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 age of YAC128 mice that are transgenic for a yeast artificial chromosome carrying human HTT with an e

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

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

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

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

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

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

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

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

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

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

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

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

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

52 Using both yeast artificial chromosome clones and total human genom

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 The yeast artificial chromosome contig consists of 71 clones

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

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

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

80 A yeast artificial chromosome contig was constructed over

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

82 Yeast artificial chromosomes covering this region have b

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

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

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

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

87 Yeast artificial chromosome-fluorescence in situ hybridi

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

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

90 500 kb spanning the MYCN locus by subcloning yeast artificial chromosomes into cosmids.

91 Each yeast artificial chromosome is first subcloned into cosm

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

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

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

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

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

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

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

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

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

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

102 ession in human erythroid cells, beta-globin yeast artificial chromosome mice, and sickle cell diseas

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

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

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

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

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

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

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

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

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

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

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

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

115 Using a yeast artificial chromosome system that can detect both

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

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

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

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

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

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

122 The modification of yeast artificial chromosomes through homologous recombin

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

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

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

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

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

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

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

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

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

132 Using yeast artificial chromosomes, we have estimated the dist

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

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

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

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

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

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

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

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

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

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

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

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

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

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

147 A yeast artificial chromosome (YAC) clone that encompassed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 -1, and were used to construct an ca. 700 kb yeast artificial chromosome (YAC) contig.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

218 Yeast artificial chromosome (YAC) transgenesis is associ

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

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

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

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

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

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

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

226 Rice yeast artificial chromosome (YAC), bacterial artificial

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

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

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

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

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

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

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

234 Yeast Artificial Chromosomes (YAC) have been isolated fr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

266 Circular yeast artificial chromosomes (YACs) provide significant

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

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

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

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

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

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

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

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

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

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

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

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

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

280 .4 cM, comparable to the cloning capacity of yeast artificial chromosomes (YACs).

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

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

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

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

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

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