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1  are located in the gut, salivary gland, and tracheae.
2  in the salivary glands, proventriculus, and tracheae.
3 ular infiltrates or fibrosis in transplanted tracheae.
4              Wild-type mice rejected CD40-/- tracheae.
5 ands, intersegmental grooves, and developing tracheae.
6 igger the wingless cascade in the developing tracheae.
7 e, and promotes tube elongation in embryonic tracheae.
8 inished in ribbon mutant salivary glands and tracheae.
9  deficiencies for the Spp gene had defective tracheae and died as larvae.
10  subsequent pertussis aerosol challenge from tracheae and lungs (defined as protection), but there wa
11 en other tubular epithelia (salivary glands, tracheae, and hindgut) in much same manner as they alter
12 promotes apical membrane expansion in larval tracheae, and promotes tube elongation in embryonic trac
13      Here, we show that the adult intestinal tracheae are dynamic and respond to enteric infection, o
14    Here, we show that, although other larval tracheae are remodeled after L3, most tracheal branches
15 jectories and branching pattern of the brain tracheae are surprisingly variable.
16                                              Tracheae deficient in Duox, or deficient in both Duox an
17 f B-cell-deficient mice to reject allogeneic tracheae demonstrated that B-cell CD40-mediated response
18        The ability of mice to reject CD40-/- tracheae demonstrated that host, not donor, CD40 is requ
19                                              Tracheae from 30 hamsters (xenografts) or 23 Brown-Norwa
20 croscopic studies demonstrate that all brain tracheae grow in direct contact with the glial cell proc
21 extended to morphogenesis of the respiratory tracheae in Drosophila.
22            Work in other systems (Drosophila tracheae, MDCK models) suggests that the mitogen-activat
23 ding gut, imaginal discs, neurons, fat body, tracheae, muscles and hemocytes, for up to 8 h.
24                                       Larval tracheae of Drosophila harbour progenitors of the adult
25 type mice in clearing this pathogen from the tracheae of naive recipient mice.
26                                          The tracheae of ten domestic male pigs, weighing 40 +/- 2 kg
27 and real three-dimensional geometries of the tracheae of the bush cricket Copiphora gorgonensis.
28                         Moreover, the broken tracheae release air into the host, which the larval jew
29 al jewel wasps destroy the dorsal vessel and tracheae (respiratory system) in the thorax of their coc
30        Ultrastructural examination of mutant tracheae reveals defects in cell-extracellular matrix co
31 sudden release of air from the host's broken tracheae, suggests the larva taps into the host respirat
32 crease in mucociliary clearance in explanted tracheae that was Trpm5- and M3R-mediated.
33  remodeling of Drosophila respiratory tubes (tracheae) that elongate continually during larval growth
34                             In ribbon mutant tracheae, the dorsal trunk fails to form, and ventral br
35 omen, making gas exchange through the narrow tracheae (Tr) challenging for the elongated Pr.
36    Wild-type larvae possess only two central tracheae, typically associated with the mushroom body an
37                                       BALB/c tracheae were heterotopically transplanted into C3H mice
38                            C57BL/6 or BALB/c tracheae were implanted into wild-type control, CD28-/-,
39                                              Tracheae were transplanted into B-cell-deficient mice to
40 cted with host or donor CD40, CD40-deficient tracheae were transplanted into CD40L+/+, CD40+/+ wild-t
41 te were significantly increased in xenograft tracheae when compared with the allografts.
42 These trends suggest the space available for tracheae within the leg may ultimately limit the maximum