13 results on '"Alagramam, K. N."'
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2. Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein
3. ACF7 Is a Hair-Bundle Antecedent, Positioned to Integrate Cuticular Plate Actin and Somatic Tubulin
4. Noddy, a Mouse Harboring a Missense Mutation in Protocadherin-15, Reveals the Impact of Disrupting a Critical Interaction Site between Tip-Link Cadherins in Inner Ear Hair Cells
5. The Mechanosensory Structure of the Hair Cell Requires Clarin-1, a Protein Encoded by Usher Syndrome III Causative Gene
6. Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation
7. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
8. A New Mouse Insertional Mutation That Causes Sensorineural Deafness and Vestibular Defects
9. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
10. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
11. A new mouse insertional mutation that causes sensorineural deafness and vestibular defects
12. Erratum: Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (Human Molecular Genetics (2001) vol. 10 (1709-1718))
13. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
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