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1 f four immunoglobulin-like domains forming a horseshoe.
2 tely above the hollow space formed by the TM horseshoe.
7 o sites located at opposite ends of the TLR3 horseshoe, and an intermolecular contact between the two
8 like protein (NIPBL) induced the assembly of horseshoe, banded, ringed and hypersegmented nuclear str
10 ) from two species of bats: the wild greater horseshoe bat (Rhinolophus ferrumequinum) and the greate
11 Bats, particularly the long-lived greater horseshoe bat (Rhinolophus ferrumequinum), provide a rar
12 ct, sympatric size morphs of the large-eared horseshoe bat (Rhinolophus philippinensis) echolocate at
15 S protein selectively abrogated the usage of horseshoe bat and pangolin ACE2 but enhanced the usage o
16 itro to show that, unlike its non-prenylated horseshoe bat descendants, RhinoCA OAS1 successfully blo
18 iruses traveled at rates approximating their horseshoe bat hosts and circulated in Asia for millennia
20 new chromosomal-level genome assemblies for horseshoe bat species (Rhinolophus) and three close rela
22 a novel sarbecovirus (RhGB01) from a British horseshoe bat, at the western extreme of the rhinolophid
30 and show that, during their diversification, horseshoe bats underwent extensive chromosomal rearrange
31 selection taking place in Sarbecoviruses in horseshoe bats versus the early SARS-CoV-2 evolution in
32 ity in the PB while spontaneously vocalizing horseshoe bats were provoked to emit either short, singl
33 SARS-CoV and SARS-CoV-2 were circulating in horseshoe bats, confirming their importance as the reser
34 d microbats from the families Rhinolophidae (horseshoe bats, Old World leaf-nosed bats) and Megaderma
35 h morphological characteristics, shared with horseshoe bats, suggest that there has been convergent e
41 med that the L1 molecule is primarily in the horseshoe conformation in solution, and we have visualiz
42 the interface of Ig1 and Ig4 to stabilize a horseshoe conformation of L1 that favors homophilic bind
43 We arrived at a model in which BTX adopts a horseshoe conformation with the horseshoe plane normal t
47 rvature and host membrane lipids that permit horseshoe conformations are selectively recruited into t
48 ease inhibitors, and the inner lining of the horseshoe consists of the beta-stranded Leu/Ile-X-Leu/Il
49 The acrosomal process of the sperm of the horseshoe crab (Limulus polyphemus) is a unique crystall
51 (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and cone snail (Con
56 ysis clusters Limulus SAP pentraxin with the horseshoe crab C-reactive proteins (CRPs) rather than th
61 Nonetheless, a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site,
63 milarity in structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.
65 hylogenetically ancient "living fossil", the horseshoe crab Limulus polyphemus and determined the thr
74 onal structures presented here and the known horseshoe crab pentraxin sequences, suggest that adaptat
75 traxin species distinct from all other known horseshoe crab pentraxins that exist in many variant for
78 elated antibacterial protein of the Japanese horseshoe crab Tachypleus tridentatus, showed properties
79 uence comparisons between these taxa and the horseshoe crab, a chelicerate from the sister group to a
80 chondrial genomes are similar to that of the horseshoe crab, although both of the solifuges possess a
84 It has been found as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and
85 I is a 17-residue peptide isolated from the horseshoe crab, Tachypleus tridentatus.It has high antim
88 Cretotrichopsenius display the protective horseshoe-crab-shaped body form typical of many modern t
90 tribe Trichopseniini, display the protective horseshoe-crab-shaped body typical of many extant termit
91 x datasets spanning 22-46 years for Atlantic horseshoe crabs (Limulus polyphemus) in the Long Island
93 entified in mollusks, and arthropods such as horseshoe crabs and beetles, indicating that this pathwa
94 mical similarity between the Middle Triassic horseshoe crabs and their recent analogues documents ana
99 nd posterior divisions of the body of living horseshoe crabs differ in the loss of the outer and inne
100 this relatively simple eye helps explain how horseshoe crabs find mates and may lead to a better unde
101 ing arachnids as a clade and instead finding horseshoe crabs nested inside terrestrial Arachnida.
102 ultiomics of the cartilaginous book gills of horseshoe crabs reveals a developmental program shared w
104 lysis recovers marine forms (sea spiders and horseshoe crabs) as the successive sister groups of a mo
106 hology resembles that of extant Merostomata (horseshoe crabs).(5) Here, we identify preserved traces
107 ns; Chelicerata, represented by sea spiders, horseshoe crabs, and arachnids-the last including spider
109 late claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus
111 in host defense for "living fossils" such as horseshoe crabs, the role of the coagulation system in i
112 ith the Factor C, a serine protease found in horseshoe crabs, which is critical for antibacterial res
113 mes from three of the four extant species of horseshoe crabs-Carcinoscorpius rotundicauda, Limulus po
119 geometric abnormalities such as "arch" and "horseshoe" effects, potentially obscuring the impact of
120 mpare the GR2D2 estimator with the graphical horseshoe estimator in five cancer RNA-seq gene expressi
121 MT suggests that this protein would assume a horseshoe fold and lack methyltransferase activity.
122 GF signaling at the dorsal midline, whereas 'horseshoe' genes are predominantly regulated by Wnt sign
126 h myopia, three limb post-axial polydactyly, horseshoe kidney, abnormally positioned uterus and eleva
127 es, which we named KINSSHIP syndrome (KI for horseshoe kidney, NS for Nievergelt/Savarirayan type of
128 so provide insights into the pathogenesis of horseshoe kidneys and how congenital kidney defects can
133 eport, we review five transplantations using horseshoe kidneys: the largest reported institutional ex
134 resolved oxygen isotope (d(18)O) record from Horseshoe Lake (Collinsville, IL), an evaporatively infl
138 n previously proposed where chordin adopts a horseshoe-like arrangement enabling BMP binding cooperat
139 e reveals how suvorexant adopts a pi-stacked horseshoe-like conformation and binds to the receptor de
140 res, the N-terminal region of CNTN4 adopts a horseshoe-like conformation found also in CNTN2 and most
141 of TbBILBO1-NTD, which revealed a conserved horseshoe-like hydrophobic pocket formed by an unusually
142 s share common structural features such as a horseshoe-like pseudo two-fold symmetric fold, several c
143 all kinked around the hinge region forming a horseshoe-like shape, and the regions of flexibility of
145 to stochastic strange attractors exhibiting horseshoe-like structures mirroring turbulent transport
147 e extreme curvature of the viral capsid, as 'horseshoe' lipid conformations favor such curvature and
148 both Gaussian Markov random field (GMRF) and horseshoe Markov random field (HSMRF) prior distribution
151 udy demonstrates that regression models with horseshoe or lasso priors are effective for analyzing AD
152 wed peaks at both frequencies, arranged in a horseshoe pattern from posterior to anterior regions, wh
153 ntially binds at the promoters of genes with horseshoe patterns, but further from the promoters of ge
155 parse Bayesian inference via the regularized horseshoe prior to produce robust, interpretable biochem
156 y-inducing prior, the structured regularized horseshoe prior, BCGLMM effectively collaborates phyloge
158 ld detect this mass coral bleaching event at Horseshoe Reef and Cheeca Rocks in the Florida Keys.
159 ine regression (BKMR) and Bayesian penalized horseshoe regression for variable selection and then bui
162 on showed that these domains are bent into a horseshoe shape in the related molecules hemolin and axo
163 blastopore falls into two main categories: a horseshoe shape with a dorsal gap, as in Wnt8 expression
164 on micrographs, the complex has a bilobed or horseshoe shape with outer dimensions of approximately 1
165 rminal Ig-like domains of neurofascin form a horseshoe shape, akin to several other immunoglobulin su
166 ent may wrap around the MIP1alpha dimer in a horseshoe shape, facilitating the interaction of the S-d
168 hand) muscle representation surrounded by a "horseshoe"-shaped zone of proximal (shoulder and elbow)
169 A structure reported recently reveals a horseshoe-shaped arrangement of 19 transmembrane helices
171 structures also revealed that by adopting a horseshoe-shaped conformation in a deep groove, the glyc
172 EAT repeats of the scaffold A subunit form a horseshoe-shaped fold, holding the catalytic C and regul
174 y a pair of agglutinated valves, enclosing a horseshoe-shaped lophophore, supported by a lower bipart
175 eated giant cell containing a characteristic horseshoe-shaped ring of nuclei that are present within
177 n structure at 2.1 angstroms reveals a large horseshoe-shaped solenoid assembled from 23 leucine-rich
178 uggest that the basic framework of TLRs is a horseshoe-shaped solenoid that contains an extensive bet
180 I, which is anionic, also appears to use its horseshoe-shaped structure to engender long-range Coulom
181 ing indicates that Lrch4 LRRs conform to the horseshoe-shaped structure typical of LRRs in pathogen-r
185 a double addition is possible, leading to a horseshoe-shaped system comprised of seven conjugated ri
187 The gamma-secretase complex comprises a horseshoe-shaped transmembrane domain, which contains 19
188 pen, while the viral cores were cylindrical, horseshoe-shaped, or fragmented, with some particles con
191 stallization revealed that hTLR3 ECD forms a horseshoe structure similar to the recently elucidated x
192 uidic design involves a bubble anchored in a horseshoe structure which can be stimulated by a piezoel
195 is accessible from the convex side of the TM horseshoe, suggesting considerable conformational change
197 tility, whereas treatment of an asymptomatic horseshoe tear resulted in $2981/QALY ($1436/QALY).
200 ement of incident acute PVD (and symptomatic horseshoe tears) offer a low cost and a favorable cost-u