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

30 Sequencing full-length cDNAs and hybridizations using RNA populatio

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

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

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

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

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

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

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

38 Full-length cDNAs can be obtained from complex mixtures

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 Full-length cDNA clones containing the entire coding reg

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

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

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

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

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

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

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

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

74 Full-length cDNA clones provide information about intron

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

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

77 Full-length cDNA clones were identified encoding two can

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

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

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

81 We report the full-length cDNA cloning, molecular characterization and

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

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

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

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

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

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

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

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

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

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

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

93 The full-length cDNA corresponding to the differentially exp

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

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

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

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

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

99 The full length cDNA encoding the beta subunit was isolated

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 Full-length cDNAs encoding CYP79D16, CYP79A68, CYP71AN24

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

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

119 Three full-length cDNAs encoding putative isoprenoid synthases

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 We report nanopore sequencing of full-length cDNA from CLL samples with and without SF3B1

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 horbol ester (PMA) and transduction with the full-length cDNA of GLS2.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 >250,000 expressed sequence tags and 28,000 full-length cDNA sequences are available prior to the co

249 Here, we generated over 10,000,000 full-length cDNA sequences at a median accuracy of 97.9%

250 Apparent full-length cDNA sequences coding for manganese superoxi

251 Apparent full-length cDNA sequences coding respectively for mitoc

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

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

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

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

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

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

258 Using full-length cDNA sequences to identify transcription sta

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

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

261 1 OsWRKY genes, 48 of which are supported by full-length cDNA sequences.

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

263 data set to (1) show that deep and accurate full-length cDNA sequencing can be used to provide isofo

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 MS-derived sequences of natural Rhi o 2, the full-length cDNA was cloned, and expressed as recombinan

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

287 The full-length cDNA was constructed from reverse transcript

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

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

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

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

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

293 Full-length cDNAs were isolated from a Drosophila embryo

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

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

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

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

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

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

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