Janet Koster

BEng

Affiliatie UvA Amsterdam Gastroenterology Endocrinology Metabolism Other Academic Staff, Genetic Metabolic Diseases

Specialization

Focus of research

Latest publications

PEX39 facilitates the peroxisomal import of PTS2-containing proteins
Chen, W. W., Rodrigues, T. A., Wendscheck, D., Pedrosa, A. G., Yang, C., Francisco, T. N., Möcklinghoff, T., Zografakis, A., Nunes-Silva, B., Avraham, R. E., Silva, A. R., Ferreira, M. J., Das, H., Koster, J., Neuwirth, S., Bender, J., Oeljeklaus, S., Sondhi, V., Gatsogiannis, C. & Schuldiner, M. & 6 others, Zalckvar, E., Hofmann, K., Waterham, H. R., DeBerardinis, R. J., Azevedo, J. E. & Warscheid, B., 1 Aug 2025, In: Nature Cell Biology. 27, 8, p. 1256-1271 16 p.
Research output: Contribution to journal › Article › Academic › peer-review
Overexpression of PEX14 results in mistargeting to mitochondria, accompanied by organelle fragmentation and clustering in human embryonic kidney cells
Jansen, R. L. M., de Boer, R., de Lange, E. M. F., Koster, J., Vlijm, R., Waterham, H. R. & van der Klei, I. J., 1 Aug 2024, In: Biochimica et Biophysica Acta - Molecular Cell Research. 1871, 6, 119754.
Research output: Contribution to journal › Article › Academic › peer-review
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders
Kaiyrzhanov, R., Rad, A., Lin, S.-J., Bertoli-Avella, A., Kallemeijn, W. W., Godwin, A., Zaki, M. S., Huang, K., Lau, T., Petree, C., Efthymiou, S., Ghayoor Karimiani, E., Hempel, M., Normand, E. A., Rudnik-Schöneborn, S., Schatz, U. A., Baggelaar, M. P., Ilyas, M., Sultan, T. & Alvi, J. R. & 69 others, Ganieva, M., Fowler, B., Aanicai, R., Akay Tayfun, G., Al Saman, A., Alswaid, A., Amiri, N., Asilova, N., Shotelersuk, V., Yeetong, P., Azam, M., Babaei, M., Bahrami Monajemi, G., Mohammadi, P., Samie, S., Banu, S. H., Basto, J. P., Kortüm, F., Bauer, M., Bauer, P., Beetz, C., Garshasbi, M., Hameed Issa, A., Eyaid, W., Ahmed, H., Hashemi, N., Hassanpour, K., Herman, I., Ibrohimov, S., Abdul-Majeed, B. A., Imdad, M., Isrofilov, M., Kaiyal, Q., Khan, S., Kirmse, B., Koster, J., Lourenço, C. M., Mitani, T., Moldovan, O., Murphy, D., Najafi, M., Pehlivan, D., Rocha, M. E., Salpietro, V., Schmidts, M., Shalata, A., Mahroum, M., Talbeya, J. K., Taylor, R. W., Vazquez, D., Vetro, A., Waterham, H. R., Zaman, M., Schrader, T. A., Chung, W. K., Guerrini, R., Lupski, J. R., Gleeson, J., Suri, M., Jamshidi, Y., Bhatia, K. P., Vona, B., Schrader, M., Severino, M., Guille, M., Tate, E. W., Varshney, G. K., Houlden, H. & Maroofian, R., 4 Apr 2024, In: Brain.
Research output: Contribution to journal › Article › Academic › peer-review
All publications

Janet Koster

Specialization

Focus of research

PEX39 facilitates the peroxisomal import of PTS2-containing proteins

Overexpression of PEX14 results in mistargeting to mitochondria, accompanied by organelle fragmentation and clustering in human embryonic kidney cells

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

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