ライフサイエンスコーパス: non-classical

1 assembled MHCI proteins, both classical and non-classical.

2 the plasmon in such stacks is unambiguously non-classical.

3 , characterized as classical inflammatory or non-classical.

4 g has been increasingly investigated for its non-classical actions in stimulation of innate immunity

5 esistance to kynurenic acid which suggests a non-classical activation of NMDA receptors by mitochondr

6 AtAGP30 is a non-classical AGP core protein from Arabidopsis that is

7 This cDNA, DcAGP1, encodes a new class of non-classical' AGP with strong similarity to a family of

8 Identification of novel, non-classical and druggable AR-target genes may provide

9 changed over time with an increasing rate of non-classical and subclinical phenotypes.

10 emble antithrombin III-binding classical and non-classical anticoagulant polysaccharide structures fo

11 nhibited by classical antifolates but not by non-classical antifolates or biopterin.

12 down of TbFT1-3 increased susceptibly to the non-classical antifolates pyrimethamine and nolatrexed.

13 s antigen-dependent activation, primarily by non-classical antigen-presenting cells.

14 nduced cell death may be occurring through a non-classical apoptosis pathway that is not dependent on

15 three-dimensional suprastructures which have non-classical architectures (non-Archimedean/Platonic so

16 and/or persistent collateral sensitivity to non-classical BCR-ABL1 drugs arises in emergent tumor su

17 (or triggered) single-photon sources exhibit non-classical behaviour in that they emit, with a high d

18 This non-classical behaviour of the electrical conductance an

19 the Bell inequality was designed to test for non-classical behaviour without assuming the applicabili

20 was inactive against glycine receptor, its "non-classical" binding sites on alpha7 nAChR should be w

21 luster containing B. inopinata and the other non-classical Brucella species but also revealed signifi

22 We have identified a non-classical cadherin, Cad74A, as a putative adhesion g

23 Thus, non-classical cadherins that function in adhesion are li

24 tivate endothelial nitric oxide (eNOS) via a non-classical, "calcium-independent" pathway.

25 c molecules, mostly lipids, presented by the non-classical CD1 family (CD1a-e).

26 cially for proinflammatory and profibrogenic non-classical CD14 + CD16+ monocytes.

27 osely with circulating monocytes, especially non-classical CD14+ CD16+ monocytes, which were found to

28 delta T-cell receptor and its ligand, T22, a non-classical class I major histocompatibility complex (

29 isms of regulation is the recognition of the non-classical class I MHC molecule HLA-E, in complex wit

30 ctive peptides is generated by processing at non-classical cleavage sites that do not contain basic r

31 Neither the peptidases responsible for non-classical cleavages nor the compartment involved in

32 te of an atomic memory is transformed into a non-classical collective atomic state by Rydberg-level i

33 k interactions do not allow fast creation of non-classical collective states.

34 proband with femorogluteal lipodystrophy and non classical congenital adrenal hyperplasia, and an ess

35 s stages of differentiation, we identified a non-classical consensus splicing sequence in intron 2 ad

36 Here we report non-classical correlations between single photons and ph

37 At the macroscopic optical-field level non-classical correlations can also be important, as in

38 Compared to previous investigations of non-classical correlations for photon pairs produced in

39 ton pairs-discrete light quanta that exhibit non-classical correlations-play a crucial role in quantu

40 The results shed new light on non-classical crystallization mechanisms and have implic

41 Thromboxane synthase (TXAS) is a "non-classical" cytochrome P450.

42 ferating cell nuclear antigen (PCNA) and two non-classical DNA polymerases, Rev1 and DNA polymerase e

43 l theories with maximal certainty have their non-classical dynamics absolutely restricted to only the

44 also plays a positive role as the enabler of non-classical dynamics in an interferometer.

45 abilistic theories this heavily curtails the non-classical dynamics.

46 ry minimizes certainty in return for maximal non-classical dynamics.

47 ion processing and metrology applications, a non-classical emitter of single photons is required.

48 his increase in expression was mostly due to non-classical enhancer activity within the intron, and m

49 synaptotagmin-1 is able to utilize the FGF-1 non-classical exocytotic pathway and that the release of

50 s: 1) classical (malabsorption syndrome); 2) non-classical (extraintestinal and/or gastrointestinal s

51 ified as classical fast spiking (n = 10), as non-classical fast spiking (n = 3, including one burst-f

52 nstrate a mechanism that is able to transfer non-classical features imprinted on the state of a matte

53 tum physics relies on detectors sensitive to non-classical features of systems, enabling precise test

54 in biology requires clear identification of non-classical features that these processes can exhibit

55 om temperature can manifest and benefit from non-classical fluctuations of collective pigment motions

56 This supports non-classical formation of aragonite within both a synth

57 y, alerts us to the increasing evidence for 'non-classical' forms of protein translocation that may i

58 prisingly, paternally-expressed genes of the non-classical gene imprinted network were strikingly enr

59 controlling adaptation to such environments, non-classical genetic effects are likely to be observed.

60 e tomographically verify preservation of the non-classical Greenberger-Horne-Zeilinger state.

61 Human leucocyte antigen-G (HLA-G) is a non-classical HLA class I molecule demonstrated original

62 ally identifies the dosage contribution of a non-classical HLA gene to disease etiology.

63 risk of a synonymous mutation at HLA-DOA, a non-classical HLA gene, on anti-citrullinated protein au

64 LA class I-derived peptides displayed on the non-classical HLA-E for recognition by CD94-NKG2 recepto

65 Here, we will discuss non-classical immunoregulatory properties of C3 and C5 c

66 The presence of the observed strong non-classical induction force implied that energies of n

67 hat the heritable variations are produced by non-classical inheritance systems, including non-DNA inh

68 tein inhibitor, DARPin E2_79, acts through a non-classical inhibition mechanism, not only blocking Ig

69 itial state of sufficient purity to create a non-classical, inseparable state.

70 both classical TPRT-mediated insertions and non-classical insertions.

71 These results suggest that SAMHD1 is a non-classical interferon-stimulated gene regulated throu

72 Chloride intracellular channels (CLIC) are non-classical ion channels lacking a signal sequence for

73 h atypical language laterality also included non-classical language areas such as the superior and mi

74 he demonstration of these capabilities using non-classical light remains challenging.

75 providing direct evidence for a solid-state non-classical light source, this result proves that a si

76 Non-classical light sources offer a myriad of possibilit

77 uantum electrodynamic techniques or prepared non-classical light sources.

78 t on-chip photon correlation measurements of non-classical light.

79 The non-classical major histocompatibility complex (MHC) hom

80 Disruption of the non-classical Major Histocompatibility Complex (MHC) Ib

81 The protein HLA-E is a non-classical major histocompatibility complex (MHC) mol

82 ss potential implications on the notion that non-classical major histocompatibility complex (MHC) mol

83 altering and/or mimicking: (1) classical and non-classical major histocompatibility complex (MHC) pro

84 tructural characterizations of classical and non-classical major histocompatibility complex class II

85 It encodes the beta subunit of the non-classical major histocompatibility complex class II

86 Qa-1 epitopes, the peptides that bind to non-classical major histocompatibility complex Ib Qa-1 m

87 at recognize lipid antigens presented by the non-classical Major Histocompatibility Complex molecule

88 d mTOR pathways, and provide an example of a non-classical means for SHH-mediated protein regulation

89 These results together reveal a non-classical mechanism by which VDR acts as a c-Jun/AP-

90 The present study describes a non-classical mechanism that does not require internaliz

91 /ZMYND10) are very frequently inactivated by non-classical mechanisms such as promoter hypermethylati

92 ion could be mediated by allosteric or other non-classical mechanisms.

93 turn inhibits c-Jun-dependent cell death by non-classical mechanisms.

94 Calpain 5 (CAPN5) is a non-classical member of the calpain family.

95 However, little is known about how these non-classical MHC class I (MHCI) molecules diverged from

96 epending on type, interact with classical or non-classical MHC class I antigens of the adaptive immun

97 ure NKT cells are positively selected by the non-classical MHC class I molecule CD1d, which is expres

98 natural killer-cell receptor), often bind to non-classical MHC class I molecules, such as the human M

99 We and others have demonstrated that the non-classical MHC I molecule HLA-E can present pathogen-

100 assical MHC (MHC-Ia), we have shown that the non-classical MHC molecule (MHC-Ib) H2-M3 was a ligand f

101 cells recognize glycolipids presented by the non-classical MHC molecule CD1d.

102 The non-classical MHC molecule T22 represents the best chara

103 HLA-F, a non-classical MHC molecule, is not known to present pept

104 to the medulla, included cells restricted by non-classical MHC molecules and expressed the receptor N

105 ovel insights into the role of classical and non-classical MHC molecules in graft rejection.

106 microbial non-peptidic antigens presented by non-classical MHC MR1.

107 bond strengths and a recent structure of the non-classical MHCII protein HLA-DO reveal changes in the

108 overview of the regions within classical and non-classical MHCII proteins that display conformational

109 w that Salmonella can exploit mammalian cell non-classical microRNA processing machinery to further p

110 non-classical states of motion by capturing non-classical microwave signals prepared by the most coh

111 recognize antigens presented by a variety of non-classical molecules.

112 Non-classical monoamine recognition evolved in two steps

113 n blood contains classical, intermediate and non-classical monocyte subsets that each express charact

114 IKV infection was observed, in contrast to a non-classical monocyte-mediated M2-skewed immunosuppress

115 CD16(-) classical monocytes, CD14(+)CD16(++) non-classical monocytes and CD14(++)CD16(+) intermediate

116 The DCs originate from non-classical monocytes and form stable, cognate interac

117 ing of blood monocyte subsets indicates that non-classical monocytes are biased progenitors of altern

118 Here, we demonstrate that circulating non-classical monocytes are directly recruited to polyme

119 a previously unknown role for blood-derived non-classical monocytes as contributors to alternatively

120 t cancer, and levels of these miRs in CD115+ non-classical monocytes correlates with metastatic tumor

121 advanced stages of PAOD, while classical and non-classical monocytes displayed no such trend.

122 inated more frequently from intermediate and non-classical monocytes in CF patients.

123 n exacerbated M2-skewed immunosuppression of non-classical monocytes in conjunction with a global sup

124 recruitment kinetics and functional role of non-classical monocytes remains unclear.

125 ll molecule FTY720 recruits S1PR3-expressing non-classical monocytes that support vascular remodeling

126 vation and P2X7R activity were comparable in non-classical monocytes to other subsets: their diminish

127 Here we show that primary human non-classical monocytes, exposed to LPS or LPS + BzATP (

128 intermediate monocytes, and CD14(+)CD16 ++: non-classical monocytes.

129 pression, cytokine and chemokine levels, and non-classical monocytes; 3) gene signature of leukocyte

130 An archetype of such non-classical motion is tunnelling through an energy bar

131 a single atom unequivocally demonstrated the non-classical nature of radiation.

132 ffect of directed emission combined with the non-classical nature of the emitted light.

133 Schwarz inequality is clear evidence for the non-classical nature of the mechanical state generated.

134 Recently, examples of non-classical neurotransmission have also been reported,

135 ha, but repressed by treatment of cells with non-classical NF-kappaB activators, anthracyclins and UV

136 previously unsuspected role of M64 within a non-classical NLS may contribute to its invariance among

137 aused by the impaired function of a flanking non-classical nuclear localization signal (NLS).

138 ave been proposed as intermediate species in non-classical nucleation processes.

139 nsformation of a classical state to a highly non-classical one and a Gaussian state to a non-Gaussian

140 ent, and stable generation and processing of non-classical optical states.

141 s evolved a new way to recognize amines in a non-classical orientation.

142 g and antibunching simultaneously is a fully non-classical outcome of the wave-particle duality of ph

143 Transglutaminase 2 (TG2) is secreted by a non-classical pathway into the extracellular space, wher

144 nalyses suggest that SGSs are secreted via a non-classical pathway that involves cleavage into a 300-

145 The proposed model for ClyA represents a non-classical pathway to attack eukaryotic host cells.

146 rs bind to and are internalized by ECs via a non-classical pathway, CAM-mediated endocytosis.

147 g the possibility of its being secreted by a non-classical pathway, which is not clearly understood.

148 athrin machinery and mediate signalling via 'non-classical' pathways.

149 one disorder in the native-state can lead to non-classical Phi(M)-values (Phi(M) > 1) in the rate-det

150 g excited spin qubits can act as a source of non-classical phonons.

151 s are a unique and exciting nanomaterial for non-classical photocatalytic mineralization of organic c

152 Non-classical photon correlations between the emission f

153 ed detector is subsequently used to estimate non-classical photon number states.

154 th by a factor of 7.47 under preservation of non-classical photon-number statistics.

155 The results demonstrate the necessity of a non-classical picture for this class of microscopic syst

156 ta has distinct effects on classical PKC and non-classical PKC activity.

157 nstitutive and autonomous Ca(2+)-independent non-classical PKC activity.

158 ificity for moesin and with activation under non-classical PKC conditions.

159 of facilitating selection of the appropriate non-classical polymerase and polymerase-switching events

160 In the symptomatic group the non-classical prevailed over the classical phenotype (66

161 d cell-coupling in the proximal kidney via a non-classical pro-fibrotic mechanism and the data provid

162 f these steroid-peptide links, especially on non-classical progesterone actions through allopregnanol

163 suring the Husimi Q function and confirm the non-classical properties of these transient states by ca

164 therefore suggest that investigation of the non-classical properties of vibrational motions assistin

165 lar cartilage vesicles (ACVs) participate in non-classical protein secretion, intercellular communica

166 erfamily can participate in the catalysis of non-classical reactions.

167 Models seeking to explain these non-classical receptive field (nCRF) effects in terms of

168 results reveal possibly a context-dependent, non-classical regulatory role for SOX9.

169 ssical class I genes, two CD1 genes and some non-classical Rfp-Y genes are known in chicken, and all

170 o Here, we show that AChE plays an essential non-classical role in vertebrate gut morphogenesis.

171 To explore the 'non-classical' role of AChE, we examined embryos mutant

172 te that AChE is dispensable for its proposed non-classical roles in muscle fiber formation and sensor

173 n addition, AChE is thought to play several 'non-classical' roles that do not require catalytic funct

174 n processing T. gondii oocysts, in line with non-classical routes of infection, and open new perspect

175 Perhaps most excitingly, phenoxazines have "non-classical" RTA activity, where they trap >2 peroxyl

176 ain, is believed to play a major role in the non-classical secretion of the aFGF release complex medi

177 Non-classical secretory vesicles, collectively referred

178 ion of two gold centers to enforce selective non-classical sigma,pi-activation with bifunctional subs

179 miR-744 also enhanced the activation of non-classical signal components, such as ERK and p38.

180 ignaling, but may activate MAPK to occur via non-classical signaling intermediates.

181 mediated chemoattraction represents a novel, non-classical signaling system that has therapeutic pote

182 eriochlorophylls coordinated by LH2 act as a non-classical single-photon emitter.

183 This allows measurement-based non-classical state preparation, which has been applied

184 Preparation of these non-classical states in resonators is non-trivial due to

185 s process, it should be possible to generate non-classical states of light by measurement and perform

186 To create and manipulate non-classical states of light for quantum information pr

187 The generation of non-classical states of light is of fundamental scientif

188 The deterministic generation of non-classical states of light, including squeezed states

189 rthermore, it will enable the preparation of non-classical states of motion by capturing non-classica

190 pid advances in the control and detection of non-classical states of motion, possibly even testing qu

191 categorized into classical, intermediate or non-classical subsets, and subsequently differentiated i

192 During the evolution, non-classical superpositions of coherent states (that is

193 On one extreme, non-classical theories with maximal certainty have their

194 We test various "non-classical" transcription activators (comprising a co

195 Recently, FH gene was also identified as a "non-classical" tumor suppressor gene and heterozygous mu

196 These include a non-classical tyrosine motif that serves as the signal f

197 Existence of the non-classical VDR pathway was suggested by a requirement

198 the yeast vacuole/lysosome by a constitutive non-classical vesicular transport mechanism, the cytopla

199 y fibres are primarily due to differences in non-classical, voltage-dependent ion channels, active cl