Hair-Bundle Links: Genetics as the Gateway to Function
Author:
Publisher
Cold Spring Harbor Laboratory
Subject
General Biochemistry, Genetics and Molecular Biology
Reference133 articles.
1. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells
2. Interactions in the network of Usher syndrome type 1 proteins
3. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
4. The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15
5. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
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4. Unique transcriptomes of sensory and non-sensory neurons: insights from Splicing Regulatory States;Molecular Systems Biology;2024-03-04
5. PKHD1L1 is required for stereocilia bundle maintenance, durable hearing function and resilience to noise exposure;2024-03-04
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