戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top