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Volumn 62, Issue 9, 1998, Pages 1826-1829

A rapid method for disrupting genes in the escherichia coli genome

Author keywords

E. sherichia coli; Gene disruption; Genome analysis; Plasmid vector

Indexed keywords

ARTICLE; BACTERIAL GENE; BACTERIAL GENOME; ESCHERICHIA COLI; GENETIC PROCEDURES; GENETICS;

EID: 0032153603     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.62.1826     Document Type: Article
Times cited : (12)

References (12)
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    • Use of bacteriophage X recombination functions to promote gene replacement in
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  • 7
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    • Replacement and amplification of bacterial genes with sequences altered
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    • Vivo transfer of chromosomal mutation onto multicopy plasmids utilizing polA strains: Cloning of an ompR2 mutation in Escherichia coli K-12
    • Saarilhti, H. T., and Palva, E. T., In vivo transfer of chromosomal mutation onto multicopy plasmids utilizing polA strains: cloning of an ompR2 mutation in Escherichia coli K-12. FEMS Microbiol. Lett., 26, 27-33 (1985).
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    • Saarilhti, H.T.1    Palva, E.T.2
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    • Molecular analysis by deletion and site directed mutagenesis of the cis-acting upstream sequence involved in activation of the ompF promoter in Escherichia coli
    • Kato, M., Aiba, H., and Mizuno, T., Molecular analysis by deletion and site directed mutagenesis of the cis-acting upstream sequence involved in activation of the ompF promoter in Escherichia coli. J. Biochem. (Tokyo), 105, 341-347 (1989).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.