ライフサイエンスコーパス: DNA marker

1 e the most intensively researched epigenetic DNA marker.

2 nostic chloroplast DNA and nuclear ribosomal DNA markers.

3 etically, we isolated a number of sex-linked DNA markers.

4 ly analyze agarose gel images of polymorphic DNA markers.

5 ting physical and sequence maps and numerous DNA markers.

6 d by the loss of jiggling motion of specific DNA markers.

7 s on commonly used short tandem repeat (STR) DNA markers.

8 region-specific DNA for cloning of genes or DNA markers.

9 of an appropriately dense set of polymorphic DNA markers.

10 which contains 456 bacterial clones and 202 DNA markers.

11 pressed hazelnut oil based on microsatellite DNA markers.

12 y genetic map consisting of easily genotyped DNA markers.

13 7 amplified fragment length polymorphisms as DNA markers.

14 de search for linkage, using 290 polymorphic DNA markers.

15 for a tilapia, Oreochromis niloticus, using DNA markers.

16 ouston) and in Jamaica, using nine autosomal DNA markers.

17 be constructed guided by the transmission of DNA markers.

18 D7S688 spanning the TCRB locus were used as DNA markers.

19 four sequence-tagged site (STS) loci, and 10 DNA markers.

20 entification may benefit from the identified DNA markers.

21 milar to previous phylogenies produced using DNA markers.

22 olecular analyses of chloroplast and nuclear DNA markers.

23 acer (ITS) and large subunit (LSU) ribosomal DNA markers.

24 celerated significantly the decay of all the DNA markers.

25 enetic differentiation identified by nuclear DNA markers.

26 ble for parent-rated anxiety and genome-wide DNA markers.

27 the estimation of genetic linkage maps from DNA markers.

28 reservative, which reduced detection of some DNA markers.

29 was done using 21 additional closely spaced DNA markers.

30 hecking consensus maps of contigs, and using DNA markers.

31 ting soybean composite genetic map using 388 DNA markers.

32 were mapped using polymorphic microsatellite DNA markers.

33 rmination of serotype in Salmonella based on DNA markers.

34 tomated linkage mapping of human polymorphic DNA markers.

35 manually and by screening the BACs with 367 DNA markers.

36 33 allozyme loci, which were used as nuclear DNA markers.

37 man electroencephalogram in conjunction with DNA markers.

38 Of the map's 758 DNA markers, 136 have multiple locations in the NRY, ref

39 Bulked segregant analysis revealed two DNA markers (28-178 and 23-201) within 10 cM of these lo

40 hromosome 1q were evaluated by genotyping 16 DNA markers across 107 centimorgans of this chromosome i

41 phocyte proportions in B6SJLF2 mice by using DNA markers adjacent to these mapped QTLs and found that

42 f double-stranded DNA fragments with various DNA markers, agarose gel concentrations, and field stren

43 Such DNA markers allow the identification of maize genomic DN

44 Many DNA markers anchored sets of 2-8 different contigs.

45 inkage map constructed with 1236 polymorphic DNA markers and 14 erythrocyte antigens and serum protei

46 ence for genetic linkage between polymorphic DNA markers and 15 putative IDDM susceptibility loci, de

47 has been constructed by hybridization of 69 DNA markers and 61 YAC end probes to gridded arrays of Y

48 such as locus-specific sequence-tagged site DNA markers and bacterial artificial chromosome contigs

49 indicate that the association between NOTCH4 DNA markers and bipolar disorder is related to altered f

50 d the SphI cleavage sites resulting in these DNA markers and derived a comprehensive map for the RH l

51 From 1.7 million DNA markers and g scores at ages 7 and 12 on 2875 childr

52 se competing hypotheses using microsatellite DNA markers and lynx samples from 17 collection sites in

53 ses for meta-analysis of association between DNA markers and phenotypes of medical and/or social conc

54 ese mapping approaches and to identify novel DNA markers and probes for the BLM candidate region, a c

55 ed inbred strains of M. hapla that differ in DNA markers and produced hybrids and F(2) lines.

56 atistically estimate the association between DNA markers and regions of a genome (quantitative trait

57 investigations will require large numbers of DNA markers and the technology to screen large populatio

58 apped to cosmid 126D1 at the mfd41 (D17S261) DNA marker, and their conceptual translation showed homo

59 we could distinguish by using microsatellite-DNA markers, and developed an allele-specific quantitati

60 s, larger sample sizes, a greater density of DNA markers, and more-sophisticated statistical modeling

61 ome (YAC) clones ordered with respect to 142 DNA markers, approximately one probe every 110 kb.

62 luable where nonrecombining, gender-specific DNA markers are desired, including forensic investigatio

63 Transferable DNA markers are essential for breeding and genetics.

64 n of gene order that is revealed when common DNA markers are mapped in different species.

65 Although DNA markers are very powerful for distinguishing among i

66 Using the intensity level of the probe (or a DNA marker) as a reference, we efficiently sort the FCS

67 o tags for targeting and detecting the HIV-1 DNA marker, as opposed to using bare AuNPs in LF strips.

68 1:1 for the presence or absence of dominant DNA markers, as would be expected if sister chromosomes

69 orphic DNA markers is an invaluable tool for DNA marker-assisted breeding, positional cloning, and a

70 are the segregation ratios of microsatellite DNA markers at 6 hr and 2-3 months postfertilization in

71 nk bipolar affective disorder to polymorphic DNA markers at or near the gene for tyrosine hydroxylase

72 nalysis was performed using four polymorphic DNA markers at the MEN1 gene locus; D11S480, PYGM, D11S4

73 Both reproductive biology-based and DNA marker-based studies indicate that genders have sepa

74 efined the location of the ODDD gene between DNA markers D6S266/D6S261 (centromeric) and D6S1639 (tel

75 The strongest linkage was to DNA marker D6S433 (Zmax = 8.96, thetamax = 0.001).

76 rn of allelic loss using nine microsatellite DNA markers (D9S177, D9S303, D9S778, D9S171, D12S1015, D

77 Error within a DNA marker dataset can result in reduced statistical pow

78 In general, the microbial DNA markers demonstrated a higher fecal concentration th

79 Significant variations in DNA marker density are related to possible centromeric r

80 A commercially available DNA marker derived from pUC19 was quantified by dPCR and

81 This map and the DNA markers derived from it were instrumental in the rec

82 DNA markers described herein facilitate cloning of genes

83 The DNA markers described in this paper are the starting poi

84 Advances in genetic resources, DNA markers, DNA sequence information, and gene expressi

85 ic mobility similar to that of 270-kb linear DNA markers during clamped homogeneous electric field ge

86 nts to a 180-kb interval that was flanked by DNA markers DXS705 and DXS741.

87 vered a novel THD signature sequence between DNA markers DXS87 and DXS366.

88 nts as highly sensitive endogenous cell-free DNA markers, enabling the relative abundance measurement

89 as validated using a series of LG23-specific DNA markers (five SNPs with highest association to sex f

90 isolating rare cells on the basis of RNA or DNA markers, followed by bulk or single-cell transcripto

91 itutes the first report of a pseudoautosomal DNA marker for plant sex chromosomes.

92 We found a DNA marker for the HD gene in 1983-the first marker to b

93 hromosome systematically with a dense map of DNA markers for allelic associations with g.

94 ercial vegetable oils for the application of DNA markers for food safety and traceability.

95 Despite the promise of using DNA markers for the early detection of cancer, none has

96 To resolve this conflict and develop useful DNA markers for this gene, we isolated and characterized

97 Because DNA markers from the region did not identify intact yeas

98 were not macroscopically blood-stained, two DNA markers gave an informative and correct result, iden

99 Results of this study suggest that DNA markers H-ND6, H-ND5, and Pig-2-Bac may be among the

100 Efforts to discover resistance genes and DNA markers have been dominated by candidate gene and qu

101 Microsatellite DNA markers have been widely used as a tool for the dete

102 In the first generation of plant genomics, DNA markers have refined some perceptions of genetic var

103 genetics model results in a distribution of DNA marker heterozygosities and linkage disequilibria th

104 tegies, independent contig building methods, DNA marker hybridization, and different fingerprinting m

105 A SNP-based DNA marker in the coding region accurately predicted phe

106 analyzed the inheritance of 443 polymorphic DNA markers in 22 recombinant cloned progeny derived fro

107 n ash (Fraxinus pennsylvanica) contains 1201 DNA markers in 23 linkage groups spanning 2008.87cM.

108 erns on chromosome 11q13 using 8 polymorphic DNA markers in 44 different MEN1 tumors from parathyroid

109 To provide rapid and accurate detection of DNA markers in a straightforward, inexpensive, and multi

110 By sequencing high-resolution DNA markers in over 4000 topsoil samples from natural an

111 al importance for identifying locus-specific DNA markers in tetraploid cottons including leading cult

112 preparations and by analysis of polymorphic DNA markers in the patients and their available parents.

113 Previously reported linkage between BP and DNA markers in the pericentromeric region of chromosome

114 e in a set of U.S. winter wheat and identify DNA markers in these regions, we conducted a genome-wide

115 studies with polymerase chain reaction-based DNA markers in two large pedigrees recently localized th

116 The analysis for chromosome 16 specific DNA markers, in revertant clones of senescent microcell

117 rosatellite and random amplified polymorphic DNA markers indicated that the mutants mapped to two sit

118 However, additional codominant DNA marker information in the affected region excluded t

119 a selection method for HAP varieties with a DNA marker is suggested.

120 coverage of the rice genome with polymorphic DNA markers is an invaluable tool for DNA marker-assiste

121 The use of various kinds of nuclear DNA markers is increasing, as are multiple locus studies

122 Linkage testing with DNA markers is still required for patients with multiple

123 erequisite for the development of diagnostic DNA markers is the genetic dissection of the factors tha

124 um L., involving 335 markers, including RFLP DNA markers, isozymes, seed storage proteins, rRNA, and

125 identify two randomly amplified polymorphic DNA markers linked to Ma3.

126 Availability of DNA markers linked to R1R2R3 genes would allow efficient

127 We searched for DNA markers linked to this major gene using the techniqu

128 ticle, we consider the analysis of biallelic DNA marker loci and human quantitative trait loci in set

129 The anonymous DNA marker locus D17S938, linked to adRP locus RP13 on c

130 inkage was achieved with several polymorphic DNA markers mapping to chromosome 6p12-p21 (maximal 2-po

131 We aimed to identify and validate methylated DNA markers (MDMs) for HCC detection.

132 We aimed to evaluate the use of methylated DNA markers (MDMs) from biliary brushings to enhance MBS

133 Physical mapping was accomplished by 179 DNA markers mostly representing expressed genes using 41

134 Evaluation of DNA markers near CpCYC-b revealed a recombination hot sp

135 kage of the Htg9.1 phenotype with a specific DNA marker (NM4182) located on a single genomic sequence

136 In contrast, no chloroplast DNA or ribosomal DNA markers of H. debilis ssp. cucumerifolius were found

137 texanus had chloroplast DNA and/or ribosomal DNA markers of H. debilis ssp. cucumerifolius.

138 The analysis of intracellular RNA and DNA markers of HBV replication and examination of HBV RN

139 By identifying novel DNA markers of insecticide resistance, this study opens

140 1A, 1B, and 1D were generated by mapping 50 DNA markers on 56 single-break deletion lines.

141 map of single nucleotide polymorphism (SNP) DNA markers on chromosome 15q25-q26 to maximize the info

142 the alpha-synuclein gene and closely linked DNA markers on chromosome 4q and the APOE epsilon4 allel

143 tipoint mapping method and eight informative DNA markers on chromosome 6 (D6S461, D6S276, D6S105, D6S

144 nt article describes linkage analysis of 310 DNA markers on chromosomes 1, 5p, 6, 8, 10q, 11q, and 12

145 linkage maps of loci defined by polymorphic DNA markers on rat chromosome 1 were constructed by geno

146 assessed for LOH using eight microsatellite DNA markers on six chromosomes.

147 lyzing the methylation status of polymorphic DNA markers on X-linked genes because extensive de novo

148 ne when using randomly amplified polymorphic DNA markers, or as has occurred with human genetic linka

149 ence or absence of a series of Y-chromosomal DNA markers, or sequence-tagged sites (STSs).

150 lower mosaic virus 35S promoter)) and non-GM DNA marker (papain) in 15 min.

151 satellite and mitochondrial (control region) DNA markers provided mixed evidence for roundscale spear

152 Previous Y chromosome and mitochondrial DNA markers provided no support for their claimed Greek

153 ation, calibrated with dPCR or IDMS measured DNA markers, provides an effective method for certifying

154 study of S. damnosum s.l. using a repetitive DNA marker, pSO11, are presented.

155 Sera were analyzed for two methylated DNA markers: RASSF1A and RAR-beta2.

156 Nuclear DNA markers reflect a species tree consistent with expec

157 Tr129 and the DNA markers reported here are useful resources for impro

158 f the tribe based on nuclear and chloroplast DNA markers, representing the most in-depth reconstructi

159 n changes in metabolite profiles or based on DNA markers, require advanced and expensive instrumentat

160 vary from study to study on the basis of the DNA markers, sample size, relative-pair types, and pedig

161 using three independent sets of polymorphic DNA markers, sampling 30 loci distributed across all nuc

162 In stage 1, 65 DNA markers selected from the chicken genetic maps were

163 ffect sizes ranged from moderate for urinary DNA markers (SMD = 0.44 [95% CI, 0.20-0.68]; P < .001) t

164 .68]; P < .001) to very large for blood cell DNA markers (SMD = 1.12 [95% CI, 0.69-1.55; P < .001).

165 Genotyping of DNA markers spanning 8 genes for autosomal dominant HCM

166 Evaluation of polymorphic DNA markers spanning chromosome 1 demonstrated that the

167 Linkage analysis for polymorphic DNA markers spanning the X chromosome established linkag

168 The DNA markers spread rapidly in both the CCH and CCC after

169 dered as important candidate genes for maize DNA marker studies.

170 ed fragment length polymorphism is a popular DNA marker technique that has applications in multiple f

171 hat encompassed 1.05 Gb and 404 high-quality DNA markers that anchored 742 contigs.

172 ld therefore greatly benefit from diagnostic DNA markers that can be applied early in the breeding cy

173 henotype, and neither TR locus was linked to DNA markers that flank a major-effect locus for life cyc

174 Using highly polymorphic DNA markers that flank the KLF4 locus, we found evidence

175 e can be calculated using these saliva-based DNA markers that risk stratifies patients on a scale of

176 ocus on putative virulence genes and neutral DNA markers that were likely to be phylogenetically info

177 set of AFLP primers amplified 28 single-copy DNA markers that were useful for identifying overlapping

178 es to human obesity, we examined polymorphic DNA markers that, by virtue of syntenic relationships to

179 hich is expression profiled and genotyped at DNA markers throughout the genome, can reveal regulatory

180 A DNA marker tightly linked to flesh color colocalized on

181 DNA markers tightly linked to quantitative resistance lo

182 were identified and anchored to the nearest DNA marker to form 10,172 homeologous marker sets.

183 Here we use autosomal, paternal and maternal DNA markers to (1) test the hypothesis that Inuit dogs h

184 FLP (amplified fragment length polymorphism) DNA markers to analyze 78 B. anthracis isolates and six

185 knowledge, we used nuclear and mitochondrial DNA markers to assess genetic diversity, gene flow and t

186 s issue of Cell, Metzger et al. use forensic DNA markers to demonstrate that the leukemia cells have

187 We used live trapping, telemetry and DNA markers to determine social and fitness measures.

188 o this end, we used 1170 genome-wide nuclear DNA markers to examine phylogenetic relationships betwee

189 were allelotyped for 10 genes and 49 random DNA markers to identify the smallest region of overlap i

190 port the first application of microsatellite DNA markers to investigate population subdivision in Atl

191 we use microsatellite DNA and mitochondrial DNA markers to investigate the evolutionary mechanisms t

192 mponent, a genomewide search for linkages of DNA markers to percent body fat is ongoing in Pima India

193 for saturating a small targeted region with DNA markers, TRS should facilitate gene isolation from d

194 a gigas, using a total of 102 microsatellite DNA markers typed in 11-day-old larvae from three famili

195 Our data consists of 14 microsatellite DNA markers, typed from pooled DNA samples from [Formula

196 Using available regional DNA markers, we constructed a yeast artificial chromosom

197 taking advantage of a cluster of visible and DNA markers, we identified three D. mauritiana factors i

198 Using microsatellite DNA markers, we show here that chimerism in marmoset (Ca

199 plified fragment-length polymorphism nuclear DNA markers, we show that the introduced white sucker (C

200 etic stock identification from seven nuclear DNA markers, we showed that catches at the two sites in

201 Based on previous genetic mapping, DNA markers were developed that localized the genetic ba

202 A total of 17 DNA markers were genotyped from this region of chromosom

203 order detachment rate coefficients, kdet, of DNA markers were greater ( approximately 1 h(-1)) than k

204 order attachment rate coefficients (katt) of DNA markers were greater ( approximately 10 h(-1)) than

205 Twenty-one dominant PCR-based DNA markers were identified as linked to Ctv by bulked s

206 The DNA markers were introduced into the environment through

207 DNAm-age and mitochondrial DNA markers were measured from participant blood samples

208 Random amplified polymorphic DNA markers were scored from the haploid drone fathers o

209 The DNA markers were stable for 1 month in the environment.

210 Microsatellite DNA markers were studied in 656 families with two or mor

211 Twelve polymorphic DNA markers were tested to identify possible genetic alt

212 The microbial DNA markers were the three human-associated (BacH, HF183

213 DNA markers were used to follow the fate of the F and M

214 or a bivalve mollusc that use microsatellite DNA markers, which should enable them to be transferred

215 genome-wide scan included 403 microsatellite DNA markers with an average spacing of 9 cM.

216 A genomewide map of 310 microsatellite DNA markers with average spacing of 11 centimorgans was

217 ffers from previous studies based on various DNA markers, with respect to topology and inter-lineage

218 The AluVpA DNA marker within intron 5 of the interferon-alpha recep