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1  associated with AAT [1.19 (1.03, 1.37)] and NEO [1.22 (1.04, 1.44)].
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
4      To date, large-scale identification of (neo-)Ags from DNA sequencing data has mainly relied on p
5 uced an augmentation of glial progeny in the neo- and archicortex.
6            Chlorogenic acid and its isomers (neo- and cryptochlorogenic acid) were the major polyphen
7                                     However, neo- and d-chiro-inositol hexakisphosphates were recentl
8                     We synthesized authentic neo- and D-chiro-IP(6) and used them to identify signals
9 phorus in soils and reveal the prevalence of neo- and D-chiro-IP(6) in the environment.
10  on the new signal assignments revealed that neo- and D-chiro-IP(6) occur widely in both terrestrial
11 forms strong reciprocal connections with the neo- and entorhinal cortex (EC).
12                Hybrids generated by crossing neo- and established tetraploids exhibit intermediate ph
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
17 w that mountainous areas are centres of both neo- and paleo-endemism.
18                     Pyramidal cell layers in neo- and paleocortex had a balance of mRNAs that was sig
19 D8(+) T cell responses against tumor-derived neo- and self-antigens via dermal DCs.
20 tumors within the mice as compared with both neo- and soluble syndecan-1-transfected cells.
21 d additional motifs, which may contribute to neo- and sub-functionalization of these proteins.
22 , whereas Kv3.2 is abundantly represented in neo- and subcortical regions.
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
28 rces to expand the repertoire of targetable (neo-)antigens and improve therapeutic outcomes.
29   In a gene-trap mouse model with a beta-gal+neo (beta-geo) insertion in the endogenous RPTP-kappa ge
30 sing the green fluorescent protein (GFP) and neo (conferring resistance to G418).
31 specifically in TF1-PR cells, but not in TF1-neo (control) cells.
32  brain in the heterozygous (HET) zQ175 delta-neo (DN) mouse model at 3, 6, and 10 months of age, usin
33 h later, and triggers a marked transition in neo-/entorhinal cortical activity.
34   coefficient: 1.33; 95% CI: 1.05, 1.69) and NEO (exp.
35 CI: 1.1, 1.7), and chronic inflammation with NEO (exp.
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
39 nuated working memory impairment in NMDA Nr1(neo-/-) mice.
40                                  Mobile WACh NEO (MWACh NEO) was a parallel, unblinded and individual
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
43 ON (15-acetyl-deoxynivalenol), T2-Tetrol and NEO (Neosolaniol).
44  Previously we showed that Ani (anisodamine)/Neo (neostigmine) combination produced anti-shock effect
45                          Participants of the NEO (Netherlands Epidemiology of Obesity) study (n=5630)
46            In transgenic neurotrophin-3 lacZ-neo (NT-3(lacZneo)) mice, in which the coding region for
47 ly complement definitive therapy with either neo- or adjuvant therapy to improve prognosis.
48 eater tendency toward lysosomal leakage than neo- or apoE3-transfected cells.
49 lants, likely occurring through processes of neo- or sub-functionalization.
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
52 effectively than stimulation with WT or MC38-Neo (p < 0.05).
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
55 4,306 islands, and identified 142 sites with neo-, paleo-, mixed and super-endemism.
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
58       Jejunal polyposis was advanced in 21% (neo- SS III or IV).
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