ライフサイエンスコーパス: expression library

1 reen a neonatal rat dorsal root ganglia cDNA expression library.

2 ns, were used to screen a B. microti genomic expression library.

3 in vitro and screened a C. albicans genomic expression library.

4 post-DLI responder sera to screen a CML cDNA expression library.

5 resorption surface with an osteoblast phage expression library.

6 receptor, we screened a RAW 264.7 cell cDNA expression library.

7 he constituent enzymes using a combinatorial expression library.

8 t was complemented with Cn var. grubii yeast expression library.

9 brid screening of a human mammary gland cDNA expression library.

10 om a chronic myelogenous leukemia (CML) cDNA expression library.

11 ike factor from a mouse dorsal root ganglion expression library.

12 y screening a lambdaGEX phage HeLa cell cDNA expression library.

13 o directly screen an M. tuberculosis genomic expression library.

14 (iGb(3) synthase) from a rat placental cDNA expression library.

15 fore used to screen a B. burgdorferi genomic expression library.

16 ed mice were used to screen a P. yoelii cDNA expression library.

17 tivity, from a human cervical carcinoma cell expression library.

18 human sperm antigen by screening of a testis expression library.

19 e immune serum was used to screen a CEF cDNA expression library.

20 n SPH-binding factor (hSBF) from a HeLa cell expression library.

21 has been isolated from a tobacco lambda gt11 expression library.

22 l antibody 58K-9) to screen a rat liver cDNA expression library.

23 s transformed with an Arabidopsis cDNA yeast expression library.

24 d mice to screen an L. major amastigote cDNA expression library.

25 of DNA was used to screen a lambdagt11 cDNA expression library.

26 ene by screening a P. yoelii lambda-Zap cDNA expression library.

27 hospecific antiserum to screen a phosphatase expression library.

28 in, designated Aed a 3, was isolated from an expression library.

29 d to directly screen a P. gingivalis genomic expression library.

30 y completed Saccharomyces cerevisiae protein expression library.

31 differential screen of a P. falciparum cDNA expression library.

32 opulations that have been transduced with an expression library.

33 icking variants from a randomly mutated SapI expression library.

34 ression (RAGE) to create genome-wide protein expression libraries.

35 enced after immunoscreening T.aquaticus YT-1 expression libraries.

36 tiserum is used to screen bacteriophage cDNA expression libraries.

37 usly described CT genes in normal and cancer expression libraries.

38 to 16 antibiotics from 21 faecal metagenomic expression libraries.

39 the respective SAGE (Serial Analysis of Gene Expression) libraries.

40 lated and used to screen a glioblastoma cDNA expression library, 28 gene products were identified.

41 Using this serum for screening a human cDNA expression library a 2.5 kb cDNA clone was isolated whic

42 clonal antibody used to screen a human liver expression library allowed the isolation of a 1.2-kb clo

43 Combinatorial cloning and expression library analysis were used to determine the e

44 Combinatorial cloning and expression library analysis were used to isolate human a

45 EREX (Serologic Analysis of Recombinant cDNA Expression Libraries) analysis.

46 n and mouse homologs were isolated from cDNA expression libraries and designated HEL308.

47 on channel cloning by screening of mammalian expression libraries and discovery of compounds that cor

48 produced and screened two keratinocyte cDNA expression libraries and identified a previously sequenc

49 in factors in adult and embryonic mouse skin expression libraries and isolated a factor that is highl

50 o-hybrid system was applied to a mouse tooth expression library and a tuftelin-interacting protein (T

51 as bait, we screened a human T cell-enriched expression library and identified a gene encoding the gC

52 inhibitory activity of OMgp, we screened an expression library and identified the Nogo receptor (NgR

53 een a Leishmania amazonensis amastigote cDNA expression library and obtained the full-length gene tha

54 made a differentiated rat Sertoli cell cDNA expression library and screened it using the yeast two-h

55 d from a 43(HIV) lambda ZAP Escherichia coli expression library and screened with a panel of rabbit a

56 this yeast strain with an Arabidopsis yeast expression library and selected sterol prototrophs to ob

57 antiserum was used to screen a tobacco cDNA expression library and three distinct immunoreactive cDN

58 ose replica filter lifts from a plasmid cDNA expression library and treatment of the filters with chl

59 constructed 12 SAGE (serial analysis of gene expression) libraries and sequenced 606 532 tags.

60 eened by SEREX (serological analysis of cDNA expression libraries), and 43 genes were isolated, 2 of

61 lar antigens was used to immunoscreen a cDNA expression library, and a full length cDNA clone was iso

62 used to screen a lambdaZapII C. burnetii DNA expression library, and an immunoreactive clone was iden

63 n a B. burgdorferi genomic DNA lambda vector expression library, and an immunoreactive clone was isol

64 infected with a retroviral human heart cDNA expression library, and apoptosis was induced in virus-i

65 uman HDAC1 protein was used to screen a cDNA expression library, and one of the clones identified enc

66 g 10A-Ras cells with a MDA-MB-231 retroviral expression library, and selecting with Latrunculin-A rep

67 Using an expression library approach, we isolated a cDNA from HeL

68 pe-specific and developmental stage-specific expression libraries are rapidly enhancing the power of

69 t encodes Ecgp by screening of an HBMEC cDNA expression library as well as by 5' rapid amplification

70 d as a probe to screen a human placenta cDNA expression library by Far Western analysis.

71 show that a cDNA isolated from a rat testis expression library by interactive cloning using the regu

72 DNA was partially isolated from a HepG2 cell expression library by screening with the promoter-linked

73 We screened a chicken embryo cDNA expression library by using a peptide derived from the R

74 ied a positive clone from a human heart cDNA expression library by using an alkaline phosphatase-kall

75 t a cDNA clone, isolated from a keratinocyte expression library by using immunoaffinity-purified OCP

76 the antigen was isolated from a bEND.3 pCDM8 expression library by using transient expression in COS-

77 Transdominant genetics using expression libraries can identify proteins and peptides

78 zation of a herpes simplex virus (HSV)-based expression library consisting of cDNAs derived from PC12

79 e element B sequence as a probe to screen an expression library constructed from mRNA obtained from t

80 protein X, we screened a phage display cDNA expression library constructed from prion-infected neuro

81 ol CRE oligodeoxynucleotide and a human cDNA expression library constructed in phage lambda.

82 An inducible protein expression library, constructed from genomic DNA isolate

83 Here, we report the generation of an expression library containing a large and diverse repert

84 Here, we use a vaccinia virus (VACV) expression library containing each of the predicted 258

85 psid protein of feline calicivirus (FCV), an expression library containing random, short (100- to 200

86 A small protein expression library, corresponding to approximately 0.1x

87 By screening a rat lung expression library coupled with rapid amplification of c

88 ubtract in silico known human sequences from expression library data sets, leaving candidate nonhuman

89 A cDNA expression library derived from an IFN-gamma-stimulated

90 A cDNA expression library derived from HuH-7 mRNA was transfect

91 interact with GATE, we have screened a cDNA expression library derived from IFN-gamma-stimulated mur

92 A complementary DNA expression library derived from marrow samples from myel

93 anscribed/translated cDNAs from a small pool expression library derived from mouse spleen.

94 Direct functional screening of a cDNA expression library derived from primary porcine alveolar

95 accines were prepared by transferring a cDNA expression library derived from SB5b cells, a breast can

96 We utilized a cDNA expression library derived from the B6SutA(1) mouse myel

97 ation of second-generation short hairpin RNA expression libraries designed using an increased knowled

98 Transfection of CD4- 293T cells with a cDNA expression library developed from a podocyte cell line d

99 d from a Brugia malayi infective-stage larva expression library encoded a 12.5-kDa protein product (B

100 Using expression libraries encoding RNAs predisposed to formin

101 ng from oligonucleotides and construction of expression libraries enriched for ORFs.

102 through random mutagenesis or by introducing expression libraries, followed by selection of mutant or

103 Screening of expression libraries for bioactive clones that modulate

104 Using this yeast assay, we screened expression libraries for cDNAs from the plant, Lycopersi

105 ical for virus replication, we screened cDNA expression libraries for genes or gene fragments that co

106 ential utility of this and similarly derived expression libraries for genome-wide approaches to ident

107 oline core motif were recovered by screening expression libraries for ligands of the FE65 WW domain.

108 Therefore, we screened keratinocyte cDNA expression libraries for the putative inhibitor.

109 peroxidase to screen a barley aleurone cDNA expression library for CaM binding proteins.

110 cDNA from immature pea seeds by screening an expression library for enzyme activity.

111 to screen a human breast tissue hybrid cDNA expression library for genes encoding the proteins bindi

112 tivated in breast cancer, we screened a cDNA expression library for genes that mediate EGF-independen

113 wo-hybrid screen of a HeLa cell-derived cDNA expression library for human factors interacting with th

114 110) in the CD11b promoter, we probed a cDNA expression library for interacting proteins.

115 We screened a human osteoclast (OCL) cDNA expression library for OCL inhibitory factors and identi

116 We screened a human lung cDNA expression library for potential CaMKI substrates by sol

117 substrates, we screened an RBL-2H3 bacterial expression library for proteins that were tyrosine phosp

118 We therefore screened a colon expression library for regulators of u-PAR promoter acti

119 The screening of cDNA expression libraries from human tumors with serum antibo

120 Viral vector-based gene expression libraries from normal or diseased tissues off

121 We constructed a complementary DNA expression library from activated human CD3+ T cells, an

122 Probing of a lambdagt11 expression library from an induced myelomonocytic cell l

123 A cDNA expression library from Brassica juncea was introduced i

124 1H system to screen a salt induced rice cDNA expression library from Hasawi.

125 A lambdagt11 expression library from mouse brain was screened with ra

126 To this end, we constructed an expression library from the silk glands of the ghost mot

127 Here we describe the first genomic DNA expression library generated using the high-capacity her

128 calmodulin (CaM) to screen a corn root cDNA expression library has led to the isolation of a CaM-bin

129 rological analysis of recombinant tumor cDNA expression libraries) has been applied to several differ

130 as retrovirus-mediated mutagenesis and cDNA expression libraries have contributed greatly to our und

131 ag-pol, codon-optimized (CO) gag-pol, and an expression library immunization (ELI) vaccine geneticall

132 s recently developed against HIV-1 using the expression library immunization approach.

133 avium subsp. paratuberculosis infection with expression library immunization.

134 We are therefore exploring random RNA expression libraries in Escherichia coli to search for s

135 ze the power of serological analysis of cDNA expression libraries in identifying new human tumor anti

136 de a relatively general method for screening expression libraries in mammalian cells.

137 ells were transfected with an antisense cDNA expression library in an episomal vector followed by sel

138 rio cholerae O1, and used to probe a genomic expression library in Escherichia coli constructed from

139 used it to screen an M. tuberculosis genomic expression library in Escherichia coli.

140 promoter, we screened a mouse limb bud cDNA expression library in the yeast one-hybrid screening sys

141 transduced a C2C12 myoblast cDNA retroviral expression library into Ba/F3 cells and panned infected

142 tance to TAM, we introduced full-length cDNA expression library into estrogen receptor-positive MCF7

143 imental approach involved creation of tagged expression libraries, introduction of these libraries in

144 al use of antibody phage display and antigen expression libraries is developed and applied to a donor

145 Concurrently, an expression library made from USG3 genomic DNA was screen

146 tion of the lipoamidase gene by screening an expression library made in an unusual cosmid vector in w

147 cDNA expression library methods are usually cell-type depende

148 Serological analysis of recombinant cDNA expression libraries of human cancer has identified a nu

149 Using an approach based on Escherichia coli expression libraries of random Ad3 and Ad14p1 fiber knob

150 oviral gene transfer to create combinatorial expression libraries of trafficking signal variants in m

151 Serial analysis of gene expression libraries of two normal pancreatic ductal cel

152 In an expression library of a patient with LAgP, PMNs were scr

153 Ad35 knob-CD46 interaction, we generated an expression library of Ad35 knobs with random mutations a

154 From an Escherichia coli expression library of adenovirus type 35 fiber knob muta

155 or 1 (HAVcr-1) cDNA was isolated from a cDNA expression library of African green monkey kidney (AGMK)

156 By immunoscreening an expression library of B. cenocepacia isolate BC7, we ide

157 DTS analysis of 9,026 20-bp tags from an expression library of BCBL-1 cells infected with Kaposi'

158 racellular phase of the life cycle, a lambda expression library of Chlamydia psittaci DNA was differe

159 We then screened a novel expression library of filarial antigens displayed on the

160 ITT consists of a retroviral cDNA expression library of fusion proteins consisting of a Le

161 We performed immunoscreening of an expression library of genomic DNA from a human isolate o

162 pressed during incipient, subclinical TB, an expression library of M. tuberculosis genomic DNA was sc

163 its were identified by immunoscreening of an expression library of M. tuberculosis genomic DNA with s

164 um tuberculosis by the immunoscreening of an expression library of M. tuberculosis genomic DNA with s

165 Bacillus anthracis Sterne (pXO1(+), pXO2(-)) expression library of putative spore surface (spore-asso

166 A retroviral expression library of random cDNA fragments was construc

167 By screening an expression library of random rRNA fragments, we identifi

168 REB, of 2575 bp length, was isolated from an expression library of RL95 cells with a multimer of the

169 39-kDa protein and was used to screen a cDNA expression library of T. vaginalis.

170 work we generated a Saccharomyces cerevisiae expression library of the A. thaliana Sultr1;2 gene with

171 s tolerance profiles, and built differential expression library of their transcripts under control an

172 first selected from a Xenopus laevis oocyte expression library on the basis of the ability of the fu

173 atabase with data from several human cardiac expression libraries, phenotypic data from OMIM and data

174 e promoter region of GluB-1 as bait and cDNA expression libraries prepared from developing rice panic

175 oforms from Arabidopsis, we screened several expression libraries prepared from flower meristem, seed

176 signaling, we used 35S-labeled CaM to screen expression libraries prepared from tissues that were eit

177 se responses, we screened an autologous cDNA expression library prepared from a densely infiltrated m

178 2+)/CaM in tuberization, we have screened an expression library prepared from developing tubers with

179 We screened a phage expression library prepared from HeLa cDNA and identifie

180 ACV strain Western Reserve (VACV-WR) plasmid expression library, produced previously for proteome mic

181 A cDNA expression library representing the wheat transcriptome

182 Deep sequencing of digital gene expression libraries, representing three biological repl

183 study, we show that a screen of a lambdagt11 expression library resulted in the isolation of an appro

184 Immunoprobing of a hippocampal-expression library resulted in the isolation of EFA6A, a

185 The transfection of COS cells with cDNA expression libraries results in activation of luciferase

186 antigen by using a differential immunologic expression library screen.

187 Using proteomic analysis and gene expression library screening in a previous project, we i

188 The usage of this randomized ssDNA expression library screening technology to selectively m

189 Expression library screening with NF-muNR binding sites

190 Yeast two-hybrid, cDNA expression library screening, and coimmunoprecipitation

191 ction, representational difference analysis, expression library screening, and host gene expression p

192 sponsive region of the COL7A1 promoter in an expression library screening.

193 uced factors by biochemical purification and expression library screening.

194 Serological analyses of recombinant cDNA expression libraries (SEREX), has recently emerged as a

195 Three phage clones from a B. burgdorferi DNA expression library synthesized a 30 kDa antigen that was

196 the construction and application of a shRNA expression library targeting 9,610 human and 5,563 mouse

197 creen in murine ES (mES) cells using a shRNA expression library targeting murine transcriptional regu

198 By varying repeat length, we generated expression libraries that incrementally and predictably

199 to select PI-SceI variants from a randomized expression library that bind to different DNA substrates

200 ) receptors were used as probes to screen an expression library that was prepared from a highly TGFbe

201 th the recent development of siRNA and shRNA expression libraries, the application of RNAi technology

202 When used to screen a mouse liver cDNA expression library, this antibody exclusively recognized

203 We used silk gland expression libraries to address a long-standing controve

204 In this study, we screened a retrovirus expression library to identify EC membrane antigens dete

205 rbed IRS was used to screen a B. burgdorferi expression library to identify immunoreactive phage clon

206 used serologic analysis of recombinant cDNA expression library to screen the sera of MGUS patients t

207 rological analysis of recombinant tumor cDNA expression libraries) to different tumor types has led t

208 a gain-of-function screen, using an egg cDNA expression library, to identify an orphan G protein-coup

209 By using retroviral cDNA expression libraries, transduced selector cells expressi

210 ned HGE agent and Ehrlichia equi genomic DNA expression libraries using polyclonal equine E. equi ant

211 ction based screening of an Arabidopsis cDNA expression library using a 35S calmodulin (CaM) probe.

212 ne cDNA encoding NSGPx, isolated from a lung expression library using a polymerase chain reaction pro

213 cloned by screening a Leishmania major cDNA expression library using a rabbit antiserum.

214 midis attachment to collagen, we screened an expression library using digoxigenin-labeled collagen as

215 1, VL2 and VL3, from a human brain stem cDNA expression library using four tandem repeats of the 26-b

216 iginally cloned from a 3T3-L1 adipocyte cDNA expression library using full-length c-Cbl as a bait.

217 ed by interaction screening of a human brain expression library using the human erythroid spectrin (a

218 ory element was isolated by screening a cDNA expression library using the Southwestern technique.

219 The discovery that expression libraries, using Escherichia coli or yeast, p

220 ible, randomized single-stranded DNA (ssDNA) expression library was constructed and screened for cond

221 e to high salinity, a salt-induced rice cDNA expression library was constructed and subsequently scre

222 enotype (Hasawi), a salt-stress-induced cDNA expression library was constructed and subsequently scre

223 h for an etiologic agent of KS, a phage cDNA expression library was constructed from the aorto-iliac

224 A retroviral cDNA expression library was constructed from the EGFR-positiv

225 A B. burgdorferi genomic expression library was differentially probed with sera f

226 p. paratuberculosis sequences, a genomic DNA expression library was generated and subdivided into poo

227 A plasmid DNA expression library was generated from cecal bacteria of

228 To determine the identity of BID, an expression library was ligand screened with the BID-bind

229 gamma-linolenic acid (GLA) (18:3n-6), a cDNA expression library was made from the fungus Mortierella

230 e host, an I. scapularis salivary gland cDNA expression library was probed with serum from tick-immun

231 ng an antibody raised to Zm GST V-VI, a cDNA expression library was screened and a Zm GST V clone ide

232 A mouse limb bud cDNA expression library was screened by the Saccharomyces cer

233 A bovine liver cDNA expression library was screened for clones that compleme

234 A meningococcal genomic expression library was screened for potent CD4+ T-cell a

235 A Xenopus oocyte expression library was screened for proteins that bind t

236 An Arabidopsis cDNA expression library was screened in yeast for clones that

237 transcriptional regulation, a HeLa cell cDNA expression library was screened using a yeast two-hybrid

238 tify novel PPAR-interacting proteins, a cDNA expression library was screened with bacterially express

239 embrane proteins, a 3T3-F442A adipocyte cDNA expression library was screened with non-tyrosine-phosph

240 A T. vaginalis cDNA expression library was screened with pooled sera from pa

241 A Borrelia burgdorferi N40 genomic expression library was screened with serum from actively

242 recognized by the host, a Bartonella genomic expression library was screened with serum from an infec

243 A human peripheral blood T cell cDNA expression library was screened with the K12-Fc protein,

244 ort to find additional MDT genes, an E. coli expression library was selected for increased survival t

245 llular receptor for this virus, a mouse cDNA expression library was transfected into Cos-7 monkey kid

246 By antibody screening of an expression library we have identified and partially char

247 ss-excised Staphylococcus aureus lambdaZapII expression library, we cloned an operon encoding a novel

248 Using a genomic expression library, we determined that the clone recogni

249 to screen a human breast tissue hybrid cDNA expression library, we found that the zinc-finger transc

250 to screen a human breast tissue hybrid cDNA expression library, we have found that four orphan/nucle

251 By screening a mouse cDNA expression library, we have identified an ubiquitously e

252 NIH3T3 transfected with a human marrow cDNA expression library, we identified a putative annexin II

253 eptide as a probe to screen the human testis expression library, we identified an androgen-enhanced A

254 Screening a genomic expression library, we identified C. albicans Set1p as a

255 gh functional screening of a cellular kinase expression library, we identified mitogen-activated prot

256 Through screening of a lambda phage expression library, we identified one of these as the no

257 eled GRP1 probe to screen a mouse brain cDNA expression library, we isolated a cDNA clone encoding a

258 Using antibodies against rib43a to screen an expression library, we recovered a full-length cDNA clon

259 g 77,746 genes in 10 serial analysis of gene expression libraries were analyzed.

260 First, cDNA expression libraries were constructed from life cycle st

261 Soil metagenomic expression libraries were constructed with DNA samples p

262 Expression libraries were made from GT:CD46 and GTKO por

263 irus, noninfectible cells transduced with an expression library were challenged with a selectable pse

264 (MBP-1) from a human cervical carcinoma cell expression library which negatively regulates c-myc prom

265 library, a literature repository and a gene expression library will provide support to the burgeonin

266 ng proteins that is based on probing plasmid expression libraries with [alpha-32P]GTP.

267 otein-protein interaction-based screening of expression libraries with CaM.

268 teins have been isolated by screening lambda expression libraries with DNA probes containing their bi

269 atus and Lytechinus variegatus, by screening expression libraries with monoclonal antibodies to hyali

270 erculosis (H37Rv and Erdman strains) genomic expression libraries with pooled sera from patients with

271 creening of L. interrogans and L. kirschneri expression libraries with sera from leptospirosis patien

272 We have screened a human cDNA expression library with a digoxygenin-labelled protein p

273 creened a Mycobacterium tuberculosis genomic expression library with a pool of sera from patients dia

274 g sciellin by screening a human keratinocyte expression library with a sciellin-specific monoclonal a

275 We screened a Xenopus laevis oocyte cDNA expression library with a Src homology 3 (SH3) class II

276 To isolate mammalian Vg1 we screened a mouse expression library with a Vg1-specific monoclonal antibo

277 ed At14a, was isolated by immunoscreening an expression library with an anti-integrin antibody.

278 that bind to this region, we screened a cDNA expression library with an RNA probe containing this seq

279 artonella vinsonii subsp. berkhoffii genomic expression library with anti-Bartonella antibodies led t

280 that was isolated by immunoscreening a cDNA expression library with autoantibodies from patients wit

281 Hybridization screening of a lambda gt11 expression library with BG16.21 revealed two transcripts

282 A was cloned by screening an Ehrlichia canis expression library with convalescent dog sera, which res

283 d by differentially probing a B. burgdorferi expression library with CSF and sera from patients with

284 Immunoscreening of an expression library with monospecific antibody resulted i

285 We therefore screened a Xenopus expression library with Nck SH3 domains to identify Nck-

286 vel tumor antigens by immunoscreening a cDNA expression library with ovarian cancer patient serum.

287 assays for B. microti, we screened a genomic expression library with patient serum pools.

288 n, GRIN1, was identified by screening a cDNA expression library with phosphorylated GTPgammaS-G(z)alp

289 the GVM response, we screened a myeloma cDNA expression library with post-DLI serum from 4 patients w

290 mor destruction, we screened a melanoma cDNA expression library with postimmunization sera from a lon

291 y probing an aoHGE lambda ZAP II genomic DNA expression library with sera from aoHGE-infected mice.

292 By screening an L. infantum expression library with sera from human VL patients or i

293 screened a murine renal cell carcinoma cDNA expression library with sera from mice vaccinated with i

294 s faecium by screening an E. faecium genomic expression library with sera from patients with E. faeci

295 iral protein antigens by screening a genomic expression library with serum from a rabbit hyperimmuniz

296 was isolated by screening a wheat seed cDNA expression library with serum IgE from wheat food-allerg

297 l analysis of a recombinant lung cancer cDNA expression library with the autologous patient serum led

298 Screening of a HeLa cDNA expression library with the C-rich strand of a PDGF-A si

299 Screening of an expression library with the MCAT1 element yielded a cDNA

300 Probing a cerebellar expression library with TrAb sera from patients with Hod