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

1 express HbS after transfer of a 240-kb betas yeast artificial chromosome.

2 a 27-kb region around the Hoxc8 gene from a yeast artificial chromosome.

3 insert cloning systems such as bacterial and yeast artificial chromosomes.

4 maps for large genomic clones, possibly even yeast artificial chromosomes.

5 nel of rodent-human somatic cell hybrids and yeast artificial chromosomes.

6 s and identifying actin gene locations among yeast artificial chromosomes.

7 such as bacteriophage P1 clones, cosmids, or yeast artificial chromosomes.

8 flanking markers are contained in a 1,240-kb yeast artificial chromosome, a region small enough to pr

9 ids, genome-wide radiation hybrids, and mega-yeast artificial chromosome analysis.

10 globin locus residing on a 248-kb beta-locus yeast artificial chromosome and analyzed its function in

11 Here we report a map of yeast artificial chromosome and bacterial artificial chr

12 Flanking markers were identified and a yeast artificial chromosome and cosmid contig of the reg

13 n and the entire beta-globin gene locus in a yeast artificial chromosome and in 2 globin promoter-rep

14 ing this motif in a 248 kb beta-globin locus yeast artificial chromosome and measuring the activity o

15 cts or large, almost authentic, transloci on yeast artificial chromosomes and undergo B-cell-specific

16 'HS2 was recombined into a beta-globin locus yeast artificial chromosome, and transgenic mice were pr

17 al chromosome showed that it was in the same yeast artificial chromosome as the gene encoding liver g

18 irst to map the MEN1 region physically using yeast artificial chromosome, bacterial artificial chromo

19 ation of fluorescence in situ hybridization, yeast artificial chromosome, bacterial artificial chromo

20 ped in Xp22.2 by Southern blot analysis on a yeast artificial chromosome/bacterial artificial chromos

21 The YAC (yeast artificial chromosome)-based physical map of chrom

22 as found to be refractory to cloning in YAC (yeast artificial chromosome)-based vectors, a P1 artific

23 previous high level expression results with yeast artificial chromosome-based mouse Igkappa transgen

24 A yeast artificial chromosome-based physical map suggests

25 Using yeast artificial chromosome-based single-copy isotransge

26 eleted upon V kappa-J kappa joining, we used yeast artificial chromosome-based techniques to fuse dis

27 In addition, again using yeast artificial chromosome-based technology, we created

28 Yeast artificial chromosome-based transgenesis was used

29 with mice carrying a human beta-globin locus yeast artificial chromosome (beta YAC), and analyzed glo

30 ent of 5'HS4 from a 248 kb beta-globin locus yeast artificial chromosome (beta-YAC) and analyzed glob

31 A promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells

32 these possibilities, human beta-globin locus yeast artificial chromosome (beta-YAC) lines were produc

33 of fetal hemoglobin human beta-globin locus yeast artificial chromosome (beta-YAC) mice, showing tha

34 in the context of a human beta-globin locus yeast artificial chromosome (beta-YAC) results in profou

35 tionally silenced in adult beta-globin locus yeast artificial chromosome (beta-YAC) transgenic mice,

36 in the context of a human beta-globin locus yeast artificial chromosome (betaYAC) and analyzed the e

37 ning the entire human beta-globin locus as a yeast artificial chromosome (betaYAC) transgene.

38 s of a set of mice transgenic for a modified yeast artificial chromosome carrying the human PAX6 locu

39 tamine neurotoxicity, we introduced human AR yeast artificial chromosomes carrying either 20 or 100 C

40 romosome 12, MLF2 was found to reside on the yeast artificial chromosome clone 765b9.

41 of a human disease gene in the context of a yeast artificial chromosome clone containing endogenous

42 Physical mapping using a rat yeast artificial chromosome clone shows that the alterna

43 n of expanded CAG repeat motifs into a 250kb yeast artificial chromosome clone spanning the MJD1 locu

44 ht chain transgene is derived in part from a yeast artificial chromosome clone that includes nearly h

45 The psoriasin gene was present on a 380-kb yeast artificial chromosome clone that was previously ma

46 ntaining the Mep1b gene were obtained from a yeast artificial chromosome clone using polymerase chain

47 markers mi69 and ASB2, which is covered by a yeast artificial chromosome clone, CIC9E2, on chromosome

48 ized the human LMX1.1 gene to three CEPH "B" yeast artificial chromosome clones (907A11, 935B12, and

49 The gene was localized to four CEPH "B" yeast artificial chromosome clones (914B4, 951G9, 981D6,

50 u hybridization mapping of the corresponding yeast artificial chromosome clones and sequence-tagged s

51 Using both yeast artificial chromosome clones and total human genom

52 The use of these yeast artificial chromosome clones as a probe for fluore

53 ntified three highly overlapping nonchimeric yeast artificial chromosome clones containing the apex o

54 is gene were isolated by hybrid capture with yeast artificial chromosome clones covering the deletion

55 A set of yeast artificial chromosome clones has been ordered into

56 The contigs combine 75 yeast artificial chromosome clones, 12 bacterial artific

57 Here we use specialized linear yeast artificial chromosome clones, each carrying a larg

58 ted a topologic map of the 9p21 region using yeast artificial chromosome clones, pulse-field gel elec

59 hromosome by means of chromosome 22-specific yeast artificial chromosome clones.

60 was previously used to capture inserts from yeast artificial chromosome clones.

61 most efficient first step is isolating YAC (Yeast Artificial Chromosome) clones.

62 , the single transgenic made with the 560 kb yeast artificial chromosome construct containing the tTA

63 rm in HT1080 cells after transfecting linear yeast artificial chromosome constructs minimally contain

64 e expression, mutant human beta-globin locus yeast artificial chromosome constructs were used, each h

65 Treatment of transgenic mice expressing a yeast artificial chromosome containing 128 CAG repeats (

66 induced by HO endonuclease in a dispensable yeast artificial chromosome containing human DNA.

67 Thus, identification of a yeast artificial chromosome containing the candidate loc

68 The KO mice with the yeast artificial chromosome containing the human FMR1 ge

69 have recently shown that Fmr1KO mice with a yeast artificial chromosome containing the human FMR1 ge

70 generated a line of transgenic mice using a yeast artificial chromosome containing the Ret mutation

71 netic and physical mapping of scm identified yeast artificial chromosomes containing an exon of mdab1

72 ransgenic mice were generated by transfer of yeast artificial chromosomes containing the entire human

73 Here, we report the construction of a 20-Mb yeast artificial chromosome contig and a high-resolution

74 er of cancer cell lines after isolation of a yeast artificial chromosome contig and development of ST

75 The yeast artificial chromosome contig consists of 71 clones

76 known mammalian ARF genes, to a well-defined yeast artificial chromosome contig on human chromosome 7

77 ned approximately 2-3 Mb, as determined by a yeast artificial chromosome contig reported to cover thi

78 The NTS gene is located on a yeast artificial chromosome contig that contains several

79 A yeast artificial chromosome contig was constructed over

80 Starting with yeast artificial chromosome contigs from the 7q31.3 and

81 Yeast artificial chromosomes covering this region have b

82 However, it is difficult to purify intact yeast artificial chromosome DNA at a concentration suffi

83 tlc1-human allele, and sequencing of rescued yeast artificial chromosome ends has verified the additi

84 re identical to those of C. elegans cosmids, yeast artificial chromosomes, expressed sequence tags, o

85 Chinese hamster ovary cells containing the yeast artificial chromosome F136C5 (alphaYAC) respond to

86 Yeast artificial chromosome-fluorescence in situ hybridi

87 etional analysis across the 450-kb region by yeast-artificial-chromosome fragmentation and phage P1 c

88 In contrast to BAC and yeast artificial chromosome HD mouse models that express

89 500 kb spanning the MYCN locus by subcloning yeast artificial chromosomes into cosmids.

90 Each yeast artificial chromosome is first subcloned into cosm

91 f sequence conservation, using as template a yeast artificial chromosome known to contain both interl

92 Differential genomic blotting using a yeast artificial chromosome known to contain the PAR-1 a

93 nic mouse lines carrying a beta-globin locus yeast artificial chromosome lacking the LCR to determine

94 Using clones derived from four yeast artificial chromosome libraries, a contig has been

95 urospora crassa was cloned previously from a yeast artificial chromosome library and was found to be

96 tude du Polymorphisme Humain megabase-insert yeast artificial chromosome library, which contains info

97 n a set of two radiation hybrid panels and a yeast artificial chromosome library.

98 and screening of a chromosome-specific YAC (yeast artificial chromosome) library revealed that the g

99 CR-based screening to construct a continuous yeast artificial chromosome map covering >20 mb in human

100 enetic maps, expressed sequence tags (ESTs), yeast artificial chromosome maps, bacterial artificial c

101 The map comprises a contig of 14 overlapping yeast artificial chromosomes onto which we positioned 25

102 recombination in yeast, either as part of a yeast artificial chromosome or in a yeast-E. coli shuttl

103 iled physical map of nearly 2 Mb, containing yeast artificial chromosomes, P1-derived artificial chro

104 Fluorescence in situ hybridization using a yeast artificial chromosome physically mapped AVPR1A to

105 Fluorescence in situ hybridization of yeast artificial chromosome probes encompassing these lo

106 rescence in situ hybridization analysis with yeast artificial chromosome probes.

107 A yeast artificial chromosome sequence-tagged site-based (

108 The physical mapping of this gene to a yeast artificial chromosome showed that it was in the sa

109 e mapped six novel ESTs to a 15-Mb contig of yeast artificial chromosomes spanning the critical regio

110 A positional cloning strategy using yeast artificial chromosomes spanning the HPS locus was

111 In our study, we used a yeast artificial chromosome, spanning the entire area wh

112 fingerprinting and previously characterized yeast artificial chromosomes subcloned into cosmids and

113 Using a yeast artificial chromosome system that can detect both

114 in gene 3' enhancer, by deleting them from a yeast artificial chromosome that spans the human beta-gl

115 This region was contained in a single yeast artificial chromosome that was 220 kb long.

116 n any of the overlapping parental BACs and a yeast artificial chromosome that were originally tested

117 nd by hybridization to two overlapping human yeast artificial chromosomes that are located in 4q22.

118 roblasts transformed with multiple copies of yeast artificial chromosomes that contain the full-lengt

119 f genomic DNA from higher eukaryotes such as yeast artificial chromosomes, the delitto perfetto strat

120 The modification of yeast artificial chromosomes through homologous recombin

121 Based on electrophoretic analysis of yeast artificial chromosomes, TNFR2 maps within 400 kb o

122 -in, pop-out" gene targeting in a human apoB yeast artificial chromosome to introduce nonsense mutati

123 d 3' end of the gene were subcloned from the yeast artificial chromosomes to enable untranscribed DNA

124 +/-) with mice harboring a human beta-globin yeast artificial chromosome transgene.

125 We report that single-copy yeast artificial chromosome transgenes containing an unm

126 Human beta-globin locus yeast artificial chromosome transgenic mice display corr

127 Characterization of the largest element in yeast artificial chromosome transgenic mice revealed it

128 We analyzed two sets of human yeast artificial chromosome transgenic mice that contain

129 ial and brain tissue derived from Huntington yeast artificial chromosome transgenic mice.

130 Using yeast artificial chromosomes, we have estimated the dist

131 The mutant yeast artificial chromosomes, which coded for the trunca

132 -p21, composed of 205 loci, connected by 480 yeast artificial chromosomes, with average interlocus di

133 e chain reaction the localization of ATIC to yeast artificial chromosome (YAC) 914E7 previously repor

134 ion and characterization of newly identified yeast artificial chromosome (YAC) and bacterial artifici

135 pulsed-field gel electrophoresis (PFGE), and yeast artificial chromosome (YAC) and bacterial artifici

136 Both yeast artificial chromosome (YAC) and bacterial clone-ba

137 hromosome arm deletions were evaluated using yeast artificial chromosome (YAC) and P1 probes.

138 d it up in Saccharomyces cerevisiae, using a yeast artificial chromosome (YAC) base.

139 eplaced with the PyE within the context of a yeast artificial chromosome (YAC) bearing the whole locu

140 thin their life span, we decided to obtain a yeast artificial chromosome (YAC) carrying the AR gene a

141 ed the core elements within the context of a yeast artificial chromosome (YAC) carrying the entire lo

142 We have shown previously that a 320 kb yeast artificial chromosome (YAC) carrying the intact hu

143 a new hybrid vector, pTARBAC1, containing a yeast artificial chromosome (YAC) cassette (a yeast sele

144 by direct complementary DNA selection from a yeast artificial chromosome (YAC) clone containing a 650

145 A yeast artificial chromosome (YAC) clone that encompassed

146 A 420 kb yeast artificial chromosome (YAC) clone, extending well

147 kers from the region did not identify intact yeast artificial chromosome (YAC) clones after screening

148 n myeloid hematopoietic cells, we introduced yeast artificial chromosome (YAC) clones and derivatives

149 cosmid clones to three partially overlapping yeast artificial chromosome (YAC) clones and determined

150 e sequence length polymorphisms (SSLPs) from yeast artificial chromosome (YAC) clones containing regi

151 Employing a PCR-based strategy, yeast artificial chromosome (YAC) clones containing the

152 ll hybrids, and five independent overlapping yeast artificial chromosome (YAC) clones containing the

153 in situ hybridization with a panel of mapped yeast artificial chromosome (YAC) clones from 7q to exam

154 We have isolated 48 yeast artificial chromosome (YAC) clones from a 4 cM/27

155 s on human metaphase chromosomes of over 950 yeast artificial chromosome (YAC) clones from the CEPH l

156 ysical map of P1 (PAC), bacterial (BAC), and yeast artificial chromosome (YAC) clones of this interva

157 The physical map consists of a contig of 420 yeast artificial chromosome (YAC) clones ordered with re

158 ites (STSs) within the region, a total of 21 yeast artificial chromosome (YAC) clones were isolated a

159 Yeast artificial chromosome (YAC) clones were used to de

160 have integrated into 721.174 two overlapping yeast artificial chromosome (YAC) clones which cover the

161 the long arm of the human X chromosome using yeast artificial chromosome (YAC) clones.

162 nalysis was performed with several 8p11 CEPH yeast artificial chromosome (YAC) clones.

163 of bacterial artificial chromosome (BAC) and yeast artificial chromosome (YAC) clones.

164 re constructed from multimegabase contigs of yeast artificial chromosome (YAC) clones; 2) they are in

165 ping data from reduced radiation 8p hybrids, yeast artificial chromosome (YAC) co-localisation of mar

166 verexpressing the human VPAC(2)R gene from a yeast artificial chromosome (YAC) construct.

167 previously reported the generation of human yeast artificial chromosome (YAC) constructs encompassin

168 bout 50 kb from the IgH intron enhancer in a yeast artificial chromosome (YAC) containing a 220 kb re

169 rand break (DSB) within a 360-kb dispensable yeast artificial chromosome (YAC) containing human DNA (

170 y studying the transcriptional activity of a yeast artificial chromosome (YAC) containing Igf2 and H1

171 ferred by this element by deleting it from a yeast artificial chromosome (YAC) containing the entire

172 roplasts that results in the generation of a yeast artificial chromosome (YAC) containing the gene of

173 Deletion of the DHS from a 310-kb yeast artificial chromosome (YAC) containing the human C

174 nic mice by pronuclear injection of a 380 kb yeast artificial chromosome (YAC) containing the human P

175 a 6-kbp promoter fragment nor even a 120-kbp yeast artificial chromosome (YAC) containing the whole G

176 mouse chromosome 1 and the construction of a yeast artificial chromosome (YAC) contig across this reg

177 ning efforts to identify the RMD-1 TSG(s), a yeast artificial chromosome (YAC) contig consisting of 1

178 A yeast artificial chromosome (YAC) contig containing 22 Y

179 We constructed a yeast artificial chromosome (YAC) contig covering the de

180 Here we describe a yeast artificial chromosome (YAC) contig covering the di

181 We then developed a yeast artificial chromosome (YAC) contig for this region

182 The telomeric end of the contig overlaps a yeast artificial chromosome (YAC) contig from Xq24-q26 a

183 A yeast artificial chromosome (YAC) contig is described th

184 cute insulin response, we have constructed a yeast artificial chromosome (YAC) contig map that spans

185 in head and neck squamous cell carcinoma, a yeast artificial chromosome (YAC) contig spanning the en

186 lable regional DNA markers, we constructed a yeast artificial chromosome (YAC) contig that contained

187 The final assembly consists of a yeast artificial chromosome (YAC) contig with 42 members

188 We have constructed a yeast artificial chromosome (YAC) contig, extending from

189 -1, and were used to construct an ca. 700 kb yeast artificial chromosome (YAC) contig.

190 f other cereal genomes, has resulted in rice yeast artificial chromosome (YAC) contigs spanning parts

191 ability of foreign telomeres to complement a yeast artificial chromosome (YAC) deficient by one telom

192 available that allow the transfer of intact yeast artificial chromosome (YAC) DNA into transgenic mi

193 nd approach, MACs were formed from a defined yeast artificial chromosome (YAC) DNA molecule containin

194 gration to specific single-copy sites within yeast artificial chromosome (YAC) insert DNA.

195 which facilitates the rapid modification of yeast artificial chromosome (YAC) insert DNA.

196 We have aligned yeast artificial chromosome (YAC) inserts in a contig sp

197 We show here that a 250 kbp GATA-2 yeast artificial chromosome (YAC) is expressed strongly

198 nts with four Arabidopsis, ecotype Columbia, yeast artificial chromosome (YAC) libraries.

199 d-tagged sites (STSs) against a large-insert yeast artificial chromosome (YAC) library and then integ

200 struction and characterization of an arrayed yeast artificial chromosome (YAC) library for the rat ge

201 We have constructed a zebrafish yeast artificial chromosome (YAC) library using genomic

202 gene members on this cluster, a human CEPH B yeast artificial chromosome (YAC) library was screened b

203 Introduction of a 1.1 Mb fragmented yeast artificial chromosome (YAC) mapping to this region

204 curately in transgenic mice that carry large yeast artificial chromosome (YAC) or ligated cosmid cons

205 l artificial chromosome (BAC) contigs from a yeast artificial chromosome (YAC) physical map is descri

206 A yeast artificial chromosome (YAC) physical map of chromo

207 In addition, we mapped SOCS2 by yeast artificial chromosome (YAC) pool screening to YAC

208 omosome 13q12 region by cytogenetic mapping, yeast artificial chromosome (YAC) pool screening, and ra

209 lting BAC contigs and oriented them within a yeast artificial chromosome (YAC) scaffold by observing

210 From a human chromosome Xq25-specific yeast artificial chromosome (YAC) sublibrary, five YACs

211 ave focused on strategies that would utilize yeast artificial chromosome (YAC) technology, thus permi

212 able transfection of an approximately 620-kb yeast artificial chromosome (YAC) that carried the entir

213 We then compared expression from a 310 kb yeast artificial chromosome (YAC) that contains the enti

214 ome (HAC) vector was constructed from a 1-Mb yeast artificial chromosome (YAC) that was selected base

215 We subsequently showed that a 271-kbp yeast artificial chromosome (YAC) transgene could fully

216 Yeast artificial chromosome (YAC) transgenesis is associ

217 herapeutic approaches to fragile X syndrome, yeast artificial chromosome (YAC) transgenic mice were g

218 Here, we used a yeast artificial chromosome (YAC) transgenic mouse model

219 ism and A beta deposition in a genomic-based yeast artificial chromosome (YAC) transgenic mouse model

220 ucted a YAC/STS contig map by initiating two yeast artificial chromosome (YAC) walks from the markers

221 In a yeast artificial chromosome (YAC) we have engineered an

222 Here we describe transgenic mice carrying a yeast artificial chromosome (YAC) with the intact human

223 transgenic mouse line bearing a 662-kb Gata3 yeast artificial chromosome (YAC), and these animals (te

224 Rice yeast artificial chromosome (YAC), bacterial artificial

225 A yeast artificial chromosome (YAC), P1, and cosmid clone

226 wing introduction of the human APP gene in a yeast artificial chromosome (YAC), we examined the effec

227 letion critical region was assembled using a yeast artificial chromosome (YAC)-based isolation and bi

228 udy was to assess the feasibility of using a yeast artificial chromosome (YAC)-based reporter gene co

229 Using a yeast artificial chromosome (YAC)-based sequence-tagged

230 nts with an increased loss of an ADE2-marked yeast artificial chromosome (YAC).

231 b in size from complex genomes as a circular yeast artificial chromosome (YAC).

232 Yeast Artificial Chromosomes (YAC) have been isolated fr

233 A method for linking any standard yeast artificial chromosomes (YAC) is described.

234 earlier study, Fmr1 knockout mice carrying a yeast-artificial chromosome (YAC) transgene that over-ex

235 ecently we described the identification of a yeast artificial chromosome, YAC 927G4, that spans a tra

236 In previous studies with the yeast artificial chromosome (YAC128) transgenic HD mouse

237 for physical mapping consists of contigs of yeast artificial chromosome (YACs), large vectors that a

238 ave introduced two different CFTR-containing yeast artificial chromosomes (YACs) (320 and 620 kb) int

239 een mapped at seven-fold average coverage in yeast artificial chromosomes (YACs) and 100 kb inter-seq

240 Through molecular analysis using yeast artificial chromosomes (YACs) and cosmid clones, t

241 a large human locus, overlapping regions on yeast artificial chromosomes (YACs) and cosmids were lin

242 Yeast artificial chromosomes (YACs) are a common tool fo

243 demonstrate here that human genes present on yeast artificial chromosomes (YACs) are transcribed in y

244 We have used RARE cleavage to cut yeast artificial chromosomes (YACs) at specific EcoRI si

245 rt the isolation and characterization of two yeast artificial chromosomes (YACs) bearing the murine G

246 ment of a system for shuttling DNA cloned as yeast artificial chromosomes (YACs) between yeast and ma

247 stability by generating transgenic mice with yeast artificial chromosomes (YACs) carrying AR CAG repe

248 ouse antibody production and engineered with yeast artificial chromosomes (YACs) containing different

249 Nearly all the M1-selected transformants had yeast artificial chromosomes (YACs) containing human DNA

250 accurately a variety of linear and circular yeast artificial chromosomes (YACs) containing human DNA

251 Procedures for introducing yeast artificial chromosomes (YACs) containing large gen

252 n can be used to assess gene expression from yeast artificial chromosomes (YACs) containing the 230 k

253 beta production in vivo, we have introduced yeast artificial chromosomes (YACs) containing the entir

254 We propose a new method for segregation of yeast artificial chromosomes (YACs) from endogenous yeas

255 Forty-three yeast artificial chromosomes (YACs) from the X chromosom

256 ve isolation of human DNAs as large circular yeast artificial chromosomes (YACs) from two rodent/huma

257 ransgenesis with large DNA molecules such as yeast artificial chromosomes (YACs) has an advantage ove

258 simple and rapid assay for GCRs, exploiting yeast artificial chromosomes (YACs) in Saccharomyces cer

259 ic stem (ES) cell lines containing different yeast artificial chromosomes (YACs) integrated into the

260 en established to convert pYAC4-based linear yeast artificial chromosomes (YACs) into circular chromo

261 describe a modified protocol for introducing yeast artificial chromosomes (YACs) into murine embryoni

262 expressed sequence tags (ESTs) identified 33 yeast artificial chromosomes (YACs) or P1 clones, which

263 (FISH) was then performed using a series of yeast artificial chromosomes (YACs) ordered in the CDR,

264 Circular yeast artificial chromosomes (YACs) provide significant

265 ange restriction mapping was performed using yeast artificial chromosomes (YACs) spanning approximate

266 ndidate interval for NP-C, three overlapping yeast artificial chromosomes (YACs) spanning the 1 centi

267 The PDE10A gene was mapped to three yeast artificial chromosomes (YACs) that contain human D

268 ective isolations of the entire HPRT gene as yeast artificial chromosomes (YACs) that extended from t

269 r transgenic mice, containing four different yeast artificial chromosomes (YACs) that together cover

270 We isolated two murine yeast artificial chromosomes (YACs) that, when introduce

271 some sequences in the form of large circular yeast artificial chromosomes (YACs) up to 170 kb in size

272 isolated the region between these markers in yeast artificial chromosomes (YACs) using a combination

273 murine cells, a transgenesis system based on yeast artificial chromosomes (YACs) was established for

274 equence-tagged site (STS) content mapping in yeast artificial chromosomes (YACs) was used to cover th

275 An approach is described to modify yeast artificial chromosomes (YACs) with cassettes that

276 bility of human DNA contained in dispensable yeast artificial chromosomes (YACs) within the yeast Sac

277 The map comprises a contig of 84 overlapping yeast artificial chromosomes (YACs), P1 artificial chrom

278 .4 cM, comparable to the cloning capacity of yeast artificial chromosomes (YACs).

279 ique of exon trapping to human chromosome 21 yeast artificial chromosomes (YACs).

280 human DNA during transformation to generate yeast artificial chromosomes (YACs).

281 insertions into two different mouse-derived yeast artificial chromosomes (YACs).

282 zation of a Chlamydomonas genomic library in yeast artificial chromosomes (YACs).

283 somatic cell and radiation hybrid panels and yeast artificial chromosomes (YACs).

284 a coli P1 artificial chromosomes (PACs) into yeast artificial chromosomes (YACs).