Nicola Strenzke

BetaIVSigma1 spectrin stabilizes the nodes of Ranvier and axon initial segments.

Expression pattern and functional characterization of connexin29 in transgenic mice.

CSPalpha-deficiency causes massive and rapid photoreceptor degeneration.

Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV.

Complexin-I is required for high-fidelity transmission at the endbulb of Held auditory synapse.

The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing.

Onset coding is degraded in auditory nerve fibers from mutant mice lacking synaptic ribbons.

Hearing requires otoferlin-dependent efficient replenishment of synaptic vesicles in hair cells.

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome.

Bassoon and the synaptic ribbon organize Ca²+ channels and vesicles to add release sites and promote refilling.

Connexin32 can restore hearing in connexin26 deficient mice.

Mice do not require auditory input for the normal development of their ultrasonic vocalizations.

Deletion of the presynaptic scaffold CAST reduces active zone size in rod photoreceptors and impairs visual processing.

A critical role for the cholesterol-associated proteolipids PLP and M6B in myelination of the central nervous system.

Disruption of the presynaptic cytomatrix protein bassoon degrades ribbon anchorage, multiquantal release, and sound encoding at the hair cell afferent synapse.

Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling.

Concurrent maturation of inner hair cell synaptic Ca2+ influx and auditory nerve spontaneous activity around hearing onset in mice.

Mastoid cavity obliteration and Vibrant Soundbridge implantation for patients with mixed hearing loss.

Bassoon-disruption slows vesicle replenishment and induces homeostatic plasticity at a CNS synapse.

Optogenetic stimulation of the auditory pathway.

The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice.