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1 te sRNAs, a third of which were validated by northern blot analysis.
2 sts, was confirmed by both real-time PCR and Northern blot analysis.
3 xL, an anti-apoptotic gene, was evaluated by Northern blot analysis.
4 hese microarray results were confirmed using northern blot analysis.
5 oop position and expression as determined by northern blot analysis.
6 , uterus, testis, and placenta, as judged by Northern blot analysis.
7 infection in mice with Sy2, as determined by Northern blot analysis.
8 r cell cultures were evaluated by RT-PCR and Northern blot analysis.
9 in endothelial cells that were verifiable by Northern blot analysis.
10 detection of internalized siRNA by modified Northern blot analysis.
11 2 expression when analyzed by immunoblot and Northern blot analysis.
12 This result was confirmed by Northern blot analysis.
13 that miR-3676 and miR-4521 are tsRNAs using Northern blot analysis.
14 These results were further confirmed by Northern blot analysis.
15 f prostate cancer, as detected by RT-PCR and Northern blot analysis.
16 on by cJun and JunB of 10 candidate genes by Northern blot analysis.
17 transcripts were independently reproduced by Northern blot analysis.
18 noma (HCC) microarray study and confirmed by Northern blot analysis.
19 ption polymerase chain reaction (RT-PCR) and Northern blot analysis.
20 AGT mRNA expression was determined by Northern blot analysis.
21 orn mouse kidney was confirmed by RT-PCR and Northern blot analysis.
22 re confirmed by reverse transcription-PCR or Northern blot analysis.
23 on is restricted to prostate and placenta by Northern blot analysis.
24 of these eight novel miRNAs was confirmed by Northern blot analysis.
25 A species (NP, F, HN, and L) was examined by Northern blot analysis.
26 e LPS binding protein CD14 were confirmed by Northern blot analysis.
27 miRNAs is validated by quantitative PCR and northern blot analysis.
28 Preferential gene induction was verified by Northern blot analysis.
29 ceptor for alpha-MSH (MC1-R), as assessed by Northern blot analysis.
30 by cDNA microarray analysis and confirmed by Northern blot analysis.
31 The mRNA expression pattern was examined by Northern blot analysis.
32 fter Dex treatment, a result consistent with Northern blot analysis.
33 ression was demonstrated in transformants by northern-blot analysis.
34 sequent confirmation of mir expression using northern-blot analysis.
35 in vivo primer extension experiments and by Northern blotting analysis.
36 K-i was detected in embryonic fibroblasts by Northern blotting analysis.
37 rimer extension experiments, consistent with Northern blotting analysis.
38 be found in the higher primate species with Northern blot analysis, a potential alternative explanat
39 to a 10-fold decrease in HCV replication by Northern blot analysis and 21% specific lysis of FCA1 ce
45 ally investigated six novel candidates using Northern blot analysis and found expression of three can
46 es throughout the whole plant as revealed by northern blot analysis and gene fusion assay of RIE1 pro
51 phy to detect the presence of MMP-2, and for Northern blot analysis and in situ hybridization with MT
52 sed on the extended UGT1 locus combined with Northern blot analysis and in situ hybridization, we det
55 d in various human tissues and cell lines by Northern blot analysis and multiple tissue expression ar
56 transcription-polymerase chain reaction and Northern blot analysis and of protein expression by West
60 lone that expressed GSTP1 mRNA determined by Northern blot analysis and quantitative reverse transcri
65 characterized the expression of this gene by Northern blotting analysis and in situ hybridization to
66 U gene in infected cells was demonstrated by Northern blot analysis, and bicistronic N-U mRNA was als
67 time reverse transcription-PCR, confirmed by Northern blot analysis, and correlated with the presence
68 y expressed in vascular endothelial cells by Northern blot analysis, and immunohistochemical staining
69 rythroid-specific expression was detected by Northern blot analysis, and maximal expression during th
70 ed by nuclear in vitro transcription run-on, northern blot analysis, and quantitative polymerase chai
72 ression, as measured by luciferase assay and Northern blot analysis, at concentrations of 10 and 30 m
95 ption polymerase chain reaction (RT-PCR) and northern blot analysis demonstrated reduced expression o
116 the count of cell number for proliferation, Northern blot analysis for gene expression (up to 10 day
117 adult cadaveric donors and were assessed by Northern blot analysis for growth and melanogenic respon
121 findings were validated by real-time PCR and Northern blot analysis in an independent panel of colon
124 of S100A4 in the cornea was determined using Northern blot analysis, in situ hybridization, and immun
125 d during chondrocyte maturation, as shown by Northern blot analysis, in situ hybridization, and real-
130 transcriptase-polymerase chain reaction and Northern blot analysis indicated that both groES and gro
141 transcription-polymerase chain reaction and Northern blot analysis indicated that VHL mRNA levels we
152 NAs (miRNAs), six of which were confirmed by Northern blot analysis, leaving four as provisional.
156 of these same genes was also investigated by northern blot analysis of anther RNA isolated from wild-
157 ss total maternal-UBE3A RNA was confirmed by Northern blot analysis of cell lines carrying 15q11- q13
158 ementary tissues in the developing limb, and Northern blot analysis of chick limb bud mRNA shows that
162 ay, electrophoretic mobility shift assay and Northern blot analysis of expression of endogenous kappa
164 is mutation was confirmed by high-resolution Northern blot analysis of heart tissue from both familie
172 NA recovery, DNA fragmentation patterns, and Northern blot analysis of retinal heme oxygenase (HO)-1
176 , site-directed mutagenesis experiments, and Northern blot analysis of RNA produced by constructs ind
179 creased in Jnk2(-/-) mice with CIA, EMSA and Northern blot analysis of total joint extracts revealed
182 alter expression of HRPAP20 was evaluated by Northern blot analysis of total RNA obtained from PRL-st
190 screening of an albumen gland cDNA library, Northern blot analysis, purification, characterization,
191 multiple molecular techniques, which include Northern blot analysis, real-time PCR, miRNA microarray,
197 al samples by quantitative real-time PCR and Northern blot analysis revealed an inverse correlation b
225 ugh cidABC transcription was not detected by Northern blot analysis, reverse transcriptase PCR reveal
226 lization was determined at the mRNA level by Northern blot analysis, RT-PCR, and in situ hybridizatio
228 features of IMPDH1 in the retina, including Northern blot analysis, serial analysis of gene expressi
231 transcription polymerase chain reaction and Northern blot analysis showed decreased amounts of ap65
237 transcriptase polymerase chain reaction and Northern blot analysis showed that both rap1A and rap1B
247 Intriguingly, in situ hybridization and Northern blot analysis showed that the expression of PME
255 2 cluster of snoRNAs by RNase protection and northern blot analysis shows that the MBII-52 expressing
260 atabases, RT-PCR, in situ hybridization, and Northern blot analysis that cells in the mouse retina ex
265 Quantitative polymerase chain reaction and northern blot analysis verified that bound mRNA remained
272 m (ArsRS) in this acid-inducible regulation, Northern blot analysis was performed with RNAs isolated
281 ing an miRNA microarray screen, confirmed by Northern blot analysis, we defined a set of seven miRNAs
283 ing a combination of microarray analysis and Northern blot analysis, we found that an anti-apoptotic
284 xamining the expression pattern of miRNAs by Northern blot analysis, we found that Drosophila miRNAs
289 rse-transcription polymerase chain reaction, Northern blot analysis, Western blot analysis, and funct
290 tion of the VEGF promoter were determined by Northern blot analysis, Western blot analysis, and use o
291 be performed using alternative methods (eg, Northern blot analysis, Western blot, immunohistochemist
292 e newly synthesized RNA was characterized by Northern blot analysis, which demonstrated the productio
293 nscription and replication was determined by Northern blot analysis, which examined full-length antig
294 ription run-on assays, promoter studies, and Northern blot analysis, while stability of the COL1A1 an
295 or H37Rv, and the total RNA was subjected to Northern blot analysis with a (32)P-labeled probe derive
299 small RNA substrates were probed directly by Northern blot analysis with RNA from the RNase P TS muta
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