ZFIN ID: ZDB-PERS-080428-2
Zaucker, Andreas
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Affiliation: Ferenc Müller Lab
Address: Department of Medical and Molecular Genetics Division of Reproductive and Child Health Institute of Biomedical Research University of Birmingham, B15 2TT Edgbaston, Birmingham, D-76021 United Kingdom
Country: United Kingdom
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BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Weger, M., Diotel, N., Weger, B.D., Beil, T., Zaucker, A., Eachus, H.L., Oakes, J.A., do Rego, J.L., Storbeck, K.H., Gut, P., Straehle, U., Rastegar, S., Mueller, F., Krone, N. (2018) Expression and activity profiling of the steroidogenic enzymes of glucocorticoid biosynthesis and the fdx1 co-factors in zebrafish. Journal of neuroendocrinology. 30(4):e12586
Eachus, H., Zaucker, A., Oakes, J.A., Griffin, A., Weger, M., Güran, T., Taylor, A., Harris, A., Greenfield, A., Quanson, J.L., Storbeck, K.H., Cunliffe, V.T., Müller, F., Krone, N. (2017) Genetic disruption of 21-hydroxylase in zebrafish causes interrenal hyperplasia. Endocrinology. 158(12):4165-4173
Griffin, A., Parajes, S., Weger, M., Zaucker, A., Taylor, A.E., O'Neil, D.M., Müller, F., Krone, N. (2016) Ferredoxin 1b (Fdx1b) is the essential mitochondrial redox partner for cortisol biosynthesis in zebrafish. Endocrinology. 157(3):1122-34
Zaucker, A., Bodur, T., Roest Crollius, H., Hadzhiev, Y., Gehrig, J., Loosli, F., Watson, C., Müller, F. (2014) Description of Embryonic Development of Spotted Green Pufferfish (Tetraodon nigroviridis). Zebrafish. 11(6):509-17
Zaucker, A., Mercurio, S., Sternheim, N., Talbot, W.S., and Marlow, F.L. (2013) notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish. Disease models & mechanisms. 6(5):1246-59
Cullinane, A.R., Straatman-Iwanowska, A., Zaucker, A., Wakabayashi, Y., Bruce, C.K., Luo, G., Rahman, F., Gürakan, F., Utine, E., Ozkan, T.B., Denecke, J., Vukovic, J., Di Rocco, M., Mandel, H., Cangul, H., Matthews, R.P., Thomas, S.G., Rappoport, J.Z., Arias, I.M., Wolburg, H., Knisely, A.S., Kelly, D.A., Muller, F., Maher, E.R., and Gissen, P. (2010) Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization. Nature Genetics. 42(4):303-312
Csenki, Z., Zaucker, A., Kovacs, B., Hadzhiev, Y., Hegyi, R., Lefler, K.K., Muller, T., Kovacs, R., Urbanyi, B., Varadi, L., and Muller, F. (2010) Intraovarian transplantation of stage I-II follicles results in viable zebrafish embryos. The International journal of developmental biology. 54(4):585-589
Gehrig, J., Reischl, M., Kalmar, E., Ferg, M., Hadzhiev, Y., Zaucker, A., Song, C., Schindler, S., Liebel, U., and Muller, F. (2009) Automated high-throughput mapping of promoter-enhancer interactions in zebrafish embryos. Nature Methods. 6(12):911-916

NON-ZEBRAFISH PUBLICATIONS