ライフサイエンスコーパス: RPP

1 RPP correction did not improve reproducibility for eithe

2 RPP microarrays were used to profile the phosphorylation

3 RPP microarrays, prepared using simple procedures and st

4 RPP modifiers did not improve SE prediction beyond RPPs

5 RPP was effective only when it was added before assembly

6 lateral heterostructures from various n = 2 RPPs that are more stable against anion interdiffusion a

7 In this configuration, the chiral 2D RPP perovskites offer a significant chiroptical response

8 chirality-regulated spin-polarization of 2D RPP/NPLs hybrid perovskite thin films has significantly

9 Optimized n = 4 RPP solar cells had PCEs of 13% with significant potenti

10 e archaeal RPR is associated with at least 4 RPPs, which function in pairs (RPP21-RPP29 and RPP30-POP

11 the Pfu RPR and RNase P holoenzyme (RPR + 5 RPPs) traverse different Mg2+-dependent paths to converg

12 DCA did not affect RPP but normalized dP/dt in HYP.

13 out RNase P proteins (RPPs), addition of all RPPs lowers the Mg2+ requirement to ~10-20 mM and improv

14 proportion of admissions were similar among RPP-negative and RVP-negative patients (85.3 and 87.1%,

15 DBP and RPP significantly higher in order "A" compared to order

16 SS increased HR and RPP in both orders, while reducing the rMSSD index and S

17 therapy had significantly lower BP, HR, and RPP at 5 and 7 metabolic equivalents (METs) and peak exe

18 Significantly lower exercise BP, HR, and RPP levels are achieved with beta-blocker-based therapy

19 To understand the Mg2+- and RPP-dependent structural changes that increase activity,

20 plasma membrane proteins per 5 minutes, and RPP suppressed 50% of production.

21 e in antibiotic duration in RVP-positive and RPP-positive patients with abnormal chest imaging (6.2 a

22 In RVP-positive and RPP-positive patients, 68.9 and 44.5% of those with norm

23 The average TATs for the RVP and RPP were 27.9 and 3.0 h, respectively (P < 0.0001).

24 n of 34.6 +/- 2.77 nanomoles superoxide, and RPP inhibited 60% of production.

25 5%) were positive for SARS-CoV-2 and another RPP-covered respiratory virus.

26 The four archaeal RPPs have eukaryotic homologs and function as heterodime

27 leavage results from the ability of archaeal RPPs to selectively increase the RPR's apparent rate of

28 tively, these results indicate that archaeal RPPs are able to compensate for structural defects in th

29 ing our previous finding that these archaeal RPPs function as two binary RPP complexes (POP5*RPP30 an

30 eriolar diameter decreased by 17% and 29% at RPP of 130 and 160 mmHg, respectively.

31 ap of this binary complex with the bacterial RPP and highlights their shared recognition of a phyloge

32 Moreover, POP5*RPP30, like the bacterial RPP, helps normalize the RPR's rates of cleavage of non-

33 difiers did not improve SE prediction beyond RPPs presence/absence ( p = 0.8).

34 air (RPP21-RPP29) had no effect; both binary RPP complexes significantly reduced the monovalent and d

35 t these archaeal RPPs function as two binary RPP complexes (POP5*RPP30 and RPP21*RPP29), we prepared

36 roxide, and production was suppressed 72% by RPP.

37 he possible inhibition of this activation by RPP.

38 RPR function might imply that their cognate RPPs provide the functional groups that make up the acti

39 In contrast, RPPs with n 3 form more diffuse lateral heterojunctions,

40 ts on resistance mediated by seven different RPP (recognition of Peronospora parasitica) genes.

41 tructure of a TRBV4-1(+) TCR-HLA-B*07:02/EBV(RPP) complex, which provides a molecular basis for the o

42 After stimulation with the HLA-B*0702/EBV(RPP) peptide, the production of IL-2, perforin, and gran

43 However, the magnitude of the HLA-B*0702/EBV(RPP)-specific and HLA-B*0702/CMV(TPR)-specific CD8(+) T

44 revalence of MS patients with HLA-B*0702/EBV(RPP)-specific CD8(+) T cells ex vivo.

45 yme B and the cytotoxicity of HLA-B*0702/EBV(RPP)-specific CD8(+) T cells were decreased.

46 Similar TCRs were identified in EBV(RPP)-specific CD8(+) T cell repertoires across multiple

47 g residues 379-387 of EBNA-3 (RPPIFIRRL [EBV(RPP)]).

48 The EBV(RPP) CD8(+) T cell response was common among both EBV-se

49 nse mutants on resistance specified by eight RPP genes (for resistance to Peronospora parasitica) exp

50 artially ameliorated upon addition of either RPP pair.

51 Astat-Dx RP assay in comparison to the ePlex RPP assay for the detection of respiratory pathogens.

52 ndromic testing systems, including the ePlex RPP assay, is the ability to generate cycle threshold (C

53 tory targets that were detected by the ePlex RPP assay.

54 samples that were not detected by the ePlex RPP assay.

55 64.6, and 55.7% were identified by the ePlex RPP, NxTAG RPP, and Mycoplasma Direct assays, respective

56 ion compared with placebo and controlled for RPP was reduced by 22.3% on ranolazine 500 mg bid (p = 0

57 Current models for RPP action are derived from 7.2- to 16-A resolution stru

58 l RNase P comprises an RPR and at least four RPPs, which have eukaryal homologs and function as two b

59 omprises one catalytic RPR and at least four RPPs.

60 Despite substantially greater RPP increases relative to baseline during beta1-AR (HCF,

61 nstrated that single-crystalline lead halide RPP nanosheets possess unprecedentedly large nonlinear r

62 For every SD decrease in RPP reactivity with mental stress, the adjusted hazard r

63 is increased by the hypoxia-induced fall in RPP rather than by an increase in renal sympathetic acti

64 hypoxia is predominantly due to the fall in RPP.

65 gulatory responses induced by an increase in RPP, and this response was not further impaired by papil

66 r breathing were mediated by the increase in RPP; neither plasma ANP nor renin activity change in the

67 ositive to any of the 16 pathogen targets in RPP and any household member tested positive for SARS-Co

68 Here, we show that halide miscibility in RPPs decreases with perovskite layer thickness (n), enab

69 Cold pressor test increased RPP similarly in both groups (53+/-26% versus 46+/-26%),

70 The increased RPP to the right kidney accounted for differences in ren

71 acterial pathogens than it is to other known RPP genes.

72 (beta1, 39%; beta2, 34%), despite the large RPP difference between the groups.

73 yet the direct and general growth of lateral RPP heterostructures remains challenging.

74 uct reactivity was calculated as the maximum RPP during a standardized mental stress test minus the R

75 1,183 +/- 1857 mm Hg/min; 75.5 +/- 12.9 min, RPP and heart rate, respectively; systolic blood pressur

76 Hg/min; 151 +/- 19.1 mm Hg; 197 +/- 8.6 min; RPP, systolic blood pressure and heart rate, respectivel

77 Moreover, one pair of Mja RPPs (POP5-RPP30) enhanced k(obs) for the RPR-catalyzed

78 ction was estimated by adding 0.20 microg/ml RPP.

79 coincubated with and without 0.25 microg/ml RPP.

80 tory pathogen panel (RPP), the Luminex NxTAG RPP, the ELITech ELITe InGenius Mycoplasma MGB research

81 5.7% were identified by the ePlex RPP, NxTAG RPP, and Mycoplasma Direct assays, respectively.

82 We first show the application of RPP microarrays to the study of signaling kinetics and p

83 We conclude that elevations of RPP contribute significantly to the fibrosis and epithel

84 er, the power conversion efficiency (PCE) of RPP cells remains inferior to 3D perovskite-based cells.

85 ogen gene expression; (b) acute reduction of RPP for 3 h could stimulate renin gene expression in the

86 Reduction of RPP to 60 mmHg for 3 h in these animals had little effec

87 se-urethane anaesthetised rats, reduction of RPP to 60 mmHg for 3 h in vehicle or losartan-treated (5

88 Following reduction of RPP to 60 mmHg for 3 h, plasma renin activity was increa

89 not apparent during short-term reduction of RPP.

90 current model for the mechanism of action of RPPs proposes that drug release is indirect and achieved

91 d from 7.2- to 16-A resolution structures of RPPs bound to vacant or nontranslating ribosomes.

92 l than the minor reductions in heart rate or RPP, suggesting that ranolazine's beneficial mechanism o

93 -protein interactions between L7Ae and other RPPs.

94 stablished ePlex Respiratory Pathogen Panel (RPP) assay, for which we used 287 respiratory samples fr

95 he GenMark ePlex respiratory pathogen panel (RPP), the Luminex NxTAG RPP, the ELITech ELITe InGenius

96 ing a commercial respiratory pathogen panel (RPP).

97 y the recognition of Peronospora parasitica (RPP)2 (At) locus in Arabidopsis accession Columbia (Col-

98 ance (Recognition of Peronospora parasitica [RPP]) gene products triggers localized cell death (a hyp

99 advantage of Radiographic Pulmonary Pattern (RPP).

100 and periodic electroencephalogram patterns (RPPs) associated with SE and seizures.

101 2D Ruddlesden-Popper perovskite (RPP) solar cells have excellent environmental stability.

102 R)- and (S)-2D Ruddlesden-Popper perovskite (RPP)/NPL hybrids.

103 l (2D) Ruddlesden-Popper halide perovskites (RPPs) show suppressed and anisotropic ion diffusion that

104 d Ruddlesden-Popper-type halide perovskites (RPPs) with tunable ultraviolet-to-visible direct bandgap

105 ctions are studied by Real Physical Picture (RPP) model.

106 espite significant progress in cloning plant RPP genes and characterizing essential plant components

107 ent basal MABP and renal perfusion pressure (RPP) from falling after addition of Losartan and to keep

108 died the impact of renal perfusion pressure (RPP) on the development of renal injury in this model.

109 influence of acute renal perfusion pressure (RPP) reduction on renin release, renal renin and angiote

110 V were absent when renal perfusion pressure (RPP) was prevented from rising during air breathing by u

111 step increases in renal perfusion pressure (RPP).

112 Baseline rate-pressure product (RPP) (6559+/-1590 versus 7144+/-1157 bpmxmm Hg) and MBF

113 % to 26% reduction in rate pressure product (RPP) and impaired dP/dt versus SHAM (P<0.05).

114 , heart rate (HR) and rate-pressure product (RPP) at maximal and submaximal workloads were assessed.

115 nt depression and the rate-pressure product (RPP) during exercise to determine whether ranolazine's m

116 similar increases in rate-pressure product (RPP) in smokers and nonsmokers.

117 5 and 5 minutes for a rate-pressure product (RPP) less than 20% baseline.

118 blood pressure (DBP), rate-pressure product (RPP) oxygen saturation (SpO(2)), and heart rate variabil

119 The rate-pressure product (RPP) was calculated as the mean systolic blood pressure

120 mula: see text]O(2)), rate pressure product (RPP), CP and VP compared to those only diagnosed with HF

121 ventricular systolic blood pressure product (RPP).

122 lso normalized to the rate.pressure product (RPP).

123 urements were made of rate-pressure product (RPP=LV developed pressure x heart rate), phosphorus-cont

124 ch we termed regeneration-promoting program (RPP), is essential for proper repair.

125 ly downregulated by an RPE-generated protein RPP.

126 The bacterial RNase P protein (RPP) aids RNase P RNA (RPR) catalysis by promoting subst

127 c RNase P RNA (RPR) and one RNase P protein (RPP), have helped understand the pleiotropic roles (incl

128 veloped a multiplexed reverse phase protein (RPP) microarray platform for simultaneous monitoring of

129 tinal pigment epithelial protective protein (RPP) was described, which suppresses the superoxide gene

130 rchaeal RPR active without RNase P proteins (RPPs), addition of all RPPs lowers the Mg2+ requirement

131 R) and a varying number of RNase P proteins (RPPs): 1 in bacteria, at least 4 in archaea and 9 in euk

132 and one copy each of five RNase P proteins (RPPs; POP5, RPP30, RPP21, RPP29, L7Ae).

133 Ribosome protection proteins (RPPs) confer resistance to tetracycline by binding to th

134 Ribosome protection proteins (RPPs) confer tetracycline resistance by binding to the r

135 Robustified projection pursuit (RPP) was used for statistical analysis using RNA as a su

136 method using robustified projection pursuit (RPP).

137 30 and RPP21*RPP29), we prepared recombinant RPP pairs from three archaea and established interchange

138 VP) or respiratory pathogen panel (ePlex RP; RPP) within 48 h of presentation.

139 ng refractive index near resonance, a single RPP crystal can exhibit different nonlinear functionalit

140 Neural Networks (CNN) to detect specifically RPP from feline TR images has not been investigated.

141 the "Trp-cage" peptide (NLY IQW LKD GGP SSG RPP PS).

142 ropic ion diffusion that could enable stable RPP heterostructures, yet the direct and general growth

143 ne essential RNA (RPR) and protein subunits (RPPs) numbering one in bacteria, and at least four in ar

144 ver, the number of RNase P protein subunits (RPPs) varies from 1 in bacteria to 9 or 10 in eukarya.

145 nucleotide C1054 of the 16S rRNA, such that RPP action uses Pro509, rather than Y506/Y507, to direct

146 The results suggest that RPPs are efficient nonlinear materials in the visible wa

147 The RPP and ST-segment depression were assessed before start

148 The RPP increased by a mean (SD) of 77.1% (23.1%) during men

149 ectively), despite comparable changes in the RPP (P = NS).

150 d repair-macrophage identity develops in the RPP at the transcriptional level and how induced macroph

151 ated by the spacer and A-site cations in the RPP structures.

152 Fewer patients were admitted in the RPP-positive compared to the RVP-positive group (76.9 an

153 ercise despite an additional increase in the RPP.

154 a standardized mental stress test minus the RPP at rest.

155 ason for the reduction in fill factor of the RPP devices.

156 yo-electron microscopy reconstruction of the RPP TetM in complex with a translating ribosome at 3.9-A

157 Here we report a cryo-EM structure of the RPP TetM in complex with the 70S ribosome at 7.2-A resol

158 rug-binding site induced upon binding of the RPP to the ribosome.

159 family member, GDF-15, as a component of the RPP.

160 family member, GDF-15, as a component of the RPP.

161 d it had weak-to-intermediate effects on the RPP genes.

162 renal arteries; during the same period, the RPP to the right kidney rose to 164 +/- 8 mmHg.

163 MBF normalized to the RPP (derived from the ratio of MBF ([milliliters per gra

164 of salt-induced hypertension over 2 wk, the RPP to the left kidney was maintained at control levels

165 t necessary for resistance mediated by these RPP genes.

166 1-2/ndr1-1 background, suggesting that these RPP genes operate additively through EDS1, NDR1 and as-y

167 bidopsis genes following activation of three RPP genes directed against the pathogenic oomycete Peron

168 of MBF ([milliliters per gram per minute] to RPP [beats per minute times millimeters of mercury] time

169 WT control mice exhibited typical RPP-dependent vasoconstriction that was significantly at

170 V-2, all household specimens were tested via RPP if the index child's day 0 specimen tested positive

171 citon resonance of the thinnest qunatum-well RPPs, boosting the nonlinear response.

172 In the pooled sample, when RPP reactivity to mental stress was added to a model inc

173 n groups (48+/-36% versus 48+/-28%), whereas RPP again increased similarly in the 2 groups (59+/-30%

174 cus furiosus (Pfu) RPR, either alone or with RPPs pre-tRNA.