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1 Cerebral cortex was snap frozen.
2 or intraperitoneal injection of cocaine and snap frozen.
3 r either transmission electron microscopy or snap frozen.
4 ter lobectomy, tumor and lung specimens were snap frozen.
5 muscles from both hindlimbs were removed and snap-frozen.
6 eft carotids and contralateral controls were snap-frozen.
7 % of gestation, newborn and adult sheep were snap frozen after four 6-mg dexamethasone or placebo inj
17 control and FSHD deltoid and biceps muscles, snap-frozen at resting length, were cryosectioned, indir
19 titative proteomics and phosphoproteomics on snap-frozen biopsies of hepatocellular carcinoma (HCC) a
25 and age-matched oxygen-treated animals were snap frozen for immunohistochemical analysis with antibo
28 mogeneous ex vivo tumor samples, sections of snap frozen human breast cancer murine xenografts were s
31 te (3.2%) tubes, centrifuged, and the plasma snap frozen in liquid N2 and stored at -80 degrees C.
32 kidneys (n = 4, each group) were harvested, snap frozen in liquid nitrogen, and analyzed for CaR mes
36 sh specimens of 62 periampullary tumors were snap-frozen in liquid nitrogen and adjacent tissue was f
40 al hepatic gene expression was determined in snap-frozen liver biopsy specimens from 4 groups: (1) pa
41 cific CD8(+) T cells in peripheral blood and snap-frozen liver biopsy specimens of two chimpanzees (P
42 similar studies, our data were obtained from snap-frozen needle HCC biopsies (n=52) matched with thei
43 patients underwent colectomy and harvest and snap-freezing of normal mucosa, adenoma, and carcinoma.
44 leus-plantaris muscle group was isolated and snap frozen, or underwent 30 min of electrically evoked
46 more efficiently than long amplicons both in snap-frozen (P = 0.0006) and FFPE (P = 0.0152) tissues.
47 njection, at which time brains were removed, snap frozen, sectioned and quantitatively analyzed for f
48 rectus EOMs attached and TAs were dissected, snap frozen, serially sectioned, and stained for acetylc
49 oduced results similar to that obtained from snap-frozen specimens, although the protein quantity was
52 reperfusion, LPO was determined by assay of snap frozen tissue for thiobarbituric acid (TBA) concent
54 eeze-fracture electron microscopy of unfixed snap-frozen tissue samples confirmed this supramolecular
57 anomas, using early-passage cell strains and snap-frozen tissues (n = 18 and n = 24, respectively) co
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