A Highly Efficient Escherichia coli-Based Chromosome Engineering System Adapted for Recombinogenic Targeting and Subcloning of BAC DNA
Top Cited Papers
- 1 April 2001
- Vol. 73 (1), 56-65
- https://doi.org/10.1006/geno.2000.6451
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Targeted Mutagenesis of the Endogenous Mouse Mis Gene PromoterCell, 1999
- Rapid modification of bacterial artificial chromosomes by ET- recombinationNucleic Acids Research, 1999
- Efficient and precise engineering of a 200 kb β-globin human/bacterial artificial chromosome in E. coli DH10B using an inducible homologous recombination systemGene Therapy, 1999
- Generalized lacZ expression with the ROSA26 Cre reporter strainNature Genetics, 1999
- Improved properties of FLP recombinase evolved by cycling mutagenesisNature Biotechnology, 1998
- Methods for generating precise deletions and insertions in the genome of wild-type Escherichia coli: application to open reading frame characterizationJournal of Bacteriology, 1997
- Functional Identification of the Mouse Circadian Clock Gene by Transgenic BAC RescueCell, 1997
- Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.Proceedings of the National Academy of Sciences, 1992
- Neuron Specific Enolase, A Clinically Useful Marker for Neurons and Neuroendocrine CellsAnnual Review of Neuroscience, 1987
- Cosmid DNA packaging in vivoGene, 1982