FACULTAD DE CIENCIAS
Facultad/Centro de investigación
Instituto de Biología Molecular de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Biología Molecular de Barcelona (16)
2023
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Plastic degradation by insect hexamerins: Near-atomic resolution structures of the polyethylene-degrading proteins from the wax worm saliva
Science advances, Vol. 9, Núm. 38, pp. eadi6813
2022
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Wax worm saliva and the enzymes therein are the key to polyethylene degradation by Galleria mellonella
Nature Communications, Vol. 13, Núm. 1
2021
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Influence of core extension and side chain nature in targeting G-quadruplex structures with perylene monoimide derivatives
Bioorganic Chemistry, Vol. 108
2015
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Chemical speciation of MeHg+ and Hg2+ in aqueous solution and HEK cells nuclei by means of DNA interacting fluorogenic probes
Chemical Science, Vol. 6, Núm. 7, pp. 3757-3764
2006
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A microarray-based detection system for genetically modified (GM) food ingredients
Plant Molecular Biology, Vol. 61, Núm. 1-2, pp. 123-139
2005
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Interlaboratory transfer of a PCR multiplex method for simultaneous detection of four genetically modified maize lines: Bt11, MON810, T25, and GA21
Journal of Agricultural and Food Chemistry, Vol. 53, Núm. 9, pp. 3333-3337
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Real-time polymerase chain reaction based assays for quantitative detection of barley, rice, sunflower, and wheat
Journal of Agricultural and Food Chemistry, Vol. 53, Núm. 18, pp. 7003-7009
2004
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Development and comparison of four real-time polymerase chain reaction systems for specific detection and quantification of Zea mays L.
Journal of Agricultural and Food Chemistry, Vol. 52, Núm. 15, pp. 4632-4637
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Development of real-time PCR systems based on SYBR® Green I, Amplifluor™ and TaqMan® technologies for specific quantitative detection of the transgenic maize event GA21
Journal of Cereal Science, Vol. 39, Núm. 1, pp. 99-107
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Quantitative Detection of Listeria monocytogenes and Listeria innocua by Real-Time PCR: Assessment of hly, iap, and lin02483 Targets and AmpliFluor Technology
Applied and Environmental Microbiology, Vol. 70, Núm. 3, pp. 1366-1377
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Simultaneous quantitative detection of Listeria spp. and Listeria monocytogenes using a duplex real-time PCR-based assay
FEMS Microbiology Letters, Vol. 233, Núm. 2, pp. 257-267
2003
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A rapid and direct real time PCR-based method for identification of Salmonella spp.
Journal of Microbiological Methods, Vol. 54, Núm. 3, pp. 381-390
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A specific real-time quantitative PCR detection system for event MON810 in maize YieldGard® based on the 3′-transgene integration sequence
Transgenic Research, Vol. 12, Núm. 2, pp. 179-189
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Development of melting temperature-based SYBR Green I polymerase chain reaction methods for multiplex genetically modified organism detection
Analytical Biochemistry, Vol. 323, Núm. 2, pp. 164-170
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Real-time and conventional polymerase chain reaction systems based on the metallo-carboxypeptidase inhibitor gene for specific detection and quantification of potato and tomato in processed food
Journal of Food Protection, Vol. 66, Núm. 6, pp. 1063-1070
2001
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A rapeseed-specific gene, Acetyl-CoA carboxylase, can be used as a reference for qualitative and real-time quantitative PCR detection of transgenes from mixed food samples
Journal of Agricultural and Food Chemistry, Vol. 49, Núm. 8, pp. 3622-3627