Researcher Portfolio
Tefs, Cindy
Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. E.-D. Schulze, Max Planck Institute for Biogeochemistry, Max Planck Society, Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. S. E. Trumbore, Max Planck Institute for Biogeochemistry, Max Planck Society
Researcher Profile
Position: Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. E.-D. Schulze, Max Planck Institute for Biogeochemistry, Max Planck Society
Position: Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. S. E. Trumbore, Max Planck Institute for Biogeochemistry, Max Planck Society
Researcher ID: https://pure.mpg.de/cone/persons/resource/persons62575
Publications
(1 - 25 of 30)
: Simard, M.-L., Mourier, A., Greaves, L. C., Taylor, R. W., & Stewart, J. (2018). A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency. J Pathol, 245(3), 311-323. doi:10.1002/path.5084. [PubMan] : Kauppila, J. H. K., Bonekamp, N., Mourier, A., Isokallio, M., Just, A., Kauppila, T., Stewart, J., & Larsson, N. (2018). Base-excision repair deficiency alone or combined with increased oxidative stress does not increase mtDNA point mutations in mice. Nucleic Acids Res, 46(13), 6642-6669. doi:10.1093/nar/gky456. [PubMan] : Kühl, I., Miranda, M., Atanassov, I., Kuznetsova, I., Hinze, Y., Mourier, A., Filipovska, A., & Larsson, N. (2017). Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals. Elife, 6. doi:10.7554/eLife.30952. [PubMan] : Brandt, T., Mourier, A., Tain, L. S., Partridge, L., Larsson, N.-G., & Kühlbrandt, W. (2017). Changes of mitochondrial ultrastructure and function during ageing in mice and Drosophila. eLife, 6: e24662. doi:10.7554/eLife.24662. [PubMan] : Brandt, T., Mourier, A., Tain, L. S., Partridge, L., Larsson, N., & Kuhlbrandt, W. (2017). Changes of mitochondrial ultrastructure and function during ageing in mice and Drosophila. Elife, 6. doi:10.7554/eLife.24662. [PubMan] : Kauppila, J. H. K., Baines, H. L., Bratic, A., Simard, M.-L., Freyer, C., Mourier, A., Stamp, C., Filograna, R., Larsson, N., Greaves, L. C., & Stewart, J. B. (2016). A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. Cell Rep, 16(11), 2980-90. doi:10.1016/j.celrep.2016.08.037. [PubMan] : Perez-Perez, R., Lobo-Jarne, T., Milenkovic, D., Mourier, A., Bratic, A., Garcia-Bartolome, A., Fernandez-Vizarra, E., Cadenas, S., Delmiro, A., Garcia-Consuegra, I., Arenas, J., Martin, M. A., Larsson, N., & Ugalde, C. (2016). COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep, 16(9), 2387-98. doi:10.1016/j.celrep.2016.07.081. [PubMan] : Kühl, I., Miranda, M., Posse, V., Milenkovic, D., Mourier, A., Siira, S. J., Bonekamp, N., Neumann, U., Filipovska, A., Polosa, P. L., Gustafsson, C. M., & Larsson, N. (2016). POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. Sci Adv, 2(8), e1600963. doi:10.1126/sciadv.1600963. [PubMan] : Rackham, O., Busch, J. D., Matic, S., Siira, S. J., Kuznetsova, I., Atanassov, I., Ermer, J. A., Shearwood, A. M., Richman, T. R., Stewart, J. B., Mourier, A., Milenkovic, D., Larsson, N., & Filipovska, A. (2016). Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly. Cell Rep, 16(7), 1874-90. doi:10.1016/j.celrep.2016.07.031. [PubMan] : Ramos, E., Larsson, N., & Mourier, A. (2016). Bioenergetic roles of mitochondrial fusion. Biochim Biophys Acta, 1857(8), 1277-83. doi:10.1016/j.bbabio.2016.04.002. [PubMan] : Rackham, O., Busch, J. D., Matic, S., Siira, S., Kuznetsova, I., Atanassov, I., Ermer, J., Shearwood, A.-M.-J., Richman, T., Stewart, J. B., Mourier, A., Milenkovic, D., Larsson, N., & Filipovska, A. (2016). Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly. Cell Reports, 16(7), 1874-1890. doi:http://dx.doi.org/10.1016/j.celrep.2016.07.031. [PubMan] : Kauppila, J. H. K., Baines, H. L., Bratic, A., Simard, M.-L., Freyer, C., Mourier, A., Stamp, C., Filograna, R., Larsson, N., Greaves, L. C., & Stewart, J. B. (2016). A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. Cell reports, 16(11), 2980-2990. doi:10.1016/j.celrep.2016.08.037. [PubMan] : Kühl, I., Miranda, M., Posse, V., Milenkovic, D., Mourier, A., Siira, S. J., Bonekamp, N. A., Neumann, U., Filipovska, A., Polosa, P. L., Gustafsson, C. M., & Larsson, N. (2016). POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. Science advances, 2(8), e1600963. doi:10.1126/sciadv.1600963. [PubMan] : Lagouge, M., Mourier, A., Lee, H., Spahr, H., Wai, T., Kukat, C., Ramos, E., Motori, E., Busch, J. D., Siira, S., Kremmer, E., Filipovska, A., & Larsson, N. (2015). SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation. PLoS Genet, 11(8), e1005423. doi:10.1371/journal.pgen.1005423. [PubMan] : Freyer, C., Stranneheim, H., Naess, K., Mourier, A., Felser, A., Maffezzini, C., Lesko, N., Bruhn, H., Engvall, M., Wibom, R., Barbaro, M., Hinze, Y., Magnusson, M., Andeer, R., Zetterstrom, R. H., von Dobeln, U., Wredenberg, A., & Wedell, A. (2015). Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid. J Med Genet, 52(11), 779-83. doi:10.1136/jmedgenet-2015-102986. [PubMan] : Mourier, A., Motori, E., Brandt, T., Lagouge, M., Atanassov, I., Galinier, A., Rappl, G., Brodesser, S., Hultenby, K., Dieterich, C., & Larsson, N. (2015). Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels. J Cell Biol, 208(4), 429-42. doi:10.1083/jcb.201411100. [PubMan] : Mourier, A., Motori, E., Brandt, T., Lagouge, M., Atanassov, I., Galinier, A., Rappl, G., Brodesser, S., Hultenby, K., Dieterich, C., & Larsson, N.-G. (2015). Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels. The Journal of Cell Biology: JCB, 208(4), 429-442. doi:10.1083/jcb.201411100. [PubMan] : Mourier, A., Matic, S., Ruzzenente, B., Larsson, N., & Milenkovic, D. (2014). The respiratory chain supercomplex organization is independent of COX7a2l isoforms. Cell Metab, 20(6), 1069-75. doi:10.1016/j.cmet.2014.11.005. [PubMan] : Baggio, F., Bratic, A., Mourier, A., Kauppila, T. E. S., Tain, L. S., Kukat, C., Habermann, B., Partridge, L., & Larsson, N. (2014). Drosophila melanogaster LRPPRC2 is involved in coordination of mitochondrial translation. Nucleic Acids Res, 42(22), 13920-38. doi:10.1093/nar/gku1132. [PubMan] : Kühl, I., Kukat, C., Ruzzenente, B., Milenkovic, D., Mourier, A., Miranda, M., Koolmeister, C., Falkenberg, M., & Larsson, N. (2014). POLRMT does not transcribe nuclear genes. Nature, 514(7521), E7-11. doi:10.1038/nature13690. [PubMan] : Vernochet, C., Damilano, F., Mourier, A., Bezy, O., Mori, M. A., Smyth, G., Rosenzweig, A., Larsson, N., & Kahn, C. R. (2014). Adipose tissue mitochondrial dysfunction triggers a lipodystrophic syndrome with insulin resistance, hepatosteatosis, and cardiovascular complications. Faseb j, 28(10), 4408-19. doi:10.1096/fj.14-253971. [PubMan] : Mourier, A., Ruzzenente, B., Brandt, T., Kuhlbrandt, W., & Larsson, N. (2014). Loss of LRPPRC causes ATP synthase deficiency. Hum Mol Genet, 23(10), 2580-92. doi:10.1093/hmg/ddt652. [PubMan] : Ross, J. M., Stewart, J. B., Hagstrom, E., Brene, S., Mourier, A., Coppotelli, G., Freyer, C., Lagouge, M., Hoffer, B. J., Olson, L., & Larsson, N. (2013). Germline mitochondrial DNA mutations aggravate ageing and can impair brain development. Nature, 501(7467), 412-5. doi:10.1038/nature12474. [PubMan] : Baggio, F., Bratic, A., Mourier, A., Kukat, C., Habermann, B., Partridge, L., & Larsson, N. (2013). Role of the mitochondrial protein LRPPRC2 in Drosophila melanogaster. MITOCHONDRION, 13(6), 909-909. doi:10.1016/j.mito.2013.07.032. [PubMan] : Wredenberg, A., Lagouge, M., Bratic, A., Metodiev, M. D., Spahr, H., Mourier, A., Freyer, C., Ruzzenente, B., Tain, L. S., Grönke, S., Baggio, F., Kukat, C., Kremmer, E., Wibom, R., Polosa, P. L., Habermann, B., Partridge, L., Park, C. B., & Larsson, N. (2013). MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals. PLoS Genet, 9(1), e1003178. doi:10.1371/journal.pgen.1003178. [PubMan]