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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 for activating dppMX expression in posterior spiracles.
5 a homologue of Drosophila melanogaster empty spiracles.
6 ping the adult legs and the larval posterior spiracles.
7 s air contact across the posterior breathing spiracles.
8 ox-regulated gene network from the posterior spiracles(10) and have since diversified in morphology i
9 try, including endoskeletal enclosure of the spiracle and a lateral cranial canal.
10 which generate the adult tracheal tubes, the spiracle and the epidermis surrounding the spiracle.
11 like segmentation genes orthodenticle, empty spiracles and buttonhead (btd) are expressed and require
12 so tested using promoter elements from empty spiracles and Distal-less, two genes known to be directl
13 normal functions: formation of the posterior spiracles and specification of an eighth abdominal denti
14                    Anatomical details of the spiracles and tracheal tubes are described, images prese
15 nd wide rather than long and thin, while the spiracles are flat instead of dome-shaped.
16 , from which nicotine is exhaled through the spiracles as an antispider signal.
17 otein induces organogenesis of the posterior spiracles by coordinating an organ-specific gene network
18 as exchange cycle (DGC) starts with a closed-spiracle (C) phase, during which little external gas exc
19                                           In spiracle cells, the down-regulation of polarity and E-ca
20 are two rounds of Dpp signaling in posterior spiracle development.
21 little effect on the activation of the empty spiracles element.
22 al fashion with the cephalic gap genes empty spiracles (ems) and buttonhead (btd) to assign segmental
23 odenticle (otd), buttonhead (btd), and empty spiracles (ems), which are expressed in partially overla
24 te homeobox gene related to Drosophila empty spiracles (ems)] RGCs in mouse neocortex and chick foreb
25 triguingly, several aspects of dpp posterior spiracle expression and function are similar to demonstr
26 change takes place, followed by a fluttering-spiracle (F) phase, which is usually dominated by diffus
27 d is necessary for designating the posterior spiracle field.
28 he previous observations of their effects on spiracle formation.
29 ired to activate dpp expression in posterior spiracle formation.
30 2, a human homologue of the Drosophila empty spiracles gene is a homeodomain-containing transcription
31 marker MDM panel (homeobox A1 [HOXA1], empty spiracles homeobox 1 [EMX1], AK055957, endothelin-conver
32 ls that is found embedded in the wall of the spiracle in many non-teleost jawed fishes.
33                                  The role of spiracles in polypterid respiration has been unclear, wi
34 he second round appears necessary for proper spiracle internal morphology and fusion with the remaind
35 video, kinematic and pressure data that show spiracle-mediated aspiration accounts for up to 93% of a
36                                      Second, spiracle morphogenesis requires the input of both trh an
37             The DGC is terminated by an open-spiracle (O) phase, during which accumulated CO2 escapes
38 nal running through the leg from an acoustic spiracle on the thorax.
39 le respiratory gases only through valve-like spiracles on their thorax and abdomen, making gas exchan
40  tetrapods, in having large paired openings (spiracles) on top of their head.
41 tein cannot activate its direct target empty spiracles or other downstream genes while it can functio
42 RNA and protein followed sequentially by the spiracle, the dorsal intrasegmental annuli, the interann
43          Transcriptional activation of empty spiracles, the Drosophila ortholog of EMX2, by Abdominal
44 ansfers sound from the mesothoracic acoustic spiracle to the internal side of the ear drums in the le
45 tion are compensated for by the simultaneous spiracle up-regulation of guanine nucleotide exchange fa
46 hat polypterids could inhale air through the spiracles, while later reports have largely dismissed su
47 arity in the size and position of polypterid spiracles with those of some stem tetrapods suggests tha