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2 ith ILC do not seem to benefit as much from (neo-)adjuvant chemotherapy as patients with NST, althoug
3 rom fifteen protected forests throughout the Neo-, Afro-, and Asian tropics were identified from syst
10 on the new signal assignments revealed that neo- and D-chiro-IP(6) occur widely in both terrestrial
13 recombinant human (rh) BDNF into the rodent neo- and limbic cortex and used a turkey anti-BDNF antib
14 a new method called categorical analysis of neo- and paleo-endemism (CANAPE) that allows, for the fi
15 xonomic and phylogenetic plant diversity and neo- and paleo-endemism by generating a novel dated tree
16 quantitative distinction between centres of neo- and paleo-endemism, useful to the conservation deci
23 deas that epigenetic modifications can drive neo- and subfunctionalization in evolution by gene dupli
24 xed selection compared to BZR1, hallmarks of neo- and subfunctionalization, and dynamic HSP90 client
25 ication, and point mutations coupled to gene neo- and subfunctionalizations were involved in the evol
26 ontaining nonrandom concentrations of young (neo-) and old (paleo-) endemic taxa were identified usin
27 e control cultures, the L-RRE-neo-, L-TR/TAT-neo-, and L-M10-SN-transduced cultures displayed up to 1
29 In a gene-trap mouse model with a beta-gal+neo (beta-geo) insertion in the endogenous RPTP-kappa ge
32 brain in the heterozygous (HET) zQ175 delta-neo (DN) mouse model at 3, 6, and 10 months of age, usin
36 uro (puromycin-resistant 293 cells) and MDBK-Neo (G418-resistant MDBK cells) cell lines for total cel
37 "other" inositols (cis-, epi-, allo-, muco-, neo-, L-chiro-, D-chiro-, and scyllo-) and derivatives r
38 ompared with the control cultures, the L-RRE-neo-, L-TR/TAT-neo-, and L-M10-SN-transduced cultures di
41 to receive treatment with either the ACURATE neo (n=398) or the CoreValve Evolut bioprostheses (n=398
42 implantation with the self-expanding ACURATE neo (NEO) did not meet noninferiority compared with the
44 Previously we showed that Ani (anisodamine)/Neo (neostigmine) combination produced anti-shock effect
50 similar evolutionary outcomes by independent neo- or subfunctionalization processes during the evolut
51 ication may have allowed hox13 duplicates to neo- or subfunctionalize, ultimately contributing to the
53 4+ T-cell functionality decreased after both neo (P = .0025) and recall (P = .0080) MML vaccination.
54 ells that produced IgA in response to either neo (P = .0221) or recall (P = .0356) MML vaccinations w
56 We previously observed that in newly formed (neo-)polyploids of Arabidopsis arenosa, synapsis defects
57 ay that uses a neomycin phosphotransferase ( neo ) retrotransposition cassette to determine relative
59 epair of I-SceI nuclease-induced DSBs in one neo (the recipient) required a choice between two donor
60 Colocalization of cross-linked fibrin and neo (used to replace TM) reveals that fibrin is deposite
61 es, we synchronized human leukemia Jurkat T, Neo (using aphidicolin), breast cancer MCF-7, normal fib