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1 f four immunoglobulin-like domains forming a horseshoe.
2 tely above the hollow space formed by the TM horseshoe.
3            Treatment decisions for stones in horseshoe and ectopic kidneys can be challenging, and mu
4                              Urolithiasis in horseshoe and ectopic kidneys presents unique challenges
5 the protein, weakening the bonds forming the horseshoe and permitting the molecule to extend.
6 o sites located at opposite ends of the TLR3 horseshoe, and an intermolecular contact between the two
7 SARS)-like CoV was identified in the Chinese horseshoe bat (Rhinolophidae) in 2005.
8 ct, sympatric size morphs of the large-eared horseshoe bat (Rhinolophus philippinensis) echolocate at
9 V, which is currently circulating in Chinese horseshoe bat populations.
10 treetlights along commuting routes of lesser horseshoe bats (Rhinolophus hipposideros).
11                                              Horseshoe bats are a diverse Old World family (Rhinoloph
12          Moreover, because call frequency in horseshoe bats has a dual function in resource acquisiti
13                         We used echolocating horseshoe bats to investigate the role of the midbrain a
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
17 uency in a highly vocal mammal, echolocating horseshoe bats.
18 tion, in an isolated larynx preparation from horseshoe bats.
19                      The structures reveal a horseshoe configuration, with variable residues of D2 an
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
23 a compact shape consistent with the expected horseshoe conformation.
24 mmunoglobulin domains (Ig1-4), arranged in a horseshoe conformation.
25 brane-derived lipids which adopt a U-shaped 'horseshoe' conformation.
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
29 ng that powers the acrosomal reaction of the horseshoe crab (Limulus polyphemus) sperm.
30 (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and cone snail (Con
31 mage reconstruction of myosin filaments from horseshoe crab (Limulus) muscle.
32 crobial peptide present in leukocytes of the horseshoe crab (Tachypleus tridentatus).
33                        Here, cysteine 271 of horseshoe crab arginine kinase has been mutated to serin
34 ysis clusters Limulus SAP pentraxin with the horseshoe crab C-reactive proteins (CRPs) rather than th
35 RP, which are 51% identical, and 31-35% with horseshoe crab CRPs.
36                  Here we report a new fossil horseshoe crab from the mid-Silurian Lagerstatte in Here
37  Middle Triassic (ca. 244 million years old) horseshoe crab from Yunnan Province, SW China.
38     Nonetheless, a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site,
39 erial lipopolysaccharide-binding lectin from horseshoe crab hemocytes.
40 milarity in structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.
41                          Rhabdom shedding in horseshoe crab lateral eye photoreceptors was studied wi
42 hylogenetically ancient "living fossil", the horseshoe crab Limulus polyphemus and determined the thr
43                    The photoreceptors of the horseshoe crab Limulus polyphemus are classical preparat
44                      The lateral eyes of the horseshoe crab Limulus polyphemus undergo dramatic daily
45                                       In the horseshoe crab Limulus polyphemus, enhanced phosphorylat
46  edulis and the telson levator muscle of the horseshoe crab Limulus polyphemus.
47 ational polymorphism from populations of the horseshoe crab Limulus polyphemus.
48  all other known chelicerates, including the horseshoe crab Limulus polyphemus.
49 eactions of the sea cucumber Thyone, and the horseshoe crab Limulus.
50 eceptors from the ventral optic nerve of the horseshoe crab Limulus.
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
53 ghly conserved N terminus of all other known horseshoe crab pentraxins.
54  system, the actin-based acrosomal bundle of horseshoe crab sperm.
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
58 cloning of the choline co-transporter in the horseshoe crab, Limulus polyphemus.
59 by one sensory organ, the lateral eye of the horseshoe crab, Limulus polyphemus.
60 s and is found in the plasma of the American horseshoe crab, Limulus polyphemus.
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
63 s of bacteria and a clotting factor from the horseshoe crab.
64 s are of similar sizes to those found in the horseshoe crab.
65    Cretotrichopsenius display the protective horseshoe-crab-shaped body form typical of many modern t
66  all of which possess specialized swollen or horseshoe-crab-shaped body plans.
67 tribe Trichopseniini, display the protective horseshoe-crab-shaped body typical of many extant termit
68 presentatives of Chelicerata, which includes horseshoe crabs and arachnids.
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
71                                              Horseshoe crabs are classic "living fossils", supposedly
72                                   The living horseshoe crabs are remnants of a much larger diversity
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
75 ates (which includes spiders, scorpions, and horseshoe crabs).
76 late claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus
77                  The existence of WGD in the horseshoe crabs, noted for relative morphological stasis
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
81 nd fine setae permits comparison with extant horseshoe crabs.
82 revealed in the appendages of two species of horseshoe crabs.
83 MT suggests that this protein would assume a horseshoe fold and lack methyltransferase activity.
84 ependent packing patterns, reveals a pair of horseshoes in trans-synaptic adhesion mode.
85                          Oxygen atoms at the horseshoe inner surface constitute a transient binding s
86                                  These Ig1-4 horseshoes interact in a novel back-to-back orientation
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
89                        Experience with donor horseshoe kidneys for transplantation is very limited.
90 , but resulted in kidney fusions, resembling horseshoe kidneys in humans.
91 m data revealed good graft survival of donor horseshoe kidneys in renal transplantation.
92                                   Currently, horseshoe kidneys may be underutilized for transplantati
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
99  would extend outward on the outer face of a horseshoe-like structure.
100 etrical circular toroids but in less regular horseshoe-like structures.
101 e extreme curvature of the viral capsid, as 'horseshoe' lipid conformations favor such curvature and
102 ine residues; it adopts a shape similar to a horseshoe of dimensions 125 x 80 x 40 A.
103 wed peaks at both frequencies, arranged in a horseshoe pattern from posterior to anterior regions, wh
104 BTX adopts a horseshoe conformation with the horseshoe plane normal to the pore axis.
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
109 s to be elongated, with no indication of the horseshoe shape.
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
112 )is on the front face) and loop 2, forming a horseshoe-shaped arrangement.
113 EAT repeats of the scaffold A subunit form a horseshoe-shaped fold, holding the catalytic C and regul
114                       Rpn3/5/6/7/9/12 form a horseshoe-shaped heterohexamer, which connects to the CP
115 y a pair of agglutinated valves, enclosing a horseshoe-shaped lophophore, supported by a lower bipart
116 n the flagella, the majority is found in two horseshoe-shaped rings around the basal bodies.
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
119                                  The overall horseshoe-shaped structure of the TLR3-ECD is formed by
120 I, which is anionic, also appears to use its horseshoe-shaped structure to engender long-range Coulom
121                         TFIID is a trilobed, horseshoe-shaped structure, with TFIIA and TFIIB bound o
122 ether show that chordin indeed has a compact horseshoe-shaped structure.
123            First, we observed a constrained, horseshoe-shaped substrate pocket, formed from an alpha-
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
127                                VPS35 forms a horseshoe-shaped, right-handed, alpha-helical solenoid,
128                 LRRs are known to assume the horseshoe structure in ribonuclease inhibitors, and the
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
131 on the concave surface of the characteristic horseshoe structure.
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).
134                   Treatment of a symptomatic horseshoe tear resulted in a net cost savings of $1749 (
135 ement of incident acute PVD (and symptomatic horseshoe tears) offer a low cost and a favorable cost-u

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