ライフサイエンスコーパス: self-recognition

1 carbohydrates that are crucial for self/non-self recognition.

2 se to pathogens and vaccines and in self/non-self recognition.

3 ity characterized by extensive plasticity of self recognition.

4 cells during education for improved missing-self recognition.

5 cell tolerance and MHC-I-independent missing-self recognition.

6 the polymorphic S-locus determines self/non-self recognition.

7 rcinogenesis through MHC-I-dependent missing-self recognition.

8 ivate immune signaling in the absence of non-self recognition.

9 fit is weighed against the cost of potential self recognition.

10 are involved in barrier defense and self/non-self recognition.

11 ingle-cell identities that underlie neuronal self-recognition.

12 ial outcomes may be related to sex-divergent self-recognition.

13 ssential metabolic enzyme enabling plant non-self-recognition.

14 represent a second system for murine NK-cell self-recognition.

15 recognition, axon fasciculation, and neuron self-recognition.

16 t the cell surface and contributes to immune self-recognition.

17 pes have shown convincing evidence of mirror self-recognition.

18 arise from an intermediate state of loss of self-recognition.

19 sification among other genes involved in non-self-recognition.

20 ible relationship to traditional measures of self-recognition.

21 ot, by themselves, be reliable indicators of self-recognition.

22 lecules within nucleoprotein filament--i.e., self-recognition.

23 were formed, which suggests a high-fidelity self-recognition.

24 self-junctions and may be a feature of cell self-recognition.

25 ant roles in intercellular communication and self-recognition.

26 cells optimally suited for efficient missing self-recognition.

27 ulation on body-awareness can be extended to self-recognition.

28 ically tractable ancient model of eukaryotic self-recognition.

29 details of nonself lipid discrimination and self-recognition.

30 gulatory requirements imposed by the risk of self-recognition.

31 phism, are ancient determinants of self-/non-self-recognition.

32 , synthetic flexibility and a capability for self-recognition.

33 e cell surface, presumably to avoid "missing self" recognition.

34 the killing of allogeneic cells via "missing self" recognition.

35 What is the basis of self recognition?

36 rent genetic mechanisms trigger death by non-self recognition and death by various environmental onsl

37 insects and has been implicated both in non-self recognition and in resistance to a variety of paras

38 insights into this biological system of non-self recognition and response activation.

39 ed both genes are required for efficient non-self recognition and successful mating, as assessed by p

40 is a close connection between the Q-score of self recognition and the relative foldability (Theta) of

41 these systems function in bacterial self/non-self recognition and thereby play an important role in m

42 tions between pollen and pistil proteins as "self" recognition and/or rejection mechanisms to prevent

43 Ureas are well-known for self-recognition and aggregation behavior, resulting in

44 (TLRs) 7 and 9 exposes the host to potential self-recognition and autoimmunity.

45 in axon and dendritic patterning and neuron self-recognition and avoidance.

46 ided insights into the mechanisms underlying self-recognition and escape from thymic deletion.

47 her segments possibly correspond to sites of self-recognition and interaction with the other degrados

48 ings suggest a possible dissociation between self-recognition and more generalized face processing wi

49 ral patterning functions, including neuronal self-recognition and non-self-discrimination to direct s

50 dendrites and axons, demonstrating a role in self-recognition and repulsion leading to self-avoidance

51 ium between a compact form, showing specific self-recognition and resistance to proteolysis, and an e

52 ly on cell surface cues that govern cellular self-recognition and selective interactions with appropr

53 n guidance and synaptic adhesion, as well as self-recognition and self-avoidance, depending on the ne

54 la Dscam1 receptor is important for neuronal self-recognition and self-avoidance.

55 enable the fabrication of devices with both self-recognition and self-regulating functionality.

56 molecular and biochemical basis of self/non-self-recognition and self-rejection.

57 or tolerance maintenance under conditions of self-recognition and strong costimulation.

58 ls that play essential roles in establishing self-recognition and tolerance, with important implicati

59 w that the SpoIVB PDZ domain is required for self-recognition and trans cleavage of SpoIVB and is pro

60 haviors including food acquisition, self/non-self recognition, and intraspecific communication.

61 clude studies of imitation, tool use, mirror self-recognition, and the potential for attribution of m

62 activity and protein modification can direct self recognition are beginning to be unearthed.

63 Antagonistic interactions and non-self recognition are likely to promote microbial diversi

64 feature and contingency of movement cues to self-recognition are discussed.

65 (+) T cells expressing markers of heightened self-recognition are selectively retained, but not clona

66 This work brings attention to the role of "self-recognition" as a dynamic interaction between dendr

67 Kzeta knockout mice display improved missing self recognition, as evidenced by enhanced rejection of

68 rucial role of inhibitory HLA-C receptors in self-recognition, as well as NK cell education and respo

69 Our results indicate that self recognition associated with the development of MS i

70 The potential for self-recognition at a species level, and subsequent skel

71 es in their mixed solutions, demonstrating a self-recognition behavior between two highly similar mac

72 This self-recognition behavior can be explained by the slight

73 we map genetic factors underlying color and self-recognition behavior of genetic similarity in both

74 udy of the location of genes responsible for self-recognition behavior, recognition of blue color, an

75 new study finds that rhesus monkeys display self-recognition behaviors toward a mirror after multimo

76 ed natural transplantation reaction, whereby self-recognition between colonies leads to formation of

77 s an adhesion molecule in axon growth and in self-recognition between dendrites of the same neuron.

78 Self-/non-self-recognition between pollen and pistil is regulated

79 e molecules, including Dscams and Pcdhgs, in self-recognition, but repulsive molecular mechanisms rem

80 KLRG1 mediates missing self recognition by binding to a highly conserved site o

81 were later scored for behavioral indices of self-recognition by a trained observer who was blind to

82 t an initial kissing hairpin forms following self-recognition by autocomplementary RNA loops, leading

83 es from neurons, which depends on homophilic self-recognition by Dscams.

84 e mechanisms, driven by the need to maintain self-recognition by innate immune cells, while escaping

85 he first time, that disruption of inhibitory self-recognition can efficiently promote ADCC in a human

86 Self-recognition can often lead to repulsion, a process

87 ay play a role in the Pcdh-mediated neuronal self-recognition code.

88 that short CDR3s increase the potential for self-recognition, conferring heightened risk of autoimmu

89 s but also decreases the formation of strong self-recognition contacts between beta-strands with high

90 Domain-swapped contacts compete with self-recognition contacts in forming various trapped sta

91 The impaired missing self recognition could not be overcome through cytokine

92 Despite this requirement for self-recognition during development, mature T cells do n

93 s shed new light into the connection between self-recognition during positive selection and recogniti

94 Here we show that post-thymic self-recognition facilitates the antigen reactivity of m

95 tion by nonexpressing flo1 cells by self/non-self recognition: FLO1(+) cells preferentially stick to

96 Because alleles at self-recognition genes are under balancing selection, th

97 s observation is consistent with deletion of self-recognition genes as a mechanism for the evolution

98 expressed in the fetus has the property of "self-recognition." Green-beard effects have many formal

99 Structural studies of missing self recognition have focused on NK receptors that bind

100 isplay CD47-although signaling mechanisms in self-recognition have remained largely unknown.

101 + cells is more pronounced in the context of self-recognition (HLA matching, indirect presentation).

102 irst in vivo evidence for MHC-independent NK self-recognition in a bone marrow rejection assay.

103 dition to using the mark test to demonstrate self-recognition in a regular mirror, we exposed six fem

104 to complex biological molecules, such as the self-recognition in dilute solutions.

105 rtant for cell-cell communication, molecular self-recognition in neurons, and innate immune defenses.

106 le physiological consequences of glutathione self-recognition in such processes as abnormal protein a

107 des neurons with a unique molecular code for self-recognition in the nervous system.

108 ontribution to phagocytosis, suggesting that self-recognition inhibits contractile engulfment.

109 1B(lo) NK subset and MHC-I-dependent missing-self recognition intact.

110 ing: in the context of the Pot1 protein, DNA self-recognition involving base-stacking and unusual G-T

111 Self recognition is based on allele-specific interaction

112 he question of whether a similar paradigm of self recognition is implicated in the development of mul

113 In contrast, MHC-I-dependent missing-self recognition is preserved in Nkrp1b(-/-) mice.

114 s from those of other neurons, and that this self-recognition is essential for wiring the Drosophila

115 sations and recall our recent actions; (iii) self-recognition; (iv) the awareness of awareness; and (

116 The high-fidelity self-recognition ligation afforded facile access to the

117 Recent studies now indicate that prion self-recognition may be an important factor in both the

118 including the Solanaceae, and this self/non-self recognition mechanism between pollen and pistil is

119 This self-recognition mechanism is a novel peripheral compone

120 These roles of PAPC constitute a self/non-self-recognition mechanism that determines the site of b

121 Here we report of a self-recognition mechanism that has a novel role in moto

122 ssembly, and thus providing a size-dependent self-recognition mechanism.

123 The collaborative non-self recognition model predicts that, for any S-haplotyp

124 The collaborative non-self-recognition model for S-RNase-based self-incompatib

125 dered an indicator of self-awareness, mirror self-recognition (MSR) has long seemed limited to humans

126 Specificity in plant non-self-recognition occurs either directly by perception of

127 t the distortion must be rationalized before self-recognition occurs.

128 for NKR-P1B(B6) in MHC-I-independent missing-self recognition of Clr-b in vivo.

129 Missing self recognition of MHC class I molecules is mediated in

130 le for NKR-P1B:Clr-b interactions in missing-self recognition of normal hematopoietic cells and sugge

131 loaded strongly on the probe question about self-recognition of alcohol-related problems and AD crit

132 Upon self-recognition of beta(2)-microglobulin (beta(2)M) mol

133 ted with Crohn's disease, where breakdown in self-recognition of commensal bacteria leads to gastroin

134 A new study has found that self-recognition of the octopus's skin by its suckers in

135 ptor-ligand system in a new form of "missing self-recognition" of tumor cells.

136 species result in mortality if there is no 'self-recognition' on a broad species level.

137 Chiral self-sorting (also known as chiral self-recognition or chiral self-discrimination) is funda

138 Cell-cycle, proliferation, death, and self-recognition pathways were altered in this radiogeno

139 a anserina participates in a fungal self/non-self recognition phenomenon called heterokaryon incompat

140 We report a self-recognition phenomenon based on an assembly process

141 mong alleles in the diploid parent determine self-recognition phenotypes of both pollen and stigma.

142 peting demands of nonself discrimination and self-recognition place limitations on the mechanisms by

143 tures, resulting in the transfer of "altered self" recognition potential among leukocyte lineages.

144 s of secondary determinants that sustain the self-recognition process during disease progression.

145 nd reflect genetic strategies for biological self-recognition processes in other species.

146 omise CD47's interaction with the macrophage self-recognition receptor signal regulatory protein alph

147 Non-self recognition resulting in programmed cell death is a

148 receptors, thus perturbing induction of the self-recognition signal.

149 as been designed to bind at the amyloid-beta self-recognition site and prevent amyloid-beta from misf

150 ofibrils and monomers, HSA targets key Abeta self-recognition sites spanning the beta strands found i

151 he ectodomain surface, including the site of self-recognition, suggest a model for protein assembly o

152 Vegetative incompatibility is a self/non-self recognition system that inhibits virus transmission

153 complex class I (MHC-I)-independent missing-self recognition system that monitors cellular Clr-b lev

154 A non-self-recognition system called vegetative incompatibilit

155 Despite self-recognition, T cells remain tolerant even in the se

156 he hallmark empirical assessment, the mirror self-recognition test, focuses on an animal's ability to

157 ydroids have evolved a molecular strategy of self-recognition that is unique among characterized allo

158 that determine the exquisite specificity of self-recognition; these data suggest that direct interac

159 ins (Saguinus oedipus) emitted indicative of self-recognition to a mirror was compared with the frequ

160 sp33 uses protein unfolding as a switch from self-recognition to high-affinity client binding.

161 We found that the consequence of self-recognition via TLR8 results in a constellation of

162 f the negative regulator CD5 correlates with self-recognition, we studied CD5(lo) and CD5(hi) naive C

163 e regions of interest (ROIs) associated with self-recognition were examined using a general linear mo

164 r in both studies, but behavioral indices of self-recognition were not consistently generated by the

165 ay a vital role in NK cell-mediated "missing-self" recognition, which contributes to NK cell activati

166 s is necessary and sufficient for attractive self-recognition, which is mediated by differential cell

167 Dscam isoforms on the cell surface underlie self-recognition, while the cytoplasmic tail converts th

168 arly, recent work in animal tool use, mirror self-recognition (with all its contentious issues), and

169 rituximab with an Ab that blocks inhibitory self-recognition yielded increased NK cell-mediated targ