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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 dentify in cultured cells and to validate in isolated tissues.
4 udy of T-cell subsets in peripheral blood or isolated tissues.
5   The ability to stimulate select neurons in isolated tissue and in living animals is important for i
6 ntricular cell types previously described in isolated tissues and cells are maintained in intact cani
7 e M cell to date has been accomplished using isolated tissues and cells.
8                            Even when freshly isolated tissues are used, they are almost always derive
9 lthough devoid of activity in a classic B(1) isolated tissue assay, B(1) antagonist activity for 1 wa
10 rexone (6) were synthesized and evaluated in isolated tissue assays in vitro and in vivo in mouse ant
11                                           In isolated tissue assays, inosine (1 mM) significantly dec
12                                           We isolated tissues at the site of blastogenesis onset and
13 s of coronary arteries were determined using isolated tissue baths and isometric tension recording.
14                       RCH can be elicited in isolated tissues ex vivo, suggesting cold-sensing and do
15 ctions on action potential duration (APD) in isolated tissue experiments.
16 ll restoration of biological activity to the isolated tissue factor ectodomain via the engineering of
17                                          All isolated tissues fibrillated spontaneously.
18                                              Isolated tissue from CO2-exposed toadfish also exhibited
19                                          LCM-isolated tissues from patient-matched normal, ductal car
20    MMAPPR can exploit RNA-seq data sets from isolated tissues or whole organisms that are used for ge
21 o control cardiac rhythm in the whole heart, isolated tissue preparations and single cardiomyocytes.
22 1 was confirmed in pharmacologically defined isolated tissue preparations.
23 nce of glutamate receptors (GluRs) in living isolated tissue preparations.
24                                              Isolated tissues showed immunohistochemical and biophysi
25 hat transcription is activated by a recently isolated tissue-specific bHLH protein, BETA2, heterodime
26 ting Gal4-VP16 gene/enhancer trap vector, we isolated tissue-specific drivers that regulate expressio
27              Molecular analysis, using newly isolated tissue-specific markers, shows that the ventral
28                       Previous studies using isolated tissues suggest that the colonic H, K-ATPase (c
29          All animals production from freshly isolated tissue was measured by a NO*-specific microelec
30 an be determined by counting PRP activity of isolated tissues, whereas digital whole-body autoradiogr

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