ライフサイエンスコーパス: gene analysis

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

2 ated transcription as determined by reporter gene analysis.

3 Precollected blood was used for gene analysis.

4 ions for whole genome scanning and candidate gene analysis.

5 aemoproteins was investigated using reporter gene analysis.

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

7 function undetected by traditional reporter gene analysis.

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

9 were investigated with linkage and candidate gene analysis.

10 sequence that we have identified by reporter gene analysis.

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

12 consented for germline cancer predisposition gene analysis.

13 nt of tissue origin that is seen with coding gene analysis.

14 tes with built-in tools to enhance essential-gene analysis.

15 ron microscopy (TEM), Raman spectroscopy and gene analysis.

16 poxia response element binding, and reporter gene analysis.

17 ng on the patient and his parents for causal gene analysis.

18 ing metagenomic and differentially expressed gene analysis.

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

20 ve genome sequencing accompanied by targeted gene analysis.

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

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

23 ed to support clinical studies beyond single gene analysis.

24 ences that cannot be discerned by individual gene analysis.

25 umably by ANME-2a/b as indicated by 16S rRNA gene analysis.

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

27 dressing problems associated with individual gene analysis.

28 robust than the results based on individual gene analysis.

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

30 results of neutrophil studies and candidate gene analysis.

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

32 Search Tool for the Retrieval of Interacting Genes analysis.

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

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

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

36 integration method designed for atlas-scale gene analysis across cell types and tissues.

37 Moreover, comparative gene analysis allowed us to discover brittle star-specif

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

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

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

41 Reporter gene analysis and electrophoretic mobility shift assays

42 Reporter gene analysis and EMSA demonstrated that hTLR9 gene tran

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

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

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

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

47 Furthermore, reporter gene analysis and proliferation assays supported a criti

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

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

50 Marker gene analysis and staining for hemoglobin revealed that

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

52 performed single-cell RNA sequencing, marker gene analysis, and functional studies to examine how YAP

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

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

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

56 agnetic resonance imaging, histological, and gene analysis approaches in living and nonliving human f

57 quencing-based techniques for immunoglobulin gene analysis are labor-intensive and rely on attaining

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

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

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

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

62 Target gene analysis by Affymetrix expression profiling shows t

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

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

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

66 r dissimilarity and differentially expressed gene analysis categorized those clusters into three grou

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

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

69 daSNV target gene analysis, combined with daSNV editing, underscored

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

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

72 16S ribosomal RNA gene analysis demonstrated that dusp6-deficient mice har

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

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

75 Reporter gene analysis demonstrates that these genes have distinc

76 From candidate gene analysis, DNAm levels at the 6 CpGs at age 2 were a

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

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

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

80 of plasma proteins, coagulation studies, and gene analysis for changes in immune and metabolic profil

81 ell clustering, immune phenotyping, and risk gene analysis for children with undifferentiated colitis

82 Candidate gene analysis for the resistance locus on chromosome 5 i

83 e-fractionated manipulation experiments with gene analysis further reveal niche partitioning of ammon

84 In a candidate gene analysis, GBA variants were also identified to be a

85 iologist to perform differentially expressed gene analysis, gene ontology and pathway enrichment anal

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

87 High-throughput phylogenetic 16S rRNA gene analysis has permitted to thoroughly delve into mic

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

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

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

91 In single-gene analysis, high-sensitivity CRP levels were signific

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

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

94 However, de novo significantly mutated gene analysis identified genes not previously reported i

95 Immediate early gene analysis identified T-types exhibiting preferential

96 Target gene analysis implicated FOXO and RUNX1 regulation, soma

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

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

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

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

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

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

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

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

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

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

107 Gene analysis indicated that both hormones decreased PLI

108 Functional gene analysis indicated that both membrane damage and in

109 Marker gene analysis indicated that both sets of cells differen

110 Functional gene analysis indicated that genes involved in developme

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

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

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

114 on, gene fold change, and spatially variable gene analysis, introducing false positive and false nega

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

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

117 Protein or gene analysis may indicate molecular phenotypes within t

118 SCLC DDR phenotypes, we developed a new DDR gene analysis method and applied it to SCLC clinical sam

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

120 Conventional gene analysis methods lack the spatiotemporal resolution

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

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

123 emained unchanged for decades and functional gene analysis of Agrobacterium has been hampered by time

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

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

126 RNA sequencing and gene analysis of extracted RNA from treated cancer cells

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

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

129 ping of Hnf4a binding sites and differential gene analysis of Hnf4a mutant kidneys identified direct

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

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

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

133 nd breastfeeding outcomes, and run candidate-gene analysis of methylation sites associated with BMI i

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

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

136 sent a genomic, transcriptomic and metabolic gene analysis of six of the most widely used HEK293 cell

137 Reporter gene analysis of the human SDH2 promoter indicates that

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

139 ion myocardial infarction (STEMI), a gene-by-gene analysis of the platelet gene expression identified

140 Reporter gene analysis of this region in endothelial cells demons

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

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

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

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

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

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

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

148 Candidate gene analysis on MMTV-Cre;Vangl2(flox/flox) and Vangl2(L

149 a mutational signature and candidate driver gene analysis on these lesions.

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

151 2 diabetes have been identified by candidate gene analysis or positional cloning.

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

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

154 Marker gene analysis placed Gcm2 downstream of the known transc

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

156 t mass spectrometry [MALDI-TOF MS], 16S rRNA gene analysis) proved challenging to confidently disting

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

158 Immunoglobulin gene analysis provides fundamental insight into B cell r

159 Gene analysis revealed a cytosine to thymidine transitio

160 Secretome gene analysis revealed a highly connected network of int

161 Targeted gene analysis revealed increased expression in PI3K whic

162 Culture-independent 16S rRNA gene analysis revealed that both bacteria and archaea we

163 Gene analysis revealed that expression of integrin a(3)

164 Gene analysis revealed that overall expression of mRNAs

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

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

167 16S rRNA gene analysis revealed that the population of Bifidobact

168 Reporter gene analysis revealed that these genes are expressed in

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

170 Candidate gene analysis reveals downregulation of Dkk1 in the digi

171 ssment or violence as part of the Stress and Gene Analysis (SAGA) study, a cross-sectional nationally

172 sectional study were women in the Stress-And-Gene-Analysis (SAGA) cohort who answered the question re

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

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

175 18S rRNA gene analysis showed pico-prymnesiophytes belonged to br

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

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

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

179 Multivariate gene analysis showed that ameloblastoma cells downregula

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

181 Reporter gene analysis showed that the activation of Cyp7b1 gene

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

183 Comparative gene analysis shows that amniote egg proteins have evolv

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

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

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

187 erns and providing interpretable subcellular gene analysis, such as defining the gene importance scor

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

189 Comparative gene analysis supported the ancestral pairings of CSF1R/

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

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

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

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

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

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

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

197 nd an accessible online database for gene-by-gene analysis to aid in correct cell identification and

198 tool samples were subjected to both 16S rRNA gene analysis to assess beta-diversity and untargeted me

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

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

201 herapeutic strategies based on single driver gene analysis to discovery based on interactions between

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

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

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

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

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

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

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

209 ssess optimal sample processing for 16S rRNA gene analysis using paired-end Illumina MiSeq technology

210 l concentration required to perform 16S rRNA gene analysis using three different DNA extraction proto

211 Functional gene analysis was indicative of a response of the microb

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

213 Gene analysis was performed on microdissected tissue sam

214 Furthermore, over-representation gene analysis was performed to identify pathways that we

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

216 mozygosity mapping with subsequent candidate gene analysis was performed.

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

218 Faecal 16S ribosomal RNA gene analysis was undertaken.

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

220 Tumor gene analysis was used in 21 of 64 patients (33%), and c

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

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

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

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

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

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

227 To demonstrate BOLORAMIS for multiplexed gene analysis, we targeted 96 mRNAs within a co-culture

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

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

230 Feature reduction and functional gene analysis were used to compare proteomic and transcr

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

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

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

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

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

236 Parallel gene analysis with microarrays provides a rapid and effi

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

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