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1 tained random sequences of 9 or 18 nt in the intercistronic region.
2 e 5' leader sequence of the CLN3 mRNA in the intercistronic region.
3 having translated the uORF despite the short intercistronic region.
4 ependent attenuator located in the tyrS-pdxY intercistronic region.
5 iption terminator element located within the intercistronic region.
6 n, are present in the pyrR-pyrP or pyrP-pyrB intercistronic regions.
7 e utilization phenotype lay in the abgR-abgA intercistronic region and appeared to allow the expressi
9 yrP gene encoding a uracil permease, a 13-nt intercistronic region, and the pyrB gene encoding aspart
10 other internal promoter lay in the secG-yvaK intercistronic region, and this activity (P(B)) was depe
11 olytic processing in the 3' untranslated and intercistronic regions, and sites within the coding regi
12 found at the Shine-Dalgarno sequences and in intercistronic regions are processed with higher efficie
15 ate the presence of an extra promoter in the intercistronic region, creating what has been termed a "
16 this method, the presence of an IRES in the intercistronic region facilitates the translation of Gal
21 resence of the TEV 5' leader sequence in the intercistronic region increased expression of the second
22 uced the 5'-UTR of mouse Kv1.4 mRNA into the intercistronic region of a bicistronic vector containing
23 leader, as well as the common exon into the intercistronic region of a dicistronic luciferase constr
24 number of copies of this IRES module in the intercistronic region of a dicistronic mRNA strongly enh
25 otes internal initiation when present in the intercistronic region of a dicistronic mRNA, indicating
26 translation in vivo even when present in the intercistronic region of a discistronic mRNA, indicating
30 Here, we report mutational analysis of the intercistronic region of this operon by linker scan anal
31 Furthermore, this element is predicted in intercistronic regions of numerous operons of C. elegans
32 protein for the operon, a 39-nucleotide (nt) intercistronic region, the pyrP gene encoding a uracil p
33 licing is exclusively to SL1 and there is no intercistronic region; the polyadenylation signal is onl
34 ond cistron and 18 random nucleotides in the intercistronic region was introduced into a yeast strain
35 -ctaC'-lacZ fusion (containing the ctaB-ctaC intercistronic region) was placed at a remote nonessenti
36 rter containing the GATA-4 5'-UTR within the intercistronic region, we demonstrate that this leader s
37 rs MgrA and NorG and shares a 420-nucleotide intercistronic region with the divergently transcribed p
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