Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

28 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
In vitro insertional mutagenesis with a selectable DNA fragment.
Prentki P, Krisch HM. Prentki P, et al. Gene. 1984 Sep;29(3):303-13. doi: 10.1016/0378-1119(84)90059-3. Gene. 1984. PMID: 6237955
Sequence analysis and transcription of the apxI operon (hemolysin I) from Actinobacillus pleuropneumoniae.
Frey J, Haldimann A, Nicolet J, Boffini A, Prentki P. Frey J, et al. Among authors: prentki p. Gene. 1994 May 3;142(1):97-102. doi: 10.1016/0378-1119(94)90361-1. Gene. 1994. PMID: 8181764
A modified pBR322 vector with improved properties for the cloning, recovery, and sequencing of blunt-ended DNA fragments.
Prentki P, Krisch HM. Prentki P, et al. Gene. 1982 Feb;17(2):189-96. doi: 10.1016/0378-1119(82)90072-5. Gene. 1982. PMID: 6282713
The plasmid cloning vector pBR325 contains a 482 base-pair-long inverted duplication.
Prentki P, Karch F, Iida S, Meyer J. Prentki P, et al. Gene. 1981 Sep;14(4):289-99. doi: 10.1016/0378-1119(81)90161-x. Gene. 1981. PMID: 6271628
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 …
Omegon-Km: a transposable element designed for in vivo insertional mutagenesis and cloning of genes in gram-negative bacteria.
Fellay R, Krisch HM, Prentki P, Frey J. Fellay R, et al. Among authors: prentki p. Gene. 1989;76(2):215-26. doi: 10.1016/0378-1119(89)90162-5. Gene. 1989. PMID: 2546859
Nucleotide sequence of the classical lacZ deletion delta M15.
Prentki P. Prentki P. Gene. 1992 Dec 1;122(1):231-2. doi: 10.1016/0378-1119(92)90056-u. Gene. 1992. PMID: 1339377 No abstract available.
Plasmid vectors for selecting IS1-promoted deletions in cloned DNA: sequence analysis of the omega interposon.
Prentki P, Binda A, Epstein A. Prentki P, et al. Gene. 1991 Jul 15;103(1):17-23. doi: 10.1016/0378-1119(91)90385-o. Gene. 1991. PMID: 1652541
Functional promoters created by the insertion of transposable element IS1.
Prentki P, Teter B, Chandler M, Galas DJ. Prentki P, et al. J Mol Biol. 1986 Oct 5;191(3):383-93. doi: 10.1016/0022-2836(86)90134-8. J Mol Biol. 1986. PMID: 3029382
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 rem …
This processing of the gene 32 mRNA was observed in RNase III or P-deficient strains of Escherichia coli. However, after infection of …
28 results
Jump to page
Feedback