A rapid and simple method for inactivating chromosomal genes in Yersinia (Q41465604)

1 October 2017

A rapid and simple method for inactivating chromosomal genes in Yersinia (English)

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1 October 2017

4

Jean Marc Ghigo

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1 October 2017

Anne Derbise

1

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1 October 2017

Biliana Lesic

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2

1 reference

1 October 2017

Denis Dacheux

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3

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1 October 2017

Elisabeth Carniel

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5

1 reference

1 October 2017

1 September 2003

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FEMS Immunology and Medical Microbiology

1 October 2017

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1 October 2017

38

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1 October 2017

2

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1 October 2017

113-116

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A rapid method for efficient gene replacement in the filamentous fungus Aspergillus nidulans

1 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

Use of bacteriophage lambda recombination functions to promote gene replacement in Escherichia coli

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

A correction in the nucleotide sequence of the Tn903 kanamycin resistance determinant in pUC4K.

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

PCR-synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

A highly efficient electroporation system for transformation of Yersinia

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

The high-pathogenicity island of Yersinia pseudotuberculosis can be inserted into any of the three chromosomal asn tRNA genes

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

Characterization of the O-antigen gene clusters of Yersinia pseudotuberculosis and the cryptic O-antigen gene cluster of Yersinia pestis shows that the plague bacillus is most closely related to and has evolved from Y. pseudotuberculosis serotype O:

1 reference

https://api.crossref.org/works/10.1016%2FS0928-8244%2803%2900181-0

7 January 2021

10.1016/S0928-8244(03)00181-0

Identifiers

DOI

1 reference

1 October 2017

1 reference