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1 wth, and abrogated development of the dorsal air sacs.
2 were assessed for inability to colonize the air sac and cause septicemia in 2-week-old white Leghorn
3 rtedly depends on bellowslike ventilation by air sacs and may have evolved to meet the high aerobic d
5 Caudally positioned abdominal and thoracic air sacs are critical components of the avian aspiration
6 re development was seen in an in vivo dorsal air sac assay of glioblastoma cells with downregulated c
7 heal systems, the mechanisms of tracheal and air sac compression in insects, and the function of both
11 d injection of air into the cranial thoracic air sac during song elicited a compensatory reduction in
13 Injection of purified SpeB alone into a skin air sac failed to induce any significant tissue damage;
14 tion: a dense, thick and downturned rostrum; air sac fossae; cranial asymmetry; and exceptionally bro
21 n this isolate was injected into mice via an air sac model for skin infection, organisms recovered fr
23 zation in vivo as determined by mouse dorsal air sac model, and conditioned medium from Ad-MMP-2-Si-i
26 ute to the development of lesions within the air sacs of birds but is not required for subsequent gen
28 however, when they were injected into a skin air sac on outbred CD1 mice, all mice injected with M1 i
33 eal organ grows from an epithelial tube (the air sac primordium (ASP)) that arises during the third l
37 f a custom-built fast valve connected to the air sac system, we achieved partial or total silencing o
39 t birds, evidence for cervical and abdominal air-sac systems in non-avian theropods, along with thora
41 respiratory system includes high-compliance air sacs that ventilate a dorsally fixed, non-expanding
42 anchless(FGF)-dependent growth of the dorsal air sacs, the major tracheal organs of the adult fly.
44 and other granulocytes that infiltrated the air sac were quantitated by single-color flow cytometry.
45 n alligator, an amphibious ectotherm without air sacs, which suggests that this pattern dates back to
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