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1 cid secretion when the sensor approached the isolated tissue.
2  in order to improve the preservation of the isolated tissue.
3 udy of T-cell subsets in peripheral blood or isolated tissues.
4 dentify in cultured cells and to validate in isolated tissues.
5 on within the intact organism but not within isolated tissues.
6   The ability to stimulate select neurons in isolated tissue and in living animals is important for i
7 exing technologies applied to the imaging of isolated tissues and cells and to non-invasive whole-bod
8 ntricular cell types previously described in isolated tissues and cells are maintained in intact cani
9 e M cell to date has been accomplished using isolated tissues and cells.
10 ardiac contractility and calcium handling in isolated tissues and myocytes and analyzed mitochondrial
11                            Even when freshly isolated tissues are used, they are almost always derive
12 lthough devoid of activity in a classic B(1) isolated tissue assay, B(1) antagonist activity for 1 wa
13 rexone (6) were synthesized and evaluated in isolated tissue assays in vitro and in vivo in mouse ant
14                                           In isolated tissue assays, inosine (1 mM) significantly dec
15                                           We isolated tissues at the site of blastogenesis onset and
16 s of coronary arteries were determined using isolated tissue baths and isometric tension recording.
17 ngs from Sprague Dawley rats were mounted in isolated tissue baths with (+) and without (-) PVAT.
18 d assay that evaluates pattern separation in isolated tissue by controlling and recording the input a
19                        In cultured cells and isolated tissues, ceramides perturb mitochondrial functi
20                       RCH can be elicited in isolated tissues ex vivo, suggesting cold-sensing and do
21 ctions on action potential duration (APD) in isolated tissue experiments.
22 ll restoration of biological activity to the isolated tissue factor ectodomain via the engineering of
23                                          All isolated tissues fibrillated spontaneously.
24                                              Isolated tissue from CO2-exposed toadfish also exhibited
25                                          LCM-isolated tissues from patient-matched normal, ductal car
26    MMAPPR can exploit RNA-seq data sets from isolated tissues or whole organisms that are used for ge
27 o control cardiac rhythm in the whole heart, isolated tissue preparations and single cardiomyocytes.
28 1 was confirmed in pharmacologically defined isolated tissue preparations.
29 nce of glutamate receptors (GluRs) in living isolated tissue preparations.
30 ed us to maximize proteome coverage of laser-isolated tissue samples containing nanogram levels of pr
31                                              Isolated tissues showed immunohistochemical and biophysi
32 hat transcription is activated by a recently isolated tissue-specific bHLH protein, BETA2, heterodime
33 ting Gal4-VP16 gene/enhancer trap vector, we isolated tissue-specific drivers that regulate expressio
34              Molecular analysis, using newly isolated tissue-specific markers, shows that the ventral
35                       Previous studies using isolated tissues suggest that the colonic H, K-ATPase (c
36         Water was added by injection into an isolated tissue volume (a 20 mm diameter disk of 5 mm th
37          All animals production from freshly isolated tissue was measured by a NO*-specific microelec
38 an be determined by counting PRP activity of isolated tissues, whereas digital whole-body autoradiogr