Jeanne Boyer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Jeanne Boyer has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Agnès Thierry
Department of Genomes and Genetics, Institut Pasteur, CNRS UMR3525, F75724 Paris, France
1 shared publication - Bernard Dujon
Department of Genomes and Genetics, Institut Pasteur, CNRS UMR3525, F75724 Paris, France
1 shared publication - Christophe Hennequin
Unité de Génétique Moléculaire des Levures (URA2171 CNRS and UFR 927 Université Pierre et Marie Curie)
1 shared publication - Cécile Fairhead
Université Paris-Sud XI, CNRS UMR 8621, Institut de Génétique et Microbiologie, Orsay, France
1 shared publication - Emmanuel Talla
Unité de Génétique Moléculaire des Levures (URA2171 CNRS and UFR 927 Université Pierre et Marie Curie)
1 shared publication - Emmanuelle Fabre
Université Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, Paris, France
1 shared publication
Latest Publications
- Open Access
- 31 August 2004
- Published by Springer Nature in Genome Biology
- Vol. 5 (9) , R72
Large-scale exploration of growth inhibition caused by overexpression of genomic fragments in Saccharomyces cerevisiae
We have screened the genome of Saccharomyces cerevisiae for fragments that confer a growth-retardation phenotype when overexpressed in a multicopy plasmid with a tetracycline-regulatable (Tet-off) promoter. We selected 714 such fragments with a mean size of 700 base-pairs out of around 84,000 clones tested. These include 493 in-frame open reading frame fragments corresponding to 454 distinct genes (of which 91 are of unknown function), and 162 out-of-frame, antisense and intergenic genomic fragments, representing the largest collection of toxic inserts published so far in yeast.
- 31 August 2004
- Published by Springer Nature in Genome Biology
- Vol. 5 (9) , R72
Open AccessLarge-scale exploration of growth inhibition caused by overexpression of genomic fragments in Saccharomyces cerevisiae
We have screened the genome of Saccharomyces cerevisiae for fragments that confer a growth-retardation phenotype when overexpressed in a multicopy plasmid with a tetracycline-regulatable (Tet-off) promoter. We selected 714 such fragments with a mean size of 700 base-pairs out of around 84,000 clones tested. These include 493 in-frame open reading frame fragments corresponding to 454 distinct genes (of which 91 are of unknown function), and 162 out-of-frame, antisense and intergenic genomic fragments, representing the largest collection of toxic inserts published so far in yeast.