ライフサイエンスコーパス: cloned

1 e been mapped, no resistance genes have been cloned.

2 over the parental clone were FACS-sorted and cloned.

3 ength cDNA of the 14,538-nt viral genome was cloned.

4 y mu opioid receptor subtypes that have been cloned.

5 96 (15%) of the GTs coded by rice have been cloned.

6 and minor allergens have been identified and cloned.

7 We cloned 10 virus-specific TCRs targeting 5 different viru

8 Here we have cloned 113 human monoclonal antibodies (mAbs) specific f

9 was sensitive enough to detect one copy of a cloned 23S-5S IGS fragment from "CandidatusRickettsia am

10 In the study, we cloned 643 bp RFRP cDNA from the striped hamster hypotha

11 We cloned 9 individual domains that compose the entire RPM-

12 We identified and cloned a family of three inositol hexakisphosphate kinas

13 In this work we cloned a full-length cDNA encoding an LPXRFa precursor i

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

15 In this study, we cloned a full-length sequence for the Gnih precursor of

16 We cloned a full-size Tg coding sequence from western clawe

17 We identified a L. edodes C-S lyase (Lecsl), cloned a gene of Csl encoded Lecsl and then combined mod

18 We then cloned a hpRNA targeting YFP under the regulation of the

19 We have cloned a miR395 gene from rice (Oryza sativa) and studie

20 ignaling mutants in Arabidopsis thaliana, we cloned a mutant allele of a gene that encodes a protein

21 e trait locus (QTL) analysis, identified and cloned a novel cinnamyl alcohol dehydrogenase allele (Sb

22 Here, we have identified and cloned a pollen-expressed P. rhoeas threonine-aspartate-

23 In this study, we cloned a representative set of mAbs elicited by a model

24 We cloned a set of P5betaR genes from angiosperm plant spec

25 Ectopic overexpression of the newly cloned AA-enriched variant, PIK3CD-S, in EA PCa cell lin

26 The cloned acHCN gene was expressed in Xenopus oocytes, whic

27 control CER3 transcript levels directly, we cloned additional genes identified in our suppressor scr

28 All cloned AHAs could restore immune effector functions to p

29 I-2 produced by recombinant strains carrying cloned AI synthase genes, increased survival of V. chole

30 Here we have cloned all three zebrafish amigos and show that amigo1 i

31 ition, compounds that acted as agonists at a cloned alpha-like BiOctR also induced a hyperactivity re

32 pression and its up-regulation in cancer, we cloned an approximately 1.6-kb promoter segment of the h

33 In this study, we cloned an isopentenyl pyrophosphate isomerase (IPPI) cDN

34 In this study, we cloned and analyzed chromosome markers from cultivated p

35 One of the predicted lancelet BCOL proteins, cloned and analyzed for carotenoid cleavage activity in

36 ptide (Ntcp) from the respective species was cloned and analyzed for HBV and HDV receptor activity in

37 S-821 forms tetramers instead of trimers, we cloned and analyzed its psaL gene.

38 We cloned and analyzed the expression of the genes Emx1, Lh

39 In this study, we cloned and analyzed the MSTN gene (Sc-MSTN) from razor c

40 cal steps toward (iso)eugenol production, we cloned and characterized a caffeoyl-coenzyme A O-methylt

41 To test this hypothesis we first cloned and characterized ALOX15 orthologs of selected Ca

42 luding six alpha and five beta subunits were cloned and characterized from silkworm.

43 s study, a full-length cDNA encoding CPR was cloned and characterized from T. cinnabarinus (designate

44 Here we cloned and characterized rare affinity-matured human NAN

45 Here we have cloned and characterized the iridoid synthase enzyme fro

46 Two decades later, it was cloned and characterized to be a transmembrane mucin, MU

47 In both diseases, the autoantigens have been cloned and characterized; pemphigus antigens are desmogl

48 se two receptor genes along with CsPYL1 were cloned and expressed in a heterologous system.

49 Here, the tth111IIRM gene was cloned and expressed in E. coli, and Tth111II was purifi

50 ermophilic archaeron Sulfolobus tokodaii was cloned and expressed in E. coli.

51 se from Narcissus sp. and Galanthus spp. was cloned and expressed in Escherichia coli Biochemical ana

52 Therefore, this gene was cloned and expressed in Escherichia coli, and the result

53 gulated at different moisture gradients, was cloned and expressed in tobacco.

54 llular and neck domain of human langerin was cloned and expressed to produce a recombinant active tri

55 ormation, but not in diploids that have been cloned and frozen.

56 Here we cloned and functionally characterized NCCbeta from the E

57 keeping genes selected from C. maculata were cloned and investigated.

58 get protein for DMI fungicides (VvCYP51) was cloned and investigated.

59 lergen Bet v 1 was the first such gene to be cloned and its product characterized.

60 This gene was cloned and over-expressed in Escherichia coli BL21(DE3).

61 The recombinant allergen was cloned and purified, showing similar IgE reactivity in v

62 Its promoter gm-hir1 was cloned and revealed to strongly express a fluorescence r

63 igh throughput methods to sequence 18S rRNA, cloned and sequenced 28S rRNA and microscopically counte

64 We cloned and sequenced a number of Tth111II star sites whi

65 from genetically diverse almond samples was cloned and sequenced and then analyzed for changes affec

66 AA adjacent to TAP2 as in domestic ducks, we cloned and sequenced genomic UAA-TAP2 fragments from all

67 We have previously cloned and sequenced the lnm gene cluster from Streptomy

68 We cloned and sequenced the promoter of the DBR2 gene from

69 We recovered mRNA from PBMCs from two cats, cloned and sequenced the variable and constant domains o

70 These viruses were also cloned and sequenced through Sanger sequencing to confir

71 The cDNA of the mature trypsin was cloned and sequenced.

72 etabolic regulation, the Leishmania GMPR was cloned and shown to be sufficient to complement the guaC

73 aspase genes were identified, the cDNAs were cloned and the recombinant enzymes were obtained after t

74 The gene was cloned and the sequence was codon optimized and expresse

75 genomic DNA containing the Cnn2 promoter was cloned, and a nested set of 5' truncations was studied.

76 The major Siberian hamster allergen was cloned, and allergenic properties were characterized, pr

77 We purified, cloned, and characterized 13 IgGs specific for several t

78 From this screening strategy, we identified, cloned, and characterized spe-45, a gene that encodes an

79 he typical stacked-brick binding pattern was cloned, and deletion of the cluster was performed.

80 Many of these genes have been cloned, and disruptions of their functions are associate

81 om Escherichia coli The gene was identified, cloned, and functionally expressed in the Omp-deficient

82 d prospectively isolate TEPs, we identified, cloned, and generated recombinant zebrafish thrombopoiet

83 ural and biochemical studies, we identified, cloned, and partially characterized bacterial homologues

84 The majority of antibodies that we isolated, cloned, and sequenced belonged to the IgM isotype of the

85 Using an IgG4-specific RT-PCR, we amplified, cloned, and sequenced IgG4 H chain transcripts of PBMCs

86 IgE transcripts were amplified, cloned, and sequenced using RT-PCR.

87 lthy volunteers were primed to piperacillin, cloned, and subjected to the similar analyses.

88 ion, a putative transformer2 gene (tra2) was cloned, and the structural feature and expression profil

89 in the biosynthesis pathway of melanin, were cloned, and their temporal expression patterns in the in

90 These variants were cloned, and then expressed using the magnICON transient

91 ver, the long-standing question of whether a cloned animal undergoes an accelerated aging process is

92 rtunity to study the health and longevity of cloned animals compared with their cell donors.

93 The health of cloned animals generated by somatic-cell nuclear transfe

94 ing of somatic cells to enable production of cloned animals.

95 ility of early-onset age-related diseases in cloned animals.

96 Nonpathogenic TC-derived virus N13R10 (cloned as a bacterial artificial chromosome [BAC]) has a

97 Here, FEN1 was cloned as a suppressor of transcriptional gene silencing

98 The strain C500 has been cloned as an infectious, pathogenic bacterial artificial

99 s with "matched" heavy and light chains were cloned as IgG1, and those of high affinity for specific

100 nd resistance, whereas overexpression of the cloned ATHB13 in Col-0 and Col-eds1-2 backgrounds result

101 egments on mature peptide part of MAF-1 were cloned, based on the primers designed according to the c

102 by two methods (HhaI-assay and sequencing of cloned bisulfite PCR products).

103 the evolution of this regulatory circuit, we cloned both ABA-signaling elements, SLAC1 and OST1, from

104 We have cloned both; while highly conserved in domain organizati

105 Expression of cloned BSH enzymes in the gastrointestinal tract of gnot

106 A second C5a receptor, C5L2, has also been cloned but has received much less attention because its

107 pacX was cloned by impala transposon mutagenesis.

108 g a region of interest that are subsequently cloned by recombination into a luciferase reporter vecto

109 yamine oxidase (PAO) gene was identified and cloned by screening suppression subtractive hybridisatio

110 Emb14 was cloned by transposon tagging and was confirmed by analys

111 We then generated recombinant viruses from cloned cDNAs prepared to the antigenomic RNAs both of th

112 a major disruption of signaling between the cloned conceptus and the endometrium, particularly the i

113 Our results support a "bottleneck" model for cloned conceptus survival during the periimplantation pe

114 that might be affected by the presence of a cloned conceptus, ultimately leading to mortality before

115 sed genes were affected by the presence of a cloned conceptus, whereas at d 34, approximately 36% and

116 Here we present the first individually cloned CRISPR-Cas9 genome wide arrayed sgRNA libraries c

117 he plasma of the animal from which they were cloned, demonstrating the power of mAb isolation for a d

118 opments that have led to the production of a cloned DI RNA that is highly active in preclinical studi

119 Bait-prey junctions are cloned directly from isolated genomic DNA using LAM-PCR

120 The longevity of both the donor and the cloned dog was close to the median lifespan of Afghan ho

121 vity and health of Snuppy, the world's first cloned dog, and its somatic cell donor, Tai, a male Afgh

122 ein the Bcr 3' untranslated region (UTR) was cloned downstream of a luciferase reporter showed repres

123 enylate/uridylate-rich elements (AREs), were cloned downstream of a reporter gene.

124 re lost in embryonic stem (ES) cells, and ES-cloned embryos show RNF12-dependent Xist expression.

125 d apoptotic status of bovine preimplantation cloned embryos.

126 ing to developmental failure in somatic cell cloned embryos.

127 rophage-tropic proteins, while the remaining cloned env genes encoded R5 T cell-tropic proteins.

128 PIEZO1 is a recently cloned eukaryotic cation-selective channel that opens wi

129 In this study, we cloned, expressed and characterized all of the glycoside

130 As a proof of principle we have cloned, expressed and characterized functional recombina

131 We successfully cloned, expressed and purified this putative cysteine pr

132 Here, we cloned, expressed, and characterized Rab5a and Rab5b fro

133 Here, we cloned, expressed, and characterized the GTPase LdSar1 a

134 In this study, Stt7 kinase has been cloned, expressed, and purified in a heterologous host.

135 We have cloned, expressed, and purified the CutC GRE and the act

136 Similarly, surface phenotypes of individual cloned fibroblast-like cells exhibit significant variati

137 We identified and cloned four AQPs from C. lectularius, assessed tissue an

138 In this study, we identified and cloned four OsCAF1 genes (OsCAF1A, OsCAF1B, OsCAF1G, and

139 e the means for future functional studies we cloned FoxP4 from zebra finches and compared regional an

140 mately 91% sequence identity to Bet v 7) was cloned from a cDNA library and expressed in Escherichia

141 striking differences in protein yields when cloned from a chloramphenicol resistant vector into an i

142 first-in-class, monoclonal antibody (MABp1) cloned from a human being to target interleukin-1alpha,

143 IgG AHAs cloned from a single human donor exhibited restricted sp

144 k contrast to reports on Dolly (first animal cloned from adult cells) whose diagnoses of osteoarthrit

145 Luc, which expresses an env gene (C.Du151.2) cloned from an acute heterosexually infected woman and a

146 However, TCRs cloned from an effective and one of two ineffective clon

147 tylserotonin-O-methyltransferase (ASMT), was cloned from apple rootstock, Malus zumi.

148 lum, and although alpha-like OctRs have been cloned from Balanus improvisus (BiOctR) and Drosophila m

149 Drug-specific T cells were cloned from blood and inflamed skin, and cellular phenot

150 le fragment complementation system for COase cloned from Chromobacterium sp.

151 nsLTPs-encoding cDNA and gene sequences were cloned from Coffea arabica and Coffea canephora species.

152 antiporter-encoding genes were isolated and cloned from complementary DNA (EcNHX1-EcNHX4).

153 The MfR protein subunits Met and SRC, cloned from Daphnia pulex, were fused to the fluorophore

154 a panel of human recombinant antibodies was cloned from different B cell subpopulations, and the pre

155 Here, we survey 332 NBS-LRR genes cloned from five resistant Oryza sativa (rice) cultivars

156 ear transfer to generate three lines of mice cloned from iNKT nuclei.

157 4, CYP71AP13, CYP71AU50, and CYP736A117 were cloned from P. mume 'Nanko' using publicly available P.

158 By studying antibodies cloned from patients with heterologous secondary infecti

159 -forming (cbv1) and accessory beta1 subunits cloned from rat cerebral artery myocytes.

160 Fertile mice were cloned from several neurons, establishing the compatibil

161 Monoclonal antibodies were expression cloned from single PCs of patients either isolated from

162 , Vps20, Vps24, Snf7, Vps46, and Vps60) were cloned from Spodoptera frugiperda Using a viral compleme

163 A type 2 metallothionein gene, SsMT2, was cloned from Suaeda salsa, a salt- and alkali-tolerant pl

164 The HCV1406 TCR was cloned from T cells that expanded when a hepatitis C vir

165 quence identity with a proteinase previously cloned from the American cockroach (Per a 10).

166 The two genes were cloned from the chromosome of Pseudomonas aeruginosa.

167 re found in CD247 complementary DNAs (cDNAs) cloned from the patient as well as in cDNA and genomic D

168 raniol into the secologanin pathway was also cloned from the trancriptome resource.

169 BOLTING time control 1 (BTC1) gene has been cloned from this locus.

170 Here, we examine 3,000 Mb of metagenomic DNA cloned from three phenotypically distinct patients for e

171 SlCAT2 was cloned from tomato flower cDNA, over-produced in Escheri

172 we previously observed that anti-RhD (D) Igs cloned from two donors, hyperimmunized with D(+) erythro

173 emical function of two members of this group cloned from V. minor (VmPiNMT) and R. serpentina (RsPiNM

174 s been implicated in bystander apoptosis, we cloned full-length Envs from plasma of viremic patients

175 We cloned full-length GLP-1 receptor (GLP-1R) mRNA from a h

176 To address this systematically, we cloned full-length open reading frames of alternatively

177 We positionally cloned fzt and discovered that it contains a mutation in

178 ations above wild-type levels via exogenous, cloned-gene expression compensated for inefficient B pro

179 Cloned genes in the vicinity of the four QTLs were also

180 It is now possible to deliver cloned genes safely and stably to specific retinal cell

181 ficient cloning trap, but also may allow any cloned genes to be expressed as His-tagged fusion protei

182 omerulonephritis QTL (Crgn) and positionally cloned genes underlying Crgn1 and Crgn2, which accounted

183 We cloned genetically divergent env genes from the plasma o

184 We cloned genomic DNA from two males hemizygous for the lon

185 By homology search, we also identified and cloned GPCAT genes from three plant species.

186 emical validation, a full-length ZmTps21 was cloned, heterologously expressed in Escherichia coli, an

187 noxy)pyrrolidine-2-carboxylic acid (1b), for cloned homomeric kainic acid receptors subtype 1 (GluK1)

188 shown to change the activity of CHRMs using cloned human CHRMs and CHRM knockout mice but not human

189 Earlier, we had cloned IG20 cDNA from a human insulinoma and had shown t

190 The cloned IgG-specific AHA-variable regions were mutated fr

191 responsible for the mutant wax phenotype was cloned in a forward genetic screen and identified to enc

192 ating stable cell lines the sgRNAs have been cloned in a lentivirus backbone containing PiggyBac tran

193 ic G protein-coupled receptors (GPCRs) to be cloned in any organism.

194 Salmonella typhimurium InvA gene sequences (cloned in E. coli and after 30-cycle PCR) with SYBR((R))

195 ted unique signaling capabilities, have been cloned in fetal brain tissue.

196 BRCA1 was positionally cloned in September 1994.

197 liver a 152 kb herpes simplex virus 1 genome cloned in yeast into mammalian cells to produce infectio

198 organization of any mega-sized DNA molecules cloned in yeast, facilitating the construction of design

199 Genomes can be cloned; individuals cannot.

200 lg) was covalently linked to a RMR motif and cloned into a bacterial expression system for protein pr

201 The full-length cDNA was cloned into a baculovirus expression vector, and recombi

202 s that adopted a G-quadruplex structure were cloned into a luciferase dual vector and examined for th

203 omain from the collagen alpha3(IV) chain was cloned into a mammalian expression vector, pCI-neo, with

204 native flanking sequences were amplified and cloned into a pCAG-eGFP vector directed by the ubiquitou

205 VHH) were isolated, transcribed to cDNA, and cloned into a phagemid vector for phage display library

206 , a codon-optimized gene was synthesized and cloned into a recombinant modified vaccinia virus Ankara

207 l receptor (TCR) alpha- and beta-chains were cloned into a retroviral vector.

208 terleukins and chemokines, were individually cloned into adeno-associated viral vectors.

209 hromosome, are synthesized in vitro and then cloned into allelic exchange vectors using standard proc

210 mplified from patient-derived serum samples, cloned into an expression vector, and used to generate v

211 A full-length Cx43 cloned into mammalian expression vector pCI-neo was used

212 he resulting chimeric mouse-human genes were cloned into plant expression vectors for stable nuclear

213 us regions of the HABP2 promoter region were cloned into reporter constructs, and the promoter activi

214 the protease gene, cathepsin S (Rs-cps), was cloned into the binary vector pFGC5941 in the forward an

215 lls, a sequence encoding Cre recombinase was cloned into the Il22 locus, and IL22(Cre) mice were cros

216 9 and 36 residues from the C-terminus, were cloned into the recombinant expression vector pET-28a-Pe

217 TRPM2, the second subfamily member to be cloned, is expressed in many tissues including brain, he

218 ck garden ant (Lasius niger), identified and cloned its cognate receptor and determined its pharmacol

219 they block native Kv1.3 in human T cells and cloned Kv1.3 stably expressed in L929 mouse fibroblasts.

220 Similar effects were seen on gating of cloned Kv4.2 channels, but the inhibition was less prono

221 Currents from cloned Kv4.3 channels expressed in HEK-293 cells were in

222 ssays and sequence analysis of single-colony cloned M. genitalium organisms.

223 F) binding sites in the AaTPS1 promoter, and cloned members of both TF classes were able to activate

224 ase resistance (R) genes were identified and cloned more than two decades ago.

225 Here, we reported a newly cloned mosquito Aedes (Ae.) aegypti salivary allergen.

226 Here, we cloned multiple Env sequences from 7 HIV-2-infected pati

227 In this study, we cloned multiple laforin orthologs, established a purific

228 to monitor the growth of pools of previously cloned mutants and reproducibly differentiated between d

229 gsk3, tkl3, and PBANKA_082960 by genotyping cloned mutants.

230 key factors to control viral replication we cloned Mx1 cDNAs from three bat families, Pteropodidae,

231 iological screening against several types of cloned nAChRs expressed in Xenopus laevis oocytes.

232 Here we cloned naked mole-rat ASIC3 (nmrASIC3) and used a cell-s

233 We cloned nod positionally and found that it encodes CELL N

234 Analysis of cloned Ntcp from all species revealed a pronounced role

235 Four HCN subunits have been cloned, of which HCN1 and HCN2 subunits are predominantl

236 We cloned one of these antibodies, 3H3, from memory B cells

237 M. tuberculosis DapE (MtDapE) was cloned, over-expressed and purified as an N-terminal hex

238 lic archaeon Archaeoglobus fulgidus has been cloned, over-expressed in Escherichia coli and biochemic

239 KEY MESSAGE: The vacuolar SlCAT2 was cloned, over-produced in E. coli and reconstituted in pr

240 Consequently, both enzymes were cloned, overexpressed, and purified as recombinant prote

241 ide with novel biochemical functionality, we cloned PawS1 genes and showed that this dual destiny is

242 iminosum DNA was confirmed by sequencing the cloned PCR products, and while alignment of the ITS ampl

243 Jurkat cells and in vitro methylation of the cloned PLS3 promoter suppressed luciferase expression in

244 f nematode effectors in parasitic plants, we cloned predicted effectors genes from Heterodera avenae

245 roducts was assessed by Sanger sequencing of cloned products.

246 qubit at room temperature, which stores the cloned quantum states for a millisecond under ambient co

247 If several cloned R genes were available, it would be possible to p

248 ies of >55 nM were found for all other human-cloned receptor subtypes tested.

249 for the missing ARPP phosphatase were found, cloned, recombinantly expressed, and purified.

250 rim5 homologues restricted any of a panel of cloned retroviruses.

251 hat introduction of additional copies of the cloned rstC gene instead of infection with RS1varphi was

252 er studies using recA deletion mutants and a cloned rstC gene showed that the excision event was recA

253 We cloned sabaeus CD4 and 10 candidate coreceptors.

254 A recombinant Asd(+) plasmid pCZ1 with the cloned Salmonella Choleraesuis O-antigen gene cluster wa

255 s) can support full-term development of semi-cloned (SC) embryos upon injection into MII oocytes and

256 Although when cloned separately, a single SaPI gene totally blocks pha

257 DNA of the protein was cloned, sequenced, and expressed, confirming its identit

258 Phylogenetic analysis of the cloned sequences demonstrated a high diversity of unchar

259 arative genomic hybridization, mate pair and cloned sequences, and FISH analyses, we have identified

260 recent report detailing the health status of cloned sheep concluded that the animals had aged normall

261 sure measurements in 13 aged (7-9 years old) cloned sheep, including four derived from the cell line

262 urally conceived sheep, and our healthy aged cloned sheep.

263 l long-term health effects in a cohort of 13 cloned sheep.

264 The RON3 gene was map-based cloned starting from the ron3-1 leaf mutant and found to

265 the previously identified 32 aa peptide was cloned successfully.

266 We cloned the avian ortholog of C2CD3 and found its express

267 We cloned the cDNA of SLC44A4 from human colonic epithelial

268 a simpler assay, we previously purified and cloned the diagnostic glycoproteins in the LLGP fraction

269 We cloned the effector gene AvrPm3(a2/f2) from locus_2, whi

270 We cloned the entire genome of M. mycoides in yeast and use

271 We cloned the FZL gene based on the lesion mimic phenotype

272 all BPL cells express CD19, and we recently cloned the gene encoding a natural ligand of the human C

273 ene expression, we previously identified and cloned the gene encoding apolipoprotein O (APOO), which

274 We cloned the gene encoding the Yellow Fluorescence Protein

275 ly in Nicotiana benthamiana and isolated and cloned the genes encoding the isoenzymes with plastidic

276 d the NTS neuronal networks in zebrafish and cloned the genes encoding the NTS neuropeptide and recep

277 Previously, we have cloned the lnm gene cluster from S. atroolivaceus S-140

278 To test this hypothesis, we cloned the lux quorum-sensing (QS) system and a GFP repo

279 Therefore, we cloned the maize Tel2 and Tti1 homologs and showed that

280 We cloned the prototypic EBV-neutralizing antibody, 72A1, a

281 us for mutants defective in IT formation and cloned the responsible gene, ERN1, encoding an AP2/ERF t

282 ry with a crude Arabidopsis seed extract, we cloned the single-domain antigen-binding fragments from

283 conserved in an invertebrate SLO2 channel we cloned the SLO2 channel fromDrosophila(dSLO2) and compar

284 We previously cloned the taqIIRM gene, purified the recombinant protei

285 e contribution to CD8(+) T-cell function, we cloned the TCR alpha and beta chain genes from one effec

286 The gene was cloned, the protein was overexpressed in Escherichia col

287 Two homologs of the TVA receptor have been cloned: the original quail TVA receptor, which has been

288 Since we cloned this enzyme from cDNA, we know that the gene in q

289 and crop species, and although none has been cloned to date, transcript profiling experiments have id

290 The selected plants were cloned to reduce genetic variability within each genotyp

291 omic annotations for a recently positionally-cloned Tst gene (Thiosulfate Sulfur Transferase, synonym

292 Recently we cloned two catalase-lipoxygenase fusion protein genes (a

293 nonetheless reversible for wild-type and sub-cloned U2OS cells, except for lasting genomic difference

294 Identified putative promoters were cloned upstream of GFP.

295 mportant genes in vivo, their promoters were cloned upstream of the luxCDABE operon, and luciferase e

296 Domestic animals can be cloned using techniques such as embryo splitting and nuc

297 The cloned viruses revealed typical acute and set point vira

298 s are not yet fully understood, we generated cloned viruses with all the necessary characteristic of

299 Using sequences we cloned, we retrodict the likely stepwise creation of Paw

300 %) of CAZy defined Arabidopsis GTs have been cloned, while 96 (15%) of the GTs coded by rice have bee