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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 RNA gene (SL RNA) repeat is present in large multicopy arrays and has been used as a marker for the d
9 the hypodermis and vulva when expressed from multicopy arrays.
10 ated against single-copy (pyrG and ARG4) and multicopy (arsC) controls.
11 om the beta-lactamase signal sequence in the multicopy Asd(+) pYA3493 vector to create pYA3494.
12 ates independent of copy number variation in multicopy ChrY gene families that influence susceptibili
13 ral variation in copy number of Sly and Rbmy multicopy ChrY genes.
14 ify novel mutator effects resulting from the multicopy cloning (MCC) of specific genes and therefore
15                                            A multicopy cloning approach was used to search for metage
16 with flanking SNP genotypes, the majority of multicopy CNPs do not (40% with r > 0.8).
17  range from 28 to 348 bp, and the lengths of multicopy CREE appear mainly in the ranges of 154 to 156
18 ies demonstrated that deletion of the entire multicopy cysteine protease B (CPB) gene array in L. mex
19 ive to QseBC was mapped, and single-copy and multicopy deletion analyses were performed to determine
20 t, the native tatA gene of Prov. stuartii in multicopy did not suppress an aarA mutation.
21 yed octapeptides and avidity effect of their multicopy display on the phage scaffold, good biocompati
22                 We determined the single and multicopy distribution of distinct viral cell junctions
23 -Asp-pThr-Asp motifs, recently identified as multicopy docking sites within Mdc1, are evolutionarily
24 s tended to be differentially expressed, and multicopy duplicate genes were likely to diverge express
25                             A screen using a multicopy E. coli library led to identification of the r
26 t to (i) complementation; (ii) dominance and multicopy effects; (iii) interaction with wild-type FliH
27                       Ty1 transcription of a multicopy element expressed from the GAL1 promoter aboli
28                                      Because multicopy elements can facilitate genomic recombination
29  of the null mutant with the LmGT4 gene on a multicopy episomal expression vector also reverted these
30 atent, with the viral genome persisting as a multicopy episome and expressing only a small subset of
31 binding to KSHV terminal repeat DNA mediates multicopy episome persistence.
32 circularized viral genome is maintained as a multicopy episome.
33 asmids to persist in dividing human cells as multicopy episomes that attach to chromosomes during mit
34 virus (EBV) establishes latent infections as multicopy episomes with complex patterns of viral gene t
35 fA or mifB increased flagellin levels, while multicopy expression decreased them.
36                                              Multicopy expression of brlR in a DeltasagS mutant resto
37              In contrast to the csrA mutant, multicopy expression of csrA repressed transcription fro
38 ster carrier Nfu and partially suppressed by multicopy expression of either sufA or nfu, suggesting f
39     This inhibition can be suppressed by the multicopy expression of mex67 suggesting that Mex67p can
40                                 Furthermore, multicopy expression of mifA induced other phenotypes kn
41                                              Multicopy expression of msc1 robustly suppresses a tempe
42                       Finally, we found that multicopy expression of sypG resulted in robust biofilm
43 boratory conditions, but could be induced by multicopy expression of sypG, which encodes a response r
44  biofilm formation and a hyperswarmer, while multicopy expression of this gene promotes sessility.
45                                              Multicopy expression plasmids encoding essential MOB1 or
46                     A series of SSB-encoding multicopy expression plasmids were introduced into reeng
47                                              Multicopy extragenic suppressors were selected in strain
48                                              Multicopy FAA4 could not suppress the growth defect in t
49        Ribosomal RNAs (rRNAs) are encoded by multicopy families of identical genes.
50 ated Bcl-X(L) transgenic mice that contain a multicopy Flag-tagged mouse Bcl-x(Flag) transgene driven
51                      Moreover, ftsA R286W or multicopy ftsQAZ, which can largely bypass the requireme
52               Intragenomic variation of this multicopy gene can interfere with accurate phylogenetic
53          Nevertheless, their genomes harbour multicopy gene clusters that were named potential mobile
54  be used as a general method to downregulate multicopy gene families in P. falciparum.
55      The distinction between single-copy and multicopy gene families is reflected in their functional
56  regulation also likely applies to the other multicopy gene families of P. falciparum.
57 asite Plasmodium falciparum contains several multicopy gene families, including var, rifin, stevor an
58                      Here, we report that 33 multicopy gene families, representing approximately 273
59 nsertions upstream of tDNAs in two different multicopy gene families.
60 en, a protein called PfEMP1, is encoded by a multicopy gene family called var.
61                                      The var multicopy gene family encodes Plasmodium falciparum eryt
62                                  The patatin multicopy gene family encodes the major storage protein
63 f variable antigens, encoded by members of a multicopy gene family named var.
64 nia in immunosuppressed patients, contains a multicopy gene family that encodes the major surface gly
65 ocyte membrane protein-1" encoded by the var multicopy gene family.
66                          MSG is encoded by a multicopy gene family; in two specific forms of rat-deri
67 ntagonists in this conflict are the X-linked multicopy gene Xmr and its multicopy MSYq-linked relativ
68                      In contrast, paralogous multicopy genes are found in the highly recombining regi
69                        Furthermore, X-linked multicopy genes exhibit a similar degree of expression a
70 entical X chromosome and CNV in Y chromosome multicopy genes exhibit sperm head abnormalities and fem
71  genome stability and organelle function and multicopy genes in signaling, transport, and metabolism.
72 test the hypothesis that CNV in Y chromosome multicopy genes influences the paternal parent-of-origin
73                 The X chromosome carries two multicopy genes related to Sly: Slx and Slxl1.
74 an and mouse sex chromosomes are enriched in multicopy genes required for postmeiotic differentiation
75 ntified on the bovine MSY (12 single- and 16 multicopy genes), 16 are bovid specific.
76 c family of miRNAs encoded by closely spaced multicopy genes.
77  vulgare) and Brassica oleracea by targeting multicopy genes.
78  copy number variation (CNV) in Y chromosome multicopy genes.
79 nce in CNV between homologous X:Y chromosome multicopy genes.
80 coli, genes encoding Vgr are associated with multicopy genetic elements designated Rhs (rearrangement
81                                            A multicopy genomic fragment from a tumor two-dimensional
82                                          The multicopy human U2 small nuclear (sn)RNA genes are trans
83 milies being either primarily single-copy or multicopy in all species.
84 ously published M. tuberculosis strains with multicopy inhA or kasAB plasmids, were tested for their
85 rtussis, and B. holmesii was developed using multicopy insertion sequences (ISs) in combination with
86      We used a unique system consisting of a multicopy integration of an estrogen receptor responsive
87 lating cells, which may obviate the need for multicopy integration to achieve high-level expression a
88 t host and thus bypasses the requirement for multicopy Kan(r); faa and ssrA mutants are additive in t
89 NA (tmRNA) (encoded by ssrA), coupled with a multicopy kanamycin resistance determinant, suppressed b
90 nii, in which the homologous PRT-1 genes are multicopy, kex1 is a single-copy gene encoding a protein
91                                          The multicopy kinetoplast DNA (kDNA) probes were the most se
92 ocumented, are also unusual in their lack of multicopy LINE-like and gypsy-like retrotransposons, gro
93                                     The Mlp (multicopy lipoproteins) family is one of many paralogous
94  point of view, our results suggest that the multicopy MD simulation approach is very useful when stu
95                                          The multicopy model demonstrates the range of atomic displac
96           To address this, we have performed multicopy molecular dynamics (MD) simulations of RT in t
97 e DNA damage sensitivity of a chk1 mutant by multicopy msc1 also requires pht1.
98                     Suppression of cnp1-1 by multicopy msc1 requires pht1.
99 Synonymous substitution rate analyses of the multicopy MSY genes indicated that two major periods of
100  are the X-linked multicopy gene Xmr and its multicopy MSYq-linked relative Sly, which are upregulate
101  regulatory mechanism controlling dispersed, multicopy MuDR/Mu elements responsible for Mutator activ
102 od stage, known as PfEMP1 and encoded by the multicopy multigene family known as the var genes.
103  conjugated to gold nanoparticles, yielding 'multicopy-multivalent' nanoscale glycoconjugates.
104 immune response are encoded in the genome as multicopy, nonallelic gene families.
105  and animal papillomavirus DNA replicates as multicopy nuclear plasmids.
106 ry components of the ribosome are encoded by multicopy nuclear ribosomal RNA (rRNA) genes: 28/26S, 18
107 -producing mutants, such as grrSA containing multicopies of the amyR gene.
108                                              Multicopy overexpression of flp-21 transformed wild soci
109 e hyperfimbriated phenotype conferred by the multicopy oxyR plasmid was absent in a type I fimbrial m
110                                            A multicopy p1 allele, P1-wr (white pericarp/red cob) is e
111 ion and small RNA targeting, relating to the multicopy paralogous genes generated from whole genome t
112 hed at centromeres, TET/JBP transposons, and multicopy paralogous genes that are not expressed, but r
113 n in plants is often associated with complex multicopy patterns of transgene integration at the same
114           In a comparison of single-copy and multicopy PCR targets in 70 tissue samples, the sensitiv
115               Nevertheless, the detection of multicopy pfmdr1 in African parasites suggests a high po
116     Second, in medium that lacked thymidine, multicopy phtC(+) or phtD(+) alleles enhanced the surviv
117                                              Multicopy plasmepsin 2 constitutes a surrogate molecular
118 treated with dihydroartemisinin-piperaquine, multicopy plasmepsin 2 in the sample collected before tr
119 day 42 fell below 90% when the proportion of multicopy plasmepsin 2 parasites exceeded 22%.
120 l and temporal increase of the proportion of multicopy plasmepsin 2 parasites was highly correlated w
121                                              Multicopy plasmepsin 2 predicted dihydroartemisinin-pipe
122                        However, grvA(+) on a multicopy plasmid also conferred the antivirulence pheno
123  mutation in acrR or acrAB expression from a multicopy plasmid also suppressed the TolCP246R,S350C de
124 decarboxylase defect was complemented from a multicopy plasmid and in single copy.
125 onsequences of overexpression of tnaC from a multicopy plasmid and observed that under inducing condi
126  the C-terminal 53 amino acids of MutS) on a multicopy plasmid are proficient for mutation avoidance.
127 nhibited by an oversupply of DnaA and that a multicopy plasmid carrying rcbA neutralizes this inhibit
128 eplication and distribution of the bacterial multicopy plasmid ColE1 in a population of exponentially
129           Expression of ptsP in trans from a multicopy plasmid complemented the lysC mutant, suggesti
130                    Expression of ExsD from a multicopy plasmid completely repressed transcription of
131                                  Further, in multicopy plasmid concatamers, each intron could only si
132 antly higher in the snr-1 mutant harboring a multicopy plasmid containing snr-1.
133                                       When a multicopy plasmid containing the amyR gene was introduce
134 igen gene promoter or in a strain carrying a multicopy plasmid containing the entire B. cereus plc-sp
135 in place of WT ftsA or with ftsA* alone on a multicopy plasmid divide mostly normally, whether they a
136 hromosomal DeltaacrB mutant transformed with multicopy plasmid encoding MdtM suggested a functional s
137                                            A multicopy plasmid encoding NarU complemented a narK muta
138  outer membrane phospholipase gene pldA on a multicopy plasmid in a vpsC or vacJ mutant restored its
139 heterocyst differentiation when present on a multicopy plasmid in Anabaena sp. PCC 7120.
140 t create mutator phenotypes when put on to a multicopy plasmid in Escherichia coli.
141  complemented by providing the ler gene on a multicopy plasmid in trans.
142 type strain, while expression of YggX from a multicopy plasmid increased the aconitase levels above t
143 NAIII in trans to the MW2 arlRS mutant via a multicopy plasmid induced autolysis in this MRSA strain.
144              Elevated dnaA expression from a multicopy plasmid induces more frequent initiation from
145   We demonstrate that DksA expression from a multicopy plasmid is necessary and sufficient for suppre
146 f the CCU/CCA/CCG-decoding tRNA(Pr)(o)3 on a multicopy plasmid leads to suppression of several +1 fra
147                                            A multicopy plasmid library of the E. coli genome can then
148 ion of the multidrug transporter MdfA from a multicopy plasmid or by growth at pH 6.0.
149  expressed either from the trc promoter on a multicopy plasmid or from the endogenous dsbA promoter b
150                                    The small multicopy plasmid pAMalpha1 (9.75 kb) encoding tetracycl
151 e its role further, comW was cloned into the multicopy plasmid pMSP3535, under the control of a nisin
152  When induced for expression, baeR cloned in multicopy plasmid pTrc99A significantly increased the re
153 d over-expression of the DinG protein from a multicopy plasmid result in a slight reduction of UV res
154                             We localized the multicopy plasmid RK2 in Escherichia coli and found that
155         Increased expression of GlxII from a multicopy plasmid sensitizes E. coli to MG.
156 partitioning locus STB of the 2mum circle--a multicopy plasmid that resides in the yeast nucleus and
157 ains containing the B. cereus plcR gene on a multicopy plasmid under control of the strong B. anthrac
158 fragments between 3 and 5 kbp in length on a multicopy plasmid vector that was transformed into E. co
159 ontaining the intact groES-groEL operon on a multicopy plasmid was generated and used to demonstrate
160 some of the TBP mutations is suppressed by a multicopy plasmid with SNR6 or by an spt3 mutation.
161         When virADeltaR was expressed from a multicopy plasmid, both sugar and the phenolic inducer w
162 ntify the genes which, when expressed from a multicopy plasmid, can restore the growth defect of the
163                        When expressed from a multicopy plasmid, DsrA was stable in both wild-type and
164 tein was expressed in the hetF mutant from a multicopy plasmid, HetR-GFP accumulated nonspecifically
165 erhelicase mutant, and when expressed from a multicopy plasmid, it results in UV sensitivity (UV(s)),
166  When each of the genes was expressed from a multicopy plasmid, M. smegmatis exported comparable prop
167              We visualized the location of a multicopy plasmid, pHP13, in living cells of Bacillus su
168 1 gene and/or the mobN1 gene was cloned on a multicopy plasmid, production of the protein was constit
169  product, when either mutated or cloned on a multicopy plasmid, seems to be capable of compensating f
170 brial phenotype in strains bearing oxyR on a multicopy plasmid.
171 o the sigma(K)-controlled gerE promoter on a multicopy plasmid.
172 oside (IPTG)-inducible promoter present on a multicopy plasmid.
173 l extract of a strain expressing mpaA from a multicopy plasmid.
174 could be complemented by providing cbpA on a multicopy plasmid.
175 g partition sites of P1 inserted in a small, multicopy plasmid.
176 A-K2378, a strain overexpressing norA from a multicopy plasmid.
177  expressed from a constitutive promoter on a multicopy plasmid.
178 d when expressed from a strong promoter on a multicopy plasmid.
179         Our results suggest a model in which multicopy plasmids are not always randomly diffusing thr
180 lly constitutive not only when produced from multicopy plasmids but also at a single-copy gene dosage
181            Furthermore, the stabilization of multicopy plasmids by Rcd is shown to be tryptophanase d
182                                              Multicopy plasmids carrying mutS alleles that are domina
183                                 In addition, multicopy plasmids containing the LSB6 gene directed the
184                Expression of efflux pumps on multicopy plasmids did not improve endogenous FFA produc
185    While the expression of these proteins on multicopy plasmids did not improve production over the b
186                                In this work, multicopy plasmids expressing either inhA or kasA genes
187                                              Multicopy plasmids expressing either ntrC or nifA from a
188                                              Multicopy plasmids expressing v-SNAREs Gos1p or Ykt6p, b
189  mltG was initially isolated in a screen for multicopy plasmids generating a lethal phenotype in cell
190                                              Multicopy plasmids in Escherichia coli are not randomly
191 harvesting complex components expressed from multicopy plasmids in strains in which the corresponding
192 o- to four-times-higher values obtained from multicopy plasmids in stringent cells and eight-times-hi
193       Experiments with ftsQAZ and ftsQA*Z on multicopy plasmids indicate that ftsQAZzipA+ and ftsQA*Z
194           Thus Rcd-mediated stabilization of multicopy plasmids is dependent upon indole acting as a
195            Here we show that expression from multicopy plasmids of mutant cspA mRNAs bearing nonsense
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 ee distinct genetic regions when harbored on multicopy plasmids.
202 n: a novel thrombin inhibitor derived from a multicopy precursor in the salivary glands of the ixodid
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  lines of evidence that a eutherian-specific multicopy retrogene, DUX4, encodes a transcription facto
207 ared origin of the two resistance-conferring multicopy Rhg1 groups and subsequent independent evoluti
208  find that SCN resistance is associated with multicopy Rhg1 haplotypes that form two distinct groups.
209                            Subdomains of the multicopy ribosomal DNA locus containing transcription u
210 lies on detecting one of the subunits of the multicopy rRNA genes.
211                                              Multicopy rscS1 activated transcription of genes within
212                                     Finally, multicopy rscS1 provided a colonization advantage over c
213  Saccharomyces cerevisiae 2-mum plasmid is a multicopy selfish genome that resides in the nucleus.
214 cular type of error in the reference genome: multicopy sequences which have been incorrectly assemble
215  OY-M genome, primarily as a result of fewer multicopy sequences, including PMUs.
216 imum lifespan was significantly increased by multicopy SGS1.
217 i, which is responsible for the synthesis of multicopy single-stranded DNA-Ec86.
218 oli and are responsible for the synthesis of multicopy single-stranded DNA.
219 uces a unique RNA-DNA hybrid molecule called multicopy single-stranded DNA.
220 , this 6-AU sensitivity can be suppressed by multicopy SNR6 or BRF1.
221                                          The multicopy subunit c of the H(+)-transporting F1Fo ATP sy
222                                              Multicopy suppression analysis implicates TPR9 in Brf1 b
223  high-mobility-group protein Nhp6, including multicopy suppression and synthetic lethality.
224  predicted target-replacer gene pairs in new multicopy suppression experiments.
225 he apparent affinities determined by in vivo multicopy suppression experiments.
226                     We use PROPER to predict multicopy suppression in Escherichia coli, achieving hig
227 rowth with pyruvate as the carbon source and multicopy suppression suggest that several other transam
228 ty is typically studied experimentally using multicopy suppression, in which over-expression of a pro
229 in B6), which we validate experimentally via multicopy suppression.
230  Proteus mirabilis, tatA was identified as a multicopy suppressor and restored extracellular signal p
231                                      Using a multicopy suppressor assay to identify genes that suppre
232                     Msc1 was identified as a multicopy suppressor capable of facilitating survival in
233                                 It acts as a multicopy suppressor for dnaJ mutations and functions in
234  Escherichia coli, is known to function as a multicopy suppressor for dnaJ mutations and to bind nons
235 e recently observed that KsgA functions as a multicopy suppressor for the cold-sensitive cell growth
236                                      Through multicopy suppressor mutagenesis, we have identified a n
237    RbfA, a 30S ribosome-binding factor, is a multicopy suppressor of a cold-sensitive C23U mutation o
238 complex), which was originally isolated as a multicopy suppressor of a cytochrome b mRNA translation
239  encodes a putative Hsp90 co-chaperone, as a multicopy suppressor of a temperature-sensitive allele (
240                     SCD5 was identified as a multicopy suppressor of clathrin HC-deficient yeast.
241 ste 12 (Su(z)12), Extra Sex Combs (ESC), and Multicopy Suppressor of IRA 1 (MSI1), and functions in m
242                    SLY41 was identified as a multicopy suppressor of loss of Ypt1, a Rab GTPase essen
243           SUR7 was originally described as a multicopy suppressor of rvs167, whose product is an acti
244     The transcription factors Msn2 and Msn4 (multicopy suppressor of SNF1 mutation proteins 2 and 4)
245 p1 and the proteasome is mediated by Sts1, a multicopy suppressor of srp1-49.
246     We isolated a novel gene, alp16(+), as a multicopy suppressor of temperature-sensitive alp6-719 m
247 des C, C, and A to the 3' end of tRNAs, is a multicopy suppressor of the defect in tRNA nuclear expor
248  isolated the transcription factor MBP1 as a multicopy suppressor of the growth and alpha-factor resp
249                We report here that SGS1 is a multicopy suppressor of the methyl methanesulphonate (MM
250 he pleiotropic drug resistance network, as a multicopy suppressor of the mitochondrial import defects
251 e identified a truncated allele of dam1 as a multicopy suppressor of the sensitivity of cdc13-117 (cy
252 NA processing and degradation pathways, is a multicopy suppressor of the synthetic lethality and of t
253          DksA was originally identified as a multicopy suppressor of the temperature sensitivity caus
254 ified the ribosome binding protein Stm1 as a multicopy suppressor of the temperature sensitivity of t
255                          SecA functions as a multicopy suppressor of the temperature-sensitive phenot
256 ized open reading frame YER074W-A as a novel multicopy suppressor of the thermosensitive yip1-4 strai
257                                            A multicopy suppressor screen for genes capable of returni
258                               We conducted a multicopy suppressor screen for genes that suppress the
259                                            A multicopy suppressor screen revealed six genes, the over
260  network t-SNARE Sed5p, also functioned as a multicopy suppressor.
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 D23 and DDI1 were identified in a screen for multicopy suppressors of the temperature-sensitivity of
271                                              Multicopy suppressors of these insertions led to identif
272                              A screening for multicopy suppressors of these Vpr activities in fission
273 re we identify several HAL genes that act as multicopy suppressors of this sensitivity and are connec
274 ia coli porin regulation was discovered from multicopy suppressors that permitted growth of cells exp
275 ESS1 in transcription by studying one of its multicopy suppressors, BYE1.
276 gene copies present in a hypermethylated and multicopy tandem array.
277 rDNA) genes in eukaryotes are organized into multicopy tandem arrays and transcribed by RNA polymeras
278  genomes by inserting site-specifically into multicopy target sites, thereby avoiding random disrupti
279 oth the deletion and/or the transposition of multicopy TEs associated with 2b-induced hypomethylation
280 ermatogenesis genes expressed premeiosis and multicopy testis genes.
281 c interaction between the instability of the multicopy transgene and the Werner Syndrome gene.
282 SID-1 is required for efficient silencing of multicopy transgenes, indicating that mobile silencing s
283  facilitating the rapid dissemination of the multicopy transposons in a weedy population.
284                                              Multicopy transposons rapidly disseminate through popula
285                            We speculate that multicopy transposons, carrying both fitness and unfitne
286                                          The multicopy trr1 gene fragments in P. carinii are not tran
287                     Phage HLIPs cluster with multicopy types found exclusively in Prochlorocococus, s
288 te that mutation of Rnu2-8, one of the mouse multicopy U2 snRNA genes, causes ataxia and neurodegener
289 table and correlated with methylation of the multicopy UAS.
290 een fluorescent protein (GFP) gene through a multicopy, upstream activator sequence (UAS).
291 al switches between different members of the multicopy var gene family.
292  in Plasmodium falciparum is mediated by the multicopy var gene family.
293  switches in expression among members of the multicopy var gene family.
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

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