ライフサイエンスコーパス: spiracle

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1 ch10, Spiracular Branch10, and the Posterior Spiracle).

2 e spiracle and the epidermis surrounding the spiracle.

3 the embryo to generate the larval posterior spiracle.

4 s air contact across the posterior breathing spiracles.

5 for activating dppMX expression in posterior spiracles.

6 a homologue of Drosophila melanogaster empty spiracles.

7 ping the adult legs and the larval posterior spiracles.

8 try, including endoskeletal enclosure of the spiracle and a lateral cranial canal.

9 which generate the adult tracheal tubes, the spiracle and the epidermis surrounding the spiracle.

10 like segmentation genes orthodenticle, empty spiracles and buttonhead (btd) are expressed and require

11 so tested using promoter elements from empty spiracles and Distal-less, two genes known to be directl

12 normal functions: formation of the posterior spiracles and specification of an eighth abdominal denti

13 nd wide rather than long and thin, while the spiracles are flat instead of dome-shaped.

14 , from which nicotine is exhaled through the spiracles as an antispider signal.

15 otein induces organogenesis of the posterior spiracles by coordinating an organ-specific gene network

16 as exchange cycle (DGC) starts with a closed-spiracle (C) phase, during which little external gas exc

17 In spiracle cells, the down-regulation of polarity and E-ca

18 are two rounds of Dpp signaling in posterior spiracle development.

19 little effect on the activation of the empty spiracles element.

20 al fashion with the cephalic gap genes empty spiracles (ems) and buttonhead (btd) to assign segmental

21 odenticle (otd), buttonhead (btd), and empty spiracles (ems), which are expressed in partially overla

22 te homeobox gene related to Drosophila empty spiracles (ems)] RGCs in mouse neocortex and chick foreb

23 triguingly, several aspects of dpp posterior spiracle expression and function are similar to demonstr

24 change takes place, followed by a fluttering-spiracle (F) phase, which is usually dominated by diffus

25 d is necessary for designating the posterior spiracle field.

26 ired to activate dpp expression in posterior spiracle formation.

27 2, a human homologue of the Drosophila empty spiracles gene is a homeodomain-containing transcription

28 The role of spiracles in polypterid respiration has been unclear, wi

29 he second round appears necessary for proper spiracle internal morphology and fusion with the remaind

30 video, kinematic and pressure data that show spiracle-mediated aspiration accounts for up to 93% of a

31 The DGC is terminated by an open-spiracle (O) phase, during which accumulated CO2 escapes

32 tetrapods, in having large paired openings (spiracles) on top of their head.

33 tein cannot activate its direct target empty spiracles or other downstream genes while it can functio

34 RNA and protein followed sequentially by the spiracle, the dorsal intrasegmental annuli, the interann

35 Transcriptional activation of empty spiracles, the Drosophila ortholog of EMX2, by Abdominal

36 tion are compensated for by the simultaneous spiracle up-regulation of guanine nucleotide exchange fa

37 hat polypterids could inhale air through the spiracles, while later reports have largely dismissed su

38 arity in the size and position of polypterid spiracles with those of some stem tetrapods suggests tha

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