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1 of a cartilage-specific promoter, and then these transgenic mice were used for a genetic rescue of abnormalities in Crtl1
6 21 (human melanoma)-bearing severe combined immunodeficient mice were used for biodistribution, PET imaging, and determin
8 Splenocytes from C57BL/6 J (B6) AID(-/-) mice were used for determining in vitro proliferation respons
9 Different sets of mouse mandibular incisors of C57BL/6 mice were used for dissections and microCT reconstructions.
10 gous db/m+, db/db, and db/db catalase (CAT)-transgenic (Tg) mice were used for DNA chip microarray analysis.
12 y the mechanism of this suppression, samples from 5-day BDL mice were used for evaluation of liver injury.
14 Mouse C2C12 myoblasts and normal FVB/N mice were used for in vitro and in vivo confirmation, respect
15 Conditional polycystin-2-knockout (Pkd2KO) mice were used for in vivo studies and to isolate cystic chol
18 cipients, and syngeneic C3H/HeJ-gld (CD95 ligand-deficient) mice were used for normal C3H/HeJ recipients.
21 runcations that have been previously analyzed in transgenic mice were used for production of stably transfected mouse ery
27 In initial experiments, 10-month-old mice were used for the single treatment with 9-cis-R-Ac or th
31 plenocytes from G-CSF-mobilized perforin-deficient (pfp-/-) mice were used for transplantation, 90% of recipients died of
32 ich culture from wild-type (WT) and InsP(3)R2 knockout (KO) mice were used for western blots, confocal immunofluorescence
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