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1                             Upon systemic or intrasplenic administration into mice reconstituted with
2  and CCR7 was determined after intracameral, intrasplenic, and subcutaneous transplantation of uveal
3  of HSCs in vivo, we developed a protocol of intrasplenic artery injection to directly deliver HSCs i
4 han precapillary resistance, thus increasing intrasplenic capillary hydrostatic pressure (P(c)) and f
5 or rats treated with carbon tetrachloride or intrasplenic cell transplantation and healthy Wistar rat
6 but did not deteriorate in animals receiving intrasplenic hepatocyte transplantation (G1) (P <.01).
7  improved toward normal in animals receiving intrasplenic hepatocyte transplantation (P <. 01).
8                       In laboratory animals, intrasplenic hepatocyte transplantation corrects the phy
9                   Our data also suggest that intrasplenic hepatocyte transplantation may provide a me
10 SG mice even when delayed until 3 days after intrasplenic HIV-1 inoculation.
11                                Patients with intrasplenic hyperattenuating foci on portal venous phas
12                                     A single intrasplenic (i.s.) delivery of A-NK cells (1 x 10(7)) a
13  NK cell depletion from PBMCs prior to their intrasplenic injection abrogated the suppression of in v
14  woodchuck hepatocytes were transplanted via intrasplenic injection and were found to integrate into
15 s introduced into the portal circulation via intrasplenic injection are immunogenic not tolerogenic a
16 ha1-antitrypsin (hA1AT) were transplanted by intrasplenic injection into host mice and the secreted h
17 emoval of NK cells from human PBMCs prior to intrasplenic injection into NSG mice completely abrogate
18 -Luc), and the ACE-CD vector was infused via intrasplenic injection into the portal circulation.
19          Fifty percent of rats that received intrasplenic injection of 10 x 10(6) primary Lewis rat h
20                        Groups then underwent intrasplenic injection of 10(6) Morris hepatoma cells, f
21 hepatocytes showed that adult rats tolerated intrasplenic injection of a large cell number in single
22 role of Cten in metastasis was tested by (a) intrasplenic injection of CRC cells stably transfected w
23  of syngeneic rat bone marrow cells (G4); or intrasplenic injection of Dulbecco's modified Eagle medi
24                             Animals received intrasplenic injection of fluorescently labeled human st
25               Group 3 (n = 16) rats received intrasplenic injection of isolated hepatocytes (2.5 x 10
26                                   Similarly, intrasplenic injection of LLC cells resulted in rapid co
27 enic CD11b-diphtheria toxin receptor mice by intrasplenic injection of MC38 colon and Lewis lung carc
28                          Results showed that intrasplenic injection of purified, donor-strain-specifi
29 almatians that underwent sham laparotomy and intrasplenic injection of saline solution; CsA given alo
30  liver metastasis mouse model established by intrasplenic injection of the human colon cancer cell li
31 d in the liver metastases that resulted from intrasplenic injection of the tumor cells in transgenic
32                                              Intrasplenic injection of tumor cells has long been know
33                                       Direct intrasplenic injection produced engraftment that was far
34 ve within the livers of nude mice 24 h after intrasplenic injection than weakly metastatic clone A ce
35 nic mice were transplanted into host mice by intrasplenic injection, and subsequent survival of the t
36                                        After intrasplenic injection, galectin-3 cDNA transfected BT54
37 ection, in lungs (67 +/- 9%); however, after intrasplenic injection, only some LSEC remained in the s
38 he formation of hepatic metastases following intrasplenic injection, suggesting that it did inhibit e
39                                           On intrasplenic injection, transplanted hepatocytes immedia
40  injection and in the liver and spleen after intrasplenic injection, without translocations into pulm
41 d the number of hepatic metastases following intrasplenic injection.
42 idase were transplanted into Agxt-/- mice by intrasplenic injection.
43  efficient formation of liver metastasis via intrasplenic injection.
44 tases from pancreatic cancer were induced by intrasplenic injections of Capan1 or AsPC1 cells in nude
45 iorized livers of three groups of mice after intrasplenic inoculation of human colon cancer cells.
46 ted liver metastasis in C57BL/6 mice through intrasplenic inoculation of MC38 colon carcinoma cells.
47 h develop productive in vivo infection after intrasplenic inoculation with HIV-1.
48 a decreased number of gross metastases in an intrasplenic model of liver metastasis.
49 evere combined immunodeficiency mice through intrasplenic or intraportal routes.
50 ed the incidence of hepatic metastases after intrasplenic/portal inoculation of colon carcinoma cells
51          AI4 T cells only underwent vigorous intrasplenic proliferation in NOD.IFN-gamma(null) recipi
52                                          For intrasplenic pseudoaneurysm, arterial phase imaging was
53 30 with splenic active bleeding, and 30 with intrasplenic pseudoaneurysm.
54 on of carbon tetrachloride were subjected to intrasplenic rat or porcine hepatocyte transplantation.
55 fectively by the intraportal rather than the intrasplenic route.
56 ol C57BL/6 mice via the tail vein, s.c., and intrasplenic routes.
57 p 4 (n = 12) sham-transplanted rats received intrasplenic saline infusion, and after 3 days they were
58 nd partial hepatectomy with/without a single intrasplenic, syngeneic hepatocyte transplantation.
59 the differentiation of intrahepatic, but not intrasplenic, Th17 cells in wild-type mice, whereas the
60  emphasizing the importance of MZ B cells in intrasplenic trafficking of bound substrates.
61                               In conclusion, intrasplenic transplantation of allogeneic hepatocytes p
62          Compared to sham-operated controls, intrasplenic transplantation of CD47-deficient OVA(+) he
63                                              Intrasplenic transplantation of F344 rat hepatocytes fol
64 ocrotaline was given followed 1 day later by intrasplenic transplantation of healthy C57BL/6 mouse he
65                                      Indeed, intrasplenic transplantation of Id1(+/+) or Id1(-/-) LSE
66                                 Importantly, intrasplenic transplantation of SCL-overexpressing hESC-
67 on and warm ischemia-reperfusion followed by intrasplenic transplantation of syngeneic F344 rat hepat
68                             Animals received intrasplenic transplantation of syngeneic rat hepatocyte
69 lls that formed tumours after intravenous or intrasplenic transplantation, particularly among ineffic
70 epatocytes were retained in the spleen after intrasplenic transplantation.
71 nsion pattern similar to those observed with intrasplenic transplantation.
72 blastoma (HB) is limited to subcutaneous and intrasplenic xenograft models that do not recapitulate t

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