戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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 o land, a behavior similar to that of extant horseshoe crabs.
5 revealed in the appendages of two species of horseshoe crabs.
6 es, and marine sea spiders (pycnogonids) and horseshoe crabs.
7 vely, of chelicerate groups like spiders and horseshoe crabs.
8 nd fine setae permits comparison with extant horseshoe crabs.
9 hology resembles that of extant Merostomata (horseshoe crabs).(5) Here, we identify preserved traces
10 uence comparisons between these taxa and the horseshoe crab, a chelicerate from the sister group to a
11 chondrial genomes are similar to that of the horseshoe crab, although both of the solifuges possess a
12     The presence of marine species including horseshoe crab and green algae support a warmer climate
13 presentatives of Chelicerata, which includes horseshoe crabs and arachnids.
14 entified in mollusks, and arthropods such as horseshoe crabs and beetles, indicating that this pathwa
15 mical similarity between the Middle Triassic horseshoe crabs and their recent analogues documents ana
16 ns; Chelicerata, represented by sea spiders, horseshoe crabs, and arachnids-the last including spider
17 e: rhinoceroses, pangolins, bears, sturgeon, horseshoe crabs, and caterpillar fungus.
18 late claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus
19                                              Horseshoe crabs are an ancient species facing modern thr
20                                              Horseshoe crabs are archetypal marine chelicerates with
21                                              Horseshoe crabs are classic "living fossils", supposedly
22                                   The living horseshoe crabs are remnants of a much larger diversity
23                        Here, cysteine 271 of horseshoe crab arginine kinase has been mutated to serin
24 lysis recovers marine forms (sea spiders and horseshoe crabs) as the successive sister groups of a mo
25 ysis clusters Limulus SAP pentraxin with the horseshoe crab C-reactive proteins (CRPs) rather than th
26 mes from three of the four extant species of horseshoe crabs-Carcinoscorpius rotundicauda, Limulus po
27 RP, which are 51% identical, and 31-35% with horseshoe crab CRPs.
28 nd posterior divisions of the body of living horseshoe crabs differ in the loss of the outer and inne
29 this relatively simple eye helps explain how horseshoe crabs find mates and may lead to a better unde
30                  Here we report a new fossil horseshoe crab from the mid-Silurian Lagerstatte in Here
31  Middle Triassic (ca. 244 million years old) horseshoe crab from Yunnan Province, SW China.
32                                    The major horseshoe crab groups are thought to have arisen in the
33     Nonetheless, a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site,
34 erial lipopolysaccharide-binding lectin from horseshoe crab hemocytes.
35 milarity in structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.
36                          Rhabdom shedding in horseshoe crab lateral eye photoreceptors was studied wi
37 hylogenetically ancient "living fossil", the horseshoe crab Limulus polyphemus and determined the thr
38                    The photoreceptors of the horseshoe crab Limulus polyphemus are classical preparat
39                      The lateral eyes of the horseshoe crab Limulus polyphemus undergo dramatic daily
40                                       In the horseshoe crab Limulus polyphemus, enhanced phosphorylat
41  all other known chelicerates, including the horseshoe crab Limulus polyphemus.
42  edulis and the telson levator muscle of the horseshoe crab Limulus polyphemus.
43 ational polymorphism from populations of the horseshoe crab Limulus polyphemus.
44 eactions of the sea cucumber Thyone, and the horseshoe crab Limulus.
45 eceptors from the ventral optic nerve of the horseshoe crab Limulus.
46    The acrosomal process of the sperm of the horseshoe crab (Limulus polyphemus) is a unique crystall
47 ng that powers the acrosomal reaction of the horseshoe crab (Limulus polyphemus) sperm.
48 (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and cone snail (Con
49 mage reconstruction of myosin filaments from horseshoe crab (Limulus) muscle.
50 x datasets spanning 22-46 years for Atlantic horseshoe crabs (Limulus polyphemus) in the Long Island
51 cloning of the choline co-transporter in the horseshoe crab, Limulus polyphemus.
52 by one sensory organ, the lateral eye of the horseshoe crab, Limulus polyphemus.
53 s and is found in the plasma of the American horseshoe crab, Limulus polyphemus.
54    It has been found as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and
55 ing arachnids as a clade and instead finding horseshoe crabs nested inside terrestrial Arachnida.
56                  The existence of WGD in the horseshoe crabs, noted for relative morphological stasis
57 onal structures presented here and the known horseshoe crab pentraxin sequences, suggest that adaptat
58 traxin species distinct from all other known horseshoe crab pentraxins that exist in many variant for
59 ghly conserved N terminus of all other known horseshoe crab pentraxins.
60 ultiomics of the cartilaginous book gills of horseshoe crabs reveals a developmental program shared w
61    Cretotrichopsenius display the protective horseshoe-crab-shaped body form typical of many modern t
62  all of which possess specialized swollen or horseshoe-crab-shaped body plans.
63 tribe Trichopseniini, display the protective horseshoe-crab-shaped body typical of many extant termit
64  system, the actin-based acrosomal bundle of horseshoe crab sperm.
65 elated antibacterial protein of the Japanese horseshoe crab Tachypleus tridentatus, showed properties
66 crobial peptide present in leukocytes of the horseshoe crab (Tachypleus tridentatus).
67  I is a 17-residue peptide isolated from the horseshoe crab, Tachypleus tridentatus.It has high antim
68 in host defense for "living fossils" such as horseshoe crabs, the role of the coagulation system in i
69                              However, modern horseshoe crabs undertake amphibious excursions onto lan
70 ith the Factor C, a serine protease found in horseshoe crabs, which is critical for antibacterial res