ライフサイエンスコーパス: chelicerate

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1 chondrial rRNA structures of a hexapod and a chelicerate.

2 inities to pancrustacean WYR was observed in chelicerates.

3 tacea, and an alliance between myriapods and chelicerates.

4 mnants of a much larger diversity of aquatic chelicerates.

5 tream of where they are typically located in chelicerates.

6 ve been analyzed in insects, crustaceans and chelicerates.

7 stral domain similar to that found in modern chelicerates.

8 erbivores that are very distantly related to chelicerates.

9 chelate first appendage is consistent with a chelicerate affinity for the pycnogonids.

10 Of note, other arthropods such as chelicerates and crustaceans express two dsx genes, both

11 round patterns characterizing onychophorans, chelicerates and mandibulates are likely to have diverge

12 debate was stimulated recently by studies in chelicerates and myriapods that show that neural precurs

13 In the remaining euarthropod groups, the chelicerates and myriapods, a single-minded homologue ha

14 ed in insects and several representatives of chelicerates and myriapods, while data on crustaceans ar

15 many cases intermediate between those of the chelicerates and those of the insects and crustaceans, c

16 umber of studies in insects, crustaceans and chelicerates, and is important for the correct reconstru

17 n segment (protocerebrum) of mandibulate and chelicerate arthropods and the nonganglionic brains of p

18 hat a true biramous limb was once present in chelicerates as well as in the mandibulates.

19 s); in the remaining euarthropod groups, the chelicerates (e.g. spiders) and myriapods (e.g. milliped

20 ed by segmental stripes, while myriapods and chelicerates exhibit segmental stripes that form early i

21 between these taxa and the horseshoe crab, a chelicerate from the sister group to arachnids.

22 nguish some groups of arachnids, distinguish chelicerates from other arthropods, and further clarify

23 ore the last common ancestor of these marine chelicerates >135 million years ago.

24 fied in the spider Achaearanea tepidariorum (chelicerate), however, the gene is not expressed in the

25 ifferent from the pattern in all other known chelicerates, including the horseshoe crab Limulus polyp

26 The chelicerate Limulus polyphemus, all isopod crustaceans t

27 nd the longest contiguous fragments with the chelicerate Limulus polyphemus.

28 Chelicerate mites diverged from other arthropod lineages

29 tin was not identified in representatives of chelicerates, myriapods, or any species outside Pancrust

30 s (insects/crustaceans) or precursor groups (chelicerates/myriapods) per hemi-segment.

31 ancestor or whether myriapods group with the chelicerates (Myriochelata).

32 tionship to 46 other insect, crustacean, and chelicerate opsin sequences.

33 rown-group euarthropods near the ancestry of chelicerates, or a segmented ecdysozoan lineage with con

34 are observed in both our fossil and outgroup chelicerate orders.

35 he shared neural characters of myriapods and chelicerates represent derived characters that support t

36 pair-rule patterning in either myriapods or chelicerates, suggesting that the early pair-rule expres

37 that differs in location from those of other chelicerates, suggesting that these translocations occur

38 he development of mechanosensory organs in a chelicerate, the spider Cupiennius salei.

39 most basally branching arthropod clade, the chelicerates (which includes spiders, scorpions, and hor

40 Spiders belong to the chelicerates, which is an arthropod group that branches

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