ライフサイエンスコーパス: bi-

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

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

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

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

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

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

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

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

9 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

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

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

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

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

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

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

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

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

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

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

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

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

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

23 Bi- and multivariable logistic regression, Kaplan-Meier

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

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

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

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

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

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

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

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

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

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

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

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

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

37 Bi- and tri-antennary oligosaccharides with bisecting Gl

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

39 Bi- and tri-exponential models for ultrasensitive assay

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

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

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

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

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

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

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

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

48 Bi- and triantennary structures, with and without lactos

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Bi- and trilayer graphene have attracted intensive inter

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

125 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.

126 % identity with AGXT2L1 and AGXT2L2) forming bi- or tri-functional proteins with a putative kinase be

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

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

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

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

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

132 11.2DS (Df1/+ and Tbx1(+/-)) presenting with bi- or unilateral OME, the fourth pharyngeal arch-derive

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 2As on the expression of proteins encoded in bi-, tri-, or quad-cistronic constructs.

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