ライフサイエンスコーパス: SAGE

1 and sequential analysis of gene expression (SAGE).

2 iling by serial analysis of gene expression (SAGE).

3 milar to serial analysis of gene expression (SAGE).

4 es using serial analysis of gene expression (SAGE).

5 er using serial analysis of gene expression (SAGE).

6 's Survey of Global Ageing and Adult Health (SAGE).

7 with microarray and the future potential of SAGE.

8 oprecipitation (ChIP) with a modification of SAGE.

9 e facilitated by the enhanced method of Long SAGE.

10 .05 in the large CHS study, but not in CAPPS/SAGE.

11 ociation of C15orf53 with SC was observed in SAGE.

12 lareol, a diterpene-diol isolated from Clary sage.

13 rior transcriptome studies by microarray and SAGE.

14 egano+sage; oregano+sage+5%honey and oregano+sage+10%honey.

15 ration were oregano+sage+5%honey and oregano+sage+10%honey.

16 ib-sib correlations were calculated with the SAGE 5.0 program FCOR, to estimate heritability of retin

17 ylated hydroxytoluene; oregano+sage; oregano+sage+5%honey and oregano+sage+10%honey.

18 lues after 96h of refrigeration were oregano+sage+5%honey and oregano+sage+10%honey.

19 tolerability of brexanolone (USAN; formerly SAGE-547 Injection), a proprietary, aqueous formulation

20 udy investigated brexanolone (USAN; formerly SAGE-547 injection), an intravenous formulation of allop

21 SAGE 7.0 software was used for the analysis of data obta

22 Here, we characterize Sage, a bHLH transcription factor expressed exclusively

23 In this study, we have identified sage, a salivary-specific bHLH protein as a new heterodi

24 heather (Mg, Na), bearberry (Ba, Fe, Pb) and sage (Ag) honeys.

25 h and U), common heather (Co, K, Mg, Na, V), sage (Ag, Cd, Cu), and bearberry (Ba, Fe, Pb, Sb, Zn).

26 ding to 26,502 transcripts were sequenced in SAGE analyses.

27 SAGE analysis comparing normal to Fuchs' endothelium dem

28 lts show the power of combined array CGH and SAGE analysis for the identification of candidate amplic

29 SAGE analysis indicates that genes that are on the same

30 By SAGE analysis, the genes expressed by EPC are more simil

31 ancies that could have been resolved by long SAGE and 10-20% of the short SAGE tags had no obvious ma

32 Although SAGE and Affymetrix chip expression levels showed a sign

33 Here we apply a combination of SAGE and chromatin immunoprecipitation (ChIP) protocols

34 qualitative expression signals obtained from SAGE and EST data with those from GeneChip arrays showed

35 We show that both Sage and Fkh are required for the expression of Sage tar

36 already established in other cell types, and Sage and Fkh cannot alter the fate of most embryonic cel

37 Sage and Fkh drive expression of the bZip transcription

38 Sage target genes, and that co-expression of Sage and Fkh is sufficient to drive target gene expressi

39 However, most of the reports on SAGE and germ cell development are limited to descriptiv

40 ata sets obtained by different technologies (SAGE and high-density oligonucleotide chip arrays) and c

41 differentially regulated genes identified by SAGE and interrogated ADPKD patient samples.

42 eristic of sequencing-based methods, such as SAGE and Long SAGE is the unavoidable occurrence of arti

43 small insert sizes associated with existing SAGE and LongSAGE protocols.

44 atabase by the same tissue type used by both SAGE and microarray analysis; then the multiple UniGene

45 ained by integrating expressed sequence tag, SAGE and microarray datasets.

46 including gene expression analysis from EST, SAGE and microarray projects and proteomics studies.

47 t impressions in the graves include stems of sage and other Lamiaceae (Labiatae; mint family) or Scro

48 echanisms responsible for these abilities of sage and thyme have not been fully understood yet.

49 such as serial analysis of gene expression (SAGE) and mass spectrometry proteomic technology.

50 we used serial analysis of gene expression (SAGE) and microarray analysis to compare the gene expres

51 We used serial analysis of gene expression (SAGE) and microarray analysis to identify changes in gen

52 rs since serial analysis of gene expression (SAGE) and microarray hybridization techniques were simul

53 e Study of Addiction: Genes and Environment (SAGE) and the Australian Twin Family Study of AUDs (OZAL

54 tudy of Addiction: Genetics and Environment (SAGE) and the Collaborative Study on the Genetics of Alc

55 tudy of Addiction: Genetics and Environment (SAGE), and 2644 cases and 494 controls from our own stud

56 h, using serial analysis of gene expression (SAGE), and compared the profiles on-line with other glan

57 n (MACS), Dutch (PIAMA), Canadian (CAPPS and SAGE), and German (GINIplus and LISAplus) birth cohorts

58 tudy of Addiction: Genetics and Environment [SAGE], and International Consortium on the Genetics of H

59 est the idea, we developed a tissue-specific SAGE annotation database based on microarray data ().

60 These latter SAGE applications are facilitated by the enhanced method

61 STs) and serial analysis of gene expression (SAGE), are also included.

62 and NGS-based classification is compared to SAGE-based classification and classification directly on

63 reads, NGS-based classification outperforms SAGE-based classification.

64 ples (COGA: best P = 1.7 x 10-6, R2 = 0.026; SAGE: best P = .001, R2 = 0.01; Yale-Penn: best P = .035

65 from Escherichia coli, Artemisia tridentata (sage brush), Pyrococcus furiosus, and Methanobacter ther

66 ce of the recommended schedule of IPV by the SAGE, but the evidence was largely from developed countr

67 We demonstrate over simulated data that SAGE can be used to infer correct haplotypes of the high

68 rts, CHS (Children's Health Study) and CAPPS/SAGE (Canadian Asthma Primary Prevention Study/Study of

69 siteFiNDER|3D can be accessed at: 'http://sage.csb.yale.edu/sitefinder3d' and requires, at a minim

70 pithelium were in general agreement with the SAGE data and showed that these proteins are also expres

71 rably more information can be extracted from SAGE data by carrying out a systematic analysis of both

72 The SAGE data could also be well fit by a Monte Carlo model

73 the PN9 and mature mouse cornea, the present SAGE data demonstrate dynamic changes in gene expression

74 r study highlights the benefits of exploring SAGE data for comprehensive identification of human anti

75 inal transcripts, the quantitative nature of SAGE data for differentially expressed genes, the reprod

76 Vast amounts of SAGE data have been collected and more than a thousand S

77 informatic analyses using recently published SAGE data on the transcriptome of mouse type A spermatog

78 RA2 rs279858 association was observed in the SAGE data sets with a combined P of 9 x 10(-6) (OR=1.17

79 This detailed analysis of the SAGE data shows first that while there is evidence of al

80 However, analysis of our SAGE data shows that antisense transcripts are probably

81 ures should aid the proper interpretation of SAGE data to address biological and medical questions.

82 , we use a computational biology analysis of SAGE data to assess the abundance and distribution of se

83 is review focuses on the general features of SAGE data, including the specificity of SAGE tags with r

84 hen comparing mouse with human breast cancer SAGE data.

85 ne genes which are consistent with available SAGE data.

86 sing the serial analysis of gene expression (SAGE) data in all 130 deduced BTB/POZ genes.

87 CGH and serial analysis of gene expression (SAGE) data to correlate copy number and expression level

88 sing our serial analysis of gene expression (SAGE) data, as well as public SAGE databases that contai

89 g public Serial Analysis of Gene Expression (SAGE) data, we found that the intronic poly(A) site is u

90 retinal serial analysis of gene expression (SAGE) data.

91 tudy of Addiction: Genetics and Environment (SAGE) data.

92 GE is the first publicly available web-based SAGE database on male gonad development that covers six

93 ion patterns of five genes selected from the SAGE database.

94 ne expression (SAGE) data, as well as public SAGE databases that contained a total of 137 SAGE librar

95 EST) and serial analysis of gene expression (SAGE) databases was enzyme quiescin Q6 sulfhydryl oxidas

96 tudy of Addiction: Genetics and Environment (SAGE) dataset, we tested for association of CHRNB3-A6 SN

97 Overall, the incorporation of sage decoction in the daily diet or its use as a complem

98 Serial analysis of gene expression (SAGE) demonstrated that more than 90% of those host gene

99 tudy of Addiction: Genetics and Environment (SAGE) demonstrates that applying the multivariate associ

100 The Study Assessing Goals in the Elderly (SAGE) demonstrates that older men and women with coronar

101 SAGE-derived endothelial cell gene expression patterns f

102 lso confirmed the differential expression of SAGE-discovered genes within the initial set of five cel

103 y use of serial analysis of gene expression (SAGE) do not match these genes.

104 nscientious prothrombin time monitoring, and sage dosage adjustment remain paramount in warfarin mana

105 eing a remote detection technique, the Hyper-SAGE effect is further enhanced in situations where the

106 according to ISO 9909 and GDC standards for sage EO quality, revealing compliance for only 10 popula

107 e (HS) sampling in the quality assessment of sage EO.

108 for rapid screening in quality assessment of sage EOs.

109 rable benefits, also being an alternative to sage essential oils that can display some toxic effects.

110 rimental methods such as tiling arrays or 5' SAGE/EST sequencing have recently lead to much larger da

111 is issue of Immunity, Wing et al. (2014) and Sage et al. (2014) demonstrate that CTLA-4 is a critical

112 STAGE is conceptually based on SAGE, except that the input is ChIP-enriched DNA.

113 This constrains the design of SAGE experiments intended to determine biological comple

114 nt genes within collections of microarray or SAGE experiments.

115 tag based expression (EBE) experiments and 5 SAGE experiments.

116 QSOX1 mRNA levels, based on SAGE expression data, did not correlate with either Estr

117 encapsulates stabilised with gum arabic and sage extract (SOE) exhibited significantly higher encaps

118 l polymer, gum arabic as wall co-polymer and sage extract as wall stabiliser was spray dried using a

119 The encapsulates containing sage extract showed a lower rate of lipid oxidation duri

120 Rosemary and sage extracts represented promising technological option

121 activated in breast cancer that traditional SAGE failed to call.

122 lial aggregation analysis was performed, and SAGE FCOR was used to quantify the total genetic contrib

123 h boosts expression of Sage-Fkh targets, and Sage, Fkh and Sens colocalize on SG chromosomes.

124 Importantly, expression of Sage-Fkh target genes appears to simply add to the tissu

125 Senseless (Sens), which boosts expression of Sage-Fkh targets, and Sage, Fkh and Sens colocalize on S

126 The botanical origin of lumichrome from sage flower was assessed by analysing bee-stomach extrac

127 ation of serial analysis of gene expression (SAGE) for this purpose.

128 Raw data were analyzed using SAGE (GE) software.

129 Raw data was preprocessed using SAGE (GE) software.

130 lp offset the adverse effects of wildfire on sage-grouse and other wildlife populations.

131 ng effects from wildfire nullified pulses of sage-grouse population growth that typically follow year

132 ldfire has contributed strongly to declining sage-grouse populations over the past 30 y at large spat

133 ontinue unabated, model projections indicate sage-grouse populations will be reduced to 43% of their

134 ffective population sizes for two polygynous sage-grouse species and compared them to estimates from

135 of a sagebrush-obligate species, the greater sage-grouse, across the Great Basin of western North Ame

136 The principle of SAGE has been developed to address specific issues such

137 Since its invention, SAGE has been widely applied to analyzing gene expressio

138 c Advisory Group of Experts on Immunization (SAGE) has recommended introduction of at least 1 dose of

139 diastase activity were studied in Dalmatian sage honey.

140 ified by serial analysis of gene expression (SAGE); however, its function in epithelial ion transport

141 Americans, Asthma, Genes, and Environments (SAGE II).

142 nalysis, serial analysis of gene expression (SAGE), immunohistochemistry, transcript sequencing, and

143 ignal amplification by gas extraction (Hyper-SAGE) in both NMR spectra and magnetic resonance images

144 dded multiple large-scale datasets including SAGE, interactome, 3D protein structure datasets and NCB

145 nder two different conditions suggested that SAGE is a reliable and reproducible technique for use in

146 SAGE is a technique that allows the rapid, quantitative

147 os have a phenotype similar to sens and that sage is necessary to maintain expression of sens in the

148 We show that Sage is required for late SG survival and normal tube mo

149 uencing-based methods, such as SAGE and Long SAGE is the unavoidable occurrence of artifact sequences

150 Serial analysis of gene expression (SAGE) is a method for identifying and quantifying transc

151 Serial analysis of gene expression (SAGE) is a method used to obtain comprehensive, unbiased

152 Serial Analysis of Gene Expression (SAGE) is a powerful technology for measuring global gene

153 Serial Analysis of Gene Expression (SAGE) is a powerful tool for genome-wide transcription s

154 Serial analysis of gene expression (SAGE) is a widely used technique for large-scale transcr

155 Salvia divinorum commonly known as diviner's sage, is an ethnomedicinal plant of the mint family (Lam

156 gulate expression of PH4alphaSG2, as well as sage itself, and to indirectly regulate expression of PH

157 ation (LAAPPI) and LDTD-APPI mass spectra of sage leaves (Salvia officinalis) using a field-deployabl

158 analysis of polar and nonpolar compounds in sage leaves and chili pepper.

159 an Gastrointestinal and Endoscopic Surgeons (SAGES) led to the promulgation of a formalised countrywi

160 compared with 25 of our human breast cancer SAGE libraries (>2.5 million human breast-specific tags)

161 We apply SAGEScreen to Long SAGE libraries and compare error rates for several proce

162 g the authors' multidonor-derived retina/RPE SAGE libraries and existing single-donor retina/RPE libr

163 he rat limbal and central corneal epithelial SAGE libraries consisted of 41,894 and 40,691 tags, resp

164 esent study, the comprehensive annotation of SAGE libraries derived from an asexual stage population

165 In this study, we generated three SAGE libraries from melanoma tissues.

166 two retinal pigment epithelium (RPE)/choroid SAGE libraries made from matched macula or midperipheral

167 ze of a transcriptome is ill-determined from SAGE libraries of even moderately large size.

168 SAGE databases that contained a total of 137 SAGE libraries representing a wide variety of normal and

169 SAGE libraries representing control and TNT-exposed seed

170 genes most highly expressed in our melanoma SAGE libraries was a calcium-regulated gene, calpain 3 (

171 Tags with a total count of > or =20 in three SAGE libraries were examined.

172 levels of gene expression between groups of SAGE libraries, the libraries within each group are ofte

173 a and publicly available normal human tissue SAGE libraries.

174 enerated serial analysis of gene expression (SAGE) libraries from two distinct populations of single,

175 Serial analysis of gene expression (SAGE) libraries generated from the tumor cell lines were

176 et of 11 serial analysis of gene expression (SAGE) libraries was analyzed using a combination of supe

177 Serial analysis of gene expression (SAGE) libraries were constructed and analyzed, and in si

178 s agent, serial analysis of gene expression (SAGE) libraries were generated for three sensitive and t

179 uencing and sampling errors was applied to a SAGE library (137 832 tags) obtained from mouse embryoni

180 rently altered cancer expression in the CGAP SAGE library collection-often in keeping with predicted

181 ditis elegans using a public tissue-specific SAGE library data set.

182 The sequence coverage of each SAGE library is beyond 150K, 'which is the most extensiv

183 elopment, with 150,000 sequence tags in each SAGE library.

184 ompared with previously published normal EOM SAGE library.

185 e latest Serial Analysis of Gene Expression (SAGE) library data derived a complete list of 459 genes

186 Several SAGE-like methods have also been developed for the genom

187 The comparative analysis of mouse and human SAGE mammary cancer data validates this p53 null mouse t

188 ifloral, heather, common heather, bearberry, sage, mandarin orange-blossom and honeydew) collected in

189 John's Wort, sage, marjoram and thyme were assayed.

190 dually required for SLS production, and that sagE may further serve an immunity function.

191 ibutions indicate limitations in the EBE and SAGE methods at both high- and low-expression levels.

192 n of various biological data, including EST, SAGE, microarray and annotation data.

193 oupled with targeted xenon biosensors, Hyper-SAGE offers another path to highly sensitive molecular i

194 One limitation of using SAGE on an organism with a complex genome and lacking de

195 Comparison of SAGE-Seq and traditional SAGE on normal and cancerous breast tissues reveals high

196 erformed serial analysis of gene expression (SAGE) on CD15(+) myeloid progenitor cells from 22 AML pa

197 s (WHO) Strategic Advisory Group of Experts (SAGE) on Immunization recommended conducting this synchr

198 12, the Strategic Advisory Group of Experts (SAGE) on Immunization recommended universal IPV introduc

199 The effect of combinations of sage, oregano and honey on lipid oxidation in cooked chi

200 : control; butylated hydroxytoluene; oregano+sage; oregano+sage+5%honey and oregano+sage+10%honey.

201 The synergistic efficacy of gum arabic and sage polyphenols in stabilising capsule wall and protect

202 Sage Products, US National Institutes of Health.

203 y discovering a fusion transcript based on a SAGE profile and for the first time precisely describes

204 sed on a serial analysis of gene expression (SAGE) profile of the MYCN-amplified NB cell line IMR-5.

205 the clinical validation data demonstrate how SAGE profiles can highlight specific links between signa

206 Since the original SAGE protocol was developed in a short-tag (10-bp) forma

207 SAGE provided quantitative measurements of >20,000 trans

208 Serial analysis of gene expression (SAGE) provides a global analysis platform for profiling

209 Serial analysis of gene expression (SAGE) provides an alternative, with additional advantage

210 ta were organized with the use of NUD-IST 4 (Sage Publications Software) and were analyzed by the con

211 (WHO's) Strategic Advisory Group of Experts (SAGE) recommended that all 126 countries using only oral

212 sufficient evidence to determine whether the SAGE-recommended IPV schedule for the polio endgame woul

213 In 2013, SAGE reiterated the importance of attaining the long-ter

214 have been collected and more than a thousand SAGE-related studies have been published since the mid-1

215 rated by Serial Analysis of Gene Expression (SAGE) representing major stages in mouse male germ cell

216 Our SAGE results and the clinical validation data demonstrat

217 SAGE results converged with previous microarray analysis

218 The SAGE results extend the database of genes expressed in t

219 In addition, our data suggest that sage RNAi embryos have a phenotype similar to sens and t

220 unifloral honey types showed that Dalmatian sage (S. officinalis L.) honey is characterised by unusu

221 lementation, we show sagA, sagB, sagC, sagD, sagE, sagF and sagG are each individually required for S

222 , the active component of the hallucinogenic sage Salvia divinorum, is an apparently selective and hi

223 and methanol/water (80:20, v/v) extracts of sage (Salvia officinalis L.) were evaluated and characte

224 sessment of essential oil (EO) from culinary sage (Salvia officinalis L., Lamiaceae) is limited by th

225 a xpiperita), melissa (Melissa officinalis), sage (Salvia officinalis), nettle (Urtica dioica), linde

226 hin MARCH6 and ROPN1L were replicated in the SAGE sample (p<0.05).

227 A replication study was conducted using the SAGE sample with 762 individuals.

228 The resulting Java-based tool, called SAGE (Scoring function for Assembled GEnomes), is freely

229 Comparison of SAGE-Seq and traditional SAGE on normal and cancerous br

230 SAGE-Seq is a powerful method for the identification of

231 SAGE-Seq is able to identify genes and pathways abnormal

232 breast tissues reveals higher sensitivity of SAGE-Seq to detect less-abundant genes, including those

233 ication of ultra high-throughput sequencing, SAGE-Seq, for the accurate quantification of normal and

234 SAGE (Serial Analysis of Gene Expression) can be used to

235 SAGE (serial analysis of gene expression) detects transc

236 n craniofacial structures, we constructed 12 SAGE (serial analysis of gene expression) libraries and

237 were determined by sequencing the respective SAGE (Serial Analysis of Gene Expression) libraries.

238 In fact, we have previously utilized SAGE (serial analysis of gene expression) to identify ab

239 ethylation-specific digital karyotyping) and SAGE (serial analysis of gene expression).

240 rrelations were calculated using FCOR in the SAGE software package.

241 rn, honeydew, heather, lime, mint, rapeseed, sage, strawberry tree, sulla flower, savory and thistle)

242 In the Successful AGing Evaluation (SAGE) study, the authors used a structured multicohort d

243 UniGene clusters assigned to the nonspecific SAGE tag are searched in the database under the matched

244 ue in differential gene expression analysis, SAGE tag collections afford abundant information on the

245 However, to fully exploit the value of large SAGE tag datasets, it is desirable to account for and co

246 The nonspecific SAGE tag is first matched to the database by the same ti

247 By analysis of a highly expressed SAGE tag not matching a Unigene cluster we identified fo

248 s of gene expression (SAGE), we identified a SAGE tag that was present only in invasive breast carcin

249 The transcript corresponding to this SAGE tag, dermcidin (DCD), encodes a secreted protein no

250 Because of the limited length, many SAGE tags are shared by transcripts from different genes

251 Our study shows that most of the unmatched SAGE tags are truly novel SAGE tags that originated from

252 When the SAGE tags expressed within these cell line libraries wer

253 difications have been made to produce longer SAGE tags for more precise gene identification and to de

254 Examination of 71,930 Long SAGE tags generated from six libraries derived from two

255 novel procedures to characterise, in detail, SAGE tags generated from the whole grain transcriptome o

256 esolved by long SAGE and 10-20% of the short SAGE tags had no obvious match to currently annotated hu

257 omparing the use of 10-bp SAGE tags to 17-bp SAGE tags indicated that the short SAGE technology was m

258 Nine different SAGE tags matching mitochondrial sequences accounted for

259 e that can be used to identify the antisense SAGE tags originated from the antisense strand of known

260 uracy of gene annotation for the nonspecific SAGE tags should be significantly improved.

261 neoplastic tissues, we identified five novel SAGE tags specifically expressed in ovarian cancer.

262 t of the unmatched SAGE tags are truly novel SAGE tags that originated from novel transcripts not yet

263 titative analysis comparing the use of 10-bp SAGE tags to 17-bp SAGE tags indicated that the short SA

264 s of SAGE data, including the specificity of SAGE tags with respect to their original transcripts, th

265 iled analysis of transcriptome data, such as SAGE tags, is essential to understand fully the factors

266 From a total of 1,247,535 SAGE tags, we identified 2,604 transcripts whose express

267 anscripts, including the three most abundant SAGE tags, which did not correspond to any known genes o

268 n antisense ESTs and 3198 are mapped only by SAGE tags.

269 resent the specific gene for the nonspecific SAGE tags.

270 useful source for annotating the nonspecific SAGE tags.

271 STs, and serial analysis of gene expression (SAGE) tags, and performed an extensive annotation on thi

272 Hyper-SAGE takes advantage of a change in physical phase to in

273 e and Fkh are required for the expression of Sage target genes, and that co-expression of Sage and Fk

274 We find that many Sage targets, identified by microarray analysis, encode

275 sing the serial analysis of gene expression (SAGE) technique.

276 In this review, a summary of the advances in SAGE technology and its unique attributes and potential

277 to 17-bp SAGE tags indicated that the short SAGE technology was more efficient at identifying differ

278 Previous studies using SAGE (the Study of Addiction: Genetics and Environment)

279 udy of Addiction, Genetics, and Environment (SAGE); the Yale-Penn genetic study of substance dependen

280 ith the salivary gland-specific bHLH protein Sage to directly regulate expression of PH4alphaSG2, as

281 Here, we use 5' SAGE to map 5' TSS in S.cerevisiae.

282 nderlies serial analysis of gene expression (SAGE) to analyze mutations that result from DNA synthesi

283 we used serial analysis of gene expression (SAGE) to compare transcripts in wild-type and Pti4-expre

284 we used serial analysis of gene expression (SAGE) to identify genes expressed in two normal substant

285 From the training set of 21,321 unique SAGE transcript tags derived from 11 libraries, five gen

286 Data were collected for the SAGE trial from 1990 to 2007 and for the ICGHD from 2004

287 The combination of ChIP, RDA and SAGE-type methods has advantages over other similar stra

288 A comparison study of short SAGE versus GeneChip and long SAGE was conducted to dete

289 study of short SAGE versus GeneChip and long SAGE was conducted to determine if data were interchange

290 markers, serial analysis of gene expression (SAGE) was done on three samples from the same patient: n

291 Serial analysis of gene expression (SAGE) was performed on postnatal day (PN)9 and adult mou

292 Serial analysis of gene expression (SAGE) was performed to identify and quantify gene transc

293 Serial analysis of gene expression (SAGE) was used to determine alterations in the EOM trans

294 Serial analysis of gene expression (SAGE) was used to obtain gene expression profiles of nor

295 Using serial analysis of gene expression (SAGE), we identified a SAGE tag that was present only in

296 Effect estimates in CAPPS and SAGE were also conflicting but not significant (0.63 [0.

297 Different populations (30) of culinary sage were assessed using GC/FID/MS analysis of the hydro

298 s, the reproducibility, the comparability of SAGE with microarray and the future potential of SAGE.

299 The analysis of phenolic extracts of sage without parathion showed that irradiation decreased

300 of transcript abundance and determined that SAGE yielded quantitatively reliable data.