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1 Several of these changes were confirmed by Northern blot analyses.
2 CK are detected only in skin by Southern and Northern blot analyses.
3 ne brain, by using in situ hybridization and northern blot analyses.
4 of phospholamban transcripts was examined by Northern blot analyses.
5 artilage but not normal cartilage by PCR and Northern blot analyses.
6 uct was used as a probe in Southern blot and Northern blot analyses.
7 ytometry and at the level of mRNA by PCR and Northern blot analyses.
8 pairs identified in dsRNAs were confirmed by Northern blot analyses.
9 ion, Western blot, immunohistochemistry, and Northern blot analyses.
10 n as confirmed by transcriptional fusion and Northern blot analyses.
11 utant by either reverse transcriptase PCR or Northern blot analyses.
12 Results were confirmed by microarray and Northern blot analyses.
13 achieved, as confirmed by PCR, Southern, and Northern blot analyses.
14 eting was demonstrated by flow cytometry and Northern blot analyses.
15 regulation of these operons were examined by Northern blot analyses.
16 ses at that time, as shown by microarray and Northern blot analyses.
17 el by Western blot, immunoprecipitation, and Northern blot analyses.
18 cistronic transcripts were not detectable on Northern blot analyses.
19 tinct tissue-specific expression patterns by Northern blot analyses.
20 tive reverse transcription-PCR (qRT-PCR) and Northern blot analyses.
21 tive AP-2B gene was confirmed by RT--PCR and Northern blot analyses.
22 describe expression in L. pennellii through northern-blot analyses.
23 house-grown banana plants were determined by northern-blot analyses.
24 ression using quantitative real-time PCR and Northern blots analyses.
27 veolin-1alpha, an identification verified by Northern blot analyses and by the cloning of a cDNA usin
31 ld restore GADD45beta expression in HepG2 in Northern blot analyses and quantitative real-time polyme
36 ed by genomic Southern blot, immunoblot, and Northern blot analyses, and two-dimensional gel electrop
37 evels of endogenous D3 mRNA, as indicated by Northern blot analyses, and was significantly reduced wh
45 transcriptase polymerase chain reaction and Northern blot analyses demonstrate that neither CIITA no
55 isolated from endotoxin-exposed rat livers, Northern blot analyses demonstrated that Kupffer cells b
63 duction of IL-2R components was derived from northern blot analyses demonstrating TIF-induced decreas
66 and WEHV2 were also similar to that of WDSV; Northern blot analyses detected only low levels of the o
68 xpression profiling using DNA microarray and northern-blot analyses identified 82 transcript types fr
69 ession of an AM receptor was not detected by Northern blot analyses in either embryo or trophoblast g
78 and polyamine transport and metabolism, and Northern blot analyses indicate that the AbcR sRNAs acce
88 In agreement, strand-specific RT-PCR and Northern blot analyses indicated that antisense transcri
98 oarray and/or quantitative real-time PCR and northern blot analyses, microRNA-218 (miR-218) was speci
99 out using a conventional dicistronic vector, Northern blot analyses might not be sensitive enough to
100 oliferation and colony reduction assays, and Northern blot analyses, neither blocking of the binding
106 he N-terminal amino acid residues of ACC2 in Northern blot analyses of different human and mouse tiss
114 nd 15.5 days of gestation, respectively, and Northern blot analyses of RNAs from dissected embryos re
118 RNase protection, in situ hybridization, and Northern blot analyses of wild-type and germ-cell-defici
119 mRNA species are detectable in the brain by Northern blot analyses or in neuroblastoma cell lines.
126 sense construct was verified by Southern and Northern blot analyses, respectively, and resulted in de
129 miquantitative reverse transcription-PCR and Northern blot analyses, resulting in confirmation of six
160 tions, enzyme-linked immunosorbent assay and Northern blot analyses showed downregulation of VEGF in
162 s transduced with retroviral constructs, and Northern blot analyses showed high steady-state antisens
164 ptase-polymerase chain reaction (RT-PCR) and Northern blot analyses showed that C(6)-ceramide signifi
167 Furthermore, reverse transcriptase PCR and Northern blot analyses showed that cpb2 genes in all of
170 ults of OLE1 promoter-lacZ reporter gene and Northern blot analyses showed that hypoxia- and cobalt-i
177 ure rodent microRNAs and quantitative RT-PCR/Northern blot analyses showed that Trx1 upregulates memb
179 onal analyses by transient transfections and Northern blot analyses suggest APBP-1 has the capacity t
186 ith the use of polymerase chain reaction and Northern blot analyses, the NPC in HSMCs was identified
187 , we have used reverse transcription-PCR and Northern blot analyses to ascertain the spectrum of SPC
190 is study, we used proteomics and Western and Northern blotting analyses to demonstrate that alcohol d
191 ssed for immunocytochemistry and Western and Northern blot analyses, to determine stromal cell densit
194 d proteins and RNA collected for western and northern blot analyses using antibodies specific for alp
197 a late transcript of 1.8 kb are detected in Northern blot analyses using probes containing the EICP0
199 of the cDNA partial TIP-B1 clone, as well as Northern blot analyses using the cDNA insert as a probe,
205 re, through in vivo cross-linking assays and Northern blot analyses, we have demonstrated that Ets-1
206 Using 3'-rapid amplification cDNA end and Northern blot analyses, we identified the complete 3'-un
208 roarray, reverse transcription (RT)-PCR, and Northern blotting analyses, we identified 11 virally enc
209 ic techniques, and in situ hybridization and Northern blot analyses were conducted to characterize, l
210 erence, bfpA-cat transcriptional fusions and northern blot analyses were employed to monitor bfpA exp
211 nzyme-linked immunosorbent assay (ELISA) and Northern blot analyses were performed to determine secre
214 d in chronic diarrheas, cDNA microarrays and Northern blot analyses were used to compare global mRNA
216 n was glycoxidized in vitro, and Western and Northern blot analyses were used to investigate NOSIII e
219 o these two regulatory regions, we performed Northern blot analyses, which showed the presence of ets
222 ls during gizzard development by Western and Northern blot analyses, with a large increase just prece
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