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1 h intermediate or high specific activity and none of 6 (0%) mice treated with low specific activity or formulation demons
5 Finally, CD4+ T cells from arthritic mice treated with CM-MSC showed increases in FOXP3 and IL-4 e
7 3(+) LSCs derived from preneoplastic livers of beta2SP(+/-) mice treated with interleukin-6 (pIL6; (IL6) beta2SP(+/-) LSC
9 Moreover, CMs isolated from transverse aortic constriction mice treated with MR-409 showed improved contractility and re
11 Lineage tracing using Rosa-td tomato (Col2-Cre-ERT2) mice treated with tamoxifen indicated that the same Col2 expr
12 Furthermore, TAMs isolated from IH-exposed mice treated with celecoxib reduced the proliferation of LLC1
13 Analysis of plasma and lung tissues from SEB-exposed mice treated with abatacept demonstrated significantly lower
14 Oxygen consumption in freshly isolated mitochondria from mice treated with Honokiol showed enhanced mitochondrial resp
16 In xenograft models of EOC using SKOV3ip1 or HeyA8, mice treated with the combination of itraconazole and paclita
17 The reduction in urinary oxalate excretion in hyperoxaluric mice treated with O. formigenes CM reflects the in vivo reten
19 Human AML cells from terminally ill mice treated with chemotherapy (chemoAML) had higher lipid co
21 ogether with a decreased expression of cleaved caspase-3 in mice treated with 6-OHDA or rotenone.
24 cells, but not progenitor proliferation, is interrupted in mice treated with a hedgehog (Hh) pathway inhibitor (HPI), an
27 was consistent with the restoration of the CHS response in mice treated with the DNA demethylating agent, 5-aza-2'-deoxy
29 that lipogenesis is dispensable for liver tumorigenesis in mice treated with DEN, and identifies an important role for A
30 ing CRISPR-Cas9 genome editing in transplantable tumours in mice treated with immunotherapy to discover previously undesc
32 Despite the absence of diabetes, NOD mice treated with anti-CSF-1 receptor starting at 3 or 10 wk
39 Skin inflammation significantly improved in KC-Tie2 mice treated with each of the antibodies targeting IL-23, IL-
41 obtained from Cbx3/HP1gamma-insufficient mice or wild type mice treated with Cbx3/HP1gamma-insufficient CD8(+) T cells,
44 was not observed in Ig-treated Rag1(-/-) mice or wild-type mice treated with anti-type I IFNR alone.
47 y tumorigenic and metastatic, whereas those derived from WT mice treated with pIL6 ((IL6) WT LSCs) had significantly less
48 ER stress markers were increased in the lungs of healthy WT mice treated with recombinant murine CIRP, but not in the lun
50 er binding to CNS synaptosomes isolated from wild type (wt) mice treated with NIR light was significantly reduced and the
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