Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss von Honda, Keiji, Griffith, Andrew J.

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TMC1 and TMC2 Are Components of the Mechanotransduction Channel in Hair Cells of the Mammalian Inner Ear von Pan, Bifeng, Géléoc, Gwenaelle S., Asai, Yukako, Horwitz, Geoffrey C., Kurima, Kiyoto, Ishikawa, Kotaro, Kawashima, Yoshiyuki, Griffith, Andrew J., Holt, Jeffrey R.

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TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia von Kurima, Kiyoto, Ebrahim, Seham, Pan, Bifeng, Sedlacek, Miloslav, Sengupta, Prabuddha, Millis, Bryan A., Cui, Runjia, Nakanishi, Hiroshi, Fujikawa, Taro, Kawashima, Yoshiyuki, Choi, Byung Yoon, Monahan, Kelly, Holt, Jeffrey R., Griffith, Andrew J., Kachar, Bechara

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Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes von Kawashima, Yoshiyuki, Géléoc, Gwenaëlle S G, Kurima, Kiyoto, Labay, Valentina, Lelli, Andrea, Asai, Yukako, Makishima, Tomoko, Wu, Doris K, Della Santina, Charles C, Holt, Jeffrey R, Griffith, Andrew J

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Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularis von Strepay, Dillon, Olszewski, Rafal T., Nixon, Sydney, Korrapati, Soumya, Adadey, Samuel, Griffith, Andrew J., Su, Yijun, Liu, Jiamin, Vishwasrao, Harshad, Gu, Shoujun, Saunders, Thomas, Roux, Isabelle, Hoa, Michael

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Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis von Hertzano, Ronna, Elkon, Ran, Kurima, Kiyoto, Morrisson, Annie, Chan, Siaw-Lin, Sallin, Michelle, Biedlingmaier, Andrew, Darling, Douglas S, Griffith, Andrew J, Eisenman, David J, Strome, Scott E

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SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice von Li, Xiangming, Sanneman, Joel D, Harbidge, Donald G, Zhou, Fei, Ito, Taku, Nelson, Raoul, Picard, Nicolas, Chambrey, Régine, Eladari, Dominique, Miesner, Tracy, Griffith, Andrew J, Marcus, Daniel C, Wangemann, Philine

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Acute genetic ablation of pendrin lowers blood pressure in mice von Trepiccione, Francesco, Soukaseum, Christelle, Baudrie, Veronique, Kumai, Yusuke, Teulon, Jacques, Villoutreix, Bruno, Cornière, Nicolas, Wangemann, Philine, Griffith, Andrew J, Byung Choi, Yoon, Hadchouel, Juliette, Chambrey, Regine, Eladari, Dominique

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Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome von Nishio, Ayako, Ito, Taku, Cheng, Hui, Fitzgerald, Tracy S, Wangemann, Philine, Griffith, Andrew J

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Dissection of the Endolymphatic Sac from Mice von Honda, Keiji, Lee, Hyun Jae, Griffith, Andrew J., Roux, Isabelle

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Genetic Hearing Loss Associated With Autoinflammation von Nakanishi, Hiroshi, Prakash, Pragya, Ito, Taku, Kim, H. Jeffrey, Brewer, Carmen C., Harrow, Danielle, Roux, Isabelle, Hosokawa, Seiji, Griffith, Andrew J.

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Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria von Adeyemo, Adebolajo, Faridi, Rabia, Chattaraj, Parna, Yousaf, Rizwan, Tona, Risa, Okorie, Samuel, Bharadwaj, Thashi, Nouel-Saied, Liz M, Acharya, Anushree, Schrauwen, Isabelle, Morell, Robert J, Leal, Suzanne M, Friedman, Thomas B, Griffith, Andrew J, Roux, Isabelle

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Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing von Kitajiri, Shin-ichiro, Sakamoto, Takeshi, Belyantseva, Inna A., Goodyear, Richard J., Stepanyan, Ruben, Fujiwara, Ikuko, Bird, Jonathan E., Riazuddin, Saima, Riazuddin, Sheikh, Ahmed, Zubair M., Hinshaw, Jenny E., Sellers, James, Bartles, James R., Hammer, John A., Richardson, Guy P., Griffith, Andrew J., Frolenkov, Gregory I., Friedman, Thomas B.

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Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome von Sethna, Saumil, Zein, Wadih M., Riaz, Sehar, Giese, Arnaud Pj, Schultz, Julie M., Duncan, Todd, Hufnagel, Robert B., Brewer, Carmen C., Griffith, Andrew J., Redmond, T. Michael, Riazuddin, Saima, Friedman, Thomas B., Ahmed, Zubair M.

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Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function von Nakanishi, Hiroshi, Kurima, Kiyoto, Pan, Bifeng, Wangemann, Philine, Fitzgerald, Tracy S., Géléoc, Gwenaëlle S., Holt, Jeffrey R., Griffith, Andrew J.

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Slc26a4 -insufficiency causes fluctuating hearing loss and stria vascularis dysfunction von Ito, Taku, Li, Xiangming, Kurima, Kiyoto, Choi, Byung Yoon, Wangemann, Philine, Griffith, Andrew J

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Molecular architecture underlying fluid absorption by the developing inner ear von Honda, Keiji, Kim, Sung Huhn, Kelly, Michael C, Burns, Joseph C, Constance, Laura, Li, Xiangming, Zhou, Fei, Hoa, Michael, Kelley, Matthew W, Wangemann, Philine, Morell, Robert J, Griffith, Andrew J

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Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86 von Rehman, Atteeq U., Santos-Cortez, Regie Lyn P., Morell, Robert J., Drummond, Meghan C., Ito, Taku, Lee, Kwanghyuk, Khan, Asma A., Basra, Muhammad Asim R., Wasif, Naveed, Ayub, Muhammad, Ali, Rana A., Raza, Syed I., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael, Riazuddin, Saima, Billington, Neil, Khan, Shaheen N., Friedman, Penelope L., Griffith, Andrew J., Ahmad, Wasim, Riazuddin, Sheikh, Leal, Suzanne M., Friedman, Thomas B.

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Cochlear Pathomorphogenesis of Incomplete Partition Type II in Slc26a4-Null Mice von Ito, Taku, Fujikawa, Taro, Honda, Keiji, Makabe, Ayane, Watanabe, Hiroki, Bai, Jing, Kawashima, Yoshiyuki, Miwa, Toru, Griffith, Andrew J., Tsutsumi, Takeshi

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Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction Channels von Makabe, Ayane, Kawashima, Yoshiyuki, Sakamaki, Yuriko, Maruyama, Ayako, Fujikawa, Taro, Ito, Taku, Kurima, Kiyoto, Griffith, Andrew J., Tsutsumi, Takeshi

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