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7 on the new signal assignments revealed that neo- and D-chiro-IP(6) occur widely in both terrestrial
9 recombinant human (rh) BDNF into the rodent neo- and limbic cortex and used a turkey anti-BDNF antib
10 a new method called categorical analysis of neo- and paleo-endemism (CANAPE) that allows, for the fi
11 quantitative distinction between centres of neo- and paleo-endemism, useful to the conservation deci
16 deas that epigenetic modifications can drive neo- and subfunctionalization in evolution by gene dupli
17 xed selection compared to BZR1, hallmarks of neo- and subfunctionalization, and dynamic HSP90 client
18 e control cultures, the L-RRE-neo-, L-TR/TAT-neo-, and L-M10-SN-transduced cultures displayed up to 1
19 In a gene-trap mouse model with a beta-gal+neo (beta-geo) insertion in the endogenous RPTP-kappa ge
22 uro (puromycin-resistant 293 cells) and MDBK-Neo (G418-resistant MDBK cells) cell lines for total cel
23 "other" inositols (cis-, epi-, allo-, muco-, neo-, L-chiro-, D-chiro-, and scyllo-) and derivatives r
24 ompared with the control cultures, the L-RRE-neo-, L-TR/TAT-neo-, and L-M10-SN-transduced cultures di
27 Previously we showed that Ani (anisodamine)/Neo (neostigmine) combination produced anti-shock effect
31 similar evolutionary outcomes by independent neo- or subfunctionalization processes during the evolut
33 4+ T-cell functionality decreased after both neo (P = .0025) and recall (P = .0080) MML vaccination.
34 ells that produced IgA in response to either neo (P = .0221) or recall (P = .0356) MML vaccinations w
35 ay that uses a neomycin phosphotransferase ( neo ) retrotransposition cassette to determine relative
36 epair of I-SceI nuclease-induced DSBs in one neo (the recipient) required a choice between two donor
37 Colocalization of cross-linked fibrin and neo (used to replace TM) reveals that fibrin is deposite
38 es, we synchronized human leukemia Jurkat T, Neo (using aphidicolin), breast cancer MCF-7, normal fib
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