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Nicola Strenzke - Publications

Affiliations: 
Institute of Auditory Neuroscience University of Goettingen Medical School 
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51 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
2025 Oestreicher D, Malpede AM, Reitmeier A, Bräuer CP, Schoch L, Strenzke N, Pangrsic T. Noise-induced ribbon synapse loss in the mouse basal cochlear region does not reduce inner hair cell exocytosis. Frontiers in Cellular Neuroscience. 18: 1523978. PMID 39839350 DOI: 10.3389/fncel.2024.1523978  0.363
2024 Oestreicher D, Chepurwar S, Kusch K, Rankovic V, Jung S, Strenzke N, Pangrsic T. CaBP1 and 2 enable sustained Ca1.3 calcium currents and synaptic transmission in inner hair cells. Elife. 13. PMID 39718549 DOI: 10.7554/eLife.93646  0.738
2024 Dörje NM, Shvachiy L, Kück F, Outeiro TF, Strenzke N, Beutner D, Setz C. Age-related alterations in efferent medial olivocochlear-outer hair cell and primary auditory ribbon synapses in CBA/J mice. Frontiers in Cellular Neuroscience. 18: 1412450. PMID 38988659 DOI: 10.3389/fncel.2024.1412450  0.376
2023 Chen H, Monga M, Fang Q, Slitin L, Neef J, Chepurwar SS, Mingroni Netto RC, Lezirovitz K, Tabith A, Benseler F, Brose N, Kusch K, Wichmann C, Strenzke N, Vona B, et al. Ca2+-binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing. Protein & Cell. PMID 38066594 DOI: 10.1093/procel/pwad058  0.701
2023 Michanski S, Kapoor R, Steyer AM, Möbius W, Früholz I, Ackermann F, Gültas M, Garner CC, Hamra FK, Neef J, Strenzke N, Moser T, Wichmann C. Piccolino is required for ribbon architecture at cochlear inner hair cell synapses and for hearing. Embo Reports. e56702. PMID 37477166 DOI: 10.15252/embr.202256702  0.479
2022 Hausrat TJ, Vogl C, Neef J, Schweizer M, Yee BK, Strenzke N, Kneussel M. 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. PMID 36518539 DOI: 10.3389/fcell.2022.987691  0.377
2022 Chepurwar S, von Loh SM, Wigger DC, Neef J, Frommolt P, Beutner D, Lang-Roth R, Kubisch C, Strenzke N, Volk AE. A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2. Human Molecular Genetics. PMID 36300302 DOI: 10.1093/hmg/ddac267  0.718
2022 Maul A, Huebner AK, Strenzke N, Moser T, Rübsamen R, Jovanovic S, Hübner CA. 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. PMID 35129434 DOI: 10.7554/eLife.72251  0.4
2021 Stalmann U, Franke AJ, Al-Moyed H, Strenzke N, Reisinger E. 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. PMID 34335185 DOI: 10.3389/fncel.2021.677543  0.315
2019 Kroll J, Jaime Tobón LM, Vogl C, Neef J, Kondratiuk I, König M, Strenzke N, Wichmann C, Milosevic I, Moser T. Endophilin-A regulates presynaptic Ca influx and synaptic vesicle recycling in auditory hair cells. The Embo Journal. PMID 30733243 DOI: 10.15252/Embj.2018100116  0.489
2018 Haag N, Schüler S, Nietzsche S, Hübner CA, Strenzke N, Qualmann B, Kessels MM. 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. PMID 30157434 DOI: 10.1016/J.Celrep.2018.07.087  0.352
2018 Cruces-Solís H, Jing Z, Babaev O, Rubin J, Gür B, Krueger-Burg D, Strenzke N, de Hoz L. Auditory midbrain coding of statistical learning that results from discontinuous sensory stimulation. Plos Biology. 16: e2005114. PMID 30048446 DOI: 10.1371/Journal.Pbio.2005114  0.361
2018 Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, et al. Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Human Genetics. PMID 29435658 DOI: 10.1007/S00439-018-1870-7  0.311
2018 Jean P, Lopez de la Morena D, Michanski S, Jaime Tobón LM, Chakrabarti R, Picher MM, Neef J, Jung S, Gültas M, Maxeiner S, Neef A, Wichmann C, Strenzke N, Grabner C, Moser T. The synaptic ribbon is critical for sound encoding at high rates and with temporal precision. Elife. 7. PMID 29328020 DOI: 10.7554/Elife.29275  0.559
2018 Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, et al. The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Human Genetics. PMID 29305691 DOI: 10.1007/S00439-017-1862-Z  0.442
2017 Vogl C, Butola T, Haag N, Hausrat TJ, Leitner MG, Moutschen M, Lefèbvre PP, Speckmann C, Garrett L, Becker L, Fuchs H, Hrabe de Angelis M, Nietzsche S, Kessels MM, Oliver D, ... ... Strenzke N, et al. The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing. Embo Reports. PMID 28893864 DOI: 10.15252/Embr.201643689  0.462
2017 Lukashkina VA, Levic S, Lukashkin AN, Strenzke N, Russell IJ. A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanics. Nature Communications. 8: 14530. PMID 28220769 DOI: 10.1038/ncomms14530  0.314
2017 Picher MM, Gehrt A, Meese S, Ivanovic A, Predoehl F, Jung S, Schrauwen I, Dragonetti AG, Colombo R, Van Camp G, Strenzke N, Moser T. Ca(2+)-binding protein 2 inhibits Ca(2+)-channel inactivation in mouse inner hair cells. Proceedings of the National Academy of Sciences of the United States of America. PMID 28183797 DOI: 10.1073/Pnas.1617533114  0.556
2016 Strenzke N, Chakrabarti R, Al-Moyed H, Müller A, Hoch G, Pangrsic T, Yamanbaeva G, Lenz C, Pan KT, Auge E, Geiss-Friedlander R, Urlaub H, Brose N, Wichmann C, Reisinger E. Hair cell synaptic dysfunction, auditory fatigue and thermal sensitivity in otoferlin Ile515Thr mutants. The Embo Journal. PMID 27729456 DOI: 10.15252/Embj.201694564  0.509
2016 Ohn TL, Rutherford MA, Jing Z, Jung S, Duque-Afonso CJ, Hoch G, Picher MM, Scharinger A, Strenzke N, Moser T. Hair cells use active zones with different voltage dependence of Ca2+ influx to decompose sounds into complementary neural codes. Proceedings of the National Academy of Sciences of the United States of America. PMID 27462107 DOI: 10.1073/Pnas.1605737113  0.488
2016 Vogl C, Panou I, Yamanbaeva G, Wichmann C, Mangosing SJ, Vilardi F, Indzhykulian AA, Pangršič T, Santarelli R, Rodriguez-Ballesteros M, Weber T, Jung S, Cardenas E, Wu X, Wojcik SM, ... ... Strenzke N, et al. Tryptophan-rich basic protein (WRB) mediates insertion of the tail-anchored protein otoferlin and is required for hair cell exocytosis and hearing. The Embo Journal. PMID 27458190 DOI: 10.15252/Embj.201593565  0.543
2016 Sommen M, Schrauwen I, Vandeweyer G, Boeckx N, Corneveaux JJ, van den Ende J, Boudewyns A, De Leenheer E, Janssens S, Claes K, Verstreken M, Strenzke N, Predöhl F, Wuyts W, Mortier G, et al. DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined With a Mutation Classification System. Human Mutation. PMID 27068579 DOI: 10.1002/Humu.22999  0.338
2015 Jung S, Maritzen T, Wichmann C, Jing Z, Neef A, Revelo NH, Al-Moyed H, Meese S, Wojcik SM, Panou I, Bulut H, Schu P, Ficner R, Reisinger E, Rizzoli SO, ... ... Strenzke N, et al. Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing. The Embo Journal. PMID 26446278 DOI: 10.15252/Embj.201591885  0.419
2015 Moser T, Strenzke N. Synaptic encoding and processing of auditory information in physiology and disease. Hearing Research. PMID 26119179 DOI: 10.1016/J.Heares.2015.06.015  0.403
2015 Jung S, Oshima-Takago T, Chakrabarti R, Wong AB, Jing Z, Yamanbaeva G, Picher MM, Wojcik SM, Göttfert F, Predoehl F, Michel K, Hell SW, Schoch S, Strenzke N, Wichmann C, et al. Rab3-interacting molecules 2α and 2β promote the abundance of voltage-gated CaV1.3 Ca2+ channels at hair cell active zones. Proceedings of the National Academy of Sciences of the United States of America. 112: E3141-9. PMID 26034270 DOI: 10.1073/Pnas.1417207112  0.532
2015 Pangrši? T, Gabrielaitis M, Michanski S, Schwaller B, Wolf F, Strenzke N, Moser T. EF-hand protein Ca2+ buffers regulate Ca2+ influx and exocytosis in sensory hair cells. Proceedings of the National Academy of Sciences of the United States of America. 112: E1028-37. PMID 25691754 DOI: 10.1073/Pnas.1416424112  0.483
2014 Hernandez VH, Gehrt A, Jing Z, Hoch G, Jeschke M, Strenzke N, Moser T. Optogenetic stimulation of the auditory nerve. Journal of Visualized Experiments : Jove. e52069. PMID 25350571 DOI: 10.3791/52069  0.384
2014 Bosen F, Schütz M, Beinhauer A, Strenzke N, Franz T, Willecke K. The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice. Febs Letters. 588: 1795-801. PMID 24685692 DOI: 10.1016/J.Febslet.2014.03.040  0.374
2014 Hernandez VH, Gehrt A, Reuter K, Jing Z, Jeschke M, Mendoza Schulz A, Hoch G, Bartels M, Vogt G, Garnham CW, Yawo H, Fukazawa Y, Augustine GJ, Bamberg E, Kügler S, ... ... Strenzke N, et al. Optogenetic stimulation of the auditory pathway. The Journal of Clinical Investigation. 124: 1114-29. PMID 24509078 DOI: 10.1172/Jci69050  0.381
2014 Mendoza Schulz A, Jing Z, Sánchez Caro JM, Wetzel F, Dresbach T, Strenzke N, Wichmann C, Moser T. Bassoon-disruption slows vesicle replenishment and induces homeostatic plasticity at a CNS synapse. The Embo Journal. 33: 512-27. PMID 24442636 DOI: 10.1002/Embj.201385887  0.502
2013 Wong AB, Jing Z, Rutherford MA, Frank T, Strenzke N, Moser T. Concurrent maturation of inner hair cell synaptic Ca2+ influx and auditory nerve spontaneous activity around hearing onset in mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 10661-6. PMID 23804089 DOI: 10.1523/Jneurosci.1215-13.2013  0.543
2013 Lipstein N, Sakaba T, Cooper BH, Lin KH, Strenzke N, Ashery U, Rhee JS, Taschenberger H, Neher E, Brose N. Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling. Neuron. 79: 82-96. PMID 23770256 DOI: 10.1016/J.Neuron.2013.05.011  0.468
2013 El-Kordi A, Kästner A, Grube S, Klugmann M, Begemann M, Sperling S, Hammerschmidt K, Hammer C, Stepniak B, Patzig J, de Monasterio-Schrader P, Strenzke N, Flügge G, Werner HB, Pawlak R, et al. A single gene defect causing claustrophobia. Translational Psychiatry. 3: e254. PMID 23632458 DOI: 10.1038/Tp.2013.28  0.321
2013 Jing Z, Rutherford MA, Takago H, Frank T, Fejtova A, Khimich D, Moser T, Strenzke N. Disruption of the presynaptic cytomatrix protein bassoon degrades ribbon anchorage, multiquantal release, and sound encoding at the hair cell afferent synapse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 4456-67. PMID 23467361 DOI: 10.1523/Jneurosci.3491-12.2013  0.582
2012 tom Dieck S, Specht D, Strenzke N, Hida Y, Krishnamoorthy V, Schmidt KF, Inoue E, Ishizaki H, Tanaka-Okamoto M, Miyoshi J, Hagiwara A, Brandstätter JH, Löwel S, Gollisch T, Ohtsuka T, et al. Deletion of the presynaptic scaffold CAST reduces active zone size in rod photoreceptors and impairs visual processing. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 12192-203. PMID 22933801 DOI: 10.1523/Jneurosci.0752-12.2012  0.448
2012 Hammerschmidt K, Reisinger E, Westekemper K, Ehrenreich L, Strenzke N, Fischer J. Mice do not require auditory input for the normal development of their ultrasonic vocalizations. Bmc Neuroscience. 13: 40. PMID 22533376 DOI: 10.1186/1471-2202-13-40  0.41
2012 Pangrsic T, Strenzke N, Schwaller B, Moser T. The Role of Mobile Calcium Buffers in Synaptic Transmission at the Inner Hair Cell Ribbon Synapse Biophysical Journal. 102: 319a. DOI: 10.1016/J.Bpj.2011.11.1752  0.533
2011 Degen J, Schütz M, Dicke N, Strenzke N, Jokwitz M, Moser T, Willecke K. Connexin32 can restore hearing in connexin26 deficient mice. European Journal of Cell Biology. 90: 817-24. PMID 21813206 DOI: 10.1016/J.Ejcb.2011.05.001  0.422
2011 Schütz M, Auth T, Gehrt A, Bosen F, Körber I, Strenzke N, Moser T, Willecke K. The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome. Human Molecular Genetics. 20: 28-39. PMID 20926451 DOI: 10.1093/Hmg/Ddq429  0.439
2010 Frank T, Rutherford MA, Strenzke N, Neef A, PangrÅ¡ič T, Khimich D, Fejtova A, Fetjova A, Gundelfinger ED, Liberman MC, Harke B, Bryan KE, Lee A, Egner A, Riedel D, et al. Bassoon and the synaptic ribbon organize Ca²+ channels and vesicles to add release sites and promote refilling. Neuron. 68: 724-38. PMID 21092861 DOI: 10.1016/J.Neuron.2010.10.027  0.623
2010 Pangrsic T, Lasarow L, Reuter K, Takago H, Schwander M, Riedel D, Frank T, Tarantino LM, Bailey JS, Strenzke N, Brose N, Müller U, Reisinger E, Moser T. Hearing requires otoferlin-dependent efficient replenishment of synaptic vesicles in hair cells. Nature Neuroscience. 13: 869-76. PMID 20562868 DOI: 10.1038/Nn.2578  0.526
2010 Buran BN, Strenzke N, Neef A, Gundelfinger ED, Moser T, Liberman MC. Onset coding is degraded in auditory nerve fibers from mutant mice lacking synaptic ribbons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 7587-97. PMID 20519533 DOI: 10.1523/Jneurosci.0389-10.2010  0.727
2010 Frank T, Rutherford MA, Strenzke N, Neef A, Pangrši? T, Khimich D, Fejtova A, Gundelfinger ED, Liberman MC, Harke B, Bryan KE, Lee A, Egner A, Riedel D, Moser T. Bassoon and the Synaptic Ribbon Organize Ca2+ Channels and Vesicles to Add Release Sites and Promote Refilling Neuron. 68: 1202. DOI: 10.1016/j.neuron.2010.12.020  0.524
2009 Neef J, Gehrt A, Bulankina AV, Meyer AC, Riedel D, Gregg RG, Strenzke N, Moser T. The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 10730-40. PMID 19710324 DOI: 10.1523/Jneurosci.1577-09.2009  0.45
2009 Strenzke N, Chanda S, Kopp-Scheinpflug C, Khimich D, Reim K, Bulankina AV, Neef A, Wolf F, Brose N, Xu-Friedman MA, Moser T. Complexin-I is required for high-fidelity transmission at the endbulb of Held auditory synapse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 7991-8004. PMID 19553439 DOI: 10.1523/Jneurosci.0632-09.2009  0.582
2008 Rickheit G, Maier H, Strenzke N, Andreescu CE, De Zeeuw CI, Muenscher A, Zdebik AA, Jentsch TJ. Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV. The Embo Journal. 27: 2907-17. PMID 18833191 DOI: 10.1038/Emboj.2008.203  0.415
2008 Strenzke N, Pauli-Magnus D, Meyer A, Brandt A, Maier H, Moser T. Update on physiology and pathophysiology of the inner ear : PPPathomechanisms of sensorineural hearing loss | Update zur Physiologie und Pathophysiologie des Innenohrs : Pathomechanismen der Sensorineuralen Schwerhörigkeit Hno. 56: 27-36. PMID 18210004 DOI: 10.1007/S00106-007-1640-7  0.371
2007 Pauli-Magnus D, Hoch G, Strenzke N, Anderson S, Jentsch TJ, Moser T. Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses. Neuroscience. 149: 673-84. PMID 17869440 DOI: 10.1016/J.Neuroscience.2007.08.010  0.518
2006 Schmitz F, Tabares L, Khimich D, Strenzke N, de la Villa-Polo P, Castellano-Muñoz M, Bulankina A, Moser T, Fernández-Chacón R, Südhof TC. CSPalpha-deficiency causes massive and rapid photoreceptor degeneration. Proceedings of the National Academy of Sciences of the United States of America. 103: 2926-31. PMID 16477021 DOI: 10.1073/Pnas.0510060103  0.491
2006 Eiberger J, Kibschull M, Strenzke N, Schober A, Büssow H, Wessig C, Djahed S, Reucher H, Koch DA, Lautermann J, Moser T, Winterhager E, Willecke K. Expression pattern and functional characterization of connexin29 in transgenic mice. Glia. 53: 601-11. PMID 16435366 DOI: 10.1002/Glia.20315  0.389
2004 Lacas-Gervais S, Guo J, Strenzke N, Scarfone E, Kolpe M, Jahkel M, De Camilli P, Moser T, Rasband MN, Solimena M. BetaIVSigma1 spectrin stabilizes the nodes of Ranvier and axon initial segments. The Journal of Cell Biology. 166: 983-90. PMID 15381686 DOI: 10.1083/Jcb.200408007  0.323
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