ライフサイエンスコーパス: complementary DNA

1 7A) variants were generated in the mouse VWF complementary DNA.

2 lver nanoparticles (AgNPs) in the absence of complementary DNA.

3 ce at neutral pH that repels the hybridizing complementary DNA.

4 nterfering with efficient synthesis of viral complementary DNA.

5 ons was compared with the reference Na(v)1.7 complementary DNA.

6 single base pair mismatch between probe and complementary DNA.

7 are complex and identifiable only in cloned complementary DNA.

8 th constructed samples containing mutant and complementary DNA.

9 opulations of tethered vesicles that display complementary DNA.

10 noparticles modified with a different target complementary DNA.

11 A was extracted and reverse transcribed into complementary DNA.

12 be strands display very high affinity toward complementary DNA.

13 sity of the ssDNA probe, and hybridized with complementary DNA.

14 d be rescued by both human and zebrafish at3 complementary DNAs.

15 er and human TLR4 were transfected with CFTR complementary DNAs.

16 y, prefers forked substrate DNAs and anneals complementary DNAs.

17 lysis led to the identification of eight TPS complementary DNAs.

18 tifiable only in complementary DNA or cloned complementary DNA, 3 of which are novel.

19 erized the enzymes encoded by three of these complementary DNAs: a monoterpene synthase that belongs

20 ted adenovirus containing the angiopoietin-1 complementary DNA (AdAng1), on survival and lung injury

21 tified duplications 55 kilobases upstream of complementary DNA AK123120 (P = 3.6 x 10(-6)).

22 imens were processed by sequence-independent complementary DNA amplification and next-generation sequ

23 sequent translational frameshift as shown by complementary DNA analysis.

24 to aptamer molecules pre-hybridized to their complementary DNA anchor molecules immobilized on the gr

25 50% change in fluorescence intensity between complementary DNA and 1 base mismatch DNA which shows th

26 uctures consisting of mRNA hybridized to the complementary DNA and a single-stranded DNA loop, are fo

27 high sensitivity (0.7859 m(0)pM(-1)) towards complementary DNA and can be used to detect it in the co

28 Subsequently, we analyzed complementary DNA and evaluated the methylation status o

29 Furthermore, sequence analyses of ZmYuc1 complementary DNA and genomic clones revealed many chang

30 entrations by investigating the annealing of complementary DNA and RNA hairpins derived from the tran

31 te relevant biological interactions based on complementary DNA and RNA oligonucleotides that could be

32 n is moderately stabilizing when paired with complementary DNA and RNA, but less stabilizing than bot

33 te that it is destabilizing when paired with complementary DNA and RNA.

34 Variations were reproduced in the ABCB4 complementary DNA and the mutants, thus obtained, expres

35 itivities for a series of concentrations for complementary DNA and wild type versus mutant DNA hybrid

36 irus 2/2 (rAAV2/2) vector carrying the RPE65 complementary DNA, and measured visual function over the

37 Two squalene synthase (SS)-like complementary DNAs are identified in race L with one enc

38 n that becomes linear via hybridization to a complementary DNA) are described.

39 nd TGF-beta1-mediated signaling pathways and complementary DNA arrays.

40 and exchange that requires two base pairs of complementary DNA at the site of cleavage; a sequence id

41 n of the subjects' lymphocytes with KINDLIN3 complementary DNA but not CALDAGGEF1 cDNA reverses the L

42 es are not only restricted to protein-coding complementary DNAs but also include short hairpin RNAs a

43 ng human IGFBP-3 (Ad3), IGFBP-5 (Ad5), or no complementary DNA (cAd).

44 ies specific tmRNA molecules are targeted by complementary DNA capture probes that are covalently att

45 ncing (FISSEQ), in which stably cross-linked complementary DNA (cDNA) amplicons are sequenced within

46 ods typically require RNA to be converted to complementary DNA (cDNA) before measurements, even thoug

47 Ratios in complementary DNA (cDNA) dilution assays from qPCR data

48 and functional cloning, we have identified a complementary DNA (cDNA) encoding a bona fide FcmuR in h

49 ing polyA capture, 3' rapid amplification of complementary DNA (cDNA) ends, full-length cDNAs, and RN

50 In this study, we isolated a 1,520-bp complementary DNA (cDNA) for mimosinase from L. leucocep

51 d the murine phenylalanine hydroxylase (Pah) complementary DNA (cDNA) from a liver-specific promoter

52 With probe complementary DNA (cDNA) immobilized on the PEPS surface

53 When the complementary DNA (cDNA) is added, the thickness of the

54 differential gene expression analysis using complementary DNA (cDNA) libraries has been improved.

55 Using a subtracted complementary DNA (cDNA) library and sequence informatio

56 diated polymerase chain reaction (LMPCR) and complementary DNA (cDNA) library construction.

57 rther advance its utility in high-throughput complementary DNA (cDNA) library screening, we report th

58 teracting protein by screening a human liver complementary DNA (cDNA) library using mammalian two-hyb

59 a cells with a pooled lentivirus-based human complementary DNA (cDNA) library, transfected the cells

60 combined laser capture microdissection with complementary DNA (cDNA) microarray analysis.

61 r stem/progenitor cells (FLSPC) versus AL by complementary DNA (cDNA) microarray technology.

62 human HCC gene expression data obtained from complementary DNA (cDNA) microarrays and corresponding D

63 d discriminant analysis typically applied to complementary DNA (cDNA) microarrays.

64 ndividuals and 756 additional sequences from complementary DNA (cDNA) of seven of those individuals.

65 Aptamer-complementary DNA (cDNA) oligonucleotides were tested to

66 Compared with complementary DNA (cDNA) or messenger RNA (mRNA) microar

67 Analysis of allelic imbalance in complementary DNA (cDNA) samples from human liver (n = 2

68 the sea floor, represented by over 1 billion complementary DNA (cDNA) sequence reads.

69 Several procedures for RNA extraction and complementary DNA (cDNA) synthesis were compared for the

70 s inhibiting reverse transcription and viral complementary DNA (cDNA) synthesis.

71 ine brain endothelial cells (ECs) with MMP-9 complementary DNA (cDNA) using pc DNA3.1 (+)/Myc-His A e

72 struct containing full-length mouse fetuin-A complementary DNA (cDNA), linked to a His-tag, to the li

73 As previously noted, the positions of complementary DNA (cDNA)-starts depend on cDNA length in

74 orescence enhancement in the presence of its complementary DNA (cDNA).

75 e nucleotide polymorphisms (SNPs) in SLC22A1 complementary DNA (cDNA).

76 cells by supplementation with wild-type K14 complementary DNA (cDNA).

77 adeno-associated virus (AAV) carrying RPE65 complementary DNA (cDNA).

78 was replaced with a lacZ (beta-gal) reporter complementary DNA (cDNA; IkappaB alpha(+/lacZ)) suggests

79 Multiple mutations were found in CD247 complementary DNAs (cDNAs) cloned from the patient as we

80 functionally characterized three strawberry complementary DNAs (cDNAs) that encode proteins with hig

81 have cloned rat ALT isoenzyme ALT1 and ALT2 complementary DNAs (cDNAs), examined their tissue expres

82 Here we report the complementary DNA cloning and systematic analysis of all

83 Based on transcriptome analysis, full-length complementary DNA cloning, and characterization of expre

84 ated SPR chip has been used to detect target complementary DNA concentration by monitoring the change

85 coma cells were transiently transfected with complementary DNA constructs encoding cd-rap, in the pre

86 The expression of a complementary DNA containing only the coding region of M

87 We cloned a full-length complementary DNA (cotton PHYTOCYANIN-LIKE ARABINOGALACT

88 tocol for converting regular DNA into pseudo-complementary DNA could improve the performance of oligo

89 able, ultraviolet light-based method to bond complementary DNA covalently.

90 Restriction factors, such as the retroviral complementary DNA deaminase APOBEC3G, are cellular prote

91 of crystal structures of cLNA modified self-complementary DNA decamer duplexes revealed that the met

92 the wild-type complementary DNA, the mutant complementary DNA depressed VWF secretion, although mult

93 Ectopic expression of a HAB1 complementary DNA derived from wild-type mRNAs partially

94 Complementary DNAs derived from the LCM-collected SAMs w

95 Upon hybridization with its complementary DNA, desorption of the nanostructures take

96 For this purpose we chose a non-self-complementary DNA duplex containing the biologically-rel

97 material for nanoscale construction because complementary DNA duplexes are programmable and structur

98 encoding genes were isolated and cloned from complementary DNA (EcNHX1-EcNHX4).

99 A complementary DNA encoding either Cre recombinase or a t

100 eno-associated virus serotype 9 carrying SMN complementary DNA encoding the missing SMN protein.

101 Morphology was specifically restored by complementary DNAs encoding forms of muskelin with full

102 tion of C4 photosynthesis in this group, the complementary DNAs encoding four distinct beta-carbonic

103 ALK complementary DNAs encoding the F1174L and R1275Q varian

104 ne reporter analysis, rapid amplification of complementary DNA ends (RACE), chemical inhibition exper

105 Using 5' Rapid amplification of complementary DNA ends (RACE), two transcriptional start

106 RNA ligase-mediated rapid amplification of complementary DNA ends analysis validated SQUAMOSA PROMO

107 ' RNA ligase-mediated rapid amplification of complementary DNA ends identified 2 novel ERBB4-truncate

108 Using rapid amplification of 5' complementary DNA ends in human brain, we identified a p

109 Here we combined 5' rapid amplification of complementary DNA ends PCR with deep sequencing to quant

110 ining of double-strand breaks (DSBs) with no complementary DNA ends that rely primarily on MMEJ repai

111 dentified by 5' RACE (rapid amplification of complementary DNA ends).

112 ction, polyA tail, 3' rapid amplification of complementary DNA ends, Southern blot, immunoblot, histo

113 as then assayed by 5' rapid amplification of complementary DNA ends.

114 polymorphism, markers, QTL and alignments to complementary DNAs, ESTs and protein homologs.

115 LX2 cells transfected with AZIN1 full-length complementary DNA expressed 35% less collagen I mRNA (P

116 hereas the control reporter is an intronless complementary DNA expression cassette.

117 We employed a designed complementary DNA featuring a guanine-rich section in it

118 four output files: a gene prediction file, a complementary DNA file, an alignment file, and a gene fe

119 peptide encompassing the H3.3K27M mutation, complementary DNA for T cell receptor (TCR) alpha- and b

120 In this study, complementary DNAs for each gene were overexpressed to d

121 eq for mapping transcribed regions, in which complementary DNA fragments are subjected to high-throug

122 In this study, we sequenced complementary DNA fragments of cultured human B-cells an

123 The biosensor has the ability to detect complementary DNA fragments with a detection limit down

124 criptomes on the basis of deep sequencing of complementary DNA fragments, yielding a digital inventor

125 found in 4 of 5 patients, and sequencing of complementary DNA from affected patients confirmed that

126 Sequence analysis of aggrecan complementary DNA from an affected individual revealed h

127 in reaction on the affected exon junction in complementary DNA from blood total RNA.

128 We sequenced complementary DNA from bone marrow of 47 refractory anem

129 ptome variation across mammals, we sequenced complementary DNA from nine tissues from four mammals an

130 amplified by polymerase chain reaction using complementary DNA from renal tissue and cloned in frame

131 Coexpression of Fah complementary DNA from the transposon vector allowed for

132 We sequenced polyadenylated RNA-derived complementary DNAs from 92 psoriatic and 82 normal punch

133 When complementary DNAs from barley MTs were expressed in Cu-

134 e probes which have been hybridized to their complementary DNA, GNPs and MNPs, via the hydrogen, elec

135 ing reverse transcription and formation of a complementary DNA, has been observed in the non-homologo

136 kinetics for different DNA sequences, where complementary DNA homopolymers are adsorbed faster than

137 Here, we show by expression of the des complementary DNA in Escherichia coli that DES has the c

138 d virus vector (AAV) expressing a normal ND4 complementary DNA in patients with a G to A mutation at

139 expression of a Brassica napus ACBP (BnACBP) complementary DNA in the developing seeds of Arabidopsis

140 by adenoviral expression of a CaR antisense complementary DNA inhibited Ca(2+)(o)-induced activation

141 pod super green fluorescent protein (copGFP) complementary DNA, inserted at the Kit locus, were gener

142 ribonucleases, DSB repair proceeds through a complementary DNA intermediate, whereas in their absence

143 Transient transfection of AZIN1 SV2 complementary DNA into LX2 cells reduced collagen I gene

144 tion of Gp1ba promoter-driven human alphaIIb complementary DNA into the AAVS1 locus of iPSCs led to h

145 al of our strategy by targeting a corrective complementary DNA into the IL2RG gene of HSCs from healt

146 Sequence analysis was performed on viral complementary DNA isolated from serum specimens collecte

147 n reaction and direct RNA sequencing without complementary DNA isolation.

148 xtracellular coding region of a maize zmbri1 complementary DNA knocked down the expression of all fiv

149 assembled 277,224,180 Illumina reads from 12 complementary DNA libraries to build what is to our know

150 Complementary DNA libraries were sequenced by Solexa.

151 yzed from GT:CD46 and GTKO porcine aortic EC complementary DNA libraries, respectively.

152 In a functional screen of mammalian complementary DNA libraries, we identified moesin as a n

153 rstand the PA pathway in tea, we generated a complementary DNA library from leaf tissue of the bliste

154 Using a complementary DNA library screen, we identified the tran

155 Here we show, using an iterative complementary DNA library screening approach, that human

156 as used as bait to screen a yeast two-hybrid complementary DNA library specific for regenerating live

157 cising floral organs, and used to generate a complementary DNA library.

158 ture, and self-complementary versus non-self-complementary DNA linker strands (1- versus 2-component

159 and fusion are mediated by hybridization of complementary DNA-lipid conjugates inserted into the two

160 We previously showed that complementary DNA-lipids, inserted into small unilamella

161 lls were similarly analyzed and also used in complementary DNA microarray analyses.

162 Laser capture microdissection-coupled complementary DNA microarray analysis is a powerful tool

163 Complementary DNA microarray analysis was performed on I

164 the hippocampus was analyzed by genome-wide complementary DNA microarray analysis.

165 rom 9 obese subjects was analyzed by using a complementary DNA microarray at baseline after weight lo

166 Multiple biological and technical complementary DNA microarray replicates allowed rigorous

167 A recent complementary DNA microarray study identified a gene-exp

168 New molecular technologies such as complementary-DNA microarray have the potential to incre

169 cluded hepatic gene expression profile using complementary DNA microarrays, genotype at the IL28B SNP

170 cooling, over several days, of solutions of complementary-DNA-modified nanoparticles through the mel

171 noparticles mediated by interactions between complementary DNA molecules attached to the nanoparticle

172 s with perfect-matched and single-mismatched complementary DNA molecules were examined by using circu

173 s of the long-range stem interaction using a complementary DNA oligomer, which effectively shifts the

174 proach, linear copolymers were prepared from complementary DNA oligomers containing covalently attach

175 reduced through hybridization with a set of complementary DNA oligomers labeled with a fluorescence

176 achieved by annealing two partly-overlapping complementary DNA oligonucleotides for insertion into an

177 bit the nucleocapsid-chaperoned annealing of complementary DNA oligonucleotides to the TAR and RRE-II

178 which are novel; and 6 identifiable only in complementary DNA or cloned complementary DNA, 3 of whic

179 that ubiquitously expressed the human Foxm1b complementary DNA or mice in which the Foxm1 fl/fl targe

180 mixed samples, SC probes covalently capture complementary DNA or RNA oligo targets and reject two-nu

181 oorthogonal cycloaddition in the presence of complementary DNA or RNA templates.

182 ave a higher melting temperature with either complementary DNA or RNA, whereas the remaining PMO anal

183 ere engineered to express an inducible Mist1 complementary DNA or to express a short hairpin RNA that

184 es were validated using individual sgRNA and complementary DNA overexpression.

185 Here we use pyrosequencing of complementary DNA-PCR amplicons as a general approach to

186 m tests and overexpression of wild-type RGP2 complementary DNA placed under the control of the 35S pr

187 2-aminoethylglycyl (aeg)-PNA is better with complementary DNA (PNA:DNA) than with complementary RNA

188 hybridized with excess fluorescently labeled complementary DNA probes.

189 sed 454 sequencing to generate 391,157 brain complementary DNA reads, resulting in robust hits to 301

190 ominent increases in thermal affinity toward complementary DNA relative to reference strands (average

191 ric selectivity: Hybridization kinetics with complementary DNA remains nearly unaffected, but interac

192 Overexpression of complementary DNA represents the most commonly used gain

193 Complementary DNA rescue and localization experiments in

194 Sequencing of complementary DNA revealed heterozygous transcripts lack

195 applied direct high-throughput sequencing of complementary DNAs (RNA-Seq), supplemented with data fro

196 between the lower portion of DNA S1 and its complementary DNA S2 formed an identical double-stranded

197 er portion of DNA S1 was hybridized with its complementary DNA S3 modified on AuNPs to bring the DNA

198 ingle-stranded DNA (ssDNA), or dimeric, self-complementary DNA (scDNA) genomes.

199 Functional complementary DNA selection for a receptor mediating KSH

200 h a retroviral vector encoding the human ADA complementary DNA sequence (GSK2696273) as part of singl

201 These results suggest that annealing of self-complementary DNA sequence engages an alternative telome

202 inant products (derived from the full-length complementary DNA sequence of human factor VIII), second

203 Using Fc as a quencher label on a complementary DNA sequence, an intramolecular ECL quench

204 eaks in DNA upon RNA-guided recognition of a complementary DNA sequence, which strictly requires the

205 ology search and engages in pairing with the complementary DNA sequence.

206 fied samples were also tested for binding of complementary DNA sequences and the results were less st

207 to form pcPNA-pcPNA duplexes but can bind to complementary DNA sequences by Watson-Crick pairing via

208 driven by native regulatory regions and from complementary DNA sequences driven by the constitutive m

209 he reversibility of the interactions between complementary DNA sequences is an advantage.

210 nscriptomic' studies have reported that many complementary DNA sequences shared no significant homolo

211 gated to proteins of interest, contain short complementary DNA sequences that provide additional bind

212 to form pcPNA-pcPNA duplexes but can bind to complementary DNA sequences via double duplex-invasion c

213 No-complementary and complementary DNA sequences were clearly discriminated a

214 on containing PcGs binding sites and miR-223 complementary DNA sequences, evolutionarily conserved in

215 Moreover, upon comparison of DNA and complementary DNA sequences, we discovered cytidine-to-u

216 ng or other techniques based on annealing of complementary DNA sequences.

217 ive to the presence of a large excess of non-complementary DNA sequences.

218 cid bases (LNAs) have increased affinity for complementary DNA sequences.

219 cell adhesion to other surfaces coated with complementary DNA sequences.

220 anding of psoriasis, we used high-throughput complementary DNA sequencing (RNA-seq) to assay the tran

221 polymerase chain reaction with cloning, and complementary DNA sequencing were used to confirm pathog

222 ree multigene cassettes containing up to six complementary DNAs/short hairpin RNAs.

223 on of the synthesis and properties of pseudo-complementary DNA should lead to an ideal target for use

224 atched that encoded by a recently identified complementary DNA (SlGOMT1) from a white campion flower

225 eloped for MBs, we report on the analysis of complementary DNAs specific for fruitless (fru) and Ods-

226 double stranded DNA (dsDNA, hybridized), non-complementary DNA (ssDNA, un-hybridized) and single nucl

227 and microscale self-assembly processes, with complementary DNA "sticky ends" as one of the most notab

228 erature induced melting transition of a self-complementary DNA strand covalently attached at the 5' e

229 d in a surface-tethered vesicle encounters a complementary DNA strand from another vesicle indicates

230 Changes in surface stress occur when one complementary DNA strand melts and diffuses away from th

231 y hRad52 occurred most efficiently when each complementary DNA strand or each ssDNA-hRPA complex was

232 We then site-selectively attached the complementary DNA strand to the N-terminus of a protein.

233 a heterogeneous competitive exchange with a complementary DNA strand which breaks PSA-aptamer intera

234 hich unwinds this intermediate to reveal the complementary DNA strand with a 5'-end that is degraded

235 A hybridized to RNA, as well as the expelled complementary DNA strand.

236 t of one DNA strand while annealing a second complementary DNA strand.

237 cent bases, most of which are purines of the complementary DNA strand.

238 viral RNA that is hybridized at one end to a complementary DNA strand.

239 The chemical bond between the two complementary DNA strands can be reversibly broken upon

240 LGA alone shows minimal DNA loading, and non-complementary DNA strands do not get encapsulated within

241 tches that could arise during replication of complementary DNA strands to account for any particular

242 model system that uses the hybridization of complementary DNA strands to model the formation of the

243 (5' to 3' translocase), that operate on the complementary DNA strands to unwind duplex DNA.

244 The rezipping force of two complementary DNA strands under tension has been measure

245 N-terminal region of Rad52, which can anneal complementary DNA strands, and is independent of its Rad

246 terstrand cross-links (ICLs) covalently link complementary DNA strands, block DNA replication, and tr

247 Transcription requires unwinding complementary DNA strands, generating torsional stress,

248 es are prepared through the self-assembly of complementary DNA strands.

249 RNAs (miRNAs) can be produced from the fully complementary DNA strands.

250 recognition and highly selective binding of complementary DNA strands.

251 recently shown to also facilitate pairing of complementary DNA strands.

252 cripts, and protein-binding sites on the two complementary DNA strands.

253 o those of bimolecular association of small, complementary DNA strands.

254 thesized, and hybridize efficiently with the complementary DNA strands.

255 small interfering DNAs guide TtAgo to cleave complementary DNA strands.

256 interleukin-2 receptor gamma-chain (gammac) complementary DNA successfully restored immunity in most

257 and chromosomal integration of nascent viral complementary DNA suppressed.

258 eled DNA oligonucleotides to bind and unbind complementary DNA suspended between two trapped beads.

259 ously perform proximity extension assays and complementary DNA synthesis in the same reaction.

260 ermore, we demonstrate that the amount of L1 complementary DNA synthesized by L1 reverse transcriptas

261 PNAs were found to be specific toward their complementary DNA target as seen from their significantl

262 B. melitensis) based on the screening of its complementary DNA target by using two different newly de

263 ne-reactive commercial microarray slides and complementary DNA target hybridization using fluorescenc

264 ates of individual probes in the presence of complementary DNA target influences the electrode potent

265 analyte (Bmax) values for the interaction of complementary DNA target with the immobilized DNA probes

266 wing a high degree of specificity toward the complementary DNA target, as well as single-base mismatc

267 uctance of the nanotube in the presence of a complementary DNA target.

268 to form an "E-DNA" sensor responsive to its complementary DNA target.

269 tal data showed that the interaction between complementary DNA targets and probe 1 is more effective

270 ense) uses CRISPR RNA (crRNA) guides to bind complementary DNA targets at sites adjacent to a trinucl

271 acids) display extraordinary affinity toward complementary DNA targets due to favorable preorganizati

272 ) enabled sensitive detection and capture of complementary DNA targets in the presence of complex med

273 zed MO or DNA "probe" strands hybridize with complementary DNA "targets" from solution, both the MO-D

274 d in a predetermined linear arrangement to a complementary DNA template that was chemoselectively mod

275 e-DNA (P-DNA) molecules on a surface through complementary DNA tethers directing cells to adhere and

276 A detection without reverse transcription to complementary DNA that is faster, simpler, and less pron

277 ected in equal quantities with the wild-type complementary DNA, the mutant complementary DNA depresse

278 biotinylated DNA probes with mutant DNA and complementary DNA, the resulting duplex DNA helixes were

279 ong biotinylated DNA probes, mutant DNA, and complementary DNA, the resulting duplex DNA helixes were

280 ately stable parallel stranded duplexes with complementary DNA, they do not form stable hybrids with

281 , was used in combination with a fluorescent complementary DNA to create dense clusters of fluorescen

282 rrection of ribosomal protein deficiency via complementary DNA transfer into the "safe harbor" AAVS1

283 e model expressing a full-length ATXN2(Q127)-complementary DNA under control of the Pcp2 promoter (a

284 notype of eda9 was complemented with an EDA9 complementary DNA under the control of a 35S promoter (P

285 mRNA expression by targeted resequencing of complementary DNA using single-molecule molecular invers

286 everse transcriptases, produce virus-derived complementary DNAs (vDNA).

287 replications of DPV measurement of 0.2microM complementary DNA was 4.88%.

288 Norovirus complementary DNA was amplified by overlapping polymeras

289 Hg(2+) leads to DNA hybridization, in which complementary DNA was captured onto the biosensor surfac

290 equence of the 5'-flanking region of mVGLUT2 complementary DNA was cloned.

291 METHODS AND Complementary DNA was prepared from C57BL/6-mice subject

292 The porcine complementary DNA was recovered by polymerase chain reac

293 injection of adenovirus expressing the HNF6 complementary DNA was used to increase hepatic HNF6 leve

294 4A, E562A, and E564A mutants containing self-complementary DNA were compared with virus containing si

295 Transporter complementary DNAs were also expressed in the companion

296 Complementary DNAs were transfected into HEK293 cells.

297 acid (Fc-PNA) and a Fc-PNA hybridized with a complementary DNA, while the DNA polymerase-assisted tar

298 detection limit of approximately 500 aM for complementary DNA with a linear dynamic range up to 10(-

299 idizing these fluorescent oligomers to short complementary DNAs with varied bases opposite the xDNA b

300 ence of a DNA toehold in a similar manner to complementary DNA, with kinetic details specific to the