ライフサイエンスコーパス: previously characterized

1 mary endosymbiont), Sodalis and Wolbachia as previously characterized.

2 d antimicrobial benzo[c]phenanthridines were previously characterized.

3 individual activation dynamics have not been previously characterized.

4 nto the discovery of CO2 -fixing enzymes not previously characterized.

5 Its function in these cells has not been previously characterized.

6 nscriptional activation by CtBP has not been previously characterized.

7 elates to transmission clusters has not been previously characterized.

8 inated coccidioidomycosis (DCM) has not been previously characterized.

9 atrophy on SW-AF imaging, which has not been previously characterized.

10 tivity for SP enrichment, which has not been previously characterized.

11 brane helices that form a binding pocket not previously characterized.

12 od in breast cancer metastases have not been previously characterized.

13 a wider range of developmental programs than previously characterized.

14 metry imaging (MSI) experiments has not been previously characterized.

15 action mechanism involves protonation of the previously characterized 1,2-mu peroxy Fe(III)Fe(III) (P

16 ae that were serologically distinct from the previously characterized 15 serovars were described, and

17 We previously characterized 3 SitAI toxin/immunity pairs th

18 ng an observational meta-analysis design, we previously characterized a gain-of-function microRNA-410

19 We previously characterized a murine model of neurogenic bl

20 ode a human IgA1 protease gene, igaA, and we previously characterized a novel human IgA1 protease gen

21 We have previously characterized a panel of anti-TG2 mAbs genera

22 We previously characterized a recombinant neprilysin that c

23 We have previously characterized a reporter of Nr4a1 transcripti

24 We previously characterized a wide array of transcriptomic

25 e chronic constriction injury pain model) of previously characterized A3AR agonist, 2-(3,4-difluoroph

26 In contrast to most previously characterized accuracy modulators, including

27 l adhesion (FA) system that is distinct from previously characterized actin/FA structures.

28 A in GLUT4 trafficking is independent of its previously characterized activity in ER exit site format

29 In the latter experiment, previously characterized adducts, both expected and unex

30 rdingly, ouchless mutants fail to complement previously characterized adgra2 mutants and exhibit high

31 Cross-comparison of AmbO5 with a previously characterized aliphatic halogenase homolog We

32 Previously characterized ALK, NTRK1, and PAX3 fusions we

33 onserved surface on GS that is distinct from previously characterized allosteric and binding surfaces

34 We previously characterized alpha-helical cytotoxic islet a

35 hitecture and assembly mechanism relative to previously characterized AMA-RON2 complexes.

36 4), as a novel amyloidogenic protein with no previously characterized amyloid-prone domains.

37 We previously characterized an isolate that exhibited great

38 ring INsertion) through COINd, have not been previously characterized and consist entirely of imperfe

39 tified three thorax-specific neuroblasts not previously characterized and show that HOX genes confine

40 racterized here include 13 that had not been previously characterized and that collectively explain a

41 binding mode similar to AZ11645373 and other previously characterized antagonists.

42 s using these antibodies, in addition to the previously characterized anti-tau oligomer antibody T22.

43 he transgenic lines described here and those previously characterized appear to result from different

44 We previously characterized Arabidopsis thaliana mutants wi

45 study shows that Drosophila KDM4A (dKDM4A), previously characterized as a euchromatic histone H3 K36

46 istant member of the CARF domain superfamily previously characterized as a Mn(2+)-dependent deadenyla

47 it heterozygous (gamma2(+/-)) mice, which we previously characterized as a model animal with construc

48 Although BAK1 was previously characterized as a negative regulator of cell

49 The hypothesis was that isolates that were previously characterized as contagious would be identifi

50 s and mice, an NMDAR-independent form of LTP previously characterized as dependent on voltage-gated C

51 expression patterns of six ABC transporters previously characterized as differentially expressed in

52 d proteins from the D. reducens proteome not previously characterized as iron reductases.

53 strate that mGlu1 receptors, which have been previously characterized as oncogenes, also behave like

54 NtEXO70A1a localized to the small area previously characterized as the site of exocytosis in th

55 es quick screening of IAA conjugates in both previously characterized as well as uncharacterized spec

56 In previously characterized ASD risk loci, we identified 49

57 Previously characterized bacterial beta-etherases are ho

58 pecificity for Tyr over Phe as compared with previously characterized bacterial enzymes, consistent w

59 is homologous in structure and activity to a previously characterized bacterial thiaminase I.

60 In contrast to previously characterized bacteriophage satellites, expre

61 identified based on sequence similarity to a previously characterized binding site for HetR in the pr

62 The enzyme has been previously characterized biochemically in fungi, but no

63 bacteriological medium were mediated by the previously characterized biofilm factors poly-N-acetyl g

64 adhesion molecule-1, and leptin, as well as previously characterized biomarkers, including neuron-sp

65 All previously characterized broadly neutralizing antibodies

66 Fe=CCH(3)](+) are discussed in comparison to previously characterized, but heterosubstituted, iron ca

67 tudy, high- and low-fidelity CHIKV variants, previously characterized by altered in vitro population

68 lates that had FKS1 HS1 and FKS2 HS1 domains previously characterized by DNA sequencing.

69 When applied to 312 P. acnes isolates previously characterized by MLST and representing types

70 One hundred fifty samples previously characterized by Sanger sequencing were evalu

71 cal environment of the Ppant arm of two ACPs previously characterized by solution NMR, and was used t

72 al propagation in nanomagnet chains has been previously characterized by static magnetic imaging expe

73 was undertaken in a large cohort of 43 cases previously characterized by targeted next-generation seq

74 g results of 100 nasopharyngeal swab samples previously characterized by the Stanford Health Care EUA

75 y P. aeruginosa and 30 A. baumannii isolates previously characterized by whole-genome sequencing from

76 treme N terminus of Psd2p (C2-1) as well the previously characterized C2 domain of Psd2p (C2-2).

77 of acidic lipopeptides that is distinct from previously characterized calcium-dependent antibiotics i

78 Fe-4S] cluster binding pocket, distinct from previously characterized canonical sigma704-bound transc

79 Here we report that, unlike previously characterized cell lineages, differentiation

80 tational framework improves the detection of previously characterized cell-cycle genes compared to ap

81 We previously characterized central projections of cutaneou

82 Using previously characterized CHIKV fidelity variants, we add

83 ded paratope that differs significantly from previously characterized Chlamydiaceae-specific mAbs des

84 ns of conserved RNA structure, including all previously characterized cis-acting regulatory elements

85 CKAMP52 and CKAMP59-that, together with the previously characterized CKAMP44, constitute a novel fam

86 Furthermore, in contrast to previously characterized CLE genes expressed in the wood

87 Similar to previously characterized Cln3 mutant mouse lines, this n

88 k discharge (SD) and glow discharge (GD), as previously characterized cold plasma systems, were used

89 te selective connections of these cells with previously characterized components of the circuit.

90 d compare the activity of these compounds to previously characterized compounds that act at the PAR1

91 A therapeutic vaccine platform that has been previously characterized consists of heat-killed recombi

92 educed Gd-MoFeP is structurally identical to previously characterized counterparts around the FeMo-co

93 of approximately 240 pN, well below that of previously characterized covalent mechanophores.

94 o bin- or locus-specific biases accounts for previously characterized covariates impacting Hi-C conta

95 CP-overexpression (OX) cells compared with a previously characterized cp-knockdown line.

96 ly voltage dependent, in contrast to that in previously characterized cryptophyte ACRs, indicating di

97 gulation are common elements shared with the previously characterized CsLycB2a promoter, and these sh

98 combined with mRNA expression profiling and previously characterized data on a large set of kinase i

99 We selected 24 diverse samples from a previously characterized data set derived from DNA extra

100 ment, caused considerable production of some previously characterized DBPs in addition to novel bromi

101 utations were clearly distinct from a set of previously characterized DCM mutations.

102 e the utility of our method by perturbing 40 previously characterized developmental genes in variants

103 Ace2/Swi5 paralogs, they are associated with previously characterized differences in posttranslationa

104 ne strong association on chromosome 5 near a previously characterized disease resistance gene.

105 Previously characterized disease-causing mutations in IG

106 Ag that was significantly more potent than a previously characterized dNKT cell Ag, mammalian phospha

107 in maize resistance to SCMV, differing from previously characterized dominant or recessive potyvirus

108 We demonstrate on four previously characterized drug effect data sets that appl

109 ired for the hallmark inflammatory responses previously characterized during murine vaginitis.

110 r run lengths and higher velocities than the previously characterized dynein activator bicaudal D2 (B

111 inal alpha-arrestin domain and proximal to a previously characterized E3 ubiquitin ligase-binding sit

112 ehaved differently from one another and from previously characterized (early deletional) responses of

113 We compared these with previously characterized EAST/SeSAME mutants (G77R and A

114 We have previously characterized eIF4E1b as a component of the C

115 We have previously characterized electrophysiological properties

116 We find that this cluster as well as the previously characterized endocrocin (enc) cluster both c

117 It had a similar K(m) and V(max) to previously characterized enzymes using sucrose as a subs

118 BIS1 acted in a complementary manner to the previously characterized ethylene response factor Octade

119 ncluding mature tissues, where expression of previously characterized Exo70 genes is usually absent.

120 te EVs that are similar in size and shape to previously characterized exosomes from other organisms a

121 rehensive molecular phylogeny, including all previously characterized family members.

122 ditional acid, the latter being related to a previously characterized [Fe(NNH(2))](+) intermediate of

123 both monooxygenases are distinct from those previously characterized for DMNT and TMTT synthesis in

124 rrelation with ZPA- and AER-expressed genes, previously characterized functional ZPA and AER enhancer

125 rein, we demonstrate that in addition to its previously characterized functions, B1 inhibits vaccinia

126 t its properties closely resemble those of a previously characterized fungal homolog, afTMEM16.

127 ms in disease progression in addition to the previously characterized fusobacteria, proteobacteria, f

128 ts phylogenetic relationships with the other previously characterized GALVs.

129 Also, the previously characterized gene clusters escaping XCI in h

130 the KnowEnG Knowledge Network collection of previously characterized gene-gene interactions.

131 candidate selected regions that include both previously characterized genes (e.g., transcription elon

132 powdery mildew susceptibility identified two previously characterized genes affecting the acetylation

133 In addition to cloning variants of previously characterized genes, specifically CsTPS14CT [

134 eing differentially regulated, including the previously characterized glucose and xylose transporter

135 glyoxalases that are not redundant with the previously characterized glutathione-dependent GLO1/GLO2

136 We previously characterized HAIYPRH, from the M13-based Ph.

137 me of day-dependent response, including many previously characterized heat-response genes.

138 f aptamer-conjugated PSi biosensors, where a previously characterized his-tag binding aptamer (6H7) i

139 complexes: NAP-1, NLP, and nucleophosmin are previously characterized histone chaperones, and TAP/p32

140 kinetics of the PfSET7 enzyme are similar to previously characterized histone methyltransferase enzym

141 As for previously characterized histone SET domain proteins, th

142 acteristics of the accessions disclosed both previously characterized (HMA4, HMA3) and new candidate

143 In contrast to previously characterized homologs, both of these protein

144 We have previously characterized HTLV-3- and HTLV-4-encoded anti

145 tes are observed, the second of which is the previously characterized I(core) millisecond intermediat

146 at IGMT5, a gene with moderate similarity to previously characterized IGMTs, encodes the methyltransf

147 Here, we examined the role of previously characterized IGR IRES mutations on viral yie

148 exhibited a metabolic burden similar to that previously characterized in aneuploid yeast and cultured

149 tor-1 (TCF1, encoded by Tcf7), a protein not previously characterized in beta cells.

150 h they are relatively rare, niches have been previously characterized in both the brain and spinal co

151 that an allosteric site, the "minor pocket," previously characterized in CXC chemokine receptors-1 an

152 les of dynamic polymerase exchange have been previously characterized in model systems provided by co

153 The polymers used were previously characterized in moisture content, ash and ni

154 These include events previously characterized in the context of myotonic dyst

155 entifies a two-component system (KinB-AlgB), previously characterized in the regulation of Pseudomona

156 ts contains a conserved GT-1 domain that was previously characterized in transcription factors that f

157 l (7DHC) metabolism initiated by CYP11A1 and previously characterized in vitro, occur in vivo, we ana

158 appeared parallel at the molecular level to previously characterized incompatibilities, but also rai

159 atis that has evolved independently from the previously characterized interaction between bacterial t

160 Validation of SynAg with 89 previously characterized interactions shows a log-linear

161 This set of putative PPIs included both previously characterized interactors, along with a large

162 31)P NMR spectroscopy and by comparison with previously characterized intermediates observed in the p

163 ribed S. aureus genotype B was present among previously characterized isolates from cases of bovine i

164 ntly less affected in Gnaq(d/d) mice than in previously characterized Kiss1r(-/-) or Kiss1r(d/d) mice

165 uronide substrates inefficiently compared to previously characterized L1 GUS enzymes like E. coli GUS

166 The previously characterized L407F mutant allele of Arabidop

167 gnals, including three rare variants, at two previously characterized loci: FGB and IRF1.

168 Remarkably, and in contrast to all previously characterized LPMOs, which are active only on

169 This method distinguished previously characterized lung- and liver- targeting nano

170 lysis), a conservation not observed in other previously characterized lytic transglycosylase families

171 The proper expression of two previously characterized MATE flavonoid transporters MtM

172 The peptide backbone is distinct from all previously characterized Mbns, and the post-translationa

173 we incorporated patient-derived stroma in a previously characterized MCF7-derived in vitro duct mode

174 gs to the amidohydrolase superfamily, unlike previously characterized MCP hydrolases, which are serin

175 In addition to the previously characterized mechanism of action of CX-5461

176 vidence to suggest that hPolbeta follows the previously characterized mechanisms of D-stereoselectivi

177 y of the pSHP2-expressing cell population to previously characterized meristematic domains, further s

178 mplement largely resembled the activity of a previously characterized metalloproteinase of T. forsyth

179 Unlike previously characterized MIA-producing plants, C. acumin

180 developed myeloid disease, whereas all other previously characterized mice deficient in both cNHEJ an

181 assessed in comparison to culture using 690 previously characterized microbial isolates.

182 lay mixed mechanisms of action compared with previously characterized modulators of other mAChRs.

183 Previously characterized monoclonal antibodies that bloc

184 We have previously characterized mouse CMV (MCMV)-encoded immune

185 measuring thrombus contraction in vivo and a previously characterized mouse line with a defect in int

186 g (ECC) in ventricular cardiomyocytes from a previously characterized mouse model of chronic sympathe

187 We have previously characterized mouse models recapitulating hum

188 ck in mouse cells is not attributable to the previously characterized mouse restriction factor Fv1.

189 Unlike previously characterized mucosal responses, T cell respo

190 We previously characterized multiple mouse monoclonal antib

191 Unlike the previously characterized Muscleblind (Mbl) circular RNA,

192 A previously characterized mutant, Gp59-I87A, exhibits mar

193 formation of amyloidogenic fragments in the previously characterized mutants.

194 We have previously characterized mutations in a Caenorhabditis e

195 ssessing the effect of expression levels and previously characterized mutations on BAR.

196 We had previously characterized N,N-diethyl-N'-phenylpiperazine

197 Their diversity and similarities with previously characterized natural killer (NK) cells and l

198 .2 genes encoding the NDUFS8 subunit and the previously characterized ndufs4 CI mutant.

199 served YXXXY motif that is used by all other previously characterized NEAT domains to coordinate iron

200 nd to be regulated by NF addition, including previously characterized NF-induced marker genes.

201 The previously characterized noncoding RNA that regulates ex

202 sponsible for SPI-1 repression have not been previously characterized, nor have the bacterial signali

203 nal sequence that does not correspond to any previously characterized NRPS domain.

204 arities and is only distantly related to all previously characterized NTTs.

205 the number of known off-targets for certain previously characterized nucleases more than tenfold.

206 lex" that is heterogeneously formed from our previously characterized Nup54.Nup58 and Nup54.Nup62 int

207 s of this transition, but in contrast to the previously characterized oligogenic basis of a pollinato

208 inally, detailed expression analyses for the previously characterized organ boundary gene candidate N

209 operate through a different pathway from the previously characterized OXI1-dependent response to path

210 e wild type level of PAS susceptibility in a previously characterized PAS resistant strain of M. tube

211 , is catabolized to alpha-ketoglutarate by a previously characterized pathway.

212 This binding site is distinct from those of previously characterized PCu(A)C domains but resembles c

213 and function of PDZ2as, in comparison to the previously characterized PDZ2 domain.

214 ethanolamine desaturase and suggest that the previously characterized phenotype of Tmem189-deficient

215 rogen bond with phosphate that is typical of previously characterized phosphate-binding proteins, but

216 Progeny from a cross between hms-1 and the previously characterized PME inhibitor5 overexpression l

217 Contrary to previously characterized Pol epsilon cancer variants, th

218 ke an exonuclease active site mutant that we previously characterized, POLE cancer mutants readily dr

219 particles that have largely been stripped of previously characterized pre-40S components, but retain

220 reactive descending neurons are identical to previously characterized primary commissure pioneer (PNP

221 eplication termination that is distinct from previously characterized prokaryotic mechanisms.

222 iptional start sites (TSS) and is defined by previously characterized promoter-associated chromatin m

223 three showed no substantial homology to any previously characterized protein in the NCBI database.

224 earches failed to reveal similarities to any previously characterized protein or domain.

225 Most previously characterized proteins that are required for

226 Moreover, mph2-and previously characterized PSII repair-defective mutants-e

227 In addition to recapitulating previously characterized regulons, we discovered 454 nov

228 le retaining a local conformation similar to previously characterized repeat proteins of the same cla

229 ptococcus pyogenes, SEER identifies relevant previously characterized resistance determinants for sev

230 their rapid elimination failed to elicit the previously characterized response to intranasal inoculat

231 nstrated among Rtn4, Ceg9, and atlastin 1, a previously characterized reticulon interacting partner.

232 We conclude that dKDM4A, in addition to its previously characterized role in euchromatin, utilizes b

233 ate this function to be independent of their previously characterized role in the DNA damage response

234 ires the alpha7 tail binding site, besides a previously characterized Rpt5 binding site.

235 mple sequencing data from varying numbers of previously characterized samples at varying depths of co

236 Among 270 additional previously characterized samples, both multiplex panels

237 represents a novel fold that is unrelated to previously characterized secretion chaperones.

238 o not encode any discernable similarities to previously characterized sequences were identified.

239 lar basis of these effects, mutation of four previously characterized serines within the Kv3.4 N-term

240 HIV and Treponema pallidum antibodies in 450 previously characterized serum specimens.

241 We have previously characterized several steps in the avenacin p

242 looked for somatic mutations by identifying previously characterized single-nucleotide variants and

243 We previously characterized SLC, a stem-loop structure in t

244 e simulations, benzene is released through a previously characterized, sparsely populated room-temper

245 variants in the current study, as well as in previously characterized species A and J viruses infecti

246 Here, we report that the previously characterized splicing kinase SRPK1 initiates

247 nd transducing germinant signals relative to previously characterized spore formers.

248 ding protein different in structure from all previously characterized ssDNA binding proteins.

249 Mice were infected with the previously characterized straight-rod Deltapgp1 and Delt

250 d most other homologs, is not present in the previously characterized streptococcal OatA.

251 of the other serotypes, which have not been previously characterized: [structure: see text] Common a

252 Abeta antibody binding sites, distinct from previously characterized structures.

253 Interestingly, unlike previously characterized subcompartments, these interact

254 M2-A1-N1-T1-E2-H3), the same as those of the previously characterized symptomatic N155 Vellore isolat

255 S. marcescens Db10 genome that included the previously characterized systems, sdeXY, sdeAB, and sdeC

256 Furthermore, the previously characterized Td oxygen sensor ODP influences

257 We recover TS/CYP gene pairs for previously characterized terpene metabolic gene clusters

258 gnizing group 2 influenza A viruses has been previously characterized that binds to a highly conserve

259 Using atomic force microscopy, we previously characterized the disruption of model membran

260 We previously characterized the Enpp1(asj) mutant mouse as

261 While we have previously characterized the expression profiles of majo

262 We previously characterized the key role of volume-regulate

263 We previously characterized the link between WNT7A and the

264 We previously characterized the Mdr2(Abcb4)(-/-) mouse as a

265 We have previously characterized the metabolic defects associate

266 We have previously characterized the robust penetrance of a hete

267 We previously characterized the role of two highly conserve

268 We previously characterized the TRN-SR2 binding interface i

269 between the S-methylcysteine residue and the previously characterized thioglycine, 5-(S)-methylargini

270 We have previously characterized three monodomain ARO/CYCs: ZhuI

271 Bacterial isolates previously characterized through whole-genome sequencing

272 ive-fold lower Michaelis Constant (Km ) than previously characterized TNT-active Arabidopsis thaliana

273 ted cells also upregulated several genes not previously characterized to be antiviral, such as RND1,

274 y, and has structural features distinct from previously characterized TOG domains.

275 e that distinguishes SusC-like proteins from previously characterized TonB-dependent transporters.

276 The previously characterized topological nature of the band

277 the codon for pyrrolysine that distinguishes previously characterized trimethylamine methyltransferas

278 A previously characterized triplex DNA-specific antibody (

279 Previously characterized trisolvated dimeric enolates un

280 We previously characterized Tspan8 for its ability to promp

281 Our laboratory previously characterized Tsr4 as a 40S biogenesis factor

282 We have previously characterized two EHDs (EH domain containing

283 We have previously characterized two SNARE proteins, secretory p

284 We previously characterized two tau strains that stably mai

285 Previously characterized Type I systems use two identica

286 yCas9 using a different mechanism than other previously characterized Type II-A Acrs.

287 Although the previously characterized ultrafast indicators iGlu(u) an

288 induced neutrophil transepithelial migration previously characterized using cell line-based models.

289 ty, we compared V. splendidus 13B01 with the previously characterized V. splendidus 12B01, which has

290 A previously characterized version of Cdc42p, Cdc42p(E100A

291 mens, and found that they clustered with two previously characterized Vibrio navarrensis isolates in

292 Compared to previously characterized viruses expressing amino-termin

293 dentified genes encoding known receptors for previously characterized viruses of Escherichia coli (ph

294 wed patterns of connectivity consistent with previously characterized visual system connections, and

295 In this instance and in contrast to the previously characterized visual system, endocytosis from

296 We used wild-type VP35 and previously characterized VP35 mutants to clarify VP35-DC

297 ng at frq functions in a parallel pathway to previously characterized VVD-dependent silencing and is

298 Unlike previously characterized wHTH proteins, PCG2-DBD utilize

299 nsferase GCN5 ((Gcn5(hat/hat) )), which were previously characterized with respect to their exencepha

300 n from diunsaturated fatty acids produced by previously characterized Z11-desaturase/conjugase MsexD2