Year |
Citation |
Score |
2022 |
Tuschl K, White RJ, Trivedi C, Valdivia LE, Niklaus S, Bianco IH, Dadswell C, González-Méndez R, Sealy IM, Neuhauss SCF, Houart C, Rihel J, Wilson SW, Busch-Nentwich EM. Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish. Disease Models & Mechanisms. PMID 35514229 DOI: 10.1242/dmm.044594 |
0.339 |
|
2022 |
White RJ, Mackay E, Wilson SW, Busch-Nentwich EM. Allele-specific gene expression can underlie altered transcript abundance in zebrafish mutants. Elife. 11. PMID 35175196 DOI: 10.7554/eLife.72825 |
0.328 |
|
2019 |
Weiner AMJ, Scampoli NL, Steeman TJ, Dooley CM, Busch-Nentwich EM, Kelsh RN, Calcaterra NB. Dicer1 is required for pigment cell and craniofacial development in zebrafish. Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms. 1862: 472-485. PMID 30840854 DOI: 10.1016/j.bbagrm.2019.02.005 |
0.315 |
|
2019 |
Lush ME, Diaz DC, Koenecke N, Baek S, Boldt H, St Peter MK, Gaitan-Escudero T, Romero-Carvajal A, Busch-Nentwich EM, Perera AG, Hall KE, Peak A, Haug JS, Piotrowski T. scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling. Elife. 8. PMID 30681411 DOI: 10.7554/Elife.44431 |
0.321 |
|
2018 |
Perez-Garcia V, Fineberg E, Wilson R, Murray A, Mazzeo CI, Tudor C, Sienerth A, White JK, Tuck E, Ryder EJ, Gleeson D, Siragher E, Wardle-Jones H, Staudt N, Wali N, ... ... Busch-Nentwich EM, et al. Placentation defects are highly prevalent in embryonic lethal mouse mutants. Nature. PMID 29539633 DOI: 10.1038/Nature26002 |
0.308 |
|
2017 |
Anderson JL, Mulligan TS, Shen MC, Wang H, Scahill CM, Tan FJ, Du SJ, Busch-Nentwich EM, Farber SA. 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. PMID 29161261 DOI: 10.1371/journal.pgen.1007105 |
0.301 |
|
2017 |
Henke K, Daane JM, Hawkins MB, Dooley CM, Busch-Nentwich EM, Stemple DL, Harris MP. Genetic Screen for Post-embryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form. Genetics. PMID 28835471 DOI: 10.1534/Genetics.117.300187 |
0.334 |
|
2017 |
Erickson T, Morgan CP, Olt J, Hardy K, Busch-Nentwich EM, Maeda R, Clemens-Grisham R, Krey JF, Nechiporuk AV, Barr-Gillespie PG, Marcotti W, Nicolson T. Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt). Elife. 6. PMID 28534737 DOI: 10.7554/Elife.28474 |
0.702 |
|
2017 |
Erickson T, Morgan CP, Olt J, Hardy K, Busch-Nentwich E, Maeda R, Clemens R, Krey JF, Nechiporuk A, Barr-Gillespie PG, Marcotti W, Nicolson T. Author response: Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt) Elife. DOI: 10.7554/Elife.28474.020 |
0.661 |
|
2008 |
Obholzer N, Wolfson S, Trapani JG, Mo W, Nechiporuk A, Busch-Nentwich E, Seiler C, Sidi S, Söllner C, Duncan RN, Boehland A, Nicolson T. 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. PMID 18305245 DOI: 10.1523/Jneurosci.5230-07.2008 |
0.539 |
|
2007 |
Geisler R, Rauch GJ, Geiger-Rudolph S, Albrecht A, van Bebber F, Berger A, Busch-Nentwich E, Dahm R, Dekens MP, Dooley C, Elli AF, Gehring I, Geiger H, Geisler M, Glaser S, et al. Large-scale mapping of mutations affecting zebrafish development. Bmc Genomics. 8: 11. PMID 17212827 DOI: 10.1186/1471-2164-8-11 |
0.63 |
|
2004 |
Sidi S, Busch-Nentwich E, Friedrich R, Schoenberger U, Nicolson T. gemini encodes a zebrafish L-type calcium channel that localizes at sensory hair cell ribbon synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 4213-23. PMID 15115817 DOI: 10.1523/JNEUROSCI.0223-04.2004 |
0.714 |
|
2004 |
Busch-Nentwich E, Söllner C, Roehl H, Nicolson T. The deafness gene dfna5 is crucial for ugdh expression and HA production in the developing ear in zebrafish. Development (Cambridge, England). 131: 943-51. PMID 14736743 DOI: 10.1242/dev.00961 |
0.615 |
|
2003 |
Söllner C, Burghammer M, Busch-Nentwich E, Berger J, Schwarz H, Riekel C, Nicolson T. Control of crystal size and lattice formation by starmaker in otolith biomineralization. Science (New York, N.Y.). 302: 282-6. PMID 14551434 DOI: 10.1126/science.1088443 |
0.571 |
|
Show low-probability matches. |