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

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

6 NA enriched via hybridization with bacterial artificial chromosomes.

7 nsformation with linked multigenes and plant artificial chromosomes.

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

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

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

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

12 mbryonic stem cells (ES cells) and bacterial artificial chromosomes and have used it to classify 17 s

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

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

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

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

17 Artificial chromosomes are useful in making functional v

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

19 ext of the infection have utilized bacterial artificial chromosomes as vectors to generate mutant vir

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

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

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

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

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

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

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

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

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

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

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

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

32 ping of 30 genetic marker-anchored bacterial artificial chromosome (BAC) clones on the pachytene chro

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

34 for receptor activity conferred by bacterial artificial chromosome (BAC) clones spanning the region.

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

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

37 Through the analysis of bacterial artificial chromosome (BAC) clones, pulsed-field gel ele

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 2, COMT and ARVCF, on behaviors in bacterial artificial chromosome (BAC) transgenic (TG) mice.

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

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

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

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

84 Bacteria artificial chromosome (BAC) transgenic mice expressing t

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

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

87 Using bacterial artificial chromosome (BAC) transgenic mice that express

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

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

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

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

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

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

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

95 Bacterial artificial chromosome (BAC) vectors enable stable clonin

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

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

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

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

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

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

102 A bacterial artificial chromosome (BAC)-based physical map of the ap

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

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

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

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

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

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

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

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

111 man mutant huntingtin (fl-mhtt), a bacterial artificial chromosome (BAC)-mediated transgenic mouse mo

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

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

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

115 encoding the first 8 exons using a bacterial artificial chromosome (BAC).

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

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

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

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

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

121 Bacterial artificial chromosomes (BACs) are capable of propagating

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

123 demonstrate intact modification of bacterial artificial chromosomes (BACs) containing long arrays of

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

125 Bacterial artificial chromosomes (BACs) derived from genomes of la

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

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

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

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

130 Thirty-two ASGR bacterial artificial chromosomes (BACs) isolated from both species

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 Initially, bacterial artificial chromosome clone recombineering and tradition

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

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

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

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

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

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

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

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

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

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

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

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 The KO mice with the yeast artificial chromosome containing the human FMR1 gene had

168 recently shown that Fmr1KO mice with a yeast artificial chromosome containing the human FMR1 gene hav

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

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

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

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 Using bacterial artificial chromosome-driven, miRNA silencing technology

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

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

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

180 A bacterial artificial chromosome encompassing the full Bcl11b gene

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

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

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

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

185 Interphase bacterial artificial chromosome fluorescence in situ hybridization

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

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

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

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

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

191 We have used a human artificial chromosome (HAC) to manipulate the epigenetic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 genome"), which were all cloned as bacterial artificial chromosomes in Escherichia coli.

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

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

209 including expressed sequence tags, bacterial artificial chromosome libraries, physical and genetic ma

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

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

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

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

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

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

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

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

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

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

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

221 1(McKrae) genome was cloned into a bacterial artificial chromosome plasmid (McKbac) and utilized to c

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

223 through expressed sequence tags or bacterial artificial chromosomes produced comparative assignments

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

225 Using bacterial artificial chromosome recombineering, we generated trans

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

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

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

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

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

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

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

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

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

235 Mutagenesis using a VZV bacterial artificial chromosome system showed that ORF23 was dispe

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

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

238 The advent of bacterial artificial chromosome technologies has enabled engineeri

239 Using bacterial artificial chromosome technology, we generated cells exp

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

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

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

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

244 of the overlapping parental BACs and a yeast artificial chromosome that were originally tested do not

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

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

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

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

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

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

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

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

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

254 essed at physiological levels from bacterial artificial chromosome transgenes.

255 Complementation using bacterial artificial chromosome transgenesis implicated zinc finge

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

257 Using a bacterial artificial chromosome transgenic approach, we establishe

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

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

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

261 ut patch recordings in slices from bacterial artificial chromosome transgenic mice examined the role

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

263 This study utilized bacterial artificial chromosome transgenic mice expressing ERbeta

264 ectly test this idea, we developed bacterial artificial chromosome transgenic mice that allowed the a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

283 we generated CD80-eCFP mice using bacterial artificial chromosome transgenic technology.

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

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

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

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

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

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

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

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

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

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

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

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

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

297 r study, Fmr1 knockout mice carrying a yeast-artificial chromosome (YAC) transgene that over-expresse

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

299 ize from complex genomes as a circular yeast artificial chromosome (YAC).

300 Circular yeast artificial chromosomes (YACs) provide significant advant