ライフサイエンスコーパス: tracheae

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1 e, and promotes tube elongation in embryonic tracheae.

2 are located in the gut, salivary gland, and tracheae.

3 in the salivary glands, proventriculus, and tracheae.

4 ular infiltrates or fibrosis in transplanted tracheae.

5 Wild-type mice rejected CD40-/- tracheae.

6 ands, intersegmental grooves, and developing tracheae.

7 igger the wingless cascade in the developing 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, although other larval tracheae are remodeled after L3, most tracheal branches

14 jectories and branching pattern of the brain tracheae are surprisingly variable.

15 f B-cell-deficient mice to reject allogeneic tracheae demonstrated that B-cell CD40-mediated response

16 The ability of mice to reject CD40-/- tracheae demonstrated that host, not donor, CD40 is requ

17 Tracheae from 30 hamsters (xenografts) or 23 Brown-Norwa

18 croscopic studies demonstrate that all brain tracheae grow in direct contact with the glial cell proc

19 extended to morphogenesis of the respiratory tracheae in Drosophila.

20 Work in other systems (Drosophila tracheae, MDCK models) suggests that the mitogen-activat

21 type mice in clearing this pathogen from the tracheae of naive recipient mice.

22 The tracheae of ten domestic male pigs, weighing 40 +/- 2 kg

23 Ultrastructural examination of mutant tracheae reveals defects in cell-extracellular matrix co

24 remodeling of Drosophila respiratory tubes (tracheae) that elongate continually during larval growth

25 In ribbon mutant tracheae, the dorsal trunk fails to form, and ventral br

26 Wild-type larvae possess only two central tracheae, typically associated with the mushroom body an

27 BALB/c tracheae were heterotopically transplanted into C3H mice

28 C57BL/6 or BALB/c tracheae were implanted into wild-type control, CD28-/-,

29 Tracheae were transplanted into B-cell-deficient mice to

30 cted with host or donor CD40, CD40-deficient tracheae were transplanted into CD40L+/+, CD40+/+ wild-t

31 te were significantly increased in xenograft tracheae when compared with the allografts.

32 These trends suggest the space available for tracheae within the leg may ultimately limit the maximum

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