A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae. (original) (raw)
Nucleic Acids Res. 1993 Jul 11; 21(14): 3329–3330.
Centre de Génétique Moléculaire du Centre National de la Recherche Scientifique, Laboratoire Propre Associé à l'Université Pierre-et-Marie-Curie, Gif-sur-Yvette, France.
Full text
Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (231K), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Oliver SG, van der Aart QJ, Agostoni-Carbone ML, Aigle M, Alberghina L, Alexandraki D, Antoine G, Anwar R, Ballesta JP, Benit P, et al. The complete DNA sequence of yeast chromosome III. Nature. 1992 May 7;357(6373):38–46. [PubMed] [Google Scholar]
- Gietz D, St Jean A, Woods RA, Schiestl RH. Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Res. 1992 Mar 25;20(6):1425–1425. [PMC free article] [PubMed] [Google Scholar]
- Struhl K. Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8419–8423. [PMC free article] [PubMed] [Google Scholar]
Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press