ライフサイエンスコーパス: rapid amplification of cDNA ends

1 the longest cDNA clones obtained by 5'-RACE (rapid amplification of cDNA ends).

2 ain reaction (RT-PCR) and by 5' and 3' RACE (rapid amplification of cDNA ends).

3 ts were detected by 5' and 3' RACE analysis (rapid amplification of cDNA ends).

4 sue growth factor) as a probe and by 5'RACE (rapid amplification of cDNA ends).

5 tained and verified through RT-PCR and RACE (rapid amplification of cDNA ends).

6 d mapped its transcription start sites by 5'-rapid amplification of cDNA ends.

7 MEC cDNA expression library as well as by 5' rapid amplification of cDNA ends.

8 equencing, reverse transcription-PCR, and 5'-rapid amplification of cDNA ends.

9 from the start codon, was determined by 5'- rapid amplification of cDNA ends.

10 eneration a full-length cDNA using 5' and 3' rapid amplification of cDNA ends.

11 on with degenerate primers and by 5'- and 3'-rapid amplification of cDNA ends.

12 IA (TFIIIA) was cloned by degenerate PCR and rapid amplification of cDNA ends.

13 ed by primer extension, as well as 5' and 3' rapid amplification of cDNA ends.

14 the expressed sequence tag and performing 5'-rapid amplification of cDNA ends.

15 nicum using reverse transcription PCR and 3'-rapid amplification of cDNA ends.

16 ranscription start site was determined by 5'-rapid amplification of cDNA ends.

17 ne and retrieval of the remaining cDNA by 5' rapid amplification of cDNA ends.

18 quence tags, PCR of human heart cDNA, and 5'-rapid amplification of cDNA ends.

19 se searching, polymerase chain reaction, and rapid amplification of cDNA ends.

20 ly spliced cDNA (U16+), was identified by 5' rapid amplification of cDNA ends.

21 use transcript sequence was determined using rapid amplification of cDNA ends.

22 DNA clones isolated by library screening and rapid amplification of cDNA ends.

23 as mapped by tiled array and confirmed by 5' rapid amplification of cDNA ends.

24 the missing 3' sequences were obtained by 3'-rapid amplification of cDNA ends.

25 PC-TP was cloned by library screening and 5'-rapid amplification of cDNA ends.

26 cription-polymerase chain reaction and 5'/3'-rapid amplification of cDNA ends.

27 thern blots (3.7 kb) was determined using 3' rapid amplification of cDNA ends.

28 anscriptase-polymerase chain reaction and 3' rapid amplification of cDNA ends.

29 human WIN cDNAs by library screening and 5'-rapid amplification of cDNA ends.

30 sozyme (RMPK) was cloned using the method of rapid amplification of cDNA ends.

31 from the purified protein and by 5'- and 3'-rapid amplification of cDNA ends.

32 nal regions of the genome were determined by rapid amplification of cDNA ends.

33 c fos clone using degenerate PCR followed by Rapid Amplification of cDNA Ends.

34 nt virus mRNA molecules was determined by 3' rapid amplification of cDNA ends.

35 using degenerate oligonucleotides, PCR, and rapid amplification of cDNA ends.

36 cDNA were subsequently captured by 5' and 3' rapid amplification of cDNA ends.

37 tion of lambda gt11 library screening and 3' rapid amplification of cDNA ends (3'-RACE).

38 etermined by both S1 nuclease mapping and 5' rapid amplification of cDNA ends (5' RACE) to be located

39 a range of tissues using the technique of 5' rapid amplification of cDNA ends (5' RACE).

40 5'-Rapid amplification of cDNA ends (5'-RACE) analysis show

41 Both 5'-rapid amplification of cDNA ends (5'-RACE) and 3'-RACE t

42 5'-rapid amplification of cDNA ends (5'-RACE) and computati

43 Nuclease protection and 5'-rapid amplification of cDNA ends (5'-RACE) revealed five

44 Rapid amplification of cDNA ends (5'-RACE) was used to i

45 Using the technique of rapid amplification of cDNA ends, a full-length cDNA of

46 on a partial amino acid sequence, 5'- and 3'-rapid amplification of cDNA ends allowed the generation

47 Furthermore, both primer extension and 5'-rapid amplification of cDNA ends analyses identified mul

48 5'-rapid amplification of cDNA ends analyses of RNA prepare

49 Polymerase chain reaction and 5'-rapid amplification of cDNA ends analyses revealed the t

50 ocytic cDNA library as well as by 5'- and 3'-rapid amplification of cDNA ends analyses.

51 ime polymerase chain reaction, and 3' and 5' rapid amplification of cDNA ends analyses.

52 However, Northern blot and 5' RACE (rapid amplification of cDNA ends) analyses indicated tha

53 Bioinformatic and 5'RACE (rapid amplification of cDNA ends) analyses of the 5' gen

54 cDNA sequencing and 5' rapid amplification of cDNA ends analysis demonstrate th

55 5'-Rapid amplification of cDNA ends analysis demonstrated t

56 rn blotting, phage library screening, and 5' rapid amplification of cDNA ends analysis in the region

57 Northern blot and 5' rapid amplification of cDNA ends analysis of antigenome

58 Rapid amplification of cDNA ends analysis of hTR-/hTERT-

59 5'-Rapid amplification of cDNA ends analysis of intestinal

60 5' Rapid amplification of cDNA ends analysis of mouse mRNA

61 In 5'-rapid amplification of cDNA ends analysis of purified mR

62 Rapid amplification of cDNA ends analysis revealed that

63 a combination of cDNA library screening and rapid amplification of cDNA ends analysis, a novel human

64 the transcription start point (TSP) using 5' rapid amplification of cDNA ends analysis, the 5' promot

65 Using a combination of 5' rapid amplification of cDNA ends analysis, transient tra

66 Rather, using 5'-rapid amplification of cDNA ends analysis, we demonstrat

67 Using 5'-rapid amplification of cDNA ends analysis, we extended t

68 By combining RNase protection and rapid amplification of cDNA ends analysis, we have deter

69 ranscription start site, as determined by 5' rapid amplification of cDNA ends analysis.

70 Using 5' RACE (rapid amplification of cDNA ends) analysis, multiple tra

71 the gene trap transcripts are obtained by 5' rapid amplification of cDNA ends and are sequenced to de

72 The missing 5' sequences were obtained by 5'-rapid amplification of cDNA ends and by analysis of an N

73 Rapid amplification of cDNA ends and cDNA sequencing stu

74 homolog was isolated by a combination of 5'-rapid amplification of cDNA ends and direct polymerase c

75 h Mrf2 cDNA by cDNA library screening and 5' rapid amplification of cDNA ends and identified two isof

76 We show by rapid amplification of cDNA ends and Northern blotting t

77 l-treated human THP-1 cells together with 5'-rapid amplification of cDNA ends and polymerase chain re

78 5' rapid amplification of cDNA ends and primer extension sh

79 criptional start sites were identified by 5'-rapid amplification of cDNA ends and primer extension.

80 A combination of rapid amplification of cDNA ends and reverse transcripta

81 start site (+1), which was determined by 5' rapid amplification of cDNA ends and RNase protection as

82 upstream from the translation start site by rapid amplification of cDNA ends and RNase protection as

83 The full-length cDNA was obtained by 5' rapid amplification of cDNA ends and RT-PCR.

84 By 5'-rapid amplification of cDNA ends and S1 nuclease protect

85 rent variants of the exchanger, we used both rapid amplification of cDNA ends and S1 nuclease protect

86 Using 5'- and 3'-rapid amplification of cDNA ends and two cDNA libraries,

87 lobulin-like molecules, we utilized 3' RACE (rapid amplification of cDNA ends) and a highly conserved

88 flow designed to address this based on RACE (rapid amplification of cDNA ends) and long-read RNA sequ

89 of the K12 transcript was mapped by 5' RACE (rapid amplification of cDNA ends) and S1 nuclease protec

90 ript 1 (LT1) and LT2, by cDNA sequencing, 5' rapid amplification of cDNA ends, and primer extension a

91 the gene was mapped by RNase protection, 5' rapid amplification of cDNA ends, and primer extension e

92 Screening of a rat heart cDNA library, 5'-rapid amplification of cDNA ends, and RNase protection a

93 Further FISH, 5'-rapid amplification of cDNA ends, and RT-PCR analyses di

94 rge flgBCDEFGHIJKL operon were determined by rapid amplification of cDNA ends, and secretion of the F

95 nt study, mouse PAP7 cDNA was extended by 5'-rapid amplification of cDNA ends; and a 3432 bp sequence

96 5'- and 3'-rapid amplification of cDNA ends approaches were carried

97 We have performed 5' rapid amplification of cDNA ends as well as a nuclease p

98 By 5'-rapid amplification of cDNA ends assay and DNA sequencin

99 Primer extension and RACE (rapid amplification of cDNA ends) assays were used to id

100 ated from normal human melanocyte cDNA by 5'-rapid amplification of cDNA ends based on the homology t

101 We carried out 5' rapid amplification of cDNA ends beginning with mRNA fro

102 onucleotide-directed RNase H cleavage and 5' rapid amplification of cDNA ends both indicate that the

103 and 237 bp, respectively) were amplified by rapid amplification of cDNA ends, cloned and sequenced.

104 cDNA (4.4 kb) was amplified by rapid amplification of cDNA ends, cloned, and sequenced

105 Rapid amplification of cDNA ends cloning mapped transcri

106 the trapped LPS-response genes via 5' RACE (rapid amplification of cDNA ends) cloning identified nov

107 ewly discovered first exon, identified by 5'-rapid amplification of cDNA ends, consists of a 5'-untra

108 clone and subsequent analyses of products of rapid amplification of cDNA ends coupled with S1 nucleas

109 5'-RACE (rapid amplification of cDNA ends) data indicate the pres

110 ethod described here comprises a modified 5'-rapid amplification of cDNA ends, deep sequencing of 3'

111 The mapping of 5' mRNA ends using rapid amplification of cDNA ends defined a promoter with

112 ecific oligonucleotide probes followed by 5' rapid amplification of cDNA ends detects an antisense sm

113 5'-RNA ligase-mediated rapid amplification of cDNA ends evaluation of ICA1 tran

114 Rapid-amplification-of-cDNA-ends experiments indicated t

115 Results of RNA ligase mediated rapid amplification of cDNA ends followed by sequence de

116 Real time PCR and 5'-rapid amplification of cDNA ends followed by Southern bl

117 e full-length cDNA was isolated by 3' and 5' rapid amplification of cDNA ends from mouse liver.

118 g portion of the coding sequence by 5' RACE (rapid amplification of cDNA ends), full-length cDNA was

119 quent reverse transcription-PCR (RT-PCR) and rapid amplification of cDNA ends generated a complete ge

120 a combination of cDNA library screening and rapid amplification of cDNA ends has permitted the isola

121 V5 outlier expression by RNA ligase-mediated rapid amplification of cDNA ends identified one case wit

122 Analyses using 5' rapid amplification of cDNA ends identified the transcri

123 RACE (Rapid Amplification of cDNA Ends) identified a 1.5-Kb tr

124 Database analysis and 5'-RACE (rapid amplification of cDNA ends) identified a 4191 bp c

125 cells and liver; however, 5'-RACE analysis (rapid amplification of cDNA ends) identified AS mRNA spe

126 Finally, our 5' rapid amplification of cDNA ends in conjunction with spl

127 the analysis of hsd2 transcripts by 5' RACE (rapid amplification of cDNA ends) indicates that inversi

128 HSCs and erythroid cells was confirmed by 5'-rapid amplification of cDNA ends, indicating that at lea

129 DeltarcrR-P and DeltarcrR-NP strains, and 5' Rapid Amplification of cDNA Ends mapped the 5' terminus

130 , reverse transcription-PCR (RT-PCR), the 5' rapid amplification of cDNA ends method (5'RACE), and im

131 its transcription initiation sites by the 5'-rapid amplification of cDNA ends method.

132 gene (300 bp) was amplified by means of the rapid-amplification-of-cDNA-ends method, cloned and sequ

133 ng, quantitative PCR, Northern blotting, and rapid amplification of cDNA ends methods.

134 Results of 5'-rapid amplification of cDNA ends, Northern analysis, N-t

135 loning by a combination of sib selection and rapid amplification of cDNA ends of a cDNA encoding a ne

136 tained from an expressed sequence tag and 5'-rapid amplification of cDNA ends of a mouse liver cDNA l

137 5'-Rapid amplification of cDNA ends of a selected band, seq

138 Rapid amplification of cDNA ends of clone 17a revealed a

139 Primer extension and 5'-rapid amplification of cDNA ends of distal colon RNA wer

140 searches of the GenBank databases and by 5' rapid amplification of cDNA ends of human brain cDNAs.

141 Based on these sequences, rapid amplification of cDNA ends of human mammary gland

142 Analysis by 5' rapid amplification of cDNA ends of liver mRNA from thes

143 ntity of the clone, and after both 5' and 3' rapid amplification of cDNA ends, oligonucleotide primer

144 Using RT-PCR and 3'- and 5'-rapid amplification of cDNA ends on toad cardiac mRNA, w

145 nspection of the Mct8 promoter region and 5'-rapid amplification of cDNA ends PCR analysis in F9 cell

146 Rapid amplification of cDNA ends PCR yielded a 536-bp MA

147 ed using reverse transcription-PCR (RT-PCR), rapid amplification of cDNA ends PCR, RNA dot blotting,

148 lin heavy-chain transcripts, as shown by PCR-rapid amplification of cDNA ends (PCR-RACE).

149 mykiss) Mx cDNAs were cloned by using RACE (rapid amplification of cDNA ends) PCR and were designate

150 'New RACE' (rapid amplification of cDNA ends) PCR is a method for ob

151 RACE (rapid amplification of cDNA ends) PCR is useful for quic

152 e divergent transcripts were mapped using 5' rapid amplification of cDNA ends-PCR (RACE-PCR), and str

153 ll-length cDNA of the enzyme was obtained by rapid amplification of cDNA ends-PCR amplification of cD

154 However, rapid amplification of cDNA ends-PCR and lacZ fusion exp

155 Rapid amplification of cDNA ends-PCR was used to confirm

156 ng cDNA clones by hot start, seminested, and rapid amplification of cDNA ends-PCR.

157 cross-linking family 7 (mACF7) by sequential rapid amplification of cDNA ends-PCR.

158 e analysis of 50 TCR beta clones obtained by rapid amplification of cDNA ends per culture.

159 Oligo/RNase H cleavage analysis and rapid amplification of cDNA ends-poly(A) test both confi

160 we cloned one of the trapped genes using 5' rapid amplification of cDNA ends polymerase chain reacti

161 g a rat lung expression library coupled with rapid amplification of cDNA ends polymerase chain reacti

162 nucleotides apart, were identified using 5'-rapid amplification of cDNA ends polymerase chain reacti

163 RNKp30 cDNA was cloned by 5' rapid amplification of cDNA ends polymerase chain reacti

164 This was possible through the use of rapid amplification of cDNA ends-polymerase chain reacti

165 was confirmed by Poly(A) Polymerase-Mediated Rapid Amplification of cDNA Ends (PPM-RACE).

166 By 5' rapid amplification of cDNA ends, primer extension analy

167 P mRNA was cloned after amplification by the rapid amplification of cDNA ends procedure, and a part o

168 We used a 5' rapid amplification of cDNA ends procedure, followed by

169 Using a 5' rapid amplification of cDNA ends procedure, the transcri

170 ntified in four of these lines by using a 5' rapid amplification of cDNA ends protocol.

171 d by primer extension studies and a modified rapid amplification of cDNA ends protocol.

172 The 5' end of the cDNA was cloned using a 5'-rapid amplification of cDNA ends protocol.

173 ial Display Polymerase Chain Reaction and 5' Rapid Amplification of cDNA Ends protocols, we isolated

174 ssion of ETV4 using quantitative PCR, and by rapid amplification of cDNA ends, quantitative PCR, and

175 5' rapid amplification of cDNA ends (RACE) analyses of RNAs

176 3'-Rapid amplification of cDNA ends (RACE) analyses of the

177 5' rapid amplification of cDNA ends (RACE) and deletion ana

178 rmination sites, and splicing patterns using rapid amplification of cDNA ends (RACE) and full-length

179 is facilitated by cloning methods such as 5'-Rapid Amplification of cDNA Ends (RACE) and inverse poly

180 By using both rapid amplification of cDNA ends (RACE) and Northern blo

181 To characterize these mutations, 3' rapid amplification of cDNA ends (RACE) and polymerase c

182 e correct cDNA sequence was determined by 5' rapid amplification of cDNA ends (RACE) and primer exten

183 Rapid amplification of cDNA ends (RACE) and RNase protec

184 th cDNA of the human hSmad5 (hSmad5) gene by rapid amplification of cDNA ends (RACE) and then determi

185 ovel combination of techniques including the rapid amplification of cDNA ends (RACE) and tiling array

186 ipherin/rds (srds) cDNA were isolated by the rapid amplification of cDNA ends (RACE) approach.

187 s identified by primer extension assay and a rapid amplification of cDNA ends (RACE) assay.

188 Cloning and sequence analyses of 5'-rapid amplification of cDNA ends (RACE) cDNAs from human

189 Limited 5' and 3' rapid amplification of cDNA ends (RACE) experiments and

190 Primer extension, RNase protection, and rapid amplification of cDNA ends (RACE) experiments indi

191 utational and experimental platform adapting rapid amplification of cDNA ends (RACE) for large-scale

192 se eosinophil and lung cDNA libraries and by rapid amplification of cDNA ends (RACE) from liver, sple

193 Northern blot analysis and 3' rapid amplification of cDNA ends (RACE) in placenta conf

194 Rapid amplification of cDNA ends (RACE) is widely used t

195 from complex mixtures of cellular mRNA using rapid amplification of cDNA ends (RACE) PCR as long as p

196 Results from rapid amplification of cDNA ends (RACE) PCR suggest that

197 plice variant, beta(2b), from heart using 5' rapid amplification of cDNA ends (RACE) PCR.

198 3' rapid amplification of cDNA ends (RACE) polymerase chain

199 The rapid amplification of cDNA ends (RACE) procedure is a w

200 uencing multiple clones from each 5'- and 3'-rapid amplification of cDNA ends (RACE) product and asse

201 Using a 3' rapid amplification of cDNA ends (RACE) protocol, HD-5 w

202 5'-Rapid amplification of cDNA ends (RACE) revealed an alte

203 5'- and 3'-Rapid Amplification of cDNA Ends (RACE) revealed IGH/CHS

204 We have used rapid amplification of cDNA ends (RACE) to identify mult

205 Rapid amplification of cDNA ends (RACE) was performed on

206 Rapid amplification of cDNA ends (RACE) was used to obta

207 gene structures, a high-throughput method of rapid amplification of cDNA ends (RACE) was used to obta

208 by sequencing of EST clones and products of rapid amplification of cDNA ends (RACE), an mRNA that en

209 tion (PCR) amplification products, 5' and 3' rapid amplification of cDNA ends (RACE), and by helper p

210 HV) using next-generation RNA sequencing, 3' rapid amplification of cDNA ends (RACE), and tiled micro

211 ription-polymerase chain reactions (RT-PCR), rapid amplification of cDNA ends (RACE), and transient e

212 ing the GFP reporter system combined with 5' rapid amplification of cDNA ends (RACE), in vitro transc

213 This study detected by rapid amplification of cDNA ends (RACE), primer extensio

214 Using rapid amplification of cDNA ends (RACE), reverse-transcr

215 Finally, using 5' rapid amplification of cDNA ends (RACE), two transcripti

216 tion (RT-PCR), in combination with 5' and 3' rapid amplification of cDNA ends (RACE), was used to clo

217 Using 3' rapid amplification of cDNA ends (RACE), we mapped the 3

218 By using 5' rapid amplification of cDNA ends (RACE), we mapped two H

219 Rapid amplification of cDNA ends (RACE)-PCR extension of

220 ssion/1/1918 (H1N1) virus were determined by rapid amplification of cDNA ends (RACE).

221 owed by recovery of full-size transcripts by rapid amplification of cDNA ends (RACE).

222 ption-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE).

223 ere discovered in the present study by using rapid amplification of cDNA ends (RACE).

224 ion of cDNA library screening, RT-PCR and 5' rapid amplification of cDNA ends (RACE).

225 cation of the endogenous gene possible by 5' rapid amplification of cDNA ends (RACE).

226 ainder of the cDNA was obtained by 5' and 3' rapid amplification of cDNA ends (RACE).

227 splice variants of CTGF were assessed by 5' Rapid Amplification of cDNA Ends (RACE).

228 NA isolated from Pacific hagfish brain using rapid amplification of cDNA ends (RACE).

229 The missing 5' end was isolated using rapid amplification of cDNA ends (RACE).

230 coding the MIP prepropeptide was isolated by rapid amplification of cDNA ends (RACE).

231 tic cells (FSDDC) by subtractive cloning and rapid amplification of cDNA ends (RACE).

232 The 5'-rapid amplification of cDNA ends results and the differe

233 Analyses by Northern blotting and rapid amplification of cDNA ends revealed that gene 4 is

234 ts of Tap1 and Lmp2 mRNA in NOD mice, and 5'-rapid amplification of cDNA ends revealed the loss of a

235 Northern blot analysis and 5' rapid amplification of cDNA ends revealed two transcript

236 fH transcriptional start sites by 5'RACE (5' rapid amplification of cDNA ends) revealed that these 5'

237 A 5' rapid amplification of cDNA ends reveals that mouse E-Tm

238 We used 5' RNA ligase-mediated rapid amplification of cDNA ends (RLM-RACE) and RT-PCR t

239 dentified by full-length RNA ligase-mediated rapid amplification of cDNA ends (RLM-RACE) between -61

240 5' RNA ligase-mediated rapid amplification of cDNA ends (RLM-RACE) PCR analysis

241 (CAGE) tags, 1.2 million RNA ligase mediated rapid amplification of cDNA ends (RLM-RACE) reads, and 5

242 Using 5'-rapid amplification of cDNA ends, RNase protection assay

243 NA by a combination of techniques: 5' and 3' rapid amplification of cDNA ends, RT-PCR, and searching

244 Analysis of one tumor by 3' rapid amplification of cDNA ends showed altered transcri

245 Use of a 3' RACE (rapid amplification of cDNA ends) strategy with a degene

246 are not present, and primer extension and 5'-rapid amplification of cDNA ends studies suggest that tr

247 nternal promoters were detected using the 5' rapid amplification of cDNA ends system.

248 onal start site has been mapped using the 5' rapid amplification of cDNA ends technique, and this sta

249 nd using the polymerase chain reaction-based rapid amplification of cDNA ends technique, three forms

250 ain reaction (RT-PCR) in conjunction with 5'-rapid amplification of cDNA ends technique, we have clon

251 Using the nested 5'-rapid amplification of cDNA ends technique, we obtained

252 ii was obtained using an RNA ligase-mediated rapid amplification of cDNA ends technique.

253 as the nucleotide sequences were obtained by rapid amplification of cDNA ends technique.

254 full-length cDNA was cloned by the 5'-RACE (rapid amplification of cDNA ends) technique and sequence

255 MRG1 (MSG1-Related Gene 1), by the 5'-RACE (rapid amplification of cDNA ends) technique.

256 A combination of genomic, cDNA and 3' rapid amplification of cDNA ends techniques was used to

257 entified using polymerase chain reaction and rapid amplification of cDNA ends techniques.

258 By using S1 nuclease and 5'- rapid amplification of cDNA ends, the cap sites for the

259 rt site(s) of the IA-2 gene was mapped by 5' rapid amplification of cDNA ends to 97 bp upstream of th

260 f degenerate oligonucleotides and 5'- and 3'-rapid amplification of cDNA ends to clone two cDNAs of 2

261 We used rapid amplification of cDNA ends to clone two new isofor

262 We performed 5'-rapid amplification of cDNA ends to determine the transc

263 We used rapid amplification of cDNA ends to identify a chimeric

264 Using RNA ligase-mediated rapid amplification of cDNA ends to identify novel trans

265 We used 3' rapid amplification of cDNA ends to profile expression o

266 ites are identified for the TREX genes using rapid amplification of cDNA ends to recover the 5'-flank

267 of a PC12 cDNA library, followed by 5' RACE (rapid amplification of cDNA ends) to determine the 5' en

268 c fusions, reverse transcriptase PCR, and 5' rapid amplification of cDNA ends, to localize and identi

269 The full cDNA by 5' rapid amplification of cDNA ends was 0.4 kilobase pair,

270 Rapid amplification of cDNA ends was employed to obtain

271 Rapid amplification of cDNA ends was used to clone cDNAs

272 Genome analysis and 5'-rapid amplification of cDNA ends was used to clone the f

273 Rapid amplification of cDNA ends was used to identify a

274 transcription-polymerase chain reaction and rapid amplification of cDNA ends, we cloned a full-lengt

275 y, via both RNase protection analysis and 5'-rapid amplification of cDNA ends, we determined the tran

276 Using PCR and rapid amplification of cDNA ends, we discovered several

277 Using 3' rapid amplification of cDNA ends, we have amplified two

278 Using 3' rapid amplification of cDNA ends, we have identified a c

279 Using RPA, primer extension assay and 5' rapid amplification of cDNA ends, we were able to demons

280 Marathon cDNA amplification and 5'-rapid amplification of cDNA ends were used to confirm th

281 Primer extension analysis and 5'-rapid amplification of cDNA ends were used to identify t

282 5' and 3' rapid amplifications of cDNA ends were used to obtain th

283 of 69 rpoH-dependent genes using 5' RACE (5' rapid amplification of cDNA ends), which allowed us to d

284 IA and IB, were identified by performing 5'-rapid amplification of cDNA ends with human liver cDNA a

285 Rapid amplification of cDNA ends with PCR, sequences fro

286 5'-Rapid amplification of cDNA ends with templates from mul

287 untranslated region (3'UTR), we performed 3' rapid amplification of cDNA ends with the S1 parental co

288 ronal channel SCN8A, we carried out 5'-RACE (rapid amplification of cDNA ends) with RNA from human an

289 Human brain cDNA library screening and 5' rapid amplification of cDNA ends yielded full-length DEN

290 This approach, together with 5'and 3' rapid amplification of cDNA ends, yielded a human cDNA t

291 This approach, together with 5'-rapid amplification of cDNA ends, yielded a human cDNA t