Mike Gerards (M.)
Key publicaties
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Hemel, I. M. G. M., Knoops, K., Lopez-Iglesias, C., & Gerards, M. (2025). The Curse of the Red Pearl: A Fibroblast-Specific Pearl-Necklace Mitochondrial Phenotype Caused by Phototoxicity. Biomolecules, 15(2), Article 304. https://doi.org/10.3390/biom15020304Meer informatie over deze publicatie
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Hemel, I. M. G. M., Arts, I. C. W., Moerel, M., & Gerards, M. (2025). The Matrix of Mitochondrial Imaging: Exploring Spatial Dimensions. Biomolecules, 15(2), Article 229. https://doi.org/10.3390/biom15020229Meer informatie over deze publicatie
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Hemel, I. M. G. M., Steen, C., Denil, S. L. I. J., Ertaylan, G., Kutmon, M., Adriaens, M., & Gerards, M. (2025). The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphology. Mitochondrion, 81, Article 102008. https://doi.org/10.1016/j.mito.2025.102008Meer informatie over deze publicatie
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Hemel, I. M. G. M., Sarantidou, R., & Gerards, M. (2021). It takes two to tango: The essential role of ER-mitochondrial contact sites in mitochondrial dynamics. International Journal of Biochemistry & Cell Biology, 141, Article 106101. https://doi.org/10.1016/j.biocel.2021.106101Meer informatie over deze publicatie
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Hemel, I. M. G. M., Engelen, B. P. H., Luber, N., & Gerards, M. (2021). A hitchhiker's guide to mitochondrial quantification. Mitochondrion, 59, 216-224. https://doi.org/10.1016/j.mito.2021.06.005Meer informatie over deze publicatie
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Gerards, M., van den Bosch, B. J. C., Danhauser, K., Serre, V., van Weeghel, M., Wanders, R. J. A., Nicolaes, G. A. F., Sluiter, W., Schoonderwoerd, K., Scholte, H. R., Prokisch, H., Rötig, A., de Coo, I. F. M., & Smeets, H. J. M. (2011). Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene. Brain, 134(Pt 1), 210-219. https://doi.org/10.1093/brain/awq273Meer informatie over deze publicatie
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Gerards, M., Sluiter, W., van den Bosch, B. J. C., de Wit, L. E. A., Calis, C. M. H., Frentzen, M., Akbari, H., Schoonderwoerd, K., Scholte, H. R., Jongbloed, R. J., Hendrickx, A. T. M., de Coo, I. F. M., & Smeets, H. J. M. (2010). Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. Journal of Medical Genetics, 47(8), 507-12. https://doi.org/10.1136/jmg.2009.067553Meer informatie over deze publicatie
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Gerards, M., Cannino, G., de Cozar, J. M. G., & Jacobs, H. T. (2018). Intracellular vesicle trafficking plays an essential role in mitochondrial quality control. Molecular Biology of the Cell, 29(7), 809-819. https://doi.org/10.1091/mbc.E17-10-0619Meer informatie over deze publicatie
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Gonzalez de Cozar, J. M., Gerards, M., Teeri, E., George, J., Dufour, E., Jacobs, H. T., & Joers, P. (2019). RNase H1 promotes replication fork progression through oppositely transcribed regions of Drosophila mitochondrial DNA. Journal of Biological Chemistry, 294(12), 4331-4344. https://doi.org/10.1074/jbc.RA118.007015Meer informatie over deze publicatie
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Fukuoh, A., Cannino, G., Gerards, M., Buckley, S., Kazancioglu, S., Scialo, F., Lihavainen, E., Ribeiro, A., Dufour, E., & Jacobs, H. T. (2014). Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthase. Molecular Systems Biology, 10(6), Article 734. https://doi.org/10.15252/msb.20145117Meer informatie over deze publicatie