ライフサイエンスコーパス: full-length cDNA

1 -protein coding RNA (now approximately 7% of full-length cDNAs).

2 t the mutations did not lower the amounts of full-length cDNA.

3 lt in W446G, was identified in the patient's full-length cDNA.

4 n sequence information was used to isolate a full-length cDNA.

5 y cells by amplification of the transfected, full-length cDNA.

6 rification of its antigen and cloning of its full-length cDNA.

7 /brevican, but not when transfected with the full-length cDNA.

8 duction in the formation of intermediate and full-length cDNA.

9 an the entire genome were used to generate a full-length cDNA.

10 , and U87-MG glioblastoma) with human plgf-2 full-length cDNA.

11 a total of 3160 (59%) completely sequenced, full-length cDNAs.

12 d an RNA-capture method for rapid cloning of full-length cDNAs.

13 t multiple sites, may require screening many full-length cDNAs.

14 pporting information for annotated genes and full-length cDNAs.

15 the human genes based on known proteins and full-length cDNAs.

16 rried out by cloning and characterization of full-length cDNAs.

17 Two full-length cDNAs (1,179 bp each), ReCHS1 and ReCHS2, en

18 h the antisense orientation of the HRG-beta2 full-length cDNA (231/ASPOOL, 231/AS31 and Hs578T/AS15).

19 Full-length cDNA analysis provided evidence for decrease

20 An apparently full-length cDNA and a 2.8-kb genomic fragment containin

21 pe by site-directed mutagenesis of a VSIV-GI full-length cDNA and analysis of the recovered engineere

22 We now isolated the corresponding full-length cDNA and determined that the predicted gene

23 Here we report the identification of full-length cDNA and elucidation of genomic organization

24 We have cloned the full-length cDNA and genomic region of a human prostate

25 Sequencing the full-length cDNA and several hundred basepairs of genomi

26 lation and molecular characterization of the full-length cDNA and the determination of the genomic DN

27 With the full-length cDNAs and a lentiviral vector system, we wer

28 s were generated from libraries enriched for full-length cDNAs and analyzed to identify candidate ful

29 Here we report the isolation of full-length cDNAs and genomic clones for the murine Pb99

30 With this EST as a starting point, full-length cDNAs and genomic coding sequences from upla

31 Sequencing full-length cDNAs and hybridizations using RNA populatio

32 d by scrutiny of our collection of sequenced full-length cDNAs and much larger collection of 5'-ESTs,

33 ecent integration of large datasets of mouse full-length cDNAs and radiation-hybrid mapped ESTs, the

34 lification of complementary DNA (cDNA) ends, full-length cDNAs, and RNA-seq, we defined approximately

35 demonstrate that RNA transcripts from GBV-C full-length cDNA are infectious in primary CD4-positive

36 The full-length cDNAs are 2,141 bp for PDE11A2 and 2205 bp f

37 /pool, </=1 molecule/gene for most genes) of full-length cDNAs are amplified, fragmented and short-re

38 We obtained full-length cDNA by hybridization screening of mouse eos

39 However, we were able to clone four full-length cDNAs by screening the same latex cDNA libra

40 Full-length cDNAs can be obtained from complex mixtures

41 A 1,734-bp full-length cDNA clone (accession no. AF196292) encoding

42 We have isolated a full-length cDNA clone (thymic stromal origin (TSO)-1C12

43 The process of obtaining a full-length cDNA clone can be highly time and labor inte

44 fied, and using the methods of proteomics, a full-length cDNA clone encoding an enzyme matching the p

45 A full-length cDNA clone encoding hebraein was isolated fr

46 We isolated a full-length cDNA clone of amphioxus AmphiNk2-tin, an NK2

47 dividually by site-directed mutagenesis on a full-length cDNA clone of BC.

48 ort the construction and the properties of a full-length cDNA clone of HRV16, pR16.11, which produces

49 of the spliced, polyadenylated BART RNAs, a full-length cDNA clone of one of the BART isoforms was o

50 We used a full-length cDNA clone of ONNV to construct a series of

51 ethal neurological disease, we constructed a full-length cDNA clone of silver-haired bat-associated R

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

53 xovirus genes in JPV, a plasmid containing a full-length cDNA clone of the genome of JPV was construc

54 We inserted a full-length cDNA clone of the genomic RNA of the dicistr

55 tant P coding sequences were inserted into a full-length cDNA clone of VSV, and the virus recovery, k

56 ted JE virus SA14-14-2 vaccine strain into a full-length cDNA clone of YF 17D virus.

57 We first constructed a stable full-length cDNA clone of ZIKV in a novel linear vector

58 A full-length cDNA clone predicts a novel vertebrate-speci

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

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

61 RNA transcribed from the full-length cDNA clone was highly infectious upon transf

62 amplification and cDNA library screening, a full-length cDNA clone with a 1,167-bp open reading fram

63 verse transcription-PCR and assembled into a full-length cDNA clone, clone C, which contained 14 muta

64 ations were subsequently incorporated into a full-length cDNA clone.

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

66 Thus, obtaining full-length cDNA clones and sequences for most or all ge

67 Full-length cDNA clones containing the entire coding reg

68 We have sequenced two full-length cDNA clones corresponding to the human sedli

69 the isolation and sequencing of genomic and full-length cDNA clones encoding DC3.

70 The isolation of full-length cDNA clones for each of these candidate gene

71 organs (i.e., rhinophores), we isolated five full-length cDNA clones from an A. californica central n

72 We aligned full-length cDNA clones from the Mammalian Gene Collecti

73 for defining the coding region of genes, and full-length cDNA clones have proven to be useful for inv

74 on factor genes that were not represented by full-length cDNA clones in our Drosophila Gene Collectio

75 otype, and cell tropism of IBDV, we prepared full-length cDNA clones of a virulent strain, Irwin Moul

76 Full-length cDNA clones provide information about intron

77 d useful cDNA libraries for the isolation of full-length cDNA clones that are not yet available in th

78 subunits from cultured cells and identified full-length cDNA clones using amino acid sequences from

79 Full-length cDNA clones were identified encoding two can

80 s for JHM.SD and JHM.WU and, utilizing these full-length cDNA clones, constructed chimeric viruses an

81 -sRNAs) by using differential RNA selection, full-length cDNA cloning and 454 transcriptome sequencin

82 d candidate diterpene synthase sequences for full-length cDNA cloning and functional characterization

83 Full-length cDNA coding for dentin matrix protein 1 (DMP

84 We found mostly novel full-length cDNA coding for metalloproteases (P-II and P

85 Here, we report a full-length cDNA coding for the human homolog of yeast R

86 The full-length cDNA coding for the N-benzoyltransferase has

87 We have thus identified dozens of full-length cDNAs coding for proteins with sequence homo

88 d from our collection compared with the KOME full-length cDNA collection.

89 Three full-length cDNAs containing these distinct TSSs were re

90 The amino acid sequence of KIP1 deduced from full-length cDNA contains an EF-hand Ca(2+)-binding moti

91 omplex isoforms because it fails to sequence full-length cDNA copies of RNA molecules.

92 A full-length cDNA copy of the Cowden PEC genome was clone

93 w pathway presumably involves synthesis of a full-length cDNA copy of the inserted intron RNA, with c

94 We have isolated nearly full length cDNAs corresponding to the five proximal gen

95 The full-length cDNA corresponding to the differentially exp

96 ause they were not found in previous EST and full-length cDNA datasets.

97 egulate ADPRH gene expression, we cloned the full-length cDNA, determined the genomic structure of mo

98 Its full-length cDNA encoded a 493-aa protein that has only

99 The full-length cDNA encodes a predicted protein of 806 amin

100 The full-length cDNA encodes a type-I IPPI containing a plas

101 The full length cDNA encoding the beta subunit was isolated

102 The full-length cDNA encoding a novel atRDH, RDH10, was clon

103 identify all genes expressed in human EC, a full-length cDNA encoding a potential secreted protein h

104 o test this idea in soybean (Glycine max), a full-length cDNA encoding a putative ortholog of AGL15 w

105 e selected EST clones was used to generate a full-length cDNA encoding a putative seven transmembrane

106 We have isolated a full-length cDNA encoding a putative ultraviolet (UV)-se

107 A full-length cDNA encoding a secreted orthologue of the h

108 In this work we cloned a full-length cDNA encoding an LPXRFa precursor in the Eur

109 In this study, a full-length cDNA encoding CPR was cloned and characteriz

110 Full-length cDNA encoding human and mouse ACSBG2 was clo

111 lyses, the cloning and characterization of a full-length cDNA encoding mouse EMSP1, and the localizat

112 ribe the cloning and characterization of the full-length cDNA encoding OsGR3, a chloroplast-localized

113 We generated a full-length cDNA encoding the entire mouse bamacan/SMC3

114 Here we report the cloning of a full-length cDNA encoding the human ortholog (HSulf-1) o

115 We have cloned a full-length cDNA encoding the M(r) approximately 70,000

116 To address this we have cloned a full-length cDNA encoding the P. xylostella RyR and esta

117 The full-length cDNA encoding this novel CAATCH1 (cation-ani

118 Full-length cDNAs encoding CYP79D16, CYP79A68, CYP71AN24

119 Among the differentially expressed genes, full-length cDNAs encoding homologs of a PR5, a sunflowe

120 Three full-length cDNAs encoding PEPC were isolated from H. ve

121 Three full-length cDNAs encoding putative isoprenoid synthases

122 Full-length cDNAs encoding the alpha- and beta-subunits

123 of cDNA ends on toad cardiac mRNA, we cloned full-length cDNAs encoding two alternatively spliced var

124 P450s in this species, we have cloned three full-length cDNAs encoding two CYP4M subfamily members a

125 eveloped to facilitate production of a mouse full-length cDNA encyclopedia representing approximately

126 erated 3' ESTs and the existing sequences of full-length cDNAs, ESTs, and serial analysis of gene exp

127 involved in resistance to TAM, we introduced full-length cDNA expression library into estrogen recept

128 Expression of these two full-length cDNAs failed to form HNK-1 glycan nor to add

129 o recognize and provide coverage of 78 maize full-length cDNAs (FLCs).

130 In the current report we have cloned a full length cDNA for a human paralogue of CRB1 called Cr

131 NA ends) PCR is useful for quickly obtaining full length cDNAs for mRNAs for which only part of the s

132 Therefore, we cloned full-length cDNA for a human homolog of BGM, and we inve

133 A full-length cDNA for Arabidopsis PLD zeta 1 has been ide

134 rotein (pIRES2-EGFP) or a plasmid containing full-length cDNA for both E2F2 and EGFP (pIRES2-E2F2/EGF

135 We isolated, cloned and sequenced the full-length cDNA for chicken c-Cbl and constructed antis

136 gent and either a control plasmid containing full-length cDNA for enhanced green fluorescent protein

137 The full-length cDNA for GGH, subcloned into a constitutive

138 We have isolated the full-length cDNA for human ATP-binding cassette, sub-fam

139 We expressed the full-length cDNA for human PLCgamma2 in bacteria and pur

140 a-estradiol (E2) affinity column we cloned a full-length cDNA for IEBP from the estrogen-resistant NW

141 The full-length cDNA for L552S comprises 770 bp and encodes

142 of cDNA ends) PCR is a method for obtaining full-length cDNA for mRNA for which only part of the seq

143 olation and functional characterization of a full-length cDNA for one of the novel genes, designated

144 Here, we report the cloning of the full-length cDNA for porcine NRAMP1, which had over 85%

145 We have now characterized the full-length cDNA for the murine orthologue that encodes

146 ived from a construct containing GFP and the full-length cDNA for the rat 14 kDa MBP was reduced when

147 First, we amplified and sequenced the full-length cDNA for the zebrafish TOR ortholog (ztor).

148 We recovered high-quality, full-length cDNAs for 72 genes and variously compromised

149 Two different full-length cDNAs for cinnamate 4-hydroxylase (C4H1 and

150 between the ClpR proteins, we overexpressed full-length cDNAs for ClpR1, R2, R3, R4 in clpr1, clpr2

151 Full-length cDNAs for DNA ligase IV and the alpha and be

152 system was demonstrated through isolation of full-length cDNAs for five genes of interest, including

153 We characterized full-length cDNAs for human and mouse UBE3B, a novel HEC

154 Full-length cDNAs for N. virens GKalpha and GKbeta were

155 ification of cDNA ends was used to clone the full-length cDNA from a mouse mastocytoma cell line.

156 rthern blot analysis and was used to clone a full-length cDNA from a mouse mixed germ cell cDNA libra

157 formation we then isolated the corresponding full-length cDNA from etiolated Arabidopsis cotyledons a

158 cules and random isolation of any partial or full-length cDNA from in planta genomic libraries.

159 The synthesis of accurate, full-length cDNA from low-abundance RNA and the subseque

160 We describe the cloning of a 2.5-kb full-length cDNA from rat distal colon that encodes 438

161 ntact ABCC13 ortholog, we have sequenced the full-length cDNA from rhesus macaque, which contains an

162 on introduced into a 7-kb plasmid containing full-length cDNA from the p53 gene.

163 We constructed a full-length cDNA from the plasma of a person with chroni

164 a pair of homeologous CesA2 genes and their full-length cDNAs from allotetraploid cotton.

165 This approach for cloning full-length cDNAs from available ESTs or partial cDNA se

166 Through the analysis of hundreds of full-length cDNAs from fifteen species representing all

167 Analysis of full-length cDNAs from five different mouse strains defi

168 ion of 5'-ESTs, together with another set of full-length cDNAs from Salk/Stanford/Plant Gene Expressi

169 Thirteen full-length cDNAs from the FANTOM2 set were mapped to th

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

171 tudy, we have isolated and characterized the full-length cDNA, gDNA and a putative promoter of a RIOK

172 zation images are available from analysis of full-length cDNA-green fluorescent protein (GFP) fusions

173 The full-length cDNA has an open reading frame of 2094 base

174 The full-length cDNA has an ORF of 1,320 bp corresponding to

175 The full-length cDNA has an ORF of 1,335 bases and encodes a

176 Because the full-length cDNA has not been reported, we cloned the fu

177 s, followed by cloning and sequencing of the full-length cDNA, identified this approximately 220 kDa

178 Expression of the full-length cDNA in COS cells induces sialic-acid depend

179 ains of Ty3 IN cause reduced accumulation of full-length cDNA in the viruslike particles.

180 creening a transcription factor array of 704 full-length cDNAs in murine C2C12 myoblasts following co

181 ouse cDNA 2) project, which aimed to collect full-length cDNAs inclusively from mouse tissues, and fo

182 In this study, a full-length cDNA infectious clone was generated from a l

183 overlapping transcript alignments (ESTs and full-length cDNAs) into maximal alignment assemblies, th

184 The full-length cDNA is 5 kb long and encodes a protein of 1

185 Full-length cDNA is then synthesized from purified EST-s

186 ed on discoveries using technologies such as full-length cDNA libraries and whole genome tiling micro

187 ucted 21 regular, normalized, and subtracted full-length cDNA libraries from brains of zebra finches

188 TIF-seq entails the generation of full-length cDNA libraries, followed by their circulariz

189 tor seed endosperm by shotgun transforming a full-length cDNA library into an FAH12-expressing Arabid

190 st genes are created in a single step from a full-length cDNA library.

191 However, detection of full-length cDNAs, lower levels of sequence divergence a

192 ermits both targeted isolation of individual full-length cDNA molecules and random isolation of any p

193 By means of RACE PCR, three full-length cDNAs not reported previously in the rat wer

194 A full length cDNA of GSTT (1417 base pairs) was isolated

195 This gene, with a full-length cDNA of 3 kb, is expressed in normal colon a

196 Based on the cDNA fragment sequence, a full-length cDNA of 858 bp that contains an open reading

197 We isolated a full-length cDNA of a group B MPK (PgMPK4) from pearl mi

198 The full-length cDNA of a putative diterpene synthase was is

199 In addition, we have identified full-length cDNA of DARPP-32 (GenBank accession number A

200 Phylogenetic analysis of the full-length cDNA of DgGS1-1 indicates affinities with cy

201 Analysis and cloning of a full-length cDNA of one of the overexpressed mRNAs revea

202 The full-length cDNA of PDE7B is 2399 bp, and its ORF sequen

203 s transformed with an amplicon consisting of full-length cDNA of potato leafroll virus (PLRV) express

204 We cloned full-length cDNA of RV-A16, A36, B52, B72, C2, C15, and

205 d induce hypovirulence in S. sclerotiorum, a full-length cDNA of the 14,538-nt viral genome was clone

206 The inserted cDNA corresponds to a full-length cDNA of the AtPP2CA gene, encoding a protein

207 span the entire genome, we have assembled a full-length cDNA of the SARS-CoV Urbani strain, and have

208 We have determined the full-length cDNA of this enzyme, which includes two puta

209 e of a 340-nucleotide RNA component, and the full-length cDNA of this RNA was found to be identical i

210 To investigate this proposal, we cloned the full-length cDNA of three canine beta-defensin isoforms

211 k PMCA trafficking in live cells we cloned a full-length cDNA of Xenopus PMCA1, and show that GFP-tag

212 Full-length cDNAs of each product were obtained using RA

213 We obtained the full-length cDNAs of HIF-1alpha and HIF-2alpha, and part

214 olecules involved in brain function.We found full-length cDNAs of many known brain genes and discover

215 To recover virus from molecular clones, full-length cDNAs of PaV RNAs 1 and 2 were cotranscribed

216 max (soybean), we transiently overexpressed full-length cDNAs of soybean genes that are highly induc

217 of ecdysteroids in the molt regulation, the full-length cDNAs of the blue crab, Callinectes sapidus

218 Full-length cDNAs of zCOX-1 and zCOX-2 were cloned and a

219 sults are achieved with spliced alignment of full-length cDNAs or multiple expressed sequence tags (E

220 pliced alignment with source-native ESTs and full-length cDNAs or non-native probes derived from puta

221 n the form of a rice expressed sequence tag, full-length cDNA, or plant homolog from our comparative

222 for transcriptional evidence-known proteins, full-length cDNAs, or expressed sequence tags (ESTs)-in

223 able, however, concerning genomic structure, full-length cDNA, potential transcript variants, or loca

224 The human full-length cDNA previously was described as influenza v

225 at the RIDE system can isolate low-abundance full-length cDNAs previously unattainable by conventiona

226 Bacterial expression of a full-length cDNA produces a 45 kDa protein.

227 removed during the assembly of the complete full-length cDNA product, allowing reassembly without th

228 e data sources: (1) experimentally supported full-length cDNA, promoter and first exon sequences; (2)

229 Availability of a SARS-CoV full-length cDNA provides a template for manipulation of

230 We identified, cloned, and sequenced five full-length cDNAs representing a novel gene family, and

231 In this work an apparent full length cDNA sequence coding for a catalase (HvCatal

232 Here we present the full-length cDNA sequence (11,166 bp) of VERL from the r

233 The full-length cDNA sequence for this molecule was obtained

234 MdCrzR deduced from the full-length cDNA sequence is a 655-amino acid polypeptid

235 The full-length cDNA sequence of ACDP1 consists of 5898 bp a

236 Here, we report the full-length cDNA sequence of croaker elovl4, which conta

237 The full-length cDNA sequence of four structural isoforms of

238 The full-length cDNA sequence of Hyp-1 is 782 nucleotides in

239 The full-length cDNA sequence of L1-dsRNA/SsMBV1 comprises t

240 of cDNA sequence enabling rapid retrieval of full-length cDNA sequence of novel genes.

241 The full-length cDNA sequence of PKD1L1, determined from hum

242 nd used to design PCR primers to acquire the full-length cDNA sequence.

243 Full length cDNA sequences are an important resource for

244 nt years, largely due to the availability of full length cDNA sequences derived from many tissues.

245 Ovca-DRA full length cDNA sequences exhibited >99% identity.

246 The full length cDNA sequences of tyrosine hydroxylase (TH)

247 thon has been developed and applied to maize full length cDNA sequences to identify, classify, and lo

248 based on previously unreleased high-quality full-length cDNA sequences and a second based on the set

249 In addition to the 38 OsWAKs with full-length cDNA sequences and the 11 with rice expresse

250 >250,000 expressed sequence tags and 28,000 full-length cDNA sequences are available prior to the co

251 Apparent full-length cDNA sequences coding for manganese superoxi

252 Apparent full-length cDNA sequences coding respectively for mitoc

253 Full-length cDNA sequences encoding CfTX-A and -B and a

254 hain reaction techniques were used to obtain full-length cDNA sequences encoding the purified protein

255 ential roles in spermatogenesis, we obtained full-length cDNA sequences for all known Y genes and the

256 Full-length cDNA sequences for both mouse and human poly

257 In sum, the full-length cDNA sequences of these 14 new trichomonasvi

258 Genomic and full-length cDNA sequences provide opportunities for und

259 Using full-length cDNA sequences to identify transcription sta

260 Full-length cDNA sequences were cloned, and their subcel

261 For these genes, full-length cDNA sequences were used to cluster 212 EST

262 1 OsWRKY genes, 48 of which are supported by full-length cDNA sequences.

263 ty of the resulting isotigs do not represent full-length cDNA sequences.

264 rapid amplification of cDNA ends (RACE) and full-length cDNA sequencing, revealed four independent p

265 mains incompletely annotated, with a partial full-length cDNA set available, and with many TF/CoREG g

266 Isolation of the full-length cDNA showed EndoPDI to be a 48 kDa protein t

267 Analysis of full-length cDNAs showed that at least five different Dc

268 ther key features include random priming for full-length cDNA synthesis and gel-free library purifica

269 RNA was extracted, full-length cDNA synthesized, and PCR performed for mito

270 From a cDNA library, three similar full-length cDNAs, termed LSLa, LSLb, and LSLc, were gen

271 A ends allowed the generation of two similar full-length cDNAs, termed PALa and PALb, each of which h

272 the deduced amino acid sequence derived from full-length cDNA that do not show any deletion or mutati

273 Putative exons were used to isolate a full-length cDNA that encodes a protein of 411 amino aci

274 The full-length cDNA that encodes the beta subunit of human

275 ng known TSSs from over 5700 different human full-length cDNAs, this study extracted a set of 4737 di

276 Here, two ELO full-length cDNAs (TmELO1, TmELO2) from the yellow mealw

277 ina RNA-seq and Pacific Biosciences (PacBio) full-length cDNAs to identify 104,091 high-confidence pr

278 e annotated by spliced alignment of ESTs and full-length cDNAs to their respective complete genome se

279 al copy of the AtCPSF73-I gene, that is, the full-length cDNA under the control of its native promote

280 -base pair fragment allowed the generation a full-length cDNA using 5' and 3' rapid amplification of

281 nces derived from Csp24 peptide fragments, a full-length cDNA was cloned and shown to contain multipl

282 Subsequently full-length cDNA was cloned by the 5'-RACE (rapid amplif

283 The full-length cDNA was cloned into a baculovirus expressio

284 A full-length cDNA was cloned which encodes a putative pep

285 Functional analysis of the isolated full-length cDNA was conducted in tobacco suspension cel

286 The full-length cDNA was constructed from reverse transcript

287 Overexpression of Hi95 full-length cDNA was found toxic for many types of cultu

288 uclear localization of the 18-kDa FGF-2, its full-length cDNA was fused to that of green fluorescent

289 Based upon this sequence, a full-length cDNA was isolated and predicted to encode a

290 unction of TOM1L1 is unclear, the rat TOM1L1 full-length cDNA was isolated and used to express the pr

291 The full-length cDNA was obtained by the 5' Cap capture meth

292 Full-length cDNAs were isolated from a Drosophila embryo

293 was differentially screened, and two related full-length cDNAs were molecularly characterized: tsetse

294 to homogeneity, peptides were sequenced and full-length cDNAs were obtained.

295 PGC-1alpha gene transcription, 10,000 human full-length cDNAs were screened for induction of the PGC

296 A total of 20,704 predicted human full-length cDNAs were tested for induction of the IL-8

297 ase reporter assay for identification of the full-length cDNA, which includes the transcription initi

298 e selectively enriched and sequenced copepod full-length cDNAs, which led to the characterization of

299 the assembled cDNA contig revealed a 1743-bp full-length cDNA with 1098-bp open reading frame.

300 A full-length cDNA with an ORF of 855 nt and yielding a ap