1 ption for the ARR5 gene was identified using
primer extension analysis.
2 from the ATG translation initiation site by
primer extension analysis.
3 tes of both xenA and xenB were identified by
primer extension analysis.
4 omoter could be mapped 5' to ureI (PureI) by
primer extension analysis.
5 is result was confirmed by single-nucleotide
primer extension analysis.
6 ranscription initiation were established via
primer extension analysis.
7 he transcription start site was mapped using
primer extension analysis.
8 coli, and cleavage sites were identified by
primer extension analysis.
9 ied all three transcriptional start sites by
primer extension analysis.
10 cription start sites for each gene mapped by
primer extension analysis.
11 transcriptional start site was identified by
primer extension analysis.
12 oriented phzA and phzR genes were mapped by
primer extension analysis.
13 f salA, syrP, and syrB1, respectively, using
primer extension analysis.
14 r the qsc1 and qsc2 operons and for glyA via
primer extension analysis.
15 of the heme utilization genes were mapped by
primer extension analysis.
16 transcription start site were determined by
primer extension analysis.
17 acterized by Northern blot hybridization and
primer extension analysis.
18 iation codon was identified and confirmed by
primer extension analysis.
19 or mntH in B. abortus 2308 was determined by
primer extension analysis.
20 expression were determined by lac fusion and
primer extension analysis.
21 e primary transcription start site mapped by
primer extension analysis.
22 coli DH5 alpha background, as determined by
primer-extension analysis.
23 Using
primer extension analysis,
a putative, proximal, nitroge
24 Based on
primer extension analysis,
a single cap site is located
25 Primer extension analysis and 5'-rapid amplification of
26 Primer extension analysis and 5'-rapid amplification of
27 rs, designated P1 and P2, were identified by
primer extension analysis and are located 288 and 173 bp
28 Primer extension analysis and investigation of mRNA from
29 Primer extension analysis and Northern hybridization wit
30 Both
primer extension analysis and promoter fusion studies sh
31 Using
primer extension analysis and reporter assays, we show t
32 Primer extension analysis and RNase protection assays re
33 nscription initiation site was identified by
primer extension analysis and S1 nuclease mapping.
34 Primer extension analysis and S1 nuclease protection exp
35 Primer extension analysis and site-directed mutagenesis
36 art site of the VLCAD gene was determined by
primer extension analysis and the overlapping structure
37 he B. burgdorferi lon gene was identified by
primer extension analysis and the potential promoter did
38 were previously identified in HL-60 cells by
primer extension analysis and were observed to increase
39 Primer-extension analysis and Northern blotting of total
40 scriptional start site of fegA was mapped by
primer extension analysis,
and a putative Fur-binding si
41 anscription initiation site as determined by
primer extension analysis,
and a putative polyadenylatio
42 By 5' rapid amplification of cDNA ends,
primer extension analysis,
and nuclease protection assay
43 The transcription start site is defined by
primer extension analysis,
and the 5'-flanking region ha
44 gene transcription start site was mapped by
primer extension analysis,
and the activity of the IGRP
45 (selective 2'-hydroxyl acylation analyzed by
primer extension) analysis,
and toeprinting, we found th
46 he promoter for the che operon was mapped by
primer extension analysis as well as by the construction
47 ysis of site-specific mutations coupled with
primer extension analysis authenticated the sigma(N)-dep
48 We examined
primer extension analysis by matrix-assisted laser desor
49 Primer extension analysis confirmed that cotB mRNA incre
50 Primer extension analysis confirmed that P1 is the cAMP
51 Northern blotting and
primer extension analysis defined the tsp for each gene
52 Primer extension analysis demonstrated that the transcri
53 Primer extension analysis demonstrated the presence of a
54 Primer extension analysis detected a transcript that cou
55 Primer extension analysis determined that fimW transcrip
56 Primer extension analysis determined that the transcript
57 ear-consensus promoter upstream of mcp1, and
primer extension analysis employing T. pallidum RNA reve
58 Primer extension analysis has identified a major transcr
59 Primer extension analysis identified a consensus sigma70
60 Primer extension analysis identified a late promoter mot
61 Primer extension analysis identified a major transcripti
62 Primer extension analysis identified a number of potenti
63 Primer extension analysis identified a promoter consensu
64 Primer extension analysis identified a promoter upstream
65 Primer extension analysis identified a putative promoter
66 5'-flanking region have been sequenced, and
primer extension analysis identified a single major tran
67 Primer extension analysis identified a transcription sta
68 Primer extension analysis identified a transcriptional s
69 Primer extension analysis identified a transcriptional s
70 Primer extension analysis identified a transcriptional s
71 Primer extension analysis identified a transcriptional s
72 Primer extension analysis identified an apparent transcr
73 Primer extension analysis identified single or multiple
74 Primer extension analysis identified the 5' end of a tra
75 Primer extension analysis identified the presence of a s
76 Primer extension analysis identified the transcriptional
77 Primer extension analysis identified two adjacent transc
78 Primer extension analysis identified two rpoS transcript
79 Primer extension analysis identified two transcription s
80 ription assays, using a plasmid template and
primer extension analysis,
identified three major dad tr
81 A
primer extension analysis identifies a single transcript
82 es of the two promoters were demonstrated by
primer extension analysis,
in vitro transcription experi
83 Nuclease protection analysis and
primer extension analysis indicate no aberrant transcrip
84 Reverse transcriptase PCR and
primer extension analysis indicate that both lgtF and rf
85 Primer extension analysis indicated one transcription st
86 Quantitative
primer extension analysis indicated that cbt1 null strai
87 Primer extension analysis indicated that the ccmK, rbcL
88 Primer extension analysis indicated that the stem-loop s
89 Primer extension analysis indicated that these AGAT repe
90 Primer extension analysis indicated that transcription i
91 Primer extension analysis indicated that xylF transcript
92 Primer extension analysis indicated two transcriptional
93 Primer extension analysis indicates that sigX transcript
94 Primer extension analysis indicates that the A. aegypti
95 Primer extension analysis indicates that the mgc1 RNA st
96 Primer extension analysis indicates that transcription s
97 anomalous assignment for the start site when
primer extension analysis is used.
98 Primer extension analysis localized an iron-regulated tr
99 Primer extension analysis localized one promoter for the
100 Primer extension analysis localized two transcription in
101 Primer extension analysis located a single transcription
102 Primer extension analysis located the transcription star
103 Primer extension analysis mapped the transcriptional sta
104 When HBV RNAs were examined by
primer extension analysis,
novel core- and precore-speci
105 Primer extension analysis of 16S rRNA fragments revealed
106 start sites of the RC24 gene were mapped by
primer extension analysis of both rice native RNA and in
107 Primer extension analysis of C/EBP-epsilon mRNA detected
108 Primer extension analysis of cloned PCR fragments found
109 Primer extension analysis of E. coli revealed the presen
110 th defects in swimming motility coupled with
primer extension analysis of flagellar and chemotaxis tr
111 Primer extension analysis of ftpA confirmed the lack of
112 High-resolution
primer extension analysis of hem mRNA reveals the presen
113 transcription start sites were identified by
primer extension analysis of human brain and lymphoblast
114 Primer extension analysis of intron-containing transcrip
115 transposons, and retroposons were applied to
primer extension analysis of kidney poly(A) mRNA.
116 Primer extension analysis of merA mRNA predicted a nonca
117 Primer extension analysis of mRNAs prepared from batch-g
118 Primer extension analysis of RNA extracted from circulat
119 Primer extension analysis of RNA from cultures that were
120 Primer extension analysis of RNA from wild-type classica
121 Primer extension analysis of RNA isolated from growing,
122 e 5' end of the transcript was determined by
primer extension analysis of RNA isolated from HK022 lys
123 ion start point (tsp) of KOR-3 was mapped by
primer extension analysis of RNAs synthesized either in
124 The transcription start point, defined by
primer extension analysis of schistosome RNA, begins at
125 Using
primer extension analysis of several test mRNAs, we show
126 In this report,
primer extension analysis of splicing intermediates was
127 Primer extension analysis of spx RNA shows the same addi
128 Primer extension analysis of the asr transcript revealed
129 ression of a downstream bcp-lacZ fusion, and
primer extension analysis of the bcp promoter region dem
130 , and examined the accumulation of fbpA mRNA
Primer extension analysis of the fbpA promoter region in
131 Primer extension analysis of the fleQ transcript reveale
132 Primer extension analysis of the gcvR promoter region id
133 Primer extension analysis of the gene revealed two major
134 re promoter activity is further confirmed by
primer extension analysis of the HBV core RNAs, showing
135 Primer extension analysis of the hemR gene revealed that
136 Primer extension analysis of the mlp mRNA transcripts su
137 Primer extension analysis of the mRNA from genes associa
138 Promoter resections and
primer extension analysis of the repABC promoter region
139 Primer extension analysis of the rot promoter revealed a
140 Pulse-chase, Northern, and
primer extension analysis of the rRNA biosynthetic pathw
141 Selective 2'-hydroxyl acylation analyzed by
primer extension analysis of the secondary structure of
142 Primer extension analysis of this region with mouse live
143 Primer extension analysis of this upstream region in two
144 Primer extension analysis of total RNA from infected cel
145 Primer extension analysis of transcripts from the psbD-L
146 Primer extension analysis of yolk sac, fetal liver and b
147 tion site of the TASR gene was determined by
primer extension; analysis of the TASR promoter revealed
148 Primer extension analysis placed the transcriptional sta
149 Primer-extension analysis reported here indicates that i
150 Primer extension analysis revealed a common major transc
151 Primer extension analysis revealed a major transcription
152 Primer extension analysis revealed a putative transcript
153 Primer extension analysis revealed an unusual promoter r
154 Primer extension analysis revealed four putative transcr
155 Primer extension analysis revealed multiple transcriptio
156 Primer extension analysis revealed multiple transcriptio
157 Primer extension analysis revealed one major transcripti
158 Primer extension analysis revealed that during both oxid
159 Primer extension analysis revealed that MazF-cd cleaved
160 Primer extension analysis revealed that one of these ope
161 Primer extension analysis revealed that the B. subtilis
162 Nevertheless, in both P- and P+ cells,
primer extension analysis revealed that the same four ma
163 The S1-nuclease mapping and
primer extension analysis revealed that there is a singl
164 RT-PCR and
primer extension analysis revealed that this gene cluste
165 Primer extension analysis revealed the presence of two c
166 Primer extension analysis revealed the transcription sta
167 wo types of AhpC mutants were identical, and
primer extension analysis revealed their transcription s
168 Primer extension analysis revealed two closely spaced tr
169 egments derived from this genomic region and
primer-extension analysis revealed the presence of a sec
170 cZ-alb and lacZ-sbo gene fusions, along with
primer extension analysis,
revealed that the sbo-alb gen
171 Primer extension analysis reveals that increasing concen
172 Reverse transcription
primer extension analysis reveals that rRNA extracted fr
173 Our
primer extension analysis reveals the existence of two t
174 However, our data from
primer extension analysis,
S1 nuclease mapping, beta-gal
175 Primer extension analysis showed that both promoters ove
176 Primer extension analysis showed that for plasmids conta
177 ion of a plasmid containing rDNA followed by
primer extension analysis showed that overexpression of
178 Primer extension analysis showed that RNA 5' ends mappin
179 Both Northern blot and
primer extension analysis showed that the polymerase res
180 Quantitative
primer extension analysis showed that the promoter from
181 Slot blot hybridization experiments and
primer extension analysis showed that transcription of t
182 The
primer extension analysis showed the presence of a putat
183 ach other was consistent with the results of
primer extension analysis showing a greater multiple and
184 Primer extension analysis shows that Bm1 repeats are tra
185 Primer extension analysis supported the use of putative
186 By using a cspD-lacZ fusion and
primer extension analysis,
the expression of cspD was fo
187 Using
primer extension analysis,
the promoter of the nag opero
188 Based on reverse transcription-PCR and
primer extension analysis,
this flaA homolog and five ch
189 malA transcription start site was located by
primer extension analysis to a guanine residue 8 bp 5' o
190 the llal 6.9 kb transcript was determined by
primer extension analysis to be 254 bp upstream from the
191 were identified by cDNA cloning and used for
primer extension analysis to compare the basal and stres
192 virus RNA from purified components and used
primer extension analysis to confirm the fidelity of 48S
193 We utilized
primer extension analysis to demonstrate that the diverg
194 Here we employ
primer extension analysis to identify the transcriptiona
195 We used
primer extension analysis to map the transcriptional sta
196 e transcription start site was determined by
primer-extension analysis to be 69bp upstream of the tra
197 Primer extension analysis uncovered a second intergenic
198 ative promoter element was identified by RNA
primer extension analysis upstream of the ABCD operon, w
199 Primer extension analysis using 1A and 1B gene-specific
200 S) of the MMV FLt promoter was determined by
primer extension analysis using total RNA isolated from
201 Primer extension analysis using two 30-mer oligonucleoti
202 Primer extension analysis,
using two primers simultaneou
203 Quantitative
primer extension analysis verified the induction of indi
204 Selective 2'-hydroxyl acylation analyzed by
primer extension analysis was consistent with a 13-base
205 Primer extension analysis was performed with synthetic n
206 Primer extension analysis was used to determine transcri
207 Primer extension analysis was used to identify the putat
208 Primer extension analysis was used to map the transcript
209 transcription initiation site, determined by
primer extension analysis,
was 169 nucleotides upstream
210 ratio of P2 to P1 transcripts, determined by
primer extension analysis,
was high for the strong rrnO
211 By using
primer extension analysis we identified the fabH promote
212 By using fusions to lacZ and
primer extension analysis,
we found that six of the seve
213 Through
primer extension analysis,
we found that the transcripti
214 By
primer extension analysis,
we have determined the transc
215 Using
primer extension analysis,
we identified two potential t
216 ined full-length antigenome and mRNA, and by
primer extension analysis,
which examined antigenome and
217 cross-link site on TAR RNA was determined by
primer extension analysis,
which revealed that Asp41 of
218 Primer extension analysis with E. coli RNA from five M.
219 Primer extension analysis with NIH3T3 cells revealed sta
220 Primer extension analysis with poly(A)+ RNA from culture
221 Primer extension analysis with total RNA from NIH3T3 cel