ライフサイエンスコーパス: anti-

1 the NHC backbone (vs the initially expected anti).

2 ucleobase into two different domains (syn or anti).

3 ers (cis/syn, cis/anti, trans/syn, and trans/anti).

4 hoxy group is oriented toward the other (syn-anti).

5 "Pro") or away from it, toward its reverse ("Anti").

6 naute-like gene) that are antimorphic [alg-1(anti)].

7 on correlated with ribosome affinity for the anti (1,4)-regioisomers as revealed by measured Kd value

8 nocyclohexane can be differentiated using Sc[anti-(-)-1](2) in the same ligand displacement assay.

9 of compound 6 can be fixed predominantly to anti (17a and 17b) by introducing bulky alkyl groups (e.

10 acquired for 2 h after a bolus injection of anti-(18)F-FACBC (366 +/- 51 MBq).

11 Pelvic nodal status correlated with anti-(18)F-FACBC findings in 7 of 9 patients and was ind

12 s after intravenous injection of 300-410 MBq anti-(18)F-FACBC followed by static body images.

13 evaluated the whole-body radiation burden of anti-(18)F-FACBC in humans.

14 Anti-(18)F-FACBC is a promising radiotracer for imaging

15 The present study examines anti-(18)F-FACBC uptake in patients with newly diagnosed

16 e that an approximately 370-MBq injection of anti-(18)F-FACBC yields good imaging and acceptable dosi

17 3-(18)F-fluorocyclobutane-1-carboxylic acid (anti-(18)F-FACBC) is a recently developed ligand that pe

18 3-(18)F-fluorocyclobutane-1-carboxylic acid (anti-(18)F-FACBC)is a synthetic l-leucine analog that ha

19 The conformation of the trans-anti-(1S,2R,3S,4R)-N(2)-[1-(1,2,3,4-tetrahydro-2,3,4-tri

20 a right-handed helix with all nucleotides in anti, 2'-deoxyribose conformations within the C2'-endo/C

21 P (4b) with epi-isozizaene synthase gave [11(anti)-(2)H]epi-isozizaene (3b), indicating that the S(N)

22 levels of spontaneously appearing monoclonal anti-(2-->8)-alpha-Neu5Ac did not cause autoimmunity.

23 The lack of pathology mediated by anti-(2-->8)-alpha-Neu5Ac may be explained by different

24 Natural, anti-(2-->8)-alpha-Neu5Ac present in most adults, vaccin

25 by the unusual physicochemical properties of anti-(2-->8)-alpha-Neu5Ac.

26 Synthesis of a variety of 8,16-disubstituted-anti-[2.2]metacyclophanedienes (CPD) with alkenyl and al

27 mbinant DH4 with chemoenzymatically prepared anti-(2R,3R)-2-methyl-3-hydroxypentanoyl-ACP (2a-ACP) ga

28 EBS [KS6][AT6], DEBS ACP6, and TYLS KR1 gave anti-(2R,3R)-6-ACP that underwent syn dehydration cataly

29 y syn-dehydration of the ACP-bound substrate anti-(2R,3R,4S,5R)-2,4-dimethyl-3,5-dihydroxyheptanoyl-A

30 e syn-(2S,3R)-2b-ACP, syn-(2R,3S)-2c-ACP, or anti-(2S,3S)-2d-ACP generated in situ by DEBS KR1, DEBS

31 4, with a 20-fold greater kcat/K(m) than the anti-(2S,3S)-diketide-SNAC 14, and a 40-fold advantage o

32 ree isomeric forms with hydrides in syn (2), anti (3), and cis (4) conformations have been characteri

33 y of previously unavailable (3E)-2,5-syn-2,6-anti-, (3E)-2,5-anti-2,6-anti-, and (3E)-2,5-anti-2,6-sy

34 (OHMT)Cl in solution as a mixture of syn and anti (60:40 at 0.015 M) nitrile-free isomers, but these

35 99m)TcO]depreotide (6.58% ID/g) than for the anti [(99m)TcO]depreotide (3.38% ID/g).

36 formed on Sprague-Dawley rats using syn- and anti-(99m)Tc-L- and -D-MAEC coinjected with (131)I-OIH.

37 The clearances of syn- and anti-(99m)Tc-L-MAEC in the rats were higher than the cle

38 a clearance ratio in humans ranged from 45% (anti-(99m)Tc-L-MAEC) to 74% (syn-(99m)Tc-D-MAEC) with th

39 (rGGCAAGCCU)(2) duplex has sheared A(anti).A(anti) (A.A trans Hoogsteen/Sugar-edge) pairs in which th

40 The 5'(rGGCAAGCCU)(2) duplex has sheared A(anti).A(anti) (A.A trans Hoogsteen/Sugar-edge) pairs in

41 he N(CH2)3N units on each side are in doubly anti (aa) conformations that put the aryl rings as far a

42 ting Ab-54149 than an antibody purified from anti- Ab-54149 EPS serum.

43 ogen-containing coronene-type molecules like anti-(ab)2-PBI 15, syn-(ab)2-PBI 16, and syn-(ab)2-PTE 1

44 tion having one PD(+) ring syn and the other anti (abbreviated uns) was seen, and the relative amount

45 When SO2 is anti, addition is not observed.

46 rotonated retinal photoproducts, 13-trans/15-anti (all-trans) and 13-cis/15-syn, after relaxation to

47 odies (mAb), designed to stimulate immunity [anti-(alpha)-CD137, alpha-CD40] or relieve immunosuppres

48 pid syndrome, or red blood cells coated with anti-(alpha)-Rh(D) antibodies that mediate hemolysis in

49 sensing element as it is functionalised with anti-(alpha-synuclein) antibodies using a dual strategy:

50 This produces two FMN conformations (syn and anti) analogous to DNA.

51 sing 2-nitrobenzaldehyde (up to 93:7 dr (syn:anti) and 93% ee).

52 in various orientations [C*C, A*G, and G*G (anti) and A*G and G*G (syn)] and compare the results to

53 or the purine base, as expected for A(syn)*T(anti) and G(syn)*C(+)(anti) HG base pairing, HG type hyd

54 x predominantly adopts anticonformation ( 2A-anti) and possesses triplet ground state.

55 s performed with beta-hydroxy aldehydes 37a (anti) and the corresponding p-methoxybenzyl (PMB) ether

56 having the same G-arrangement (anti:anti:syn:anti) and the top G-tetrad having the reversed G-arrange

57 le (3E)-2,5-syn-2,6-anti-, (3E)-2,5-anti-2,6-anti-, and (3E)-2,5-anti-2,6-syn-substituted enediols, a

58 symmetric (er > 99:1) total synthesis of (+)-anti- and (-)-syn-mefloquine hydrochloride from a common

59 ymmetric (>99:1 e.r.) total synthesis of (+)-anti- and (-)-syn-mefloquine hydrochloride from a common

60 stallographic analysis of derivatives of (+)-anti- and (-)-syn-mefloquine is used to lay to rest a 40

61 The synthetic (+)-anti- and (-)-syn-mefloquine samples were derivatized wi

62 and these are subsequently converted to (+)-anti- and (-)-syn-mefloquine, respectively.

63 nd these are subsequently converted into (+)-anti- and (-)-syn-mefloquine, respectively.

64 crotyl reagents afford the corresponding 1,3-anti- and 1,3-syn-methyl-substituted "homocrotylated" al

65 Surprisingly, 2,3-anti- and 2,3-syn-alpha-methyl-beta-hydroxy aldehydes re

66 2 (X = Mg) appearing as transitional between anti- and nonhomoaromatic.

67 idely used, either to evaluate the effect of anti- and pro-angiogenesis drugs of interest, or to test

68 ngaging in protein-protein interactions with anti- and pro-apoptotic Bcl2 family members, thereby exe

69 dihydrodiol and BPDE-2 treatment, changes in anti- and pro-apoptotic events in the Bcl-2 family of pr

70 We provide evidence that B56epsilon has both anti- and pro-apoptotic functions.

71 Dimeric interactions among anti- and pro-apoptotic members of the BCL-2 protein fam

72 Dissection of anti- and pro-apoptotic signalling events triggered by T

73 ein transduction to identify novel, opposing anti- and pro-cytokine-inducing roles for RhoA in the re

74 t directly affect the expression of Foxp3 or anti- and pro-inflammatory cytokines in T(reg) cells, su

75 or necrosis factor-alpha (TNF-alpha) are key anti- and pro-inflammatory mediators elicited during the

76 PARs exhibit both anti- and pro-inflammatory properties, although recent e

77 us, Paneth cell lysozyme balances intestinal anti- and pro-inflammatory responses, with implications

78 aging to date and the first to discriminate anti- and pro-longevity genes, revealing new insights on

79 Tiam1 and P-Rex1, two Rac GEFs, promote Rac1 anti- and pro-migratory signalling cascades, respectivel

80 l is proposed for quantifying simultaneously anti- and pro-oxidant activities as function of concentr

81 -induced dysregulations of the expression of anti- and pro-oxidant enzymes, mitochondrial biogenesis

82 ous redox agent that can function as both an anti- and pro-oxidant.

83 al conditions, polyphenols may manifest both anti- and pro-oxidative activity.

84 the cardiovascular system and linked them to anti- and pro-thrombotic effects of aspirin.

85 phages have been shown previously to be both anti- and proangiogenic, and their role in regulating an

86 At 7 weeks, a combination of nonclassic anti- and proapoptosis genes appear to be involved in ph

87 Both anti- and proapoptotic activities have been reported to

88 Anti- and proapoptotic BCL-2 family proteins not only re

89 upt the protein-protein interactions between anti- and proapoptotic Bcl-2 proteins.

90 Bcl-2 family proteins include anti- and proapoptotic factors that play important roles

91 DL(Healthy) on the activation of endothelial anti- and proapoptotic pathways and to determine which c

92 Here we studied interactions among anti- and proapoptotic proteins of the Bcl-2 family in l

93 the first to show that Hax-1 is a family of anti- and proapoptotic regulators that may modulate cell

94 s a pleiotropic cytokine that activates both anti- and proapoptotic signaling pathways, with cell fat

95 CP in modulating the responses between these anti- and profibrotic cytokines in the initiation and pr

96 pe I IFNs regulate the balance between IL-10 anti- and proinflammatory activity, and provide insight

97 We hypothesized that anti- and proinflammatory dimensions of beta-arrestin2 a

98 appaB (nuclear factor kappaB), expression of anti- and proinflammatory factors and of the MAP (mitoge

99 was undertaken in order to exploit both the anti- and proinflammatory properties attributed to the v

100 That a T4SS can have anti- and prokilling effects on different targets, inclu

101 ferentiation remains elusive given that both anti- and promyogenic activities have been described.

102 In this study, we have identified both anti- and proviral roles of autophagy in the compatible

103 Dechlorane Plus (anti- and syn-) and alpha- and beta-tetrabromoethylcyclo

104 f this reaction are seen in the synthesis of anti- and syn-1,3 amino alcohol vitamin D3 analogue inte

105 determine how pol beta discriminates between anti- and syn-8-oxoG, we introduced a point mutation (R2

106 Moreover, both the anti- and syn-BrP-LPA significantly reduced tumors at 3

107 roup increases the energy difference between anti- and syn-chairs with primary amino acid catalysts a

108 n has dual coding potential by virtue of its anti- and syn-conformations, base pairing with cytosine

109 (BTBPE), and hexabromocyclododecane (HBCDD), anti- and syn-Dechlorane plus were detected at levels co

110 N2-H)(.) is corroborated by DFT studies, and anti- and syn-dG(N2-H)(.) are resolved for the first tim

111 ion results in stereodivergent products with anti- and syn-diastereomers both in good diastereoselect

112 bstituted cryptophanes gives rise to the two anti- and syn-diastereomers.

113 the assignment of the stereochemistry of the anti- and syn-diepoxy and -tetraepoxy derivatives as wel

114 s, trans-dihydrodiols, and the corresponding anti- and syn-diol epoxides.

115 NA complex has 8-oxoG in equilibrium between anti- and syn-forms.

116 elected by Bs-FtsZ, while Mj-FtsZ binds both anti- and syn-geometries.

117 Parallel anti- and syn-photocycles now explain inactivation and i

118 throughput, quantitative, and translational (anti-) angiogenesis and antiangiogenesis research.

119 led multiple anti-anti conformations, no syn-anti <--> anti-anti transformations were observed.

120 ow quite different relative stabilities: syn-anti > anti-anti > anti-syn > syn-syn.

121 ferent relative stabilities: syn-anti > anti-anti > anti-syn > syn-syn.

122 diastereoselective syntheses of a variety of anti, anti-stereotriads, the direct synthesis of which h

123 and to determine the lower cut-off value of anti- anti-TTG level that best predicts CD in children w

124 nges in expression of critical pro-, but not anti-, apoptotic genes.

125 n be partially attributed to alterations in (anti)-apoptotic gene expression.

126 8), microRNA guide strand selection by ALG-1(anti) appeared normal, but microRNA* strand release was

127 some microRNA* strands present in the ALG-1(anti) Argonaute far in excess of the corresponding matur

128 ation of the absolute stereochemistry of (+)-anti- as well as (-)-syn-mefloquine.

129 when the damaged base is syn than when it is anti, at the higher temperature.

130 m the dual coding potential where 8-oxo-dGTP(anti) base pairs with cytosine and 8-oxo-dGTP(syn) uses

131 simple model accurately predicts the bonding/anti- bonding modes that are measured experimentally.

132 he two distinct CH3CHOO conformers, syn- and anti-, both of which react readily with SO2 and with NO2

133 ailable for these 10S (+)- and 10R (-)-trans-anti -[BP]-N(2)-dG adducts in double-stranded deoxyoligo

134 ene-derived N (2)-dG adduct, 10 S(+)- trans- anti-[BP]- N (2)-dG ([BP]G*), reveal that an incoming dA

135 We investigated the 10S (+)-trans-anti-[BP]-N(2)-2'-deoxyguanosine (G*) adduct in double-s

136 pyrene-derived N(2)-dG adduct, 10S-(+)-trans-anti-[BP]-N(2)-dG ([BP]G*), is processed in Dpo4, the we

137 vironmental carcinogen, is the 10S (+)-trans-anti-[BP]-N(2)-dG adduct (G*), which resides in the B-DN

138 corporation opposite the bulky 10S (+)-trans-anti-[BP]-N(2)-dG adduct by Dpo4.

139 The 10S (+)-trans-anti-[BP]-N(2)-dG adduct can cause all three base substi

140 mental observations concerning the (+)-trans-anti-[BP]-N(2)-dG adduct in double-stranded DNA with the

141 We modeled the (+)-trans-anti-[BP]-N(2)-dG adduct opposite incoming dGTP, dTTP an

142 Dpo4 is able to bypass the 10S (+)-trans-anti-[BP]-N(2)-dG adduct, albeit to a lesser extent than

143 attacks DNA to form the major 10S (+)-trans-anti-[BP]-N(2)-dG adduct, which has been shown to be mut

144 group of guanine to form the major (+)-trans-anti-[BP]-N(2)-dG adduct.

145 The dN:(+)-trans-anti-[BP]-N(2)-dG base-pair is strained to shield the bu

146 utational studies suggest that 10S (+)-trans-anti-[BP]-N(2)-dG can be accommodated in the active site

147 zation of each nucleotide opposite (+)-trans-anti-[BP]-N(2)-dG in the +1 position (T > G > A > or = C

148 eferential insertion of A opposite (+)-trans-anti-[BP]-N(2)-dG is independent of the sequence context

149 In addition, extension past (+)-trans-anti-[BP]-N(2)-dG may pose a greater block to a high fid

150 While the dATP: (+)-trans-anti-[BP]-N(2)-dG pair was well accommodated within the

151 Bulky adducts such as (+)-trans-anti-[BP]-N(2)-dG primarily block DNA replication, but a

152 udies of nucleotide incorporation, (+)-trans-anti-[BP]-N(2)-dG was modeled in the syn conformation in

153 ss of the base positioned opposite (+)-trans-anti-[BP]-N(2)-dG, extension of the primer past the lesi

154 exocyclic amino group of guanine ((+)-trans-anti-[BP]-N(2)-dG, or G*).

155 er-extension of each base opposite (+)-trans-anti-[BP]-N(2)-dG, we carried out molecular modeling and

156 n intermediate preference opposite (+)-trans-anti-[BP]-N(2)-dG, were accommodated reasonably well, bu

157 ernary complex containing this 10S (+)-trans-anti-[BP]-N(6)-dA adduct in the templating position with

158 formations of the 10S (+)- and 10R (-)-trans-anti-[BP]-N(6)-dA adducts through molecular dynamics (MD

159 dies have been carried out for 10S-(+)-trans-anti-[BP]-N2-dG ((+)-ta-[BP]G), a lesion derived from th

160 [a]pyrene-derived N2-dG adduct, 10S(+)-trans-anti-[BP]-N2-dG ([BP]G*), is processed in a well-charact

161 bserved for the stereoisomeric 10S (+)-trans-anti-[BP]G adduct in both the C-[BP]G and meC-[BP]G sequ

162 d NMR study indicates that the 10R (-)-trans-anti-[BP]G adduct undergoes a transition from a minor gr

163 enine, forming bulky (+)-1R- or (-)-1S-trans-anti-[BPh]-N6-dA adducts.

164 lammatory response syndrome (CARS; excessive anti-, but no/low proinflammatory mediators).

165 These observations have demonstrated that an anti- but not proapoptotic activity is the prevailing ev

166 dry mouth but F = 0, increased expression of anti- CA6 was noted compared to the F <1 group (p = .032

167 shed a role of vascular-disrupting agents as anti- cancer agents.

168 he total (CD68(+)), pro- (CD14(+) = M1), and anti- (CD206(+) = M2) inflammatory macrophages, crown-li

169 ) binds only to chains rotated 19.5 degrees (anti-) clockwise from the [001] direction.

170 enger) strands, and immunoprecipitated ALG-1(anti) complexes contained nonstoichiometric yields of ma

171 nd protein populations associated with ALG-1(anti) complexes in vivo.

172 uorophenyl) TEFDDOL, a quite unusual "pseudo-anti" conformation of the diol, with no intramolecular (

173 i conformations in RNA and (high-anti)-(high-anti) conformations in DNA.

174 ted) conformer of both molecules to the syn (anti) conformer.

175 ar-reaching analogies are established among (anti-) cooperative collective behaviors in chemical kine

176 ly associated with RA (P<10(-4)): *0301 with anti- cyclic citrullinated peptide-negative RA and *0701

177 this slow motion, in contrast to the 8-oxoG (anti):dCTP system.

178 rough a S(N)1 mechanism with very high (>95% anti) diastereocontrol.

179 and cis-epoxides lead to opposite ( syn and anti) diastereoisomers of the addition products.

180 n) and benzo[c]phenanthrene (BcPh) series 2 (anti) diol epoxides.

181 IgA anti-tissue transglutaminase and/or IgA anti- endomysium permitted diagnosis or exclusion of CD

182 collective behaviors in chemical kinetics, (anti-)ferromagnetic spin models in statistical mechanics

183 Phase boundaries in multiferroics, in which (anti-)ferromagnetic, ferroelectric and ferroelastic orde

184 one- and two-dimensional spin systems with (anti)-ferromagnetic interactions controlled by their sym

185 Three conformers (anti, gauche, and folded) leading to electron transfer w

186 s the cap in multiple conformations (syn and anti) giving rise to a relatively plastic and nonspecifi

187 modulation was done by treatments with DTA-1 anti- glucocorticoid-induced tumor necrosis factor recep

188 he (NIASF), no increase in the prevalence of anti- gp130-RAPS antibodies was observed in serum or syn

189 The overall anti-->syn transition rate and relative probability of t

190 oside underwent spontaneous and reproducible anti-->syn transitions.

191 expected for A(syn)*T(anti) and G(syn)*C(+)(anti) HG base pairing, HG type hydrogen bonding could on

192 ith anti-anti conformations in RNA and (high-anti)-(high-anti) conformations in DNA.

193 Anti- HNA-3a is one of the product-derived factors and a

194 ATS is similar in action to anti-(human)thymocyte globulin (ATG), which is used clin

195 The 7-phosphanorbornene anti-(i)Pr(2)NP(C(6)H(8)) could be synthesized (70% isol

196 Maternal serum concentrations of IgG anti- Ia, -Ib, -III and -V polysaccharides and anti-BP-1

197 Anti- IgG seroconversion occurred in eight -seronegative

198 in survival was found between the different anti- IgG serogroups (D-R-, D-R+, D+R-, or D+R+).

199 evels for pro (IFN-gamma and TNF-alpha)- and anti (IL-4 and IL-10)-inflammatory cytokines also were d

200 allergen inhalation and treatment trials the anti-(IL-5) therapeutic Mepolizumab).

201 Coculture with anti--IL-10 antibody increased p70 production.

202 Combined Flt3L and single-dose anti--IL-10 antibody pretreatment improved lesion cure r

203 A single dose of anti--IL-10 antibody significantly improves Flt3L immuno

204 n of (-)-8 was optimized to give 1 (syn)(/) (anti) in 85% yield and 1:1 ratio of diastereomers.

205 a postinsertional complex shows 8oG(syn).dA (anti) in a Hoogsteen-like base pair at the 3' terminus,

206 atio of the two limiting conformers (syn and anti) in solution and the extent of conjugation between

207 s exist as a mixture of E(syn)-(alpha) and Z(anti) in solution.

208 nsition states, endo-prox-anti and endo-dist-anti, in the pentadiene/PyrNO reaction, leading to nearl

209 RNA* strands were selected as guide by ALG-1(anti), indicating a defect in normal specificity of the

210 ponses by differentially regulating pro- and anti- inflammatory cytokine production in innate immune

211 modulate the expression of selected pro- and anti- inflammatory mediators such as IL-6 and IL-33.

212 ave been reported to modulate either pro- or anti- inflammatory programs, which may be specific to th

213 Homeostasis between pro- and anti- inflammatory responses induced by bacteria is crit

214 stances is linked mainly to the antioxidant, anti- inflammatory, anti-proliferative and cardioprotect

215 For 8-oxo-dGTP(anti) insertion, a novel divalent metal relieves repulsi

216 Its reversible conformational (syn and anti) interconversion and photodecomposition were observ

217 ith or without the addition of 250 microg of anti--interleukin (IL)-10 antibody on day 9.

218 the conversion of the anti (syn) to the syn (anti) isomer at 66.2 degrees C.

219 the conversion of the anti (syn) to the syn (anti) isomer at 71.0 degrees C.

220 115.2 (109.0) kJ/mol for the anti/syn- (syn/anti)-isomerization of 8 and 9, respectively.

221 ALG-1(anti) miRISC (microRNA induced silencing complex) fails

222 to three contiguous stereocentres in a (syn, anti)-mode with excellent regio and diastereoselectiviti

223 osuppressive agents CTLA4-Ig + anti-CD40L or anti-(murine)thymocyte serum (ATS).

224 Sjorgen's Syndrome (SS) and HCV, presence of anti- muscarinic receptor type 3 (M3R) antibodies in SS,

225 In addition, alg-1(anti) mutants dramatically overaccumulated microRNA* (pa

226 alg-1(anti) mutants have dramatically stronger microRNA-relate

227 (syn, Pseudomonas fluorescens, gi 70731221 ; anti, Mycobacterium smegmatis, gi 118470554 ) document t

228 Anti- N-methyl-D-aspartate receptor (NMDAR) encephalitis

229 number of PLA-positive signals generated by anti-(Nav1.5 alpha-subunit) antibodies, mainly at the pl

230 )+(R)] and the elimination mechanism (syn or anti), not substituent effects, determined the configura

231 he stereochemical configurations (syn versus anti) of the THF groups near the termini.

232 he N-heterocyclic carbene ligand IMes to fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)) cleaves the d

233 ide and the dimeric rhenium(VII) complex fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)).

234 ular flux analysis of cells transfected with anti- or pre- miR-29a confirmed that miR-29a inhibits mi

235 ve been discovered as therapeutic targets in anti- or pro-angiogenic drug development.

236 It may exhibit anti- or pro-apoptotic activity depending on the nature

237 d their ES-evoked activation produces either anti- or pro-inflammatory effects due to disease-state-d

238 at this pathway may be a suitable target for anti- or proangiogenesis strategies.

239 ssenger RNA (pre-mRNA) splicing to induce an anti- or proapoptotic response.

240 as a bifunctional regulator promoting either anti- or profibrogenic response, depending on milieu.

241 MSCs can respond to tissue injury by anti- or proinflammatory activation.

242 ies in both mice and humans suggest that the anti- or proinflammatory nature of high density lipoprot

243 The anti- or prooxidant effects of green tea catechins have

244 nin is a convergent site for the activity of anti- or propsychotic drugs, opening a possibility for n

245 possessing di- or trisubstituted alkenes and anti- or syn- relative stereochemistry at the allylic an

246 ounds, Pd(II) is capable of promoting either anti- or syn-addition.

247 with aromatic aldehydes and preparing either anti- or syn-aldol adducts with very high enantioselecti

248 ite that can tolerate 8-oxo-dG in either the anti- or syn-conformation.

249 n them, hydrogen bonds relating parallel and anti- parallel beta strands, spatial adjacencies relatin

250 Anti- PECAM/SOD, but not nontargeted counterparts, accum

251 Therefore the anti- Ph(1)-leukemia effect of the combination of BCR/AB

252 t mammary gland and the pro-(BAX:Bcl(2)) and anti-[PKC alpha*(Bcl(2)/BAX)] apoptotic ratios were eval

253 '-epi-46, and 61) and several low-micromolar anti- Plasmodium falciparum lead compounds (i.e., 46, 2,

254 Neither in vivo anti- Pp IgG antibody nor in vitro anti- Pp T-cell respo

255 r in vivo anti- Pp IgG antibody nor in vitro anti- Pp T-cell response and resultant production of RAN

256 llate (EGCG), and matrix pH (2-7) on the net anti-/pro-oxidant activity of EGCG in flaxseed oil-in-wa

257 tumor infiltrating lymphocyte (TIL)-based or anti- programmed death 1 (PD1) immunotherapy.

258 ing that quinoxaline antibiotics could exert anti- proliferative effects by inhibition of chromosomal

259 mutant ALG-1 and found that the mutant ALG-1(anti) protein fails to interact with numerous miRISC cof

260 viously shown to exhibit "pro-[PSI(+)]" and "anti-[PSI(+)]" effects, respectively.

261 he different stereochemical courses (syn and anti) result from different structural strategies for de

262 ) are compared with a commercially available anti- Salmonella antibody and the antimicrobial peptide

263 t)/anti-OH, SERO(B) at 32548 cm-1 to Gpy(up)/anti, SERO(C) at 32545 cm-1 to Gph(out)/anti, SERO(D) at

264 (up)/anti, SERO(C) at 32545 cm-1 to Gph(out)/anti, SERO(D) at 32560 cm-1 to Anti(py)/anti, SERO(E) at

265 out)/anti, SERO(D) at 32560 cm-1 to Anti(py)/anti, SERO(E) at 32537 cm-1 to Anti(up)/anti, SERO(F) at

266 (py)/anti, SERO(E) at 32537 cm-1 to Anti(up)/anti, SERO(F) at 32353 cm-1 to Gpy(out)/syn, SERO(G) at

267 ection, survival, yearly posttransplantation anti- serology, development of acute toxoplasmosis, and

268 ed on pretransplantation donor and recipient anti- serology, immunosuppression, allograft rejection,

269 clobutane species not being able to have an (anti) substituent pointing toward the HIPTO group.

270 5.2 (111.1) kJ/mol for the conversion of the anti (syn) to the syn (anti) isomer at 66.2 degrees C.

271 6.0 (112.1) kJ/mol for the conversion of the anti (syn) to the syn (anti) isomer at 71.0 degrees C.

272 rase interactions that influence templating (anti-/syn-equilibrium) of 8-oxoG while modulating fideli

273 , were asymptomatic and required no specific anti- therapy.

274 n mast cells was suppressed by anti-IL-1 and anti- thymic stromal lymphopoietin (TSLP) and was enhanc

275 tive and specific screening serologic tests (anti- tissue transglutaminase antibodies IgA [anti-TTG]

276 r tests (IgA anti-dpgli, IgG anti-dpgli, IgA anti- tissue transglutaminase, and IgA anti-endomysium)

277 ) (2) converts into its anti form [Fe(IV) (O(anti) )(TMC)(NCMe)](2+) (1) in MeCN, an isomerization fa

278 nverted these benign effects of RSFC from an anti- to a proinflammatory status.

279 Importantly, the promotion of a high anti- to pro-apoptotic Bcl-2 family member ratio by acid

280 As mice mature, BAK is converted from anti- to pro-death function in virus-infected spinal cor

281 " cytokine in cancer, changing its role from anti- to pro-tumorigenic in a context-dependent manner.

282 D74-dependent way, shifting the balance from anti- to proinflammatory cytokines in antimycobacterial

283 ansannulation reactions producing the trans, anti, trans estrane 56 in 12% overall yield.

284 xides exist as four conformers (cis/syn, cis/anti, trans/syn, and trans/anti).

285 rug conjugate (ADC) comprised of a humanized anti- Trop-2 antibody, conjugated with active metabolite

286 The in vitro and in vivo anti- Trypanosoma cruzi activity of the pyrazole-contain

287 gues with selective and significant in vitro anti- Trypanosoma cruzi activity.

288 ith siRNA-loaded NPs may exhibit synergistic anti- tumor effects.

289 ate (CL) nanoparticles to facilitate priming anti- tumor T cells by tumor lysate-loaded DC vaccine.

290 or psoriasis, but pDCs are also involved in (anti-)tumor immunity.

291 immune cells that can perform both pro- and anti- tumorigenic functions (Figure 1).

292 In contrast, Ssa1 was shown to have anti-[URE3] effects, since overexpression of Ssa1 cures

293 isease activity following 3 loading doses of anti- vascular endothelial growth factor (VEGF) agents,

294 Aflibercept has emerged as a new anti- vascular endothelial growth factor (VEGF) therapy

295 ecrosis and the mechanisms that regulate its anti- vs proapoptotic activities.

296 Western Blotting with anti- WFhb1-1 antibody revealed a significant decrease (

297 ncreases 15-syn-retinal at the expense of 15-anti, which is the predominant isomer in the wild type,

298 in polymorph A away from each other (termed anti), while in polymorph B one methoxy group is oriente

299 15, AN11251) was shown to have good in vitro anti- Wolbachia activity and physicochemical and pharmac

300 These analogs were found to be potent anti- Wolbachia antibiotics and, as such, may be useful