ライフサイエンスコーパス: multicopy

1 to amplify a species-specific region of the multicopy 18S rRNA gene, and SYBR Green was used for det

2 dependent lines of transgenic mice bearing a multicopy 413-kbp-linked Gata2 BAC transgene (bearing se

3 tation of maize carrying a tandemly repeated multicopy allele of pericarp color1 (p1) was examined us

4 Multicopy Alu elements include recently integrated subfa

5 ow of time as transgene inactivation in both multicopy and low-copy-number lines.

6 y by combining FISH with immunofluorescence; multicopy and repetitive element expression can also be

7 Genes encoding rRNA are multicopy and thus could be regulated by changing the nu

8 ss mammalian genomes, whereas most genes are multicopy and/or have lineage-specific distributions for

9 RNA gene (SL RNA) repeat is present in large multicopy arrays and has been used as a marker for the d

10 the hypodermis and vulva when expressed from multicopy arrays.

11 ated against single-copy (pyrG and ARG4) and multicopy (arsC) controls.

12 om the beta-lactamase signal sequence in the multicopy Asd(+) pYA3493 vector to create pYA3494.

13 ates independent of copy number variation in multicopy ChrY gene families that influence susceptibili

14 ral variation in copy number of Sly and Rbmy multicopy ChrY genes.

15 ify novel mutator effects resulting from the multicopy cloning (MCC) of specific genes and therefore

16 A multicopy cloning approach was used to search for metage

17 ) strand and a heavy (H) strand, exists as a multicopy closed circular genome within the mitochondria

18 with flanking SNP genotypes, the majority of multicopy CNPs do not (40% with r > 0.8).

19 range from 28 to 348 bp, and the lengths of multicopy CREE appear mainly in the ranges of 154 to 156

20 ies demonstrated that deletion of the entire multicopy cysteine protease B (CPB) gene array in L. mex

21 ive to QseBC was mapped, and single-copy and multicopy deletion analyses were performed to determine

22 t, the native tatA gene of Prov. stuartii in multicopy did not suppress an aarA mutation.

23 yed octapeptides and avidity effect of their multicopy display on the phage scaffold, good biocompati

24 We determined the single and multicopy distribution of distinct viral cell junctions

25 -Asp-pThr-Asp motifs, recently identified as multicopy docking sites within Mdc1, are evolutionarily

26 s tended to be differentially expressed, and multicopy duplicate genes were likely to diverge express

27 A screen using a multicopy E. coli library led to identification of the r

28 t to (i) complementation; (ii) dominance and multicopy effects; (iii) interaction with wild-type FliH

29 Ty1 transcription of a multicopy element expressed from the GAL1 promoter aboli

30 Because multicopy elements can facilitate genomic recombination

31 on of enrichment for repetitive and abundant multicopy elements reveals 70% of RBPs have enrichment f

32 of the null mutant with the LmGT4 gene on a multicopy episomal expression vector also reverted these

33 atent, with the viral genome persisting as a multicopy episome and expressing only a small subset of

34 binding to KSHV terminal repeat DNA mediates multicopy episome persistence.

35 circularized viral genome is maintained as a multicopy episome.

36 ) share the common property of persisting as multicopy episomes in the nuclei of rapidly dividing hos

37 virus (EBV) establishes latent infections as multicopy episomes with complex patterns of viral gene t

38 upon a stable cell line harboring a visible multicopy ER responsive transcription unit and expressin

39 fA or mifB increased flagellin levels, while multicopy expression decreased them.

40 Multicopy expression of brlR in a DeltasagS mutant resto

41 In contrast to the csrA mutant, multicopy expression of csrA repressed transcription fro

42 ster carrier Nfu and partially suppressed by multicopy expression of either sufA or nfu, suggesting f

43 This inhibition can be suppressed by the multicopy expression of mex67 suggesting that Mex67p can

44 Furthermore, multicopy expression of mifA induced other phenotypes kn

45 Multicopy expression of msc1 robustly suppresses a tempe

46 Finally, we found that multicopy expression of sypG resulted in robust biofilm

47 boratory conditions, but could be induced by multicopy expression of sypG, which encodes a response r

48 biofilm formation and a hyperswarmer, while multicopy expression of this gene promotes sessility.

49 Multicopy expression plasmids encoding essential MOB1 or

50 A series of SSB-encoding multicopy expression plasmids were introduced into reeng

51 infects cells, and its genome persists as a multicopy, extrachromosomal episome.

52 Multicopy extragenic suppressors were selected in strain

53 Multicopy FAA4 could not suppress the growth defect in t

54 Ribosomal RNAs (rRNAs) are encoded by multicopy families of identical genes.

55 ated Bcl-X(L) transgenic mice that contain a multicopy Flag-tagged mouse Bcl-x(Flag) transgene driven

56 Moreover, ftsA R286W or multicopy ftsQAZ, which can largely bypass the requireme

57 Intragenomic variation of this multicopy gene can interfere with accurate phylogenetic

58 Nevertheless, their genomes harbour multicopy gene clusters that were named potential mobile

59 be used as a general method to downregulate multicopy gene families in P. falciparum.

60 The distinction between single-copy and multicopy gene families is reflected in their functional

61 regulation also likely applies to the other multicopy gene families of P. falciparum.

62 asite Plasmodium falciparum contains several multicopy gene families, including var, rifin, stevor an

63 Here, we report that 33 multicopy gene families, representing approximately 273

64 nsertions upstream of tDNAs in two different multicopy gene families.

65 en, a protein called PfEMP1, is encoded by a multicopy gene family called var.

66 The var multicopy gene family encodes Plasmodium falciparum eryt

67 The patatin multicopy gene family encodes the major storage protein

68 f variable antigens, encoded by members of a multicopy gene family named var.

69 nia in immunosuppressed patients, contains a multicopy gene family that encodes the major surface gly

70 ocyte membrane protein-1" encoded by the var multicopy gene family.

71 MSG is encoded by a multicopy gene family; in two specific forms of rat-deri

72 ntagonists in this conflict are the X-linked multicopy gene Xmr and its multicopy MSYq-linked relativ

73 In contrast, paralogous multicopy genes are found in the highly recombining regi

74 Furthermore, X-linked multicopy genes exhibit a similar degree of expression a

75 entical X chromosome and CNV in Y chromosome multicopy genes exhibit sperm head abnormalities and fem

76 genome stability and organelle function and multicopy genes in signaling, transport, and metabolism.

77 test the hypothesis that CNV in Y chromosome multicopy genes influences the paternal parent-of-origin

78 The X chromosome carries two multicopy genes related to Sly: Slx and Slxl1.

79 an and mouse sex chromosomes are enriched in multicopy genes required for postmeiotic differentiation

80 ntified on the bovine MSY (12 single- and 16 multicopy genes), 16 are bovid specific.

81 c family of miRNAs encoded by closely spaced multicopy genes.

82 vulgare) and Brassica oleracea by targeting multicopy genes.

83 copy number variation (CNV) in Y chromosome multicopy genes.

84 nce in CNV between homologous X:Y chromosome multicopy genes.

85 We show that CbAgo targets multicopy genetic elements and suppresses the propagatio

86 The multicopy human U2 small nuclear (sn)RNA genes are trans

87 milies being either primarily single-copy or multicopy in all species.

88 as a low copy number in elasmobranchs but is multicopy in the holocephalan spotted ratfish (Hydrolagu

89 ously published M. tuberculosis strains with multicopy inhA or kasAB plasmids, were tested for their

90 rtussis, and B. holmesii was developed using multicopy insertion sequences (ISs) in combination with

91 We used a unique system consisting of a multicopy integration of an estrogen receptor responsive

92 lating cells, which may obviate the need for multicopy integration to achieve high-level expression a

93 t host and thus bypasses the requirement for multicopy Kan(r); faa and ssrA mutants are additive in t

94 NA (tmRNA) (encoded by ssrA), coupled with a multicopy kanamycin resistance determinant, suppressed b

95 nii, in which the homologous PRT-1 genes are multicopy, kex1 is a single-copy gene encoding a protein

96 The multicopy kinetoplast DNA (kDNA) probes were the most se

97 ocumented, are also unusual in their lack of multicopy LINE-like and gypsy-like retrotransposons, gro

98 The Mlp (multicopy lipoproteins) family is one of many paralogous

99 point of view, our results suggest that the multicopy MD simulation approach is very useful when stu

100 The multicopy model demonstrates the range of atomic displac

101 To address this, we have performed multicopy molecular dynamics (MD) simulations of RT in t

102 e DNA damage sensitivity of a chk1 mutant by multicopy msc1 also requires pht1.

103 Suppression of cnp1-1 by multicopy msc1 requires pht1.

104 Synonymous substitution rate analyses of the multicopy MSY genes indicated that two major periods of

105 are the X-linked multicopy gene Xmr and its multicopy MSYq-linked relative Sly, which are upregulate

106 regulatory mechanism controlling dispersed, multicopy MuDR/Mu elements responsible for Mutator activ

107 od stage, known as PfEMP1 and encoded by the multicopy multigene family known as the var genes.

108 conjugated to gold nanoparticles, yielding 'multicopy-multivalent' nanoscale glycoconjugates.

109 immune response are encoded in the genome as multicopy, nonallelic gene families.

110 host suppression of 2-micron (2mu) plasmids, multicopy nuclear parasites that have co-evolved with bu

111 and animal papillomavirus DNA replicates as multicopy nuclear plasmids.

112 ry components of the ribosome are encoded by multicopy nuclear ribosomal RNA (rRNA) genes: 28/26S, 18

113 -producing mutants, such as grrSA containing multicopies of the amyR gene.

114 Multicopy overexpression of flp-21 transformed wild soci

115 ted the bile sensitivity of DeltacspE as did multicopy overexpression of yciF.

116 e hyperfimbriated phenotype conferred by the multicopy oxyR plasmid was absent in a type I fimbrial m

117 A multicopy p1 allele, P1-wr (white pericarp/red cob) is e

118 ion and small RNA targeting, relating to the multicopy paralogous genes generated from whole genome t

119 hed at centromeres, TET/JBP transposons, and multicopy paralogous genes that are not expressed, but r

120 In a comparison of single-copy and multicopy PCR targets in 70 tissue samples, the sensitiv

121 Nevertheless, the detection of multicopy pfmdr1 in African parasites suggests a high po

122 Second, in medium that lacked thymidine, multicopy phtC(+) or phtD(+) alleles enhanced the surviv

123 Multicopy plasmepsin 2 constitutes a surrogate molecular

124 treated with dihydroartemisinin-piperaquine, multicopy plasmepsin 2 in the sample collected before tr

125 day 42 fell below 90% when the proportion of multicopy plasmepsin 2 parasites exceeded 22%.

126 l and temporal increase of the proportion of multicopy plasmepsin 2 parasites was highly correlated w

127 Multicopy plasmepsin 2 predicted dihydroartemisinin-pipe

128 However, grvA(+) on a multicopy plasmid also conferred the antivirulence pheno

129 mutation in acrR or acrAB expression from a multicopy plasmid also suppressed the TolCP246R,S350C de

130 decarboxylase defect was complemented from a multicopy plasmid and in single copy.

131 onsequences of overexpression of tnaC from a multicopy plasmid and observed that under inducing condi

132 the C-terminal 53 amino acids of MutS) on a multicopy plasmid are proficient for mutation avoidance.

133 nhibited by an oversupply of DnaA and that a multicopy plasmid carrying rcbA neutralizes this inhibit

134 eplication and distribution of the bacterial multicopy plasmid ColE1 in a population of exponentially

135 Expression of ptsP in trans from a multicopy plasmid complemented the lysC mutant, suggesti

136 Expression of ExsD from a multicopy plasmid completely repressed transcription of

137 Further, in multicopy plasmid concatamers, each intron could only si

138 antly higher in the snr-1 mutant harboring a multicopy plasmid containing snr-1.

139 When a multicopy plasmid containing the amyR gene was introduce

140 igen gene promoter or in a strain carrying a multicopy plasmid containing the entire B. cereus plc-sp

141 in place of WT ftsA or with ftsA* alone on a multicopy plasmid divide mostly normally, whether they a

142 hromosomal DeltaacrB mutant transformed with multicopy plasmid encoding MdtM suggested a functional s

143 A multicopy plasmid encoding NarU complemented a narK muta

144 outer membrane phospholipase gene pldA on a multicopy plasmid in a vpsC or vacJ mutant restored its

145 t create mutator phenotypes when put on to a multicopy plasmid in Escherichia coli.

146 complemented by providing the ler gene on a multicopy plasmid in trans.

147 type strain, while expression of YggX from a multicopy plasmid increased the aconitase levels above t

148 NAIII in trans to the MW2 arlRS mutant via a multicopy plasmid induced autolysis in this MRSA strain.

149 Elevated dnaA expression from a multicopy plasmid induces more frequent initiation from

150 We demonstrate that DksA expression from a multicopy plasmid is necessary and sufficient for suppre

151 f the CCU/CCA/CCG-decoding tRNA(Pr)(o)3 on a multicopy plasmid leads to suppression of several +1 fra

152 A multicopy plasmid library of the E. coli genome can then

153 ion of the multidrug transporter MdfA from a multicopy plasmid or by growth at pH 6.0.

154 expressed either from the trc promoter on a multicopy plasmid or from the endogenous dsbA promoter b

155 The small multicopy plasmid pAMalpha1 (9.75 kb) encoding tetracycl

156 e its role further, comW was cloned into the multicopy plasmid pMSP3535, under the control of a nisin

157 When induced for expression, baeR cloned in multicopy plasmid pTrc99A significantly increased the re

158 d over-expression of the DinG protein from a multicopy plasmid result in a slight reduction of UV res

159 Increased expression of GlxII from a multicopy plasmid sensitizes E. coli to MG.

160 partitioning locus STB of the 2mum circle--a multicopy plasmid that resides in the yeast nucleus and

161 ains containing the B. cereus plcR gene on a multicopy plasmid under control of the strong B. anthrac

162 fragments between 3 and 5 kbp in length on a multicopy plasmid vector that was transformed into E. co

163 ontaining the intact groES-groEL operon on a multicopy plasmid was generated and used to demonstrate

164 some of the TBP mutations is suppressed by a multicopy plasmid with SNR6 or by an spt3 mutation.

165 When virADeltaR was expressed from a multicopy plasmid, both sugar and the phenolic inducer w

166 ntify the genes which, when expressed from a multicopy plasmid, can restore the growth defect of the

167 When expressed from a multicopy plasmid, DsrA was stable in both wild-type and

168 erhelicase mutant, and when expressed from a multicopy plasmid, it results in UV sensitivity (UV(s)),

169 When each of the genes was expressed from a multicopy plasmid, M. smegmatis exported comparable prop

170 We visualized the location of a multicopy plasmid, pHP13, in living cells of Bacillus su

171 1 gene and/or the mobN1 gene was cloned on a multicopy plasmid, production of the protein was constit

172 product, when either mutated or cloned on a multicopy plasmid, seems to be capable of compensating f

173 expressed from a constitutive promoter on a multicopy plasmid.

174 d when expressed from a strong promoter on a multicopy plasmid.

175 brial phenotype in strains bearing oxyR on a multicopy plasmid.

176 o the sigma(K)-controlled gerE promoter on a multicopy plasmid.

177 oside (IPTG)-inducible promoter present on a multicopy plasmid.

178 l extract of a strain expressing mpaA from a multicopy plasmid.

179 could be complemented by providing cbpA on a multicopy plasmid.

180 g partition sites of P1 inserted in a small, multicopy plasmid.

181 A-K2378, a strain overexpressing norA from a multicopy plasmid.

182 lly constitutive not only when produced from multicopy plasmids but also at a single-copy gene dosage

183 Furthermore, the stabilization of multicopy plasmids by Rcd is shown to be tryptophanase d

184 Multicopy plasmids carrying mutS alleles that are domina

185 In addition, multicopy plasmids containing the LSB6 gene directed the

186 Expression of efflux pumps on multicopy plasmids did not improve endogenous FFA produc

187 While the expression of these proteins on multicopy plasmids did not improve production over the b

188 In this work, multicopy plasmids expressing either inhA or kasA genes

189 Multicopy plasmids expressing either ntrC or nifA from a

190 mltG was initially isolated in a screen for multicopy plasmids generating a lethal phenotype in cell

191 Multicopy plasmids in Escherichia coli are not randomly

192 harvesting complex components expressed from multicopy plasmids in strains in which the corresponding

193 o- to four-times-higher values obtained from multicopy plasmids in stringent cells and eight-times-hi

194 Experiments with ftsQAZ and ftsQA*Z on multicopy plasmids indicate that ftsQAZzipA+ and ftsQA*Z

195 Thus Rcd-mediated stabilization of multicopy plasmids is dependent upon indole acting as a

196 lso monitored the effects of the presence of multicopy plasmids on the position of DNA polymerase usi

197 The efficient transmission of multicopy plasmids to daughter cells at division require

198 strong inducer dependence when produced from multicopy plasmids, B. bronchiseptica B013N alcR partial

199 1.5 to 11% frameshifting when expressed from multicopy plasmids.

200 kH proteins increased uptake when encoded on multicopy plasmids.

201 n: a novel thrombin inhibitor derived from a multicopy precursor in the salivary glands of the ixodid

202 eptor-alpha in the vicinity of an integrated multicopy prolactin gene array.

203 to test E. coli strains, both in the form of multicopy recombinant plasmids and as lysogenized propha

204 Multicopy refinement using 10 atomic models and strict 2

205 thesis in plants, and they contain their own multicopy, requisite genome.

206 This response is mediated by Dux, a multicopy retrogene defining the cleavage-specific trans

207 lines of evidence that a eutherian-specific multicopy retrogene, DUX4, encodes a transcription facto

208 ared origin of the two resistance-conferring multicopy Rhg1 groups and subsequent independent evoluti

209 find that SCN resistance is associated with multicopy Rhg1 haplotypes that form two distinct groups.

210 The multicopy ribosomal DNA (rDNA) array gives origin to the

211 Subdomains of the multicopy ribosomal DNA locus containing transcription u

212 t detail, the functional organization of the multicopy rRNA gene clusters (rDNA) in the nucleolus is

213 lies on detecting one of the subunits of the multicopy rRNA genes.

214 Multicopy rscS1 activated transcription of genes within

215 Finally, multicopy rscS1 provided a colonization advantage over c

216 Saccharomyces cerevisiae 2-mum plasmid is a multicopy selfish genome that resides in the nucleus.

217 great ape common ancestor already possessed multicopy sequences homologous to most human and chimpan

218 cular type of error in the reference genome: multicopy sequences which have been incorrectly assemble

219 OY-M genome, primarily as a result of fewer multicopy sequences, including PMUs.

220 imum lifespan was significantly increased by multicopy SGS1.

221 i, which is responsible for the synthesis of multicopy single-stranded DNA-Ec86.

222 oli and are responsible for the synthesis of multicopy single-stranded DNA.

223 uces a unique RNA-DNA hybrid molecule called multicopy single-stranded DNA.

224 In this assay, multicopy small-subunit (SSU) ribosomal DNA (rDNA) seque

225 , this 6-AU sensitivity can be suppressed by multicopy SNR6 or BRF1.

226 The multicopy subunit c of the H(+)-transporting F1Fo ATP sy

227 Multicopy suppression analysis implicates TPR9 in Brf1 b

228 high-mobility-group protein Nhp6, including multicopy suppression and synthetic lethality.

229 he apparent affinities determined by in vivo multicopy suppression experiments.

230 predicted target-replacer gene pairs in new multicopy suppression experiments.

231 We use PROPER to predict multicopy suppression in Escherichia coli, achieving hig

232 rowth with pyruvate as the carbon source and multicopy suppression suggest that several other transam

233 ty is typically studied experimentally using multicopy suppression, in which over-expression of a pro

234 in B6), which we validate experimentally via multicopy suppression.

235 Proteus mirabilis, tatA was identified as a multicopy suppressor and restored extracellular signal p

236 Using a multicopy suppressor assay to identify genes that suppre

237 Msc1 was identified as a multicopy suppressor capable of facilitating survival in

238 It acts as a multicopy suppressor for dnaJ mutations and functions in

239 Escherichia coli, is known to function as a multicopy suppressor for dnaJ mutations and to bind nons

240 e recently observed that KsgA functions as a multicopy suppressor for the cold-sensitive cell growth

241 Through multicopy suppressor mutagenesis, we have identified a n

242 RbfA, a 30S ribosome-binding factor, is a multicopy suppressor of a cold-sensitive C23U mutation o

243 encodes a putative Hsp90 co-chaperone, as a multicopy suppressor of a temperature-sensitive allele (

244 SCD5 was identified as a multicopy suppressor of clathrin HC-deficient yeast.

245 ste 12 (Su(z)12), Extra Sex Combs (ESC), and Multicopy Suppressor of IRA 1 (MSI1), and functions in m

246 SLY41 was identified as a multicopy suppressor of loss of Ypt1, a Rab GTPase essen

247 SUR7 was originally described as a multicopy suppressor of rvs167, whose product is an acti

248 The transcription factors Msn2 and Msn4 (multicopy suppressor of SNF1 mutation proteins 2 and 4)

249 p1 and the proteasome is mediated by Sts1, a multicopy suppressor of srp1-49.

250 We isolated a novel gene, alp16(+), as a multicopy suppressor of temperature-sensitive alp6-719 m

251 des C, C, and A to the 3' end of tRNAs, is a multicopy suppressor of the defect in tRNA nuclear expor

252 We report here that SGS1 is a multicopy suppressor of the methyl methanesulphonate (MM

253 e identified a truncated allele of dam1 as a multicopy suppressor of the sensitivity of cdc13-117 (cy

254 NA processing and degradation pathways, is a multicopy suppressor of the synthetic lethality and of t

255 DksA was originally identified as a multicopy suppressor of the temperature sensitivity caus

256 ified the ribosome binding protein Stm1 as a multicopy suppressor of the temperature sensitivity of t

257 SecA functions as a multicopy suppressor of the temperature-sensitive phenot

258 ized open reading frame YER074W-A as a novel multicopy suppressor of the thermosensitive yip1-4 strai

259 A multicopy suppressor screen for genes capable of returni

260 A multicopy suppressor screen revealed six genes, the over

261 A screen for multicopy suppressors of a hop2-ts allele identified the

262 We performed a screen for multicopy suppressors of arp2-7 and identified SYP1, an

263 Seven multicopy suppressors of bck2Delta swi6-ts mutants were

264 ial proteins (e.g. MTCO3) were identified as multicopy suppressors of cdc13-1, suggesting the involve

265 gh three independent genome-wide screens for multicopy suppressors of each of the three Vpr activitie

266 We have identified OXA1 and TIM17 as novel multicopy suppressors of mtDNA instability in ilv5 cells

267 protein kinase C (Pkc1p), were identified as multicopy suppressors of sth1-3ts cells.

268 otential targets for Cln3/CDK, we identified multicopy suppressors of the temperature sensitivity of

269 dentify functional partners, we screened for multicopy suppressors of the temperature-sensitive ydj1-

270 Multicopy suppressors of these insertions led to identif

271 A screening for multicopy suppressors of these Vpr activities in fission

272 re we identify several HAL genes that act as multicopy suppressors of this sensitivity and are connec

273 ia coli porin regulation was discovered from multicopy suppressors that permitted growth of cells exp

274 ESS1 in transcription by studying one of its multicopy suppressors, BYE1.

275 gene copies present in a hypermethylated and multicopy tandem array.

276 rDNA) genes in eukaryotes are organized into multicopy tandem arrays and transcribed by RNA polymeras

277 genomes by inserting site-specifically into multicopy target sites, thereby avoiding random disrupti

278 oth the deletion and/or the transposition of multicopy TEs associated with 2b-induced hypomethylation

279 ermatogenesis genes expressed premeiosis and multicopy testis genes.

280 c interaction between the instability of the multicopy transgene and the Werner Syndrome gene.

281 SID-1 is required for efficient silencing of multicopy transgenes, indicating that mobile silencing s

282 facilitating the rapid dissemination of the multicopy transposons in a weedy population.

283 Multicopy transposons rapidly disseminate through popula

284 We speculate that multicopy transposons, carrying both fitness and unfitne

285 The multicopy trr1 gene fragments in P. carinii are not tran

286 Phage HLIPs cluster with multicopy types found exclusively in Prochlorocococus, s

287 te that mutation of Rnu2-8, one of the mouse multicopy U2 snRNA genes, causes ataxia and neurodegener

288 table and correlated with methylation of the multicopy UAS.

289 een fluorescent protein (GFP) gene through a multicopy, upstream activator sequence (UAS).

290 al switches between different members of the multicopy var gene family.

291 switches in expression among members of the multicopy var gene family.

292 in Plasmodium falciparum is mediated by the multicopy var gene family.

293 d vast diversity of its highly antigenic and multicopy var genes preclude such clear clustering in en

294 hese B. anthracis Spo0E-like proteins from a multicopy vector consistently resulted in a sporulation-

295 However, expression of ubiF from a multicopy vector restores growth and Q synthesis for bot

296 oduction of the 19-kDa-lipoprotein gene on a multicopy vector to produce Delta19::pSMT181.

297 en eis was introduced into M. smegmatis on a multicopy vector, sodium dodecyl sulfate-polyacrylamide

298 We report the construction of two multicopy vectors that allow overexpression of all seven

299 Multicopy Y-chromosomal genes in human and mouse have be

300 oform derived from an internal promoter in a multicopy YAC transgenic line results in a microphthalmi