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Human Molecular Genetics|September 13, 2013
CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndromeJoseph A Micucci, Wanda S Layman, Elizabeth A Hurd, et al.
Investigative Ophthalmology & Visual Science|July 2, 2026
Müller Glia-Exclusive CLRN1 Expression Drives Non-Cell-Autonomous Photoreceptor Degeneration in Usher Syndrome Type 3AYeachan Lee, Yuanyuan Gao, Van Phuc Nguyen, et al.
Translational Vision Science & Technology|February 16, 2023
USH2A Gene Mutations in Rabbits Lead to Progressive Retinal Degeneration and Hearing LossVan Phuc Nguyen, Jun Song, Diane Prieskorn, et al.
Elife|November 29, 2022
Cellular reprogramming with ATOH1, GFI1, and POU4F3 implicate epigenetic changes and cell-cell signaling as obstacles to hair cell regeneration in mature mammalsAmrita A Iyer, Ishwar Hosamani, John D Nguyen, et al.
Plos One|August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochleaMatthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 20, 2004
Identification and characterization of choline transporter-like protein 2, an inner ear glycoprotein of 68 and 72 kDa that is the target of antibody-induced hearing lossThankam S Nair, Kelley E Kozma, Nickoleta L Hoefling, et al.
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
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