ライフサイエンスコーパス: radiation hybrid

1 given pedigree or cell lines from a panel of radiation hybrids.

2 pped to chromosome 10p12-10p14 in a panel of radiation hybrids.

3 STS marker and radiation hybrid analyses mapped PFM1 to human chromosom

4 e tags (ESTs) that were previously mapped by radiation hybrid analysis and were reported to reside in

5 ome 3p21.3, whereas subsequent studies using radiation hybrid analysis localized PPP2R5C to chromosom

6 Radiation hybrid analysis mapped PRDM5 to human chromoso

7 Radiation hybrid analysis mapped the GPC6 gene to human

8 ed by fluorescence in situ hybridization and radiation hybrid analysis to chromosome 11 at band p15.5

9 The gene was mapped by radiation hybrid analysis to chromosome 3q within an int

10 s, developed by using cross-species primers, radiation hybrid analysis, and pool-and-sequence identif

11 By radiation hybrid analysis, we have determined that UNC5C

12 Using FISH and radiation hybrid analysis, we have localized ADAMTS9 to

13 markers in sequence and on genetic linkage, radiation hybrid and cytogenetic scales.

14 Both radiation hybrid and FISH analysis mapped the gene to ch

15 Radiation hybrid and fluorescence in situ hybridization

16 ene was localized to chromosome 17 q23-24 by radiation hybrid and fluorescent in situ hybridization a

17 Using zebrafish radiation hybrid and meiotic mapping panels, we determin

18 identify a human SNA EST and mapped this by radiation hybrid and physical mapping to the distal end

19 this region, we have constructed correlated radiation hybrid and YAC/BAC contig physical maps of the

20 by PCR analysis of the Genebridge 4 panel of radiation hybrids and by fluorescence in situ hybridizat

21 We mapped p73 using radiation hybrids and localized the gene to an interval

22 The generation of plant (barley) radiation hybrids and their culture in vitro is describe

23 We then used radiation-hybrid and cytogenetic maps to calculate recom

24 Marker positions on nine genetic linkage, radiation hybrid, and integrated maps of human chromosom

25 This map provides an integration of genetic, radiation hybrid, and physical mapping information for t

26 e YAC clone coverage and integrated genetic, radiation hybrid, and transcript map provide resources t

27 Unlike the existing radiation hybrid approach, this method allows us to comb

28 transcription units within the encompassing radiation hybrid bins and 7 in flanking bins.

29 ntified using a high-resolution physical and radiation hybrid breakpoint map and applied to a patient

30 n and to identify errors in the databases, a radiation hybrid breakpoint map was developed for the in

31 The study demonstrates the utility of a radiation hybrid breakpoint panel for correction of map

32 ing cytogenetics, overlapping DNA clones and radiation hybrids; but the ultimate and by far the most

33 phenotypic screening of the G3 human-hamster radiation hybrid cell line panel and confirmed the local

34 ucted by using the G3 panel of human/hamster radiation hybrid cell lines and >15,000 unique human gen

35 genomes for which a full genome sequence or radiation hybrid cell lines are unavailable.

36 It was mapped using monochromosomal and radiation hybrid cell lines to chromosomal region 14q11.

37 rs, and we have used phenotypic screening of radiation hybrid cell lines to identify the candidate lu

38 y measurements from a panel of mouse-hamster radiation hybrid cell lines.

39 44 by fluorescence in situ hybridization and radiation hybrid cell panel analyses.

40 A whole genome cattle-hamster radiation hybrid cell panel was used to construct a map

41 on interspecific backcross and whole-genome radiation hybrid cell panels.

42 of this 3-Mb locus, several markers showed a radiation hybrid clone retention rate above the average

43 Our radiation hybrid data localize NSBP1 and Nsbp1 to homolo

44 eotide polymorphisms, sequence-tagged sites, radiation hybrid data, transposon repeats, and more as a

45 ) has maintained RHdb, a public database for radiation hybrid data.

46 comparison with the genetic linkage map and radiation hybrid data.

47 ation Hybrid database, a public database for radiation hybrid data.

48 pped expressed sequence tags (ESTs) from the Radiation Hybrid Database (RHdb), and from other publish

49 The viewer gives access to the maps of the Radiation Hybrid Database at EBI.

50 formatics Institute (EBI) has maintained the Radiation Hybrid database, a public database for radiati

51 on of new, previously unmapped ESTs from the radiation hybrid databases.

52 Radiation hybrid derivatives also represent sources of r

53 ing with maize chromosome addition lines and radiation hybrid derivatives involves assays for the pre

54 ole-genome sequencing, mapping tools such as radiation hybrid DNA panels remain useful aids for seque

55 A LOD-3 radiation hybrid framework map consisting of 21 markers

56 These ESTs were placed on a radiation hybrid framework map of genetic markers spanni

57 Using radiation hybrid genotyping data, 99% of all possible ge

58 Canine PDE6D has been localized to canine radiation hybrid group 14-a, which extends conserved syn

59 e groups, 20 and 26, corresponding to canine radiation hybrid groups RH.34-a and RH.40-a.

60 n neuronal connections, interacting genes in radiation hybrids, interacting proteins in a literature

61 ise gene localization by phenotypic assay of radiation hybrids is practical and was not appreciably i

62 Screening of somatic cell hybrid and radiation hybrid lines by PCR and fluorescence in situ h

63 st comprehensive integration of cytogenetic, radiation hybrid, linkage and sequence maps of the human

64 To assign published radiation hybrid, linkage, and "syntenic" groups to chro

65 CILP was confirmed to reside at the observed radiation hybrid locus by fluorescence in situ hybridiza

66 9 addition line produced maize chromosome 9 radiation hybrids (M9RHs)-oat lines possessing different

67 Based on the resulting radiation hybrid map and our mouse genetic and physical

68 The radiation hybrid map and YAC/BAC physical map enable pre

69 mapping data for the mouse with the incoming radiation hybrid map data.

70 A high-resolution radiation hybrid map encompassing 9.5 Mb between the PLC

71 A fine-structure radiation hybrid map for the region that extends from D8

72 The radiation hybrid map has 5% error in order and 34% error

73 This radiation hybrid map has the highest resolution of any p

74 order of the polymorphic markers within this radiation hybrid map is consistent with published geneti

75 Here we report a radiation hybrid map of mouse genes, a combined project

76 We have constructed a genetic and radiation hybrid map of the centromeric portion of mouse

77 port the construction of a 1.5-Mb-resolution radiation hybrid map of the domestic cat genome.

78 n improved version of the integrated linkage-radiation hybrid map of the rat containing 2058 microsat

79 sents, for the first time, a high-resolution radiation hybrid map of wheat chromosome 1D (D genome) i

80 ous hit to WI-4874, which is at 78 cR on the radiation hybrid map, 3.36 cR, by radiation hybrid mappi

81 Of 36,678 STSs on the TNG radiation hybrid map, only 3604 (9.8%) were absent from

82 The densest linkage map combined with a radiation hybrid map, reported by Steen et al., includes

83 me 8, between markers D8S256 and D8S284 on a radiation hybrid map.

84 er localize the gene for NBS, we generated a radiation-hybrid map of markers at 8q21 and constructed

85 ntegration of the BAC fingerprint map with a radiation-hybrid map via assembled expressed sequence ta

86 dded to the Illinois-Texas 5,000-rad RH (RH, radiation hybrid) map.

87 arge datasets of mouse full-length cDNAs and radiation-hybrid mapped ESTs, the continued development

88 The previously isolated and radiation hybrid-mapped markers Bda84F03, 1QTEL019, and

89 Previously isolated and radiation hybrid-mapped markers TEL17P37, TEL17P49, and

90 l artificial chromosome (BAC) clones for the radiation hybrid-mapped markers, end sequencing of the B

91 all LOD 3 chromosomal maps consisting of 775 radiation-hybrid-mapped genetic markers and ESTs.

92 Using human radiation hybrid mapping and BAC contig construction, we

93 mapped this gene to human chromosome 4q22 by radiation hybrid mapping and by hybridization to two ove

94 This localization was confirmed by radiation hybrid mapping and coincides with that of HuR

95 locks, we analyzed 148 markers on CFA9 using radiation hybrid mapping and established a four-way comp

96 ene maps to chromosome 1q32 as determined by radiation hybrid mapping and FISH analysis.

97 length human enamelin cDNA and determined by radiation hybrid mapping and fluorescent in situ hybridi

98 Both radiation hybrid mapping and fluorescent in situ hybridi

99 somal localization of Optc was determined by radiation hybrid mapping and its genomic structure deter

100 ntiation Complex (EDC) at chromosome 1q21 by radiation hybrid mapping and STS content of genomic clon

101 By radiation hybrid mapping and the use of surrounding gene

102 By radiation hybrid mapping and the use of surrounding mark

103 Radiation hybrid mapping assigned the mda-7 gene to huma

104 Radiation hybrid mapping assigns this kallikrein-gene-ri

105 The LRP7 gene was also localized by radiation hybrid mapping between markers D11S24270 and D

106 Radiation hybrid mapping data indicate that the human lo

107 Radiation hybrid mapping data indicate that the porcine

108 Genetic linkage and radiation hybrid mapping data show that Fgd2 and the hum

109 Genetic linkage and radiation hybrid mapping data show that Fgd3 and the hum

110 Radiation hybrid mapping demonstrated that sciellin is l

111 Radiation hybrid mapping is an important technique for d

112 Radiation hybrid mapping localised disp1 to the same reg

113 rmed to originate from BAC 78138 at 19q13.3; radiation hybrid mapping localized EHD3 and EHD4 to 2p21

114 Radiation hybrid mapping localized hMARCO to chromosome

115 Radiation hybrid mapping localized human CLOCK to the lo

116 Radiation hybrid mapping localized human LMCD1 to the te

117 Radiation hybrid mapping localized the AXIN2 gene to hum

118 Radiation hybrid mapping localized the mouse gene to chr

119 Radiation hybrid mapping localized this gene to a region

120 Radiation hybrid mapping localized TR1 and TL2 to 8q24 a

121 Radiation hybrid mapping of MLP placed it between geneti

122 is supported by phylogenetic analysis and by radiation hybrid mapping of murine I-TAC (gene symbol Sc

123 Radiation hybrid mapping of Nope, Punc, and Neogenin pla

124 nalysis of molecular marker retention in our radiation hybrid mapping panel allowed the localization

125 Analysis of the GeneBridge 4 radiation hybrid mapping panel localized CACNB4 to posit

126 ailability of the zebrafish EST database and radiation hybrid mapping panels has dramatically expande

127 By somatic cell and radiation hybrid mapping panels, SNAIL was localized to

128 Using human-hamster radiation hybrid mapping panels, we mapped DLG3 to Xq13.

129 CR analysis of somatic cell hybrid (SCH) and radiation hybrid mapping panels.

130 Radiation hybrid mapping placed LIMAB1 in a 37-cR interv

131 Radiation hybrid mapping places the human tauCstF-64 gen

132 A radiation hybrid mapping population was developed from a

133 Radiation hybrid mapping revealed that 33 of the 76 zebr

134 Both genes were found to be X-linked: radiation hybrid mapping revealed that the human H9 gene

135 Radiation hybrid mapping studies indicate that the human

136 Radiation hybrid mapping studies placed the rat RISC loc

137 the BAC contig with a map of loci ordered by radiation hybrid mapping suggested the most likely genom

138 We have localized the receptor by radiation hybrid mapping to a region of about 500-kb pai

139 Human RASAL has been localized by radiation hybrid mapping to chromosome 12q23-24.

140 The human RAIDD/CRADD was mapped using radiation hybrid mapping to human chromosome 12, 2.9 cR

141 Rat Ush2a has been localized by radiation hybrid mapping to rat chromosome 13 between d1

142 stimulated peripheral blood lymphocytes and radiation hybrid mapping were used for localization of t

143 Radiation hybrid mapping with Stanford G3 and TNG panels

144 hairless, was localized in this interval by radiation hybrid mapping, and a missense mutation was fo

145 approach that is analogous to linkage or to radiation hybrid mapping, but that circumvents many of t

146 In this study, by radiation hybrid mapping, FISH analysis, BAC clone seque

147 Using T31 mouse radiation hybrid mapping, Folbp3 was mapped to a region

148 cR on the radiation hybrid map, 3.36 cR, by radiation hybrid mapping, from WI-4874.

149 Radiation hybrid mapping, Northern blot analysis, in sit

150 ion, RGD provides tools for gene prediction, radiation hybrid mapping, polymorphic marker selection a

151 By radiation hybrid mapping, the human gene was localized t

152 By radiation hybrid mapping, the human ortholog RAD51D was

153 By radiation hybrid mapping, the human TRIP6 gene was assig

154 Using radiation hybrid mapping, the MCT3 gene was mapped to ch

155 By radiation hybrid mapping, we localized CDC14A to chromos

156 By means of radiation hybrid mapping, we placed the human IRS-2 gene

157 on human chromosome 11q25, as determined by radiation hybrid mapping.

158 human chromosome 5q (near the centromere) by radiation hybrid mapping.

159 and between markers D15S209 and AFM321ZD5 by radiation hybrid mapping.

160 both fluorescence in situ hybridization and radiation hybrid mapping.

161 ificial chromosome (YAC) pool screening, and radiation hybrid mapping.

162 ce in situ hybridization, YAC screening, and radiation hybrid mapping.

163 23 regions, respectively, by cytogenetic and radiation hybrid mapping.

164 d integrated with the current genetic map by radiation hybrid mapping.

165 ed by fluorescence in situ hybridization and radiation hybrid mapping.

166 RD was localized to human chromosome 3q27 by radiation hybrid mapping.

167 tu hybridization and is linked to D10S603 by radiation hybrid mapping.

168 using fluorescent in situ hybridization and radiation hybrid mapping.

169 13 by fluorescence in situ hybridization and radiation hybrid mapping; the cDNA for the human homolog

170 The gene was mapped by high-resolution radiation-hybrid mapping to the interval between microsa

171 Using radiation-hybrid mapping, we show that the DHCR7 gene is

172 g DNA loci that exploits many advantages of 'radiation hybrid' mapping in taxa for which such hybrids

173 To date, we have generated radiation-hybrid-mapping data for >14,000 novel ESTs ide

174 er of published landmark loci in genetic and radiation hybrid maps is in general agreement.

175 other two maps used for this effort were the radiation hybrid maps of chromosome 16 from Whitehead In

176 atic cell hybrid breakpoint physical map and radiation hybrid maps of human chromosome 16 to construc

177 romosome walking, to build both physical and radiation hybrid maps of the CFA12 13-21 region.

178 describe lessons and pitfalls of developing radiation hybrid maps, using the example of mouse Chromo

179 lly as a YAC contig, incorporating data from radiation hybrid maps.

180 from large-insert clones, linkage maps, and radiation hybrid maps.

181 ed on EST sequence comparisons combined with radiation hybrid maps.

182 n contrast to other biological networks, the radiation hybrid network did not show a scale-free distr

183 hysical map of the human genome by typing of radiation hybrids or screening YAC libraries.

184 We show here that applying PCR-SSCP to a radiation hybrid panel allowed mapping and specific sequ

185 To improve sensitivity and efficiency of radiation hybrid panel analysis in comparison to gel-bas

186 We used a radiation hybrid panel and fluorescence in situ hybridiz

187 using the GeneBridge4 human/Chinese hamster radiation hybrid panel and found to be the MPZL1 gene, p

188 n the 5,000-rad horse x hamster whole-genome radiation hybrid panel and mapping 29 gene loci by fluor

189 ere, phenotypic screening of a human/hamster radiation hybrid panel identified SLC19A1, a feline redu

190 A 5000-rad whole genome radiation hybrid panel is described for the domestic cat

191 Radiation hybrid panel mapping and analysis of a deletio

192 was mapped to human chromosome 5q13.3 using radiation hybrid panel mapping and fluorescence in situ

193 Radiation hybrid panel mapping and fluorescence in situ

194 7 transition, we used a combination of mouse radiation hybrid panel mapping and physical mapping by m

195 Radiation hybrid panel mapping further located APAH1 bet

196 Radiation hybrid panel mapping has localized the human a

197 both fluorescence in-situ hybridization and radiation hybrid panel mapping studies.

198 f expression studies, sequence analyses, and radiation hybrid panel mapping.

199 ime and resources needed for construction of radiation hybrid panel marker maps and represents a sign

200 orescence in situ hybridization, analysis of radiation hybrid panel markers, and linkage analysis of

201 A radiation hybrid panel of chicken-hamster Wg3hCl2 cells

202 Analysis of the 5,000-rad horse x hamster radiation hybrid panel produced a map spanning 88 centir

203 PCR-SSCP of 93 samples from a human-hamster radiation hybrid panel revealed the location of the gene

204 curve analysis is reliable and efficient for radiation hybrid panel scoring, and is more sensitive an

205 Genomic mapping using a mouse hamster radiation hybrid panel showed these genes to reside in a

206 henotypic screening of the T31 mouse/hamster radiation hybrid panel to map the MMTV cell entry recept

207 r dissociation curve analysis in the buffalo radiation hybrid panel under a standard protocol, compar

208 A radiation hybrid panel was analyzed for chromosomal assi

209 Using the Stanford G3 radiation hybrid panel we were able to localize the geno

210 mapped in a rhesus macaque (Macaca mulatta) radiation hybrid panel with the human genome, allowing f

211 y constructed a 5000-rad cattle whole-genome radiation hybrid panel with the primary objective of int

212 c maps of 29 of these by using the T31 mouse Radiation Hybrid panel, comparison to human genomic sequ

213 Using the T31 radiation hybrid panel, mouse Treh was shown to be locat

214 by genotyping on a 5000-rad horse x hamster radiation hybrid panel, of which 28 were mapped by fluor

215 Using the INRA-Minnesota porcine radiation hybrid panel, we have constructed a human-pig

216 Using a radiation hybrid panel, we localized (MMU)Minpp1 to a re

217 clones were mapped with the aid of the LN54 radiation hybrid panel.

218 ers is approximately 118 kb using a Stanford radiation hybrid panel.

219 inbred population and the GeneBridge 4 human radiation hybrid panel.

220 lized in the genome using the GeneBridge 4.0 radiation hybrid panel.

221 b1 gene cluster were mapped in the T31 mouse radiation hybrid panel.

222 ered using the high-resolution Stanford TNG3 radiation hybrid panel.

223 ene-specific PCR primers and the GenBridge 4 radiation hybrid panel.

224 1 genes were determined by using a zebrafish radiation hybrid panel.

225 onstructed using the RHDF5000-2 whole-genome radiation hybrid panel.

226 We used a radiation-hybrid panel to map the PSDR1 gene to chromoso

227 mapped the human PITX3 gene to 10q25 using a radiation-hybrid panel.

228 Radiation-hybrid-panel mapping localized prostase to chr

229 P and Khsrp) to human chromosome 19 by using radiation hybrid panels and to mouse chromosome 17 by st

230 Radiation hybrid panels are already available for genome

231 d chromosome breakage for the GB4 and the G3 radiation hybrid panels were also evaluated.

232 f mapping tools, in the form of whole genome radiation hybrid panels, and are opening new possibiliti

233 on onto specific fragments of DNA within the radiation hybrid panels.

234 quencing projects, we have produced genetic, radiation hybrid, physical and transcript maps of the re

235 from available cytogenetic, genetic linkage, radiation hybrid, physical, and transcript-based mapping

236 ns, in addition to conventional deletion and radiation hybrid populations.

237 The integration of this approach with radiation hybrid (RH) analysis provides one of the most

238 A 10,000-rad radiation hybrid (RH) cell panel of the rhesus macaque w

239 es, we used bulk segregant analysis (BSA) of radiation hybrid (RH) cells.

240 of this interval, integrate the contig with radiation hybrid (RH) databases, and use these resources

241 omic additions with gamma rays and recovered radiation hybrid (RH) lines providing low- to medium-res

242 A comprehensive radiation hybrid (RH) map and a high resolution comparat

243 The construction of a high-resolution radiation hybrid (RH) map for SSC12 provides a unique op

244 ast and scalable strategy for constructing a radiation hybrid (RH) map from data on different RH pane

245 This study utilized the panel to construct a radiation hybrid (RH) map of bovine chromosome 19 (BTA19

246 he class II and other MHC genes, a framework radiation hybrid (RH) map of BTA23 was developed by test

247 have developed a unique comprehensive mouse radiation hybrid (RH) map of nearly 23,000 markers integ

248 To extend this power to the domestic cat, a radiation hybrid (RH) map of the cat was constructed int

249 ird-generation map and the 1.5 Mb-resolution radiation hybrid (RH) map of the cat.

250 A second-generation 5000 rad radiation hybrid (RH) map of the cattle genome was const

251 scribe the construction of a high-resolution radiation hybrid (RH) map of the domestic cat genome, wh

252 A first-generation radiation hybrid (RH) map of the equine (Equus caballus)

253 A radiation hybrid (RH) map of the equine X chromosome (EC

254 assembly packages, as well as data from the Radiation Hybrid (RH) map of the rat as part of their va

255 arkers and 687 positions of our whole-genome radiation hybrid (RH) map of the rat.

256 genetic linkage map of the rat and the first radiation hybrid (RH) map of the rat.

257 this map in addition to a newly constructed radiation hybrid (RH) map provides a comprehensive frame

258 nd 37 were positioned on the Roslin 3000-rad radiation hybrid (RH) map, with 20 assignments shared be

259 mparative map was constructed using parallel radiation hybrid (RH) mapping in conjunction with EST se

260 Radiation hybrid (RH) mapping is a powerful method for o

261 Radiation hybrid (RH) mapping is based on radiation-indu

262 Radiation hybrid (RH) mapping localized these genes to c

263 Radiation hybrid (RH) mapping provides a powerful tool f

264 A Java interface to radiation hybrid (RH) mapping software is described whic

265 se of cDNA microarrays, congenic mapping and radiation hybrid (RH) mapping to identify a defective SH

266 f the canine CNTFRalpha cDNA was cloned, and radiation hybrid (RH) mapping was used to determine the

267 Radiation hybrid (RH) mapping, a somatic cell genetic te

268 ndependent of meiotic recombination, such as radiation hybrid (RH) mapping, will aid precise anchorin

269 in a number of nonplant and plant systems is radiation hybrid (RH) mapping.

270 _tsp_map is a software package for computing radiation hybrid (RH) maps and for integrating physical

271 ly a few data types localized on genetic and radiation hybrid (RH) maps and offered only a few tools

272 Radiation hybrid (RH) maps are a useful tool for genome

273 The emergence of radiation hybrid (RH) maps, coupled with the large numbe

274 other types of genomic information, such as radiation hybrid (RH) maps, finger printed contig (FPC)

275 n fingerprint, assembled genomic contig, and radiation hybrid (RH) maps.

276 The radiation hybrid (RH) network constitutes a platform for

277 n-order anchor markers between the mouse T31 radiation hybrid (RH) panel and the recombination map ba

278 A mouse radiation hybrid (RH) panel was used to make a framework

279 on HSA11 were mapped using a cattle-hamster radiation hybrid (RH) panel.

280 for XLPRA, and on a 3000-rad canine-hamster radiation hybrid (RH) panel.

281 e tags (ESTs) and cDNA sequences on the LN54 radiation hybrid (RH) panel.

282 genome, incorporating detailed cytogenetic, radiation hybrid (RH), and meiotic information.

283 omosome-specific reagents and publication of radiation hybrid (RH), genetic linkage, and dog/human co

284 A radiation hybrid (RH)-derived physical map of 25 markers

285 tool for zebrafish gene mapping, a panel of radiation hybrids (RH) was produced by fusion of irradia

286 cDNAs representing over 30,000 radiation-hybrid (RH)-mapped human genes provide an alte

287 d joint frequency distribution in a panel of radiation hybrids (RHs).

288 ocalized MYO3A to human chromosome 10, and a radiation hybrid screen further localized it proximal to

289 We performed radiation hybrid screens to uncover direct TCR ligands a

290 Radiation hybrid studies confirmed the location on chrom

291 elate results from cytogenetic, genetic, and radiation hybrid studies to the genome sequence and comp

292 Analysis of radiation hybrids suggests that the gene order is RLF-PP

293 n genome by using a panel of 90 whole-genome radiation hybrids (the TNG panel) in conjunction with 40

294 analysis and FISH and, more precisely, using radiation hybrids to a region of markers linked to DFNA9

295 ased Stanford G3 panel of whole human genome radiation hybrids to phenotypically map the JSRV recepto

296 ouse genome using a panel of 94 whole-genome-radiation hybrids (WG-RHs) and 271 sequence-tagged sites

297 brid cell panel and a 5,000 rad whole-genome radiation hybrid (WGRH) panel.

298 We developed a whole-genome radiation hybrid (WGRH) resource and tested it by genoty

299 Radiation hybrids, which have to date been used almost e

300 aracterization of a "wide-cross whole-genome radiation hybrid" (WWRH) panel from cotton (Gossypium hi