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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  the Sinai Abbreviated Geriatric Evaluation (SAGE).
7 's Survey of Global Ageing and Adult Health (SAGE).
8 ociation of C15orf53 with SC was observed in SAGE.
9 lareol, a diterpene-diol isolated from Clary sage.
10 rior transcriptome studies by microarray and SAGE.
11  with microarray and the future potential of SAGE.
12 oprecipitation (ChIP) with a modification of SAGE.
13 e facilitated by the enhanced method of Long SAGE.
14 eporter system to identify regulators of cis-SAGe.
15 .05 in the large CHS study, but not in CAPPS/SAGE.
16 egano+sage; oregano+sage+5%honey and oregano+sage+10%honey.
17 ration were oregano+sage+5%honey and oregano+sage+10%honey.
18                            Administration of SAGE-217 daily for 14 days resulted in a reduction in de
19 line to day 15 was -17.4+/-1.3 points in the SAGE-217 group and -10.3+/-1.3 points in the placebo gro
20 he mean baseline HAM-D score was 25.2 in the SAGE-217 group and 25.7 in the placebo group.
21       Adverse events were more common in the SAGE-217 group than in the placebo group.
22        The most common adverse events in the SAGE-217 group were headache, dizziness, nausea, and som
23 domization: 45 patients were assigned to the SAGE-217 group, and 44 to the placebo group.
24 ed to determine the durability and safety of SAGE-217 in major depressive disorder and to compare SAG
25 gned them in a 1:1 ratio to receive 30 mg of SAGE-217 or placebo once daily.
26  in major depressive disorder and to compare SAGE-217 with available treatments.
27                                      Whether SAGE-217, an oral, positive allosteric modulator of GABA
28 ib-sib correlations were calculated with the SAGE 5.0 program FCOR, to estimate heritability of retin
29 ylated hydroxytoluene; oregano+sage; oregano+sage+5%honey and oregano+sage+10%honey.
30 lues after 96h of refrigeration were oregano+sage+5%honey and oregano+sage+10%honey.
31  tolerability of brexanolone (USAN; formerly SAGE-547 Injection), a proprietary, aqueous formulation
32 udy investigated brexanolone (USAN; formerly SAGE-547 injection), an intravenous formulation of allop
33                                              SAGE 7.0 software was used for the analysis of data obta
34                        Here, we characterize Sage, a bHLH transcription factor expressed exclusively
35            In this study, we have identified sage, a salivary-specific bHLH protein as a new heterodi
36 heather (Mg, Na), bearberry (Ba, Fe, Pb) and sage (Ag) honeys.
37 h and U), common heather (Co, K, Mg, Na, V), sage (Ag, Cd, Cu), and bearberry (Ba, Fe, Pb, Sb, Zn).
38 ding to 26,502 transcripts were sequenced in SAGE analyses.
39 lts show the power of combined array CGH and SAGE analysis for the identification of candidate amplic
40                                              SAGE analysis indicates that genes that are on the same
41 ancies that could have been resolved by long SAGE and 10-20% of the short SAGE tags had no obvious ma
42                                     Although SAGE and Affymetrix chip expression levels showed a sign
43  the effects of a candidate regulator on cis-SAGe and canonical splicing.
44               Here we apply a combination of SAGE and chromatin immunoprecipitation (ChIP) protocols
45 qualitative expression signals obtained from SAGE and EST data with those from GeneChip arrays showed
46                            We show that both Sage and Fkh are required for the expression of Sage tar
47 already established in other cell types, and Sage and Fkh cannot alter the fate of most embryonic cel
48                                              Sage and Fkh drive expression of the bZip transcription
49 Sage target genes, and that co-expression of Sage and Fkh is sufficient to drive target gene expressi
50              However, most of the reports on SAGE and germ cell development are limited to descriptiv
51 differentially regulated genes identified by SAGE and interrogated ADPKD patient samples.
52 eristic of sequencing-based methods, such as SAGE and Long SAGE is the unavoidable occurrence of arti
53  small insert sizes associated with existing SAGE and LongSAGE protocols.
54 atabase by the same tissue type used by both SAGE and microarray analysis; then the multiple UniGene
55 ained by integrating expressed sequence tag, SAGE and microarray datasets.
56 t impressions in the graves include stems of sage and other Lamiaceae (Labiatae; mint family) or Scro
57 echanisms responsible for these abilities of sage and thyme have not been fully understood yet.
58  such as serial analysis of gene expression (SAGE) and mass spectrometry proteomic technology.
59  we used serial analysis of gene expression (SAGE) and microarray analysis to compare the gene expres
60  We used serial analysis of gene expression (SAGE) and microarray analysis to identify changes in gen
61 e Study of Addiction: Genes and Environment (SAGE) and the Australian Twin Family Study of AUDs (OZAL
62 tudy of Addiction: Genetics and Environment (SAGE) and the Collaborative Study on the Genetics of Alc
63 tudy of Addiction: Genetics and Environment (SAGE), and 2644 cases and 494 controls from our own stud
64 n (MACS), Dutch (PIAMA), Canadian (CAPPS and SAGE), and German (GINIplus and LISAplus) birth cohorts
65 tudy of Addiction: Genetics and Environment [SAGE], and International Consortium on the Genetics of H
66 est the idea, we developed a tissue-specific SAGE annotation database based on microarray data ().
67                                 These latter SAGE applications are facilitated by the enhanced method
68  by cis-splicing between adjacent genes (cis-SAGe) are increasingly recognized as a widespread phenom
69  and NGS-based classification is compared to SAGE-based classification and classification directly on
70  reads, NGS-based classification outperforms SAGE-based classification.
71 ples (COGA: best P = 1.7 x 10-6, R2 = 0.026; SAGE: best P = .001, R2 = 0.01; Yale-Penn: best P = .035
72 from Escherichia coli, Artemisia tridentata (sage brush), Pyrococcus furiosus, and Methanobacter ther
73 ce of the recommended schedule of IPV by the SAGE, but the evidence was largely from developed countr
74      We demonstrate over simulated data that SAGE can be used to infer correct haplotypes of the high
75 rts, CHS (Children's Health Study) and CAPPS/SAGE (Canadian Asthma Primary Prevention Study/Study of
76 actors, SRRM1 and SF3B1, affect not only cis-SAGe chimeras, but also other types of chimeric RNAs in
77 pithelium were in general agreement with the SAGE data and showed that these proteins are also expres
78 rably more information can be extracted from SAGE data by carrying out a systematic analysis of both
79                                          The SAGE data could also be well fit by a Monte Carlo model
80 the PN9 and mature mouse cornea, the present SAGE data demonstrate dynamic changes in gene expression
81 r study highlights the benefits of exploring SAGE data for comprehensive identification of human anti
82 inal transcripts, the quantitative nature of SAGE data for differentially expressed genes, the reprod
83                              Vast amounts of SAGE data have been collected and more than a thousand S
84 informatic analyses using recently published SAGE data on the transcriptome of mouse type A spermatog
85 RA2 rs279858 association was observed in the SAGE data sets with a combined P of 9 x 10(-6) (OR=1.17
86                This detailed analysis of the SAGE data shows first that while there is evidence of al
87                     However, analysis of our SAGE data shows that antisense transcripts are probably
88 ures should aid the proper interpretation of SAGE data to address biological and medical questions.
89 , we use a computational biology analysis of SAGE data to assess the abundance and distribution of se
90 is review focuses on the general features of SAGE data, including the specificity of SAGE tags with r
91 hen comparing mouse with human breast cancer SAGE data.
92 ne genes which are consistent with available SAGE data.
93 sing the serial analysis of gene expression (SAGE) data in all 130 deduced BTB/POZ genes.
94  CGH and serial analysis of gene expression (SAGE) data to correlate copy number and expression level
95 g public Serial Analysis of Gene Expression (SAGE) data, we found that the intronic poly(A) site is u
96  retinal serial analysis of gene expression (SAGE) data.
97 tudy of Addiction: Genetics and Environment (SAGE) data.
98 GE is the first publicly available web-based SAGE database on male gonad development that covers six
99 EST) and serial analysis of gene expression (SAGE) databases was enzyme quiescin Q6 sulfhydryl oxidas
100 tudy of Addiction: Genetics and Environment (SAGE) dataset, we tested for association of CHRNB3-A6 SN
101                Overall, the incorporation of sage decoction in the daily diet or its use as a complem
102          Serial analysis of gene expression (SAGE) demonstrated that more than 90% of those host gene
103 tudy of Addiction: Genetics and Environment (SAGE) demonstrates that applying the multivariate associ
104    The Study Assessing Goals in the Elderly (SAGE) demonstrates that older men and women with coronar
105                                              SAGE-derived endothelial cell gene expression patterns f
106 lso confirmed the differential expression of SAGE-discovered genes within the initial set of five cel
107 nscientious prothrombin time monitoring, and sage dosage adjustment remain paramount in warfarin mana
108 eing a remote detection technique, the Hyper-SAGE effect is further enhanced in situations where the
109  according to ISO 9909 and GDC standards for sage EO quality, revealing compliance for only 10 popula
110 e (HS) sampling in the quality assessment of sage EO.
111 for rapid screening in quality assessment of sage EOs.
112 m spin-and-gradient echo echoplanar imaging (SAGE-EPI) sequence and quantitative estimates of vessel
113 rable benefits, also being an alternative to sage essential oils that can display some toxic effects.
114 rimental methods such as tiling arrays or 5' SAGE/EST sequencing have recently lead to much larger da
115 is issue of Immunity, Wing et al. (2014) and Sage et al. (2014) demonstrate that CTLA-4 is a critical
116               STAGE is conceptually based on SAGE, except that the input is ChIP-enriched DNA.
117 nt genes within collections of microarray or SAGE experiments.
118 tag based expression (EBE) experiments and 5 SAGE experiments.
119                  QSOX1 mRNA levels, based on SAGE expression data, did not correlate with either Estr
120  encapsulates stabilised with gum arabic and sage extract (SOE) exhibited significantly higher encaps
121 l polymer, gum arabic as wall co-polymer and sage extract as wall stabiliser was spray dried using a
122                  The encapsulates containing sage extract showed a lower rate of lipid oxidation duri
123                                 Rosemary and sage extracts represented promising technological option
124  activated in breast cancer that traditional SAGE failed to call.
125 lial aggregation analysis was performed, and SAGE FCOR was used to quantify the total genetic contrib
126 h boosts expression of Sage-Fkh targets, and Sage, Fkh and Sens colocalize on SG chromosomes.
127                   Importantly, expression of Sage-Fkh target genes appears to simply add to the tissu
128 Senseless (Sens), which boosts expression of Sage-Fkh targets, and Sage, Fkh and Sens colocalize on S
129      The botanical origin of lumichrome from sage flower was assessed by analysing bee-stomach extrac
130 ation of serial analysis of gene expression (SAGE) for this purpose.
131                 Raw data were analyzed using SAGE (GE) software.
132              Raw data was preprocessed using SAGE (GE) software.
133 es of high conservation concern, the greater sage-grouse (Centrocercus urophasianus; hereafter, sage-
134 lp offset the adverse effects of wildfire on sage-grouse and other wildlife populations.
135                                       Female sage-grouse exhibited intricate habitat selection patter
136 dels to a spatiotemporally robust dataset of sage-grouse nest locations and fates across wildfire-alt
137 ng effects from wildfire nullified pulses of sage-grouse population growth that typically follow year
138 ldfire has contributed strongly to declining sage-grouse populations over the past 30 y at large spat
139 ontinue unabated, model projections indicate sage-grouse populations will be reduced to 43% of their
140 ffective population sizes for two polygynous sage-grouse species and compared them to estimates from
141            Strong site fidelity likely drove sage-grouse to continue nesting in habitats degraded by
142 rouse (Centrocercus urophasianus; hereafter, sage-grouse).
143 of a sagebrush-obligate species, the greater sage-grouse, across the Great Basin of western North Ame
144                             The principle of SAGE has been developed to address specific issues such
145                         Since its invention, SAGE has been widely applied to analyzing gene expressio
146 c Advisory Group of Experts on Immunization (SAGE) has recommended introduction of at least 1 dose of
147  diastase activity were studied in Dalmatian sage honey.
148 ified by serial analysis of gene expression (SAGE); however, its function in epithelial ion transport
149  Americans, Asthma, Genes, and Environments (SAGE II).
150 nalysis, serial analysis of gene expression (SAGE), immunohistochemistry, transcript sequencing, and
151 ignal amplification by gas extraction (Hyper-SAGE) in both NMR spectra and magnetic resonance images
152 dded multiple large-scale datasets including SAGE, interactome, 3D protein structure datasets and NCB
153 nder two different conditions suggested that SAGE is a reliable and reproducible technique for use in
154                                          The SAGE is a statistically significant predictor of postope
155                                              SAGE is a technique that allows the rapid, quantitative
156                                 We show that Sage is required for late SG survival and normal tube mo
157 uencing-based methods, such as SAGE and Long SAGE is the unavoidable occurrence of artifact sequences
158          Serial analysis of gene expression (SAGE) is a method for identifying and quantifying transc
159          Serial analysis of gene expression (SAGE) is a method used to obtain comprehensive, unbiased
160          Serial Analysis of Gene Expression (SAGE) is a powerful technology for measuring global gene
161          Serial Analysis of Gene Expression (SAGE) is a powerful tool for genome-wide transcription s
162          Serial analysis of gene expression (SAGE) is a widely used technique for large-scale transcr
163 Salvia divinorum commonly known as diviner's sage, is an ethnomedicinal plant of the mint family (Lam
164                              In April, 2016, SAGE issued recommendations on the use of the first lice
165 gulate expression of PH4alphaSG2, as well as sage itself, and to indirectly regulate expression of PH
166 ation (LAAPPI) and LDTD-APPI mass spectra of sage leaves (Salvia officinalis) using a field-deployabl
167  analysis of polar and nonpolar compounds in sage leaves and chili pepper.
168 an Gastrointestinal and Endoscopic Surgeons (SAGES) led to the promulgation of a formalised countrywi
169          One example, leubethanol from Texas sage (Leucophyllum frutescens) has demonstrated activity
170  compared with 25 of our human breast cancer SAGE libraries (>2.5 million human breast-specific tags)
171                  We apply SAGEScreen to Long SAGE libraries and compare error rates for several proce
172 g the authors' multidonor-derived retina/RPE SAGE libraries and existing single-donor retina/RPE libr
173 he rat limbal and central corneal epithelial SAGE libraries consisted of 41,894 and 40,691 tags, resp
174            In this study, we generated three SAGE libraries from melanoma tissues.
175 two retinal pigment epithelium (RPE)/choroid SAGE libraries made from matched macula or midperipheral
176  genes most highly expressed in our melanoma SAGE libraries was a calcium-regulated gene, calpain 3 (
177 Tags with a total count of > or =20 in three SAGE libraries were examined.
178 a and publicly available normal human tissue SAGE libraries.
179 enerated serial analysis of gene expression (SAGE) libraries from two distinct populations of single,
180          Serial analysis of gene expression (SAGE) libraries were constructed and analyzed, and in si
181 s agent, serial analysis of gene expression (SAGE) libraries were generated for three sensitive and t
182 uencing and sampling errors was applied to a SAGE library (137 832 tags) obtained from mouse embryoni
183 rently altered cancer expression in the CGAP SAGE library collection-often in keeping with predicted
184 ditis elegans using a public tissue-specific SAGE library data set.
185                The sequence coverage of each SAGE library is beyond 150K, 'which is the most extensiv
186 elopment, with 150,000 sequence tags in each SAGE library.
187 ompared with previously published normal EOM SAGE library.
188 e latest Serial Analysis of Gene Expression (SAGE) library data derived a complete list of 459 genes
189                                      Several SAGE-like methods have also been developed for the genom
190  The comparative analysis of mouse and human SAGE mammary cancer data validates this p53 null mouse t
191 ifloral, heather, common heather, bearberry, sage, mandarin orange-blossom and honeydew) collected in
192                                 John's Wort, sage, marjoram and thyme were assayed.
193 dually required for SLS production, and that sagE may further serve an immunity function.
194 ibutions indicate limitations in the EBE and SAGE methods at both high- and low-expression levels.
195 alidated in separate validation cohorts from SAGES (n = 150 for CRP, IL-6; n = 126 for CHI3L1).
196 tic curve area under the curve (AUC) for the SAGE of 0.69, 0.77, 0.73, 0.66, and 0.78 for the above o
197 oupled with targeted xenon biosensors, Hyper-SAGE offers another path to highly sensitive molecular i
198                      One limitation of using SAGE on an organism with a complex genome and lacking de
199       Comparison of SAGE-Seq and traditional SAGE on normal and cancerous breast tissues reveals high
200 erformed serial analysis of gene expression (SAGE) on CD15(+) myeloid progenitor cells from 22 AML pa
201     The Strategic Advisory Group of Experts (SAGE) on Immunization advises WHO on global policies for
202 s (WHO) Strategic Advisory Group of Experts (SAGE) on Immunization recommended conducting this synchr
203 12, the Strategic Advisory Group of Experts (SAGE) on Immunization recommended universal IPV introduc
204                The effect of combinations of sage, oregano and honey on lipid oxidation in cooked chi
205 : control; butylated hydroxytoluene; oregano+sage; oregano+sage+5%honey and oregano+sage+10%honey.
206                                          The SAGE performed as well in predicting postoperative outco
207                                          The SAGE performs as well as other geriatric evaluations tha
208   The synergistic efficacy of gum arabic and sage polyphenols in stabilising capsule wall and protect
209                                              Sage Products, US National Institutes of Health.
210 y discovering a fusion transcript based on a SAGE profile and for the first time precisely describes
211 sed on a serial analysis of gene expression (SAGE) profile of the MYCN-amplified NB cell line IMR-5.
212 the clinical validation data demonstrate how SAGE profiles can highlight specific links between signa
213                           Since the original SAGE protocol was developed in a short-tag (10-bp) forma
214          Serial analysis of gene expression (SAGE) provides a global analysis platform for profiling
215          Serial analysis of gene expression (SAGE) provides an alternative, with additional advantage
216 ta were organized with the use of NUD-IST 4 (Sage Publications Software) and were analyzed by the con
217 (WHO's) Strategic Advisory Group of Experts (SAGE) recommended that all 126 countries using only oral
218 sufficient evidence to determine whether the SAGE-recommended IPV schedule for the polio endgame woul
219                                     In 2013, SAGE reiterated the importance of attaining the long-ter
220 have been collected and more than a thousand SAGE-related studies have been published since the mid-1
221 rated by Serial Analysis of Gene Expression (SAGE) representing major stages in mouse male germ cell
222                                          Our SAGE results and the clinical validation data demonstrat
223                                              SAGE results converged with previous microarray analysis
224                                          The SAGE results extend the database of genes expressed in t
225  unifloral honey types showed that Dalmatian sage (S. officinalis L.) honey is characterised by unusu
226                                              SAGE's working group on dengue vaccines met to discuss t
227 lementation, we show sagA, sagB, sagC, sagD, sagE, sagF and sagG are each individually required for S
228 , the active component of the hallucinogenic sage Salvia divinorum, is an apparently selective and hi
229  and methanol/water (80:20, v/v) extracts of sage (Salvia officinalis L.) were evaluated and characte
230 sessment of essential oil (EO) from culinary sage (Salvia officinalis L., Lamiaceae) is limited by th
231 a xpiperita), melissa (Melissa officinalis), sage (Salvia officinalis), nettle (Urtica dioica), linde
232 hin MARCH6 and ROPN1L were replicated in the SAGE sample (p<0.05).
233 overy results (94-108%) obtained from spiked sage sample and from cobalamin also validated the accura
234  A replication study was conducted using the SAGE sample with 762 individuals.
235                        Each unit decrease in SAGE score was significantly associated with a 51% (95%
236        The resulting Java-based tool, called SAGE (Scoring function for Assembled GEnomes), is freely
237 ority of the current distribution of coastal sage scrub fragments, with the exception of some outlyin
238                                Comparison of SAGE-Seq and traditional SAGE on normal and cancerous br
239                                              SAGE-Seq is a powerful method for the identification of
240                                              SAGE-Seq is able to identify genes and pathways abnormal
241 breast tissues reveals higher sensitivity of SAGE-Seq to detect less-abundant genes, including those
242 ication of ultra high-throughput sequencing, SAGE-Seq, for the accurate quantification of normal and
243                                              SAGE (serial analysis of gene expression) detects transc
244 n craniofacial structures, we constructed 12 SAGE (serial analysis of gene expression) libraries and
245 were determined by sequencing the respective SAGE (Serial Analysis of Gene Expression) libraries.
246 ethylation-specific digital karyotyping) and SAGE (serial analysis of gene expression).
247 rrelations were calculated using FCOR in the SAGE software package.
248 rn, honeydew, heather, lime, mint, rapeseed, sage, strawberry tree, sulla flower, savory and thistle)
249          In the Successful AGing Evaluation (SAGE) study, the authors used a structured multicohort d
250 the Successful Aging after Elective Surgery (SAGES) study was used for SOMAscan.
251 UniGene clusters assigned to the nonspecific SAGE tag are searched in the database under the matched
252 ue in differential gene expression analysis, SAGE tag collections afford abundant information on the
253 However, to fully exploit the value of large SAGE tag datasets, it is desirable to account for and co
254                              The nonspecific SAGE tag is first matched to the database by the same ti
255            By analysis of a highly expressed SAGE tag not matching a Unigene cluster we identified fo
256 s of gene expression (SAGE), we identified a SAGE tag that was present only in invasive breast carcin
257          Because of the limited length, many SAGE tags are shared by transcripts from different genes
258                                     When the SAGE tags expressed within these cell line libraries wer
259 difications have been made to produce longer SAGE tags for more precise gene identification and to de
260                   Examination of 71,930 Long SAGE tags generated from six libraries derived from two
261 novel procedures to characterise, in detail, SAGE tags generated from the whole grain transcriptome o
262 esolved by long SAGE and 10-20% of the short SAGE tags had no obvious match to currently annotated hu
263 omparing the use of 10-bp SAGE tags to 17-bp SAGE tags indicated that the short SAGE technology was m
264 e that can be used to identify the antisense SAGE tags originated from the antisense strand of known
265 uracy of gene annotation for the nonspecific SAGE tags should be significantly improved.
266 titative analysis comparing the use of 10-bp SAGE tags to 17-bp SAGE tags indicated that the short SA
267 s of SAGE data, including the specificity of SAGE tags with respect to their original transcripts, th
268 iled analysis of transcriptome data, such as SAGE tags, is essential to understand fully the factors
269                    From a total of 1,247,535 SAGE tags, we identified 2,604 transcripts whose express
270 anscripts, including the three most abundant SAGE tags, which did not correspond to any known genes o
271 n antisense ESTs and 3198 are mapped only by SAGE tags.
272 resent the specific gene for the nonspecific SAGE tags.
273 useful source for annotating the nonspecific SAGE tags.
274 STs, and serial analysis of gene expression (SAGE) tags, and performed an extensive annotation on thi
275                                        Hyper-SAGE takes advantage of a change in physical phase to in
276 e and Fkh are required for the expression of Sage target genes, and that co-expression of Sage and Fk
277                            We find that many Sage targets, identified by microarray analysis, encode
278 d to separate and preconcentrate cobalt from sage tea and vitamin B12 samples after complexing with a
279 sing the serial analysis of gene expression (SAGE) technique.
280  to 17-bp SAGE tags indicated that the short SAGE technology was more efficient at identifying differ
281                       Previous studies using SAGE (the Study of Addiction: Genetics and Environment)
282 udy of Addiction, Genetics, and Environment (SAGE); the Yale-Penn genetic study of substance dependen
283 ith the salivary gland-specific bHLH protein Sage to directly regulate expression of PH4alphaSG2, as
284                              Here, we use 5' SAGE to map 5' TSS in S.cerevisiae.
285 nderlies serial analysis of gene expression (SAGE) to analyze mutations that result from DNA synthesi
286  we used serial analysis of gene expression (SAGE) to compare transcripts in wild-type and Pti4-expre
287       From the training set of 21,321 unique SAGE transcript tags derived from 11 libraries, five gen
288                  Data were collected for the SAGE trial from 1990 to 2007 and for the ICGHD from 2004
289             The combination of ChIP, RDA and SAGE-type methods has advantages over other similar stra
290                  A comparison study of short SAGE versus GeneChip and long SAGE was conducted to dete
291 study of short SAGE versus GeneChip and long SAGE was conducted to determine if data were interchange
292                       The performance of the SAGE was then compared with 3 standard tools in its powe
293 markers, serial analysis of gene expression (SAGE) was done on three samples from the same patient: n
294          Serial analysis of gene expression (SAGE) was performed on postnatal day (PN)9 and adult mou
295          Serial analysis of gene expression (SAGE) was used to obtain gene expression profiles of nor
296    Using serial analysis of gene expression (SAGE), we identified a SAGE tag that was present only in
297                Effect estimates in CAPPS and SAGE were also conflicting but not significant (0.63 [0.
298       Different populations (30) of culinary sage were assessed using GC/FID/MS analysis of the hydro
299 s, the reproducibility, the comparability of SAGE with microarray and the future potential of SAGE.
300         The analysis of phenolic extracts of sage without parathion showed that irradiation decreased

 
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