ライフサイエンスコーパス: artificial chromosome

1 odels, the YAC128 and the BACHD (a bacterial-artificial chromosome).

2 human elastin gene contained in a bacterial artificial chromosome.

3 e LRRK2 genomic locus carried by a bacterial artificial chromosome.

4 d1 mRNA under the control of Pvalb bacterial artificial chromosome.

5 NA enriched via hybridization with bacterial artificial chromosomes.

6 nsformation with linked multigenes and plant artificial chromosomes.

7 promise as "bacterial skeletons" for housing artificial chromosomes.

8 We sequenced 12 V. monoica bacterial artificial chromosomes, 11 corresponding to the papaya X

9 By using bacterial artificial chromosome 16 (BAC16) clone carrying the full

10 ailability of the OSVP genome as a bacterial artificial chromosome allows for the rapid insertion of

11 in for kinetochore assembly, plus the use of artificial chromosomes and kinetochores to study centrom

12 gged dynein/dynactin subunits from bacterial artificial chromosomes and observed asymmetric cortical

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

14 Centromeres are at the heart of artificial chromosomes, and we have seen the birth of sy

15 Artificial chromosomes are useful in making functional v

16 enesis, a genome-wide search using bacterial artificial chromosome array comparative genomic hybridiz

17 Here, we use human artificial chromosome assembly assays to show that both

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

19 e was engineered to contain both a bacterial artificial chromosome (BAC) and the Invitrogen in vitro

20 to the retrieval construct from a bacterial artificial chromosome (BAC) by recombineering to generat

21 ned in silico and constructed on a bacterial artificial chromosome (BAC) by using a recombineering-ba

22 MDiGS combines biotinylated bacterial artificial chromosome (BAC) capture and multiplexed pool

23 A bacterial artificial chromosome (BAC) carrying the complete hCFTR

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

25 d a herpes simplex virus 2 (HSV-2) bacterial artificial chromosome (BAC) clone, bHSV2-BAC38, which co

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

27 cates generated from an infectious bacterial artificial chromosome (BAC) clone.

28 ) the problem of decoding reads to bacterial artificial chromosome (BAC) clones (in the context of th

29 By sequencing bacterial artificial chromosome (BAC) clones and the whole genome,

30 using 18 randomly selected potato bacterial artificial chromosome (BAC) clones in a set of 16 potato

31 ciences (PacBio) to sequence eight Bacterial Artificial Chromosome (BAC) clones spanning the horse MH

32 ndividually and as mixtures, of 95 bacterial artificial chromosome (BAC) clones that cover the 4.7-Mb

33 analyses, at the scale of complete bacterial artificial chromosome (BAC) clones, between the genome o

34 andom sequence reads and assembled bacterial artificial chromosome (BAC) clones, we show that it is c

35 Grk1(+)) were generated by using a bacterial artificial chromosome (BAC) construct containing mouse G

36 Here, we used a bacterial artificial chromosome (BAC) construct that expresses luc

37 ic LRRK2-G2019S protein from mouse bacterial artificial chromosome (BAC) constructs closely mimics en

38 n this report, we describe two VZV bacterial artificial chromosome (BAC) constructs with ORF54 gene d

39 e models were developed that use a Bacterial Artificial Chromosome (BAC) containing 208kb flanking th

40 tein (eGFP) under the control of a bacterial artificial chromosome (BAC) containing a very large regi

41 report transgenic mice carrying a bacterial artificial chromosome (BAC) containing the full human C9

42 In addition, a bacterial artificial chromosome (BAC) contig was constructed for t

43 ensive EST analysis, constructed a bacterial artificial chromosome (BAC) contig, and obtained a conti

44 We prepared recombinant HCMV bacterial artificial chromosome (BAC) DNAs with either one site mi

45 Using bacteria artificial chromosome (BAC) end sequences (16.9 Mb) and

46 We used an in vivo bacterial artificial chromosome (BAC) enhancer-trapping strategy i

47 tworm, using survey sequences from bacterial artificial chromosome (BAC) inserts and contigs derived

48 c mouse lines using a human IKBKAP bacterial artificial chromosome (BAC) into which we inserted the I

49 Here, we generated a bacterial artificial chromosome (BAC) KSHV recombinant virus with

50 racterization by end-sequencing of bacterial artificial chromosome (BAC) libraries derived from NOD/M

51 Two bacterial artificial chromosome (BAC) libraries of a homozygous do

52 walnut genome, we constructed two bacterial artificial chromosome (BAC) libraries, containing a tota

53 A bacterial artificial chromosome (BAC) library equivalent to 8-9 ti

54 We developed a bacterial artificial chromosome (BAC) library from an Ab10 line an

55 A Bacterial Artificial Chromosome (BAC) library was made from wild-c

56 e-genome shotgun (WGS) assembly, a bacterial artificial chromosome (BAC) physical map, and assembled

57 isolate rare (1:10,000-1:100,000) bacterial artificial chromosome (BAC) recombinants require selecta

58 Using Bacteria Artificial Chromosome (BAC) recombineering and a transge

59 esis by employing a combination of bacterial artificial chromosome (BAC) recombineering and quantitat

60 simple and efficient strategy for Bacterial Artificial Chromosome (BAC) recombineering based on co-s

61 e Bmp4 locus using two overlapping bacterial artificial chromosome (BAC) reporter transgenes.

62 Using chromatinized bacterial artificial chromosome (BAC) reporters in human fibroblas

63 pecific repression, we constructed bacterial artificial chromosome (BAC) reporters using human and mo

64 (ESC) lines containing single-copy bacterial artificial chromosome (BAC) reporters, covering hTERT an

65 ynthesis of a comprehensive set of bacterial artificial chromosome (BAC) resources for 19 Drosophila

66 rofluidics-based linked reads, and bacterial artificial chromosome (BAC) sequencing approaches.

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

68 ng a mutagenesis strategy based on bacterial artificial chromosome (BAC) technology.

69 esvirus (KSHV) has come to rely on bacterial artificial chromosome (BAC) technology.

70 work presents a novel in vivo DRD1-Bacterial Artificial Chromosome (BAC) Tet-on system allowing for t

71 loned as an infectious, pathogenic bacterial artificial chromosome (BAC) that is used to study MCF.

72 Using neuronal bacterial artificial chromosome (BAC) transfection, we found that,

73 Frameshift (MORF) allows a single Bacterial Artificial Chromosome (BAC) transgene to direct sparse l

74 knock-out mice expressing a human bacterial artificial chromosome (BAC) transgene were generated, re

75 Mice carrying bacterial artificial chromosome (BAC) transgenes have become impor

76 er, we use autonomous targeting of bacterial artificial chromosome (BAC) transgenes to reveal cis req

77 2, COMT and ARVCF, on behaviors in bacterial artificial chromosome (BAC) transgenic (TG) mice.

78 Using bacterial artificial chromosome (BAC) transgenic HeLa and mouse em

79 By generating a bacterial artificial chromosome (BAC) transgenic IL-13 reporter mo

80 Recent studies have used bacterial artificial chromosome (BAC) transgenic mice expressing c

81 increasingly relied on the use of bacterial artificial chromosome (BAC) transgenic mice expressing f

82 Bacteria artificial chromosome (BAC) transgenic mice expressing t

83 Initial studies of bacterial artificial chromosome (BAC) transgenic mice harboring th

84 Using Hdc-EGFP bacterial artificial chromosome (BAC) transgenic mice in which EGF

85 Using HDC-EGFP bacterial artificial chromosome (BAC) transgenic mice in which EGF

86 role of Gfi1 in vivo, we generated bacterial artificial chromosome (BAC) transgenic mice, in which a

87 HE to leukemogenesis by creating a bacterial artificial chromosome (BAC) transgenic model that recapi

88 Here, we demonstrate that a Esr2 bacterial artificial chromosome (BAC) transgenic mouse line that e

89 a temporal manner, we generated a bacterial artificial chromosome (BAC) transgenic mouse line, in wh

90 oped a series of conditional VIPR2 bacterial artificial chromosome (BAC) transgenic mouse models of V

91 Here we characterize two bacterial artificial chromosome (BAC) transgenic mouse strains ove

92 We used a bacterial artificial chromosome (BAC) transgenic strategy to expre

93 th different reporters in a single bacterial artificial chromosome (BAC) vector containing the mouse

94 Bacterial artificial chromosome (BAC) vectors enable stable clonin

95 an genome, the ends of a number of bacterial artificial chromosome (BAC) were sequenced, annotated an

96 In addition, we constructed a KSHV bacterial artificial chromosome (BAC) with LZ domain-deleted K-bZI

97 transgenic rat model using a human bacterial artificial chromosome (BAC), which contains the full-len

98 racy, and to a set of high-quality bacterial artificial chromosome (BAC)-based assemblies to evaluate

99 We previously reported a bacterial artificial chromosome (BAC)-based lymphatic reporter mou

100 omyelitis, using a newly developed bacterial artificial chromosome (BAC)-based MHV reverse genetics s

101 criptional activation of Hoxb13, a bacterial artificial chromosome (BAC)-based reporter gene deletion

102 In contrast, bacterial artificial chromosome (BAC)-cloned strains TB40-BAC4, FI

103 of US28 recombinant viruses in the bacterial artificial chromosome (BAC)-derived clinical HCMV strain

104 ing productive infection by either bacterial artificial chromosome (BAC)-derived virus in Jjhan cells

105 rating whole-genome shotgun reads, bacterial artificial chromosome (BAC)-end sequences and genotype-b

106 of enhanced vesicular function via bacterial artificial chromosome (BAC)-mediated overexpression of t

107 ying levels by taking advantage of bacterial artificial chromosome (BAC)-mediated transgenesis.

108 eased myelin periodicity in BACHD [bacterial artificial chromosome (BAC)-mediated transgenic model fo

109 Here, we establish bacterial artificial chromosome (BAC)-transgenic mouse lines with

110 Using a newly developed bacterial artificial chromosome (BAC)-transgenic mouse model, we d

111 V employed strain 68-1 cloned as a bacterial artificial chromosome (BAC).

112 rine prion protein (PrP) gene in a bacterial artificial chromosome (BAC).

113 oriLyt in cells harboring the KSHV bacterial artificial chromosome (BAC).

114 ity of transformation by the B95-8 bacterial artificial chromosome (BAC).IMPORTANCE Epstein-Barr viru

115 us tropicalis genomic sequences in bacterial artificial chromosomes (BAC) to analyze the genomic regi

116 -derived virus N13R10 (cloned as a bacterial artificial chromosome [BAC]) has a 4-bp deletion that di

117 ction of these mutations into KSHV bacterial artificial chromosome BAC36.

118 However, because only 6278 bacterial artificial chromosome (BACs) in the physical map were se

119 Bacterial artificial chromosomes (BACs) are capable of propagating

120 ns consisting of tandem repeats of bacterial artificial chromosomes (BACs) containing approximately 2

121 We selected physically mapped bacterial artificial chromosomes (BACs) containing Spirodela DNA i

122 ild-type and mutant gamma2 subunit bacterial artificial chromosomes (BACs) driven by a CMV promoter a

123 pecies utilized genetically mapped bacterial artificial chromosomes (BACs) from B. rapa as probes for

124 genomes, we identified orthologous bacterial artificial chromosomes (BACs) from C. arabica and C. can

125 s-1 amplicon technology to deliver bacterial artificial chromosomes (BACs) into cells by viral transd

126 Infectious bacterial artificial chromosomes (BACs) of herpesviruses are power

127 his has been accomplished by using bacterial artificial chromosomes (BACs) of related species.

128 al subcloning of DNA fragments from Bacteria Artificial Chromosomes (BACs) or other sources.

129 Bacterial artificial chromosomes (BACs) provide a stable, genetica

130 put method for the modification of bacterial artificial chromosomes (BACs) that uses a novel two-plas

131 In this study, VZV bacterial artificial chromosomes (BACs) were generated with small

132 Finally, bacterial artificial chromosomes (BACs) were isolated that contain

133 can be stabilized by cloning into bacterial artificial chromosomes (BACs), and then virus is regener

134 When recombineering bacterial artificial chromosomes (BACs), it is common practice to

135 Using Hox bacterial artificial chromosomes (BACs), transposon reporters, and

136 ons in a variety of plasmids up to bacterial artificial chromosomes (BACs; 144 kb deletion) have been

137 By using bacterial artificial chromosome-based chromosome painting, genomic

138 Bacterial artificial chromosome-based comparative chromosome paint

139 ion in vivo, we developed rK2-PVM, bacterial artificial chromosome-based recombinant PVM strain J3666

140 humanization using large compound bacterial artificial chromosome-based targeting vectors introduced

141 /DeltaLRR Z)) were generated using bacterial artificial chromosome-based targeting vectors, which all

142 pluripotent stem cells by means of bacterial artificial chromosome-based vectors and single-nucleotid

143 oter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.

144 possibilities, human beta-globin locus yeast artificial chromosome (beta-YAC) lines were produced in

145 entire ~72-kb sim cluster on a single phage artificial chromosome clone and produced simocyclinone h

146 ed the F66A mutation into BAC16 (a bacterial artificial chromosome clone containing the entire infect

147 vo infection, we have utilized the bacterial artificial chromosome clone of wild-type RRV(17577) (WT(

148 Initially, bacterial artificial chromosome clone recombineering and tradition

149 er of the desired sequences from a bacterial artificial chromosome clone to a transformation-compatib

150 An SRK-positive Bacterial Artificial Chromosome clone was found to contain complet

151 rtebrates (ring3) was found in the bacterial artificial chromosome clone, and the close linkage of ri

152 ed sequencing data from fosmid and bacterial artificial chromosome clones and sequence-captured DNA f

153 e S-locus in Petunia inflata using bacterial artificial chromosome clones collectively containing all

154 ion in permissive fibroblasts from bacterial artificial chromosome clones of the HCMV genome where UL

155 nal finishing of highly repetitive bacterial artificial chromosome clones that have proved successful

156 d recombinant wild-type and mutant bacterial artificial chromosome clones that spanned mouse and huma

157 i genome, we fingerprinted 461,706 bacterial artificial chromosome clones, assembled contigs, designe

158 t as a model and expression of the bacterial artificial chromosome construct consisting of human full

159 , Delta22 viruses recovered from a bacterial artificial chromosome contain multiple amino acid change

160 atment of transgenic mice expressing a yeast artificial chromosome containing 128 CAG repeats (YAC128

161 Recombineering of a 166-kb bacterial artificial chromosome containing 68 kb of the 5'-flankin

162 Using a bacterial artificial chromosome containing a complete recombinant

163 enerated a line of mice carrying a bacterial artificial chromosome containing exons 1 to 6 of the hum

164 rine resistin but transgenic for a bacterial artificial chromosome containing human resistin (BAC-Ret

165 an eGFP transgene inserted into a bacterial artificial chromosome containing most of the Rb gene.

166 Using a bacterial artificial chromosome containing the Gata1 gene modified

167 he mutation into a newly developed bacterial artificial chromosome containing the KSHV genome (BAC16)

168 A bacterial artificial chromosome containing the sequence of ZIKV st

169 We therefore constructed a bacterial artificial chromosome containing transgene (Tg), compris

170 nts and verified by sequencing two bacterial artificial chromosomes containing the two alleles.

171 DNA replication by KSHV in a KSHV bacterial artificial chromosome-containing cell line.

172 nce repeat markers, we developed a bacterial artificial chromosome contig for the Rpp4 locus in the s

173 rkers developed from the Wm82 Rpp4 bacterial artificial chromosome contig further defined the region

174 es will be useful for future applications in artificial chromosome design.

175 Mice overexpressing Glo1 on a Tg bacterial artificial chromosome displayed increased anxiety-like b

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

177 Using bacterial artificial chromosome-driven, miRNA silencing technology

178 he neurons expressing serotonergic bacterial artificial chromosome drivers Pet1 or Slc6a4.

179 Transgenic mice carrying a bacterial artificial chromosome encoding human VAMP7 mimicked the

180 hypersensitive site 1 (HSS1), in a bacterial artificial chromosome encoding the entire CIITA locus an

181 A bacterial artificial chromosome encompassing the full Bcl11b gene

182 s, we analysed 40,641 high-quality bacterial artificial chromosome-end sequences (BESs), representing

183 sgenic mouse lines using human CFH bacterial artificial chromosomes expressing full-length human CFH

184 ns of three transgenic mice with a bacterial artificial chromosome-expressing green fluorescent prote

185 Interphase bacterial artificial chromosome fluorescence in situ hybridization

186 onfirmed by physical mapping using bacterial artificial chromosome fluorescence in situ hybridization

187 loss of CIITA expression from the bacterial artificial chromosome following transfection into B cell

188 ence and structure guides the development of artificial chromosomes for functional cellular biology s

189 FIL3-short hairpin RNA in an Il12b-bacterial artificial chromosome-GFP reporter macrophage line.

190 We found that, in bacterial artificial chromosome-GLT1-enhanced green fluorescent pr

191 CIN based on the use of a nonessential human artificial chromosome (HAC) carrying a constitutively ex

192 In the Tc goat system, a human artificial chromosome (HAC) comprising the entire human

193 Our method uses a human artificial chromosome (HAC) expressing the GFP transgene

194 tromeric regions and in de novo formed Human Artificial Chromosome (HAC) was analyzed.

195 Human artificial chromosome (HAC)-based vectors offer a promis

196 Human artificial chromosome (HAC)-based vectors represent an a

197 Human artificial chromosome (HAC)-based vectors represent an a

198 y, from the kinetochore of a synthetic human artificial chromosome (HAC).

199 embryonic stem cells (hESc) utilizing human artificial chromosomes (HAC), which behave as autonomous

200 Human artificial chromosomes (HACs) are a potentially powerful

201 Prior human artificial chromosomes (HACs) required large arrays of c

202 mammalian cells and the development of human artificial chromosomes (HACs).

203 using an approximately 200-kb-long bacterial artificial chromosome harboring the entire Prox1 gene, t

204 In contrast to BAC and yeast artificial chromosome HD mouse models that express full-

205 uman IL-10 transgenic mouse with a bacterial artificial chromosome (hIL10BAC) in which the IL10 gene

206 utant Huntingtin (mHTT) expressing bacterial artificial chromosome Huntington's disease mice to deter

207 richment of mononucleosomal DNA by bacterial artificial chromosome hybridization, we mapped nucleosom

208 inserted by recombineering into a bacterial artificial chromosome immediately at the translation ini

209 Sequencing of a bacterial artificial chromosome in the fine mapped region led to t

210 enic mouse lines harboring a Gata1 bacterial artificial chromosome in which the G1MDR was deleted.

211 nd we used them to sequence canine bacterial artificial chromosomes in a single-molecule system that

212 By sequencing 8452 bacterial artificial chromosomes in pools, we assembled a sequence

213 onstructed Drosophila melanogaster bacterial artificial chromosome libraries with 21-kilobase and 83-

214 We screened a nurse shark bacterial artificial chromosome library and isolated clones contai

215 ated the AFGP genomic locus from a bacterial artificial chromosome library for Dissostichus mawsoni.

216 d green fluorescent protein [eGFP] bacterial artificial chromosome mice).

217 Using bacterial artificial chromosome-minigene stable cell lines, CRISPR

218 Here, a HAC (human artificial chromosome) module with a regulated centromer

219 omes were determined using an SCA2 bacterial artificial chromosome mouse model expressing polyglutami

220 on analyses of transgenic lines of bacterial artificial chromosomes of Ranbp2 harboring loss of funct

221 protein-2 (Ranbp2) and expressing bacterial artificial chromosomes of Ranbp2 with impaired C-termina

222 ags can be inserted and regions of bacterial artificial chromosomes or the E. coli genome can be subc

223 e also isolated small indel P1 phage-derived artificial chromosome (PAC) and BAC recombinants.

224 Using the P1-derived artificial chromosome (PAC) technology, we created mouse

225 A recombinant HCMV bacterial artificial chromosome plasmid (BACmid) expressing the no

226 1(McKrae) genome was cloned into a bacterial artificial chromosome plasmid (McKbac) and utilized to c

227 the CTCF-binding site in the HCMV bacterial artificial chromosome plasmid genome resulted in an abou

228 ells, as reported by recombineered bacterial artificial chromosomes producing fluorochromes.

229 Using bacterial artificial chromosome recombineering, we generated trans

230 Mice bearing a bacterial artificial chromosome reporter with a mutated RBP-J bind

231 Using chromatinized bacterial artificial chromosome reporters, we discovered that the

232 t fingerprinting of almost 600,000 bacterial artificial chromosomes representing 14-fold haploid geno

233 Here we devised a new conditional bacterial artificial chromosome rescue strategy to show, in mice,

234 e-gene deletion mutants carrying a bacterial artificial chromosome sequence and a luciferase marker i

235 Arabidopsis and publicly available bacterial artificial chromosome sequences from Thellungiella salsu

236 nes are tightly linked in HN1, and bacterial artificial chromosome sequencing confirmed that they exi

237 This generation of human artificial chromosomes should be suitable for studies of

238 encoding synaptic proteins within bacterial artificial chromosomes such that these proteins, express

239 mapping populations with published bacterial artificial chromosome survey sequence information to gen

240 conserved regions of UL33 using a bacterial artificial chromosome system.

241 rbored by transformation-competent bacterial artificial chromosomes (TACs).

242 The advent of bacterial artificial chromosome technologies has enabled engineeri

243 Using bacterial artificial chromosome technology, we generated cells exp

244 Using bacterial artificial chromosome technology, we have generated a mo

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

246 man PGC-1alpha genomic locus via a bacterial artificial chromosome (TG) and nontransgenic controls (C

247 We generated mice that carry a bacterial artificial chromosome that encompasses the entire human

248 recovered from parental Oka (pOka)-bacterial artificial chromosomes that had either the Delta491RSRR4

249 rification-tagged Eg5 from a mouse bacterial artificial chromosome (this construct was called mEg5) a

250 oned the LCL8664 rhLCV strain as a bacterial artificial chromosome to create recombinant rhLCV for in

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

252 ress full-length human mHTT from a bacterial artificial chromosome transgene (BACHD), we genetically

253 pressing caspase-11 from a C57BL/6 bacterial artificial chromosome transgene failed to secrete IL-1be

254 es were generated, each carrying a bacterial artificial chromosome transgene that mimicked Igh locus

255 his was accomplished by expressing bacterial artificial chromosome transgenes encoding wild-type (sta

256 ion is a general property of Hsp70 bacterial artificial chromosome transgenes, independent of the chr

257 essed at physiological levels from bacterial artificial chromosome transgenes.

258 Complementation using bacterial artificial chromosome transgenesis implicated zinc finge

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

260 Using a bacterial artificial chromosome transgenic approach, we establishe

261 Using bacterial artificial chromosome transgenic IL-7-Cre mice, we found

262 Wild-type and bacterial artificial chromosome transgenic mice (D1R-tomato and D2

263 ic Parkinson disease, we generated bacterial artificial chromosome transgenic mice (SNCA-OVX) that ex

264 nnelrhodopsin-2 in the striatum of bacterial artificial chromosome transgenic mice expressing Cre rec

265 This study utilized bacterial artificial chromosome transgenic mice expressing ERbeta

266 l show in this study that in novel bacterial artificial chromosome transgenic mice that express EGFP

267 )) neurons in striatal slices from bacterial artificial chromosome transgenic mice that synthesize en

268 n and D2-green fluorescent protein bacterial artificial chromosome transgenic mice that underwent chr

269 ole-cell recordings in slices from bacterial artificial chromosome transgenic mice to investigate the

270 en fluorescent protein hemizygotic bacterial artificial chromosome transgenic mice to show how dopami

271 drial roles for LRPPRC by creating bacterial artificial chromosome transgenic mice with moderately in

272 To address this, we used bacterial artificial chromosome transgenic mice, in which enhanced

273 Using bacterial artificial chromosome transgenic mice, we found that syn

274 To address this question we used bacterial artificial chromosome transgenic mice, which express EGF

275 defeat stress in D1-Cre or D2-Cre bacterial artificial chromosome transgenic mice.

276 unique necessary function using a bacterial artificial chromosome transgenic model.

277 To address this, we studied a bacterial artificial chromosome transgenic mouse expressing the A3

278 riched tumor cells, we generated a bacterial artificial chromosome transgenic mouse line expressing g

279 Although we worked with a bacterial artificial chromosome transgenic mouse line, this method

280 Using a bacterial artificial chromosome transgenic mouse line, we show tha

281 Here, we use bacterial artificial chromosome transgenic mouse models of LRRK2 t

282 We thus developed a bacterial artificial chromosome transgenic mouse, in which express

283 s disease, we have generated LRRK2 bacterial artificial chromosome transgenic rats expressing either

284 ehensive microarray analysis and a bacterial artificial chromosome transgenic system, here we identif

285 By employing a bacterial artificial chromosome transgenic system, we demonstrate

286 sing in vivo two-photon imaging of bacterial artificial chromosome transgenic zebrafish, we show that

287 oxin A under the control of a BAC (bacterial artificial chromosome) transgenic hu-man Langerin locus.

288 og1-Cre and Neurog1-CreER(T2) BAC (bacterial artificial chromosome) transgenic mice.

289 erated a novel multicistronic BAC (bacterial artificial chromosome) transgenic mouse line under the r

290 urons in vivo, we developed a BAC (bacterial artificial chromosome) transgenic mouse model expressing

291 We created bacterial artificial chromosome-transgenic mice expressing the avi

292 n this study, we generated several bacterial artificial chromosome-transgenic mice that overexpress C

293 Using bacterial artificial chromosome-transgenic mice, we demonstrate th

294 attle were generated by transferring a human artificial chromosome vector carrying the entire unrearr

295 Using a bacterial artificial chromosome vector, the 16.9-kb 18-gene cluste

296 es, and for assembly of linear constructs as artificial chromosome vectors.

297 ne2A (adora2a) receptor-containing bacterial artificial chromosome was employed to drive rM3Ds expres

298 Cells transfected with an HCMV bacterial artificial chromosome with gL deleted yielded virus that

299 enic mouse line bearing a 662-kb Gata3 yeast artificial chromosome (YAC), and these animals (termed G

300 Circular yeast artificial chromosomes (YACs) provide significant advant