Nicola Strenzke
Georg-August-Universität Göttingen
H-index: 34
Europe-Germany
Top articles of Nicola Strenzke
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing | Protein & Cell | Han Chen Mehar Monga Qinghua Fang Loujin Slitin Jakob Neef | 2024/4/1 |
Auditory synaptopathy due to defects of vesicle turnover at the hair cell synapse: causes and consequences | Laryngo-Rhino-Otologie | Nicola Strenzke Maike Pelgrim Shashank Chepurwar | 2024/5 |
Auditorische Synaptopathie durch Störungen des Vesikelumsatzes an der Haarzell-Synapse: Ursachen und Folgen | Laryngo-Rhino-Otologie | Nicola Strenzke Maike Pelgrim Shashank Chepurwar | 2024/5 |
A cure for deafness? | Med | Nicola Strenzke | 2024/4/12 |
A mouse model for DFNB93 corroborates use-dependent deterioration of Synaptic Transmission and Auditory Nerve Fiber Spiking as the underlying disease mechanism | Laryngo-Rhino-Otologie | David Oestreicher Shashank Chepurwar Vladan Rankovic Dirk Beutner Nicola Strenzke | 2023/5 |
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2 | Human Molecular Genetics | Shashank Chepurwar Sarah M von Loh Daniela C Wigger Jakob Neef Peter Frommolt | 2023/4/1 |
CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells | bioRxiv | David Oestreicher Shashank Chepurwar Kathrin Kusch Vladan Rankovic Sangyong Jung | 2023/10/17 |
Patient perspectives on the need for improved hearing rehabilitation: A qualitative survey study of German cochlear implant users | Frontiers in Neuroscience | Victoria Hunniford Robert Kühler Bettina Wolf Daniel Keppeler Nicola Strenzke | 2023/1/23 |
Piccolino is required for ribbon architecture at cochlear inner hair cell synapses and for hearing | EMBO reports | Susann Michanski Rohan Kapoor Anna M Steyer Wiebke Möbius Iris Früholz | 2023/9/6 |
Unraveling haplotype errors in the DFNA33 locus | Frontiers in Genetics | Barbara Vona Sabrina Regele Aboulfazl Rad Nicola Strenzke Justin A Pater | 2023/8/21 |
Ein Mausmodell für DFNB93 bestätigt eine nutzungsabhängige Verschlechterung der synaptischen übertragung und der Hörnervenfaseraktivität als zugrunde liegenden … | Laryngo-Rhino-Otologie | David Oestreicher Shashank Chepurwar Vladan Rankovic Dirk Beutner Nicola Strenzke | 2023/5 |
Progressive axonopathy when oligodendrocytes lack the myelin protein CMTM5 | Elife | Tobias J Buscham Maria A Eichel-Vogel Anna M Steyer Olaf Jahn Nicola Strenzke | 2022/3/11 |
Eine Mutation in Atp11a verursacht die autosomal dominant vererbte auditorische Neuropathie Typ 2 (AUNA2). | Laryngo-Rhino-Otologie | Nicola Strenzke Shashank Chepurwar Daniela Wigger Dirk Beutner Ruth Lang-Roth | 2022/5 |
The Cl--channel TMEM16A is involved in the generation of cochlear Ca2+ waves and promotes the refinement of auditory brainstem networks in mice | Elife | Alena Maul Antje Kathrin Huebner Nicola Strenzke Tobias Moser Rudolf Rübsamen | 2022/2/7 |
How are intra-and postoperatively determined thresholds of objective measures comparable in cochlear implant patients | Laryngo-Rhino-Otologie | Astrid Klinge-Strahl Jenny Blum Nicola Strenzke Dirk Beutner | 2022/5 |
Performance and self‐perceived hearing impairment after cochlear implantation in Menière's disease | Laryngoscope Investigative Otolaryngology | Christian Wrobel Nicholas F Bevis Astrid Klinge‐Strahl Nicola Strenzke Dirk Beutner | 2022/2 |
A mutation in Atp11a causes autosomal dominant inherited auditory neuropathy type 2 (AUNA2). | Laryngo-Rhino-Otologie | Nicola Strenzke Shashank Chepurwar Daniela Wigger Dirk Beutner Ruth Lang-Roth | 2022/5 |
Piccolino regulates the architecture of the ribbon at cochlear inner hair cell synapses | bioRxiv | Susann Michanski Rohan Kapoor Anna M Steyer Wiebke Möbius Iris Früholz | 2022/12/16 |
Systematic multigene panel studies in hereditary hearing loss diagnose complex inheritance patterns involving multiple genes | Laryngo-Rhino-Otologie | Virginia Dyett Christoph Braunwarth Hendrik Rosewich Alexandr Kuranov Silke Kaulfuß | 2022/5 |
Monoallelic loss of the F-actin-binding protein radixin facilitates startle reactivity and pre-pulse inhibition in mice | Frontiers in Cell and Developmental Biology | Torben J Hausrat Christian Vogl Jakob Neef Michaela Schweizer Benjamin K Yee | 2022/11/28 |
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