ライフサイエンスコーパス: cDNA library

1 l selection and regeneration of the selected cDNA library.

2 east two-hybrid screening of a bovine retina cDNA library.

3 created in a single step from a full-length cDNA library.

4 ase was isolated from a C. creticus trichome cDNA library.

5 -1), for HCV core protein from a human liver cDNA library.

6 sequences were cloned from our L. variegatus cDNA library.

7 t (LSU) cDNAs were mined from a hop trichome cDNA library.

8 d enzymes, as identified in a salivary gland cDNA library.

9 ant plants was used to construct a multiplex cDNA library.

10 rom an A. californica central nervous system cDNA library.

11 found in the sea lamprey Petromyzon marinus cDNA library.

12 a yeast two-hybrid screen with a human brain cDNA library.

13 leucine 977 was used to screen a human brain cDNA library.

14 genes was found to be overrepresented in the cDNA library.

15 in-3 (IL-3)-dependent NFS/N1.H7 myeloid cell cDNA library.

16 ressed sequence tags of the Mus musculus FGO cDNA library.

17 minus as bait was performed on a human brain cDNA library.

18 or HIG1) has been cloned from an alpha cell cDNA library.

19 uolar degeneration bodies) and a human brain cDNA library.

20 oding a serine protease using a B. divergens cDNA library.

21 haracterized and completely sequenced from a cDNA library.

22 a random selection of 420 clones from an EO cDNA library.

23 tified the human PENUMBRA from a bone marrow cDNA library.

24 using GARP as a bait to screen a human Treg cDNA library.

25 uently retrieved from a C. fleckeri tentacle cDNA library.

26 two-hybrid screen using an adult human brain cDNA library.

27 proteins from the P. papatasi salivary gland cDNA library.

28 3 in a two-hybrid screening on a mouse brain cDNA library.

29 spectively, were isolated from a coelomocyte cDNA library.

30 t a yeast two-hybrid screen of a mouse brain cDNA library.

31 and used it as a probe to screen a T. gondii cDNA library.

32 riptase polymerase chain reaction on a human cDNA library.

33 pression sequence tag clone counts in tissue cDNA libraries.

34 errepresented in regular non-tissue-targeted cDNA libraries.

35 -hybrid screening against a variety of human cDNA libraries.

36 ncoding a bona fide FcmuR in human B-lineage cDNA libraries.

37 nct TSSs were recovered in screens of cloned cDNA libraries.

38 rential gene expression between two pools of cDNA libraries.

39 eld sufficient quantities of RNA to generate cDNA libraries.

40 using deep sequencing of barcoded small RNA cDNA libraries.

41 clones from normalized, full-length-enriched cDNA libraries.

42 rom petunia (Petunia hybrida) petal-specific cDNA libraries.

43 f 6 was amplified from dog skin and bladder cDNA libraries.

44 complementation technology to screen a plant cDNA library against a bait protein directly in plants.

45 uplexes via a linker; reverse transcription; cDNA library amplification; and finally high-throughput

46 Venom gland cDNA library analysis predicted a prepropeptide structur

47 From an endothelial cDNA library analysis, 431 genes were significantly up r

48 oral symbiosis, we have constructed a set of cDNA libraries and generated and annotated ESTs from two

49 Stem cDNA libraries and latex extracts of eight opium poppy c

50 differential expression between two pools of cDNA libraries and predict putative tumour endothelial m

51 terest are selectively captured from complex cDNA libraries and sequenced to determine their absolute

52 cations as the construction of cell-specific cDNA libraries and the profiling of expressed genes and

53 icroarrays from perichondrium and periosteum cDNA libraries and used them to compare the gene express

54 eries using technologies such as full-length cDNA libraries and whole genome tiling microarrays, it i

55 A cDNA library and a custom microarray were constructed fo

56 ree putative PDAT enzymes from a castor seed cDNA library and coexpressed them with RcFAH12.

57 sed 454 pyrosequencing of a normalized adult cDNA library and de novo assembly to obtain an adult L.

58 ajor amplicons with the use of a mouse tooth cDNA library and dental cell lines.

59 RASSF2A was cloned from a brain cDNA library and directly sequenced, confirming the geno

60 uence identity to Bet v 7) was cloned from a cDNA library and expressed in Escherichia coli.

61 a two-hybrid analysis against a human brain cDNA library and identified COPS5 as a novel RanBP9-inte

62 n of a human embryonic kidney (HEK) 293 cell cDNA library and identified the catalytic subunit of the

63 d yeast two-hybrid screening against a human cDNA library and identified the non-muscle actin filamen

64 racteristic IL-17 response to screen the VSV-cDNA library and identified three different VSV-cDNA vir

65 To uncover these roles, we screened a cDNA library and isolated H-Ras-binding proteins that al

66 Using a subtracted complementary DNA (cDNA) library and sequence information about conserved c

67 the host strain was transformed with a human cDNA library, and cDNA clones that rescued growth at low

68 (Msbeta1, Msbeta2) subunits from an ice worm cDNA library, and compared their predicted amino acid se

69 AT III cDNA was amplified from a mouse brain cDNA library, and its recombinant protein was expressed

70 2 cDNA was isolated from a developing stigma cDNA library, and the corresponding gene was shown to ex

71 isolated from specimens and sorted by FACS, cDNA libraries are constructed and RNA-seq is performed,

72 ent calmodulin-binding proteins from natural cDNA libraries are presented as examples.

73 mu opioid receptor as bait and a human brain cDNA library as target, indicated that the carboxyl term

74 EST sequencing samples cDNA libraries at random, an approach that is most usefu

75 However, EST sequencing samples a cDNA library at random, and it recovers transcripts with

76 on channel gene from a Karlodinium veneficum cDNA library based on homology with known proton channel

77 ) Pv5-6 was isolated from a frond expression cDNA library based on the ability of the cDNA to increas

78 nding partners, we screened a human prostate cDNA library by the yeast two-hybrid assay using full-le

79 VSV-expressed cDNA libraries can therefore be used to identify tumor r

80 l ACC oxidase clones from loblolly pine root cDNA libraries characterized as part of an expressed seq

81 >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues and

82 tags (ESTs) derived from unamplified primary cDNA libraries constructed from mental glands of Desmogn

83 In the present work we sequenced five cDNA libraries constructed from midgut tissue from the s

84 ted Expressed Sequence Tags (ESTs) from four cDNA libraries constructed from un-normalized, normalize

85 total of 27,551 ESTs was obtained from five cDNA libraries constructed from vegetative and sporulati

86 ing a previous EST project conducted using a cDNA library constructed from hand-dissected apex tissue

87 on 1000 expressed sequence tags (EST) from a cDNA library constructed from pooled venom glands of 10

88 hain reaction (LMPCR) and complementary DNA (cDNA) library construction.

89 d the expected structures specified in their cDNA library constructions while satisfying our minimum

90 temperature and nutrients, we sequenced four cDNA libraries created from blades collected at the sea

91 Combining the cDNA library data with the latest Serial Analysis of Gen

92 e for the preparation of whole transcriptome cDNA libraries depleted of ribosomal RNA from only 1 mic

93 ollowing protocol outlines the generation of cDNA libraries derived from natural organisms as well as

94 the Gal4-based yeast two-hybrid system and a cDNA library derived from a chondrocytic cell line.

95 (CCoAOMT) was isolated from a Pinus radiata cDNA library derived from differentiating xylem.

96 poR1 as bait, we screened a yeast two-hybrid cDNA library derived from human fetal brain.

97 hput method, we developed a T7 phage display cDNA library derived from mRNA isolated from bronchoalve

98 as identified by differential screening of a cDNA library derived from sucrose-starved rice suspensio

99 ontrolling metabolic pathways, we screened a cDNA library derived from the white adipose tissue of ob

100 Multiple intravenous injections of a cDNA library, derived from human melanoma cell lines and

101 leader as a selective primer, we constructed cDNA libraries (e-cDNAs) from one marine and two freshwa

102 Partial sequencing of 5 cDNA libraries each for A. palmata and M. faveolata has

103 ased microfluidics was used to generate 1000 cDNA libraries, each from an individual pancreatic islet

104 We constructed a recombinant cDNA library encoding approximately 100 diverse GPI-anch

105 nscriptase as baits to screen an Arabidopsis cDNA library encoding proteins tagged with the C-termina

106 e up-regulated, we constructed a subtraction cDNA library enriched for differentially expressed genes

107 ally expressed TUs were identified among the cDNA libraries examined, of which 775 were differentiall

108 IF-seq entails the generation of full-length cDNA libraries, followed by their circularization and th

109 Screening cDNA libraries for genes encoding proteins that interact

110 mpal mRNA was extracted and used to generate cDNA libraries for microarray hybridization.

111 erent graft combinations was used to prepare cDNA libraries for small RNA sequencing and to analyze m

112 ne regulators, we screened a human leukocyte cDNA library for candidates that enhanced the activity o

113 Creating a cDNA library for deep mRNA sequencing (mRNAseq) is gener

114 the function of RGS9-2, we screened a human cDNA library for potential interacting proteins.

115 mpatible for PCR amplification to generate a cDNA library for RNAseq.

116 Selection from a human complementary DNA (cDNA) library for clones able to induce resistance to in

117 e for the preparation of whole-transcriptome cDNA libraries from a minute amount (500 pg) of total RN

118 ular, normalized, and subtracted full-length cDNA libraries from brains of zebra finches in 57 develo

119 We built fourteen cDNA libraries from different P. dactylifera tissues (cu

120 Stem cDNA libraries from each of the eight opium poppy cultiv

121 cDNA libraries from fetal and adult brain and ocular tis

122 Sequencing cDNA libraries from individual warm-sensitive neurons fr

123 (GO) terms, each data set was compared with cDNA libraries from intact adult stomach and small intes

124 identify such genes, we prepared subtractive cDNA libraries from murine subcutaneous (SC) or intra-ab

125 In this study, three cDNA libraries from ovules of radish before and after fe

126 system in Saccharomyces cerevisiae to screen cDNA libraries from rat ischemic myocardium, human heart

127 reparation and high-throughput sequencing of cDNA libraries from samples of small RNA is a powerful t

128 We have generated cDNA libraries from single human epidermal cells, design

129 a novel and straightforward method to clone cDNA libraries from small quantities of input RNA.

130 This method permits the generation of cDNA libraries from sub-picogram quantities of RNA robus

131 f curl virus (TYLCV), we previously compared cDNA libraries from susceptible (S) and resistant (R) to

132 By sequencing cDNA libraries from the central nervous system (CNS), we

133 quenced 1,679 random transcripts (ESTs) from cDNA libraries from the midguts of female ticks at varyi

134 This method involves fusing cDNA libraries from the tissue or cell type of interest

135 the need to generate and laboriously screen cDNA libraries from tumors and may represent a generally

136 In the present study, we have constructed cDNA libraries from two venomous structures of the cater

137 We made cDNA libraries from zebra finch (Taeniopygia guttata) br

138 en deprivation, we constructed a 3'-anchored cDNA library from 4(th) instar larvae subjected to normo

139 A cDNA library from a sample enriched for symbiont free la

140 969 reads by pyrosequencing a salivary gland cDNA library from adult females Amblyomma maculatum tick

141 LOGY AND CRITICAL FINDINGS: A salivary gland cDNA library from adult fleas was randomly sequenced, as

142 novel EHV-1 receptor was discovered using a cDNA library from equine macrophages.

143 We produced a PCR-based cDNA library from infective larvae (L3) in order to iden

144 tional regulators of T cell specification, a cDNA library from mouse Pro-T cells was screened for gen

145 nfirmed that hybrid clones identified in the cDNA library from one tissue could be reisolated in the

146 Here, we report the construction of a cDNA library from P. knowlesi, which has a lower A+T con

147 ucted and screened a single-cell subtractive cDNA library from pre-BotC inspiratory neurons.

148 been isolated by differential screening of a cDNA library from rice panicles.

149 w caffeoyl CoA OMT-like genes by screening a cDNA library from specialized hair cells of pods of the

150 For this reason, we generated a cDNA library from the intracellular amastigote form of L

151 clones were selected from an epigonal organ cDNA library from the same individual; their C region se

152 The screening of a cDNA library generated from the autologous melanoma cell

153 ty (LOH) analysis, RNA transcript profiling, cDNA library generation, proteomics discovery and signal

154 expression analysis using complementary DNA (cDNA) libraries has been improved.

155 A genetic screen of a cDNA library identified Arabidopsis kinesin light chain-

156 Functional oncogene screening of a TIC cDNA library identified Yap1 and Igf2bp3 as NANOG-depend

157 of specific, full-length clones from plasmid cDNA libraries in 5 d.

158 e latest available cell line and bulk tissue cDNA libraries in a two-step screen to predict novel tum

159 lated by functional screening of Arabidopsis cDNA libraries in E. coli.

160 performed functional screening of mammalian cDNA libraries in yeast that express the mammalian K(+)

161 a phenotype-based selection in which a total cDNA library in a retroviral vector has been introduced

162 ntified from an embryonic chicken pancreatic cDNA library in a screen for secreted factors.

163 A mouse embryo cDNA library in a yeast expression vector was used to tr

164 Using an MCF-7 cell cDNA library in a yeast two-hybrid screen, we cloned a f

165 lting from CP-r, we constructed a retroviral cDNA library in the vector pLNCX2 from KB-CP.5 (KCP.5),

166 eatment can be used to construct an intronic cDNA library, in which majority of the intron lariats ar

167 itary gland transcriptome consisting of five cDNA libraries including wild type tissue from E12.5 and

168 ted from the insects but was recognized in a cDNA library instead, the N-terminal site of signal pept

169 osperm by shotgun transforming a full-length cDNA library into an FAH12-expressing Arabidopsis line.

170 Deep sequencing of strand-specific cDNA libraries is now a ubiquitous tool for identifying

171 n a two-hybrid screen of a human bone marrow cDNA library, its most frequent partner was poly(rC) bin

172 Use of the cDNA library leads to presentation of a broad repertoire

173 In particular, the cDNA library made from brains at posthatching day 30-50,

174 We have described previously a cDNA library made from membrane-bound polysomal mRNA pre

175 A yeast two-hybrid screening of a cDNA library made from the sensory epithelium of embryon

176 Through a yeast two-hybrid screen of a cDNA library made from tissue of a failing human heart,

177 A collection of EST sequences from a cDNA library made from young E. coca leaves was employed

178 have carried out 'functional screening' of a cDNA library (made from a salt tolerant rice-Pokkali).

179 23(+68) as bait, we identified in a cochlear cDNA library MAGI-1, a MAGUK (membrane-associated guanyl

180 Detecting such transcripts in cDNA libraries may require sequencing millions of clones

181 tners for CHGA, by employing a phage display cDNA library method.

182 The cDNA library obtained from subtractive hybridization was

183 snoRNAs and scaRNAs have been obtained from cDNA libraries of capped and uncapped small RNAs using R

184 ng suppression subtractive hybridisation and cDNA libraries of cotton genotypes tolerant to Verticill

185 HCN1 message was also detected in cDNA libraries of rat cochlear inner and outer hair cell

186 Sequences from cDNA libraries of six tissues were assembled into 18 871

187 that could result in resistance to AMN107, a cDNA library of BCR-ABL mutants was introduced into Ba/F

188 ive potassium channel toxins (KTxs) from the cDNA library of M. eupeus venom glands, and we compare t

189 We show here that a cDNA library of normal tissue, expressed from a highly i

190 Excised plasmids from the cDNA library of P. vittata fronds were introduced into E

191 a transposon-based approach, we generated a cDNA library of SINV genomes with a green fluorescent pr

192 0, was characterized from the venomous gland cDNA library of the scorpion Scorpiops jendeki.

193 igenes from a subtracted, fruit development, cDNA library of watermelon were utilized to examine gene

194 this study we describe the generation of two cDNA libraries, one from placenta and one from testis, c

195 ets the stage for the effective screening of cDNA libraries or small molecules for strong modulators

196 reads sampling the viral genome population (cDNA library); our results are confirmed experimentally.

197 After linker addition, cDNA library preparation and high-throughput sequencing,

198 Here we report a unique cDNA library preparation technique that allows error det

199 By screening cDNA libraries prepared from low-molecular weight RNA fr

200 cterized using barcoded deep-sequencing of a cDNA library prepared from multiplexed RNA.

201 ecular screening of an androgenic gland (AG) cDNA library prepared from the crayfish Cherax quadricar

202 ive ACC oxidase, PtACO1, was isolated from a cDNA library produced using mRNA from lignifying xylem o

203 he user to highlight useful genes and manage cDNA library projects.

204 yeast two-hybrid screening of a human thymus cDNA library, PRP4, a serine/threonine protein kinase, w

205 Therefore, virus-expressed cDNA libraries represent a novel paradigm for cancer tre

206 t times after infection and used to generate cDNA libraries representing different temporal classes o

207 ntributors and was derived from more than 70 cDNA libraries representing diverse transcriptional prof

208 Using a lentiviral cDNA library rescue screening approach, we identified a

209 yeast two-hybrid screening of a mouse brain cDNA library, resolving and then validating interaction

210 nce tags from a range of Medicago truncatula cDNA libraries resulted in the identification of over 15

211 een blood-fed and Leishmania infected midgut cDNA libraries resulted in the identification of the tra

212 the transcripts from sugar-fed and blood-fed cDNA libraries resulted in the identification of transcr

213 Screening of a human cDNA library resulted in isolation of caspase-8 (Casp8),

214 Yeast one-hybrid screen of a human kidney cDNA library resulted in the identification of pescadill

215 Yeast two-hybrid screening of a human testis cDNA library revealed a new protein, RAD51AP2 (RAD51 Ass

216 ed cells in vitro, we performed a retroviral cDNA library screen for genes that confer resistance to

217 Here, a retroviral cDNA library screen showed that the stress-regulated pro

218 tive phosphoproteomics with mammalian kinome cDNA library screen.

219 , we discuss the relative merits of directed cDNA library screening and RT-PCR approaches.

220 The feasibility of the sdY2H assay on large cDNA library screening was demonstrated by the successfu

221 By cDNA library screening, we identified an immune cell-spe

222 tandem time-of-flight mass spectrometry and cDNA library screening, we isolated a novel member of th

223 tility in high-throughput complementary DNA (cDNA) library screening, we report the development of a

224 ified Entrez Gene parser and tools to manage cDNA library sequencing projects.

225 yeast two-hybrid screen of a human placenta cDNA library showed that NUCB2 (nucleobindin 2), via its

226 Analysis of our ON bipolar cDNA library showed that these cells express mRNAs for G

227 Analysis of cDNA libraries specific for transcripts bearing a 5'-tri

228 rver application that imports sequences from cDNA libraries, such as those generated through subtract

229 We designed a genetic selection using cDNA library suppression of 3xAsp myosin II to identify

230 s procedure, it takes about 4 d to construct cDNA libraries that are ready for sequencing.

231 T primers and processed into adapter-ligated cDNA libraries that were sequenced using an Illumina pla

232 cted from whole leaves to generate a focused cDNA library that was bi-directionally cloned into a tra

233 orescent cells and created a pure ON bipolar cDNA library that was negative for photoreceptor unique

234 using random primers in the construction of cDNA libraries, the PATHseq method recruits these short

235 To this end, we screened a kidney cDNA library through a yeast two-hybrid assay using NKCC

236 stem that facilitates the rapid screening of cDNA libraries to find signaling molecules that interact

237 Here, we use extensive sequencing of cDNA libraries to identify 9 paternally expressed and 34

238 og cells transfected with a human lymph node cDNA library to a HAVCR1/TIM1 Fc fusion protein.

239 We also used this cDNA library to confirm VirE2-interacting proteins in or

240 hybrid screen with SK1 as bait and a cardiac cDNA library to identify novel proteins involved in regu

241 en using dysbindin as bait against a cardiac cDNA library to identify the cardiac dysbindin interacto

242 ed lentivirus-based human complementary DNA (cDNA) library, transfected the cells with HCV subgenomic

243 ed expanded screening of eutherian and avian cDNA libraries using yeast-two-hybrid and split-ubiquiti

244 tners for RasGRP3, we screened a human brain cDNA library using a yeast two-hybrid approach.

245 In this study, we screened a prostate cDNA library using a yeast two-hybrid system and found t

246 Thus, we screened a cDNA library using a yeast two-hybrid system to search f

247 two-hybrid screening of a human fetal brain cDNA library using p100 as bait revealed specific intera

248 yeast two-hybrid screen of a skeletal muscle cDNA library using STARS as bait, and we identified two

249 yeast one-hybrid selection in a human brain cDNA library using the -10 Ets motif as a bait.

250 R was used to screen a mouse adrenal Y6 cell cDNA library using the bacterial two-hybrid system.

251 yeast two-hybrid selection in a human brain cDNA library using the C-terminal 415 amino acid of ERM

252 A yeast 2-hybrid screen of a human heart cDNA library using the N-terminal 273 residues of gamma2

253 y screening a human liver complementary DNA (cDNA) library using mammalian two-hybrid analysis.

254 In a yeast two-hybrid screen of mouse brain cDNA library, using the N-terminal region of human type

255 ne accumulation in hop trichomes, a trichome cDNA library was constructed and 9,816 cleansed expresse

256 A large, non-normalized cDNA library was constructed from premeiotic and meiotic

257 A normalized cDNA library was constructed from whole adults and 16,60

258 of the same histological type from which the cDNA library was derived.

259 random from an S. bicolor root hair-specific cDNA library was generated to identify candidate sequenc

260 A retroviral cDNA library was introduced into the nonmetastatic cance

261 wo-hybrid screen of an outer hair cell (OHC) cDNA library was performed.

262 A canine normalized retinal cDNA library was produced and analyzed by using a modifi

263 A cDNA library was produced and transferred into the DBAC-

264 A cDNA library was produced from mRNA isolated during the

265 To explore the basis of this lethality, a cDNA library was screened to identify proteins whose ove

266 o decipher the mechanism of action of Vpx, a cDNA library was screened with the yeast two-hybrid assa

267 Therefore, a mouse brain cDNA library was searched for novel TRPC4-interacting pr

268 Suppression Subtractive Hybridization (SSH) cDNA library, was printed and used for the comparison of

269 Based on simulation of sampling of virtual cDNA libraries, we estimate that error rates range from

270 To make cDNA libraries, we exploited the 2', 3'-cyclic phosphate

271 echnology in screening two adult human heart cDNA libraries, we identified the regulatory subunit of

272 of a bovine retinal pigment epithelium (RPE) cDNA library, we have identified elongation of very long

273 yeast two-hybrid screening of a human kidney cDNA library, we have identified the 70-kDa heat shock p

274 In a screen of a cDNA library, we identified 13 kinases whose overexpress

275 rid screening of a human embryonic stem cell cDNA library, we identified delta-catenin as a potential

276 s in a 2-hybrid screen against a rat cardiac cDNA library, we identified glycolytic enzymes (GAPDH an

277 st two-hybrid screening of adult human heart cDNA library, we identified HS-1 associated protein-1 (H

278 n aortic vascular smooth muscle cells (VSMC) cDNA library, we identified two cDNAs encoding C-termina

279 or (beta(2)AR), and fractions of a zebrafish cDNA library, we isolated a cDNA clone encoding receptor

280 By screening human cDNA library, we uncover that the Golgi resident protein

281 cDNA libraries were constructed from the following devel

282 H chain cDNA libraries were constructed from the RNA derived fro

283 ipt accumulation dynamics for ManS and GMGT, cDNA libraries were constructed using RNA isolated from

284 Two subtractive cDNA libraries were developed to study genes associated

285 From these various organs, 27 cDNA libraries were generated and sequenced, resulting i

286 Our cDNA libraries were not normalized.

287 s, most proteins in the D. variabilis midgut cDNA library were intracellular.

288 ybrid screenings of placenta and lung cancer cDNA libraries, which demonstrated that the long IDR lin

289 s approach combines genetic screens based on cDNA libraries with microarray detection methods to perm

290 st two-hybrid screen of human adult prostate cDNA library with a dominant-negative Mst1 (K59R) as bai

291 Expression screening of a cDNA library with a fusion protein containing the SH3 do

292 east two-hybrid screening of a mammary gland cDNA library with human p21-activated kinase 1 (Pak1) as

293 We screened a D. pteronyssinus expression cDNA library with IgE Abs from HDM allergic patients.

294 t two-hybrid screen of a 17-day mouse embryo cDNA library with KLF5 as bait.

295 we used a yeast two-hybrid screen of a human cDNA library with p35 as bait and isolated human septin

296 We screened a human testis cDNA library with sera from three polycythemia vera pati

297 2-hybrid screening of the human bone marrow cDNA library with the EP4 receptor as a bait identified

298 a yeast two-hybrid screen of a human kidney cDNA library with the UT-A1 intracellular loop (residues

299 P mining from 183,118 ESTs sequenced from 17 cDNA libraries yielded approximately 10,000 high-confide

300 A yeast two-hybrid screen of a human cDNA library yielded a phylogenetically conserved protei