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1            Of 160 drugs approved by the FDA (2010-2014), 40 were approved by OHOP.
2 ormed with adherence to the Swiss Animal Protection law and were approved by the regional veterinary office.
3 e with the guidelines on the use of animals in research and were approved by the animal care and use committee.
4                               Experiments involving animals were approved by the Institutional Administrative Panel on La
5                                       Eight new antibiotics were approved by the U.S. Food and Drug Administration (FDA)
6                                               Study cohorts were approved by local institutional review boards, and all p
7                                 All biological mesh devices were approved by the FDA based on substantial equivalence to
8                       Materials and Methods All experiments were approved by the institutional animal care and use commit
9                       Materials and Methods All experiments were approved by the local institutional review board and com
10 m cell research oversight committee, and animal experiments were approved by the administrative panel on laboratory anima
11                Materials and Methods All animal experiments were approved by the animal care and use committee and adhere
12                    Materials and Methods Animal experiments were approved by the institutional animal care and use commit
13                                      All animal experiments were approved by the institutional animal care committee.
14                                      All animal experiments were approved by the local ethics committee for animal experi
15                Materials and Methods The animal experiments were approved by the local ethics committee.
16                           Materials and Methods Experiments were approved by the institutional animal care and use commit
17                   Materials and Methods All rat experiments were approved by the University of Washington Institutional A
18 and surface charge of KCC-1, KCC-1-NH(2) and KCC-1-NH(2)-FA were approved by field emission scanning electron microscope
19 f 8 mug/ml and disk diffusion (30/20-mug disk) test methods were approved by the CLSI Subcommittee on Antimicrobial Susce
20 gerthella lenta (broth, 1 to 4 mug/ml; agar, 1 to 8 mug/ml) were approved by the Clinical and Laboratory Standards Instit
21           Also, the specific capturing of the nanoparticles were approved by FR-negative HEK 293 normal cells as FR-negat
22 EGISTRATIONPhase II protocols (NCT01498484 and NCT00002663) were approved by the Institutional Review Board at Memorial S
23          Between 2007 and 2020, 33 biosimilars for oncology were approved by the European Medicines Agency (EMA), 16 by t
24                                 Romidepsin and pralatrexate were approved by the US Food and Drug Administration for pati
25                        Materials and Methods All procedures were approved by the Animal Care and Use Committee and compli
26                                              All procedures were approved by the animal ethics committee.
27                                              All procedures were approved by the institutional animal care and use commit
28                        Materials and Methods All procedures were approved by the Weizmann Institutional Animal Care and U
29                 Materials and Methods All animal procedures were approved by the institutional Animal Care and Use Commit
30                                              The procedures were approved by the Institutional Animal Care and Use Commit
31                        Materials and Methods The procedures were approved by the institutional animal care committee.
32                                               All protocols were approved by the Animal Care Committee in accordance with
33                                               All protocols were approved by the internal review board, and signed inform
34                             Materials and Methods Protocols were approved by the office of biologic safety and institutio
35                                      Quality control ranges were approved by the CLSI in 2017 (broth microdilution MIC) a
36                                The specific recommendations were approved by all members of the task force and then assem
37                           Materials and Methods All studies were approved by the institutional animal care and use commit
38                                              Animal studies were approved by the Institutional Administrative Panel on La
39                    Materials and Methods All animal studies were approved by the institutional animal care and use commit
40                                              Animal studies were approved by the Institutional Animal Care and Use Commit
41                                          The animal studies were approved by the local animal ethics committee.
42                                               Human studies were approved by the institutional review board and were HIPA
43                                        Animal model studies were approved by the institutional Animal Care and Use Commit
44  disk diffusion and MIC QC ranges established in this study were approved by the CLSI Subcommittee on Antimicrobial Susce
45 l of 1358 individuals had died and had brain autopsies that were approved by board-certified neuropathologists.
46 l new drugs with initial indications for adult cancers that were approved by the US Food and Drug Administration between
47                                     For oncology drugs that were approved by the US Food and Drug Administration (FDA) an
48 r a cohort of 24 patented, injectable anticancer drugs that were approved by the US Food and Drug Administration between
49 h institution (NDA 212642 for UCLA and NDA 212643 for UCSF) were approved by the Food and Drug Administration as the firs
50 ilm-coated tablet doses of 25 mg or 35 mg once daily, which were approved by the SRAs for the children's weight band; the