Found: 8
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CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/s41467-017-00061-1
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- Publication type:
- Article
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.67361
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- Publication type:
- Article
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
- Published in:
- Nature Genetics, 2012, v. 44, n. 11, p. 1265, doi. 10.1038/ng.2426
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- Publication type:
- Article
An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003774
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- Publication type:
- Article
CIB2 regulates mTORC1 signaling and is essential for autophagy and visual function.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24056-1
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- Publication type:
- Article
Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.
- Published in:
- 2018
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- Publication type:
- journal article
Genomics of Otitis Media (OM): Molecular Genetics Approaches to Characterize Disease Pathophysiology.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00313
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- Publication type:
- Article
Radioprotective Effect of Aminothiol PrC-210 on Irradiated Inner Ear of Guinea Pig.
- Published in:
- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0143606
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- Publication type:
- Article