ライフサイエンスコーパス: cDNA sequence

1 hepatic expression, or functional change in cDNA sequence.

2 characterized, and FBN3, reported only as a cDNA sequence.

3 n-1 from human erythrocytes and reported its cDNA sequence.

4 sequence incorporated into the complete LAMP cDNA sequence.

5 equence and structure of SFXN5 confirmed the cDNA sequence.

6 e than 8 million base pairs of high-accuracy cDNA sequence.

7 iation sites located at +1 and +92 bp of the cDNA sequence.

8 bp of the 5' end of the published mGABPalpha cDNA sequence.

9 nique barcode sequences observed for a given cDNA sequence.

10 esign PCR primers to acquire the full-length cDNA sequence.

11 se discrimination between human and nonhuman cDNA sequences.

12 sulting isotigs do not represent full-length cDNA sequences.

13 rabidopsis collections and in 7% of the rice cDNA sequences.

14 es, 48 of which are supported by full-length cDNA sequences.

15 , knowledge of cattle KIR is limited to nine cDNA sequences.

16 fied by comparison of overlapping genomic or cDNA sequences.

17 deep sequencing to read the two barcodes and cDNA sequences.

18 a simple transcription unit based on limited cDNA sequencing.

19 lignments through a novel approach: targeted cDNA sequencing.

20 ns were evaluated intensively by genomic and cDNA sequencing.

21 connectivity information through paired-end cDNA sequencing.

22 Here we present the full-length cDNA sequence (11,166 bp) of VERL from the red abalone (

23 addition to these five, we identified using cDNA sequencing a unique mis-splicing variant that cause

24 ition of a total of nearly 500 million short cDNA sequences allowed construction of temporal strand-s

25 Comparative analysis of their genomic and cDNA sequences allowed us to carry out detailed annotati

26 cDNA sequence analyses indicated that these variants rep

27 ion (RT-PCR) with gene-specific primers, and cDNA sequencing analyses we determined that the novel tr

28 GmF3'H genomic and cDNA sequence analysis of color mutant lines with varyin

29 cDNA sequence analysis of SCN8A from THP-1 cells, a huma

30 so conserved in their sequence that previous cDNA sequence analysis resulted in "unigenes" that were

31 region (CTSHDelta10-21), were identified by cDNA sequence analysis.

32 rs were designed based on the (-)-trans-ISPD cDNA sequence and employed to screen a spearmint oil gla

33 ACDP4 contains 4765 bp of cDNA sequence and encodes a protein of 775 AA.

34 ACDP3 contains 3113 bp of cDNA sequence and encodes a putative protein of 707 AA.

35 Comparison of the cDNA sequence and genomic sequence identified six sedlin

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

37 Although both cDNA sequence and protein expression of activation-induc

38 ainst infection, the availability of the MBP cDNA sequence and rMBP should help develop: (i). a tear-

39 Initially, we cloned a guinea pig kisspeptin cDNA sequence and subsequently explored the distribution

40 clone set of 60,770 RIKEN full-length mouse cDNA sequences and 44,122 public mRNA sequences.

41 We report the cDNA sequences and amino acid sequences of the beta and

42 ols for preparing cDNA libraries, assembling cDNA sequences and annotating the sequence information a

43 ty to sort, filter and search for individual cDNA sequences and cDNA-genome alignments.

44 uence just upstream from the 5' end of these cDNA sequences and designated these as putative promoter

45 We characterized human and mouse SelM cDNA sequences and expressed the selenoprotein in variou

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

47 detailed analysis of a comprehensive set of cDNA sequences and proteomics data.

48 cleotide sequence determination of recovered cDNA sequences and subsequent sequence searches showed t

49 n addition to the 38 OsWAKs with full-length cDNA sequences and the 11 with rice expressed sequence t

50 A model system of two cDNA sequences and two human pregnancy hormones are used

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

52 th chronic myelogenous leukemia (CML), using cDNA sequencing and allele-specific oligonucleotide-poly

53 We employed cDNA sequencing and comparative genomics to identify add

54 sequence annotation that is complementary to cDNA sequencing and computational gene-finding methods.

55 EST/cDNA sequencing and microarray analysis show that nearly

56 ne by chromosomal mapping, linkage analysis, cDNA sequencing and mRNA rescue that the dorsalized zebr

57 Unlike conventional methods based on cDNA sequencing and restriction fragment length polymorp

58 Genomic tiling arrays, cDNA sequencing and, more recently, RNA-Seq have provide

59 ree elements: an aptamer, a short, partially cDNA sequence, and a PEG linker conjugating the aptamer

60 correct the previously published pericentrin cDNA sequence, and describe the complex expression patte

61 ne or one-to-many comparisons of genomic and cDNA sequences, and can also be effectively incorporated

62 ce in situ hybridization (FISH), genomic and cDNA sequencing, and quantitative PCR.

63 Using a single cDNA sequencing approach, we detected 1,364 unique neure

64 pressed sequence tags and 28,000 full-length cDNA sequences are available prior to the completion of

65 All NS5 cDNA sequences are encoded by three loci, of which two a

66 The EST and cDNA sequences are first clustered based on an all-versu

67 cDNA sequences are important for defining the coding reg

68 Triticeae EST and hq-cDNA sequences are mapped onto rice loci and stored in a

69 lant species for which more than 1000 EST or cDNA sequences are publicly available.

70 cDNA sequences are used to determine mRNA transcript str

71 random for its effective use in large-scale cDNA sequencing as well as interesting insight about the

72 ignment of mouse genomic sequence with mouse cDNA sequence (BC006598), using mouse genome browser, de

73 Errors are prevalent in cDNA sequences but the extent to which sequence collecti

74 is a software package not only for cleaning cDNA sequences, but also for helping to develop sequenci

75 We first created 'perfect' simulated cDNA sequences by splicing the sequences of exons in the

76 ng computational prediction and experimental cDNA sequencing, can efficiently generate the overlappin

77 report here the cloning, gene organization, cDNA sequence characterization and expression analysis o

78 also called Wnt15 and Wnt14b), including its cDNA sequence, chromosomal mapping, epithelial cell tran

79 In this work an apparent full length cDNA sequence coding for a catalase (HvCatalase) was iso

80 The cDNA sequence coding open reading frames for rabbit TLR2

81 Apparent full-length cDNA sequences coding for manganese superoxide dismutase

82 Apparent full-length cDNA sequences coding respectively for mitochondrial (Hv

83 QC, was developed to evaluate the quality of cDNA sequence collections and to revise those sequences

84 Bioinformatic analysis and cDNA sequencing confirmed the predicted length of horse

85 The full length of Sc-MSTN cDNA sequence consists of 4226 base pairs (bp), comprisi

86 Approximately 40% of the cDNA sequence corresponded to peptides that were identif

87 used to generate a cDNA library enriched in cDNA sequences corresponding to mRNA species that are sp

88 1B, and 1C) were identified from genomic and cDNA sequence data bases.

89 The FANTOM2 cDNA sequence data set is an excellent model to demonstr

90 ormation about gene structure extracted from cDNA sequence databases.

91 rgely due to the availability of full length cDNA sequences derived from many tissues.

92 Here we report that a large fraction of cDNA sequences detected in microbial metatranscriptomic

93 New cDNA sequence determinations for the BRV L1 and M2 genom

94 three residues, suggesting that the muMUC18 cDNA sequence determined in this report is correct.

95 on a comparison of genomic and corresponding cDNA sequences determined for two mitochondrial DNA-enco

96 ICAD, is correctly processed, and dff40/cad cDNA sequence does not reveal mutations altering its ami

97 Their complete cDNA sequences encode predicted peptides of 252 and 598

98 Its cDNA sequence encoded for a 303-aa protein with a calcul

99 The complete LAPSER1 cDNA sequence encodes a predicted protein containing var

100 A cDNA sequence encoding mature peptide of zebrafish somat

101 The cDNA sequence encoding O-fucosyltransferase 2 was origin

102 Analysis of cDNA sequence encoding zeta-crystallin of the tree frog

103 on of the components of CF, we have isolated cDNA sequences encoding a second component of CF, CF50.

104 icago truncatula enabled us to identify nine cDNA sequences encoding BAHD super-family enzymes that a

105 Full-length cDNA sequences encoding CfTX-A and -B and a third putati

106 Subsequently, cDNA sequences encoding rodent and human RasGRP4 protein

107 Here, we report the cloning of cDNA sequences encoding seven clusters or isoforms of th

108 The transcript for ACDP2 has 4058 bp of cDNA sequence, encoding a protein of 875 AA.

109 Here, we provide cDNA sequence evidence that the platyrrhine GH cluster a

110 This cDNA sequence exhibited 87% homology with human IL-10.

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

112 ntext of either wild-type or codon-optimized cDNA sequences expressed under control of the strong, ub

113 Genomic and cDNA sequencing followed by joint assembly is a rapid an

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

115 in spermatogenesis, we obtained full-length cDNA sequences for all known Y genes and their X chromos

116 We identified cDNA sequences for lama2, lama4 and lama5 and disrupted

117 We characterized rice cDNA sequences for OsDr1 and OsDrAp1, which encode struc

118 in pea and castor peroxisomal membranes and cDNA sequences for several 'cytosolic' MDARs, the geneti

119 We report cDNA sequences for the mouse orthologs of three of these

120 ene by RACE-PCR, and analysis of the deduced cDNA sequence found that this maternal product was appro

121 Full-length CTL2 cDNA sequenced from guinea pig inner ear has 85.9% ident

122 of cDNA ends (RACE) was used to obtain their cDNA sequences from 11 cDNA populations.

123 CE, clones from 506 genes were sequenced and cDNA sequences from 399 target genes were recovered.

124 Direct comparison and alignment of existing cDNA sequences from a related species is an effective an

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

126 leven partial mitochondrial nad5 genomic and cDNA sequences from diverse taxa of hornworts reveal 125

127 Two cDNA sequences from G. theta and one from Cryptomonas en

128 Computational analysis of cDNA sequences from multiple organisms suggests that a l

129 ucleotide discrepancies were found in 51% of cDNA sequences from one Arabidopsis cDNA collection, 89%

130 We also identified two WC1 cDNA sequences from other cattle that did not correspond

131 r sorting approximately 4 million additional cDNA sequences from over 200 plant species.

132 cDNA sequences from seven taxonomically diverse hornwort

133 Comparison of multiple cDNA sequences from several individuals reveals the pres

134 The amino acid sequences deduced from MUC18 cDNA sequences from six other mouse melanoma cell lines

135 cDNA sequences from virion RNA were synthesized, amplifi

136 A combination of mining genome and cDNA sequences from wild tomato species and S. lycopersi

137 nstrate that two rhodopsins, identified from cDNA sequences, function as low- and high-light-intensit

138 We describe the cDNA sequence, genomic organization, and splice variants

139 Here we report a comparison of cDNA sequences, genomic organization, editing site seque

140 543 base pairs upstream of the 5' end of the cDNA sequence has a glucose responsive regulatory elemen

141 Although the human MDM2 cDNA sequence has been reported, the genomic organisatio

142 acrophage colony-stimulating factor (GM-CSF) cDNA sequence has been substituted for the E3-gp19 gene

143 The ZMTX3 cDNA sequence has the greatest homology to a human seque

144 In maize, five sig cDNA sequences have been reported, and four of the produ

145 Subsequent cloning of the pool identified a cDNA sequence homologous, except for one amino acid (aa

146 The obtained cDNA sequences, homology comparisons and high-throughput

147 different sera led to the cloning of partial cDNA sequences identical to annexin XI-A.

148 ly or computationally identified, many short cDNA sequences identified as tags by use of serial analy

149 ability of an adenovirus containing a 528 bp cDNA sequence in antisense orientation to the 5' end of

150 The PLC-beta2 cDNA sequence in the patient showed no abnormalities.

151 reening identified FP-1 as the most abundant cDNA sequence in this subtraction library.

152 Here we identify mouse cDNA sequences in the FANTOM2 data set for a set of 67 h

153 premature termination codons in 4 and 42% of cDNA sequences in the respective Arabidopsis collections

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

155 Molecular cloning and cDNA sequencing in human brain revealed that NRG3 underg

156 eral binding sites upstream of the GABPalpha cDNA sequence including sites for GABP (-86, -104, -169,

157 compared to the previously published ADAMTS6 cDNA sequence, including a redefinition of the predicted

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

159 Comparison of genomic and cDNA sequences indicated that both AS-81 and AS-193 tran

160 Analysis of the complete WC1 cDNA sequences indicated that the thirteen WC1 genes cod

161 f the neuroserpin precursor deduced from its cDNA sequence indicating the entire molecule was deposit

162 calculated from ss-cDNA and double-stranded-cDNA sequencing, indicting that ss-cDNA sequencing is bo

163 We have grouped all available EST and cDNA sequences into 12,063 ACEGs (assembly of contiguous

164 By targeting FKHR cDNA sequences into the Pax3 locus of embryonic stem cel

165 MdCrzR deduced from the full-length cDNA sequence is a 655-amino acid polypeptide that conta

166 for elucidating gene structures with native cDNA sequences is cost-effective and will become even mo

167 -stranded-cDNA sequencing, indicting that ss-cDNA sequencing is both robust and appropriate for use i

168 (>95%) was observed in analogous venom gland cDNA sequences isolated (by PCR) from another saw-scaled

169 The variant AFP (vAFP) cDNA sequences isolated from a multipotent hematopoietic

170 The cDNA sequence matched contiguous genomic DNA sequences i

171 the extrapallial (EP) protein by RT-PCR and cDNA sequencing methods and by de novo peptide sequencin

172 The cDNA sequence of 1830 bp is located on gene Xq25-26 with

173 The full-length cDNA sequence of ACDP1 consists of 5898 bp and encodes a

174 iments have subsequently identified a 900-bp cDNA sequence of APeg3 from mouse brain.

175 expression plasmid (pcDNA3-ATF) containing a cDNA sequence of ATF-uPA.

176 We determined the entire cDNA sequence of Ce-kettin that encodes a protein of 472

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

178 The cDNA sequence of CYP4G19 has an open ready frame of 1638

179 The first comes from a cDNA sequence of Dfos.

180 The full-length cDNA sequence of four structural isoforms of trehalose-6

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

182 The full-length cDNA sequence of L1-dsRNA/SsMBV1 comprises two large ope

183 The complete cDNA sequence of Limulus SAP, and the derived amino acid

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

185 nization of the previously published partial cDNA sequence of MUC17.

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

187 The full-length cDNA sequence of PKD1L1, determined from human testis cD

188 In this study we determined the primary cDNA sequence of porcine Dicer (pDicer), confirmed its e

189 The complete cDNA sequence of rabbit LL was determined, and labeled L

190 The cDNA sequence of the gene has open reading frames of 106

191 The cDNA sequence of the new protein encodes 541 amino acid

192 A partial cDNA sequence of this gene, called PSGR, was recently cl

193 The cDNA sequence of this gene, which has been designated Ob

194 We furthermore report the complete cDNA sequences of 11 additional trichomonasvirus strains

195 Here, we report the complete cDNA sequences of 3 trichomonasvirus strains, one from e

196 everal potential miRNA targets were found in cDNA sequences of California poppy.

197 The cDNA sequences of CYP4AB1 and CYP4AB2 have open reading

198 d that use a liver-specific promoter and the cDNA sequences of either the human or canine heavy and l

199 , we conducted public database searches with cDNA sequences of human Siglec-5 to -10 and identified t

200 This study presents data on the cDNA sequences of lombricine kinase from two smaller oli

201 To date, cDNA sequences of one or more strains of each of three t

202 racod (Crustacea) vision, we present partial cDNA sequences of ostracod visual pigment genes (opsins)

203 The cDNA sequences of the central hypervariable region of se

204 The results of genomic and cDNA sequences of the porcine TGFBR1 gene demonstrated t

205 The cDNA sequences of the rat, cattle, pig, and dog OAS gene

206 We also analyzed cDNA sequences of the three genes that have been previou

207 In sum, the full-length cDNA sequences of these 14 new trichomonasviruses greatl

208 Analysis of the cDNA sequences of these antibodies show clustered mutati

209 The full length cDNA sequences of tyrosine hydroxylase (TH) and dopa dec

210 udy examined p44 expression and analyzed the cDNA sequences of various p44 transcripts from the splee

211 The full-length genomic and cDNA sequences of ZmMRP1 and 2 were obtained, permitting

212 cDNA sequencing of the receptor tyrosine kinase domain o

213 Notably, cDNA sequencing of Wnt/beta-catenin pathway regulatory g

214 Although high-throughput cDNA sequencing offers a unique opportunity to delineate

215 protein analytes and nontargeted immobilized cDNA sequence or antibodies.

216 ase designed to facilitate the search of EST/cDNA sequences or STS markers that can be used to repres

217 The cDNA sequences originated from independent rearrangement

218 Here we describe the details of our cDNA-sequencing pipeline, including a summary of the exp

219 carcinoma cell lines with the complete ppFur cDNA sequence (pIRES-EGFP-ppFur) or with the empty expre

220 cDNA sequences predict that the proteins have a function

221 king sequence matched the C. reinhardtii Rca cDNA sequence previously deposited in the National Cente

222 ybridized with 5760 cDNA arrays (5289 unique cDNA sequences) printed on individual microscope slides.

223 n the nucleic acid restoration of incomplete cDNA sequences prior to T7 in vitro transcription (IVT)

224 Large-scale cDNA sequencing projects and tiling array studies have r

225 ng is greatly outpacing the rate of EST- and cDNA-sequencing projects.

226 Genomic and full-length cDNA sequences provide opportunities for understanding h

227 Additional cDNA sequencing provided the previously unknown N-termin

228 Comparison of genomic with cDNA sequences provides their exon-intron structure.

229 16S rRNA cDNA sequencing, qPCR of mcrA transcripts, and functiona

230 A total of 1710 cDNA sequence reads revealed the presence of many cDNAs

231 esented by over 1 billion complementary DNA (cDNA) sequence reads.

232 We previously identified cDNA sequences representing four Arabidopsis thaliana ty

233 g focused on the generation of comprehensive cDNA-sequence resources.

234 the five in-frame AUG residues in the eIF4GI cDNA sequence resulted in loss of corresponding polypept

235 For the remaining two genes, the cDNA sequences reveal major differences with predicted g

236 hylogenetic analyses of hornwort genomic and cDNAs sequences reveal that 65 of the 94 phylogeneticall

237 Analysis of human and mouse cDNA sequences revealed mitochondrial and cytosolic tran

238 Comparative analysis of genomic and cDNA sequences revealed that the SiTf gene was comprised

239 Subsequent cDNA sequencing revealed errors in published sequences t

240 cDNA sequencing revealed the existence of structural pol

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

242 The cDNA sequence reveals it to be a POU domain factor relat

243 Recent advances in high-throughput cDNA sequencing (RNA-seq) can reveal new genes and splic

244 Strand-specific, massively parallel cDNA sequencing (RNA-seq) is a powerful tool for transcr

245 Massively parallel cDNA sequencing (RNA-Seq) provides an unbiased way to st

246 melanocyte transcriptome, massively parallel cDNA sequencing (RNA-seq) was performed on genetically m

247 (TG) neurons using the Illumina platform for cDNA sequencing (RNA-seq).

248 The cDNA sequences share total identity in their 3'-end and

249 cDNA sequences show that both RNAs encode the identical

250 -ray crystallography, both based on the same cDNA sequence, show that each aggregate is constructed f

251 The SERT cDNA sequence shows no homology to any of the known gene

252 ith antisense oligonucleotides to the cloned cDNA sequence significantly inhibited UTP- and ATP-induc

253 The full-length spurt cDNA sequence spans a genomic DNA fragment of 7,313 bp,

254 Amplifiable cDNA sequence tags were isolated by hybridization to ind

255 reverse genetics were used to isolate a new cDNA sequence that encodes for a protein assembled into

256 n questioned based on a compilation of human cDNA sequences that showed a high frequency of upstream

257 found by flow cytometry, immunoblotting and cDNA sequencing that individuals with FCGR3B-deleted all

258 embryo, a partial DNA complementary to RNA (cDNA) sequence that was later identified as the human ho

259 viding practical guidelines for interpreting cDNA sequences, the scanning model provides a theoretica

260 er of matching EST and high quality cDNA (hq-cDNA) sequences, tissue distribution and likely intron p

261 omparison of the published mouse pericentrin cDNA sequence to mouse genomic DNA sequences revealed tw

262 e mouse genome database that mapped the PAP7 cDNA sequence to the 1H4 area.

263 Matching of the cDNA sequence to the human genome revealed that the eIF2

264 Comparison of the cDNA sequence to the human genomic sequence indicates th

265 standalone program for mapping and aligning cDNA sequences to a genome.

266 Using full-length cDNA sequences to identify transcription start sites (TS

267 n developed and applied to maize full length cDNA sequences to identify, classify, and localize poten

268 Making use of available cDNA sequences to other TKDP family members and recent i

269 The alignment of full-length human cDNA sequences to the finished sequence of the human gen

270 n structures in a genome is to align spliced cDNA sequences to the genome.

271 quencing of the SSH library and matching the cDNA sequences to the P. yoelii genome yielded 25 redund

272 methods in conjunction with high throughput cDNA sequencing to determine the precise 5'-capped and 3

273 Here we used RNA-Seq, tiling microarrays and cDNA sequencing to explore the transcriptome in 30 disti

274 Canine ortholog cDNA sequence was cloned and verified using RPE/choroid

275 We detected 350 RNA editing sites when the cDNA sequence was compared to that of the genomic DNA.

276 An additional validation by RT-PCR and cDNA sequencing was successfully performed for 105 selec

277 From the cDNA sequences we assembled a unigene set of 137 distinc

278 Using the GmPGM cDNA sequence, we identified a homologous Arabidopsis th

279 With 120 Mb of cDNA sequences, we were able to identify genomic rearran

280 o coupled with reverse transcription PCR and cDNA sequencing, we have identified 4 novel isoforms of

281 27,840 independent cDNA sequences were filtered by computational subtractio

282 All other cDNA sequences were found to agree with the previous ann

283 Several different M. x giganteus C(4)-PPDK cDNA sequences were found, but putative translated prote

284 cDNA sequences were generated from developing nasturtium

285 domain) sequences, eight different Ovca-DRB cDNA sequences were identified in BHS.

286 Additionally, equivalent IgH cDNA sequences were identified in both fractions, sugges

287 rrying the region of deletions in the turkey cDNA sequences were identified.

288 The cDNA sequences were obtained by assembling their 5' and

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

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

291 verlap or immediately flank 5' ends of known cDNA sequences, while the remainder is found in other ge

292 To this end, a full-length mouse IL-17F cDNA sequence with a 483-bp coding region sequence was f

293 family member revealed an abnormally spliced cDNA sequence with skipping of exon 47.

294 rted in the literature, is based solely upon cDNA sequences with chain lengths determined according t

295 Comparison of the cDNA sequences with each other and with the mouse genomi

296 e splice events as seen in alignments of EST/cDNA sequences with genome sequences, and a database of

297 trategy is to: 1) identify windows of unique cDNA sequences with homology to each other, 2) compare t

298 that combines extremely specific 5'-complete cDNA sequencing with an integrated data analysis workflo

299 tes the utility of combining high-throughput cDNA sequencing with proteomics experiments in a target

300 odel to demonstrate the power of large-scale cDNA sequencing, with the goal of providing a full-lengt