Sonja Brosel, Ph.D. - Publications

2010 Columbia University, New York, NY 
Genetics, Molecular Biology

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Gleiss H, Encke J, Lingner A, Jennings TR, Brosel S, Kunz L, Grothe B, Pecka M. Cooperative population coding facilitates efficient sound-source separability by adaptation to input statistics. Plos Biology. 17: e3000150. PMID 31356637 DOI: 10.1371/Journal.Pbio.3000150  0.436
2017 Brosel S, Grothe B, Kunz L. An auditory brainstem nucleus as a model system for neuronal metabolic demands. The European Journal of Neuroscience. PMID 29205598 DOI: 10.1111/Ejn.13789  0.459
2015 Direnberger S, Banchi R, Brosel S, Seebacher C, Laimgruber S, Uhl R, Felmy F, Straka H, Kunz L. Analysis of signal processing in vestibular circuits with a novel light-emitting diodes-based fluorescence microscope. The European Journal of Neuroscience. 41: 1332-44. PMID 25847143 DOI: 10.1111/Ejn.12907  0.419
2012 Casarin A, Giorgi G, Pertegato V, Siviero R, Cerqua C, Doimo M, Basso G, Sacconi S, Cassina M, Rizzuto R, Brosel S, M Davidson M, Dimauro S, Schon EA, Clementi M, et al. Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations. Orphanet Journal of Rare Diseases. 7: 21. PMID 22515166 DOI: 10.1186/1750-1172-7-21  0.561
2010 Papeta N, Zheng Z, Schon EA, Brosel S, Altintas MM, Nasr SH, Reiser J, D'Agati VD, Gharavi AG. Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice. The Journal of Clinical Investigation. 120: 4055-64. PMID 20978358 DOI: 10.1172/Jci43721  0.586
2010 Brosel S, Yang H, Tanji K, Bonilla E, Schon EA. Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease. The American Journal of Pathology. 177: 2541-8. PMID 20864674 DOI: 10.2353/Ajpath.2010.100229  0.571
2010 Yang H, Brosel S, Acin-Perez R, Slavkovich V, Nishino I, Khan R, Goldberg IJ, Graziano J, Manfredi G, Schon EA. Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2. Human Molecular Genetics. 19: 170-80. PMID 19837698 DOI: 10.1093/Hmg/Ddp477  0.601
2009 Acin-Perez R, Salazar E, Brosel S, Yang H, Schon EA, Manfredi G. Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects. Embo Molecular Medicine. 1: 392-406. PMID 20049744 DOI: 10.1002/Emmm.200900046  0.553
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