ライフサイエンスコーパス: DNA marker

1 e the most intensively researched epigenetic DNA marker.

2 pressed hazelnut oil based on microsatellite DNA markers.

3 celerated significantly the decay of all the DNA markers.

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

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

6 of an appropriately dense set of polymorphic DNA markers.

7 which contains 456 bacterial clones and 202 DNA markers.

8 y genetic map consisting of easily genotyped DNA markers.

9 enetic differentiation identified by nuclear DNA markers.

10 7 amplified fragment length polymorphisms as DNA markers.

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

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

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

14 be constructed guided by the transmission of DNA markers.

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

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

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

18 the estimation of genetic linkage maps from DNA markers.

19 reservative, which reduced detection of some DNA markers.

20 was done using 21 additional closely spaced DNA markers.

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

22 ting soybean composite genetic map using 388 DNA markers.

23 were mapped using polymorphic microsatellite DNA markers.

24 rmination of serotype in Salmonella based on DNA markers.

25 tomated linkage mapping of human polymorphic DNA markers.

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

27 33 allozyme loci, which were used as nuclear DNA markers.

28 man electroencephalogram in conjunction with DNA markers.

29 nostic chloroplast DNA and nuclear ribosomal DNA markers.

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

31 ly analyze agarose gel images of polymorphic DNA markers.

32 ting physical and sequence maps and numerous DNA markers.

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

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

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

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

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

38 Such DNA markers allow the identification of maize genomic DN

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 Although DNA markers are very powerful for distinguishing among i

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

61 1:1 for the presence or absence of dominant DNA markers, as would be expected if sister chromosomes

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

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

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

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

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

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

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

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

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

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

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

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

74 DNA markers described herein facilitate cloning of genes

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 1A, 1B, and 1D were generated by mapping 50 DNA markers on 56 single-break deletion lines.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 Nuclear DNA markers reflect a species tree consistent with expec

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

157 A DNA marker tightly linked to flesh color colocalized on

158 DNA markers tightly linked to quantitative resistance lo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

178 The DNA markers were introduced into the environment through

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

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

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

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

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

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

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

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

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

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

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