ライフサイエンスコーパス: gene analysis

1 function undetected by traditional reporter gene analysis.

2 mic DNA and mRNA was performed for candidate gene analysis.

3 ated transcription as determined by reporter gene analysis.

4 Precollected blood was used for gene analysis.

5 ions for whole genome scanning and candidate gene analysis.

6 aemoproteins was investigated using reporter gene analysis.

7 ing metagenomic and differentially expressed gene analysis.

8 ies have broad application in DNA chip-based gene analysis.

9 -Proteobacteria on the basis of the 16S rRNA gene analysis.

10 were investigated with linkage and candidate gene analysis.

11 sequence that we have identified by reporter gene analysis.

12 posal of the Fugu genome as a tool for human gene analysis.

13 ic defect was detected by means of candidate gene analysis.

14 ve genome sequencing accompanied by targeted gene analysis.

15 ures were the results of ocular biometry and gene analysis.

16 via Ingenuity Pathway Analysis (IPA) and hub gene analysis.

17 ed to support clinical studies beyond single gene analysis.

18 ences that cannot be discerned by individual gene analysis.

19 ia a genome-wide linkage study and candidate gene analysis.

20 dressing problems associated with individual gene analysis.

21 robust than the results based on individual gene analysis.

22 as determined by 5' UTR and E1 (envelope 1) gene analysis.

23 results of neutrophil studies and candidate gene analysis.

24 ample of all-gene-analysis instead of single gene analysis.

25 Through complementation and reporter gene analysis, a region of INO 5'-flanking sequences was

26 In candidate-gene analysis, a SNP (rs4852279) located near the CYP26B

27 Based on a combination of enzymology and gene-analysis, a new degradative pathway for caffeine ha

28 An in silico candidate gene analysis and bioinformatics review led us to identi

29 whole-genome homozygosity mapping, candidate-gene analysis and deep sequencing, we have identified lo

30 als, and will become a valuable resource for gene analysis and discovery.

31 Reporter gene analysis and electrophoretic mobility shift assays

32 Reporter gene analysis and EMSA demonstrated that hTLR9 gene tran

33 d the Pr gene via a combination of candidate gene analysis and fine mapping.

34 Candidate gene analysis and genome scans have been employed to ide

35 lysis was conducted in PLINK using candidate-gene analysis and genome-wide analysis.

36 nd direct sequencing were used for candidate gene analysis and mutation scanning.

37 from SLE patients were explored by reporter gene analysis and real-time RT-PCR, respectively.

38 Immediate early gene analysis and single unit recordings from VMHvl duri

39 Marker gene analysis and staining for hemoglobin revealed that

40 Reporter gene analysis and use of SRDX fusions suggested that TCP

41 ic variables, mRNA expression values, single-gene analysis, and gene set enrichment analysis (GSEA).

42 Using a candidate gene analysis approach, we also identified single-nucleo

43 In a single-gene-analysis approach, estimating the variability of ea

44 rge-scale genome-wide approach and candidate gene analysis are needed.

45 ostic accuracy of multiple immune activation gene analysis as means to diagnose renal allograft rejec

46 plications have implications for mapping and gene analysis as well as the predisposition to recurrent

47 comparisons between our approach and single-gene-analysis based methods.

48 Target gene analysis by Affymetrix expression profiling shows t

49 Genome-wide target gene analysis by ChIP-seq confirmed the binding of SOC1

50 combined homozygosity mapping with candidate gene analysis by performing 'ciliopathy candidate exome

51 These cases indicate that VH gene analysis can be used to probe tumor cell behavior i

52 e 6 (AAV6) transduction, we used comparative gene analysis (CGA) combined with pathway visualization

53 human airway epithelial cells using reporter genes analysis, chromatin immunoprecipitation, small int

54 tion, while a standard univariate individual gene analysis corrected for multiple testing as well as

55 Reporter gene analysis demonstrated that 2 kb of grik5 5'-flankin

56 16S ribosomal RNA gene analysis demonstrated that dusp6-deficient mice har

57 Reporter gene analysis demonstrated that this sequence, termed "a

58 paclitaxel, differential display and single gene analysis demonstrated that transcriptional activati

59 Reporter gene analysis demonstrates that these genes have distinc

60 In family ANA, candidate gene analysis excluded linkage to loci associated with a

61 licing, which was confirmed by an individual gene analysis explaining how AGO1 controls inclusion lev

62 Notably, where single-gene analysis finds little similarity between two indepe

63 ible applications include multiple-candidate gene analysis, genomewide scans, and medical diagnostics

64 tants, structural modeling, and multispecies gene analysis have now been employed to identify a resid

65 pproaches using genetic linkage or candidate gene analysis have often been limited, costly, and slow

66 Oligogenic Linkage Analysis Routines -Major Gene Analysis) have similar type 1 and type 2 errors and

67 Reporter gene analysis identified a 5'-flanking region containing

68 atin immunoprecipitation assays and reporter gene analysis identified a functional xenobiotic respons

69 Future applications range from gene analysis in basic research to medicine, for example

70 Reporter gene analysis in COS-7 cells expressing both p65-p50 and

71 rmore, data obtained by Hoxc13/lacZ reporter gene analysis in mice that overexpress Hoxc13 suggest ne

72 a basis for positional cloning and candidate gene analysis in order to identify a gene that may be in

73 ndicating the value of reverse transcriptase gene analysis in phylogenetic and biodiversity studies.

74 Based on reporter gene analysis in roots, His1-3 is expressed almost exclu

75 We have successfully used direct gene analysis in the prenatal diagnosis of Batten's dise

76 We report on the use of direct gene analysis in the prenatal diagnosis of this disease.

77 se-depleted conditions, and in vivo reporter gene analysis indicated reduced expression of these gene

78 Global gene analysis indicated that a 2-fold increase in TGFbet

79 Functional gene analysis indicated that genes involved in developme

80 The gene analysis indicated that more than 150 genes were si

81 Reporter gene analysis indicates that 335 bp of upstream CTLA4 se

82 sed genes based on rank is an example of all-gene-analysis instead of single gene analysis.

83 T cell receptor gene analysis is a sensitive method for assessment of pe

84 Because single gene analysis is not feasible in MLS patients (all have

85 Here, we present a haplotype-mining gene-gene analysis method, which considers multi-locus data f

86 ratometry, corneal pachymetry, and candidate gene analysis (MFRP, PRSS56).

87 are also provided by this first system-wide gene analysis of a microbial community specialized towar

88 An assay based on 16S and 23S rRNA gene analysis of B. cepacia ATCC 25416 (genomovar I) was

89 Fine mapping followed by candidate gene analysis of erd - a canine hereditary retinal degen

90 l for full-length Mycobacterium tuberculosis gene analysis of first- and second-line drug resistance

91 Candidate gene analysis of GPR179 in DNA extracted from patients w

92 has the potential to be useful in candidate gene analysis of inherited diseases, the human gene for

93 were examined using immunohistochemistry and gene analysis of laser capture microdissected retina.

94 miR-192/-194 in vivo we combined Affymetrix gene analysis of liver in which miR-192/-194 had been si

95 two members of the index family and targeted gene analysis of other members of this family and of six

96 cyte cell line Mono Mac 6, based on reporter gene analysis of point mutations at a number of nuclear

97 Reporter gene analysis of the human SDH2 promoter indicates that

98 Polymerase chain reaction plus gene analysis of the microsporidian 16S ribosomal RNA ha

99 Reporter gene analysis of this region in endothelial cells demons

100 Reporter gene analysis of two regions of the human factor VII (FV

101 which is located 800 bp upstream of the MBD1 gene, analysis of the murine CGBP gene locus failed to d

102 mmon variation are described for a candidate gene, analysis of the tagSNP set can comprehensively int

103 Despite the existence of this new DSP gene, analysis of VDJ rearrangements from adult bone mar

104 transcription-PCR of cell wall biosynthetic genes, analysis of hydrolytic activities, transmission e

105 llular level, and indeed all brain-expressed genes, analysis of protein distribution (at synapses and

106 Interrogation of Nkx2-1-regulated genes, analysis of tumours at defined developmental stag

107 nic species were detected either by 16S rRNA gene analysis or by MALDI-TOF MS except for the opportun

108 2 diabetes have been identified by candidate gene analysis or positional cloning.

109 may obtain from a univariate (i.e., gene by gene) analysis package making it extremely easy to use f

110 s fall into the category of so called single-gene-analysis, performing hypothesis testing on a gene-b

111 Marker gene analysis placed Gcm2 downstream of the known transc

112 combination of genetic mapping and candidate gene analysis presents Cdkn2c, a gene encoding for cycli

113 confirming the diagnosis of PDS and ALDH7A1 gene analysis provides a means for prenatal diagnosis.

114 Gene analysis revealed a cytosine to thymidine transitio

115 Gene analysis revealed that overall expression of mRNAs

116 The VP4 gene analysis revealed that P[7] strains were closely re

117 In vitro DNA binding and in vivo reporter gene analysis revealed that siderophores are not co-repr

118 Reporter gene analysis revealed that these genes are expressed in

119 ed by secreted alkaline phosphatase reporter gene analysis revealed that transcription is supported b

120 Candidate gene analysis reveals downregulation of Dkk1 in the digi

121 es, which has been revolutionary for protein gene analysis, should also be able to address questions

122 AGP31 promoter-beta-glucuronidase reporter gene analysis showed expression in the vascular bundle t

123 18S rRNA gene analysis showed pico-prymnesiophytes belonged to br

124 Ig gene analysis showed that 7 of 13 HmAbs used the V(H)3 a

125 Reporter gene analysis showed that a 633-bp promoter fragment of

126 Prion protein gene analysis showed that all cases were homozygous for

127 Reporter gene analysis showed that RORgamma was able to induce re

128 Reporter gene analysis showed that the activation of Cyp7b1 gene

129 Moreover, reporter gene analysis shows that a transcriptional regulatory mo

130 Comparative gene analysis shows that amniote egg proteins have evolv

131 in(ogen) have been elucidated by protein and gene analysis, site-directed mutagenesis, and x-ray crys

132 le for many years and is a component of most gene analysis software packages, including the Staden Pa

133 Based on gene-by-gene analysis, some accessory genes were more prevalent

134 Reporter gene analysis suggests that Nap, Ets, Rce, and Sp1 sites

135 oyed multiple methods including differential gene analysis, suppression subtractive hybridization, an

136 ts with two mutations, indicating that other gene analysis techniques should be used before excluding

137 However, in a gene-by-gene analysis, the animal-to-animal variance is smaller

138 We present a new WWW-based tool for plant gene analysis, the Arabidopsis Co-Expression Tool (ACT),

139 By reporter gene analysis, this selectivity is also functionally pre

140 or select candidate target genes by reporter gene analysis, though many of the target genes are expre

141 es, an observation that was traced by fusion gene analysis to a mutation of the TATA box motif in the

142 We utilized reporter gene analysis to demonstrate that the MIP-MOD promoter i

143 ter characterize these cells, we used global gene analysis to determine gene expression patterns amon

144 proaches of positional cloning and candidate gene analysis to great effect, with the pivotal role of

145 GP) pseudotyped virions, we used comparative gene analysis to identify genes whose expression correla

146 We carried out a transgenic reporter gene analysis to identify region- and cell type-specific

147 multiple separate databases for variant and gene analysis, users can obtain important information by

148 Promoter deletion and luciferase reporter gene analysis using cardiac and skeletal muscle cell lin

149 ic epithelium, we performed in vivo reporter gene analysis using heterozygous Pdx1(lacZ/+) and bigeni

150 We performed a candidate gene analysis using immune, cystic fibrosis transmembran

151 Blood sampling for gene analysis was performed after informed consent was o

152 Gene analysis was performed on microdissected tissue sam

153 the role of EMP2 in the etiology of disease, gene analysis was performed to show transcripts that are

154 mozygosity mapping with subsequent candidate gene analysis was performed.

155 Finally, a novel paired gene analysis was shown to distinguish gastrointestinal

156 Immunoglobulin gene analysis was unique and demonstrated a clonal bias;

157 Using microarray gene analysis, we found that carboxyl-terminal Src kinas

158 By gene analysis, we have demonstrated that this protein be

159 een mapped to 5p13.1-q11.2, and by candidate gene analysis, we identified missense mutations in the O

160 al profiling, bioinformatics, and functional gene analysis, we identify a new axis of mosquito resist

161 ng the nucleus as the substrate for parallel gene analysis, we provide a platform for the fusion of g

162 By marker gene analysis, we show that the expression of the alpha-

163 Using differential gene analysis, we traced the unique apoptotic effect of

164 ts of cellular fatty acid (CFA) and 16S rRNA gene analysis were combined with biochemical data to ass

165 Microscopy and in situ reporter gene analysis were used to directly observe changes in b

166 ological analyses, is commonly based on gp60 gene analysis, which appears to require bespoke species-

167 nce (RNAi) is a powerful tool for functional gene analysis, which has been successfully used to down-

168 ain negative), confirmed by antigen receptor gene analysis, which showed germ line configuration.

169 These tools allow a replacement of single-gene analysis with a highly efficient whole-genome analy

170 Parallel gene analysis with microarrays provides a rapid and effi

171 tal to LTA in Jurkat cells based on reporter gene analysis, with evidence of recruitment of upstream

172 The gene analysis yielded a major revision to the yeast gene