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Items: 5

1.

Counting of viable C. burnetii cells by quantitative reverse transcription PCR using a recombinant plasmid (pCB-dotA) as a standard.

Zúniga-Navarrete F, Flores-Ramirez G, Quevedo-Díaz M, Škultéty L.

Acta Virol. 2018;62(4):409-414. doi: 10.4149/av_2018_409.

PMID:
30472871
2.

Improvement and efficient display of Bacillus thuringiensis toxins on M13 phages and ribosomes.

Pacheco S, Cantón E, Zuñiga-Navarrete F, Pecorari F, Bravo A, Soberón M.

AMB Express. 2015 Dec;5(1):73. doi: 10.1186/s13568-015-0160-1. Epub 2015 Nov 25.

3.

Identification of Bacillus thuringiensis Cry3Aa toxin domain II loop 1 as the binding site of Tenebrio molitor cadherin repeat CR12.

Zúñiga-Navarrete F, Gómez I, Peña G, Amaro I, Ortíz E, Becerril B, Ibarra JE, Bravo A, Soberón M.

Insect Biochem Mol Biol. 2015 Apr;59:50-7. doi: 10.1016/j.ibmb.2015.02.002. Epub 2015 Feb 17.

PMID:
25698611
4.

A Tenebrio molitor GPI-anchored alkaline phosphatase is involved in binding of Bacillus thuringiensis Cry3Aa to brush border membrane vesicles.

Zúñiga-Navarrete F, Gómez I, Peña G, Bravo A, Soberón M.

Peptides. 2013 Mar;41:81-6. doi: 10.1016/j.peptides.2012.05.019. Epub 2012 Jun 26.

PMID:
22743140
5.

Cadherin binding is not a limiting step for Bacillus thuringiensis subsp. israelensis Cry4Ba toxicity to Aedes aegypti larvae.

Rodríguez-Almazán C, Reyes EZ, Zúñiga-Navarrete F, Muñoz-Garay C, Gómez I, Evans AM, Likitvivatanavong S, Bravo A, Gill SS, Soberón M.

Biochem J. 2012 May 1;443(3):711-7. doi: 10.1042/BJ20111579.

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