ライフサイエンスコーパス: bi-

1 ty of immunization (0.732) and the lowest of BI (0.098).

2 y of immunization (0.418) and the highest of BI (0.323); all mRNA-1273 vaccine sequences showed the h

3 TNFR1 was associated with baseline BI (-0.93 BI points per SD increment in TNFR1; 95% confi

4 The detection limit for Bi (1.1 ng mL(-1)) is worse than with the QTA (0.16 ng m

5 pped more often with maxima along Line-P for BI (10 667 +/- 1299 copies ml(-1) ) and the tropical Atl

6 S instillation in the presence or absence of BI (15% of body surface burn) and determined the degree

7 al cation 6(+), obtained by oxidation of 2,6-bi-(2'-oxa-6'-azaadamantane-6'-yl)-2,6-diazaadamantane-2

8 thod was developed for the synthesis of 2,2'-bi-, 2,2':6',2"-ter-, and 2,2':6',2'':6'',2'''-quaterpyr

9 CuSe, while the binary-elemental Bi(2)O(3) + Bi + 3Cu + 3Se reaction generates many intermediates bef

10 rials (Bi(2)O(2)Se + Cu(2)Se and Bi(2)O(3) + Bi + 3Cu + 3Se) were studied to determine the effect of

11 -dependent binding of hydrophobic probe 1,1'-bi-(4-anili-no)naphthalene-5,5'-disulfonate (bis-ANS) to

12 quantification of (221)Fr (218 keV) and (213)Bi (440 keV).

13 rotect DNA from digestion by R.HphI or R.Ngo BI (5'TCACC 3').

14 e between the periods without and with Power BI (50.1% vs. 47.9%, P = 0.152).

15 asting showed significantly higher impact on BI (58.61% for YW, 131% for BW and 83.85% for PW) and WA

16 hrough binding with demethylated naphthol AS-BI (7-bromo-3-hydroxy-2-naphth-o-hydroxyanilide, 2) and

17 , cyclobutadiene, or benzyne, the respective bi-[8]annulenylene, [6]annuleno[8]annulene, or [6]-[8]an

18 y functional outcomes were not different for BI (95-100) (0.6, 0.4-1.1; p=0.13) or for mRS score (0.6

19 A partially ordered Pd(3)Bi (a mixed phase of intermetallic and solid solution) a

20 rs was achieved by incubating them with (213)Bi- and (188)Re-labeled mAb 18B7 or with (188)Re-9C7 mAb

21 RIT of CN with (213)Bi- and (188)Re-labeled specific mAb and of HC with (188

22 Both (213)Bi- and (211)At-labeled 201B mAb were effective therapie

23 Results: (213)Bi- and (225)Ac-L1 demonstrated specific cell uptake and

24 Results:(213)Bi- and (225)Ac-L1 demonstrated specific cell uptake and

25 Hence, SR-BI- and autophagy promote a surveillance pathway that pa

26 intestinal cholesterol absorption, blocks SR-BI- and CD36-facilitated uptake of cholesterol into COS-

27 In order to distinguish between Bi- and host-related traps and to identify their possibl

28 nd that cAMP signaling accelerates repair of bi- and mono-functional platinum-induced DNA damage.

29 in patients with HAX1 deficiency as well as bi- and monoallelic mutations in CLPB.

30 We show that CRISPR/Cas9-introduced bi- and monoallelic SNORA31 deletions render human pluri

31 piezoconductive effect observed in suspended bi- and multi-layer graphene.

32 tlight, we present the mechanisms generating bi- and multi-nucleated cardiomyocytes, and the mechanis

33 ods, aroyl-S,N-ketene acetals and subsequent bi- and multichromophores can be readily synthesized.

34 of a host of transition metal complexes with bi- and multidentate ligands discloses the distortion pa

35 available in ultrathin forms such as mono-, bi- and multilayers, which are commonly known as two-dim

36 en divorced from cytokinesis and so produces bi- and multinucleated cells.

37 quency combs can be used to generate several bi- and multiphoton entangled qubits, with direct applic

38 ation [2]catenane and other more traditional bi- and multistation molecular switches are significant.

39 Bi- and multivariable logistic regression, Kaplan-Meier

40 Bi- and multivariate analyses and machine learning algor

41 Uni-, bi- and multivariate analyses were performed using Poiss

42 We then developed bi- and multivariate models for predicting half-lives in

43 We investigate uni-, bi- and multivariate properties of sensor time series by

44 gical behavior in schizophrenia across uni-, bi- and multivariate scales and lay the groundwork for f

45 ered [Ni@[Bi6Ni6(CO)8]4- by removal of three Bi- and one Ni-atoms of two neighboring triangular faces

46 resent findings, we propose BaFe(2)O(4) as a Bi- and Pb-free model for the search of new advanced mul

47 aura coupling for the synthesis of unnatural bi- and polyaryl and heteroaryl amino acid derivatives (

48 d for the construction of such benzannulated bi- and polycyclic carbon frameworks has been developed,

49 mature cell type ('uni-lineage potential'), bi- and rarer multi-lineage progenitors were present amo

50 sive overview of the development of emerging Bi- and Sb-based as well as a new Cu, Sn, Pb, Ag, and hy

51 y and diversity of an existing collection of bi- and terphenyl compounds, we synthesized hybrid molec

52 ogenative coupling of 4-picoline to form the bi- and terpyridine.

53 Platinum(II) bi- and terpyridyl chloro complexes, Pt(dcbpy)Cl2 and [P

54 Fluorescent alpha,alpha'-diamide substituted bi- and terthiophene derivatives were prepared by Stille

55 A series of unsymmetrical bi- and tetrathiophenes have been synthesized with bipyr

56 Bi- and tri-antennary "complex type" oligosaccharides ha

57 ometry, which demonstrates a predominance of bi- and tri-antennary core-fucosylated complex type stru

58 A family of about 20 novel acidic bi- and tri-antennary N-glycans, amounting to almost hal

59 Bi- and tri-antennary oligosaccharides with bisecting Gl

60 These glycans were mainly bi- and tri-antennary sugars with up to five and seven f

61 Bi- and tri-exponential models for ultrasensitive assay

62 lacking this enzyme are more susceptible to bi- and tri-functional DNA alkylating agents with this p

63 Here we show that interlayer excitons in bi- and tri-layer 2H-MoSe(2) crystals exhibit electric-f

64 Further, we observe the bi- and tri-layer excited state (2s) interlayer excitons

65 ology but different particle density for the bi- and tri-segmented viral particles and reveal major v

66 work, we first show that estimating MI of a bi- and tri-variate Gaussian distribution using k-neares

67 of the method enables the genetic typing of bi- and triallelic single-nucleotide polymorphisms in po

68 nd to two types of asialo-glycans, namely to bi- and triantennary complex N-glycan structures (NA2/NA

69 A unified strategy for the syntheses of bi- and triantennary fully sialylated N-glycans is descr

70 The Endo-F3 mutants were able to use both bi- and triantennary glycan oxazolines as substrates for

71 ociated increase in outer arm fucose on both bi- and triantennary glycans at the N187 site of HPX.

72 Asymmetric bi- and triantennary glycans could be obtained by remova

73 difucosylated paucimannosidic forms, whereas bi- and triantennary glycans were found in both sources,

74 reviously infeasible synthesis of asymmetric bi- and triantennary N-glycans, especially with the LacN

75 phenotypes were found to be consistent with bi- and triantennary structures of complex type that exh

76 Bi- and triantennary structures, with and without lactos

77 comprised of 23 heterogeneous glycoforms of bi- and triantennary, core and terminal fucosylation, an

78 A practical one-pot synthesis of bi- and triantennated australine analogues from a pivota

79 t a one-pot Lewis acid mediated synthesis of bi- and triarylpropanal derivatives and their correspond

80 systematic access to a variety of different bi- and triaryls with good to excellent yields for the c

81 port details of the synthesis of a series of bi- and trichromophores.

82 We have now created a collection of bi- and tricongenic strains with these intervals and ass

83 ated directly with diphenylketene to produce bi- and tricyclic 3,4-dihydropyridin-2(1H)-ones; similar

84 A method for the synthesis of bi- and tricyclic amidines has been developed through co

85 give highly unusual and medicinally relevant bi- and tricyclic barbiturates.

86 Of the bi- and tricyclic classes of diterpenes found in Salvia,

87 ration for the preparation of spiro or fused bi- and tricyclic ether units prevalent in molecules for

88 yl dianion to a cyclohexasilane, we obtained bi- and tricyclic ladder cyclohexasilanes.

89 these structures to obtain extremely potent bi- and tricyclic PCSK9 inhibitor peptides.

90 of aromatic ketimines and aldimines provides bi- and tricyclic ring systems with good regioselectivit

91 d, giving rise rapidly to more complex fused bi- and tricyclic scaffolds.

92 ype rearrangement of a series of benzo-fused bi- and tricyclic sulfonamides is reported.

93 ly useful dihydrothiopyrans as well as other bi- and tricyclic sulfur-containing heterocycles are for

94 ]nonane, bicyclo[2.2.1]heptane, and selected bi- and tricyclic terpenoids.

95 A series of bi- and tricyclic, N-heterocycle-fused, beta-lactones we

96 Additionally, in the case of bi- and tricyclizations, decalins with cis stereochemist

97 metal-complexing fragments with alternating bi- and tridentate chelates has been shown to behave as

98 KOH, after acidification, directly provides bi- and tridentate ligands containing the 4-carboxy-1,8-

99 his approach was shown by the preparation of bi- and trifunctional building blocks (21 examples), whi

100 The implications for the organisation of bi- and trifunctional enzyme complexes within the folate

101 Bi- and trilayer graphene have attracted intensive inter

102 er, the synthesis of high-quality large-size bi- and trilayer graphene single crystals still remains

103 synthesis of 100 mum pyramid-like hexagonal bi- and trilayer graphene single-crystal domains on Cu f

104 ed by the controlled production of 22 mono-, bi- and trilayer graphene stacks encapsulated in hexagon

105 Hz range electromagnetic responses of mono-, bi- and trilayer WTe(2) in the same multi-terraced micro

106 atomic-scale layered structures of single-, bi- and trilayers of NbSe2 separated by PbSe layers.

107 te that photoluminescence from MoS(2) mono-, bi- and trilayers originates solely from in-plane excito

108 Finally, we show that, as in rhombohedral bi- and trilayers(20-22), integrating a transition metal

109 lene insertion into Cd{N(TMS)(2)}(2) affords bi- and trimetallic cadmium aluminyls 1 and 2, featuring

110 has been extended to the synthesis of other bi- and trimetallic nanoparticles of Pt-transition metal

111 ction highlights the catalytic activities of bi- and trimetallic NPs.

112 copic measurements revealed a combination of bi- and trimolecular reaction kinetics.

113 res exist to define the corresponding static bi- and trimolecular receptor complexes, it is evident t

114 plits into two distinct subgroups containing bi- and trinuclear metal centres.

115 counts for the magnitude and waveform of the bi- and triphasic magnetic fields evoked by somatic and

116 ion also allows for the synthesis of related bi- and triradicals.

117 ing bisecting N-acetylglucosamine along with bi- and trisialylated triantennary glycans.

118 factors, current management strategies, new bi- and trispecific T-cell engagers, combination therapi

119 heoretical and simulation-based evidence for bi- and tritrophic communities, we show that environment

120 Id-1 was widely expressed in proliferating bi- and unipotential progenitors, but its expression was

121 ten must be compatible with the synthesis of bi- and/or trivalent analogues.

122 lux through the various pathways (ABCA1-, SR-BI-, and ABCG1-mediated efflux); however, these subjects

123 ommunities with increasing complexity: uni-, bi-, and multi-directional cross-feeding of either subst

124 istic details behind the synthesis of mono-, bi-, and multimetallic nanoframes, as well as heterostru

125 ile achieving asymmetrical growth for mono-, bi-, and multimetallic systems.

126 symmetry (skewness) and modal nature (mono-, bi-, and multimodal), of a variety of different polyolef

127 Uni-, bi-, and multiphasic injection schemes were tested.

128 eving the parameters used to generate mono-, bi-, and tri-exponential TRFAs from the global analysis

129 energies were compared with those for mono-, bi-, and tri-layer graphene, as well as SiO(2) substrate

130 cs, lexical frequency, neighborhood density, bi-, and tri-phonemic probabilities.

131 ch isoform and showed the presence of mono-, bi-, and triantennary complex carbohydrate, as well as f

132 structures, including high mannose, hybrid, bi-, and triantennary oligosaccharides.

133 rescued and produced normal ratios of mono-, bi-, and tricistronic RNAs, but its replication was slow

134 loride allows the direct synthesis of mono-, bi-, and tricyclic 4,5-dihydropyrazole-5-carboxylic acid

135 se set of aza heterocycles, including mono-, bi-, and tricyclic compounds.

136 g to the formation of enantioenriched mono-, bi-, and tricyclic products.

137 In this study, a series of mono-, bi-, and tricyclic ring-fused nitrones were prepared to

138 and kinetic control with a variety of mono-, bi-, and tricyclic structures evolving under the conditi

139 gies (only 18-34 kcal mol(-1) for the mono-, bi-, and tricyclics considered).

140 Megalibraries with mono-, bi-, and trimetallic materials were synthesized, and nan

141 PR) spectroscopic characterization of mono-, bi-, and trimolecular RNA structures shows that Cm will

142 ne-based sigma-type (carbon-centered) mono-, bi-, and triradicals toward dimethyl disulfide (DMDS) we

143 the conventional infinitesimal model, uni-, bi-, and trivariate MiXeR tools, applied to GWAS summary

144 cific for rat rbA (anti-CNA3) and for rabbit BI (anti-NBI-1 and anti-NBI-2) isoforms of alpha 1A.

145 se in mean atherosclerotic lesion area in SR-BI-/- apoE-/- --> apoE-/- mice compared with SR-BI+/+ ap

146 R-BI in recipient mice reconstituted with SR-BI-/- apoE-/- bone marrow.

147 olesterol efflux from SR-BI+/+ apoE-/- or SR-BI-/- apoE-/- macrophages to HDL or apoA-I discs was det

148 ice with bone marrow cells collected from SR-BI-/- apoE-/- mice or SR-BI+/+ apoE-/- mice.

149 ined from the compound consisting of K + and Bi + at A-site.

150 ohort, including mainly MB patients with low BI (average:1), 41%(n = 14) and 44%(n = 15) were detecte

151 This indicates a more random bi--bi kinetic mechanism, in comparison to an ordered bi

152 wness), DeltaE (total different colours) and BI (Browning Index) parameters, polyphenol oxidase (PPO)

153 ms-C paradigm, but was suppressed for C-25ms-Bi (by 31%); it was unchanged for Bi only and C only.

154 (177)Lu -C-NETA and (205/6)Bi -C-NETA possess an excellent or acceptable in vivo bi

155 on examining late improvement per RMI and/or BI (eg, 5-year mortality/institutionalisation with RMI/B

156 -dependent protein kinase regulatory subunit bI (EST01644); rat integral membrane glycoprotein (EST00

157 ifurcations occur for increasing N (mono --> bi --> mono-stability), with steady states corresponding

158 bined alpha-, gamma-, and x-ray emitter (213)Bi (half-life, 46 min) is promising for radionuclide the

159 ess ratios; DOC costs (2016 US dollars); and BI (healthcare cost/prison entrant) to generalize to oth

160 with pLiv-11-directed expression of human SR-BI (hSR-BI) or human SR-BII (hSR-BII).

161 the latter are constitutively expressing SR-BI (Idla7-SR-BI).

162 ding in the PbTe-like sublattice and soft Tl-Bi (In-Bi) bonding interaction is responsible for intrin

163 J774 cells with increased expression of SR-BI (J774-SRBI cells) esterified plasma membrane choleste

164 specific Nedd4-1 or SR-BI deletion and in SR-BI (K500A/K508A) mutation mice.

165 The primary end-point was BI (laboratory-confirmed SARS-CoV-2 infection >=14 days

166 has high expression levels of recombinant SR-BI (ldlA7-SR-BI), was used to examine the effect of SR-B

167 rom 0.1 to 2.4 microM, following the order 1-BI < 4-CPI < 1-CPI < 4-PI < BEI < 1-PI.

168 mechanics, in particular with respect to the BI <--> BII backbone equilibrium, which is essential to

169 tions in sugar pucker and phosphate backbone BI <--> BII equilibria.

170 nt key factors were > 1 severe cMRI-detected BI (MO/CO:-11.27/-10.3 score points (sp), p = 0.021/0.04

171 re and subcellular localization of murine SR-BI (mSR-BI) expressed either in transfected Chinese hams

172 ective uptake of HDL CE mediated by mouse SR-BI (mSR-BI) with that mediated by rat CD36 (rCD36), a cl

173 space-saving 'end-on' configuration, or (2) bi-/multi-layer adsorption on NH(2) SAM.

174 +/- 19.5 h) versus Asians (44.1 +/- 14.0 h), Bi-/multi-racial (48.0 +/- 16.0 h), and Whites (50.2 +/-

175 e study, self-identifying as Asian (n = 32), Bi-/multi-racial (n = 10), Black (n = 22), White (n = 23

176 Ab-SA conjugate followed by 800 muCi of (213)Bi- or (90)Y-DOTA-biotin, 80% and 20%, respectively, sur

177 anced anti-tumor efficacy as compared to its bi- or mono-drug components in cell line-derived tumor x

178 Hypermutated proviruses showed bi- or mono-phasic decay, reflecting different selective

179 Terminally differentiated cardiomyocytes are bi- or multi-nucleated, or have polyploid nuclei.

180 American, Asian, Hispanic, Native American, Bi- or Multi-racial and Pacific Islander.

181 lternatives-a phenomenon known as perceptual bi- or multi-stability.

182 nted by arrays of values at linearly ordered bi- or multiallelic loci.

183 OMMs with three types of mesostructures: (i) bi- or multicontinuous, (ii) columnar, and (iii) discont

184 ed as strongly binding sites), correspond to bi- or multidentate complexation to carboxylate groups,

185 me, different populations of chains within a bi- or multimodal polyolefin product can be selectively

186 cate their DNA, and approximately 25% became bi- or multinucleated.

187 lusters of a few metal ions held in place by bi- or multipodal organic linkers.

188 ntration, and highlight the role of synaptic bi- or multistability in the stability of learned synapt

189 bility to express more than one protein from bi- or polycistronic mRNAs.

190 cular G4 approximately 1000-fold better than bi- or tetramolecular G4 DNA.

191 s) are crystalline and porous materials with bi- or three-dimensional structures built up by connecti

192 han with the 1,2-1,3-arm or 1,4-1,3-arm of a bi- or tri-antennary oligosaccharide chain of N-glycan.

193 % identity with AGXT2L1 and AGXT2L2) forming bi- or tri-functional proteins with a putative kinase be

194 ators were pronounced with varying levels of bi- or tri-national population connectivity displayed by

195 in Drosophila pupal notum, alteration of the bi- or tricellular septate junctions (SJs) triggers a me

196 of SJ integrity, caused by the depletion of bi- or tricellular SJ components, alters ESCRT-III/Vps32

197 However, mapping studies reveal these to be bi- or tricistronic mRNAs with ORF 71 located 3' to ORFs

198 found that the reaction pathways leading to bi- or tricyclic frameworks depend on the kind of haloge

199 Isochalcogenoureas (IChU) embedded in bi- or tricyclic ring systems have proven to be versatil

200 zymes within the folate pathway can occur as bi- or trifunctional complexes in bacteria and parasites

201 A promising strategy is to design Pt based bi- or trimetallic nanostructures because their unique s

202 of Wnt/beta-catenin signaling that can bind bi- or trimethylated lysine 4 of histone-3 (H3K4me(2/3))

203 Cl(-) efflux from Xenopus oocytes expressing bi- or tripartite AE2-AE1 chimeras to define TMD subregi

204 r nonlipidated multiantigenic peptides or as bi- or tripeptide constructs, were studied in a mouse na

205 11.2DS (Df1/+ and Tbx1(+/-)) presenting with bi- or unilateral OME, the fourth pharyngeal arch-derive

206 x, only a subset of which are productive for bi- (or larger) cyclization and lead to products.

207 energy of electron traps decreases with the Bi (or N)-related downward shift of the conduction band.

208 skeletal FDG uptake was categorized as uni-, bi-, or multifocal (>/= three lesions).

209 activities and structural determinants of a (bi-)polarization system encoded in free-living and oblig

210 ion was observed between CD4 cell counts and BI (r2 = 0.1617, P = 0.0463), MGI (r2 = 0.2123, P = 0.02

211 roxides are promising candidates for stable (bi-)radicals due to their high degree of spin delocaliza

212 ntly, two unique point mutations in human SR-BI - S112F or T175A - were identified in subjects with h

213 matory monocyte subtype and partially via SR-BI (scavenger receptor BI).

214 the major HDL-dependent m-RCT pathway via SR-BI (scavenger receptor class B type 1) to the liver, a C

215 density lipoprotein receptor), ABCA-1, or SR-BI (scavenger receptor class B type I) but was released

216 e high density lipoprotein (HDL) receptor SR-BI (scavenger receptor class B type I) mediates the sele

217 ivity with time kinetics parallel to anti-SR-BI (scavenger receptor class B type I), but significantl

218 in the high-density lipoprotein receptor SR-BI (scavenger receptor class B, type I) and apolipoprote

219 rs, the high-density lipoprotein receptor SR-BI (scavenger receptor class B, type I) and its adaptor

220 ent studies revealed that scavenger receptor BI (SR-BI or Scarb1) plays a critical protective role in

221 ice with liver-specific overexpression of SR-BI (SR-BI Tg mice) have been crossed onto LDL receptor-d

222 ver overexpression of the scavenger receptor BI (SR-BI Tg).

223 caveolar uptake of LDL by scavenger receptor BI (SR-BI) and activin-like kinase 1 (ALK1) and requires

224 The class B scavenger receptors BI (SR-BI) and BII (SR-BII) are high-density lipoprotein

225 Scavenger receptor BI (SR-BI) binds high density lipoproteins (HDL) with hi

226 The scavenger receptor-BI (SR-BI) delivers sterols from circulating lipoprotein

227 Scavenger receptor BI (SR-BI) facilitates the efflux of cellular cholestero

228 ptake process mediated by scavenger receptor BI (SR-BI) in vivo.

229 ptake process mediated by scavenger receptor BI (SR-BI) in vivo.

230 Scavenger receptor BI (SR-BI) is a cell surface receptor that binds high de

231 The scavenger receptor BI (SR-BI) is an HDL receptor that plays a key role in H

232 Scavenger receptor BI (SR-BI) is known to mediate the selective uptake of h

233 Scavenger receptor BI (SR-BI) is the major receptor for high-density lipopr

234 The binding of HDL to scavenger receptor-BI (SR-BI) mediates cholesterol movement.

235 r ovary cells reveal that scavenger receptor-BI (SR-BI) mediates the effects of HDL on the enzyme.

236 Scavenger receptor BI (SR-BI) mediates the selective uptake of HDL choleste

237 Scavenger receptor BI (SR-BI) mediates the selective uptake of high density

238 Scavenger receptor BI (SR-BI) mediates the selective uptake of high density

239 Scavenger receptor BI (SR-BI) mediates the selective uptake of high-density

240 until the discovery that scavenger receptor BI (SR-BI) plays an important role.

241 Here we report that scavenger receptor BI (SR-BI) prevents NO-induced cytotoxicity.

242 Based on our finding that scavenger receptor BI (SR-BI) promotes free cholesterol (FC) exchange betwe

243 s studies have shown that scavenger receptor BI (SR-BI) stimulates the bidirectional flux of free cho

244 AI (apoAI)-knockout mice, scavenger receptor BI (SR-BI) transgenic mice, and control mice were cohybr

245 his study, we report that scavenger receptor BI (SR-BI), a high density lipoprotein receptor, is a cr

246 Scavenger receptor BI (SR-BI), a putative high density lipoprotein (HDL) re

247 of these molecules is the scavenger receptor BI (SR-BI), a receptor for high density lipoprotein that

248 ad Listeria monocytogenes scavenger receptor BI (SR-BI), an anti-atherogenic lipid exchange mediator,

249 CV: the tetraspanin CD81, scavenger receptor BI (SR-BI), and the tight-junction (TJ) protein claudin

250 In contrast to scavenger receptor BI (SR-BI), another cell surface molecule capable of fac

251 ce proteins, CD81 and the Scavenger Receptor BI (SR-BI), respectively, to infect hepatocytes.

252 nsports it to the liver's scavenger receptor BI (SR-BI), where SR-BI mediates the uptake of cholester

253 tein (HDL) via binding to scavenger receptor BI (SR-BI), which is colocalized with eNOS in endothelia

254 ein (HDL) phospholipid in scavenger receptor BI (SR-BI)-mediated free cholesterol flux was examined b

255 erol by the HDL receptor, scavenger receptor BI (SR-BI).

256 HDL and knockdown of the scavenger receptor-BI (SR-BI).

257 involve the HDL receptor, scavenger receptor BI (SR-BI).

258 ransfer receptors such as scavenger receptor BI (SR-BI).

259 A mutant SR-BI (SR-BIdel509) that lacked only the leucine in the PDZ

260 The alpha-emitter, (213)Bi (T(1/2) = 45.6 min), was conjugated to a 100-nm diame

261 ous studies showed that the C terminus of SR-BI ("target peptide") binds directly to PDZ1 and influen

262 The highest yields were observed with Bi-, Te-, and Pb-based additives, and particularly from

263 ge pre-BII-cell stage, there is a shift from bi- to mono-allelic lambda5 transcription, while the sec

264 a severe differentiation blockade at the pre-BI- to pre-BII-cell transition.

265 t Asn-168 were predominantly sialylated with bi- to tetra-antennary branches, and Asn-538 and Asn-745

266 esin-mediated loop extrusion can switch from bi- to unidirectional and is controlled independently in

267 Persistently increased levels of M-CSF after BI (to 1.4+/-0.2 nmol/L [ELISA] and 29.4+/-4.9% of cross

268 Neointimal thickness increased after BI (to 4.8+/-2.9 mm(2); P<0.001 versus control), but thi

269 Sialylated bi-, tri- [mainly the (2,4)-branched isomer], tetraanten

270 Bi-, tri- and multispecific antibodies have enabled the

271 e from single to hundreds of cores in mono-, bi-, tri- and quaternary composites.

272 d binding, the binding of a series of mono-, bi-, tri- and tetravalent carboxylate ligands to Ca(II)

273 We expect that the bi-, tri-, and quad-cistronic vectors constructed here a

274 possible, for the first time, to prepare any bi-, tri-, and tetra-antennary asymmetric N-glycan from

275 vergent strategy for the rapid production of bi-, tri-, and tetra-antennary complex type N-glycans wi

276 ycans, and a remarkable diversity of complex bi-, tri-, and tetra-antennary glycans decorated with fu

277 It was found GnT-III can act on bi-, tri-, and tetra-antennary N-glycans and can also ac

278 lement of fully galactosylated or sialylated bi-, tri-, and tetra-antennary N-glycans was largely equ

279 ovide a wide range of asymmetrical bisecting bi-, tri-, and tetra-antennary N-glycans.

280 rent saccharide compositions with sialylated bi-, tri-, and tetra-antennary structures.

281 ked glycosylation sites, each varying in its bi-, tri-, and tetraantennary glycan content.

282 deficiency, affecting neutral and sialylated bi-, tri-, and tetraantennary N-glycans.

283 se analysis revealed 24 lactosamine species (bi-, tri-, and tetraantennary structures), with all bran

284 Bi-, tri-, and tetracyclic isoquinoline salts were readi

285 arbocation intermediates and accumulation of bi-, tri-, and tetracyclic sesterterpenes, revealing the

286 s matchsticks" self-assemble into multipods (bi-, tri-, and tetrapods) of varying coordination number

287 difference in biological performance between bi-, tri-, and tetravalent ligand structures while ident

288 2As on the expression of proteins encoded in bi-, tri-, or quad-cistronic constructs.

289 o complex structures such as spiro and fused bi-/tricyclic O-heterocycles from readily available prec

290 s, which readily form five- and six-membered bi-/tricyclic products.

291 the spatial arrangement of achiral or chiral bi-/tridentate ligands around an octahedral metal centre

292 ee-dimensional (3D) superconductor BaPb(1-x) Bi (x) O(3) (BPBO), which surprisingly demonstrate three