Elisabeth Busch-Nentwich
Affiliations: | University of Cambridge, Cambridge, England, United Kingdom |
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| Tuschl K, White RJ, Trivedi C, et al. (2022) Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish. Disease Models & Mechanisms |
| White RJ, Mackay E, Wilson SW, et al. (2022) Allele-specific gene expression can underlie altered transcript abundance in zebrafish mutants. Elife. 11 |
| Weiner AMJ, Scampoli NL, Steeman TJ, et al. (2019) Dicer1 is required for pigment cell and craniofacial development in zebrafish. Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms. 1862: 472-485 |
| Lush ME, Diaz DC, Koenecke N, et al. (2019) scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling. Elife. 8 |
| Perez-Garcia V, Fineberg E, Wilson R, et al. (2018) Placentation defects are highly prevalent in embryonic lethal mouse mutants. Nature |
| Anderson JL, Mulligan TS, Shen MC, et al. (2017) mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay. Plos Genetics. 13: e1007105 |
| Henke K, Daane JM, Hawkins MB, et al. (2017) Genetic Screen for Post-embryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form. Genetics |
| Erickson T, Morgan CP, Olt J, et al. (2017) Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt). Elife. 6 |
| Erickson T, Morgan CP, Olt J, et al. (2017) Author response: Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt) Elife |
| Obholzer N, Wolfson S, Trapani JG, et al. (2008) Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 2110-8 |