Nicola Strenzke

Affiliations: 
Institute of Auditory Neuroscience University of Goettingen Medical School 
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"Nicola Strenzke"
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Chen H, Monga M, Fang Q, et al. (2023) Ca2+-binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing. Protein & Cell
Michanski S, Kapoor R, Steyer AM, et al. (2023) Piccolino is required for ribbon architecture at cochlear inner hair cell synapses and for hearing. Embo Reports. e56702
Hausrat TJ, Vogl C, Neef J, et al. (2022) Monoallelic loss of the F-actin-binding protein radixin facilitates startle reactivity and pre-pulse inhibition in mice. Frontiers in Cell and Developmental Biology. 10: 987691
Chepurwar S, von Loh SM, Wigger DC, et al. (2022) A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2. Human Molecular Genetics
Maul A, Huebner AK, Strenzke N, et al. (2022) The Cl-channel TMEM16A is involved in the generation of cochlear Ca waves and promotes the refinement of auditory brainstem networks in mice. Elife. 11
Stalmann U, Franke AJ, Al-Moyed H, et al. (2021) Otoferlin Is Required for Proper Synapse Maturation and for Maintenance of Inner and Outer Hair Cells in Mouse Models for DFNB9. Frontiers in Cellular Neuroscience. 15: 677543
Kroll J, Jaime Tobón LM, Vogl C, et al. (2019) Endophilin-A regulates presynaptic Ca influx and synaptic vesicle recycling in auditory hair cells. The Embo Journal
Haag N, Schüler S, Nietzsche S, et al. (2018) The Actin Nucleator Cobl Is Critical for Centriolar Positioning, Postnatal Planar Cell Polarity Refinement, and Function of the Cochlea. Cell Reports. 24: 2418-2431.e6
Cruces-Solís H, Jing Z, Babaev O, et al. (2018) Auditory midbrain coding of statistical learning that results from discontinuous sensory stimulation. Plos Biology. 16: e2005114
Tranebjærg L, Strenzke N, Lindholm S, et al. (2018) Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Human Genetics
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