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1 the DUTT1 gene (-244 to +27 relative to the translation start site).
2 es at position -29 to -32 (counting from the translation start site).
3 le strains (86 nucleotides upstream from the translation start site).
4 ides -344 and -242 (numbered relative to the translation start site).
5 ween nucleotides -161 and -3 (in relation to translation start site).
6 normally generated by use of an alternative translation start site.
7 tional start site lies 75 bp upstream of the translation start site.
8 itiation approximately 27 bp upstream of the translation start site.
9 e initiates at position -203 relative to the translation start site.
10 onfirmed approximately 100bp upstream of the translation start site.
11 -bp fragment is located 58 bp 5' of the ptxS translation start site.
12 r (EE), located 3 kb upstream from the Hoxc8 translation start site.
13 sent between 1800 and 1100bp upstream of the translation start site.
14 art site approximately 112bp upstream of the translation start site.
15 , which is located 450bp upstream of the ATG translation start site.
16 towards a region 100-420 bp upstream of the translation start site.
17 base pairs -2,373 and -2,316 relative to the translation start site.
18 he promoter element that splice near the ATG translation start site.
19 ion site 264 base pairs (bp) upstream of the translation start site.
20 ome assembly onto mRNAs and selection of the translation start site.
21 proximately 650 base pairs upstream from the translation start site.
22 cation of cDNA ends were used to confirm the translation start site.
23 as been mapped to 478 bp upstream of the ATG translation start site.
24 which the second nucleotide of exon 2 is the translation start site.
25 transversion at position -94 relative to the translation start site.
26 approximately -793 and -268 upstream of the translation start site.
27 ating approximately 204 bp upstream from the translation start site.
28 very divergent and this aids in locating the translation start site.
29 37 kDa proteins that arise from a single AUG translation start site.
30 , which extends 4.8 kb upstream from the ATG translation start site.
31 G transversion that occurs 61 bp before the translation start site.
32 , are 176 and 170 base pairs upstream of the translation start site.
33 and -158 to -116 (43-bases), upstream of the translation start site.
34 ite is only 13 bp upstream from the putative translation start site.
35 l sequence of zipper protein to the apparent translation start site.
36 a 55-bp intron which is located close to the translation start site.
37 in their leader sequence but share a common translation start site.
38 s at 66, 69, and 96 base pairs 5' of the ATG translation start site.
39 ted within the coding region 71 bp after the translation start site.
40 beginning 2,214 nt upstream from the PDE3A1 translation start site.
41 al hundred base pairs upstream of the Rv1813 translation start site.
42 activity of NOL7 were 560 bp upstream of its translation start site.
43 arby sites, -367 and -364 bp upstream of the translation start site.
44 n several hundred base pairs upstream of the translation start site.
45 irs (bp) and its locations coincide with the translation start site.
46 ps to a position downstream of the predicted translation start site.
47 se element (CRE) 965 bp upstream of the CD1A translation start site.
48 tion initiation site 86 bp upstream from the translation start site.
49 ACE to a region 19 kb upstream of the ZFP106 translation start site.
50 n intron 2, yielding a protein with a unique translation start site.
51 s present approximately 2 kb upstream of the translation start site.
52 located at -1371 kb upstream of the Cyp2c29 translation start site.
53 kDa isoform, C/EBPalphap30, from an internal translation start site.
54 al promoter region to 321 bp upstream of the translation start site.
55 s required for oncogene silencing included a translation start site.
56 tream AUG in exon III as the first available translation start site.
57 226, -201, -146, and -102 bp relative to the translation start site.
58 tion is initiated from a conserved, intronic translation start site.
59 ites with a major site 51 nt upstream of the translation start site.
60 cription-initiation site 64 bp 5' of the ATG translation-start site.
61 uced ribosome stalling, which causes bias at translation start sites.
62 ne identification systems at finding precise translation start sites.
63 ular compartments via the use of alternative translation start sites.
64 gene; 1352 nucleotides separate the putative translation start sites.
65 gions, which are shown to be higher close to translation start sites.
66 li encodes two proteins from in-frame tandem translation start sites.
67 ulatory promoter located upstream of the CD5 translation start sites.
68 on approximately 1 kb 5' upstream of the ATG translation starting site.
70 -kb DNA fragment immediately upstream of the translation start site (-1300 to +1 bp, with the transla
71 on of 830 bp located 1986 bp upstream of the translation start site (1389 bp upstream of the transcri
72 structure of the USH3 gene, including a new translation start site, 5' untranslated region, and a tr
73 d PTEN-Long, that arises from an alternative translation start site 519 base pairs upstream of the AT
75 und between 1500 and 2186 bp upstream of the translation start site, a region that contains 1 consens
76 enced the iaaM oncogene, but deletion of the translation start site abolished the ability of the tran
77 tion site was identified upstream of the GLI translation start site along with three minor transcript
78 ription start site 27 bp upstream of the UUG translation start site and a minor transcription start s
79 nd placenta 250 and 249 bp upstream from the translation start site and a second major site at -100 b
80 TTATA-3') was located 110 bp upstream of the translation start site and appeared to be used for both
81 genomic DNA fragment upstream from the RFC1 translation start site and determined the nucleotide seq
82 hat lack the periostin gene and replaced the translation start site and first exon with a lacZ report
83 e oligodeoxynucleotides directed against the translation start site and first intron-exon splice junc
84 f sid1 mapped within 1043 bp upstream of the translation start site and include the first untranslate
86 stis transcripts regulate both the choice of translation start site and the efficiency of translation
87 isense oligonucleotides directed against the translation start site and the intron 7-8 splice donor s
89 ces immediately upstream and downstream of a translation start site and to detect the contrasting non
90 -A exchange 571 base pairs upstream from the translation start site and was present between consensus
91 erevisiae RAD52 gene contains five potential translation start sites and protein-blot analysis typica
92 nscription start site 517 bp upstream of the translation start site, and anchored PCR was performed t
93 TCGN5CGA-3' binding site within 200bp of the translation start site, and pksA and ver1 had an additio
94 itiation site approximately 116 bp 5' to the translation start site, and sequences extending to -141
95 sequence indicated an incorrectly predicted translation start site, and the corrected full-length Dt
96 ermini (105 were novel potential alternative translation start sites, and 2180 represented stable pro
97 element, the 5' untranslated region, and the translation start site are comparable in strength of the
100 ether, our results indicate that alternative translation start sites are used to generate Egr3 isofor
101 the other at -1239 to -1039, relative to the translation start site) are implicated in RANKL-induced
102 ense RNA that overlaps the transcription and translation start sites as well as the first splice dono
106 at-containing transcripts that do not have a translation start site (AUG) but contain an open-reading
107 ariations were found within 1.4 kb 5' to the translation start site between the inbred lines A/J, C57
109 hionine codons that could potentially act as translation start sites, but most mSGY protein synthesis
110 hat the fragments originate from alternative translation start sites, but their precise origin is unk
112 dentification of the S. pneumoniae RNase HII translation start site by amino-terminal sequencing of t
113 a position 152 nucleotides upstream from the translation start site by rapid amplification of cDNA en
114 om -1640 to -1287 base pairs upstream of the translation start site containing a cAMP-response elemen
116 bp or from -2312 to -10 bp (relative to the translation start site) could function as a promoter in
117 an Ik-binding site at -378 to -374 (with the translation start site designated as +1) in the mouse do
118 slation start site (-1300 to +1 bp, with the translation start site designated as +1) of the mouse DO
119 orpholino oligonucleotide (MO) targeting the translation start site die at approximately the midblast
120 DNA sequences immediately upstream of the translation start site direct expression of the beta-glu
121 in vivo experiments showed that alternative translation start sites direct the At5g32470 protein to
122 rom positions -3231 to -118 (relative to the translation start site) directed high-level expression i
123 e epitopes occurs primarily from alternative translation start sites downstream of the stop codon.
124 of the region between the transcription and translation start sites (downstream segment) was investi
125 ription start site 1594 bp upstream from the translation start site due to an intervening intron.
126 ntisense reagents complementary to the IGF1R translation start site enhance radio- and chemosensitivi
127 e located 34 nucleotides upstream of the ATG translation start site for nifH2, and a sequence resembl
128 sequence upstream of the rat cyclin B1 gene translation start site from Rattus norvegicus liver geno
131 of upstream NF-kappa B site (-533 bases from translation start site) had no effect on thrombin respon
137 n antisense oligonucleotide beginning at the translation start site in PCNA mRNA was effective in inh
138 presented by position -92 to -43 nt from the translation start site in the extended AS mRNA 5'-UTRs p
139 uanine-rich sequences positioned adjacent to translation start sites in 5'-untranslated regions (5'-U
141 APs from diverse lineages and is enriched at translation start sites in both E. coli and Bacillus sub
145 ocated between -318 and -237 relative to the translation start site is required for constitutive FasL
146 s indicate that 331 bp upstream of the HSF-1 translation start site is required for maximal basal exp
147 both isoforms is determined by which of two translation start sites is used, and only those isoforms
151 tisense oligonucleotide targeted against the translation start site of DLX-7 mRNA to inhibit its expr
153 , A or C at position 1002 numbering from the translation start site of Ik-1) within our Ikaros clones
154 promoter element immediately upstream of the translation start site of the gene, which mediated these
156 A putative promoter region located 5' of the translation start site of the human chk-alpha gene was c
157 consequence of the sequence information, the translation start site of this open reading frame has be
158 ant enrichment in the phyA transcription and translation start sites of not only H3K9/14ac and H3K27a
159 h antisense oligonucleotide sequences to the translation start sites of PKC-alpha, -beta, -gamma, -de
160 oxynucleotides (AsODNs) targeted against the translation start sites of the Kv alpha subunits Kv1.2,
162 gulatory region (P268, -444 to -177 from the translation start site) of the pea plastocyanin gene (Pe
163 tep is when the ribosomal subunits join at a translation start site on a messenger RNA to form a func
165 Moreover, the motif overlapped with the translation start sites on the plus strand of a group of
167 nstream NF-kappa B site (-223 bases from the translation start site) prevented the activation of ICAM
168 n, which removes most of smn-1 including the translation start site, produces a pleiotropic phenotype
172 Analysis of the sequence upstream of the translation start site revealed several potential Sp1-bi
173 the 5' sequences upstream of the predicated translation start sites revealed a substantial enrichmen
174 n the coding region named cHP is involved in translation start site selection as well as RNA replicat
177 re in the capsid coding region (cHP) directs translation start site selection in human and mosquito c
178 yA signals, Kozak sequences at the annotated translation start site, start codons and stop codons, co
179 tion reading frames, each driven by distinct translation start sites, start site selection of individ
181 erited mutation located close to the protein translation start site that is thought to produce a shor
182 asepairs immediately upstream of each gene's translation start site (the upstream control region (UCR
183 broad roles for mRNA context in programming translation start sites, the rate of translation elongat
184 from nucleotide -1373 to -3 (relative to the translation start site) to a luciferase reporter gene.
185 t a 1000-bp DNA fragment upstream of the ATG translation start site (TSS) had promoter activity in re
187 genome walking upstream of the canine MMP-9 translation start site using canine genomic DNA as templ
189 nscription initiation 201 bp upstream of the translation start site was found by RNase protection and
190 equences downstream of the first CAV protein translation start site was found to have significantly l
191 ive stem-loop 31 nucleotides upstream of the translation start site was required for Cgi system funct
192 (from position -222 to +102 relative to the translation start site) was replaced by plasmid sequence
193 h were focused around the phyA transcription/translation start sites, were detected within 1 h of dee
194 e region 176 to 147 bp upstream from the ATG translation start site where there are normally 5 Sp1 bi
195 een nucleotides -122 and -56 upstream of the translation start site which contains a consensus Sp1 bi
196 ical initiator methionine codon is used as a translation start site, which we term downstream ATI (dA
197 luorescent protein or CD40L) upstream of the translation start site within exon 1 allowed transgene e
198 examined approximately 2 kb upstream of the translation start site within humans and non-human prima
200 ciani et al. recently identified an internal translation start site within the M(2) receptor mRNA, di
202 be truncated to 600 bp long relative to the translation start site without affecting expression.