ライフサイエンスコーパス: nonclassical

1 Nonclassical 3C2E bonding among the C1, C1', and C2' ato

2 his article that KIR3DL2 and KIR2DS4 and the nonclassical Ag HLA-F, expressed as a free form devoid o

3 trochemical nucleation and growth supports a nonclassical aggregative growth mechanism.

4 linically relevant model systems for probing nonclassical, ancestral neurohormone functions.

5 ted with alternative activation, whereas the nonclassical and classical populations demonstrated an a

6 lammatory phenotype defined by (1) increased nonclassical and intermediate monocytes, (2) a proinflam

7 e mechanism of crystallization, classical or nonclassical; and whether quinoline antimalarials inhibi

8 is to educate the reader on the contemporary nonclassical applications of these anions.

9 Nonclassical approaches are needed because ions in biolo

10 ied enzymes differed among salt-wasting- and nonclassical-associated variants, but these differences

11 y identified in the components of the HPV is nonclassical because the mean structure of the epitope c

12 ive to Gaussian statistics--facilitates this nonclassical behavior.

13 altered in optical cavities, often inducing nonclassical behavior.

14 onfirm that aztreonam-like beta-lactams plus nonclassical beta-lactamase inhibitors, particularly avi

15 ique population of kidney T cells, depend on nonclassical beta2m molecules for homeostasis and use MH

16 his is consistent with the intermediacy of a nonclassical bicyclobutonium cation 8N.

17 approach to peptide conjugation based on the nonclassical bioisosteric replacement of the guanidine g

18 emokine receptor 2-dependent manner, and the nonclassical blood resident monocyte subset that patrols

19 IL-6) and activated monocytes (CD14dimCD16+; nonclassical) but not with markers of HIV.

20 binding fragments, including a selection of nonclassical CA II binding chemotypes, were identified.

21 , namely salt wasting, simple virilizing, or nonclassical CAH.

22 outside the context of the virus it induces nonclassical, cancer cell-specific apoptosis.

23 es indicate that the reaction proceeds via a nonclassical carbocation followed by anti-1,2-migration.

24 mited to norbornene systems proceeding via a nonclassical carbocation.

25 ving free radicals, reaction mechanisms, and nonclassical carbocations are discussed.

26 luded proving the occurrence of benzynes and nonclassical carbocations as reaction intermediates, and

27 In the case of potential nonclassical carbocations substituted with the p-(pentaf

28 et al. is based on CH5(+) and Olah's related nonclassical carbonium ion chemistry.

29 monocytes with classical CD14(++)CD16(-) and nonclassical CD14(+)CD16(++) monocytes revealed that the

30 ease in the classical (CD14(++) CD16(-)) and nonclassical (CD14(+) CD16(+)) subsets at 12 days postin

31 Nonclassical (CD14(+)CD16(++)) and intermediate (CD14(++

32 in humans and Ly6C(+)Treml4(+) in mice), and nonclassical (CD14(-)CD16(+) in humans and Ly6C(lo) in m

33 CD16(-)), intermediate (CD14(+)CD16(+)), and nonclassical (CD14(dim)CD16(+)) monocytes.

34 CD16(-)), intermediate (CD14(+)CD16(+)), and nonclassical (CD14(dim)CD16(+)) monocytes.

35 6(+) (both intermediate [CD14(+)CD16(+)] and nonclassical [CD14(dim)CD16(+)]) monocytes was increased

36 aracterized by reduced levels of circulating nonclassical CD16(+) monocytes with a poor activation pr

37 Interestingly, FACIN is a nonclassical cell surface protein, a cytosolic enzyme ac

38 erentiate sequentially into intermediate and nonclassical cells.

39 ith a distance that is relatively long for a nonclassical CF-HC hydrogen bond.

40 ho-hydrogen to participate in a stabilizing, nonclassical CH...O hydrogen bond with a ring oxygen of

41 Additional stabilizing nonclassical CH...O hydrogen-bond interactions seem to d

42 The study has shown that nonclassical channel combinations for colorimetric quant

43 Thus, protoadamantyl zwitterion has a less nonclassical character than the corresponding cation, so

44 uctural features that are similar to certain nonclassical class I genes in other vertebrates, and, un

45 Nonclassical class I MHC-like molecules are ligands for

46 Human and murine MHC nonclassical class Ib-restricted invariant T (iT) cell s

47 Nonclassical (class-Ib) major histocompatibility complex

48 s one of our examples, we apply STS to check nonclassical correlations among sites in a photosyntheti

49 rmodynamics in relation to the settlement of nonclassical correlations between the wells.

50 hese STS measures enable a new way to assess nonclassical correlations in an open quantum network, su

51 The cationic nonclassical [Cp2ZrN(SiHMe2)2](+) ([2](+)) is prepared f

52 might be reconciled by invoking a three-step nonclassical crystal growth mechanism comprising (i) doc

53 s via both conventional Ostwald ripening and nonclassical crystallization by particle attachment.

54 Although this form of nonclassical crystallization is generally described by o

55 further source of inspiration how to exploit nonclassical crystallization routes for syntheses of str

56 systems, microfluidic systems (classical and nonclassical), custom-built polymerase chain reaction de

57 -II involve both classical endolysosomal and nonclassical cytosolic pathways.

58 were identified in a 5-year-old patient with nonclassical DBA and in a 17-year-old patient with myelo

59 Patients with nonclassical DBA and other hypoproliferative anemias may

60 d origin, such as monocytes and classical or nonclassical DCs.

61 For xanthene vs xanthene-(d(2)), large, nonclassical deuterium kinetic isotope effects are rough

62 In contrast, we find that nonclassical DFG-out conformations strongly select again

63 Nonclassical diagnoses were observed more frequently in

64 support the assignment of these complexes as nonclassical dihydrogen adducts of Co(-I).

65 se had higher event rate than did those with nonclassical disease (hazard ratio for men, 5.63, 95% co

66 data on the natural course of classical and nonclassical disease in men and women.

67 e had a history of more events than men with nonclassical disease or women with either phenotype; wom

68 ely to develop complications than women with nonclassical disease.

69 These results illustrate how describing nonclassical dopant dynamics requires taking the effecti

70 The present review offers an overview of nonclassical (e.g., with no pre- or in situ activation o

71 E2 in the late stages of pregnancy through a nonclassical E2/ERalpha transrepressive pathway, directl

72 nd promote cellular immunity through diverse nonclassical effector functions.

73 ng a simple yet rigorous platform to include nonclassical effects in plasmon-enabled nanophotonic phe

74 r dynamics techniques to shed light on these nonclassical effects, which are often difficult to inves

75 bation theory and observations of pronounced nonclassical effects.

76 Simulations reveal three important nonclassical effects: the nucleation free-energy barrier

77 tric triplet (omega(flap) = 0 deg) stem from nonclassical electron delocalization in the former and t

78 ic process of recombination and propose that nonclassical excision circles are liberated during the f

79 tom and the H6 of the base, reminiscent of a nonclassical F...H hydrogen bond, could be observed.

80 osylsphingosine concentrations than men with nonclassical Fabry disease or women with either phenotyp

81 We conclude that nonclassical FD is caused by Fpn mutations that decrease

82 We further examine the nonclassical features and energy fluxes implied by the d

83 Nonclassical ferroportin disease (FD) is a form of hered

84 ssical (physicochemical and topological) and nonclassical (fingerprints) molecular descriptors of 138

85 nd that more than 50% of patients could have nonclassical food allergy, with immediate disruption of

86 iants associated with either salt-wasting or nonclassical forms of CAH were expressed, purified, and

87 Calculations suggest that the observed nonclassical fullerene could be a kinetically trapped sp

88 Using Xenopus nonclassical gene 10 tetramers and RNAi loss of function

89 equirement of the class Ib molecule, Xenopus nonclassical gene 10, in its differentiation and functio

90 c modulator provides a novel explanation for nonclassical gene regulation by (*)NO.

91 ese effects are unknown, they likely involve nonclassical genetic mechanisms.

92 ore, the GRP88 nuclear localization suggests nonclassical GPCR modes of action of the protein that co

93 at SSZ-13 grows by two concerted mechanisms: nonclassical growth involving the attachment of amorphou

94 The nonclassical H2 adduct is an intermediate in the complet

95 sequilibrium structure of both classical and nonclassical HLA genes.

96 The nonclassical HLA molecule MHC-related protein 1 (MR1) pr

97 HLA-G, a nonclassical HLA molecule uniquely expressed in the plac

98 n was circumvented by enforced expression of nonclassical HLA molecules.

99 The classical HLA-C and the nonclassical HLA-E and HLA-G molecules play important ro

100 Recent evidence identified HLA-E, a nonclassical HLA-I, as an important part of the antivira

101 ereas Ag presentation by classical and other nonclassical HLAs was unaffected.

102 at miR-152 overexpression down-regulates the nonclassical human leukocyte antigen (HLA) class I molec

103 ocatalysts toward the reaction revealed that nonclassical hydrogen bonding was involved in the stabil

104 econdary to pyroptotic lysis and in nonlytic/nonclassical IL-1beta export.

105 We report an experimental demonstration of a nonclassical imaging mechanism with super-resolving powe

106 mmunoprecipitation analyses, revealed that a nonclassical importin beta family member, IPO3, was the

107 was 0.7% (8/1078) and was 16.7% (9/54) for "nonclassical" indications (peritonitis, carcinomatosis,

108 This effect is mediated through the nonclassical inhibitory G (Galphai/0) protein.

109 articles are therefore expected to exhibit a nonclassical inhomogeneous spectral broadening due to si

110 e the output distribution resulting from the nonclassical interference of photons in an integrated ph

111 previous complexities and the first on-chip nonclassical interference with more than two photonic in

112 , eight spatial modes and many classical and nonclassical interferences.

113 precise FcgammaR repertoire on classical and nonclassical intermediate monocytes--M1 and M2c macropha

114 monocytes cocultures (IL-6(hi)) was added to nonclassical/intermediate monocyte cocultures (TNF(hi)),

115 vels of TNF were detected in cocultures with nonclassical/intermediate monocytes, the blockade of whi

116 )CD16(-) (classical) and CD14(+/dim)CD16(+) (nonclassical/intermediate), have been described.

117 characterization, and catalytic activity of nonclassical iron(II) polyhydride complexes containing t

118 vel spectroscopic capabilities provided by a nonclassical light excitation, this is of critical impor

119 The use of a nonclassical light source for studying molecular electro

120 ers in future photonic applications, such as nonclassical light sources for quantum communication or

121 erate and characterize frequency-multiplexed nonclassical light sources for quantum info-communicatio

122 Semiconductors can also be used to generate nonclassical light; in fact, CMOS-compatible silicon chi

123 rived from glioblastoma (GBM) cells involves nonclassical, lipid raft-dependent endocytosis.

124 have uncovered an immunosuppressive role for nonclassical Ly6Clo monocytes that mediates resistance t

125 rized macrophage depletion and inhibition of nonclassical macrophage migration, in addition to direct

126 Cx3cr1(-/-) mice were used to inhibit nonclassical macrophage migration.

127 , in addition to direct interactions between nonclassical macrophages and fibroblasts in angiotensin

128 Human leukocyte antigen-G (HLA-G) is a nonclassical major histocompatibility complex (MHC) clas

129 ntrolled expansion that was dependent on the nonclassical major histocompatibility complex (MHC) prot

130 Structural analysis shows FcRn is a nonclassical major histocompatibility complex Class I re

131 in human; murine H2-O) is a highly conserved nonclassical major histocompatibility complex class II (

132 pocR, suggesting it might regulate pocR in a nonclassical manner.

133 tion of eicosanoid generation in response to nonclassical MC activation mechanisms.

134 Ab-mediated immunity, while suggesting a new nonclassical mechanism of Ab function, which may apply t

135 ters in the bulk liquid is associated with a nonclassical mechanism of crystal growth and can trigger

136 Fbxo45 appears to be secreted by a nonclassical mechanism, not involving a signal peptide a

137 These nonclassical mechanisms include 1) inhibition of gut DPP

138 ves in Diabetes outlines and discusses these nonclassical mechanisms of DPP-4 inhibition.

139 cules and precursors, bridging classical and nonclassical mechanisms.

140 ive endocytosis (MEND) in BHK fibroblasts by nonclassical mechanisms.

141 ew, we discuss the evidence supporting these nonclassical megakaryocytic differentiation pathways and

142 ciency, caused by a failure to eliminate the nonclassical metabolite 1,5AG6P.

143 g frequency is blue-shifted, consistent with nonclassical metal-CO interactions.

144 repertoire presented by classical as well as nonclassical MHC class I (MHC I) molecules is altered in

145 of jawed vertebrates, we identified a third nonclassical MHC class I lineage (UDA), which is present

146 HLA-G is a nonclassical MHC class I molecule and its physiological

147 ain and recognize lipid Ags presented by the nonclassical MHC class I molecule CD1d are probably the

148 -forming NKG2D, NKG2 receptors recognize the nonclassical MHC class I molecule HLA-E, and they can be

149 on of C19MC miRNAs and the macaque placental nonclassical MHC class I molecule, Mamu-AG.

150 ctivating receptor interacting with HLA-E, a nonclassical MHC class I molecule.

151 mportant positive regulator of classical and nonclassical MHC class I molecules.

152 eign and self-lipids in association with the nonclassical MHC class I-like molecules, CD1 proteins.

153 Ag presentation via the nonclassical MHC class Ib molecule HLA-E, with nearly co

154 MHC-E is a highly conserved nonclassical MHC class Ib molecule that predominantly bi

155 a highly conserved, ubiquitously expressed, nonclassical MHC class Ib molecule with limited polymorp

156 ariant Valpha6 [iValpha6]) restricted by the nonclassical MHC class Ib molecule XNC10 in the amphibia

157 Nonclassical MHC class Ib-restricted invariant T (iT) ce

158 at were entirely restricted by MHC II or the nonclassical MHC I molecule, MHC-E.

159 d immunogenicity of peptides associated with nonclassical MHC I was increased in the absence of ERAAP

160 s onto MHC II is catalyzed by HLA-DM (DM), a nonclassical MHC II molecule.

161 Mouse CD1d is a nonclassical MHC molecule able to present lipids and gly

162 ntionally restricted by MHC class II and the nonclassical MHC-E molecule in RM.

163 l MHC class I and MHC class II molecules and nonclassical MHC-I molecules.

164 lationships, including those associated with nonclassical MHC-I, have yet to be clearly defined.

165 lity complex E (MHC-E) is a highly conserved nonclassical MHC-Ib molecule that tightly binds peptides

166 cells is controlled by the interplay of the nonclassical MHCII molecules, HLA-DM (DM) and HLA-DO (DO

167 HLA-DM, a nonclassical MHCII protein, acts as a peptide exchange c

168 its replacement with an organic results in a nonclassical mode of growth that obscures 2D layers and

169 vity in the brain, much of which can involve nonclassical modes of neuronal firing and integration.

170 tment to the site of injury, implicating the nonclassical monocyte in this process.

171 hat myeloid cells, specifically cells of the nonclassical monocyte lineage, play a direct role in the

172 ed using highly purified human classical and nonclassical monocyte subsets from a clinical cohort, al

173 )/CD16(+) intermediate and CD14(low)/CD16(+) nonclassical monocyte subsets in peripheral blood mononu

174 Accumulation of these nonclassical monocyte-derived pulmonary interstitial mac

175 Nonclassical monocytes (CD14+, CD16++), interleukin (IL)

176 , mice that have markedly reduced numbers of nonclassical monocytes (CX3CR1(-/-)) exhibited a signifi

177 ediate monocytes [IM]), and CD14(+)CD16(2+) (nonclassical monocytes [NCM]).

178 indicate that inflammatory transitional and nonclassical monocytes and CD1c+ conventional dendritic

179 an) can define slan-positive CD14(+)CD16(++) nonclassical monocytes and slan-negative CD14(++)CD16(+)

180 that, in murine hypoxia-induced PH, Ly6C(lo) nonclassical monocytes are recruited to small pulmonary

181 tribution of these monocyte subsets with the nonclassical monocytes being expanded (almost 2-fold) in

182 d hierarchical clustering, the slan-positive nonclassical monocytes cluster with monocytes and are cl

183 ly higher baseline peripheral frequencies of nonclassical monocytes compared with nonresponder patien

184 To determine if the sensing of hypoxia by nonclassical monocytes contributes to the development of

185 The viral DNA level in nonclassical monocytes correlated with the viral DNA lev

186 deposition were generated for classical and nonclassical monocytes defining enhanceosomes of the 2 m

187 CCR5, was higher, and a higher proportion of nonclassical monocytes expressed CCR1, CXCR3, and CX3CR1

188 riming them for anaerobic energy production, nonclassical monocytes expressed higher levels of oxidat

189 Nonclassical monocytes have been widely viewed as anti-i

190 Intermediate and nonclassical monocytes have longer circulating lifespans

191 ons, similar to classical, intermediate, and nonclassical monocytes in humans, based upon CD14 and CD

192 findings show that, in response to hypoxia, nonclassical monocytes in the lung sense hypoxia, infilt

193 e adhesion of classical monocytes but not of nonclassical monocytes in the mouse cremaster muscle and

194 Our data suggest a critical role for nonclassical monocytes in the pathology of TBI in mice,

195 Subsequent labeling of intermediate and nonclassical monocytes is consistent with a model of seq

196 reen fluorescent protein) mice, we show that nonclassical monocytes patrol inside healthy carotid art

197 scular space in resting organs, and Ly6c(lo) nonclassical monocytes patrol the vasculature.

198 gage ex vivo FcgammaRIIIA (CD16)-expressing, nonclassical monocytes resulting in ADCC-mediated lysis

199 d become infected and the number of infected nonclassical monocytes that transmit virus to CD4(+) and

200 intermediate monocytes are more likely than nonclassical monocytes to migrate to the lesion site.

201 Nonclassical monocytes undergo intravascular patrolling

202 ial patrolling is a prominent new feature of nonclassical monocytes with unique molecular and kinetic

203 nocyte subsets (classical, intermediate, and nonclassical monocytes) to the total viral burden in 22

204 F(V600E) was tracked to classical monocytes, nonclassical monocytes, and CD1c(+) myeloid dendritic ce

205 Both classical and nonclassical monocytes, but not CD1c(+) DCs, made foamy

206 and the functions of monocytes, particularly nonclassical monocytes, in health and disease.

207 sical and intermediate monocytes, but not in nonclassical monocytes, which nonetheless display a very

208 T1 phosphorylation in fetal intermediate and nonclassical monocytes.

209 f viral DNA in CD8(+) and CD4(+) T cells for nonclassical monocytes.

210 d a significant increase in the frequency of nonclassical monocytes.

211 ty in commonly used approaches for depleting nonclassical monocytes.

212 ced shift in myeloid cells from classical to nonclassical monocytes.

213 RATIONALE: Nonclassical mouse monocyte (CX3CR1(high), Ly-6C(low)) p

214 allization within the membrane media follows nonclassical multistep crystallization governed by the h

215 Nonclassical nanotube end-caps have been constructed fro

216 Furthermore, a nonclassical negative-binomial model was shown to correc

217 cales via both classical spike-dependent and nonclassical neuropeptide-dependent mechanisms.SIGNIFICA

218 Previous studies have implicated nonclassical NF-kappaB as a pathway important in the dev

219 sistance can occur through activation of the nonclassical NF-kappaB pathway and acquired resistance m

220 B-cell receptor and JAK/STAT signaling, the nonclassical NF-kappaB pathway, cell-cycle regulation, a

221 nt B cells, with downstream loss of MAPK and nonclassical NF-kappaB signaling.

222 associated factor 3 (TRAF3), an inhibitor of nonclassical NF-kappaB signaling.

223 n mTEC development mediated by inhibition of nonclassical NF-kappaB.

224 The larger Ga and In ions stabilize rare, nonclassical Ni-H2 adducts that catalyze olefin hydrogen

225 he interaction of TNPO1 and TNPO3 with these nonclassical NLSs may regulate the formation of membrane

226 NPO1 and Transportin-3 (TNPO3) recognize two nonclassical NLSs within the cold-inducible RNA-binding

227 Here we show that a nonclassical nuclear import pathway via IPO3 (importin 3

228 In the complex, eVP24 recognizes a unique nonclassical nuclear localization signal (NLS) binding s

229 dict that low coordination numbers result in nonclassical nucleation behavior, which we find to be es

230 These new pathways include the so-called nonclassical nucleation mechanism via the assembly of th

231 ecursor and could therefore be an example of nonclassical nucleation.

232 The nonclassical open reading frame in the FCGR2C gene (FCGR

233 g of classic, proinflammatory monocytes into nonclassical or alternative monocytes to facilitate prop

234 3213128 (compound 28a), a novel, selective, nonclassical, orally bioavailable antifolate with potent

235 rgos, and we raise the possibility that this nonclassical pathway is shared by most AAV variants, reg

236 g prospects for exerting control over such a nonclassical pathway to crystallization to design minera

237 1B10 is secreted through a lysosome-mediated nonclassical pathway, leading to an increase in the seru

238 silica molecules as primary growth units and nonclassical pathways based on the aggregation of metast

239 lite crystallization predominantly occurs by nonclassical pathways involving the attachment of comple

240 s are either known or postulated to grow via nonclassical pathways involving the initial self-assembl

241 The particles involved in these nonclassical pathways to crystallization are diverse, in

242 Materials science has been informed by nonclassical pathways to crystallization, based on biolo

243 -transmission electron microscopy, revealing nonclassical pathways via dissolution-recrystallization

244 E2 (-/-) mice lack nonclassical patrolling monocytes but preserve classical

245 The frequency of nonclassical patrolling monocytes is increased in HTLV-1

246 tumorigenesis and cancer metastasis, but how nonclassical "patrolling" monocytes (PMo) interact with

247 The role of nonclassical, patrolling monocytes in lung tumor metasta

248 or proinflammatory (CCR2(hi)CX3CR1(low)) and nonclassical, patrolling, or alternative (CCR2(low)CX3CR

249 In this article, we demonstrate that the nonclassical peroxisome proliferator 4-phenyl butyric ac

250 uantum optics, being the trigger of multiple nonclassical phenomena.

251 simple virilizing phenotypes or with milder nonclassical phenotypes.

252 mechanistic information, aimed at developing nonclassical platinum complexes that operate via mechani

253 We then describe approaches that explore nonclassical platinum(II) complexes with trans geometry

254 s and the lectin-like receptor CD94-NKG2A by nonclassical pMHC-I complexes, in each case leading to n

255 monocytes, and there is no CD14(-) CD16(+) "nonclassical" population.

256 nambiguously to specifically bind zinc via a nonclassical, potentially catalytic zinc-binding motif.

257 ss I proteins are divided into classical and nonclassical proteins.

258 four plant PUFs results in a preference for nonclassical PUF RNA target sequences.

259 Our approach incorporates nonclassical resonance shifts and surface-enabled Landau

260 tive to conventional designs, as well as new nonclassical resonant mode shapes.

261 ignaling pathway involves the synthesis of a nonclassical retinoid.

262 dehydrogenases leading to the synthesis of a nonclassical retinoid.

263 with transduction efficiency and relies on a nonclassical retrograde transport pathway that is indepe

264 Recently, nonclassical roles for GRK2 in cardiovascular disease ha

265 In this review, classical and nonclassical roles for GRK2 will be discussed, focusing

266 itro and indicates that SosV-RBP undergoes a nonclassical route of host-cell entry.

267 y synthesized HLA-A2 molecules that follow a nonclassical secretion route.

268 The Vid pathway is linked to the nonclassical secretory and internalizing pathways.

269 ss potential functions of both classical and nonclassical sHLA-I, using soluble recombinant HLA-I/pep

270 r DFT calculations reveal the formation of a nonclassical sigma-hole region with one or even two maxi

271 At the limit, the tuning transforms the nonclassical sigma-hole regions into coordination sites,

272 A major section on nonclassical (sigma or agostic) complexes includes two g

273 We observe nonclassical spectral shifts in excess of 30 per cent an

274 Although a nonclassical state from spontaneous parametric down-conv

275 Squeezed states of light are a set of nonclassical states in which the quantum fluctuations of

276 a rare phenomenon otherwise known only from nonclassical states of light like the squeezed vacuum.

277 Among the many applications of nonclassical states of light, nonlinear microscopy has t

278 trasensitive measurements of weak forces and nonclassical states of motion.

279 expressed EGFP, with increased levels in the nonclassical subset.

280 LR) agonists in classical, intermediate, and nonclassical subsets of monocytes by assessing intracell

281 subdivided into classical, intermediate, and nonclassical subsets, but there is no unequivocal strate

282 erapy agents and humanized mAbs present with nonclassical symptoms of anaphylaxis, and patients may p

283 , natural killer and natural killer T cells, nonclassical T cells, and memory B cells.

284 RNA (siRNA) knockdown studies suggested that nonclassical targets of sorafenib are important for the

285 These ex-Th17 cells are also called nonclassical Th1 cells because of their ability to produ

286 kingly, induced marked production of diverse nonclassical TH2 inflammatory mediators, including IL-22

287 allergy, regulatory immune cell subsets and nonclassical Th2-biased inflammatory mediators in the tu

288 dependently of IFN-gamma and IL-17; however, nonclassical Th22 cells have been recently identified an

289 Three nonclassical Th22 subsets constituted the majority of al

290 most efficiently triggered the expansion of nonclassical Th22 subsets from memory T cells and classi

291 Little is known about how classical and nonclassical Th22 subsets in human diseases are regulate

292 three subsets (classical, intermediate, and nonclassical) that circulate in dynamic equilibrium.

293 Our findings are independent of the specific nonclassical theory used, thus providing important insig

294 d retinoid X receptor (RXR) by classical and nonclassical THs as another molecular activity of THs.

295 dulation are reviewed, with special focus on nonclassical TLR4 ligands with a chemical structure diff

296 factors are at our disposal to switch from a nonclassical to classical mechanism.

297 We observe classical one-step pathways and nonclassical two-step pathways that proceed via a solid-

298 med) [intermediate], and CD14(neg)/CD16(hi) [nonclassical]) were examined at homeostasis and after ac

299 ation of cells (classical, intermediate, and nonclassical) with distinct functions, however, the recr

300 ial step of the synthesis is cyclization via nonclassical Wittig olefination of resin-bound esters.