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Dr Florence van Tienen (F.H.J.)

Key publications
van Tienen, F., Zelissen, R., Timmer, E., van Gisbergen, M., Lindsey, P., Quattrocelli, M., Sampaolesi, M., Mulder-den Hartog, E., de Coo, I., & Smeets, H. (2019). Healthy, mtDNA-mutation free mesoangioblasts from mtDNA patients qualify for autologous therapy. Stem Cell Research & Therapy, 10(1), Article 405. https://doi.org/10.1186/s13287-019-1510-8
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Otten, A. B. C., Kamps, R., Lindsey, P., Gerards, M., Pendeville-Samain, H., Muller, M., van Tienen, F. H. J., & Smeets, H. J. M. (2020). TfamKnockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos. Frontiers in Cell and Developmental Biology, 8, Article 381. https://doi.org/10.3389/fcell.2020.00381
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van Tienen, F. H. J., Praet, S. F., Feyter, H. M., van den Broek, N. M., Lindsey, P. J., Schoonderwoerd, K. G., Coo, I. F., Nicolay, K., Prompers, J. J., Smeets, H. J. M., & van Loon, L. J. C. (2012). Physical activity is the key determinant of skeletal muscle mitochondrial function in type 2 diabetes. Journal of Clinical Endocrinology & Metabolism, 97(9), 3261-3269. https://doi.org/10.1210/jc.2011-3454
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Recent publications
  • Ahmadian, S., Lindsey, P. J., Smeets, H. J. M., van Tienen, F. H. J., & van Zandvoort, M. A. M. J. (2024). Spinning Disk Confocal Microscopy for Optimized and Quantified Live Imaging of 3D Mitochondrial Network. International Journal of Molecular Sciences, 25(9), Article 4819. https://doi.org/10.3390/ijms25094819
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  • Smeets, H., Verbrugge, B., Bulbena, X., Hristova, L., Vogt, J., van Beckhoven, I., Allamand, V., Almekinders, J., Barquinero, J., Berreur, S., Bönnemann, C., Bouman, K., de Bruin, L., Caron, L., Damon, C., Durbeej, M., Feijen, D., Foley, R., Goncalves, A. R., ... all participants (2024). European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy. Neuromuscular Disorders, 36, 16-22. https://doi.org/10.1016/j.nmd.2024.01.001
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  • Trayford, C., Wilhalm, A., Habibovic, P., Smeets, H., van Tienen, F., & van Rijt, S. (2023). One-pot, degradable, silica nanocarriers with encapsulated oligonucleotides for mitochondrial specific targeting. Discover Nano, 18(1), Article 161. https://doi.org/10.1186/s11671-023-03926-1
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  • Vallbona-Garcia, A., Hamers, I. H. J., van Tienen, F. H. J., Ochoteco-Asensio, J., Berendschot, T. T. J. M., de Coo, I. F. M., Benedikter, B. J., Webers, C. A. B., Smeets, H. J. M., & Gorgels, T. G. M. F. (2023). Low mitochondrial DNA copy number in buffy coat DNA of primary open-angle glaucoma patients. Experimental Eye Research, 232(1), Article 109500. https://doi.org/10.1016/j.exer.2023.109500
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  • Zelissen, R., Ahmadian, S., Montilla-Rojo, J., Timmer, E., Ummelen, M., Hopman, A., Smeets, H., & van Tienen, F. (2023). Fusion of Wild-Type Mesoangioblasts with Myotubes of mtDNA Mutation Carriers Leads to a Proportional Reduction in mtDNA Mutation Load. International Journal of Molecular Sciences, 24(3), Article 2679. https://doi.org/10.3390/ijms24032679
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  • Vallbona-Garcia, A., Lindsey, P. J., Kamps, R., Stassen, A. P. M., Nguyen, N., van Tienen, F. H. J., Hamers, I. H. J., Hardij, R., van Gisbergen, M. W., Benedikter, B. J., de Coo, I. F. M., Webers, C. A. B., Gorgels, T. G. M. F., & Smeets, H. J. M. (2023). Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup. Frontiers in Ophthalmology, 3, Article 1309836. https://doi.org/10.3389/fopht.2023.1309836
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  • Hubens, W. H. G., Vallbona-Garcia, A., de Coo, I. F. M., van Tienen, F. H. J., Webers, C. A. B., Smeets, H. J. M., & Gorgels, T. G. M. F. (2022). Blood biomarkers for assessment of mitochondrial dysfunction: An expert review. Mitochondrion, 62, 187-204. https://doi.org/10.1016/j.mito.2021.10.008
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  • Guo, L., Engelen, B. P. H., Hemel, I. M. G. M., de Coo, I. F. M., Vreeburg, M., Sallevelt, S. C. E. H., Hellebrekers, D. M. E. I., Jacobs, E. H., Sadeghi-Niaraki, F., van Tienen, F. H. J., Smeets, H. J. M., & Gerards, M. (2021). Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency. European Journal of Human Genetics, 29(12), 1789-1795. https://doi.org/10.1038/s41431-021-00947-1
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  • Bouman, K., Groothuis, J. T., Doorduin, J., van Alfen, N., ten Cate, F. E. A. U., van den Heuvel, F. M. A., Nijveldt, R., van Tilburg, W. C. M., Buckens, S. C. F. M., Dittrich, A. T. M., Draaisma, J. M. T., Janssen, M. C. H., Kamsteeg, E. J., van Kleef, E. S. B., Koene, S., Smeitink, J. A. M., Kusters, B., van Tienen, F. H. J., Smeets, H. J. M., ... Voermans, N. C. (2021). Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study. BMC Neurology, 21(1), Article 313. https://doi.org/10.1186/s12883-021-02336-z
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  • Boyer, O., Butler-Browne, G., Chinoy, H., Cossu, G., Galli, F., Lilleker, J. B., Magli, A., Mouly, V., Perlingeiro, R. C. R., Previtali, S. C., Sampaolesi, M., Smeets, H., Schoewel-Wolf, V., Spuler, S., Torrente, Y., Van Tienen, F., & Study Grp (2021). Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle. Frontiers in Genetics, 12, Article 702547. https://doi.org/10.3389/fgene.2021.702547
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