(2016) Decalmodulation of Cav1 channels by CaBPs.

(2015) Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing.

(2009) Membrane targeting of the EF-hand containing calcium-sensing proteins CaBP7 and CaBP8.

(2017) Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performance.

(2014) A frameshift mutation in GRXCR2 causes recessively inherited hearing loss.

(2012) Ca2+-dependent modulation of voltage-gated Ca2+ channels.

(2022) Calcium Channels in Retinal Function and Disease.

(2016) Transcriptomic Analysis of Mouse Cochlear Supporting Cell Maturation Reveals Large-Scale Changes in Notch Responsiveness Prior to the Onset of Hearing.

(2015) Sense and specificity in neuronal calcium signalling.

(2012) Evolution and functional diversity of the Calcium Binding Proteins (CaBPs).

(2021) Current Response in Ca V 1.3(--) Mouse Vestibular and Cochlear Hair Cells.

(2022) Cation Permeability of Voltage-Gated Hair Cell Ca(2+) Channels of the Vertebrate Labyrinth.

(2009) The molecular architecture of ribbon presynaptic terminals.

(2022) Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant.

(2012) Structural basis for the regulation of L-type voltage-gated calcium channels: interactions between the N-terminal cytoplasmic domain and Ca(2+)-calmodulin.

(2010) The diverse roles of ribbon synapses in sensory neurotransmission.

(2022) Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort.

(2018) Genetics of hearing loss in the Arab population of Northern Israel.

(2018) [Molecular Understanding of Hearing - How Does This Matter to the Hearing Impaired?]

(2023) Probing the role of the C2F domain of otoferlin.

(2022) Oncomodulin (OCM) uniquely regulates calcium signaling in neonatal cochlear outer hair cells.

(2020) Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.

(2023) Mapping oto-pharyngeal development in a human inner ear organoid model.

(2021) Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors.

(2013) Apo states of calmodulin and CaBP1 control CaV1 voltage-gated calcium channel function through direct competition for the IQ domain.

(2016) Expression and Localization of CaBP Ca2+ Binding Proteins in the Mouse Cochlea.

(2018) Functions of CaBP1 and CaBP2 in the peripheral auditory system.

(2013) A phylomedicine approach to understanding the evolution of auditory sensory perception and disease in mammals.

(2021) TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling.

(2018) Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients.

(2023) Regulation of Cardiac Cav1.2 Channels by Calmodulin.

(2021) Cav1.4 dysfunction and congenital stationary night blindness type 2.

(2019) Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing.

(2010) Progress in the structural understanding of voltage-gated calcium channel (CaV) function and modulation.

(2010) Structural basis for the differential effects of CaBP1 and calmodulin on Ca(V)1.2 calcium-dependent inactivation.

(2023) Shared and organ-specific gene-expression programs during the development of the cochlea and the superior olivary complex.

(2023) Oncomodulin regulates spontaneous calcium signalling and maturation of afferent innervation in cochlear outer hair cells.

(2022) Genetics of Hearing Impairment.

(2020) RBP2 stabilizes slow Cav1.3 Ca(2+) channel inactivation properties of cochlear inner hair cells.

(2019) The co-occurrence of rare non-ocular phenotypes in patients with inherited retinal degenerations.

(2019) Ca(2+) sensor synaptotagmin-1 mediates exocytosis in mammalian photoreceptors.

(2019) Nanomachinery Organizing Release at Neuronal and Ribbon Synapses.

(2016) Lack of CaBP1Caldendrin or CaBP2 Leads to Altered Ganglion Cell Responses.

(2017) Genetic causes of moderate to severe hearing loss point to modifiers.

(2014) Calmodulin regulation (calmodulation) of voltage-gated calcium channels.

(2020) Auditory Neuropathy Spectrum Disorders: From Diagnosis to Treatment: Literature Review and Case Reports.

(2023) Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.

(2014) Localization and expression of CaBP1caldendrin in the mouse brain.

(2020) Molecular Assembly and Structural Plasticity of Sensory Ribbon Synapses-A Presynaptic Perspective.

(2012) The SNARE complex in neuronal and sensory cells.

(2021) Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.

(2019) Auditory synaptopathy, auditory neuropathy, and cochlear implantation.

(2018) Cochlear Proteins Associated with Noise-induced Hearing Loss: An Update.

(2011) Molecular biology of hearing.

(2012) EF hand-mediated Ca- and cGMP-signaling in photoreceptor synaptic terminals.

(2022) Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.

(2023) mTORC2 regulates auditory hair cell structure and function.

(2020) Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice.

(2013) From the ultrasonic to the infrared: molecular evolution and the sensory biology of bats.