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1 f four immunoglobulin-like domains forming a horseshoe.
2 tely above the hollow space formed by the TM horseshoe.
6 o sites located at opposite ends of the TLR3 horseshoe, and an intermolecular contact between the two
8 ct, sympatric size morphs of the large-eared horseshoe bat (Rhinolophus philippinensis) echolocate at
14 ity in the PB while spontaneously vocalizing horseshoe bats were provoked to emit either short, singl
15 d microbats from the families Rhinolophidae (horseshoe bats, Old World leaf-nosed bats) and Megaderma
16 h morphological characteristics, shared with horseshoe bats, suggest that there has been convergent e
20 med that the L1 molecule is primarily in the horseshoe conformation in solution, and we have visualiz
21 the interface of Ig1 and Ig4 to stabilize a horseshoe conformation of L1 that favors homophilic bind
22 We arrived at a model in which BTX adopts a horseshoe conformation with the horseshoe plane normal t
26 rvature and host membrane lipids that permit horseshoe conformations are selectively recruited into t
27 ease inhibitors, and the inner lining of the horseshoe consists of the beta-stranded Leu/Ile-X-Leu/Il
28 The acrosomal process of the sperm of the horseshoe crab (Limulus polyphemus) is a unique crystall
30 (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and cone snail (Con
34 ysis clusters Limulus SAP pentraxin with the horseshoe crab C-reactive proteins (CRPs) rather than th
38 Nonetheless, a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site,
40 milarity in structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.
42 hylogenetically ancient "living fossil", the horseshoe crab Limulus polyphemus and determined the thr
51 onal structures presented here and the known horseshoe crab pentraxin sequences, suggest that adaptat
52 traxin species distinct from all other known horseshoe crab pentraxins that exist in many variant for
55 elated antibacterial protein of the Japanese horseshoe crab Tachypleus tridentatus, showed properties
56 uence comparisons between these taxa and the horseshoe crab, a chelicerate from the sister group to a
57 chondrial genomes are similar to that of the horseshoe crab, although both of the solifuges possess a
61 It has been found as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and
62 I is a 17-residue peptide isolated from the horseshoe crab, Tachypleus tridentatus.It has high antim
65 Cretotrichopsenius display the protective horseshoe-crab-shaped body form typical of many modern t
67 tribe Trichopseniini, display the protective horseshoe-crab-shaped body typical of many extant termit
69 entified in mollusks, and arthropods such as horseshoe crabs and beetles, indicating that this pathwa
70 mical similarity between the Middle Triassic horseshoe crabs and their recent analogues documents ana
73 nd posterior divisions of the body of living horseshoe crabs differ in the loss of the outer and inne
74 this relatively simple eye helps explain how horseshoe crabs find mates and may lead to a better unde
76 late claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus
78 in host defense for "living fossils" such as horseshoe crabs, the role of the coagulation system in i
79 ith the Factor C, a serine protease found in horseshoe crabs, which is critical for antibacterial res
80 mes from three of the four extant species of horseshoe crabs-Carcinoscorpius rotundicauda, Limulus po
87 h myopia, three limb post-axial polydactyly, horseshoe kidney, abnormally positioned uterus and eleva
88 so provide insights into the pathogenesis of horseshoe kidneys and how congenital kidney defects can
93 eport, we review five transplantations using horseshoe kidneys: the largest reported institutional ex
94 n previously proposed where chordin adopts a horseshoe-like arrangement enabling BMP binding cooperat
95 e reveals how suvorexant adopts a pi-stacked horseshoe-like conformation and binds to the receptor de
96 res, the N-terminal region of CNTN4 adopts a horseshoe-like conformation found also in CNTN2 and most
97 s share common structural features such as a horseshoe-like pseudo two-fold symmetric fold, several c
98 all kinked around the hinge region forming a horseshoe-like shape, and the regions of flexibility of
101 e extreme curvature of the viral capsid, as 'horseshoe' lipid conformations favor such curvature and
103 wed peaks at both frequencies, arranged in a horseshoe pattern from posterior to anterior regions, wh
105 on showed that these domains are bent into a horseshoe shape in the related molecules hemolin and axo
106 on micrographs, the complex has a bilobed or horseshoe shape with outer dimensions of approximately 1
107 rminal Ig-like domains of neurofascin form a horseshoe shape, akin to several other immunoglobulin su
108 ent may wrap around the MIP1alpha dimer in a horseshoe shape, facilitating the interaction of the S-d
110 hand) muscle representation surrounded by a "horseshoe"-shaped zone of proximal (shoulder and elbow)
111 A structure reported recently reveals a horseshoe-shaped arrangement of 19 transmembrane helices
113 EAT repeats of the scaffold A subunit form a horseshoe-shaped fold, holding the catalytic C and regul
115 y a pair of agglutinated valves, enclosing a horseshoe-shaped lophophore, supported by a lower bipart
117 n structure at 2.1 angstroms reveals a large horseshoe-shaped solenoid assembled from 23 leucine-rich
118 uggest that the basic framework of TLRs is a horseshoe-shaped solenoid that contains an extensive bet
120 I, which is anionic, also appears to use its horseshoe-shaped structure to engender long-range Coulom
124 a double addition is possible, leading to a horseshoe-shaped system comprised of seven conjugated ri
125 The gamma-secretase complex comprises a horseshoe-shaped transmembrane domain, which contains 19
126 pen, while the viral cores were cylindrical, horseshoe-shaped, or fragmented, with some particles con
129 stallization revealed that hTLR3 ECD forms a horseshoe structure similar to the recently elucidated x
130 uidic design involves a bubble anchored in a horseshoe structure which can be stimulated by a piezoel
132 is accessible from the convex side of the TM horseshoe, suggesting considerable conformational change
133 tility, whereas treatment of an asymptomatic horseshoe tear resulted in $2981/QALY ($1436/QALY).
135 ement of incident acute PVD (and symptomatic horseshoe tears) offer a low cost and a favorable cost-u
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