1 ified for individual circRNAs by RT-qPCR and
Northern analysis.
2 small RNAs bind Hfq; five were confirmed by
Northern analysis.
3 l2 for a 24 h time course were also used for
northern analysis.
4 undetectable in thymus, spleen and brain by
Northern analysis.
5 xpressed in 4/8 ovarian cancer cell lines by
Northern analysis.
6 ndant NS5A antigen and HCV RNA detectable by
Northern analysis.
7 iles were studied during a 48-h period using
northern analysis.
8 nd then examined for messenger RNA (mRNA) by
Northern analysis.
9 in situ hybridization, Northern and reverse
Northern analysis.
10 r results were obtained using immunoblot and
Northern analysis.
11 ype 2 (TIMP-2) expression were determined by
Northern analysis.
12 not to produce enhancin gene transcripts by
Northern analysis.
13 rin homolog with expression in the kidney by
Northern analysis.
14 23 distinct new RNA species was confirmed by
Northern analysis.
15 uppression of RUNX2 mRNA was confirmed using
Northern analysis.
16 ion are detected in the spleen and thymus by
Northern analysis.
17 ators and various inhibitors, was studied by
Northern analysis.
18 D2 (a protein required for TLR4 function) by
Northern analysis.
19 ription in lytically infected fibroblasts by
Northern analysis.
20 These findings were further confirmed by
Northern analysis.
21 -nine of the most promising were examined by
Northern analysis.
22 sfection with COX-2 reporter variants and by
Northern analysis.
23 but defined transcripts were not detected by
northern analysis.
24 6 out of 9 candidate sRNAs were observed by
Northern analysis.
25 tive real-time reverse transcription-PCR and
Northern analysis,
3-day treatment with BRL 49653 and 15
26 By
Northern analysis,
a 2.4-kilobase (kb) message was obser
27 Using
northern analysis,
a 6-fold increase of tree tobacco LTP
28 ncrease in the ATF3 mRNA species detected by
Northern analysis actually encoded both full-length ATF3
29 remained undetectable in wild-type liver by
Northern analysis after tumor induction or after PH.
30 oth an increased expression of renin mRNA by
Northern analysis and elevated plasma renin concentratio
31 Northern analysis and fluorescence-activated cell sortin
32 erential expression for RNA was confirmed by
Northern analysis and for protein by immunostaining.
33 Further,
Northern analysis and immunohistochemistry of mouse test
34 mmaRIIA cDNA in hepatocytes was confirmed by
Northern analysis and immunohistochemistry.
35 Using
Northern analysis and immunoprecipitation with anti-HBc
36 By using
Northern analysis and in situ hybridization, we found th
37 Levels of RGS5 mRNA were confirmed by
Northern analysis and in situ hybridization.
38 baceous units of mouse skin as determined by
Northern analysis and in situ hybridization.
39 NA in axotomized DRG neurons was verified by
Northern analysis and in situ hybridization.
40 Northern analysis and in situ hybridizations showed that
41 trate that NPFF precursor mRNA expression by
Northern analysis and map sites of expression by in situ
42 A subset of these miRNAs were validated by
Northern analysis and miRNAs differentially responding t
43 11) showed expression of retroviral mRNA by
Northern analysis and production of functional CK beta-1
44 ld-type versus Hoxa9-deficient marrow, using
northern analysis and qRT-PCR.
45 Northern analysis and quantitative PCR with human and ra
46 Northern analysis and RNase protection assays revealed l
47 Results from
Northern analysis and tests using IGF-I analogs suggest
48 Northern analysis and transcription fusion assays showed
49 15 of these genes were subjected to
Northern analysis,
and a high percentage of them were co
50 omic hybridization, traditional Southern and
Northern analysis,
and chromosome 8 cDNA microarray expr
51 by alternative carbon source growth assays,
northern analysis,
and genome-wide expression profiling.
52 Nevertheless, immunoblotting,
Northern analysis,
and immunohistochemistry revealed tha
53 ostate carcinoma using immunohistochemistry,
Northern analysis,
and in situ hybridization.
54 NA (mRNA) expression levels were measured by
Northern analysis,
and PG loss to the medium after carti
55 and from healthy controls was quantitated by
Northern analysis,
and ras-MAPK signaling was determined
56 Here, we report the cloning, sequence,
Northern analysis,
and the embryonic expression pattern
57 ld be used to generate sgmRNAs detectable by
Northern analysis (
approximately 2 to 32 molecules per c
58 Northern analysis confirmed a 4.0-fold increase in stead
59 A combination of database search and
Northern analysis confirmed that corresponded to 3'-UTR
60 Northern analysis confirmed that DN alpha is induced by
61 Northern analysis confirmed that LUC transcript accumula
62 Northern analysis confirmed that one or more NgLTP genes
63 Northern analysis confirmed that RGS5 expression in huma
64 Northern analysis confirmed the expression of 9 of these
65 Northern analysis confirmed the NO-dependent suppression
66 Northern analysis confirmed the presence of messages of
67 Northern analysis confirmed the transcriptional activati
68 Northern analysis confirmed these findings.
69 Two major species of Xist are detectable by
Northern analysis,
consistent with differential polyaden
70 Northern analysis corroborated the lack of Egr3 in Th1 c
71 By
Northern analysis CSP-beta mRNA was present at very low
72 , as confirmed by transcriptional fusion and
Northern analysis data.
73 Northern analysis demonstrated exaggerated pulmonary PAI
74 Northern analysis demonstrated high expression levels of
75 Using either cDNA as a probe in a
Northern analysis demonstrated high levels of expression
76 Northern analysis demonstrated increased IL-2Ralpha gene
77 Moreover, immunodot blot and
Northern analysis demonstrated phosphate-dependent produ
78 Northern analysis demonstrated PTPLA is preferentially e
79 Northern analysis demonstrated that both genes are expre
80 Northern analysis demonstrated that cells containing eit
81 Additionally,
Northern analysis demonstrated that CG7780 expression is
82 Northern analysis demonstrated that CYP2N1 transcripts a
83 Northern analysis demonstrated that in S. stapfianus lea
84 ded by the mouse and Drosophila genomes, and
Northern analysis demonstrated that PACRG and parkin wer
85 Northern analysis demonstrated that PART-1 is highly exp
86 Northern analysis demonstrated that PDIP1 mRNA is presen
87 Northern analysis demonstrated that phytochrome A mRNA i
88 Northern analysis demonstrated that PSDR1 is highly expr
89 Northern analysis demonstrated that RNR1 expression is r
90 Northern analysis demonstrated that the gene is expresse
91 Northern analysis demonstrated that the Stk10 transcript
92 Northern analysis demonstrated that the transcript for C
93 Northern analysis demonstrated that the ultraviolet irra
94 Northern analysis demonstrated that TMPRSS2 is highly ex
95 Northern analysis demonstrated widespread expression of
96 Northern analysis demonstrates that cycloheximide treatm
97 Northern analysis demonstrates that ERK8 is present in a
98 Northern analysis demonstrates that SBE A mRNA is expres
99 Northern analysis demonstrates that TRAG-3 is overexpres
100 Northern analysis demonstrates widespread expression of
101 In this study, we explore via
Northern analysis details of the transcriptional regulat
102 Northern analysis detected three major transcript isofor
103 By
Northern analysis,
EST distribution and real-time quanti
104 Northern analysis established that merA transcription re
105 id X receptor (RXR) subtypes (as detected by
Northern analysis)
except RXRgamma.
106 Northern analysis excluded the possibility of an opaque
107 chilla beta-defensin-1 (cBD-1), and found by
Northern analysis expression of the corresponding mRNA i
108 Northern analysis for ALS3 expression revealed that it i
109 remaining genes, and these were screened by
Northern analysis for damage-inducible gene expression i
110 unter, and differentiation was determined by
Northern analysis for specific genes.
111 ption polymerase chain reaction (RT-PCR) and
northern analysis for the cholecystokinin (CCK(2)) recep
112 orter (cell surface galectin-3), Western and
Northern analysis (
galectin-3, MUC2), and gel filtration
113 Northern analysis identifies ETO-2 transcripts in many o
114 rocytes and U-373 MG cells, as determined by
Northern analysis,
immunocytochemical staining, and dete
115 Eotaxin mRNA was detectable by
northern analysis in BAL cells exclusively from allergen
116 In this study,
Northern analysis in both Lactococcus and Enterococcus b
117 mouse MTP, by polymerase chain reaction and
Northern analysis in non-apoB-secreting tissues, includi
118 ning single-cell MALDI-MS peptide profiling,
northern analysis,
in situ hybridization, and immunocyto
119 scripts, atr2L and atr2S, were identified by
Northern analysis;
in VSMCs, atr2S mRNA expression was m
120 Northern analysis indicated a 1.28- kilobase pair transc
121 Although
northern analysis indicated expression of the human PSGR
122 Northern analysis indicated GL50 to be present in many t
123 unofluorescence to the nucleus of cells, and
Northern analysis indicated that ELL3 is a testis-specif
124 Northern analysis indicated that expression of the NH(2)
125 Northern analysis indicated that FPN1 mRNA levels decrea
126 Northern analysis indicated that it is predominantly exp
127 Significantly, by day 12 in culture,
Northern analysis indicated that the follicle cells expr
128 Northern analysis indicates that AtCUTA mRNA is expresse
129 Northern analysis indicates that FAM3B is highly express
130 Northern analysis indicates that the gene is repressed i
131 By
Northern analysis,
it was found to be expressed in all h
132 By
Northern analysis,
liver and platelets had identically s
133 ults of 5'-rapid amplification of cDNA ends,
Northern analysis,
N-terminal sequence, and antibody rea
134 Northern analysis of a limited number of these genes val
135 Northern analysis of a merRA double mutant produced by l
136 Northern analysis of A7R5 RNA identified high levels of
137 Northern analysis of abiotic marker genes revealed that
138 specific transcripts as well as independent
northern analysis of additional mRNAs and sRNAs.
139 Northern analysis of ATPase transcripts and in vivo puls
140 Northern analysis of box C/D RNAs reveals two prominent
141 STAT-1 gene up-regulation was confirmed by
Northern analysis of cells treated with IGFBP-3 or trans
142 Northern analysis of chicken tissue shows a high level o
143 Northern analysis of Cx31.9 showed a major 4.4-kilobase
144 Northern analysis of eight mouse tissues indicated wide
145 Northern analysis of embryonic samples and multiple adul
146 Digital
northern analysis of expressed sequence tags suggested t
147 We show by
Northern analysis of fetal and adult tissues that expres
148 Northern analysis of glucotoxic HIT-T15 cells revealed n
149 Northern analysis of GRWD1 message levels in the myeloid
150 Northern analysis of key regulators of the asexual and s
151 Northern analysis of mitochondrial RNAs in an atp25 temp
152 Northern analysis of mRNA from human tissues and cell li
153 Northern analysis of multiple human tissue mRNAs demonst
154 This was confirmed by
northern analysis of native g10 transcripts in isolated
155 Northern analysis of normal human tissue showed that TME
156 Northern analysis of NSBP1/Nsbp1 shows differences in tr
157 Northern analysis of poly(A)+ RNA from tubules, whole gl
158 Northern analysis of poly(A+) mRNAs reveals two differen
159 Based on
Northern analysis of rat tissues, a 3-kilobase CaT1 tran
160 As predicted,
Northern analysis of RNA derived from the left ventricle
161 Northern analysis of RNA from hearts of those animals an
162 Northern analysis of RNA from intraerythrocytic stages o
163 Northern analysis of RNA from mouse embryos at embryonic
164 Northern analysis of RNA isolated from organs indicated
165 Northern analysis of RNA isolated from such cells after
166 Northern analysis of RNAs from multiple mouse tissues de
167 Northern analysis of Sf9 cells transfected with bacmid v
168 little cross-contamination, as determined by
Northern analysis of specific marker RNAs.
169 Northern analysis of spoT revealed detectable message at
170 ing at sites A(0), A(1) and A(2) as shown by
northern analysis of steady state levels of rRNA precurs
171 Northern analysis of steady-state RNA from strains expre
172 ctivity in culture supernatant fluids and by
Northern analysis of the alpha-toxin transcript.
173 Northern analysis of the BCSC-1 mRNA revealed a lack of
174 Northern analysis of the erythroid progenitor cells agai
175 Northern analysis of the gene family revealed tissue-spe
176 Northern analysis of the merR mutant revealed merA trans
177 Northern analysis of the mRNA of this protein showed abu
178 Northern analysis of the normal human foreskin keratinoc
179 Northern analysis of these derivatives reveals that each
180 Western and
northern analysis of these plants demonstrate 3- to 8-fo
181 Northern analysis of total kidney RNA or Western analysi
182 Northern analysis of total RNA isolated from rd7 mouse r
183 Digital
northern analysis of transcripts expressed near the thre
184 Northern analysis of viral RNA indicated that the E2 gen
185 Northern analysis on human tissues showed expression of
186 We have performed extensive
northern analysis on one of the potato GA 20-oxidase gen
187 profiles for several genes were verified via
northern analysis or quantitative reverse transcription-
188 , liver, lung, spleen, thymus, and testis by
Northern analysis or reverse transcription polymerase ch
189 Additionally, on Western and
Northern analysis,
oxysterol treatment increased two oth
190 nd in center masses of HCCs was evidenced by
Northern analysis,
real-time polymerase chain reaction a
191 RNA was detected by immunohistochemistry and
Northern analysis,
respectively.
192 Northern analysis revealed 4 species of CCR3 mRNA.
193 Northern analysis revealed a 2.1- to 2.7-fold increase i
194 Northern analysis revealed a marked reduction of Hydin m
195 Da is detected in extracts from embryos, and
Northern analysis revealed a single transcript of 1.3kb.
196 Northern analysis revealed expression of both U(1) and U
197 Northern analysis revealed expression of genes hybridizi
198 Northern analysis revealed high levels of human P2X(2) (
199 ASCL1 promoter-reporter assay and
Northern analysis revealed that ASCL1 reduction by NOTCH
200 Additional RACE and
Northern analysis revealed that at least five different
201 Northern analysis revealed that c-Maf expression increas
202 Electronic
northern analysis revealed that candidate genes are sign
203 Northern analysis revealed that Cyr61 was expressed high
204 Northern analysis revealed that E(2)-induced PP5 express
205 Northern analysis revealed that in these cells, fragment
206 sed for use by all 3 effector complexes, and
Northern analysis revealed that individual effector comp
207 of this gene from Drosophila cDNA panels and
Northern analysis revealed that it is expressed througho
208 Northern analysis revealed that many human tissues inclu
209 Northern analysis revealed that mmDjC7 mRNA (0.9 kb) is
210 Northern analysis revealed that PDGF blocked gene expres
211 e quantitative reverse-transcription PCR and
northern analysis revealed that PDI was induced within 3
212 Northern analysis revealed that the content of ADH4 mRNA
213 tream of the predicted lon coding region and
Northern analysis revealed that transcription of the nat
214 Northern analysis revealed that XEGIP is widely expresse
215 Further
Northern analysis revealed transcriptional alterations o
216 Northern analysis revealed two transcripts in embryonic
217 Northern analysis revealed wide expression in humans and
218 of putative hibernation-responsive genes by
Northern analysis,
revealed an increase in expression of
219 o a 2.7-kb mRNA species in NCI-H727 cells by
Northern analysis,
revealed no significant match to any
220 Northern analysis reveals a cPLA2-beta transcript of 8 k
221 Cross-species
Northern analysis reveals a mouse homolog of a similar s
222 Using this cDNA fragment as probe,
Northern analysis reveals a ubiquitously expressed trans
223 Northern analysis reveals expression of the bicistronic
224 Northern analysis reveals that BACE2 mRNA is expressed a
225 Northern analysis reveals that CYP2J5 transcripts are mo
226 Northern analysis reveals that CYP2J5 transcripts are mo
227 Northern analysis reveals that CYP2J9 transcripts are pr
228 Microarray screening coupled with
Northern analysis reveals that hRAD9 regulates the abund
229 Northern analysis reveals three mRNA species: a major tr
230 Northern analysis reveals two size classes of mRNA (1.8
231 sis revealed an increase in CPD protein, and
Northern analysis showed increased CPD mRNA upon stimula
232 Northern analysis showed increased OPN expression in the
233 ter protein in the inner medullary base, and
Northern analysis showed no change in urea transporter m
234 In mtGPAT(-/-) mice, PCR genotyping and
Northern analysis showed successful knockout of mtGPAT;
235 RT-PCR and
Northern analysis showed that CILP/NTPPH messenger RNA (
236 Northern analysis showed that corin mRNA was present in
237 Northern analysis showed that expression of vascular end
238 Northern analysis showed that homocysteine increased ste
239 RT-PCR and
Northern analysis showed that kat3 expression starts as
240 Northern analysis showed that mltC, which codes for a pe
241 Northern analysis showed that PRIP mRNA is ubiquitously
242 Northern analysis showed that Srg1 expression was marked
243 Northern analysis showed that stable, truncated transcri
244 Northern analysis showed that the addition of methionine
245 Northern analysis showed that the induction of cold-resp
246 Northern analysis showed that the NtER1 was rapidly indu
247 Northern analysis showed that transcription of faeB was
248 Northern analysis showed that, in both MIS-treated rats
249 Northern analysis showed TIP39 messenger RNA in multiple
250 Northern analysis showed Zip14 up-regulation was specifi
251 Northern analysis shows that LKLF is expressed in lung i
252 Northern analysis shows that Rad51l2 is expressed in sev
253 Northern analysis shows that TEC1 transcription is highe
254 Northern analysis shows that TSSa-RNAs are subsets of an
255 Northern analysis shows that Vav3 has a broad tissue exp
256 Northern analysis shows the active transcription of the
257 basal culture conditions as a 2.5-kb band on
Northern analysis,
similar to that observed in lymphocyt
258 Northern analysis suggested that Cu/ZnSOD gene expressio
259 RNA blot (
Northern) analysis suggested that the RD114 receptor is
260 Northern analysis suggests that faster sexual developmen
261 Northern analysis suggests the liver is a major site of
262 We also demonstrated by
Northern analysis that basal expression of micF is signi
263 We demonstrated by
Northern analysis that exposure of activated 3T3-L1 cell
264 As determined by
Northern analysis,
the expression of Gdf15 in liver was
265 ession of these miRNAs has been confirmed by
Northern analysis,
their ability to inhibit target gene
266 We used quantitative
Northern analysis to assay the transcript levels of thre
267 ferential dot blot hybridization and virtual
Northern analysis to be up-regulated by maternal nutrien
268 Here we used Affymetrix micro-array and
Northern analysis to demonstrate that two enzymes involv
269 combinational suppression, were subjected to
Northern analysis to elucidate their coding capacity.
270 s plus the 57 DD candidate cDNAs detected by
Northern analysis to facilitate data validation.
271 owed by separation on a sucrose gradient and
northern analysis,
to determine the number of ribosomes
272 For
Northern analysis,
total RNA was isolated on days 8, 12,
273 We demonstrate, by using
Northern analysis,
transactivation assays, and in vitro
274 Northern analysis using different regions of the ADPRH c
275 Northern analysis using exon-specific probes confirms th
276 xamined expression of 14 candidate asRNAs by
Northern analysis using RNA from wild-type E. coli and f
277 Northern analysis using the dog heart cDNA as a probe su
278 MCP-1 message as detected using
northern analysis was absent in uninjured brain, but was
279 To study expression patterns,
Northern analysis was carried out using an NHE3 cDNA to
280 Northern analysis was carried out using the total RNA is
281 Northern analysis was conducted to determine the express
282 Northern analysis was employed to investigate mRNA produ
283 Northern analysis was used to determine the effects of g
284 Northern analysis was used to determine the expression o
285 ion of several individual genes, measured by
Northern analysis,
was also consistent with the whole ge
286 325-bp cDNA fragment that, as determined by
Northern analysis,
was expressed at higher levels in ant
287 ifferential expression of PMCA, evaluated by
Northern analysis,
was found to have more than a 4.6-fol
288 Using
Northern analysis we showed a 5-6 fold increase in the l
289 By reverse transcription-PCR and
Northern analysis,
we demonstrated expression of these O
290 By genome array and
Northern analysis,
we found that genes encoding the tran
291 expression assays, equilibrium dialysis, and
northern analysis,
we show that the yybP-ykoY motif resp
292 y, nine asRNAs detected as distinct bands by
Northern analysis were differentially affected by the rn
293 njunction with RNA amplification and reverse
Northern analysis,
were used to confirm the gene express
294 transcription-polymerase chain reaction and
Northern analysis,
where antisense messages were detecte
295 sue distribution of GLUT10 was determined by
Northern analysis,
which revealed highest levels of expr
296 ribution of FCAP expression was mapped using
Northern analysis,
whole-mount in situ hybridization, an
297 Northern analysis with an Ov/Br septin 3' UTR probe reve
298 Northern analysis with probes from the remaining five be
299 c genomic RNA that was readily detectable by
northern analysis within 4 days of transfection into Huh
300 hia coli cells that can be used directly for
northern analysis without any further purification.