ライフサイエンスコーパス: cDNA

1 cDNA array and tumor microarray analysis shows that mRNA

2 cDNA with 5 A's may yield novel Gag product(s), while cD

3 cDNAs for Aggregate Spider Glue 1 (ASG1) and 2 (ASG2) ha

4 cDNAs were constructed by site-directed mutagenesis that

5 ased microfluidics was used to generate 1000 cDNA libraries, each from an individual pancreatic islet

6 ect as low as 200 ymol, corresponding to 120 cDNA molecules of L-gene Ebola virus with a limit of det

7 re we describe a method that allows up to 25 cDNAs to be assembled into a single baculoviral expressi

8 From these various organs, 27 cDNA libraries were generated and sequenced, resulting i

9 Similarly, transfection of AP-2alpha cDNA decreased TACE promoter luciferase activity, TACE e

10 ls transfected with human Kv7.2 and/or Kv7.3 cDNAs revealed that each of these four mutations stabili

11 Ebola virus with a limit of detection of 33 cDNA molecules.

12 g enzymes prior to rapid amplification of 5' cDNA ends (5' RACE) for HIV-1 RNA and quantitative rever

13 A cDNA encoding a 30-kDa Ae. aegypti salivary protein, des

14 We amplified a cDNA from the salivary glands of the tropical bont tick

15 crosomal, seed-specific class A LPAT2s and a cDNA from C. avigera var. pulcherrima (CpuLPATB) encodin

16 It was initially isolated as a cDNA partially complementing UV sensitivity in xeroderma

17 Creating a cDNA library for deep mRNA sequencing (mRNAseq) is gener

18 mpatible for PCR amplification to generate a cDNA library for RNAseq.

19 ing to VPE was found to be up-regulated in a cDNA-AFLP analysis of host responses of a wild peanut, A

20 Sequencing of a cDNA encoding ArPPLNP2 revealed that it comprises eleven

21 Here we report the identification of a cDNA for a DGAT1-type enzyme, designated CpuDGAT1, from

22 Here we report that a cDNA encoding a full-length, approximately 45-kDa K15P r

23 viral gene expression vector transferring a cDNA encoding an enzyme or channel protein, and targetin

24 Transfection of CD4- 293T cells with a cDNA expression library developed from a podocyte cell l

25 eplaced with human FGFR3(G380R) (FGFR3(ACH)) cDNA, the most common mutation in human ACH.

26 cells that were modified with the human ADA cDNA (MND-ADA) gamma-retroviral vector after conditionin

27 f iCLIP and related methods that can amplify cDNAs that truncate at crosslink sites and we show that

28 From these analyses, cDNAs for seven previously unreported LPATs were identif

29 Both PPM1D expression analysis and cDNA sequencing in EBV LCLs of individuals support the p

30 geted capture protocol to enrich VZV DNA and cDNA prior to whole-genome/transcriptome sequence analys

31 ng suppression subtractive hybridisation and cDNA libraries of cotton genotypes tolerant to Verticill

32 ment; hence, subsequent adapter ligation and cDNA amplification steps are exclusively applied to cP-c

33 encing with methylation-specific primers and cDNA analysis in patient neurons indicated selective exp

34 c 346 kb inversion in multiple probands, and cDNA sequencing and a splicing assay established that tw

35 ZO-1 small interfering RNA and cDNA transfection experiments emphasized regulation of C

36 Furthermore, using inducible RNAi and cDNA complementation (bromodomain- and ATPase-dead const

37 Fluorescence-activated cell sorting and cDNA-microarray analyses revealed that each subclone was

38 sing a CAV1 scaffolding domain construct and cDNAs encoding wild-type CAV1, and CAV1 phosphorylation

39 nteractions, and reagents such as stocks and cDNAs.

40 ve splicing events in real-time, without any cDNA synthesis or PCR amplification requirements.

41 y was up-regulated after transfection of AP1 cDNA in cells.

42 ificant conformational change of the aptamer-cDNA than the pure aptamer upon binding with P4, as conf

43 nts based on expression technologies such as cDNA microarrays, RNA-Seq, and cell imaging-based assays

44 with various expression technologies such as cDNA microarrays, RNA-Seq, and cell imaging-based assays

45 ed expanded screening of eutherian and avian cDNA libraries using yeast-two-hybrid and split-ubiquiti

46 ale (Eubalaena glacialis; family Balaenidae) cDNA derived from long-wavelength sensitive (LWS) cone o

47 The BART cDNA transcript remained primarily nuclear yet induced c

48 e DNA synthesis and release 3'-azido-blocked cDNA fragments in a process akin to dideoxy-Sanger seque

49 We then overexpressed a blw cDNA construct driven by either the AG or GT haplotype p

50 the AG haplotype also results in greater blw cDNA expression and a significant decrease in lifespan r

51 Furthermore, RT-qPCR analysis of stapes bone cDNA showed that SERPINF1-012 expression is reduced in o

52 encing was rescued by overexpression of BPTF cDNA.

53 ion by RNase I is efficient and when a broad cDNA size range is obtained.

54 By cDNA library screening, we identified an immune cell-spe

55 ysis of finger millet (Eleusine coracana) by cDNA subtraction identified drought responsive genes tha

56 northern bobwhite myoglobin were deduced by cDNA cloning of the coding sequence from mRNA.

57 Overexpression of p21(WAF1/CIP1), either by cDNA transfection or clinical drugs, preferentially impa

58 Gain and loss of function experiments by cDNA and siRNA transfection revealed profound effects of

59 fied, and most of the genes are validated by cDNA and RNA-seq data.

60 ybrid screenings of placenta and lung cancer cDNA libraries, which demonstrated that the long IDR lin

61 The CAR cDNA is genetically integrated in the T cell genome.

62 en using dysbindin as bait against a cardiac cDNA library to identify the cardiac dysbindin interacto

63 TALEN technology and a 7bp deletion in CERKL cDNA that caused the premature termination of CERKL.

64 the endogenous fusion protein or a chimeric cDNA leads to the formation of indolent liver tumors in

65 a novel and straightforward method to clone cDNA libraries from small quantities of input RNA.

66 sgene, TgAC1, consisting of Clrn1-UTR (Clrn1 cDNA including its 5' and 3' UTR) under the control of r

67 Using an NPHV consensus cDNA clone, replication was not observed in primary equi

68 now find that this is caused by constrained cDNA-ends, which can result from the sequence and struct

69 s procedure, it takes about 4 d to construct cDNA libraries that are ready for sequencing.

70 rminal sequences, based on the corresponding cDNA.

71 Transfection of the Fig4(Cys486Ser) cDNA into cultured Fig4(-/-) fibroblasts was effective i

72 id DCK gene modification, gRNA resistant DCK cDNA was created by the introduction of silent mutations

73 mutation introduced into an infectious DENV2 cDNA clone did not yield detectable virus by plaque assa

74 support the concept of retroelement-derived cDNA as key triggers of systemic autoimmunity in Trex1-d

75 ion sequencing on single glomus cell-derived cDNAs to eliminate contamination of genes derived from o

76 icon photonic microring resonators to detect cDNA reverse transcription products via a subsequent enz

77 Furthermore expression of Wdr35 disease cDNAs in Wdr35(-/-) fibroblasts revealed that the newly

78 hput method, we developed a T7 phage display cDNA library derived from mRNA isolated from bronchoalve

79 ed lentivirus-based human complementary DNA (cDNA) library, transfected the cells with HCV subgenomic

80 additional sequences from complementary DNA (cDNA) of seven of those individuals.

81 Aptamer-complementary DNA (cDNA) oligonucleotides were tested to maximize the signa

82 y noted, the positions of complementary DNA (cDNA)-starts depend on cDNA length in several iCLIP expe

83 The target complementary genomic DNA (cDNA) isolated from clinical samples of V. cholerae was

84 ions were found in CD247 complementary DNAs (cDNAs) cloned from the patient as well as in cDNA and ge

85 To rescue Kv4 complex downregulation, cDNA constructs encoding Kv4.3, KChIP1, and DPP10 were t

86 lecule to eliminate errors introduced during cDNA synthesis, PCR, and sequencing.

87 ne therapy with transfer of micro-dystrophin cDNA into muscles.

88 Ebola cDNA was amplified by rolling circle amplification (RCA)

89 insertion of IRAlu at the 3'-UTR of the EGFP cDNA led to a rhythmic circadian nuclear retention of th

90 PSE, which are orthologs of M-IPSE, from egg cDNA of S. haematobium Using PCR and immunodetection, we

91 unya fever (CHIKF) pandemic, we used an EILV cDNA clone to design a chimeric virus containing the chi

92 co-expression of 14-3-3- and AtWRI1-encoding cDNAs led to increased oil biosynthesis in Nicotiana ben

93 yed an in silico screen for cardiac-enriched cDNAs.

94 rescued by overexpression of wild-type EXTL3 cDNA.

95 iopsies were taken and total RNA extraction, cDNA synthesis and PCR was performed using 10 candidate

96 isolated from specimens and sorted by FACS, cDNA libraries are constructed and RNA-seq is performed,

97 SlCAT2 was cloned from tomato flower cDNA, over-produced in Escherichia coli and purified by

98 tected in less than 2 h without the need for cDNA synthesis or any other enzymatic reactions and with

99 role in site-specific cleavage of TR RNA for cDNA priming.

100 eps follow published methods (Smart-seq2 for cDNA synthesis and Nextera XT barcoded library preparati

101 n methods that use reverse transcriptase for cDNA synthesis of miRNA.

102 enetics system to recover UUKV entirely from cDNA clones.

103 port the generation of infectious SFTSV from cDNA clones and demonstrate that the behavior of recombi

104 293 cells stably transfected with human FSHR cDNA expressed FSHR signal.

105 by the transduction of mouse BM with fusion cDNAs derived from human leukemias.

106 eld sufficient quantities of RNA to generate cDNA libraries.

107 combinant Isfahan virus (rISFV) from genomic cDNA as a potential new vaccine vector platform.

108 proteins from the P. papatasi salivary gland cDNA library.

109 ection of cultured neurons with human GRIN2D cDNA harboring c.1999G>A leads to dendritic swelling and

110 The cloning of the H3R cDNA in 1999 by Lovenberg et al. allowed for detailed st

111 and tested on complementary ssDNA and on HAV cDNA.

112 omparison, nRT-PCR quantified the target HAV cDNA with a limit of detection of 6.4fg/microL.

113 cellular expression systems use heterologous cDNA-based vectors which express proteins well above phy

114 intracellular dNTP pools, and facilitate HIV cDNA synthesis.

115 DBR1) is not required for early steps in HIV cDNA formation but is necessary for synthesis of interme

116 improvement in RKO mice, but not NP housing cDNA.

117 e sheep expressing a human CAG-expansion HTT cDNA transgene.

118 By screening human cDNA library, we uncover that the Golgi resident protein

119 a large-scale expression screening of human cDNAs in zebrafish embryos.

120 Initially, a codon optimized idua cDNA expression cassette (opt-IDUA) was validated for ID

121 high-throughput RNA sequencing by impairing cDNA synthesis.

122 cDNAs) cloned from the patient as well as in cDNA and genomic DNA from other individuals, suggesting

123 iation and mismatches of alleles detected in cDNA and gDNA suggesting that some loci have undergone p

124 red emission) increases with the increase in cDNA concentration.

125 The WD appears to play a role in cDNA synthesis by the ORF2p molecule, despite being outs

126 leotide polymorphism (SNP) discrimination in cDNAs from human breast cancer cell lines, which makes s

127 unreported LPATs were identified, including cDNAs from Cuphea viscosissima (CvLPAT2) and Cuphea avig

128 , supplemented with sequencing of individual cDNAs.

129 ice genotype (Hasawi), a salt-stress-induced cDNA expression library was constructed and subsequently

130 aring the 197-aa deletion from an infectious cDNA clone of the highly virulent PEDV PC22A strain (inf

131 We report an infectious cDNA clone of ZIKV that was generated using a clinical i

132 The infectious cDNA clone was further used to generate a luciferase ZIK

133 underlying molecular mechanism for inhibited cDNA synthesis, we developed a deep sequencing strategy

134 SpISO-seq requires less than 1 ng of input cDNA, limiting or removing the need for prior amplificat

135 with the reverse transcription of mRNA into cDNA, a process that can introduce strong signal variati

136 ntrol groups) for reverse transcription into cDNA, preamplification and then real time quantitative p

137 -containing rhodopsin (sgRho) vs. intronless cDNA in ameliorating retinal disease phenotypes in a rho

138 n isopentenyl pyrophosphate isomerase (IPPI) cDNA, AaIPPI1, from Artemisia annua (Aa).

139 To this end, we screened a kidney cDNA library through a yeast two-hybrid assay using NKCC

140 tive phosphoproteomics with mammalian kinome cDNA library screen.

141 ssary for synthesis of intermediate and late cDNA products.

142 ced, polyadenylated BART RNAs, a full-length cDNA clone of one of the BART isoforms was obtained and

143 In this study, we constructed a full-length cDNA clone of SL-CoV WIV1 (rWIV1), an ORFX deletion muta

144 We first constructed a stable full-length cDNA clone of ZIKV in a novel linear vector from which i

145 rms because it fails to sequence full-length cDNA copies of RNA molecules.

146 The full-length cDNA encodes a type-I IPPI containing a plastid transit

147 In this work we cloned a full-length cDNA encoding an LPXRFa precursor in the European sea ba

148 In this study, a full-length cDNA encoding CPR was cloned and characterized from T. c

149 To address this we have cloned a full-length cDNA encoding the P. xylostella RyR and established clon

150 created in a single step from a full-length cDNA library.

151 We isolated a full-length cDNA of a group B MPK (PgMPK4) from pearl millet.

152 ovirulence in S. sclerotiorum, a full-length cDNA of the 14,538-nt viral genome was cloned.

153 The full-length cDNA sequence for this molecule was obtained by means of

154 Here, we report the full-length cDNA sequence of croaker elovl4, which contained 1794 bp

155 fication of cDNA ends (RACE) and full-length cDNA sequencing, revealed four independent promoters, pr

156 The full-length cDNA was cloned into a baculovirus expression vector, an

157 e isolated and characterized the full-length cDNA, gDNA and a putative promoter of a RIOK-2 protein k

158 Two full-length cDNAs (1,179 bp each), ReCHS1 and ReCHS2, encoding uniqu

159 Here, two ELO full-length cDNAs (TmELO1, TmELO2) from the yellow mealworm (Tenebri

160 Using the sequences of full-length cDNAs from W22, we found that the error rate of PacBio s

161 and Pacific Biosciences (PacBio) full-length cDNAs to identify 104,091 high-confidence protein-coding

162 y enriched and sequenced copepod full-length cDNAs, which led to the characterization of copepod tran

163 T primers and processed into adapter-ligated cDNA libraries that were sequenced using an Illumina pla

164 f lncRNAs in human CML cells using an lncRNA cDNA microarray and identified an lncRNA termed lncRNA-B

165 the mouse COX-2 gene upstream of luciferase cDNA to characterize COX-2 basal transcriptional regulat

166 ntiviral complementation with wild-type MDH2 cDNA restored MDH2 levels and mitochondrial MDH activity

167 ecome the gold standard technique to measure cDNA and gDNA levels but the resulting data can be highl

168 hybridization-based targeted RNA-Seq method, cDNA-smMIPs are a cost-effective high-throughput tool fo

169 Using over 7 million cDNA sequences from both pyrosequencing and Sanger seque

170 enerated recombinant proteins from the mouse cDNAs encoding the Hsp90alpha-Delta and wild-type Hsp90a

171 tering nanobodies using an animal-free, mRNA/cDNA display technology.

172 ns, most of which were supported by multiple cDNA evidence (72%) while only 20% of them have coding c

173 nes RNA barcoding and generation of multiple cDNA copies per RNA molecule to eliminate errors introdu

174 Using site-directed mutagenesis, cDNAs were generated in which Tyr(99) or Tyr(138) of CaM

175 observed after overexpression of the mutant cDNA.

176 When mutant cDNAs were transfected into HEK293FT cells, both variant

177 s to control viral replication we cloned Mx1 cDNAs from three bat families, Pteropodidae, Phyllostomi

178 Three mutant NCKX4 cDNAs represent mutations found in the SCL24A4 gene and

179 with AI and OCA6 into human SLC24A4 (NCKX4) cDNA leading to single residue substitutions in the muta

180 biogenesis that were corrected with NDUFAF6 cDNA transfection.

181 igenetic changes of subretinal delivering NP-cDNA vs. NP-sgRho in the RKO mouse eyes.

182 The obtained cDNA sequences were translated into protein sequences, w

183 ) Polymerase-Mediated Rapid Amplification of cDNA Ends (PPM-RACE).

184 licing patterns using rapid amplification of cDNA ends (RACE) and full-length cDNA sequencing, reveal

185 stem combined with 5' rapid amplification of cDNA ends (RACE), in vitro transcription assays, real-ti

186 Using 3' rapid amplification of cDNA ends (RACE), we mapped the 3' end of the N and NSs

187 action, and 3' and 5' rapid amplification of cDNA ends analyses.

188 orthern blotting, and rapid amplification of cDNA ends methods.

189 s this based on RACE (rapid amplification of cDNA ends) and long-read RNA sequencing.

190 me were determined by rapid amplification of cDNA ends.

191 ffected plants employing massive analysis of cDNA ends (MACE) and RT-qPCR.

192 Analysis of cDNA extracted from patient lymphocytes unexpectedly fai

193 Analysis of cDNA libraries specific for transcripts bearing a 5'-tri

194 This method permits the generation of cDNA libraries from sub-picogram quantities of RNA robus

195 Metabolic mapping of cDNA reads from strain SN2 based on KEGG pathway showed

196 Overexpression of cDNA representing SGPL1 mutations resulted in subcellula

197 y annotated using morphological profiling of cDNA constructs, via a microscopy-based Cell Painting as

198 at enable highly multiplexed resequencing of cDNA target regions of approximately 100 nucleotides and

199 Deep sequencing of cDNA corresponding to the IgH V-D-J region from the cond

200 activation domain of YAP1, and sequencing of cDNA from the patient shows it does not result in nonsen

201 reparation and high-throughput sequencing of cDNA libraries from samples of small RNA is a powerful t

202 After deep sequencing of cDNA, computational analysis yields flexibility scores f

203 eloped kinetic cross-linking and analysis of cDNAs (chiCRAC), an ultraviolet cross-linking method tha

204 us-based system allows the overexpression of cDNAs of up to 2,100 nucleotides (encoding a protein of

205 contrast, we show that a broad size range of cDNAs in iCLIP allows the cDNA-starts to efficiently del

206 of complementary DNA (cDNA)-starts depend on cDNA length in several iCLIP experiments and we now find

207 f these protein isoforms, relying instead on cDNA-based transgene expression.

208 Null-allele test on cDNA from patients' fibroblasts of both families carryin

209 we show that computational analyses based on cDNAs-starts are appropriate for such methods.

210 his EB phenotype was fully rescued by BAC or cDNA complementation but not by the reduction of p53 lev

211 ontologies, and a new collection of full ORF cDNAs.

212 ulties in cloning the full-length RPGR-ORF15 cDNA that includes a purine-rich 3'-coding region; howev

213 ntified from an embryonic chicken pancreatic cDNA library in a screen for secreted factors.

214 in 1987, leading to the cloning of the Pemt cDNA.

215 Pteris vittata Pht1 cDNAs were isolated and characterized via heterologous e

216 erent graft combinations was used to prepare cDNA libraries for small RNA sequencing and to analyze m

217 single-molecule molecular inversion probes (cDNA-smMIPs) that enable highly multiplexed resequencing

218 d RNA is then reverse-transcribed to produce cDNA, with SHAPE-modified bases leading to truncated cDN

219 body-producing B cell clones at the protein, cDNA and gDNA levels, we characterized additional LAIR1

220 Expression of each of the PvPht1 cDNAs complemented the phosphate uptake defect of a yeas

221 We deduced the full-length of the RBM28 cDNA sequence and profiled its expression patterns detec

222 icry or by overexpression a miR827-resistant cDNA of NLA produced the opposite phenotype of reduced p

223 Guide RNA resistant cDNA rescue was a legitimate strategy and multiple DCK o

224 etion with RNA interference (RNAi)-resistant cDNA constructs demonstrated that VLP formation required

225 abbits by coimmunization with the respective cDNAs.

226 d RNA and PCR amplification of the resultant cDNA with gene-specific primers demonstrated the presenc

227 Quantitative RT-PCR of retinal cDNA showed greater values for these transcripts in reti

228 etic constructs, to deliver murine rhodopsin cDNA or gDNA.

229 d a Y1H system to screen a salt induced rice cDNA expression library from Hasawi.

230 In vivo assays show that this hybrid RNA-cDNA molecule is required for mutagenic transposition, r

231 16S rRNA cDNA sequencing, qPCR of mcrA transcripts, and functiona

232 We show that a single delivery of the sans cDNA by the adenoassociated virus 8 to the inner ear of

233 Sequencing cDNA showed the splice site variant led to skipping of e

234 activity in cells transfected with SERPINB7 cDNA carrying the mutation and promoted full-length SERP

235 ed transcriptome profiling and gene-specific cDNA-pyrosequencing have documented that transcriptome s

236 Deep sequencing of strand-specific cDNA libraries is now a ubiquitous tool for identifying

237 derived primarily from alignments of spliced cDNA sequences and protein sequences.

238 e FTIR analysis of extracted RNA, ds-DNA, ss-cDNA and isolated nuclei, we verified that the spectral

239 n contain mistakes originating from standard cDNA synthesis and cloning procedures.

240 gate sequencing Adaptors to the First-strand cDNA (DLAF).

241 q method that does not involve second-strand cDNA synthesis, as we Directly Ligate sequencing Adaptor

242 As, which can be attributed to second-strand cDNA synthesis.

243 ion of its RNA genome into a double-stranded cDNA copy, which is then integrated into the host cell c

244 ssay multiplex PCR-amplified single-stranded cDNAs and easily analyse and display the captured data.

245 Subsequent cDNA amplification and next-generation sequencing succes

246 erent ratios of rat alpha4 and beta2 subunit cDNA were transfected into human embryonic kidney 293 ce

247 restingly, titrating gamma2 or delta subunit cDNA levels progressively altered GABA-evoked currents,

248 unit degradation, 10-fold less delta subunit cDNA was required to recapitulate gamma2 subunit express

249 ng technology combined with Primer ID-tagged cDNA primers to efficiently quantify HIV-1 splicing at a

250 We were able to detect amplified target cDNA in all 5 cases of enteric fever; no detectable sign

251 s of higher thermal stability with cRNA than cDNA, although destabilized compared to duplexes of stan

252 Our results suggest that cDNA of the rhodopsin transgene and bacteria backbone in

253 The cDNA clone-derived RNA is infectious in cells, generatin

254 The cDNA of the mature trypsin was cloned and sequenced.

255 The cDNA sequence of OCN predicts that, like many other pept

256 road size range of cDNAs in iCLIP allows the cDNA-starts to efficiently delineate the complete RNA-bi

257 were caused by the plasmid backbone and the cDNA of the transgene, but not the intron-containing tra

258 Here, we adapt this method to direct the cDNA synthesis specifically toward the 3UTR/poly(A) tail

259 A 300 bp specific fragment from the cDNA fragment was chosen to insert into vector pFGC1008

260 ive potassium channel toxins (KTxs) from the cDNA library of M. eupeus venom glands, and we compare t

261 ith a block of degenerate nucleotides in the cDNA primer.

262 g the pDNA-nMgO complex and detection of the cDNA was accomplished by measuring changes in PL intensi

263 necessary when the original cell line or the cDNA is unavailable.

264 s gene expression and it was proved that the cDNA fragment was relevant to the cellulose biosynthesis

265 sed on the primers designed according to the cDNA sequence of MAF-1.

266 tomato phytaspase genes were identified, the cDNAs were cloned and the recombinant enzymes were obtai

267 These cDNAs were expressed in transgenic plants of a PORB-defi

268 dine-to-uridine-driven hypermutation of this cDNA.

269 In this study, three cDNA libraries from ovules of radish before and after fe

270 ation, ordering of scaffolds by alignment to cDNA sequences, incorporation of other map and sequence

271 ethyl group on these modified bases prior to cDNA synthesis using enzymes.

272 uplexes via a linker; reverse transcription; cDNA library amplification; and finally high-throughput

273 ll-length Arabidopsis thaliana transketolase cDNA under the control of the cauliflower mosaic virus 3

274 otype after re-expression of wild-type TRMT5 cDNA in cells derived from the affected individuals.

275 th SHAPE-modified bases leading to truncated cDNA.

276 e same line reconstituted with VEC wild-type cDNA.

277 rrent gene delivery strategies routinely use cDNA-based vectors for gene targeting; however, inclusio

278 Using cDNA microarray, quantitative RT-PCR, and immunohistoche

279 Moreover, NF-kappaB upregulation using cDNA diminished the combination effect of NTP on invasio

280 s rescued by transfection of wild-type VAC14 cDNA.

281 increase of HIV-1 RT intermediates and viral cDNA in infected resting CD4 T cells.

282 d cleave A3G-edited uridine-containing viral cDNA.

283 nfectivity factor (Vif) by deaminating viral cDNA cytosines to uracils.

284 plementary ssDNA and 6.94fg/microL for viral cDNA.

285 ugh the combined effects of inhibiting viral cDNA production and cytidine-to-uridine-driven hypermuta

286 troduction of marks of DNA damage into viral cDNA, and thereby prime it for processing by DNA repair

287 troviruses must integrate their linear viral cDNA into the host genome for a productive infection.

288 onds to defects in the accumulation of viral cDNA in the nucleus.

289 IV-1 integrase (IN) for integration of viral cDNA into human chromosome is established, studies with

290 A3H, exhibited extensive comutation of viral cDNA, as determined by the frequency of G-to-A mutations

291 retrovirus integrase (IN) inserts the viral cDNA into the host DNA genome.

292 a tetramer or octamer complex with the viral cDNA long terminal repeat (LTR) ends termed an intasome.

293 ce in situ hybridization with a set of wheat cDNAs allowed the macrostructure and cross-genome homoeo

294 5 A's may yield novel Gag product(s), while cDNA with an extra base, 7 A's, may only be a minor cont

295 profiles were compared by using genome-wide cDNA microarrays and label-free quantitative proteomics,

296 ntaining fluorinated bases form hybrids with cDNA/RNA with slightly lower stability compared to that

297 s and stable structure, which interfere with cDNA synthesis.

298 a sativa by seed-specific co-expression with cDNAs for various Cuphea FatB acyl-acyl carrier protein

299 nels, we employed HEK cells transfected with cDNAs encoding three requisite receptor subtypes: alpha7

300 ovel transfection competition assay with ZnT cDNAs to confirm that the driving force for heterodimer