ライフサイエンスコーパス: cDNA clone

1 subsequently incorporated into a full-length cDNA clone.

2 ome lineage expressed from a D. melanogaster cDNA clone.

3 d with in vitro transcripts of an infectious cDNA clone.

4 alanines by mutagenesis of an infectious FCV cDNA clone.

5 t background of a recombinant VSV infectious cDNA clone.

6 t RNA synthesis pattern was recovered from a cDNA clone.

7 to the LC coding region of an infectious FCV cDNA clone.

8 with a (32)P-labeled probe derived from the cDNA clone.

9 un cloned into a modified 1a/JFH1 infectious cDNA clone.

10 l VEEV strain originating from an infectious cDNA clone.

11 al of 68,721 ESTs were generated from 68,131 cDNA clones.

12 5' sequences from about half that number of cDNA clones.

13 enetics system to recover UUKV entirely from cDNA clones.

14 oncoding transcript represented by two IMAGE cDNA clones.

15 and derived 5' ESTs from >30,000 unique rat cDNA clones.

16 as proposed from the analysis of overlapping cDNA clones.

17 rtially sequenced over 5100 random T. reesei cDNA clones.

18 ymerase in all eight independently generated cDNA clones.

19 overed from the sequence of rhabdomyosarcoma cDNA clones.

20 t sequencing or pyrosequencing of individual cDNA clones.

21 re obtained from random sequencing of 16,152 cDNA clones.

22 collections contain principally two types of cDNA clones.

23 ae by multiple chromatographic steps, led to cDNA cloning.

24 transcription-polymerase chain reaction and cDNA cloning.

25 ikely an artifactual sequence created during cDNA cloning.

26 By use of an infectious SAT2 cDNA clone, 10 structurally exposed and highly variable

27 From 6316 cDNA clones, 3980 retinal expressed sequence tags (ESTs)

28 Of 64 Webster strain cDNA clones, 56 (87.5%) were derived from a single gene,

29 A second type of cDNA clone, a 'full-ORF' (F-ORF) expression clone, is on

30 The availability of these infectious cDNA clones affords us an opportunity to understand the

31 By combining cDNA cloning, Affymetrix (Santa Clara, CA) genechips cov

32 ese strategies--sequencing randomly selected cDNA clones, aligning protein sequences identified in ot

33 By using a "pure" culture of CTV from a cDNA clone and green fluorescent protein-labeled virus w

34 mutagenized p7 of an infectious genotype 1a cDNA clone and tested RNA transcripts of each mutant for

35 MaxT permutation analysis using t tests (20 cDNA clones and 10 unique genes), significance analysis

36 ), significance analysis for microarrays (33 cDNA clones and 15 genes, at an estimated false discover

37 For example, the value of full-length cDNA clones and deep expressed sequence tag resources, o

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

39 this system is effective for both individual cDNA clones and for cDNA libraries, permitting the direc

40 erformed a gain-of-function screen of 15,779 cDNA clones and identified 40 genes affecting exon 18 of

41 se that will aid creation of functional NPHV cDNA clones and other novel tools for hepacivirus studie

42 sion in lymphocytes determined by sequencing cDNA clones and quantifying 6FAM-labeled PCR products fo

43 Analysis of cDNA clones and RT-PCR with total mRNA revealed alternat

44 Thus, obtaining full-length cDNA clones and sequences for most or all genes in an or

45 sing differential RNA selection, full-length cDNA cloning and 454 transcriptome sequencing of the ric

46 This observation has led to the cDNA cloning and characterization of a fourth SCD isofor

47 This study describes cDNA cloning and characterization of mouse RALDH4.

48 un-based approach that led ultimately to the cDNA cloning and functional characterization of many of

49 diterpene synthase sequences for full-length cDNA cloning and functional characterization.

50 ed the expression of four of the isoforms by cDNA cloning and mass spectrometric analysis of proteins

51 fragments may have arisen in the process of cDNA cloning and not from splicing abnormalities.

52 cDNA cloning and RNA sequencing (RNA-Seq) were used to i

53 B), 22 (BCL8C), 2 (BCL8D), and 10 (BCL8E) by cDNA cloning and sequence analysis.

54 cDNA cloning and sequencing has shown that allurin is a

55 Using a library of cDNAs (1.8 x 10(6) cDNA clones) and an intermittent cisplatin selection sys

56 d myosin as determined using immunoblotting, cDNA cloning, and/or LC-MS/MS.

57 chniques; functionally related sets of human cDNA clones; and genome-scale gene collections for Sacch

58 cDNA clones are valuable reagents for functional studies

59 Libraries of cDNA clones are valuable resources for analyzing the exp

60 Using a 9,280-cDNA clone array, we have compared steady-state RNA from

61 Therefore, we constructed chimeric cDNA clones between CHIKV and VEEV or SFV to probe the e

62 ibe the construction of the first human PARG cDNA clone by reverse transcription of CF3 human fibrobl

63 Open reading frames (ORFs) derived from cDNA clones can be used to generate constructs allowing

64 Using cDNA cloning, cell culture expression, and activity assa

65 SOURCE provides content both in gene and cDNA clone-centric pages, and thus simplifies analysis o

66 We have identified a putative SWI3-like cDNA clone, CHB2 (AtSWI3B), from Arabidopsis thaliana by

67 ription-PCR and assembled into a full-length cDNA clone, clone C, which contained 14 mutations compar

68 IgE-reactive cDNA clones coding for portions of high molecular weight

69 Initial sequence analysis of our murine cDNA clone collections showed that as much as 86, 45, an

70 Subsequent studies showed that the human cDNA clone complemented an ATR-deficient bacterial mutan

71 The cDNA clone comprised an open reading frame of 1461 bp en

72 and JHM.WU and, utilizing these full-length cDNA clones, constructed chimeric viruses and mapped the

73 titutional effort to identify and sequence a cDNA clone containing a complete ORF for each human and

74 The infectivity of an RUB infectious cDNA clone containing the mutations D1210A/D1217A was de

75 solated and characterized various myotrophin cDNA clones corresponding to the multiple transcripts by

76 Ps results in matches to previously reported cDNA clones, CP2, CP3, and CP4, as well as another seque

77 reveals homologies to a previously reported cDNA clone, CP8.

78 titution of G1100D in an infectious DA virus cDNA clone demonstrated a major role for this mutation i

79 Hybridomas and cDNA clones derived from the immunized mice included man

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

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

82 We identified a tomato cDNA clone, DIG3, that encodes a protein that interacts

83 created by transfection of a genotype I HDV cDNA clone directly into the liver of a woodchuck that w

84 ill summarize the major collections of human cDNA clones, discuss some limitations common to most of

85 rging from large-scale genome sequencing and cDNA cloning efforts.

86 with the EP4 receptor as a bait identified a cDNA clone encoding a 669-amino acid protein, designated

87 cles could be rescued from a full-length FCV cDNA clone encoding a nonfunctional VP2 when VP2 was pro

88 A cDNA clone encoding a presumed full-length glycine-rich

89 In this study, a cDNA clone encoding a putative ACC oxidase, PtACO1, was

90 uences identified a single full-length maize cDNA clone encoding all the peptide sequences obtained f

91 A cDNA clone encoding alpha-conotoxin GI, the first conoto

92 ing the methods of proteomics, a full-length cDNA clone encoding an enzyme matching the properties of

93 A full-length cDNA clone encoding hebraein was isolated from a cDNA li

94 s of a zebrafish cDNA library, we isolated a cDNA clone encoding receptor activity-modifying protein

95 A cDNA clone encoding the entire 14,150-nucleotide genome

96 omplementary DNA (cDNA) library to isolate a cDNA clone encoding the ferritin heavy chain polypeptide

97 A cDNA clone encoding the human B cell alloantigen DC alph

98 A cDNA clone encoding the lignin-related enzyme caffeoyl C

99 Analysis of a cDNA clone encoding the prepropeptide precursor of pl14a

100 genomes were constructed from two infectious cDNA clones encoding a virulent and an attenuated isolat

101 interaction of CB3-RD with DAF, we produced cDNA clones encoding both CB3-RD and CB3-Nancy and mutat

102 on and sequencing of genomic and full-length cDNA clones encoding DC3.

103 We isolated several related but distinct cDNA clones encoding novel structure proteins (NSP) when

104 right Yellow-2 protoplasts identified single cDNA clones encoding proteins that interact with either,

105 equence tag database, we have identified two cDNA clones encoding putative cytosolic STs.

106 trap in yeast cells was utilized to identify cDNA clones encoding putative secreted proteins.

107 Twenty-three different cDNA clones encoding putative toxins were characterized

108 the complementary DNA (cDNA) for eNOS and 23 cDNA clones encoding the Asp-His-His-Cys motif (DHHC) pa

109 cDNA clones encoding the enzyme that synthesizes CGA, hy

110 Infectious cDNA clones encoding the marker viruses also contain uni

111 Analysis of cDNA clones encoding the novel peptides as well as those

112 of 19-kD alpha-zein genes, we characterized cDNA clones encoding these proteins from a developing en

113 t here the isolation of a complementary DNA (cDNA) clone encoding one such enzyme, mannan synthase (M

114 ent HDA+SSCP patterns were detected among 33 cDNA clones examined.

115 erminus of exon 7 in all M. nemestrina TRIM5 cDNA clones examined.

116 nify analogous doubly spliced Rej mRNAs, and cDNA clones expressing two of them also showed Rej activ

117 We describe herein the cDNA cloning, expression, and characterization of a hemo

118 We have identified this factor as the novel cDNA clone FL14676485 that encodes for the human hypothe

119 Here, we report a new cDNA clone for eIF4GI that extends the 5' sequence 340 n

120 We identified a cDNA clone for epiprofin, which is preferentially expres

121 be used at any scale, from the isolation of cDNA clones for a particular gene of interest, to the im

122 The isolation of full-length cDNA clones for each of these candidate genes resulted i

123 We isolated two corresponding cDNA clones for Sfhex that encode proteins with >99% ami

124 teins led to the identification of a 4.75-kb cDNA clone from a Strongylocentrotus purpuratus ovary cD

125 A cDNA clone from human brain encoding the mammalian homol

126 We previously sequenced an R2 cDNA clone from the yellow fever mosquito, Aedes aegypti

127 Here we demonstrate that the CRSBP-1 cDNA cloned from bovine liver libraries encodes a 322-re

128 ea mays, including ESTs representing 484,032 cDNA clones from 53 libraries and 36,565 fully sequenced

129 By screening of 1500 cDNA clones from a resistant-susceptible mosquito subtra

130 , rhinophores), we isolated five full-length cDNA clones from an A. californica central nervous syste

131 cDNA microarrays with >11,000 cDNA clones from an NOD spleen cDNA library were used to

132 ecules, MHC class I genes were identified in cDNA clones from Arabian horse A2152, which presented bo

133 striction enzymes, nor the sequencing of 130 cDNA clones from benign and malignant breast tissue and

134 Approximately 2x10(6) cDNA clones from each genotype were sequenced, correspon

135 ions against a microarray consisting of 2173 cDNA clones from five pine expressed sequence tag librar

136 echniques, we measured mRNA levels in 11 283 cDNA clones from the cerebral cortex of Tg2576 mice and

137 and searching and sequencing the NF2-related cDNA clones from the IMAGE consortium.

138 We aligned full-length cDNA clones from the Mammalian Gene Collection to the hu

139 Differential display was used to isolate cDNA clones from the three species showing differential

140 cDNA clones from the UGT2A3 gene (located on chromosome

141 A total of 11,000 cDNA clones from these libraries, representing 5,866 uni

142 b genes, Ssxb1 to Ssxb12, were identified by cDNA cloning from mouse testis and mouse tumors.

143 I), and salmon GnRH (sGnRH) were isolated by cDNA cloning from the brain of the Atlantic croaker, Mic

144 The slc5a8 cDNA, cloned from mouse kidney, codes for a protein cons

145 gene encoding Cl.ir channels in heart, ClC-2 cDNAs cloned from rat (rClC-2) and guinea pig (gpClC-2)

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

147 mutations at M-58 and E-191 in the chimeric cDNA clones further improved the viability of the chimer

148 Forty-eight of 89 (54%) sequenced cDNA clones had large deletions, each beginning and/or e

149 cDNA clones harboring viral sequences were selected and

150 cDNA clones have long been valuable reagents for studyin

151 the coding region of genes, and full-length cDNA clones have proven to be useful for investigation o

152 plication of a second virus generated from a cDNA clone, HRV-C11.

153 etermine the function of CBP, an orthologous cDNA clone (Hs CBP) was isolated from the sugar beet cys

154 Random sequencing of cDNA clones identified approximately 100 unique species.

155 cDNA cloning identified a 2733-bp transcript from AT6.1

156 Extensive cDNA cloning identified long and short forms of Xtrb2, t

157 m a single human fetal fast skeletal TnTbeta cDNA clone in order to circumvent the problem of N-termi

158 tions were introduced into an infectious FCV cDNA clone in order to evaluate the functional importanc

159 We characterized nine cDNA clones in details.

160 nes that were not represented by full-length cDNA clones in our Drosophila Gene Collection.

161 Additionally, at least 55% of the cDNA clones in this study were completely or partially a

162 CHV1-EP713 infectious cDNA clones in which the p48 coding region was deleted,

163 umber alterations across 42,000 mapped human cDNA clones, in a series of 54 gliomas of varying histog

164 Sequence analysis of these cDNA clones indicates that each clone has a unique 5' UT

165 Here, we isolated a cDNA clone Ipeglu1 encoding Ipecac alkaloid beta-D-gluco

166 The complete cDNA clone is 1.6 kb, and the gene is expressed in sever

167 The full-length zebrafish CTCF cDNA clone is 4244 bp in length with an open reading fra

168 This cDNA clone is available at the American Type Culture Col

169 cDNA cloning is a central technology in molecular biolog

170 We constructed infectious cDNA clones lacking the ER retrieval signal, the endocyt

171 A cDNA clone library of the expressed 16S rRNA corroborate

172 Some but not all of these cDNA clones may represent the entire mRNA sequence, but

173 nomic hybridization (CGH) analysis of a 4559 cDNA clone microarray.

174 Two DFR cDNA clones (MtDFR1 and MtDFR2) were isolated from the m

175 In vitro transcripts from an infectious cDNA clone mutated to eliminate potential glycosylation

176 A highly reactive cDNA clone of 1,428 bp encoded a trichomonad protein of

177 A cDNA clone of 1.1 kb encoding a 108-aa polypeptide was i

178 An infectious cDNA clone of a genotype 3 strain of hepatitis E virus a

179 We isolated a full-length cDNA clone of amphioxus AmphiNk2-tin, an NK2 gene simila

180 bovine virulence, we assembled an infectious cDNA clone of an RGD-containing A(24)Cru and derived mut

181 y site-directed mutagenesis on a full-length cDNA clone of BC.

182 th open reading frame (ORF) of an infectious cDNA clone of HCV (genotype 1a, H77 strain) in the nontr

183 An infectious cDNA clone of hepatitis E virus was mutated in order to

184 The 2861 bp cDNA clone of hGC-1 contained an open reading frame of 1

185 truction and the properties of a full-length cDNA clone of HRV16, pR16.11, which produces in vitro tr

186 Here, an infectious cDNA clone of IBV was used to address the importance of

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

188 We used a full-length cDNA clone of ONNV to construct a series of mutants in w

189 ogical disease, we constructed a full-length cDNA clone of silver-haired bat-associated RV (SHBRV) st

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

191 constructs engineered based on an infectious cDNA clone of T36 isolate of CTV, including hybrids cont

192 s in JPV, a plasmid containing a full-length cDNA clone of the genome of JPV was constructed.

193 We inserted a full-length cDNA clone of the genomic RNA of the dicistrovirus Rhopa

194 nt wild-type 88-1961 strain (r88) and from a cDNA clone of the highly attenuated Jeryl Lynn vaccine s

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

196 A partial cDNA clone of the mouse orthologue was obtained by RT-PC

197 ting of combinations of genes derived from a cDNA clone of the neurovirulent wild-type 88-1961 strain

198 A cDNA clone of unknown function, DEA1, was isolated from

199 e these mutants, we engineered an infectious cDNA clone of VSV and employed N-RNA templates from thos

200 g sequences were inserted into a full-length cDNA clone of VSV, and the virus recovery, kinetics of g

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

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

203 th IFN sensitivity and virulence, infectious cDNA clones of a virulent North American strain and the

204 Three of the seven cDNA clones of centromeric genes from rice centromere 8

205 lowing inoculation with RNA transcripts from cDNA clones of hepatitis C virus (HCV).

206 transiently in HEK293 cells using expression cDNA clones of human alpha1C, alpha2delta, and beta subu

207 We have used recombinant cDNA clones of representative persistent (CR6) and nonpe

208 and in vivo characterizations of infectious cDNA clones of swine HEV.

209 In this study, cDNA clones of the cotton KCBP homolog GhKCBP were isola

210 ectious virus was recovered from each of the cDNA clones of the HN glycoprotein mutants, employing a

211 tagged oda5 allele, we isolated genomic and cDNA clones of the wild-type gene.

212 Since the development of infectious cDNA clones of viral RNA genomes and the means of delive

213 t on the purification, characterization, and cDNA cloning of a novel UGAT involved in the biosynthesi

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

215 from 53 libraries and 36,565 fully sequenced cDNA clones, out of which 31,552 clones are non-redundan

216 A full-length cDNA clone predicts a novel vertebrate-specific protein

217 es rapid subtraction hybridization (RaSH) of cDNA clones prepared from two cell populations, a driver

218 orresponding to exon 10, which is missing in cDNAs cloned previously from human tissues.

219 Full-length cDNA clones provide information about intron and exon st

220 agenesis was performed to generate three new cDNA clones (pSHEV-1, pSHEV-2, and pSHEV-3) which differ

221 tr1 by transfection with a recombinant hCtr1 cDNA clone reduced endogenous hCtr1 mRNA levels, whereas

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

223 ional analyses of the CHV-1/EP713 infectious cDNA clone, reported here, define the requirements for p

224 Partial cDNA clones represented two groups, NMTase A and NMTase

225 Incyte GeneAlbum 1-6, which contains 65,873 cDNA clones representing 33,515 individual genes.

226 Microarray analysis, including cDNA clones representing most UniGene clusters from 12p1

227 Thirty randomly selected cDNA clones representing the differentially regulated ge

228 To obtain cDNA clones representing the remaining genes, we have ge

229 tudy of their subcellular location using the cDNA clone resources of TAIR.

230 Sequence analysis of genomic DNA and cDNA clones revealed nine paralogous genes tightly clust

231 cDNA cloning revealed six SAS1B splice variants, each co

232 ies and highlights discrepancies between any cDNA clone sequence and its expected reference sequence.

233 Alignments of cDNA clone sequences with proteins show that much of the

234 nged strategy to obtain a complementary DNA (cDNA) clone set enriched in hematopoietic genes.

235 Direct cDNA cloning showed that mouse DESC1 encodes a multidoma

236 From cDNA clones showing rhizome-enriched expression, express

237 Two distinct cDNA clones showing sequence homology to higher-plant pe

238 identify the RNA activators, we developed a cDNA cloning strategy based on stringent affinity of RNA

239 A 1,086-bp reactive cDNA clone that encoded a protein of 362 amino acids wit

240 MSPE was used to isolate a novel full-length cDNA clone that encodes a 66-kDa murine G+C-rich promote

241 was screened resulting in the isolation of a cDNA clone that encodes a 738 amino acid protein (SmSmad

242 in-conjugating enzyme, have isolated a human cDNA clone that may function as a signal peptidase and h

243 Based on this screening, we identified a cDNA clone that was allowing yeast cells to grow in the

244 A cDNA clone that was isolated encoded a protein that was

245 A libraries for the isolation of full-length cDNA clones that are not yet available in the public dom

246 s transformed with a human cDNA library, and cDNA clones that rescued growth at low K(+) concentratio

247 KCC1 gene, we mapped the 5' end of the KCC1 cDNA, cloned the corresponding genomic DNA, and identifi

248 he mutagenesis of the CHV-1/EP713 infectious cDNA clone to define the requirements for p29 and p48 cl

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

250 toprotein (AFP) genes by hydridizing labeled cDNA clones to HpaII and MspI digests of DNA from differ

251 In this paper, we utilized genomic and cDNA cloning to elucidate the sequence of the 5'-region

252 generated from all these myotrophin-specific cDNA clones translate in vitro to a 12-kD protein.

253 R products representing assemblies of BAC or cDNA clones typically require maintenance, propagation,

254 om cultured cells and identified full-length cDNA clones using amino acid sequences from internal pep

255 a strategy for high-throughput sequencing of cDNA clones using the transposon Tn5.

256 Screening with a microarray containing 864 cDNA clones using wild-type and brn-3b (-/-) retinal cDN

257 cDNA cloning, using a mouse retina library or RT-PCR fro

258 on developed to help automate the process of cDNA clone validation.

259 The other three cDNA clones varied in length, but contained identical op

260 One cDNA clone was a truncated, polyadenylated version of th

261 teristics expected of the mu 3 receptor, the cDNA clone was expressed in a heterologous system.

262 A PtaAGP6 full-length cDNA clone was expressed in bacteria.

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

264 RNA transcribed from the full-length cDNA clone was highly infectious upon transfection into

265 The FL14676485 cDNA clone was isolated from a 43(HIV) lambda ZAP Escher

266 Using a candidate gene approach, a cDNA clone was isolated that was predicted to encode the

267 A full-length LapN cDNA clone was isolated, and the deduced sequence had 77

268 specific cDNA library and a full-length NEC3 cDNA clone was isolated.

269 of these cleavage sites in an infectious FCV cDNA clone was lethal for the virus, indicating that the

270 The cDNA clone was obtained and used to generate an RNAi con

271 cDNA microarray containing 7,712 macrophage cDNA clones was used to compare the transcriptional prof

272 mparative genomic DNA sequence analysis, and cDNA cloning, we found that the mouse clade B cluster at

273 Three distinct 2DL4 cDNA clones were analyzed: one encoding the "conventiona

274 tion of XyG, and partial sequences of 10,000 cDNA clones were determined.

275 ssion subtraction cDNA library from which 11 cDNA clones were found by differential dot blot hybridiz

276 Nine hundred and sixty-nine cDNA clones were found to be differentially expressed be

277 Infectious cDNA clones were generated from an epizootic subtype IC

278 Full-length cDNA clones were identified encoding two candidate enzym

279 nal genes in the 881-kb contig; 11 groups of cDNA clones were identified in addition to those for S2-

280 e bacterial IF3, several partially sequenced cDNA clones were identified, and the complete sequence w

281 Transcripts of cDNA clones were infectious when they were mechanically

282 at had been characterized previously, 14 new cDNA clones were isolated as part of this work.

283 Three cDNA clones were isolated from a porcine parotid cDNA li

284 on library and three distinct immunoreactive cDNA clones were isolated.

285 s for reverse transcriptase-PCR, and several cDNA clones were isolated.

286 the nucleotide differences between these two cDNA clones were not critical for replication.

287 sis of human draft genomic DNA, and multiple cDNA clones were obtained.

288 Over 20,000 cDNA clones were partially sequenced from a normalized (

289 apsid and ORF3 proteins, indicating that the cDNA clones were replication competent.

290 On the basis of these Cmu2 markers, 22 cDNA clones were selected from an epigonal organ cDNA li

291 To characterize this library, 25,277 cDNA clones were sequenced and aligned with various data

292 RNA transcripts of mutant poliovirus cDNA clones were transfected into HeLa cells.

293 ption-polymerase chain reaction (RT-PCR) and cDNA cloning were conducted by conventional procedures.

294 of the specific mRNA sequences (assayed with cDNA clones) were in the (A)+ class.

295 We previously isolated a partial soybean cDNA clone whose transcript abundance is increased upon

296 oarrays were generated that carry about 8500 cDNA clones with approximately 6000 obtained from mammar

297 s, we constructed a series of BUNV S segment cDNA clones with deletions in the 3' and/or 5' UTR and t

298 rsion of our strategy that can be applied to cDNA clones with large cloning vectors, thereby overcomi

299 Transfection of CVB3 cDNA clones with the 5'-terminal deletions into HeLa cel

300 Five thousand cDNA clones with very low hybridization signals were sel