ライフサイエンスコーパス: M

1 M value was determined with the HEC method at PET imagin

2 M-scores of >3 were allocated to senior surgeons.

3 M. floribunda fruit was studied to characterize its chem

4 M. gallisepticum cgMLST represents a standardized, accur

5 M. genitalium-specific serum antibodies targeting the im

6 M. lysodeikticus is a typical enzymatic substrate for ly

7 M. pneumoniae was detected by real-time PCR in 175 (5.8%

8 M. tuberculosis WhiB1 is a NO-responsive Wbl protein (ac

9 M. tuberculosis-infected IL-21R KO mice had enhanced bac

10 M.AluI, M.CviPI, M.HhaI, and M.EcoGII were able to intro

11 Met oxidation studies (pH 7, D2O, 0.01 M phosphate, 25 degrees C) monitored by (1)H NMR spectro

12 n electrochemical oxidation/reduction in 0.1 M HClO4 was studied by in situ grazing-incidence small-a

13 0.43 M HNO3 are superior to those using 0.1 M HNO3 or Aqua Regia that under- and overestimate the re

14 ting, following their first contact with 0.1 M KCl solutions.

15 -Sevcik analysis of 10 mM K3[Fe(CN)6] in 0.1 M KCl using the electrode chip gave a diffusion coeffici

16 ircuit potential of the solid contact in 0.1 M KCl.

17 Potentially, targets will be consumed at 1 M per day per reactor, demanding a 5000x unit cost reduc

18 such as trinitrotoluene (TNT) down to 10(-10)M in concentration and 2.7x10(-15)g in mass from 120nL s

19 strong Cotton effects (Deltaepsilon = +/-100 M(-1) cm(-1) at 300 nm).

20 tent with TG accumulation in the Pnpla3(148M/M) mice being caused by impaired TG mobilization from LD

21 SERRS nanoparticles with femtomolar (10(-15) M) limits of detection.

22 oM to 10mM and limit of detection of 10(-6.2)M.

23 A miR-204 mimic (miR-204 M) decreased Cav1 in endothelial cells.

24 usion complexes with baskets 1-3 (K = 6-2243 M(-1)).

25 ted motility but knockdown of acr-16+acr-26 (M- and/or N-receptors) did not.

26 Rate constants kp and 2kt, (M(-1)s(-1)) at 30 degrees C were 4.5 and 3.5x10(6) for l

27 XPB, dentin was etched and treated with 0.3 M EDC for 1 min and then bonded with the primer-bonding

28 al potentials of -157 +/- 2 mV (vs Ag/AgCl/3 M KCl) were observed, and the solid-contact reference el

29 H) (OH2)](4+) with xanthene was 2.22 x 10(3) M(-1) s(-1), 5-6 orders of magnitude faster than other r

30 easured binding constant (Kd = 5.645 x 10(3) M(-1)) indicated strong interactions between nCu particl

31 ar extinction coefficient 23.2 (+/-0.3)x10(3)M(-1)cm(-1)).

32 e constants over 2 orders of magnitude (0.36 M(-1) s(-1) < khomo < 82 M(-1) s(-1)).

33 eference genome identified approximately 7.4 M single nucleotide polymorphisms (SNPs) and 1.9 M indel

34 Model predictions using 0.43 M HNO3 are superior to those using 0.1 M HNO3 or Aqua Re

35 The 0.43 M HNO3 together with more dilute and concentrated acid e

36 electivity and efficiency (kinact/KI > 10(5) M(-1) min(-1)).

37 ntified 100% of ligands with affinities >500 M(-1) and >/=93% of all HMO ligands (hGal-1-31 of 31 lig

38 Electrical conductivity of 38.512 M.S/m, thermal conductivity of 264 W.m(-1).K(-1) and mic

39 ed proteins, we repeated the assignment in 7 M urea (pH 2.3) and in DMSO.

40 ge was obtained from 1.0x10(-8) to 4.1x10(-7)M (R(2)=0.9987) with a detection limit of 2.5x10(-9)M.

41 The dimerization rate (6.0 x 10(8) M(-1) s(-1)) and half-life (10 ns) of CO2(*-) can be eva

42 ssociation constants in the 10(-6) to 10(-8) M range.

43 of magnitude (0.36 M(-1) s(-1) < khomo < 82 M(-1) s(-1)).

44 ngle nucleotide polymorphisms (SNPs) and 1.9 M indels.

45 in neutral buffer, with a rate constant of 9 M(-1) s(-1) as measured by NMR spectroscopy.

46 +/- 0.37) x 10(9) to (8.47 +/- 0.97) x 10(9) M(-1) s(-1) and showed an increase in rate constants wit

47 thiols (with rate constants as high as 10(9) M(-1) s(-1)).

48 =0.9987) with a detection limit of 2.5x10(-9)M.

49 of naturally occurring polymorphic NucS in a M. smegmatis surrogate model, suggests the existence of

50 or in the spelling of the author Christian A.M. Wilson, which was incorrectly given as Christian M.A.

51 We model the catalytically active M-N x moieties using density functional theory and corre

52 After M. tuberculosis infection, TOLLIP-deficient monocytes de

53 Myc activation and sterol biosynthesis after M-CSF stimulation.

54 generated during host immune responses after M. tuberculosis infection of macrophages.

55 PRELP enhances host innate immunity against M. catarrhalis through increasing complement-mediated at

56 IFN-gamma and can confer protection against M. avium infection in immunocompromised mice.

57 M.AluI, M.CviPI, M.HhaI, and M.EcoGII were able to introduce (5m

58 eproducible method for differentiation among M. gallisepticum isolates.

59 the mechanism of host lipid catabolism by an M. tuberculosis enzyme, augmenting our current understan

60 he robust T cell response observed during an M. tuberculosis infection.

61 Total lipids from an M. avium subsp. paratuberculosis (Map) ovine strain (S-t

62 plitude of medium afterhyperpolarization and M-type K(+) currents were smaller, when compared to etha

63 id test to confirm isolation of M. bovis and M. caprae from veterinary specimens following culture.

64 Certain spoligotypes of M. bovis and M. caprae were not detected by the LFD in Spanish MGIT c

65 was undetectable in Drosophila S2 cells, and M. sexta Fkh (MsFkh) interacted with Relish-Rel-homology

66 Multi-channel EMG and M-mode ultrasound revealed regional differences in activ

67 ) F-orf and M-orf, respectively inside F and M mtDNAs, which are hypothesized to participate in sex d

68 , with a differentiation between NM-GHGs and M-GHGs, to further elucidate the underlying mechanisms,

69 ke M. kansasii, M. szulgai, M. gordonae, and M. asiaticum; however, in these samples, rapid growers l

70 M.AluI, M.CviPI, M.HhaI, and M.EcoGII were able to introduce (5m)C or (N6m)A into 9 g

71 peak at 75 K is attributed to the H KS and M S (saturation magnetization) whose peaks also occur at

72 s that receive nonselective input from L and M cones.

73 pical open reading frames (ORFans) F-orf and M-orf, respectively inside F and M mtDNAs, which are hyp

74 We too find ESX-1 of M. tuberculosis and M. marinum lyses host cell membranes.

75 functions, including the production of anti-M. tuberculosis cytokines and inhibition of intracellula

76 House finch-associated M. gallisepticum (HFMG) spread rapidly and increased in

77 eviously uncharacterized membrane-associated M. tuberculosis protein encoded by Rv2672 is conserved e

78 B exposure, similar to Arabidopsis UVR8, but M. polymorpha UVR8 has weaker dimers and the proteins ap

79 ly diagnose and treat tuberculosis caused by M bovis in human beings.

80 ber 2015, searching for infections caused by M. bovis-BCG.

81 of dorsal horizontal cells were dominated by M-opsin and those of ventral horizontal cells by S-opsin

82 axonal damage are not directly initiated by M. leprae but by infected macrophages that patrol axons;

83 thorium bis(carbene) complexes with trans C=M=C cores where experimental and theoretical data sugges

84 , a lymphoid organ in which microfold cells (M cells) overlay an arrangement of B cells, T cells, and

85 on, which was incorrectly given as Christian M.A.

86 A set of 296, mostly XDR, clinical M. tuberculosis isolates from four countries were subjec

87 Methyl-coenzyme M reductase (MCR), found in strictly anaerobic methanoge

88 ed PCR sequencing and metagenomics confirmed M. oralis along with 14 bacteria, including S. intermedi

89 In contrast, M. tuberculosis populations subject to less drug pressur

90 age RNA: Emr1 (F4/80), Itgam (CD11b), Csf1r (M-CSF Receptor), Itgal (CD11a), Tnf, and Nos2 Additional

91 M.AluI, M.CviPI, M.HhaI, and M.EcoGII were able to introduce (5m)C or (N6

92 ailable images, a neuroradiology fellow (M.D.M.) performed history taking and a physical examination

93 We also show that AAV delivered M-opsin localizes in the dorsal cone outer segments, and

94 to arise from the introduction of diagnostic M. genitalium nucleic acid amplification testing includi

95 ETEXT annotation factors metastatic disease (M), macrovascular involvement of all hepatic veins (V) o

96 s a competitive antagonist and distinguished M-nAChRs activated by morantel (Kb 13.9 nM), P-nAChRs ac

97 eover, c-Src activity is sufficient to drive M fate, even in nonmyeloid cells.

98 sigma-bond of metal-borane complexes (i.e., M-->BR3 ) remains limited.

99 stably halted en route to EMT in a hybrid E/M phenotype.

100 tes of Mycobacterium avium complex and eight M. simiae isolates had tedizolid MIC50s of 8 mug/ml and

101 Introducing either M D62A or D62A E181A mutations into VHSV-IVb via reverse

102 ent with an ancient origin for M. elongata - M. cysteinexigens symbiosis, most likely over 350 millio

103 y and resistance determinants within endemic M. tuberculosis populations.

104 s a critical "retrochaperone" for these ERAD-M substrates.

105 red different proposed methods of estimating M. tuberculosis prevalence, including a method described

106 HPLC chromatograms of the expected [M-H](-) ion and UV absorption revealed the presence of f

107 of action by acting either on extracellular M. tb bacterial growth only, or both intracellularly on

108 ism by macrophage colony-stimulating factor (M-CSF; inflammation resolving) and granulocyte-M-CSF (GM

109 s and chemokines in liver and VAT of HFD-fed M-JAK2(-/-) mice.

110 e available images, a neuroradiology fellow (M.D.M.) performed history taking and a physical examinat

111 For M. smegmatis TopoI-CTD, a 27-amino-acid tail that is ric

112 A significant decrease in complications for M = 0 (ie, minimal risk cases) was also identified compa

113 ermine minimum inhibitory concentrations for M. genitalium.

114 paucity of variation means that the data for M. tuberculosis are more equivocal than for the other sp

115 s host macrophage apoptosis is essential for M. tuberculosis (Mtb) to replicate intracellularly while

116 hages became necrotic, providing a niche for M. tuberculosis replication before escaping into the ext

117 es are consistent with an ancient origin for M. elongata - M. cysteinexigens symbiosis, most likely o

118 ures previously confirmed to be positive for M. tuberculosis complex (MTBC) by qPCR.

119 extraction directly from patient samples for M. tuberculosis WGS.

120 to be elicited by expression of the foreign M.HhaII Type II methytransferase (MTase), as well.

121 el and that chromatic opponency results from M-cone-driven surround inhibition mediated by wide-field

122 ), kernel-to-fruit (K/F), mesocarp-to-fruit (M/F), oil per palm (O/P) and oil-to-dry mesocarp (O/DM).

123 Goldin-Meadow & Brentari (G-M&B) challenge the traditional separation between gestur

124 ion presented by Goldin-Meadow & Brentari (G-M&B) indicates a more complex picture.

125 o adversely impacted upon the DSB-induced G2-M checkpoint, inducing a hypersensitive and prolonged ar

126 lation centered on endocycle entry at the G2-M transition as well as yet undefined roles for differen

127 Apart from being a G2/M cyclin, cyclin F functions as the substrate-binding su

128 ay impaired cell proliferation, defective G2/M arrest and increased radiochemosensitivity in lung can

129 -phase progression, overnight increase in G2/M, and cycle completion by late night.

130 ignaling genes and down-regulation of the G2/M cell-cycle marker gene, CYCB1;1 TCP20 and NLP6&7 also

131 The GAS M protein, by which strains are differentiated into >220

132 Sequence analyses of various GAS M-Prts have shown that they contain a highly conserved s

133 Thy1-GFP-M mice were used to assess microglia-mediated neuronal r

134 CSF; inflammation resolving) and granulocyte-M-CSF (GM-CSF; proinflammatory) may contribute to the in

135 e C-specific products.IMPORTANCE HIV-1 group M includes nine clades and many recombinants.

136 from the adaptive changes observed in group M Vpus (M-Vpus) were critical for the acquisition of its

137 K transition and (ii) deprotonates in K --> M transition.

138 R., Murakami, K., Irie, Y., Hentzer, M., Nielsen, T.

139 A high M-state population could be achieved by preventing repro

140 augmenting our current understanding of how M. tuberculosis meets its nutrient requirements under hy

141 IMG/M allows open access interactive analysis of publicly av

142 vide support for examining and comparing IMG/M's datasets.

143 l nonstructural protein 1 and immunoglobulin M) has greatly simplified laboratory-based dengue diagno

144 rotein, immunoglobulin G, and immunoglobulin M), and demonstrated a high correlation with an enzyme-l

145 f ZIKV was 6.2% based on ZIKV immunoglobulin M and negative for dengue reactivity.

146 nor conditional depletion of wag31 impacted M. tuberculosis susceptibility to this compound.

147 antitranscriptional activities, implicating M as a primary regulator of cytopathicity and host trans

148 Thus, alterations in M-channel activity rapidly trigger unique AIS plasticity

149 d sensitization of the defensive behavior in M. sexta.

150 In contrast, reduced epithelial damage in M-ILK-deficient mice is correlated with elevated levels

151 ere decreased, and WhiB6 was not detected in M. marinum strains lacking genes encoding ESX-1 componen

152 RBF206 Vpu are distinct from those found in M-Vpus and mediate efficient counteraction of both the l

153 expression of genes ftsZ, psbA1, and glmS in M. aeruginosa.

154 ammatory cytokine production are impaired in M-ILK-deficient mice, and activation of epithelial NF-ka

155 pAI known to inactivate plant MAP kinases in M. oryzae.

156 4P upstream of the Dif signaling proteins in M. xanthus.

157 associated with low-level BDQ resistance in M. tuberculosis Both genes encode transcriptional regula

158 ost determinants of symbiotic specificity in M. truncatula and possibly in closely related legumes th

159 trate that the levels of ESX-1 substrates in M. marinum are fine-tuned by negative feedback control,

160 independent of RpsA and trans-translation in M. tuberculosis.

161 -->S0) rate constants can be finely tuned in M-(PM')n-M compounds and (ii) demonstrate designs in whi

162 HIV infection was associated with increased M. tuberculosis Ag-induced CD4 T cell death ex vivo, ind

163 lenge demonstrates the potential of ingested M. canettii organisms to relocate to distant organs and

164 IRAK-M, also known as IRAK-3, is an inhibitor of proinflammat

165 m/z 130.1 along with side chain-specific J1 [M - 173](+) and J2 [M - 291](+) fragment ions, as well a

166 side chain-specific J1 [M - 173](+) and J2 [M - 291](+) fragment ions, as well as additional charact

167 he first total synthesis of the juvenimicin, M-4365, and rosamicin classes of macrolide antibiotics v

168 ally relevant slow growers like M. kansasii, M. szulgai, M. gordonae, and M. asiaticum; however, in t

169 Y., Kazimirova, M., Roller, L., Jobichen, C., Swaminathan, K., Mizuguchi

170 The experimental regimens kill M. tuberculosis much more rapidly than the standard regi

171 a refractory state: IL-1R-associated kinase-M, NFkB2/p100, and hypoxia-inducible factor-1alpha.

172 at, on average, smaller A cations and larger M cations result in increased SHG efficiencies.

173 ems, Mx-yM'y-MOFs, MxM'y-MOFs, and Mx(ligand-M'y)-MOFs, in which the second metal (M') incorporation

174 M2 protein) encoded by the prevalent G1-like M gene were demonstrated to be prime contributors to enh

175 nce of clinically relevant slow growers like M. kansasii, M. szulgai, M. gordonae, and M. asiaticum;

176 owever, in these samples, rapid growers like M. mageritense occurred at much higher relative abundanc

177 complexes or the [Co(II)2(bis-salophen)M2] (M = Li, Na) dimers that are present in solution in equil

178 referential attunement of the magnocellular (M) pathway to clear threat, and of the parvocellular (P)

179 Samples where many M. tuberculosis aptamers produced high signals were rare

180 S1 is a structural paralogue of hRSV matrix (M) protein.

181 ore severe quantitative metamorphopsia (mean M-score difference 0.6; 95% CI, 0.05 to 1.1, P = .01) th

182 Median M-score for complicated cases was higher (P = .022).

183 (M') incorporation occurs through (i) metal (M) replacement in the framework nodes (type I), (ii) met

184 ligand-M'y)-MOFs, in which the second metal (M') incorporation occurs through (i) metal (M) replaceme

185 e known SHG active AMCO3F (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) materials indic

186 with anhydrous HF and the superacids HF/MF5 (M=As, Sb) were investigated at temperatures below -40 de

187 In our model, M. bovis would be taken up by amoebal trophozoites, whic

188 tion is immunosuppressive due to (monocytic) M-MDSC infiltration, which results in tumor radioresista

189 served that exosomes released during a mouse M. tuberculosis infection contribute significantly to it

190 te constants can be finely tuned in M-(PM')n-M compounds and (ii) demonstrate designs in which the kI

191 ations, resulting in doped CsPb1-xMxBr3 NCs (M= Sn(2+), Cd(2+), and Zn(2+); 0 < x </= 0.1), with pres

192 mising cathode materials, Na(Li1/3 M2/3 )O2 (M: transition metals featuring stabilized M(4+) ), for f

193 We too find ESX-1 of M. tuberculosis and M. marinum lyses host cell membranes

194 uency, phenotype, and functional capacity of M. tuberculosis-specific CD4 T cells in HIV-infected and

195 buting to impaired proliferative capacity of M. tuberculosis-specific CD4 T cells in HIV-infected ind

196 The ex vivo proliferative capacity of M. tuberculosis-specific CD4 T cells was markedly impair

197 (HIV) infection revealed 19 (18.6%) cases of M. genitalium, commonly (58%) in rectal samples.

198 for disease manifestations characteristic of M. gallisepticum infection.

199 mpedes successful T cell-mediated control of M. tuberculosis have not been well defined.

200 N-gamma target genes required for control of M. tuberculosis is inducible NO synthase (iNOS).

201 , we paid attention to comprehensive data of M&A events for 40 years and derived empirical laws by ap

202 Colonization densities of M. catarrhalis, S. aureus, and P. jirovecii are unlikely

203 zymes allows rapid and specific detection of M. tuberculosis in live animals.

204 lable molecular methods for the diagnosis of M. genitalium and assays to predict the antibiotic susce

205 relevant to understanding the environment of M. tuberculosis replication in the host.

206 s surrogate model, suggests the existence of M. tuberculosis mutator strains.

207 The protein expression of M-channel subunits, KCNQ2/3 in the LHb was also smaller.

208 Monocytes also decreased the expression of M-CSFR, and low numbers of cells underwent differentiati

209 nical and histopathologic ocular findings of M. chimaera.

210 he tedizolid MIC90 values for 81 isolates of M. abscessus subsp. abscessus and 12 isolates of M. absc

211 bscessus subsp. abscessus and 12 isolates of M. abscessus subsp. massiliense were 8 mug/ml and 4 mug/

212 ison of pretreatment and relapse isolates of M. intracellulare uncovered mutations in a previously un

213 lity as a rapid test to confirm isolation of M. bovis and M. caprae from veterinary specimens followi

214 d regeneration success in cydippid larvae of M. leidyi.

215 In conclusion, the visceral mass of M. charruana contains a trypsin-like protease that can g

216 ort female pig-tailed macaques as a model of M. genitalium infection, persistence, and immune evasion

217 digan et al. (2017) use a zebrafish model of M. leprae infection to show that infected macrophages pa

218 n earlier study, we had structural models of M.tb at a proteome scale from which a set of 13,858 smal

219 ng activity in vitro against a wide panel of M. abscessus isolates and in infected macrophages.

220 whereas the intracircular photoconversion of M back to D involves only one C13=C14 double-bond isomer

221 pecially in settings where the prevalence of M. tuberculosis infection is low and environmental sensi

222 he p27-p55 operon impairs the replication of M. bovis in bovine macrophages.

223 xpression of nfnB resulted in sensitivity of M. smegmatis to 3.

224 Genomic sequences of M. tuberculosis isolates displayed significant variation

225 treatment, and public health significance of M. genitalium reviewed at the meeting is described in de

226 Certain spoligotypes of M. bovis and M. caprae were not detected by the LFD in S

227 screening programs and targeted treatment of M. genitalium improve reproductive outcomes in women are

228 A substantial increase in the abundance of [M + Na](+) adducts was observed in samples from spinal c

229 growth arrest specific protein 6, oncostatin M, hepatocyte growth factor receptor etc.

230 n of a muscarinic-sensitive K(+)-current, or M-current.

231 usters of clock neurons-morning oscillators (M cells) and evening oscillators (E cells)-are largely r

232 (L5P), yet both lipids are present in other M. avium subspecies.

233 alladium-based bimetallic nanocrystals (PdM, M = V, Mn, Fe, Co, Ni, Zn, Sn, and potentially extendabl

234 fidence interval was predominantly positive (M=0.019; CL95 -0.007-0.044), suggesting at least an addi

235 issions were 28% and 17% higher with the PPS-M compared to the SMPS for LSHFO and MGO, respectively.

236 r constructing modular hybridization probes (M-Probes) that overcomes these challenges.

237 romyographic activity (EMG), metabolic rate (M) and whole-body thermal sensation on a visual analogue

238 When tested against all cluster-related M peptides, we found that 9 of 17 (53%) paired sera had

239 wildtype allele of wag31 in APYS1-resistant M. tuberculosis was dominant and restored susceptibility

240 Mass resolution (M/DeltaM fwhm) is observed to linearly increase with har

241 no-acid substitution in RORgammat (RORgammat(M)) that 'preferentially' disrupted TH17 differentiation

242 A rough M. tuberculosis H37Rv DeltapapA1 sulfoglycolipid-deficie

243 ilibrium with the respective [Co(I)(salophen)M] complexes.

244 identified low but escalating risk of severe M. chimaera infection associated with heater-coolers wit

245 However, simultaneous M-cell spikes generated through direct current injection

246 Since M. xanthus PilB possesses conserved motifs with high aff

247 ingle-cell level in Mycobacterium smegmatis (M. smegmatis) and Mycobacterium bovis Bacillus Calmette-

248 nd its hydrophobic binding groove of the SRP M domain towards the translocon.

249 2 (M: transition metals featuring stabilized M(4+) ), for further advances in SIBs.

250 receptor potential cation channel subfamily M member 8 (TRPM8(EGFPf/+)) locus in the 3 branches.

251 a thermal treatment yields silica-supported M(III) sites for a broad range of metals.

252 t slow growers like M. kansasii, M. szulgai, M. gordonae, and M. asiaticum; however, in these samples

253 m of AIS plasticity by selectively targeting M-type K(+) channels, which predominantly localize to th

254 In summary, we demonstrate that M. tuberculosis EsxL inhibits antigen presentation by en

255 Here we show that M. robertsii mediates the saprophyte-to-insect pathogen

256 These results suggest that M-P information is processed in segregated parallel chan

257 Our findings suggest that M. sexta's sensitization occurs through central signal a

258 The M protein is the major surface-associated virulence fact

259 The M(II) centers adopt a trigonal planar geometry and inter

260 an undergo rapid internal rotation about the M-O bond.

261 Although the M-region of Sac3 was originally thought to encompass res

262 The S cones in the other species and the M/L cones in all species had a conventional topography w

263 I3K signaling pathways are restricted by the M-ILK deficiency.

264 throughout much of human visual cortex; the M-P streams are more than a convenient sorting property

265 3.05, and mg0359 was able to distinguish the M. gallisepticum ts-11 vaccine strain from field isolate

266 es simulated HeLa cells to accumulate in the M phase.

267 NASH was ameliorated in the M+G49 group, manifested by reduced inflammation, steatos

268 role in selective sensory processing in the M-cell.

269 he assignment of each Raman feature near the M or K points of the Brillouin zone.

270 The quest towards expansion of the M n+1AX n design space has been accelerated with the rec

271 t indicates that the TPR-like repeats of the M-region extend to residue 137 and that residues 90-125

272 eld isolates, whole-genome sequencing of the M. gallisepticum vaccine strain ts-11 and several "ts-11

273 Development of the M. oryzae effector-secreting biotrophic interfacial comp

274 report the identification and cloning of the M. truncatula NFS2 gene that regulates this type of spec

275 ng and the sequenced genomes compared to the M. gallisepticum Rlow reference genome.

276 designed to target 5 sequences unique to the M. gallisepticum ts-11 strain: vlhA3.04a, vlhA3.04b, vlh

277 h demyelination, while the intensity of the [M + K](+) adducts was stronger in those sections from me

278 The three M >/= 3 foreshocks all produced positive Coulomb stress

279 deletion resulted in increased adherence to M cells and, as expected, decreased adherence to Caco-2

280 s whereby HIV impairs protective immunity to M. tuberculosis, we evaluated the frequency, phenotype,

281 ected ART-treated individuals in response to M. tuberculosis antigen stimulation.

282 t overexpression of the proteins is toxic to M. smegmatis, although whether this toxicity and the ass

283 Finally, our data suggests K-to-M mutations may provide a useful strategy for altering e

284 Histone Lys-to-Met (K-to-M) mutations act as gain-of-function mutations to inhibi

285 on and ordered phases involving at least two M n+1AX n end members.

286 -43 kcal/mol binding energy, akin to typical M-M single-bond energies.

287 ICU were found to have genetically unrelated M. hominis isolates, excluding patient-to-patient transm

288 we show that the coordinatively unsaturated M(2+) sites in these materials lead to superior performa

289 tent or active TB (aTB), were screened using M.tuberculosis-specific MHC class II tetramers.

290 After the senior radiologist (V.M.C.) reviewed the radiographs, the patient was called b

291 Recovery of viable M. genitalium from lower genital tract specimens was imp

292 hat the loss of WhiB6 resulted in a virulent M. marinum strain with reduced ESX-1 secretion.

293 e adaptive changes observed in group M Vpus (M-Vpus) were critical for the acquisition of its anti-te

294 .e. long-wavelength (L)-, middle-wavelength (M)-, and short-wavelength sensitive (S)-opsins, are resp

295 ection is not exceptional compared with what M. guttatus populations may typically experience when ad

296 Here we tested whether M-P streams exist in extrastriate cortical columns, in 8

297 es, such as Prevotella in the lung, and with M. tuberculosis antigen-induced Tregs.

298 mixtures of maltodextrin (MD) combined with M and SP from flaxseed (MD:FM:FSP - 7.5:0.2:7.5%, w/w/w)

299 f Ag-specific T cells in lungs compared with M. tuberculosis-infected WT mice.

300 t alkylation of the N-H functionality within M/NH bifunctional Noyori-type catalysts leads to detrime