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Journal of Bacteriology|January 1, 1990
mprA, an Escherichia coli gene that reduces growth-phase-dependent synthesis of microcins B17 and C7 and blocks osmoinduction of proU when cloned on a high-copy-number plasmidI del Castillo, J M Gómez, F MorenoFEMS Microbiology Letters|December 4, 2001
Secretion of the Escherichia coli K-12 SheA hemolysin is independent of its cytolytic activityF J del Castillo, F Moreno, I del CastilloJournal of Bacteriology|February 27, 2001
Construction and characterization of mutations at codon 751 of the Escherichia coli gyrB gene that confer resistance to the antimicrobial peptide microcin B17 and alter the activity of DNA gyraseF J del Castillo, I del Castillo, F MorenoActa Otorrinolaringologica Espanola|January 24, 2006
[Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset]J Gallo-Terán, C Morales-Angulo, M Rodríguez-Ballesteros, et al.The EMBO Journal|February 1, 1991
The peptide antibiotic microcin B17 induces double-strand cleavage of DNA mediated by E. coli DNA gyraseJ L Vizán, C Hernández-Chico, I del Castillo, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
An unusual mechanism for resistance to the antibiotic coumermycin A1I del Castillo, J L Vizán, M C Rodríguez-Sáinz, et al.Molecular Microbiology|July 1, 1997
The Escherichia coli K-12 sheA gene encodes a 34-kDa secreted haemolysinF J del Castillo, S C Leal, F Moreno, et al.Journal of Bacteriology|June 1, 1991
Nucleotide sequence of the Escherichia coli regulatory gene mprA and construction and characterization of mprA-deficient mutantsI del Castillo, J E González-Pastor, J L San Millán, et al.Acta Otorrinolaringologica Espanola|April 27, 1999
[Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance]C Morales Angulo, I Del Castillo, M Sarduy, et al.Clinical Genetics|January 8, 2008
Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genesL Olavarrieta, C Morales-Angulo, I del Castillo, et al.Pageof 477