ライフサイエンスコーパス: structural gene

1 activity, is associated with an intact sleB structural gene.

2 reas the other group has defects in the fap1 structural gene.

3 nhancer (KE) located 113 kbp 5' to the Gata3 structural gene.

4 S, that is nearly identical to fhaB, the FHA structural gene.

5 nts, two of which reside far 3' to the Gata2 structural gene.

6 RF 9 corresponded to a previously identified structural gene.

7 re mutants affected in the ubiquitous urease structural gene.

8 ted 13.9 and 22 kb upstream from the lactase structural gene.

9 tated solely by the source of the polymerase structural gene.

10 3' primer derived from the El Tor hemolysin structural gene.

11 have been associated with a mutation in its structural gene.

12 transcription factor, signalling pathway and structural genes.

13 ich encodes the direct regulator of the SPI1 structural genes.

14 ter which controls the expression of the fim structural genes.

15 irst infected cell due to the absence of the structural genes.

16 of hilA, encoding the activator of the T3SS structural genes.

17 ressing subgenomic WNV replicons lacking the structural genes.

18 ucture that halts transcription prior to the structural genes.

19 ich encodes the direct regulator of the SPI1 structural genes.

20 ontrols expression of gene clusters encoding structural genes.

21 after the expression of at least some viral structural genes.

22 expression of metabolic, proliferative, and structural genes.

23 HilA activates the SPI1 TTSS structural genes.

24 r to allow transcription to proceed into the structural genes.

25 mirrors the expression of other anthocyanin structural genes.

26 nd in putative operons with [Fe] hydrogenase structural genes.

27 p mRNA resulting in termination prior to the structural genes.

28 and modulating a range of key regulatory and structural genes.

29 enzymes as well as the viral capsid and tail structural genes.

30 a multiple-cloning site in place of the VEE structural genes.

31 rge intergenic space existed upstream of the structural genes.

32 bearing suppressing mutations in F(1)-ATPase structural genes.

33 o assess the secrets between photons and the structural genes.

34 factors that control the expression of these structural genes.

35 as a transcriptional repressor of flavonoid structural genes.

36 network of cell type-specific signaling and structural genes.

37 oting transcription termination prior to the structural genes.

38 esentation in the genome far exceed those of structural genes.

39 plicing, but not in transcription, of muscle structural genes.

40 NT1 (ODO1) and phenylpropanoid scent-related structural genes.

41 on of Sox6 and down-regulation of slow fiber structural genes.

42 contained a transposon insertion in the Aae structural gene (aae) and tested the mutant to determine

43 ture-sensitive mutants with mutations in the structural gene (acpP) that encodes ACP have been isolat

44 al regulators of the signature flight muscle structural gene, Actin88F.

45 al activators of adult cardiac metabolic and structural genes, an.d suppressors of noncardiac lineage

46 ncer (Tce1) lying 280 kb downstream from the structural gene and demonstrated in transgenic mice that

47 e PCR (qRT-PCR) revealed that type 1 fimbria structural genes and a gene encoding a putative outer me

48 mited by low-level transcription of the sigX structural genes and by clpP, which appears to negativel

49 E16sp viruses, we have sequenced the MRE16sp structural genes and found a 90-nucleotide deletion in t

50 d a signature, "CA20", comprising centrosome structural genes and genes whose dysregulation is implic

51 vinelandii with defined deletions in the nif structural genes and in the intergenic noncoding regions

52 required for efficient expression of muscle structural genes and microRNAs.

53 ndida albicans is primarily localized within structural genes and modulates transcriptional activity.

54 gion but not the rrn P2 promoter or the rRNA structural genes and occurred with and without active tr

55 efine a regulon that includes both flagellar structural genes and other genes apparently not involved

56 edge cells showing heightened expression of structural genes and prominent sarcomeres.

57 et of genes that includes most of the virion structural genes and some genes of DNA metabolism, but t

58 A vaccine encoding wild-type or variant ZIKV structural genes and tested immunogenicity and protectio

59 lator of the flavonoid pathway, including 11 structural genes and the transcription factor An2.

60 ngly implies that parallel evolution of both structural genes and trans-factors underpins the polyphy

61 on, beginning with ureI, followed by ureABC (structural genes), and ureEFGD (accessory genes).

62 cated hundreds of kbp 5' and 3' to the Gata2 structural gene, and both are vital for embryonic develo

63 ween rs114209171, located upstream of the F8 structural gene, and thrombosis risk.

64 gene expression heritability is trans to the structural gene, and we identify several replicating tra

65 Computational methods for structural gene annotation have propelled gene discovery

66 of RNA-Seq based transcriptome profiling to structural gene annotation helped correct existing annot

67 ter a new genome is sequenced and assembled, structural gene annotation is often the first step in an

68 approaches to iteratively refine and improve structural gene annotations across multiple Aspergillus

69 Since the structural genes appear to be intact in MVA, it is hypot

70 hways, transcription factors, and downstream structural genes are conserved during vertebrate valvulo

71 -type seedlings, y1 and its target flavonoid structural genes are coordinately expressed.

72 enome into which DNA fragments harboring the structural genes are ligated and transfected directly in

73 The Xfas53 terminase and structural genes are related at a protein and gene order

74 Mutation of either arginase structural gene (ARGAH1 or ARGAH2 encoding arginine [Arg

75 After incorporating the Gata2 structural gene as well as the distant hematopoietic and

76 dy identifies H3K27me3-mediated silencing of structural genes as requisite for zebrafish heart regene

77 rofound alterations in known GATA4-regulated structural genes as well as genes with apoptotic implica

78 of these phages to identify alleles of phage structural genes associated with infectivity.

79 ent), as well as a single determinant in the structural genes at E2 243 (Leu to Ser; avirulent to vir

80 ith expression variation of a few, primarily structural, genes at terminal positions within the netwo

81 nels, function-specific building blocks, and structural gene batteries.

82 ith several antioxidant, detoxification, and structural genes being highly expressed in both the bron

83 Its structural gene, bslA, is located on the pXO1 pathogenic

84 Bacillus subtilis contains urease structural genes but lacks the accessory genes typically

85 response was eliminated by disruption of Mpf structural genes but not components required only for DN

86 ted to have mutations in both regulatory and structural genes, but the basis for this unusual phenoty

87 an antisense RNA that regulates conjugation structural genes by a transcriptional attenuation mechan

88 ruits showed a positive correlation with the structural genes Ca4H, Comt, Kas, pAmt, and AT3 expressi

89 nomic region directly upstream of the Ppp1cc structural gene can drive expression of Ppp1cc2, and rec

90 The structural gene CHI from Alium cepa increases flavonol c

91 , is divergently transcribed upstream of the structural gene cluster.

92 As in T5, the H8 structural genes clustered on the chromosome according t

93 GWAS have reported structural genes (COL6A4), inflammation-related genes (P

94 in the mutant, whereas expression of the CL structural genes CRD1 and PGS1 did not, suggesting that

95 This is achieved by expressing the nisA structural gene, cyclase (nisC) and dehydratase (nisB),

96 ain of GBS 874391 lacking the beta-hemolysin structural gene cylE and investigated the role that beta

97 tidylinositol transfer protein (SEC14) and a structural gene deletion allele (tlg2Delta) for the Tlg2

98 demonstrated that a mutant of type 1 fimbria structural genes (DeltafimAICDHF) and a ycfR mutant show

99 5, Deltalmo2186, Deltalmo2183), both sortase structural genes (DeltasrtB, DeltasrtA, DeltasrtAB), fur

100 This element, located 280 kbp 3' to the structural gene, directs both T cell- and NK cell-specif

101 ron transport chain genes, and mitochondrial structural genes, Drp1 (dynamin-related protein 1), Fis1

102 of CDV, while known late capsid and tegument structural genes (e.g., ORFs 25, 26, 64, and 67) were CD

103 leoprotein) could decrease, while the RepRNA structural gene (E2) translation increased.

104 heir current design relies on replacement of structural genes, encoded by subgenomic RNAs (SG RNA), w

105 lacking CL due to a disruption in CRD1, the structural gene encoding CL synthase, exhibit defective

106 t cells containing a disruption of CRD1, the structural gene encoding CL synthase, exhibit temperatur

107 tivity (Ts- phenotype) targeted at TIF5, the structural gene encoding eIF5 in yeast (Saccharomyces ce

108 e is known about the regulation of hchA, the structural gene encoding Hsp31.

109 ption factor, was identified within the sigL structural gene encoding sigma(L) in Bacillus subtilis.

110 neumoniae enzymes was detected alongside the structural gene encoding the putative LplA in the T.acid

111 nes (Lith6) spanning the Apobec-1 locus, the structural gene encoding the RNA-specific cytidine deami

112 ructed adenoviral vectors (Ads) that express structural genes encoding either the Cys67stop mutant pr

113 QTL, which distinguishes between cis-QTL in structural genes encoding enzymes and regulatory trans-Q

114 Structural genes encoding enzymes involved in the genera

115 scription factor and a subset of anthocyanin structural genes encoding flavonoid 3'-hydroxylase, dihy

116 Induction of the Saccharomyces MAL structural genes encoding maltose permease and maltase r

117 e in trans to the known genomic locations of structural genes, except for single cis-QTL for nitrate

118 Mutants created by disruption of the structural gene exhibited few discernible defects in res

119 irment of flight muscles, and transcripts of structural genes expressed in the flight muscles became

120 Cell-based assays show that HDAC4 represses structural gene expression via direct binding to AT-rich

121 d for efficient repression of MEF2-dependent structural gene expression, indicating a link between th

122 leading to body wall muscle improvements in structural gene expression, locomotory performance, and

123 Viral structural gene expression, viral titers, and viral spre

124 jor requirement in the maintenance of muscle structural gene expression.

125 tional regulator of muscle morphogenesis and structural gene expression.

126 pment showed MEF2 to be more dispensable for structural gene expression: after myoblast fusion, Mef2

127 This process is characterized by structural, gene expression, metabolic, and functional s

128 ssociated communities) depends upon specific structural genes (flagella, pili and exopolysaccharide b

129 n in B. burgdorferi, we inactivated the hook structural gene flgE by targeted mutagenesis.

130 he S. enterica serovar Typhimurium sigma(28) structural gene fliA was exchanged with homologs of Aqui

131 Escherichia coli defective in the sigma(28) structural gene, fliA.

132 iting/noneliciting nature of Xcc flagellins (structural gene fliC).

133 in flagellar assembly, such as the flagellin structural gene, fliC.

134 actors required for the transcription of the structural gene FLO11.

135 d for mutations in desmosomal and other skin structural genes, followed by Sanger sequencing of candi

136 re, for the first time, we have identified a structural gene for a SM synthase.

137 rcsC) and also independent of manC (cpsB), a structural gene for colanic acid synthesis.

138 tase activity in an ndk mutant, in which the structural gene for NDP kinase is disrupted, and 2) the

139 ion, these results 1) show that nSMase2 is a structural gene for nSMase, 2) suggest that nSMase2 acts

140 udied in humans: the OT receptor (OXTR), the structural gene for OT (OXT/neurophysin-I), and CD38.

141 V-1 coreceptor in macrophages, and the viral structural gene for p24 were targeted either singly or i

142 synthase (SQD2) and a point mutation in the structural gene for phosphatidylglycerolphosphate syntha

143 Sequence analysis of the structural gene for PMT, toxA, previously suggested it w

144 purification of the recombinant enzyme, the structural gene for PSase was modified by site-directed

145 itional candidate gene in this region is the structural gene for resistin, itself.

146 inferred to be read-through of spoIIIG, the structural gene for sigma(G), from the upstream spoIIG l

147 qd2 pgp1-1, carries a T-DNA insertion in the structural gene for SQDG synthase (SQD2) and a point mut

148 ymyxin resistance, we isolated FnlpxE as the structural gene for the 1-phosphatase, an inner membrane

149 These findings show that lpxE is the structural gene for the 1-phosphatase.

150 DNA insert from an active clone located the structural gene for the 4'-phosphatase, designated lpxF.

151 entire biosynthetic machinery as well as the structural gene for the enzyme.

152 Escherichia coli confirmed that APP1 is the structural gene for the enzyme.

153 We also identified the structural gene for the H. pylori lipid A pEtN transfera

154 One of these orthologs, Hp0021, is the structural gene for the lipid A 1-phosphatase and is req

155 thermosensitive allele (sec14-1(ts)) of the structural gene for the major yeast phosphatidylinositol

156 nsposon mariner or targeted deletions of the structural gene for the S-layer protein Sap and the spor

157 Major findings are as follows: (1) the structural genes for 18S and 28S are highly conserved ac

158 The structural genes for As(III) oxidase (aoxAB), a c-type c

159 e cloned as candidates for nearly all of the structural genes for capsaicinoid biosynthesis.

160 highest expression in the sapwood, while the structural genes for flavonoid biosynthesis were up-regu

161 was evaluated in Vero cells, which lack the structural genes for IFN-alpha/beta and would preclude c

162 amino acids each were identified throughout structural genes for MLV and ATP.

163 yla involving both transposable elements and structural genes for normal housekeeping functions.

164 ant vaccine viruses expressing the prM and E structural genes for serotypes 1, 3, and 4 in the DENVax

165 loned and sequenced, which revealed that the structural genes for soluble methane monooxygenase, mmoX

166 Transcription of the Bacillus anthracis structural genes for the anthrax toxin proteins and bios

167 Expression of the structural genes for the anthrax toxin proteins is coord

168 , as in most prokaryotes, contains the eight structural genes for the F-ATPase (ATP synthase), which

169 These include calY and inhA1, structural genes for the metalloproteases camelysin and

170 Mutants lacking one or more of the structural genes for the toxin proteins, i.e., protectiv

171 onship between the Arabidopsis MYB triad and structural genes from primary and phenylpropanoid metabo

172 es from gRNA while permitting translation of structural genes from sgRNA1.

173 trans resulted in the expression of the late structural gene gag by nonintegrated HIV DNA.

174 ver, we did not find evidence that the major structural gene gag drives this correlation, highlightin

175 nes rather than a dominant role of the major structural gene gagIMPORTANCE HIV disease progression is

176 le embryonic cells, where 25-30% of X-linked structural genes have been reported to escape inactivati

177 f 7-bp repeats upstream of the HMW1 and HMW2 structural genes (hmw1A and hmw2A, respectively).

178 circuits controlling the expression of a key structural gene in a primitive light-sensing system.

179 g an in-frame deletion of the FHA or the PRN structural gene in a virulent B. bronchiseptica swine is

180 e apoB gene is located much farther from its structural gene in the intestine than in the liver.

181 s, such as MyoD and/or Myf5, and some muscle structural genes in a population of cells that continues

182 module has sufficient physics to control key structural genes in both development and disease.

183 find that frameshifting has persisted in two structural genes in budding yeasts, ABP140 and EST3 for

184 re alternative splicing of large, repetitive structural genes in muscles.

185 Deletion of individual Pho structural genes in suppressed strains did not identify

186 or the expression of only a subset of muscle structural genes in the adult.

187 red mRNA and protein levels of mitochondrial structural genes in the frontal cortex of patients with

188 The structural genes in the highly conserved carotenoid bios

189 ating key staphylococcal global regulons and structural genes in vivo, thus abrogating relevant virul

190 CpG or UpA frequencies were maximised in non-structural genes (including helicase and polymerase enco

191 ndicate that differences have evolved in key structural genes, including those encoding enzymes invol

192 stribution of many classes of regulatory and structural genes, including those involved in energy met

193 Transcriptional analysis of the ytvA structural gene indicated that it provides the entry poi

194 The expression pattern of HERV-P structural genes indicates that they are actively amplif

195 the role of SRF in controlling expression of structural genes involved in conferring the myogenic phe

196 namyl alcohol dehydrogenase1 and FaEGS2, two structural genes involved in eugenol production, was dow

197 d fibre cells reveals the key regulatory and structural genes involved in fibre formation.

198 Previous studies identified regulatory and structural genes involved in the development and diversi

199 sion of additional transcription factors and structural genes involved.

200 LpxI was identified because its structural gene is located between lpxA and lpxB in Caul

201 tein A), a predicted membrane permease whose structural gene is located in an operon with ypfP, is no

202 The PIS1 structural gene is required for the synthesis of the ess

203 The transcription of the corresponding structural genes is activated by the DcuS-DcuR two-compo

204 Transcription of the Saccharomyces MAL structural genes is induced 40-fold by maltose and requi

205 observation, the deletion of hslO, the Hsp33 structural gene, is no longer tolerated in the absence o

206 ng the transcriptional activator of the SPI1 structural genes, is directly controlled by three AraC-l

207 yruvate in a manner requiring csaB, the only structural gene known to be required for S-layer assembl

208 se and leucoanthocyanidin reductase, the key structural genes leading to PA biosynthesis, in the pres

209 We analyzed the structural gene located within a region on 1q21-q23 link

210 siderable diversity in the nonstructural and structural genes, many alphaviruses belonging to differe

211 The structural gene maps revealed that the order of the head

212 Dynamic differential DNA methylation of structural genes may be one factor contributing to morph

213 Missense mutations in structural genes may become either selectively advantage

214 ing enzymes, in addition to the heptapeptide structural gene mccA, necessary for McC biosynthesis and

215 endent upon a four-gene cluster encoding the structural gene mcjA, two maturation enzymes mcjB and mc

216 S mutant transcription of both the mutacin I structural gene mutA and the mutacin I transcriptional a

217 ned the virulence of selected regulatory and structural gene mutants in the surrogate model host Caen

218 ne prophage, prophage 1 (PhiV1), encodes the structural genes necessary for phage particle production

219 The structural genes nifHDK1 were the most abundant transcri

220 Neither structural genes nor immediate-early genes were found.

221 Initially, the cells express neither cardiac structural genes nor Nkx2.5 but differentiate in vitro i

222 uced transcription of the NO reductase (NOR) structural genes, norV and norW, as monitored by lac gen

223 Disruption of pbpD, the structural gene of PBP4, in either the parental strain o

224 lysis of the cell wall identified adr as the structural gene of the pneumococcal peptidoglycan O-acet

225 ated (lacking an N-terminal signal sequence) structural gene of Thermus thermophilus cytochrome c(552

226 w that an open-reading frame proximal to the structural genes of CoFeSP encodes an ATP-dependent redu

227 ymorphism comparable to the most polymorphic structural genes of D. melanogaster.

228 Here, we identify and analyze novel putative structural genes of HERV-P in primates, human tissues, a

229 The structural genes of P23-45, most of which have no simila

230 The structural genes of phiYS40, most of which have no simil

231 YB31 is indeed involved in the regulation of structural genes of the capsaicinoid biosynthetic pathwa

232 changes in the expression of regulatory and structural genes of the oxylipin pathway and by studying

233 by transcriptional reprogramming of specific structural genes of the pathway.

234 vels of divergence and polymorphism than the structural genes of the pathway.

235 different species of plants as regulators of structural genes of the phenylpropanoid pathway; therefo

236 ng results in increased transcription of the structural genes of the tna operon.

237 e to study the structure and function of the structural genes of this important human pathogen.

238 The three structural genes of Trichophyton rubrum encoding actin (

239 virus (FL01) was generated by replacing the structural genes of type II PRRSV strain FL12 cDNA infec

240 h for the introduction of mutations into the structural genes of West Nile virus (WNV).

241 Chimeras containing all of the MHV-1 structural genes on an MHV-A59 background were able to r

242 n cassette is atypically situated within the structural gene operon and could have moved there either

243 cies can result from mutations in the mutase structural gene or from mutations that impair the acquis

244 ies can result from inborn errors in the MCM structural gene or from mutations that impair the assimi

245 nse in replicon cells and suggest a role for structural genes, or as yet unknown interactions, in the

246 oss-of-function mutations in the Na+ channel structural gene para, but enhanced by loss-of-function m

247 activate the expression of three downstream structural genes Phalaenopsis spp. Flavanone 3-hydroxyla

248 ed pilus expression due to a mutation in the structural gene pilA.

249 A conserved module of structural genes places CW02 in the T7 supergroup, membe

250 uggesting the existence of regulatory and/or structural gene polymorphisms.

251 ry transfection with core gene but not other structural genes present in the full-length replicon.

252 e transcriptional inputs (hilC and hilD) and structural genes (prgH) decay exponentially, with a char

253 ay to temporally regulate late expression of structural gene products.

254 direct interaction with both regulatory and structural genes provide evidence for EOBI's wide-rangin

255 Two structural genes, pydA and pydB, encoding a metacleavage

256 Its structural gene, ramS, is only 38 nucleotides downstream

257 oded by mutations that reside outside of the structural gene region of the genome.

258 vectors resulted in robust expression of VEE structural genes, replication of the alphavirus vector a

259 r demonstrate that, like in S. enterica, the structural genes required for the flagellar hook-basal b

260 t mutant cell lines identified variations in structural genes, resulting in amino acid changes that d

261 e show that an insertional lesion in the sap structural gene results in elongated chains of bacilli,

262 Expression analysis of flavonoid structural genes revealed the strong down-regulation of

263 Unlike all other exocyst structural genes, SEC3 is not essential for growth.

264 The SlVRSLip structural gene sequence of R and S plants was identical

265 The ZIKV structural genes showed the highest degree of insertiona

266 ession of metabolic genes, such as Nos1, and structural genes, such as Myl1, in myofibers.

267 trogenase due to mutations in Mo nitrogenase structural genes synthesized functional V and Fe nitroge

268 downregulation of the same late anthocyanin structural genes that are downregulated in ttg1 and bHLH

269 ment of AP1 transcriptional activator to the structural genes that are required for epidermal differe

270 However, the number of structural genes that can be transferred to plants is li

271 Mef2c null muscles identified several muscle structural genes that depend on MEF2C, including those e

272 entify a group of ion channel, synaptic, and structural genes that exhibit mutually correlated expres

273 ess small open reading frames (ORFs) between structural genes that have been hypothesized to play imp

274 These do not encompass the major cartilage structural genes that many consider the most likely susc

275 Analysis of muscle structural genes that produce medium (Nrap: 5 kb), large

276 could distinguish an ancient core set of 24 structural genes that were present in the common ancesto

277 ange of categories including muscle-specific structural genes, transcription factors, and ion channel

278 Several VZV regulatory and structural gene transcripts and products were detected.

279 vels of phenolic compounds and corresponding structural gene transcripts were examined in flesh and s

280 ckdown did not interrupt expression of major structural gene transcripts, and myofibrils were formed.

281 n reductions in the levels of several muscle structural gene transcripts.

282 yndrome coronavirus (SARS-CoV) contains four structural genes, two replicase-transcriptase open readi

283 Differences in miRNA expression or structural gene variants were not detected.

284 se stimulated transcription of the aflatoxin structural genes ver-1 and nor-1 to similar intermediate

285 V-nitrogenase structural genes, vnfDGK, as well as vnfEN form an opero

286 d alpha-amylase function and regulation, the structural gene was identified and disrupted and the res

287 ntaining an in-frame deletion of the bpsABCD structural genes was constructed in a wild-type swine is

288 igma factor) expression, fleB (the flagellin structural gene) was down-regulated.

289 ir requirement for colonization, most of the structural genes were also required for RscS-induced bio

290 ons in an oxyR homolog and predicted fimbria structural genes were identified.

291 aled a striking overexpression of trp operon structural genes when the strain was grown in the presen

292 he shorter transcript to nt +140 of the comX structural gene, where a unique 69-aa open reading frame

293 ontrol the expression of only the contiguous structural gene), whereas distal eQTL act in trans.

294 cin frequently harbour mutations in the mtrR structural gene, which encodes a repressor of the mtrCDE

295 y restricted unselected allelic variation in structural genes, which hinders study of the genetic rel

296 irus-infected cells suppressed expression of structural genes, while early expression was unaffected,

297 requires the coordinated activation of many structural genes whose products are required for myofibr

298 aeroides revealed patterns of coselection of structural genes with the ancillary genes identified her

299 ith mutations in methanol dehydrogenase-like structural genes xoxF1 and xoxF2, in order to obtain ins

300 previously assigned to the ubiquitous urease structural gene, yielded an F(1) having 22% +/- 11% of w