ライフサイエンスコーパス: delayed response

1 l area were either ineffective or produced a delayed response.

2 -kinase activity is required to trigger this delayed response.

3 ated AbetaPP and loss of cell viability were delayed responses.

4 rush cells (UBCs) in generating the required delayed responses.

5 opy was performed after 24 hours to evaluate delayed responses.

6 unit of RPA becomes hyperphosphorylated as a delayed response (4-8 h) to UV radiation (10-30 J/m(2)).

7 This delayed response accounted for the prolonged and exacerb

8 However, the delayed response against GP5 early in infection may cont

9 press responses, the volitional execution of delayed responses, and the anticipation of predictable e

10 nal therapy can occur, suggesting a need for delayed-response assessment.

11 In addition, a delayed response associated with 24-hour average exposur

12 In addition, growth hormone displayed a delayed response but to a higher peak level.

13 mutations to TDF were found in patients with delayed response, but all were infected with HBV genotyp

14 tibody response to HMPV infection revealed a delayed response, but passive transfer of HMPV-specific

15 We conclude that the presence of delayed responses can identify regions of hyperexcitable

16 ted by increases in eicosanoid synthesis and delayed responses characterized by sphingolipid and ster

17 e lung by HPAI, the other viruses produced a delayed response, characterized by an increase in protei

18 The expression boundary of delayed response class genes in the subepidermal fibrobl

19 In contrast, expression of genes in the delayed response class is highest in resorbing tissues a

20 e examined on a spatial working memory task (delayed response) dependent on the PFC, and on a referen

21 ves network's performance on a two-interval, delayed response discrimination task.

22 latta) and that these metrics correlate with delayed response (DR) accuracy, a well-characterized mea

23 , as measured by the average accuracy on the delayed response (DR) test.

24 All monkeys were tested on delayed response (DR), a cognitive test of working memor

25 nd cytokine expression as fundamental to the delayed response following GTN infusion, and support the

26 Likewise, TGF-beta signaling demonstrated a delayed response following LC.

27 The delayed response format was used to assess simple one-it

28 We report that COX-1 behaves as a delayed response gene in PC12 cells exposed to NGF.

29 AMP response element-dependent immediate and delayed response genes could play a pivotal role in the

30 ent with expression characteristics of other delayed response genes in PC12 cells.

31 Similarly, a group of delayed response genes including two proteolytic enzymes

32 terized by expression of immediate early and delayed response genes.

33 increase in AChR epsilon-subunit mRNA was a delayed response in C2C12 muscle cells.

34 e of neuropathic pain, whereas MMP-2 shows a delayed response in DRG satellite cells and spinal astro

35 sponse being in the deep layers and the most delayed response in the capillary bed of layer I.

36 food allergen injections induce acute and/or delayed responses in patients with EoE but not controls.

37 vation and relative levels of MnSOD revealed delayed responses in the injured cortex of TNFR-KO anima

38 regulation of transcription factors; (2) the delayed response included a high percentage of genes rel

39 Both patients and relatives had delayed response inhibition on the Stop-Signal task comp

40 The study of delayed responses may improve our understanding of the p

41 rate the steep signal-to-response curves and delayed responses observed in cells.

42 an explanation for the reduced amplitude and delayed response of the electroretinogram a-wave observe

43 inhaled nPM into the brain may contribute to delayed responses of proximal and distal brain regions,

44 We recorded the short-latency and delayed responses of STN units and frontal electrocortic

45 nges in response to immunotherapy reflecting delayed responses or therapy-induced inflammation.

46 We used a delayed response paradigm with functional MRI to examine

47 Glucose yields a delayed response pattern, similar to a hockey stick func

48 ar motor and motivational demands (rats), or delayed response performance following zero-second delay

49 crogram/kg) administration had no effects on delayed-response performance but impaired performance on

50 Stress-induced deficits in delayed-response performance were ameliorated by pretrea

51 osure to noise stress significantly impaired delayed-response performance.

52 expression patterns of stromelysin-3 and the delayed response proteinases in the head delineate separ

53 of pup exposure, while Fos B levels showed a delayed response, reaching maximal levels after 6 h.

54 TNF-alpha and inflammatory protein 10; and a delayed response resulting from CCN1-induced TNF-alpha,

55 Delayed-response sensory discrimination is believed to r

56 d in most regions in all patients; and (ii) 'delayed responses', spikes or sharp waves occurring betw

57 itial transient increase within 5 min, and a delayed response starting between 60-90 min.

58 t, Delayed Alternation task (DA) and Spatial Delayed Response task (DR).

59 All animals acquired the delayed response task and could perform at near ceiling

60 ere heritable, only performance on a spatial delayed response task and integrity of the superior long

61 pisode schizophrenia performed an oculomotor delayed response task at baseline before any drug treatm

62 only subtle increases in sensitivity on the delayed response task following ovariectomy.

63 , were trained to perform a modified spatial delayed response task in which the attentional demands o

64 The oculomotor delayed response task is a translational spatial working

65 ested aged female rhesus macaques on (1) the delayed response task of spatial working memory, (2) a v

66 cognitive function in rats as measured in a delayed response task of spatial working memory.

67 nimals performed significantly better on the delayed response task than all of the other groups for m

68 cleus accumbens neurons in rats performing a delayed response task that allowed us to dissociate the

69 y between stimulus and response in a spatial delayed response task to explore the trajectory of seria

70 social or nonsocial stimuli; subsequently, a delayed response task was implemented to assess spatial

71 opolamine on attention, but not memory, in a delayed response task were dependent on estrogen.

72 iscriminations and the accuracy on a spatial delayed response task were found to be comparable in you

73 t of Adult Reading), working memory (Spatial Delayed Response Task), memory (Visual Object Learning T

74 ion status: Digit Symbol Coding Task, Object Delayed Response Task, and immediate facial memory.

75 mals also showed improved performance in the delayed response task, but only at 30 s delays and with

76 mm apart in monkeys performing an oculomotor delayed response task.

77 the dPFC of monkeys performing an oculomotor delayed response task.

78 ing from neurons during the performance of a delayed response task.

79 el of the PFC circuit involved in oculomotor delayed response task.

80 cortex (mPFC) were studied using an operant delayed response task.

81 emembered spatial locations on an oculomotor delayed response task.

82 in deficits in the performance of a variable delayed-response task (VDR).

83 ded from the medial PFC of rats performing a delayed-response task of working memory during acute noi

84 apparatus, monkeys were trained on a spatial delayed-response task to assess spatial working memory a

85 has been shown to improve performance of the delayed-response task, a task linked to the dorsolateral

86 or "memory fields," in monkeys performing a delayed-response task.

87 healthy human subjects performed a modified delayed-response task.

88 on interleaved saccade and reach trials of a delayed-response task.

89 reach trials in at least one interval of the delayed-response task.

90 odent dorsomedial prefrontal cortex during a delayed-response task.

91 Brain imaging studies of WM using delayed response tasks (DRTs) have shown memory-load-dep

92 x has been shown to modulate visually guided delayed response tasks as well as anxiety and depression

93 sistent activity in prefrontal cortex during delayed response tasks is a putative neural correlate of

94 mpairments in compromised memory function in delayed response tasks possibly through selective increa

95 with nonhuman primates performing oculomotor delayed response tasks suggest that the apparent adverse

96 he delayed non-matching-to-sample (DNMS) and delayed response tasks.

97 as of the macaque brain, neurons fire during delayed-response tasks at a rate determined by the value

98 Our delayed-response tasks required memory for the identity

99 ction-potential discharge) and components of delayed-response tasks used to probe PFC-dependent cogni

100 To this end, we compared delayed-response tasks with identical mnemonic and atten

101 ed with memory-guided saccades in oculomotor delayed-response tasks yet has little or no effect on th

102 as exposed by single-cell recordings during delayed-response tasks.

103 ment vehicle-injected monkeys exhibited on a delayed response test of spatial working memory.

104 ove PFC-dependent cognition as measured in a delayed-response test of spatial working memory.

105 -regulation of TIMP-2 by dibutyryl cAMP is a delayed response that requires de novo protein synthesis

106 ed, in approximately 35% of nerve bundles, a delayed response that single unit analysis showed to be

107 lect mostly low-level visual processing, and delayed responses that correlate with perceptual reports

108 ve beta-band activity persisted up until the delayed response, the CPP dropped toward baseline after

109 s exhibited a severe reading impairment with delayed response times during reading aloud tasks, but n

110 al antidepressants have limited efficacy and delayed response times of weeks to months.

111 ultrasensitive dose response, accelerated or delayed response times, and tunable adaptation.

112 ulted in more polarized cells that exhibit a delayed response to a new chemoattractant source due to

113 The task required subjects to make a delayed response to a previously lighted location, with

114 ent only after metamorphosis, highlighting a delayed response to a signal released early on.

115 counts for features of the syndrome, and its delayed response to antidepressant medication, is lackin

116 depression is complicated by a variable and delayed response to antidepressant treatment.

117 tely monitored patients may be at risk for a delayed response to critical arrhythmias if the telemetr

118 presenting with signs of HGA but who have a delayed response to doxycycline therapy or negative conf

119 actures and osteonecrosis and for reduced or delayed response to enzyme replacement therapy.

120 profiles: (1) fast, (2) prolonged, and (3) a delayed response to errors, as well as a more canonical

121 1pr) and the other by a mutant promoter with delayed response to galactose induction, we found that t

122 The delayed response to GGF2 does not reflect a lack of func

123 nullify the adverse prognosis conferred by a delayed response to induction therapy.

124 ese results represent the first example of a delayed response to light relative to light-induced imme

125 Thus, TAK1 activity is induced as a delayed response to mechanical stress, and can suffice t

126 as slower than channel closing, suggesting a delayed response to membrane potential by the ligand bin

127 % of diabetic patients either lack or have a delayed response to metformin treatment, and many patien

128 Estrous females showed a delayed response to methiothepin, but there was no methi

129 A delayed response to NAC exposure was an increase in both

130 nfants and young children as a result of the delayed response to PS antigens during ontogeny.

131 We also observed a delayed response to saliva with increased densities of T

132 to what extent remissions of DMP represent a delayed response to steroids or would have occurred with

133 ght that is rapidly reversible, as well as a delayed response to stimulation in the quiescent state.

134 otypes and prior lamivudine treatment in the delayed response to TDF warrant further investigation.

135 The delayed response to therapy is consistent with that obse

136 interval [CI], .73-.93) was associated with delayed response to treatment.

137 Lower response rates and delayed responses to ibrutinib are associated with mutat

138 ignificantly decreased Cdk5 activity, showed delayed responses to painful thermal stimulation compare

139 id FA growth occurred in all cells; however, delayed responses to stretch occurred in an orientation-

140 ntional effects, in that they accelerated or delayed responses to subsequent targets.

141 The delayed response was identical to movements evoked by cl

142 Delayed response was rarely related to inappropriate the

143 The distributions of early and delayed responses were compared with the topography of s

144 Consequently, delayed responses were normal; however, the early induct

145 ngle pulse stimulation, the distributions of delayed responses were significantly associated with the

146 However, BCH produced only a delayed response, while leucine was totally ineffective

147 individuals with Turner syndrome performed a delayed-response WM task during fMRI scanning.

148 terval between the memoranda and probes of a delayed-response WM task.

149 To assess the cognitive control, we used a delayed response working memory task with pictures of va

150 emotional and nonemotional distracters on a delayed-response working memory (WM) task.