ライフサイエンスコーパス: structural gene

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

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

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

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

5 RF 9 corresponded to a previously identified structural gene.

6 re mutants affected in the ubiquitous urease structural gene.

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

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

9 3' primer derived from the El Tor hemolysin structural gene.

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

11 dons is located immediately preceding the AT structural gene.

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

13 transcription factor, signalling pathway and structural genes.

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

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

16 irst infected cell due to the absence of the 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 factors that control the expression of these structural genes.

25 as a transcriptional repressor of flavonoid structural genes.

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

27 mirrors the expression of other anthocyanin structural genes.

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

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

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

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

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

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

34 rge intergenic space existed upstream of the structural genes.

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

36 oting transcription termination prior to the structural genes.

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

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

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

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

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

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

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

44 In bacteria and archaea, the Amt structural genes (amtB) are invariably linked to glnK, w

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

46 with chromosomal deletions involving the rgg structural gene and either the rgg or gtfG promoter also

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 including conserved poxvirus replicative and structural genes and genes likely involved in virulence

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

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

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

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

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

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

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

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

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

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

71 2 fixation reductive pentose phosphate cycle structural genes are differentially controlled.

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

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

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

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

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

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

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

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

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

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

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

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

88 Single-nucleotide polymorphisms (SNPs) in structural genes can have a dramatic effect on the biolo

89 The structural gene CHI from Alium cepa increases flavonol c

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

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

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

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

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

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

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

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

98 5, Deltalmo2186, Deltalmo2183), both sortase structural genes (DeltasrtB, DeltasrtA, DeltasrtAB), fur

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

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

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

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

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

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

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

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

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

108 es revealed that the expression of nirK, the structural gene encoding nitrite reductase, in these str

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 Viral structural gene expression, viral titers, and viral spre

123 tional regulator of muscle morphogenesis and structural gene expression.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 (AhpF, Nox1, or PrxR) just downstream of the structural gene for their peroxiredoxin (Prx, AhpC) homo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 We have also characterized the 8C10 structural gene from a 129Sv/J genomic library and have

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

185 The structural genes in the highly conserved carotenoid bios

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

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

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

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

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

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

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

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

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

195 sion of additional transcription factors and structural genes involved.

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

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

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

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

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

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

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

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

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

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

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

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

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

209 Missense mutations in structural genes may become either selectively advantage

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

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

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

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

214 sequencing of Escherichia coli revealed the structural genes napFDAGHBC, which encode NapABC enzyme

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

216 The structural genes nifHDK1 were the most abundant transcri

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

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

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

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

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

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

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

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

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

226 evolutionary time.The head and tail-encoding structural genes of Mu have only very weak similarity to

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

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

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

230 Upstream from the structural genes of the membrane-bound nitrate reductase

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

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

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

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

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

236 The three structural genes of Trichophyton rubrum encoding actin (

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

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

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

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

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

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

243 quences (INS) in the coding regions of these structural genes or modification of the codon usage patt

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

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

246 activate the expression of three downstream structural genes Phalaenopsis spp.　Flavanone 3-hydroxy

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

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

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

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

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

252 efficient and stable expression of the HIV-1 structural gene products Gag and Env could be achieved b

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 Targeted mutagenesis of the putative SLS structural gene sagA in group G streptococcus eliminated

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

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

266 h lies more than 1.5 kb upstream of the setB structural gene; setA may be transcribed via readthrough

267 The ZIKV structural genes showed the highest degree of insertiona

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

286 ic analysis of the sequence flanking the CRH structural gene was used to screen for additional STRs a

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