections, signal amplification and hybridizatio
86 between B16-F1 and B16-F10 melanoma cells in cryostat sections.
87 , Cx 32, Cx 43, and Cx 50 were used to stain cryostat sections.
88 fornica and Tritonia diomedea was studied in cryostat sections.
89 eat-sensitive guidance cues preserved in the cryostat sections.
90 mated using image analysis of serial coronal cryostat sections.
91 0(6) in ultra-clean nanotube resonators at a cryostat temperature of 30 mK, where we define Q as the
92 gn and construction of a novel liquid helium cryostat that accommodates variable-sized quartz tubes/c
93  transfer them in and out of a liquid-helium cryostat that houses a superresolution fluorescence micr
94                                              Cryostat tissue sections of fixed rhesus monkey ciliary,
95 t neuropil and glia were microdissected from cryostat tissue sections of histologically severely affe
96                                              Cryostat tissue sections of the lids were stained by imm
97 ections of medulla from female rats cut on a cryostat were incubated with five concentrations of (125
98 etector operating simultaneously in the same cryostat with the qubits.