ライフサイエンスコーパス: sensing of

1 sed, absolute radio-frequency electric field sensing of 5 muV cm(-1) Hz(-1/2).

2 hown sensitive and selective electrochemical sensing of 8-oxoguanine and uracil repair glycosylase ac

3 fered a sensitive and reversible ratiometric sensing of a 0.1-pH unit change in the pH range 5.0-8.5.

4 lity of the IIDA approach is demonstrated on sensing of a phosphonate herbicide glyphosate and other

5 have rarely been exploited for the selective sensing of a protein in blood serum.

6 nomous response mobilized by STING-dependent sensing of a specific vita-PAMP and elucidate how innate

7 relating ground-based measurements to remote sensing of aerosol properties.

8 In this paper we report the sensing of aflatoxin B1(AFB1) by field effect capacitive

9 ort evidence that in Sinorhizobium meliloti, sensing of AHLs with acyl chains composed of 14 or more

10 arly imprinted polymer (MIP) for trace level sensing of alpha-fetoprotein (AFP), which is a well know

11 Sensing of amino acids causes translocation of mTORC1 to

12 This is shown for selective sensing of an anti-insulin antibody in the presence of i

13 d capability of online monitoring and remote sensing of analyte due to the fabrication of the probe o

14 ilities towards online monitoring and remote sensing of analyte.

15 iRNAs has a negligible impact on both innate sensing of and immediate response to acute viral infecti

16 nium, remarkable progress in the binding and sensing of anions has been taking place, driven in part

17 n well established, similar progress for the sensing of anions has not yet been realized.

18 been remarkable progress in the binding and sensing of anions.

19 re used for amplification of electrochemical sensing of anti-HIV replication drug i.e. deferiprone.

20 stems depend entirely on the transporter for sensing of antimicrobial peptides, suggesting a novel mo

21 The electroanalytical sensing of APAP and INH are possible with accessible lin

22 The BiO-SPEs were evaluated toward the sensing of APAP and INH in human serum, urine, saliva, a

23 strong electrocatalytic activity toward the sensing of APAP and INH with an enhanced analytical sign

24 development of a nanocarbon based anode for sensing of ascorbic acid (AA).

25 e recently been employed for resistive-pulse sensing of Au nanoparticles (AuNP) and nanoparticles wit

26 of virulence factors via the production and sensing of autoinducing peptide (AIP) signal molecules b

27 urface is induced by auxin and requires ABP1 sensing of auxin.

28 ral human antimicrobial that promotes immune sensing of bacterial and host cell death.

29 atory response is dependent on intracellular sensing of bacterial components that access the cytosoli

30 on of some intracellular bacteria, cytosolic sensing of bacterial DNA has also been implicated in eli

31 , S. aureus(LAC), through on-chip electrical sensing of bacterial lysate.

32 that enable Kretschmann-configured plasmonic sensing of bacterial toxins.

33 terol depletion and a decrease in intestinal sensing of bile acids.

34 l sciences as data storage can be coupled to sensing of biological molecules.

35 ased electrochemical sensor for an efficient sensing of biologically active drug molecule ciprofloxac

36 Furthermore, the FETs were tested for the sensing of biomolecules (bovine serum albumin (BSA) as r

37 lls modulate insulin secretion through rapid sensing of blood glucose and integration of gut-derived

38 ability to detect and avoid shading through sensing of both blue and red light wavelengths.

39 t of DNA sensing by cGAS and STING-dependent sensing of c-di-AMP.

40 umor necrosis factor (TNF) produced upon TLR sensing of C. burnetii NMII was required to control bact

41 Sensing of C3 in the cytosol activated mitochondrial ant

42 rd a nanoliter-scale dip sensor for the dual sensing of Ca(2+) and Cd(2+) was demonstrated using micr

43 hose proper interpretation will allow remote sensing of calving processes occurring at increasing num

44 ate that a major mechanism for innate immune sensing of cancer occurs via the host STING pathway, wit

45 by the hydrogels, these results reveal cell sensing of cell volume confinement as an adhesion-indepe

46 thermore, TLR2 but not TLR4 was critical for sensing of cell wall extracts and whole corynebacteria.

47 These studies demonstrate that internal sensing of changes in pAg metabolite concentrations by B

48 l of the expression of regulatory microRNAs, sensing of changes in the environment by use of riboswit

49 to show simple colorimetric enantioselective sensing of chiral species with a fast readout in less th

50 Using optical sensing of chloramphenicol as a proof of concept, we sho

51 It allows fluorescent, ratiometric sensing of chloride ions across the entire physiological

52 Single-layer EPADs for sensing of chloride ions include wax-defined sample and

53 These results reveal innate immune sensing of circRNA and highlight introns-the predominant

54 etabolic demand by modulating the access and sensing of circulating molecules.

55 lysis bears high potential for environmental sensing of climate relevant gases and noninvasive early

56 latory elements is present to facilitate the sensing of CO2 availability, to regulate the expression

57 x 10(-9)M, indicating its potential for the sensing of COD in clinical samples and pharmaceutical fo

58 ellent electrocatalytic response towards the sensing of COD with a wide linear response range of 2.0

59 electrocatalyst toward the electroanalytical sensing of codeine phosphate (COD).

60 ce and humans, the events that lead from the sensing of cold to the development of beige fat remain p

61 Molecular hosts capable of chiroptical sensing of complexed guest molecules offer an attractive

62 Host sensing of corynebacteria is largely uncharacterized, al

63 Japanese cedar pollen, and the histochemical sensing of Cry j 2 in ruptured Japanese cedar pollen.

64 used in a drain source configuration for the sensing of cTnI.

65 a novel and sensitive probe for the optical sensing of cyanide ion (CN(-)) and 2-mercaptobenzothiazo

66 nt evidence has indicated that innate immune sensing of cytosolic DNA in dendritic cells via the host

67 Sensing of cytosolic nucleotides is a critical initial s

68 2D-hBN is utilized toward the sensing of DA in the presence of the common interferents

69 he electrochemical detection/electrochemical sensing of DA.

70 Sensing of dietary triacylglycerol in the proximal small

71 the basis for development of single-molecule sensing of differently ubiquitinated substrates with dif

72 tion activates inflammasomes, and identifies sensing of disturbances in intracellular ionic concentra

73 To enable dynamic sensing of divalent cations via PAI, we have engineered

74 ridized dsDNA could be used for quantitative sensing of DNA concentration.

75 , in CD11c+ cells, suggesting that cytosolic sensing of DNA from tumor cells is enhanced by anti-CD47

76 owed by Toll-like receptor 9 (TLR9)-mediated sensing of DNA in phagosomes.

77 use of surface plasmon resonance for direct sensing of DNA/GO binding.

78 idelity, achieved by label-free simultaneous sensing of DNA/RNA, hemoglobins, and lipids.

79 electrocatalyst toward the electroanalytical sensing of dopamine (DA).

80 varian cancer (OC), DNMTis trigger cytosolic sensing of double-stranded RNA (dsRNA) causing a type I

81 dimensional mapping of the axon diameter and sensing of dynamic changes in the substructure of myelin

82 This integration is hypothesized to mediate sensing of ECM rigidity, but parsing the function of nuc

83 ethod of charge state-dependent fluorescence sensing of electrochemical potentials.

84 gated bile acids and demonstrated intestinal sensing of elevated bile acid levels in plasma in mice.

85 t a platform for the ratiometric fluorescent sensing of endogenously generated gaseous transmitter H2

86 Although the sensing of endoplasmic reticulum (ER) Ca(2+) stores by S

87 suggesting that YopK limits the induction or sensing of endosomal membrane damage by components of th

88 nstrates a physiological role of TLR8 in the sensing of entire S. aureus in human primary phagocytes,

89 When pathogens enter the host, sensing of environmental cues activates the expression o

90 These findings establish the link between sensing of environmental cues by the external proteins a

91 ood at the molecular level about the initial sensing of environmental stress.

92 teractions Lamellipodin mediates directional sensing of epidermal growth factor (EGF) gradients and i

93 nal cues during spontaneous polarization and sensing of external cues during directional motility.

94 Evidence in plants supports the sensing of extracellular DNA by PRRs, leading to calcium

95 he HasR receptor plays a primary role in the sensing of extracellular heme and a supplementary role i

96 the usage of different integrin subtypes and sensing of extracellular matrix proteins.

97 surface of most cells, are important to the sensing of extracellular signals, and make a driving for

98 urrently, mechanisms underlying the gradient sensing of fibroblasts remain poorly understood.

99 nistic basis for models to describe gradient sensing of fibroblasts.

100 re, we present a method that exploits the pH sensing of flagellated bacteria to realize robust drift

101 TLR5-mediated sensing of flagellin promoted plasma cell differentiatio

102 n elegant navigational strategy based on the sensing of flow velocity gradients and provide a compreh

103 This approach for colorimetric sensing of fluoride by ring-opening of the otherwise pho

104 Despite its ubiquity during the binding and sensing of fluoride, the role of bifluoride (HF2(-)) and

105 tability of our SHP-OP SERS platform for the sensing of food toxins in real samples.

106 formation allowing for sub-diffraction-limit sensing of, for instance, magnetic or electric fields wi

107 s, and for the realization of ultrasensitive sensing of force and motion.

108 The sensing of foreign agents by the innate and adaptive imm

109 The field of cellular sensing of foreign DNA is in its infancy, but our curren

110 nterferon and proinflammatory responses upon sensing of foreign DNA.

111 abricated on an electrode for optoelectronic sensing of fowl adenoviruses (FAdVs).

112 This paper demonstrates the direct sensing of glucose at physiologically relevant concentra

113 nitoring, as well as selective and sensitive sensing of glucose in mammalian blood.

114 Automated amperometric sensing of glucose solutions in microtiter-plate wells u

115 onitoring (CGM) technologies enable frequent sensing of glucose to inform exogenous insulin delivery

116 o broaden the application of electrochemical sensing of glucose, we fabricated, for the first time, a

117 Moreover, in vitro glucose sensing of glucose-inhibitory neurons from the ventromed

118 of biosensing scaffold for the amperometric sensing of H2O2 and total cholesterol in human serum are

119 Amperometric sensing of H2O2 at 0.2 nM level without any redox mediat

120 The data indicate that sensing of HCV infection by RIG-I and TLR3 leads to dire

121 ts into potential roles of GraS in S. aureus sensing of HD-CAPs to induce adaptive survival responses

122 rene@ZnO is coated over copper layer for the sensing of heparin.

123 these findings suggest that innate iNKT cell sensing of HIV-1 infection in DCs is an early immune det

124 n natural HIV infection modulated normal pDC sensing of HIV.

125 The recurrent sensing of HNO uncovered with the study of Cu(II) azamac

126 on AGM pDC, which did not preclude efficient sensing of host-adapted viruses.

127 molecular pattern-sensing pathways, wherein sensing of host-derived DNA limits immune-mediated damag

128 Thus, sensing of HSV-1 infection in the CNS by microglia throu

129 ission probe for the fluorescent ratiometric sensing of hydrogen peroxide (H2O2), enzyme activity, an

130 roxidase enzyme (HRP) for bioelectrochemical sensing of hydrogen peroxide for the first time.

131 been exploited for the selective fluorescent sensing of hydrogen pyrophosphate anion.

132 Here, we report that the sensing of IAV RNA by retinoic acid inducible gene I (RI

133 Our findings show that sensing of IL-1 cytokines during colonization promotes i

134 The mechanism of innate immune sensing of immunogenic tumors leading to adaptive T cell

135 to inhibit Toll-like receptor (TLR) 7 and 8 sensing of immunostimulatory RNA, independent of their m

136 In cells, sensing of increased levels of reactive oxygen species (

137 host defense pathway is orchestrated by the sensing of infection by DAI/ZBP-1, engagement of the kin

138 Further analysis suggests that molecular sensing of infection might have a similar pathogenic rol

139 Fpr3 has been implicated in the sensing of infection-associated olfactory cues, but its

140 roles of NOD1 and NOD2 to encompass not only sensing of infections with viruses and parasites but als

141 ntibiotic-resistant infections, non-invasive sensing of infectious diseases is increasingly important

142 Innate sensing of influenza virus infection induces activation

143 ld be implemented in other systems and drive sensing of integrity and response by regeneration in oth

144 This global coupling impairs sensing of internal cues during spontaneous polarization

145 lic GMP-AMP (cGAMP) synthase (cGAS) mediated sensing of irradiated-tumor cells in DCs.

146 ferent ionophores, allowing the simultaneous sensing of K and Na ions using a flow cell.

147 lytical device (EmuPADs) for electrochemical sensing of ketamine.

148 te dehydrogenase (LDH) was developed for the sensing of l-lactate.

149 a d-states changes during CO2 chemoresistive sensing of La2O2CO3.

150 analytical efficacy is explored towards the sensing of lactate in model (buffer) solutions and is fo

151 PECT-MP for improving capabilities of remote sensing of leaf photosynthetic pigments (chlorophyll a,

152 Sensing of lipopolysaccharide (LPS) in the cytosol trigg

153 mmasome field, focusing mainly on the innate sensing of LPS.

154 This new effect enhances the sensing of magnetic switching, which has potential usage

155 irst example where the transport and not the sensing of major constituents of the plant host is the c

156 nate immune receptors have a key role in the sensing of malaria and initiating immune responses.

157 nally, SPR methodology was developed for the sensing of malarial antibodies.

158 Colorimetric as well as fluorogenic sensing of maleic acid among various carboxylic acids wa

159 esearchers for the optical visualization and sensing of many biological interactions as well as detec

160 oll-like receptor 7 (TLR7) were critical for sensing of MERS-CoV by pDCs.

161 f Thr172 phosphorylation.AMPK is involved in sensing of metabolic stress.

162 The real-time sensing of metal ions at point of care requires integrat

163 This immune layer involves sensing of microbe-associated molecular patterns (MAMPs)

164 oth locally and systemically, requires tonic sensing of microbes and complex feedback loops between i

165 1-activating multiprotein complex that links sensing of microbial and stress products to activation o

166 t is sustained through the host's continuous sensing of microbial factors and the generation of a tol

167 Our results reveal that simultaneous sensing of microbial ligands and virulence factors by TL

168 Smartphone image-based sensing of microfluidic paper analytical devices (muPADs

169 In resistive pulse sensing of microRNA biomarkers, selectivity is achieved

170 tive ionophores dedicated to electrochemical sensing of molecular ions.

171 rified IL-electrode interfaces for selective sensing of molecules with a kinetic size resolution of 0

172 ma by these cell populations required IL-18, sensing of mycobacterial viability, Mtb protein 6-kDa ea

173 of the R753Q TLR2 polymorphism on macrophage sensing of Mycobacterium smegmatis Upon infection with M

174 molecular pattern that may facilitate immune sensing of myeloma tumors and modulate the tolerogenic c

175 and clay) based modified electrodes for the sensing of NADH.

176 We hypothesized that sensing of necrotic cells by DNGR-1 plays a determinant

177 The electrochemical sensing of new psychoactive substance(s) (NPSs), synthet

178 The electrochemical sensing of new psychoactive substances, synthetic cannab

179 This study suggests that sensing of NHDC by a bacterial plasma membrane receptor

180 ll AIEgens are fruitfully employed for rapid sensing of nitroaromatic compounds (NACs) where picric a

181 here was little evidence of cytosolic immune sensing of NMII, as there was a lack of inflammasome act

182 nanoporous structure for the electrochemical sensing of NO, which was fabricated via a facile electro

183 The proposed label free sensing of nonlethal effect of model amyloid protein at

184 only human cathelicidin LL-37 triggers rapid sensing of nucleic acids by plasmacytoid dendritic cells

185 The sensing of nucleic acids by receptors of the innate immu

186 Sensing of nucleic acids by TLRs is crucial in the host

187 Our results demonstrate that aberrant sensing of nucleic acids can cause immune upregulation.

188 Cytosolic sensing of nucleic acids initiates tightly regulated pro

189 Innate sensing of nucleic acids lies at the heart of antiviral

190 des mechanisms of kin selection, single-cell sensing of nutrient depletion and the stringent response

191 mechanisms function to tightly regulate the sensing of nutrient depletion, the aggregation of popula

192 pathways, which coordinate together for the sensing of nutrient state and regulation of gene transcr

193 ed KIN as a critical regulator that mediates sensing of nutrients and controls a transcriptional resp

194 Comprehensive sensing of only 0.5 mg of a crude reaction mixture of an

195 The developed approach could be adopted for sensing of other viruses.

196 d into main sections on direct spectroscopic sensing of oxygen, on absorptiometric and luminescent pr

197 tributions provides evidence for logarithmic sensing of oxygen, which enhances sensing in low oxygen

198 e Vgamma9Vdelta2 T cell response begins with sensing of pAg via the intracellular domain of the butyr

199 f an inflammasome complex requires cytosolic sensing of pathogen-associated molecular patterns or dan

200 tured aptasensor for label free impedimetric sensing of pathogenic bacteria E. coli O78:K80:H11.

201 nts with nanomaterials for the detection and sensing of pathogenic bacteria.

202 of AMPs is an important component of innate sensing of pathogens and may play an important role in t

203 ]-containing) proteins mediate innate immune sensing of pathogens in mammals and plants.

204 inds Syk through a hemITAM motif and couples sensing of pathogens such as fungi to induction of innat

205 e protein that is critical for innate immune sensing of pathogens.

206 platforms for both the lumenal and cytosolic sensing of pathogens.

207 Intracellular sensing of pathologically relevant biomolecules could pr

208 Heightened RIG-I sensing of PB2-627E nucleocapsids correlates with previo

209 The sensing of physical force, mechanosensation, underlies t

210 e mediated by the same cellular pathway, but sensing of physical stimuli remains poorly understood.

211 Interoception is the sensing of physiological signals originating inside the

212 t to an evolutionary conserved mechanism for sensing of plant surfaces among distantly related powder

213 CDS are devoid of >4 consecutive AAA codons, sensing of prematurely placed polyA tails by a specializ

214 These findings support intracellular sensing of prenyl pyrophosphates by BTN3A1 rather than e

215 Vernalization, sensing of prolonged cold, is important for seasonal flo

216 excellent performance in the separation and sensing of propofol molecules in the human plasma sample

217 Refractive index-based sensing of prostate specific antigen (PSA) both in buffe

218 The capacity for multiplexed sensing of protease activity was demonstrated using thes

219 metal-free chemosensor for highly selective sensing of pyrophosphate (PPi) anion in physiological me

220 Our investigations indicate that sensing of reactive species by DksA redox active thiols

221 nables acute myeloid leukemia cells to evade sensing of retrotransposons by innate immune receptors.

222 Here, we show how upstream sensing of retroviral reverse transcripts integrates wit

223 erived dendritic cells here showed that TLR8 sensing of RNA ORN versus imidazoquinoline translates to

224 toplasmic RNA helicase RIG-I mediates innate sensing of RNA viruses.

225 In this study, we found that MyD88-dependent sensing of S. aureus by dermal macrophages (Mvarphi) con

226 ion of IFN-beta was induced by TLR8-mediated sensing of S. aureus RNA, which triggered IRF5 nuclear a

227 that this demonstrates the first large-scale sensing of sarcomere dynamics in vivo, which is a necess

228 diting by two ADARs, ADAR1 and ADAR2, in the sensing of self-RNA in the absence of pathogen infection

229 We found that GC B cell-intrinsic sensing of self-RNA, but not self-DNA, released from dea

230 This probe proved successful for chirality sensing of several compounds, but in situ IR monitoring

231 echano-associated biologic processes such as sensing of shear stress, particularly in the vasculature

232 Here, we show that highly multiplexed sensing of single molecules can be achieved with solid-s

233 ible protein 16 (IFI16) were involved in the sensing of siRNA and DNA, respectively.

234 icate based on the production, secretion and sensing of small inducer molecules.

235 regulatory elements that directly couple the sensing of small molecules to gene expression.

236 Recent advances in the remote sensing of solar-induced chlorophyll fluorescence (SIF)

237 growth during development is achieved by the sensing of spatial and nutritional boundaries.

238 These findings demonstrate that sensing of specific commensals primes inflammatory signa

239 regulatory mechanisms underlying intestinal sensing of specific nutrients, especially micronutrients

240 ed atomic-scale spatial resolution in remote sensing of spins may ultimately allow the structural ima

241 Taken together, MyD88-dependent sensing of staphylococci by resident dermal Mvarphis is

242 *reporter dye combinations (for differential sensing of steroids) to the real-time monitoring of chem

243 Applying YC sensing of stromal Ca(2+) dynamics to single chloroplast

244 dance with respect to circadian time, or the sensing of sugars to feedback to the circadian oscillato

245 involving TGF-beta1 and BMP6 may control the sensing of systemic and/or hepatic iron levels.

246 d a platform for the ratiometric fluorescent sensing of targeted proteins by conjugating conjoined pr

247 inoic acid-inducible gene-I (RIG-I)-mediated sensing of the 5'-epsilon region of HBV pregenomic RNA.

248 es a more reliable, selective and controlled sensing of the analyte.

249 al influence of PII-receptor interaction and sensing of the ATP/ADP ratio.

250 dependent signal transduction allows complex sensing of the environment and, combined with its broad

251 thus implicating UBL1 in G protein-mediated sensing of the external environment.

252 e nucleotide pools rather than from a direct sensing of the extracellular purine content of the envir

253 While gustatory sensing of the five primary flavors (sweet, salty, sour,

254 We find that necroptosis requires sensing of the genomic RNA within incoming virus particl

255 g mechanism, we found that the combinatorial sensing of the innate TLR2 ligands and the adaptive TH2

256 terials should be useful for next-generation sensing of the intracellular milieu.

257 cyt c/H2O2 reaction system for the real-time sensing of the kinetics of biological processes without

258 making them most suitable for intracellular sensing of the lysosomal protease cathepsin B.

259 Finally, TLR5-mediated sensing of the microbiota also impacted antibody respons

260 Toll-like receptor (TLR)-mediated sensing of the microbiota contributes to gut homeostasis

261 evel of temporal control can be achieved for sensing of the new target molecule.

262 pin 1, the PBD is the site of PA binding and sensing of the PA electrostatic charge.

263 ter configuration for the continuous in vivo sensing of the partial pressure of oxygen (PO2) in blood

264 in 10 minutes, while demonstrating multiplex sensing of the PDGF and a target DNA in the same solutio

265 abscission pathway, allows for high-affinity sensing of the peptide hormone by binding to an Arg-His-

266 Upon sensing of the peptide pheromone cCF10, Enterococcus fae

267 ignal detection to be used for nano-photonic sensing of the proximity of fluorophores.

268 using the tip for simultaneous delivery and sensing of the reaction rate.

269 Hyphal maintenance requires active sensing of the surrounding environment, leading to exclu

270 igh as approximately 40 and refractive index sensing of the surrounding medium as high as 1245 nm/RIU

271 ial in pDCs but not in cDCs, indicating that sensing of the viral genome by pDCs activates cDCs in tr

272 regulatory strategies that allow "stochastic sensing" of the environment.

273 Sensing of these DNA fragments results in pyroptosis, a

274 Direct sensing of TLR agonists by CMP induced rapid proliferati

275 ent with gp96 participating in high-affinity sensing of TLR ligands in addition to its role as a TLR

276 n of behavior, pharmacology, in vivo surface sensing of translation (SUnSET) and DiOlistic labeling w

277 It also gives rise to direct sensing of triacetone triperoxide (TATP) explosive throu

278 Portable sensing of trimethylamine vapors at ppb concentrations i

279 In this work, we study the role in pH sensing of two regions of the ectodomain enriched in aci

280 ustenance of growth are achieved through the sensing of two unidentified prey-derived cues.

281 Continuous sensing of uric acid was also performed using this biose

282 Early sensing of viral components or infection-induced tissue

283 The sensing of viral DNA is an essential step of cellular im

284 rging evidence has challenged the dogma that sensing of viral DNA occurs exclusively in sub-cellular

285 The sensing of viral DNA was shown to occur both in the cyto

286 rfering RNA production following cytoplasmic sensing of viral dsRNA.

287 eptor in an inactive state and attenuate its sensing of viral RNA (vRNA).

288 FN production during viral infection and the sensing of viral RNA is regulated by adenosine deaminase

289 codes an RIG-I-like receptor involved in the sensing of viral RNA.

290 signaling activity, its significance for the sensing of viral RNAs remains unclear.

291 the presence of viral RNAs, promoting RIG-I sensing of viral RNAs.

292 or viral load measurement through electrical sensing of viruses on a flexible plastic microchip with

293 mmunoassays, detection of microorganisms, to sensing of viruses.

294 osan is fabricated over silver layer for the sensing of VK1 whereas core shell nanostructure of polyb

295 tion of an MOF coating opens the way for the sensing of volatile organic compounds (VOCs) in gaseous

296 a new class of materials for chemiresistive sensing of volatile organic compounds (VOCs).

297 mples of the use of zeolites and MOFs in the sensing of water vapour, oxygen, NOx, carbon monoxide an

298 As such, remarkable sensing of water-soluble organic compounds with a sensit

299 Since a few years, the acoustic sensing of whole cell is the focus of increasing interes

300 N terminus of YscF is interference with host sensing of YscF, consistent with Y. pestis pathogenesis.