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Artificial transposable elements in the study of the ends of IS1.
Prentki P, Pham MH, Gamas P, Chandler M, Galas DJ. Prentki P, et al. Gene. 1987;61(1):91-101. doi: 10.1016/0378-1119(87)90368-4. Gene. 1987. PMID: 2832256
We have constructed artificial IS1-based transposons by attaching synthetic oligodeoxynucleotides, corresponding to the sequence of the ends of IS1, to a selectable DNA segment ['omega' fragment; Prentki and Krisch, Gene 29 (1984) 303-313]. ...
We have constructed artificial IS1-based transposons by attaching synthetic oligodeoxynucleotides, corresponding to the sequence of the ends …
Processing of unstable bacteriophage T4 gene 32 mRNAs into a stable species requires Escherichia coli ribonuclease E.
Mudd EA, Prentki P, Belin D, Krisch HM. Mudd EA, et al. Among authors: Prentki P. EMBO J. 1988 Nov;7(11):3601-7. EMBO J. 1988. PMID: 3061803 Free PMC article.
This processing of the gene 32 mRNA was observed in RNase III or P-deficient strains of Escherichia coli. However, after infection of an RNase E-deficient strain, the amount of processed transcript was significantly reduced while the levels of the precursor transcripts remained high. ...
This processing of the gene 32 mRNA was observed in RNase III or P-deficient strains of Escherichia coli. However, after infection of …
Incompatibility between pSC101 and lambda dv replicons.
Ekaterinaki N, Prentki P. Ekaterinaki N, et al. Among authors: Prentki P. Res Microbiol. 1991 May;142(4):381-7. doi: 10.1016/0923-2508(91)90107-l. Res Microbiol. 1991. PMID: 1831282
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