ライフサイエンスコーパス: bacterial artificial chromosome

1 HD mouse models, the YAC128 and the BACHD (a bacterial-artificial chromosome).

2 ) into the human elastin gene contained in a bacterial artificial chromosome.

3 tein in the LRRK2 genomic locus carried by a bacterial artificial chromosome.

4 emented on the HSV-1(F) genome cloned into a bacterial artificial chromosome.

5 cted using the HSV-1(F) genome cloned into a bacterial artificial chromosome.

6 fically Gad1 mRNA under the control of Pvalb bacterial artificial chromosome.

7 leosomal DNA enriched via hybridization with bacterial artificial chromosomes.

8 We sequenced 12 V. monoica bacterial artificial chromosomes, 11 corresponding to th

9 By using bacterial artificial chromosome 16 (BAC16) clone carryin

10 The availability of the OSVP genome as a bacterial artificial chromosome allows for the rapid ins

11 ng mouse embryonic stem cells (ES cells) and bacterial artificial chromosomes and have used it to cla

12 n (LAP)-tagged dynein/dynactin subunits from bacterial artificial chromosomes and observed asymmetric

13 Large-insert BAC (bacterial artificial chromosome) and BIBAC (binary BAC)

14 oma pathogenesis, a genome-wide search using bacterial artificial chromosome array comparative genomi

15 n the context of the infection have utilized bacterial artificial chromosomes as vectors to generate

16 Using an angiotensin receptor bacterial artificial chromosome (BAC) and enhanced green

17 or backbone was engineered to contain both a bacterial artificial chromosome (BAC) and the Invitrogen

18 n one exon to the retrieval construct from a bacterial artificial chromosome (BAC) by recombineering

19 irst designed in silico and constructed on a bacterial artificial chromosome (BAC) by using a recombi

20 MDiGS combines biotinylated bacterial artificial chromosome (BAC) capture and multip

21 A bacterial artificial chromosome (BAC) carrying the compl

22 We have constructed a BHV-1 bacterial artificial chromosome (BAC) clone by inserting

23 generated through end sequencing of a potato bacterial artificial chromosome (BAC) clone library (87

24 The bacterial artificial chromosome (BAC) clone Merlin (ME)

25 gles), we generated a full-length infectious bacterial artificial chromosome (BAC) clone of the P-Oka

26 constructed a herpes simplex virus 2 (HSV-2) bacterial artificial chromosome (BAC) clone, bHSV2-BAC38

27 The transfer of a 150-kb bacterial artificial chromosome (BAC) clone, RP364B14, c

28 MDV replicates generated from an infectious bacterial artificial chromosome (BAC) clone.

29 omains: (i) the problem of decoding reads to bacterial artificial chromosome (BAC) clones (in the con

30 By sequencing bacterial artificial chromosome (BAC) clones and the who

31 H analysis using 18 randomly selected potato bacterial artificial chromosome (BAC) clones in a set of

32 (FISH) mapping of 30 genetic marker-anchored bacterial artificial chromosome (BAC) clones on the pach

33 assaying for receptor activity conferred by bacterial artificial chromosome (BAC) clones spanning th

34 cific Biosciences (PacBio) to sequence eight Bacterial Artificial Chromosome (BAC) clones spanning th

35 nalysis, individually and as mixtures, of 95 bacterial artificial chromosome (BAC) clones that cover

36 mparative analyses, at the scale of complete bacterial artificial chromosome (BAC) clones, between th

37 Through the analysis of bacterial artificial chromosome (BAC) clones, pulsed-fie

38 ome from random sequence reads and assembled bacterial artificial chromosome (BAC) clones, we show th

39 nic mice (Grk1(+)) were generated by using a bacterial artificial chromosome (BAC) construct containi

40 Here, we used a bacterial artificial chromosome (BAC) construct that exp

41 e pathogenic LRRK2-G2019S protein from mouse bacterial artificial chromosome (BAC) constructs closely

42 In this report, we describe two VZV bacterial artificial chromosome (BAC) constructs with OR

43 genic mouse models were developed that use a Bacterial Artificial Chromosome (BAC) containing 208kb f

44 escent protein (eGFP) under the control of a bacterial artificial chromosome (BAC) containing a very

45 Here we report transgenic mice carrying a bacterial artificial chromosome (BAC) containing the ful

46 In addition, a bacterial artificial chromosome (BAC) contig was constru

47 formed extensive EST analysis, constructed a bacterial artificial chromosome (BAC) contig, and obtain

48 We prepared recombinant HCMV bacterial artificial chromosome (BAC) DNAs with either o

49 We used an in vivo bacterial artificial chromosome (BAC) enhancer-trapping

50 ture gene Nkx2.5, using a luciferase knockin bacterial artificial chromosome (BAC) in mouse P19CL6 pl

51 n corn rootworm, using survey sequences from bacterial artificial chromosome (BAC) inserts and contig

52 transgenic mouse lines using a human IKBKAP bacterial artificial chromosome (BAC) into which we inse

53 Here, we generated a bacterial artificial chromosome (BAC) KSHV recombinant v

54 nt and characterization by end-sequencing of bacterial artificial chromosome (BAC) libraries derived

55 Two bacterial artificial chromosome (BAC) libraries of a hom

56 ion of the walnut genome, we constructed two bacterial artificial chromosome (BAC) libraries, contain

57 A bacterial artificial chromosome (BAC) library equivalent

58 We developed a bacterial artificial chromosome (BAC) library from an Ab

59 A Bacterial Artificial Chromosome (BAC) library was made f

60 ude a whole-genome shotgun (WGS) assembly, a bacterial artificial chromosome (BAC) physical map, and

61 methods to isolate rare (1:10,000-1:100,000) bacterial artificial chromosome (BAC) recombinants requi

62 his hypothesis by employing a combination of bacterial artificial chromosome (BAC) recombineering and

63 A simple and efficient strategy for Bacterial Artificial Chromosome (BAC) recombineering bas

64 d the mouse Bmp4 locus using two overlapping bacterial artificial chromosome (BAC) reporter transgene

65 Using chromatinized bacterial artificial chromosome (BAC) reporters in human

66 is human-specific repression, we constructed bacterial artificial chromosome (BAC) reporters using hu

67 stem cell (ESC) lines containing single-copy bacterial artificial chromosome (BAC) reporters, coverin

68 he first synthesis of a comprehensive set of bacterial artificial chromosome (BAC) resources for 19 D

69 pping, microfluidics-based linked reads, and bacterial artificial chromosome (BAC) sequencing approac

70 uses (BAC-DeltaK8 and BAC-stopK8) by using a bacterial artificial chromosome (BAC) system.

71 iated herpesvirus (KSHV) has come to rely on bacterial artificial chromosome (BAC) technology.

72 erated using a mutagenesis strategy based on bacterial artificial chromosome (BAC) technology.

73 e present work presents a novel in vivo DRD1-Bacterial Artificial Chromosome (BAC) Tet-on system allo

74 has been cloned as an infectious, pathogenic bacterial artificial chromosome (BAC) that is used to st

75 Using neuronal bacterial artificial chromosome (BAC) transfection, we f

76 ith Repeat Frameshift (MORF) allows a single Bacterial Artificial Chromosome (BAC) transgene to direc

77 Pcsk9 knock-out mice expressing a human bacterial artificial chromosome (BAC) transgene were gen

78 Mice carrying bacterial artificial chromosome (BAC) transgenes have be

79 n this paper, we use autonomous targeting of bacterial artificial chromosome (BAC) transgenes to reve

80 enes TXNRD2, COMT and ARVCF, on behaviors in bacterial artificial chromosome (BAC) transgenic (TG) mi

81 Using bacterial artificial chromosome (BAC) transgenic HeLa an

82 By generating a bacterial artificial chromosome (BAC) transgenic IL-13 r

83 Recent studies have used bacterial artificial chromosome (BAC) transgenic mice ex

84 ntrol have increasingly relied on the use of bacterial artificial chromosome (BAC) transgenic mice ex

85 Initial studies of bacterial artificial chromosome (BAC) transgenic mice ha

86 Using Hdc-EGFP bacterial artificial chromosome (BAC) transgenic mice in

87 Using HDC-EGFP bacterial artificial chromosome (BAC) transgenic mice in

88 Using bacterial artificial chromosome (BAC) transgenic mice th

89 ssess the role of Gfi1 in vivo, we generated bacterial artificial chromosome (BAC) transgenic mice, i

90 ion of G2DHE to leukemogenesis by creating a bacterial artificial chromosome (BAC) transgenic model t

91 r cells in a temporal manner, we generated a bacterial artificial chromosome (BAC) transgenic mouse l

92 Here, we demonstrate that a Esr2 bacterial artificial chromosome (BAC) transgenic mouse l

93 have developed a series of conditional VIPR2 bacterial artificial chromosome (BAC) transgenic mouse m

94 Here we characterize two bacterial artificial chromosome (BAC) transgenic mouse s

95 We used a bacterial artificial chromosome (BAC) transgenic strateg

96 e genes with different reporters in a single bacterial artificial chromosome (BAC) vector containing

97 Bacterial artificial chromosome (BAC) vectors enable sta

98 common bean genome, the ends of a number of bacterial artificial chromosome (BAC) were sequenced, an

99 iral genome, we generated a recombinant HHV8 bacterial artificial chromosome (BAC) with a deletion in

100 In addition, we constructed a KSHV bacterial artificial chromosome (BAC) with LZ domain-del

101 ted an HD transgenic rat model using a human bacterial artificial chromosome (BAC), which contains th

102 scale accuracy, and to a set of high-quality bacterial artificial chromosome (BAC)-based assemblies t

103 We previously reported a bacterial artificial chromosome (BAC)-based lymphatic re

104 c encephalomyelitis, using a newly developed bacterial artificial chromosome (BAC)-based MHV reverse

105 A bacterial artificial chromosome (BAC)-based physical map

106 cted transcriptional activation of Hoxb13, a bacterial artificial chromosome (BAC)-based reporter gen

107 In contrast, bacterial artificial chromosome (BAC)-cloned strains TB4

108 d a panel of US28 recombinant viruses in the bacterial artificial chromosome (BAC)-derived clinical H

109 ressed during productive infection by either bacterial artificial chromosome (BAC)-derived virus in J

110 e by integrating whole-genome shotgun reads, bacterial artificial chromosome (BAC)-end sequences and

111 use model of enhanced vesicular function via bacterial artificial chromosome (BAC)-mediated overexpre

112 ted to varying levels by taking advantage of bacterial artificial chromosome (BAC)-mediated transgene

113 s and increased myelin periodicity in BACHD [bacterial artificial chromosome (BAC)-mediated transgeni

114 -length human mutant huntingtin (fl-mhtt), a bacterial artificial chromosome (BAC)-mediated transgeni

115 Here, we establish bacterial artificial chromosome (BAC)-transgenic mouse l

116 Using a newly developed bacterial artificial chromosome (BAC)-transgenic mouse m

117 with RhCMV employed strain 68-1 cloned as a bacterial artificial chromosome (BAC).

118 of the murine prion protein (PrP) gene in a bacterial artificial chromosome (BAC).

119 fs within oriLyt in cells harboring the KSHV bacterial artificial chromosome (BAC).

120 ted Disc1 encoding the first 8 exons using a bacterial artificial chromosome (BAC).

121 d the quality of transformation by the B95-8 bacterial artificial chromosome (BAC).IMPORTANCE Epstein

122 y of Xenopus tropicalis genomic sequences in bacterial artificial chromosomes (BAC) to analyze the ge

123 hogenic TC-derived virus N13R10 (cloned as a bacterial artificial chromosome [BAC]) has a 4-bp deleti

124 by introduction of these mutations into KSHV bacterial artificial chromosome BAC36.

125 However, because only 6278 bacterial artificial chromosome (BACs) in the physical m

126 Bacterial artificial chromosomes (BACs) are capable of p

127 some regions consisting of tandem repeats of bacterial artificial chromosomes (BACs) containing appro

128 imized to demonstrate intact modification of bacterial artificial chromosomes (BACs) containing long

129 We selected physically mapped bacterial artificial chromosomes (BACs) containing Spiro

130 Bacterial artificial chromosomes (BACs) derived from gen

131 enerated wild-type and mutant gamma2 subunit bacterial artificial chromosomes (BACs) driven by a CMV

132 Brassica species utilized genetically mapped bacterial artificial chromosomes (BACs) from B. rapa as

133 ta coffee genomes, we identified orthologous bacterial artificial chromosomes (BACs) from C. arabica

134 mplex virus-1 amplicon technology to deliver bacterial artificial chromosomes (BACs) into cells by vi

135 ingle, contiguous piece of DNA by fusing two bacterial artificial chromosomes (BACs) into one, we for

136 Thirty-two ASGR bacterial artificial chromosomes (BACs) isolated from bo

137 Infectious bacterial artificial chromosomes (BACs) of herpesviruses

138 elegans, this has been accomplished by using bacterial artificial chromosomes (BACs) of related speci

139 Bacterial artificial chromosomes (BACs) provide a stable

140 gh-throughput method for the modification of bacterial artificial chromosomes (BACs) that uses a nove

141 In this study, VZV bacterial artificial chromosomes (BACs) were generated w

142 Finally, bacterial artificial chromosomes (BACs) were isolated th

143 Bacterial artificial chromosomes (BACs) were retrofitted

144 MV genomes can be stabilized by cloning into bacterial artificial chromosomes (BACs), and then virus

145 When recombineering bacterial artificial chromosomes (BACs), it is common pr

146 Using Hox bacterial artificial chromosomes (BACs), transposon repo

147 t CCV genome as three overlapping subgenomic bacterial artificial chromosomes (BACs).

148 Modifications in a variety of plasmids up to bacterial artificial chromosomes (BACs; 144 kb deletion)

149 By using bacterial artificial chromosome-based chromosome paintin

150 Bacterial artificial chromosome-based comparative chromo

151 ute infection in vivo, we developed rK2-PVM, bacterial artificial chromosome-based recombinant PVM st

152 se genetic humanization using large compound bacterial artificial chromosome-based targeting vectors

153 DeltaLRR Z/DeltaLRR Z)) were generated using bacterial artificial chromosome-based targeting vectors,

154 in human pluripotent stem cells by means of bacterial artificial chromosome-based vectors and single

155 However, a TR-deleted HVS bacterial artificial chromosome can form replication com

156 e introduced the F66A mutation into BAC16 (a bacterial artificial chromosome clone containing the ent

157 ring de novo infection, we have utilized the bacterial artificial chromosome clone of wild-type RRV(1

158 Initially, bacterial artificial chromosome clone recombineering and

159 the transfer of the desired sequences from a bacterial artificial chromosome clone to a transformatio

160 An SRK-positive Bacterial Artificial Chromosome clone was found to conta

161 l other vertebrates (ring3) was found in the bacterial artificial chromosome clone, and the close lin

162 e integrated sequencing data from fosmid and bacterial artificial chromosome clones and sequence-capt

163 type of the S-locus in Petunia inflata using bacterial artificial chromosome clones collectively cont

164 ute infection in permissive fibroblasts from bacterial artificial chromosome clones of the HCMV genom

165 computational finishing of highly repetitive bacterial artificial chromosome clones that have proved

166 constructed recombinant wild-type and mutant bacterial artificial chromosome clones that spanned mous

167 e. tauschii genome, we fingerprinted 461,706 bacterial artificial chromosome clones, assembled contig

168 oth the rat as a model and expression of the bacterial artificial chromosome construct consisting of

169 y contrast, Delta22 viruses recovered from a bacterial artificial chromosome contain multiple amino a

170 Recombineering of a 166-kb bacterial artificial chromosome containing 68 kb of the

171 Using a bacterial artificial chromosome containing a complete re

172 In this study, we used a bacterial artificial chromosome containing a wild-type (

173 ases, we generated a line of mice carrying a bacterial artificial chromosome containing exons 1 to 6

174 lacking murine resistin but transgenic for a bacterial artificial chromosome containing human resisti

175 e carrying an eGFP transgene inserted into a bacterial artificial chromosome containing most of the R

176 Using a bacterial artificial chromosome containing the Gata1 gen

177 troduced the mutation into a newly developed bacterial artificial chromosome containing the KSHV geno

178 were generated by pronuclear injection of a bacterial artificial chromosome containing the mouse DAT

179 A bacterial artificial chromosome containing the sequence

180 We therefore constructed a bacterial artificial chromosome containing transgene (Tg

181 ied fragments and verified by sequencing two bacterial artificial chromosomes containing the two alle

182 ession and DNA replication by KSHV in a KSHV bacterial artificial chromosome-containing cell line.

183 mple sequence repeat markers, we developed a bacterial artificial chromosome contig for the Rpp4 locu

184 itional markers developed from the Wm82 Rpp4 bacterial artificial chromosome contig further defined t

185 Mice overexpressing Glo1 on a Tg bacterial artificial chromosome displayed increased anxi

186 logenin X (Amelx-iCre) with a large (250-kb) bacterial artificial chromosome DNA vector.

187 Using bacterial artificial chromosome-driven, miRNA silencing

188 ox) in raphe neurons expressing serotonergic bacterial artificial chromosome drivers Pet1 or Slc6a4.

189 Transgenic mice carrying a bacterial artificial chromosome encoding human VAMP7 mim

190 t, termed hypersensitive site 1 (HSS1), in a bacterial artificial chromosome encoding the entire CIIT

191 A bacterial artificial chromosome encompassing the full Bc

192 c resources, we analysed 40,641 high-quality bacterial artificial chromosome-end sequences (BESs), re

193 eated transgenic mouse lines using human CFH bacterial artificial chromosomes expressing full-length

194 t the brains of three transgenic mice with a bacterial artificial chromosome-expressing green fluores

195 some, as confirmed by physical mapping using bacterial artificial chromosome fluorescence in situ hyb

196 Interphase bacterial artificial chromosome fluorescence in situ hyb

197 a complete loss of CIITA expression from the bacterial artificial chromosome following transfection i

198 ented by NFIL3-short hairpin RNA in an Il12b-bacterial artificial chromosome-GFP reporter macrophage

199 We found that, in bacterial artificial chromosome-GLT1-enhanced green fluo

200 Generated using an approximately 200-kb-long bacterial artificial chromosome harboring the entire Pro

201 reated a human IL-10 transgenic mouse with a bacterial artificial chromosome (hIL10BAC) in which the

202 We used mutant Huntingtin (mHTT) expressing bacterial artificial chromosome Huntington's disease mic

203 ased on enrichment of mononucleosomal DNA by bacterial artificial chromosome hybridization, we mapped

204 t has been inserted by recombineering into a bacterial artificial chromosome immediately at the trans

205 ver-expressing the Cx26 gene from a modified bacterial artificial chromosome in the Cx30(-/-) backgro

206 Sequencing of a bacterial artificial chromosome in the fine mapped regio

207 ted transgenic mouse lines harboring a Gata1 bacterial artificial chromosome in which the G1MDR was d

208 eotides, and we used them to sequence canine bacterial artificial chromosomes in a single-molecule sy

209 kb ("1/4 genome"), which were all cloned as bacterial artificial chromosomes in Escherichia coli.

210 By sequencing 8452 bacterial artificial chromosomes in pools, we assembled

211 We constructed Drosophila melanogaster bacterial artificial chromosome libraries with 21-kiloba

212 esources, including expressed sequence tags, bacterial artificial chromosome libraries, physical and

213 We screened a nurse shark bacterial artificial chromosome library and isolated clo

214 n, we isolated the AFGP genomic locus from a bacterial artificial chromosome library for Dissostichus

215 enerated Grhl3-expressing curly tail mice by bacterial artificial chromosome-mediated transgenesis an

216 CK-enhanced green fluorescent protein [eGFP] bacterial artificial chromosome mice).

217 Using bacterial artificial chromosome-minigene stable cell lin

218 transcriptomes were determined using an SCA2 bacterial artificial chromosome mouse model expressing p

219 plementation analyses of transgenic lines of bacterial artificial chromosomes of Ranbp2 harboring los

220 an-binding protein-2 (Ranbp2) and expressing bacterial artificial chromosomes of Ranbp2 with impaired

221 de, gene tags can be inserted and regions of bacterial artificial chromosomes or the E. coli genome c

222 A recombinant HCMV bacterial artificial chromosome plasmid (BACmid) express

223 , the HSV-1(McKrae) genome was cloned into a bacterial artificial chromosome plasmid (McKbac) and uti

224 eletion of the CTCF-binding site in the HCMV bacterial artificial chromosome plasmid genome resulted

225 ith genes through expressed sequence tags or bacterial artificial chromosomes produced comparative as

226 in these cells, as reported by recombineered bacterial artificial chromosomes producing fluorochromes

227 Using bacterial artificial chromosome recombineering, we gener

228 ncy) mice induce re-expression of a Rag2-GFP bacterial artificial chromosome reporter as well as wild

229 Mice bearing a bacterial artificial chromosome reporter with a mutated

230 Using chromatinized bacterial artificial chromosome reporters, we discovered

231 ion content fingerprinting of almost 600,000 bacterial artificial chromosomes representing 14-fold ha

232 Here we devised a new conditional bacterial artificial chromosome rescue strategy to show,

233 ry of whole-gene deletion mutants carrying a bacterial artificial chromosome sequence and a luciferas

234 ions from Arabidopsis and publicly available bacterial artificial chromosome sequences from Thellungi

235 t these genes are tightly linked in HN1, and bacterial artificial chromosome sequencing confirmed tha

236 nomic loci encoding synaptic proteins within bacterial artificial chromosomes such that these protein

237 ls of two mapping populations with published bacterial artificial chromosome survey sequence informat

238 Mutagenesis using a VZV bacterial artificial chromosome system showed that ORF23

239 n the most conserved regions of UL33 using a bacterial artificial chromosome system.

240 nterest harbored by transformation-competent bacterial artificial chromosomes (TACs).

241 The advent of bacterial artificial chromosome technologies has enabled

242 Using bacterial artificial chromosome technology, we generated

243 Using bacterial artificial chromosome technology, we have gene

244 nstructed a wild-type (WT) HCMV genome using bacterial artificial chromosome technology.

245 ing the human PGC-1alpha genomic locus via a bacterial artificial chromosome (TG) and nontransgenic c

246 We generated mice that carry a bacterial artificial chromosome that encompasses the ent

247 genic zebrafish line that carries a modified bacterial artificial chromosome that expresses green flu

248 s VZV was recovered from parental Oka (pOka)-bacterial artificial chromosomes that had either the Del

249 ffinity purification-tagged Eg5 from a mouse bacterial artificial chromosome (this construct was call

250 We cloned the LCL8664 rhLCV strain as a bacterial artificial chromosome to create recombinant rh

251 mutations were engineered into the CMV Towne bacterial artificial chromosome (Towne-BAC) genome, repl

252 e mice express full-length human mHTT from a bacterial artificial chromosome transgene (BACHD), we ge

253 ophages expressing caspase-11 from a C57BL/6 bacterial artificial chromosome transgene failed to secr

254 mouse lines were generated, each carrying a bacterial artificial chromosome transgene that mimicked

255 This was accomplished by expressing bacterial artificial chromosome transgenes encoding wild

256 e association is a general property of Hsp70 bacterial artificial chromosome transgenes, independent

257 y and expressed at physiological levels from bacterial artificial chromosome transgenes.

258 Complementation using bacterial artificial chromosome transgenesis implicated

259 RESEARCH DESIGN AND We used bacterial artificial chromosome transgenesis to generate

260 Using a bacterial artificial chromosome transgenic approach, we

261 Using bacterial artificial chromosome transgenic IL-7-Cre mice

262 Wild-type and bacterial artificial chromosome transgenic mice (D1R-tom

263 and sporadic Parkinson disease, we generated bacterial artificial chromosome transgenic mice (SNCA-OV

264 outside-out patch recordings in slices from bacterial artificial chromosome transgenic mice examined

265 This study utilized bacterial artificial chromosome transgenic mice expressi

266 ion of channelrhodopsin-2 in the striatum of bacterial artificial chromosome transgenic mice expressi

267 To directly test this idea, we developed bacterial artificial chromosome transgenic mice that all

268 We will show in this study that in novel bacterial artificial chromosome transgenic mice that exp

269 sing (TH(+)) neurons in striatal slices from bacterial artificial chromosome transgenic mice that syn

270 ent protein and D2-green fluorescent protein bacterial artificial chromosome transgenic mice that und

271 we used whole-cell recordings in slices from bacterial artificial chromosome transgenic mice to inves

272 ce and green fluorescent protein hemizygotic bacterial artificial chromosome transgenic mice to show

273 ramitochondrial roles for LRPPRC by creating bacterial artificial chromosome transgenic mice with mod

274 To address this, we used bacterial artificial chromosome transgenic mice, in whic

275 Using bacterial artificial chromosome transgenic mice, we foun

276 To address this question we used bacterial artificial chromosome transgenic mice, which e

277 old social defeat stress in D1-Cre or D2-Cre bacterial artificial chromosome transgenic mice.

278 ncer has a unique necessary function using a bacterial artificial chromosome transgenic model.

279 To address this, we studied a bacterial artificial chromosome transgenic mouse express

280 n of NS-enriched tumor cells, we generated a bacterial artificial chromosome transgenic mouse line ex

281 Although we worked with a bacterial artificial chromosome transgenic mouse line, t

282 Using a bacterial artificial chromosome transgenic mouse line, w

283 Here, we use bacterial artificial chromosome transgenic mouse models

284 tory T (T reg) cell-specific, FoxP3-GFP-hCre bacterial artificial chromosome transgenic mouse was cro

285 We thus developed a bacterial artificial chromosome transgenic mouse, in whi

286 Parkinson's disease, we have generated LRRK2 bacterial artificial chromosome transgenic rats expressi

287 sing comprehensive microarray analysis and a bacterial artificial chromosome transgenic system, here

288 By employing a bacterial artificial chromosome transgenic system, we de

289 ctivation, we generated CD80-eCFP mice using bacterial artificial chromosome transgenic technology.

290 Using in vivo two-photon imaging of bacterial artificial chromosome transgenic zebrafish, we

291 phtheria toxin A under the control of a BAC (bacterial artificial chromosome) transgenic hu-man Lange

292 with Neurog1-Cre and Neurog1-CreER(T2) BAC (bacterial artificial chromosome) transgenic mice.

293 nd, we generated a novel multicistronic BAC (bacterial artificial chromosome) transgenic mouse line u

294 lian DA neurons in vivo, we developed a BAC (bacterial artificial chromosome) transgenic mouse model

295 We created bacterial artificial chromosome-transgenic mice expressi

296 In this study, we generated several bacterial artificial chromosome-transgenic mice that ove

297 Using bacterial artificial chromosome-transgenic mice, we demo

298 Using a bacterial artificial chromosome vector, the 16.9-kb 18-g

299 an adenosine2A (adora2a) receptor-containing bacterial artificial chromosome was employed to drive rM

300 Cells transfected with an HCMV bacterial artificial chromosome with gL deleted yielded