Artur Indzhykulian

Affiliations: 
University of Kentucky, Lexington, KY 
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"Artur Indzhykulian"
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Publications

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Wu X, Ivanchenko MV, Al Jandal H, et al. (2019) PKHD1L1 is a coat protein of hair-cell stereocilia and is required for normal hearing. Nature Communications. 10: 3801
György B, Meijer EJ, Ivanchenko MV, et al. (2019) Gene Transfer with AAV9-PHP.B Rescues Hearing in a Mouse Model of Usher Syndrome 3A and Transduces Hair Cells in a Non-human Primate. Molecular Therapy. Methods & Clinical Development. 13: 1-13
György B, Sage C, Indzhykulian AA, et al. (2017) Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV. Molecular Therapy : the Journal of the American Society of Gene Therapy
Vogl C, Panou I, Yamanbaeva G, et al. (2016) Tryptophan-rich basic protein (WRB) mediates insertion of the tail-anchored protein otoferlin and is required for hair cell exocytosis and hearing. The Embo Journal
Wu X, Indzhykulian AA, Niksch PD, et al. (2016) Hair-Cell Mechanotransduction Persists in TRP Channel Knockout Mice. Plos One. 11: e0155577
Indzhykulian AA, Corey DP. (2015) In the Right Place at the Right Time: Is TMC1/2 the Transduction Channel for Hearing? Cell Reports. 12: 1531-2
Fang Q, Indzhykulian AA, Mustapha M, et al. (2015) The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing. Elife. 4
Scheffer DI, Zhang DS, Shen J, et al. (2015) XIRP2, an actin-binding protein essential for inner ear hair-cell stereocilia. Cell Reports. 10: 1811-8
Indzhykulian AA, Stepanyan R, Nelina A, et al. (2013) Molecular remodeling of tip links underlies mechanosensory regeneration in auditory hair cells. Plos Biology. 11: e1001583
Riazuddin S, Belyantseva IA, Giese AP, et al. (2012) Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nature Genetics. 44: 1265-71
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