ライフサイエンスコーパス: microsatellite marker

1 n genetic clusters (as previously defined by microsatellite markers).

2 waii, USA, were genotyped (n = 600) using 12 microsatellite markers.

3 set is a powerful resource for the design of microsatellite markers.

4 adio telemetry and paternity determined with microsatellite markers.

5 led by dense map-based genome assembly using microsatellite markers.

6 ed to whole-genome LOH/AI analysis using 366 microsatellite markers.

7 using the Haseman-Elston linkage test on 404 microsatellite markers.

8 of heterozygosity/allelic imbalance with 386 microsatellite markers.

9 to 2.1 clones detected by a combination of 3 microsatellite markers.

10 king use of heterozygosity measures based on microsatellite markers.

11 51 BRCA1/2-related breast cancers, using 372 microsatellite markers.

12 ed fragment length polymorphisms (AFLPs) and microsatellite markers.

13 ture across Rum in both mtDNA haplotypes and microsatellite markers.

14 h American RA Consortium, were typed for 379 microsatellite markers.

15 herapy trials were analyzed for MSI using 11 microsatellite markers.

16 expanded genome scan was performed with 556 microsatellite markers.

17 west Ecuador using a suite of 10 polymorphic microsatellite markers.

18 Linkage analysis was performed using 416 microsatellite markers.

19 ,297 individuals from 260 families, with 391 microsatellite markers.

20 gene that is very low in heterozygosity for microsatellite markers.

21 , and a genome scan was carried out with 192 microsatellite markers.

22 studied less, and none of these studies use microsatellite markers.

23 glucose at 8 weeks and was genotyped for 80 microsatellite markers.

24 the program structure in an analysis of 378 microsatellite markers.

25 pic analyses were performed with polymorphic microsatellite markers.

26 essions of Oryza glaberrima using 93 nuclear microsatellite markers.

27 port a linkage map predominantly composed of microsatellite markers.

28 heterozygosity of closely linked polymorphic microsatellite markers.

29 10 worms was also conducted using a panel of microsatellite markers.

30 besity and normal weight using 382 autosomal microsatellite markers.

31 Genotypes were analyzed for 395 microsatellite markers.

32 e barriers between the two species, using 21 microsatellite markers.

33 ct, which hinder us from accurate genotyping microsatellite markers.

34 ndividuals were genotyped with more than 400 microsatellite markers.

35 r the SNPs, versus an average of 41% for the microsatellite markers.

36 y loci are generally conducted using 300-400 microsatellite markers.

37 sing 32 expressed sequence tag (EST)-derived microsatellite markers.

38 CRCs and adenomas were assessed by multiple microsatellite markers.

39 A genome-wide scan was performed with microsatellite markers.

40 l genome scan consisted of 395 evenly spaced microsatellite markers.

41 ) background by selection for closely linked microsatellite markers.

42 m microdissected preneoplastic lesions using microsatellite markers.

43 d confirming previous findings using neutral microsatellite markers.

44 ierarchically sampled and genotyped using 10 microsatellite markers.

45 or blood) and genotyped using 17 polymorphic microsatellite markers.

46 and segregation analysis was performed using microsatellite markers.

47 ocess of screening recombinant libraries for microsatellite markers.

48 frequency (FRE) in Drosophila montana using microsatellite markers.

49 sm arrays and linked regions evaluated using microsatellite markers.

50 rising 819 individuals, were genotyped at 46 microsatellite markers.

51 bryophyte species, Sphagnum lescurii, using microsatellite markers.

52 f the mitochondrial D-loop, 300 SNPs, and 89 microsatellite markers.

53 d by genotyping of short tandem repeat (STR) microsatellite markers.

54 ly tested in a genotyping experiment with 14 microsatellite markers.

55 separately for each population by using >370 microsatellite markers.

56 ome-wide scan and linkage analysis using 500 microsatellite markers.

57 on 174 progeny from three families using 33 microsatellite markers, a single RFLP, and 15 single nuc

58 130 microsatellite markers across the entire genome were gen

59 ss of heterozygosity analysis using multiple microsatellite markers across the genome, and real time

60 he 7p telomere was established by genotyping microsatellite markers across the telomeric region.

61 Comparative mapping of ruff microsatellite markers against the chicken (Gallus gallu

62 Dachshund and find three linked monomorphic microsatellite markers all within a 10-Mb region on chro

63 gnificant TDT-derived associations between a microsatellite marker allele and a disease.

64 dentified 92 case-control studies in which a microsatellite marker allele was found to have significa

65 In the first, an association study of 1884 microsatellite markers, allelic variants of ELP3 were as

66 total of 351 subjects were genotyped for 380 microsatellite markers along the genome at approximately

67 ried out admixture mapping using genome-scan microsatellite markers among the African American partic

68 Microsatellite marker analysis confirmed paternity and g

69 tatus, 118 patients were investigated, using microsatellite marker analysis, in addition to an earlie

70 By using a suite of 29 microsatellite markers (analyzed to confirm representati

71 netic applications, including sequencing and microsatellite marker and single nucleotide polymorphism

72 dentified and validated 8 putatively neutral microsatellite markers and 1 microsatellite marker linke

73 Fine mapping of this region using additional microsatellite markers and 10 Great Danes from a sixth p

74 nt of EBV-associated diseases, we analyzed 2 microsatellite markers and 2 SNPs located near the HLA c

75 e analyzed this 15-Mb region by genotyping 9 microsatellite markers and 36 single nucleotide polymorp

76 de myopia loci have been mapped primarily by microsatellite markers and a limited number of pedigrees

77 uals were genotyped at 14 highly polymorphic microsatellite markers and a single-nucleotide polymorph

78 ory of two of them (type A and type B) using microsatellite markers and asked whether they show signi

79 Microsatellite markers and assignment tests revealed 2 i

80 Using a set of informative microsatellite markers and F(2) generations of resistant

81 dization to those previously obtained by 399 microsatellite markers and find a high degree of concord

82 e analysis and refined the linkage area with microsatellite markers and haplotype analysis to define

83 s, supported by greatly reduced diversity in microsatellite markers and immediate recovery (heterosis

84 s study, we examined the association between microsatellite markers and levels of sex ratio bias (mei

85 ed genetic linkage map of ECB using AFLP and microsatellite markers and map the factors responsible f

86 We genotyped parasites with 18 microsatellite markers and patients for haemoglobin E, a

87 Genotypes were identified by microsatellite markers and somatic incompatibility pairi

88 fted pancreatic or biliary cancers using 386 microsatellite markers and spanning the entire genome at

89 iquantitative polymerase chain reaction with microsatellite markers and then screened for transposabl

90 and normal weight (1,020 subjects) using 21 microsatellite markers and two single nucleotide polymor

91 p of Criollo pig breeds based on a set of 24 microsatellite markers and using different criteria.

92 Single-nucleotide polymorphisms, microsatellite markers, and insertion-deletion polymorph

93 inct populations were found in England using microsatellite markers, and mitochondrial diversity was

94 using single-nucleotide polymorphism arrays, microsatellite markers, and whole-genome and Sanger sequ

95 le nucleotide polymorphism and an extragenic microsatellite marker are in linkage disequilibrium with

96 In studies where microsatellite markers are employed, it is essential tha

97 Microsatellite markers are popular genetic markers frequ

98 Highly polymorphic microsatellite markers are widely employed in population

99 r recurrence, we sought to determine whether microsatellite markers associated with breast cancer cou

100 linkage and association approaches by typing microsatellite markers at 1.2 and 0.5 cM densities, resp

101 By contrast, in the genome scan with microsatellite markers at 9 cM spacing, the maximum Z(LR

102 can for auditory-visual synesthesia with 410 microsatellite markers at 9.05 cM density in 43 multiple

103 sisted of a genome scan for linkage with 498 microsatellite markers at an average spacing of 7 cM in

104 An additional 58 microsatellite markers at approximately 2-cM density in

105 losses with the use of 21 highly polymorphic microsatellite markers at nine chromosomal sites most fr

106 We genotyped 1,058 microsatellite markers (average spacing 3.5 cM), perform

107 A whole-genome scan was performed using 404 microsatellite markers (average spacing 9 cM) and model-

108 The sensitivity of microsatellite markers BAT25, BAT26, D2S123, D5S346, and

109 s of at least 2.0 that were not found by the microsatellite markers: chromosome 8, with a maximum mod

110 Haplotype analysis using microsatellite markers close to the LIPH gene defined a

111 ase chain reaction (PCR)-based assay with 34 microsatellite markers coinciding to 2q11-2q16, nine mar

112 myopia locus in these families, polymorphic microsatellite markers covering the entire X chromosome

113 y selective DNA pooling using a panel of 198 microsatellite markers covering two-thirds of the chicke

114 n breakpoint BP3, at a position close to the microsatellite marker D15S1010 and the bacterial artific

115 mal region III (MRIII), lies between the two microsatellite markers D17S1852 and D17S954.

116 cting the maxillary central incisor with the microsatellite marker D18S64 (tightly linked to TNFRSF11

117 This linkage signal is driven mainly by the microsatellite marker D22S315 (22.59 cM), which had a si

118 d their utility is demonstrated by analyzing microsatellite marker data collected from two population

119 D2S337, and fine mapping of this region with microsatellite markers defined a minimal candidate regio

120 ion NCCCWA genetic map provides an increased microsatellite marker density and quantifies differences

121 aya (Carica papaya L.) was constructed using microsatellite markers derived from BAC end sequences an

122 map was constructed with approximately 3000 microsatellite markers developed from the reference sequ

123 semblage using mitochondrial DNA and nuclear microsatellite markers developed specifically for moa.

124 ific variation in genome stability and hence microsatellite marker development success rates.

125 Identical protocols for microsatellite marker development were implemented in th

126 For the microsatellite marker DG8S737, the -8 allele was signifi

127 Siblings and parents were genotyped for 374 microsatellite markers distributed across the 22 autosom

128 s of heterozygosity (LOH) was assessed using microsatellite markers encompassing the FABP7 gene.

129 2 children with BWS and UPD using a panel of microsatellite markers for chromosome 11.

130 The utility of the microsatellite markers for comparative mapping has been

131 Microsatellite markers for genotyping were used to asses

132 We examined 385 autosomal microsatellite markers for ND, which was assessed by smo

133 ngle-nucleotide polymorphisms (SNPs) and one microsatellite marker from the extended BDNF locus in 16

134 nt), were genotyped using highly polymorphic microsatellite markers from chromosomes 4 and 16, at an

135 the linkage and association data, which uses microsatellite markers from families informative for lin

136 backcross panel for the inheritance of five microsatellite markers from proximal Chromosome 2.

137 e diaspora of the modern cat was traced with microsatellite markers from the presumed site of domesti

138 nd characterized eight different polymorphic microsatellite markers from the sequences within and sur

139 otal hip replacement), were genotyped for 36 microsatellite markers from within a narrow interval at

140 Fine mapping the region with microsatellite markers generated a maximal multipoint LO

141 With a panel of 390 microsatellite markers genotyped in 245 U.S. and French

142 Using data from the 380 microsatellite markers genotyped in the aforementioned g

143 The results of SNP microarrays and microsatellite marker genotyping demonstrated linkage to

144 Paternity analysis based on microsatellite marker genotyping was used to infer conte

145 sing field-derived F2 isofemale families and microsatellite marker genotyping, two loci significantly

146 inimal Screening Set 2 (MSS-2) of 327 canine microsatellite markers has been multiplexed into chromos

147 iner linkage mapping using a high density of microsatellite markers has narrowed female OA susceptibi

148 olk and Texel sheep breeds were compared for microsatellite marker heterozygosity throughout seven ch

149 content associated with a traditional map of microsatellite markers (i.e., 1 marker every ~10 cM) was

150 uantitative trait linkage analysis using 261 microsatellite markers identified significant (n = 8) an

151 Recently, a microsatellite marker in intron 3 (DG10S478) and five co

152 d association was reported between JME and a microsatellite marker in the 6p21 region.

153 We have used 382 microsatellite markers in 1,297 individuals from 260 Eur

154 Genome-wide scans were performed with microsatellite markers in 12 families, and two-point lin

155 f ancestry estimations using 678 genome-wide microsatellite markers in 249 individuals from 13 admixe

156 allelic loss (FAL) was determined using 400 microsatellite markers in 81 HCCs and 77 corresponding n

157 Using 38 microsatellite markers in a pedigree of 3,147 Holstein b

158 We developed microsatellite markers in a targeted region of the Soay

159 anes from 5 pedigrees were genotyped for 280 microsatellite markers in a whole genome screen.

160 the utility and characteristics of conserved microsatellite markers in Charadriiformes (plovers, sand

161 udies of psoriasis focused on segregation of microsatellite markers in families; however, the only lo

162 We constructed genetic maps based on 353 microsatellite markers in four racial/ethnic groups: whi

163 We characterized 28 microsatellite markers in Grevy's zebra and assessed cro

164 ontrol association study using both SNPs and microsatellite markers in haplotypes matched either for

165 growth by performing Chr 1 allelotyping with microsatellite markers in microdissected tumor tissue fr

166 Our model shows that inheritance of microsatellite markers in natural tetraploids of Rorippa

167 We have studied mitochondrial DNA and microsatellite markers in nine populations from Asia, No

168 high frequency of null alleles observed for microsatellite markers in Pacific oysters.

169 We examined LOH at 7 microsatellite markers in the chromosome 3p21.3 region,

170 Similarly, we survey 302 microsatellite markers in the Dachshund and find three l

171 x determination and tail color by genotyping microsatellite markers in the F(2) progeny of a cross be

172 We genotyped a common set of 269 microsatellite markers in the three groups at the same l

173 Fine mapping with 15 additional microsatellite markers in this 11q region for the entire

174 ive single-nucleotide-polymorphism (SNP) and microsatellite markers in this critical region, with LD

175 ssociation analyses, using approximately 400 microsatellite markers, in the largest sample assembled

176 etic linkage map for Daphnia pulex using 185 microsatellite markers, including 115 new markers report

177 ase, we typed individuals for eight X-linked microsatellite markers, including several that previousl

178 Fine mapping with 17 additional microsatellite markers increased the peak to 2.61 (P=.00

179 Although co-amplification of polymorphic microsatellite markers is the current gold standard for

180 y (Vaccinium macrocarpon) genotypes based on microsatellite markers is used to highlight the capabili

181 atively neutral microsatellite markers and 1 microsatellite marker linked to the dihydropteroate synt

182 ficant linkage between the PKD phenotype and microsatellite markers linked to the feline homolog for

183 e, a total of 148 dogs were genotyped at 247 microsatellite markers located on 39 pairs of chromosome

184 We examined five polymorphic microsatellite markers located on chromosome 3p25-26 (D3

185 21 mothers, and all 24 possible sires) at 17 microsatellite marker loci and assigned paternity to all

186 cinomas) were subjected to whole genome (345-microsatellite marker) LOH analysis.

187 complex diseases, based on haplotype maps or microsatellite marker maps.

188 how high frequencies of loss of an allele at microsatellite markers near htrA1 locus on 10q26.

189 We analyzed landscape characteristics and microsatellite markers of P. leucopus populations along

190 The physical and transcription maps and the microsatellite markers of the 700-kb region of chromosom

191 at interest was aroused by reports, based on microsatellite markers, of high levels of statistically

192 iscovered a linkage of the CA phenotype to a microsatellite marker on ECA2 and identified a region of

193 ave conducted a genomewide scan by using 628 microsatellite markers on 1,890 individuals from 110 Uta

194 nomewide linkage scan with approximately 400 microsatellite markers on 23 individuals of a large four

195 The KCNJ11 and ABCC8 genes and microsatellite markers on chromosome 11 were analyzed in

196 nes encoding the K(ATP) channel subunits and microsatellite markers on chromosome 11 were analyzed in

197 SCLC cases for allelic imbalance using eight microsatellite markers on chromosome 19p, which revealed

198 de scan was performed using >382 polymorphic microsatellite markers on genomic DNA from affected and

199 ide scan was performed using 382 polymorphic microsatellite markers on genomic DNA from affected and

200 We identified 11 microsatellite markers on linkage group 3 which were lin

201 rformed in four children with CAKUT using 31 microsatellite markers on peripheral blood genomic DNA t

202 gene models, 40 marker anchors and 1053 new microsatellite markers on the map.

203 By examining more microsatellites markers on more chromosomes than previou

204 and linkage disequilibrium analyses using a microsatellite marker panel, genotyped in families to se

205 d by lower density SNP arrays or by standard microsatellite marker panels.

206 ffects on IPN resistance, using two to three microsatellite markers per linkage group.

207 Polymorphic microsatellite marker (PMM) analysis detected a total of

208 Microsatellite marker polymorphism was conserved across

209 the Satellite locus, but it was linked with microsatellite marker Ppu020.

210 Study-5 that were informative for 1p and 16q microsatellite markers (previously determined) and infor

211 Genetic cluster analysis of the microsatellite markers produced four major clusters, whi

212 This is the first study to demonstrate that microsatellite markers provide valuable information for

213 A genome scan including 380 microsatellite markers representing 29 chromosomes resul

214 Microsatellite markers, representing pairs of loci resul

215 ed agricultural fields were genotyped for 12 microsatellite markers, resulting in multiple polymorphi

216 tical analyses using chloroplast and nuclear microsatellite markers revealed evidence for both diffus

217 Microsatellite markers revealed that genetically distinc

218 Using a genome-wide microsatellite marker scan for linkage in pedigrees, we

219 We performed a whole genome microsatellite marker scan in six multiplex families wit

220 Here, we again report massive distortions of microsatellite-marker segregation ratios in two F(2) hyb

221 son of the HMA10K with the traditional 10-cM microsatellite marker set and the more dense 4-cM marker

222 Sequence analyses of these ESTs revealed microsatellite markers, single nucleotide polymorphisms,

223 9p, 10q, 17p, 17q, 18q) using 18 polymorphic microsatellite markers situated in proximity to known tu

224 nstrated LOH in at least one of the flanking microsatellite markers sJRH and D10S196 (63 kb upstream

225 Genotyping was performed using microsatellite markers spaced at approximately 10 cM int

226 scans have traditionally employed panels of microsatellite markers spaced at intervals of approximat

227 ull genome screening was performed, with 327 microsatellite markers spaced by 5 to 10 cM.

228 Although microsatellite markers spaced every 10 cM typically extr

229 ed quantitative trait locus mapping using 58 microsatellite markers spaced throughout the genome.

230 The Mammalian Genotyping Service typed 391 microsatellite markers, spaced roughly 9 cM.

231 Male carriers were genotyped using microsatellite markers spanning 20-30 cM of the Mcs1 loc

232 Microsatellite markers spanning CG5762 fail to associate

233 Six microsatellite markers spanning IBD1 were genotyped for

234 g, we genotyped 50 pedigrees with OCD, using microsatellite markers spanning the 9p24 candidate regio

235 Three hundred ninety-five highly informative microsatellite markers spanning the genome were genotype

236 een AA and the HLA loci, two genes and eight microsatellite markers spanning the HLA region were geno

237 620 of these families were also typed for 34 microsatellite markers spanning the PSORS1 interval.

238 class II genes and the identification of 23 microsatellite markers spanning this region will contrib

239 Marker associations were measured at 506 microsatellite markers spread throughout the mouse genom

240 enetic marker called SNPSTR which combines a microsatellite marker (STR) with one or more tightly lin

241 can, performed by genotyping 48 dogs for 280 microsatellite markers, suggested linkage with markers o

242 d for jal, and typed it for 93 PCR-scorable, microsatellite markers that are located throughout the m

243 data, a genome-wide scan was performed with microsatellite markers that covered the genome at 10-cM

244 QTL regions were located by association with microsatellite markers that showed significant selection

245 typing a small series of class I alleles and microsatellite markers that the extended haplotype HLA-A

246 We have analyzed genetic data for 326 microsatellite markers that were typed uniformly in a la

247 he present study, we used highly polymorphic microsatellite markers to analyze 74 Plasmodium vivax is

248 We used 10 microsatellite markers to characterize population substr

249 Finally, we developed microsatellite markers to describe the genetic structure

250 to changing climates, was assessed using ten microsatellite markers to determine mean d (2) in a subs

251 We used eight microsatellite markers to estimate genetic diversity, po

252 We used nuclear microsatellite markers to examine the genetic diversity

253 neration genetic map for rainbow trout using microsatellite markers to facilitate the identification

254 With the goal of using microsatellite markers to integrate the physical and gen

255 ochondrial genes (COI, ND1 and ND5) and nine microsatellite markers to investigate the population gen

256 Genomic DNA was scanned using microsatellite markers to localize chromosomal segments

257 We used 60 microsatellite markers to model each phenotype as a func

258 Using microsatellite markers to reclassify recurrent parasitem

259 131 cM), using 618 captive-bred birds and 34 microsatellite markers, to investigate the extent of int

260 Tightening the grid of microsatellite markers under this quantitative trait loc

261 As the microsatellite markers used differ by repeat units of 3

262 me assembly Human July 2003) as well as 8399 microsatellite markers used in the Marshfield and deCODE

263 de linkage analysis of fibromyalgia with 341 microsatellite markers, using the Haseman-Elston regress

264 n with anticoagulant rodenticides has had on microsatellite marker variation and differentiation at t

265 We found that one microsatellite marker was very strongly associated with

266 A genome scan with 494 microsatellite markers was analyzed using GENEHUNTER and

267 Fine mapping with microsatellite markers was compatible with linkage to th

268 In the current study, a genome scan with 384 microsatellite markers was performed on 587 individuals

269 rism Linkage Mapping Set version 2, with 402 microsatellite markers, was used, and, for the SNPs, the

270 The microsatellite markers we report can be easily adapted t

271 Using microsatellite markers, we assessed historical gene flow

272 Using 13 microsatellite markers, we compared 393 blue hake (Antim

273 bass (Morone saxatilis) and six multiplexed microsatellite markers, we evaluated procedures for esti

274 g the spatio-temporal frequency change of 15 microsatellite markers, we find that sigma, the standard

275 Using microsatellite markers, we observed two 3-marker minihap

276 Using microsatellite markers, we show 2 haplotypes for both th

277 onstructing a three-generation pedigree with microsatellite markers, we show that genetic effects of

278 In the case of microsatellite markers, we varied density across 11 leve

279 DNA was extracted from peripheral blood, and microsatellite markers were amplified by polymerase chai

280 eria (23% with postpartum symptoms), and 417 microsatellite markers were analyzed in multipoint allel

281 parasitemia, drug level and genotyping using microsatellite markers were assessed.

282 Inbreeding estimates based on both AFLP and microsatellite markers were found to correlate strongly

283 satellites), of which 50 gene specific and 5 microsatellite markers were generated in this study and

284 In total, 139 Microsatellite markers were genotyped across eight chrom

285 Chromosome 7 microsatellite markers were genotyped in all 12 families

286 ion genetic structure of this pest in China, microsatellite markers were obtained by AFLP of sequence

287 field center before linkage scans using 370 microsatellite markers were performed.

288 Alleles of both microsatellite markers were significantly associated wit

289 Genotype data collected for HLA-DR and 386 microsatellite markers were subjected to multipoint nonp

290 Microsatellite markers were subsequently genotyped for a

291 orphisms in TLR2 (597C-->T, 1350T-->C, and a microsatellite marker) were analyzed in 431 Ethiopian pa

292 fied fragment length polymorphism (AFLP) and microsatellite markers) were correlated with the 'real'

293 llowed by PCR genotyping of HEC (n=11) using microsatellite markers where cellular components were ge

294 iation hybrid map of the rat containing 2058 microsatellite markers which provided over 10,000 potent

295 These microsatellite markers will be the powerful tools for ge

296 -2) (TNRC15) gene, which contains the PARK11 microsatellite marker with the highest linkage score (D2

297 Linkage disequilibrium was identified for a microsatellite marker with the merle phenotype in the Sh

298 m 2,188 participants were genotyped with 405 microsatellite markers with an average intermarker dista

299 Microsatellite markers with an average spacing of 3 Mb w

300 performed in all families using polymorphic microsatellite markers with an average spacing of 5 cM.