ライフサイエンスコーパス: horseshoe crab

1 ates (which includes spiders, scorpions, and horseshoe crabs).

2 s are of similar sizes to those found in the horseshoe crab.

3 s of bacteria and a clotting factor from the horseshoe crab.

4 nd fine setae permits comparison with extant horseshoe crabs.

5 revealed in the appendages of two species of horseshoe crabs.

6 uence comparisons between these taxa and the horseshoe crab, a chelicerate from the sister group to a

7 chondrial genomes are similar to that of the horseshoe crab, although both of the solifuges possess a

8 presentatives of Chelicerata, which includes horseshoe crabs and arachnids.

9 entified in mollusks, and arthropods such as horseshoe crabs and beetles, indicating that this pathwa

10 mical similarity between the Middle Triassic horseshoe crabs and their recent analogues documents ana

11 late claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus

12 Horseshoe crabs are classic "living fossils", supposedly

13 The living horseshoe crabs are remnants of a much larger diversity

14 Here, cysteine 271 of horseshoe crab arginine kinase has been mutated to serin

15 ysis clusters Limulus SAP pentraxin with the horseshoe crab C-reactive proteins (CRPs) rather than th

16 mes from three of the four extant species of horseshoe crabs-Carcinoscorpius rotundicauda, Limulus po

17 RP, which are 51% identical, and 31-35% with horseshoe crab CRPs.

18 nd posterior divisions of the body of living horseshoe crabs differ in the loss of the outer and inne

19 this relatively simple eye helps explain how horseshoe crabs find mates and may lead to a better unde

20 Here we report a new fossil horseshoe crab from the mid-Silurian Lagerstatte in Here

21 Middle Triassic (ca. 244 million years old) horseshoe crab from Yunnan Province, SW China.

22 Nonetheless, a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site,

23 erial lipopolysaccharide-binding lectin from horseshoe crab hemocytes.

24 milarity in structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.

25 Rhabdom shedding in horseshoe crab lateral eye photoreceptors was studied wi

26 hylogenetically ancient "living fossil", the horseshoe crab Limulus polyphemus and determined the thr

27 The photoreceptors of the horseshoe crab Limulus polyphemus are classical preparat

28 The lateral eyes of the horseshoe crab Limulus polyphemus undergo dramatic daily

29 In the horseshoe crab Limulus polyphemus, enhanced phosphorylat

30 all other known chelicerates, including the horseshoe crab Limulus polyphemus.

31 edulis and the telson levator muscle of the horseshoe crab Limulus polyphemus.

32 ational polymorphism from populations of the horseshoe crab Limulus polyphemus.

33 eactions of the sea cucumber Thyone, and the horseshoe crab Limulus.

34 eceptors from the ventral optic nerve of the horseshoe crab Limulus.

35 The acrosomal process of the sperm of the horseshoe crab (Limulus polyphemus) is a unique crystall

36 ng that powers the acrosomal reaction of the horseshoe crab (Limulus polyphemus) sperm.

37 (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and cone snail (Con

38 mage reconstruction of myosin filaments from horseshoe crab (Limulus) muscle.

39 cloning of the choline co-transporter in the horseshoe crab, Limulus polyphemus.

40 by one sensory organ, the lateral eye of the horseshoe crab, Limulus polyphemus.

41 s and is found in the plasma of the American horseshoe crab, Limulus polyphemus.

42 It has been found as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and

43 The existence of WGD in the horseshoe crabs, noted for relative morphological stasis

44 onal structures presented here and the known horseshoe crab pentraxin sequences, suggest that adaptat

45 traxin species distinct from all other known horseshoe crab pentraxins that exist in many variant for

46 ghly conserved N terminus of all other known horseshoe crab pentraxins.

47 Cretotrichopsenius display the protective horseshoe-crab-shaped body form typical of many modern t

48 all of which possess specialized swollen or horseshoe-crab-shaped body plans.

49 tribe Trichopseniini, display the protective horseshoe-crab-shaped body typical of many extant termit

50 system, the actin-based acrosomal bundle of horseshoe crab sperm.

51 elated antibacterial protein of the Japanese horseshoe crab Tachypleus tridentatus, showed properties

52 crobial peptide present in leukocytes of the horseshoe crab (Tachypleus tridentatus).

53 I is a 17-residue peptide isolated from the horseshoe crab, Tachypleus tridentatus.It has high antim

54 in host defense for "living fossils" such as horseshoe crabs, the role of the coagulation system in i

55 ith the Factor C, a serine protease found in horseshoe crabs, which is critical for antibacterial res