Molecular remodeling of tip links underlies mechanosensory regeneration in auditory hair cells von Indzhykulian, Artur A, Stepanyan, Ruben, Nelina, Anastasiia, Spinelli, Kateri J, Ahmed, Zubair M, Belyantseva, Inna A, Friedman, Thomas B, Barr-Gillespie, Peter G, Frolenkov, Gregory I

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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease von Jenkinson, Emma M., Rehman, Atteeq U., Walsh, Tom, Clayton-Smith, Jill, Lee, Kwanghyuk, Morell, Robert J., Drummond, Meghan C., Khan, Shaheen N., Naeem, Muhammad Asif, Rauf, Bushra, Billington, Neil, Schultz, Julie M., Urquhart, Jill E., Lee, Ming K., Berry, Andrew, Hanley, Neil A., Mehta, Sarju, Cilliers, Deirdre, Clayton, Peter E., Kingston, Helen, Smith, Miriam J., Warner, Thomas T., Black, Graeme C., Trump, Dorothy, Davis, Julian R.E., Ahmad, Wasim, Leal, Suzanne M., Riazuddin, Sheikh, King, Mary-Claire, Friedman, Thomas B., Newman, William G.

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Pathophysiology of human hearing loss associated with variants in myosins von Miyoshi, Takushi, Belyantseva, Inna A, Sajeevadathan, Mrudhula, Friedman, Thomas B

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Growth factor and receptor malfunctions associated with human genetic deafness von Naz, Sadaf, Friedman, Thomas B.

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Tricellulin Is a Tight-Junction Protein Necessary for Hearing von Riazuddin, Saima, Ahmed, Zubair M., Fanning, Alan S., Lagziel, Ayala, Kitajiri, Shin-ichiro, Ramzan, Khushnooda, Khan, Shaheen N., Chattaraj, Parna, Friedman, Penelope L., Anderson, James M., Belyantseva, Inna A., Forge, Andrew, Riazuddin, Sheikh, Friedman, Thomas B.

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Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome von Isgrig, Kevin, Shteamer, Jack W., Belyantseva, Inna A., Drummond, Meghan C., Fitzgerald, Tracy S., Vijayakumar, Sarath, Jones, Sherri M., Griffith, Andrew J., Friedman, Thomas B., Cunningham, Lisa L., Chien, Wade W.

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Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse von Yousaf, Rizwan, Gu, Chunfang, Ahmed, Zubair M, Khan, Shaheen N, Friedman, Thomas B, Riazuddin, Sheikh, Shears, Stephen B, Riazuddin, Saima

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Interaction between the TBC1D24 TLDc domain and the KIBRA C2 domain is disrupted by two epilepsy-associated TBC1D24 missense variants von Tona, Risa, Inagaki, Sayaka, Ishibashi, Yasuko, Faridi, Rabia, Yousaf, Rizwan, Roux, Isabelle, Wilson, Elizabeth, Fenollar-Ferrer, Cristina, Chien, Wade W., Belyantseva, Inna A., Friedman, Thomas B.

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Live-cell imaging of actin dynamics reveals mechanisms of stereocilia length regulation in the inner ear von Drummond, Meghan C., Barzik, Melanie, Bird, Jonathan E., Zhang, Duan-Sun, Lechene, Claude P., Corey, David P., Cunningham, Lisa L., Friedman, Thomas B.

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Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical properties von Melli, Luca, Billington, Neil, Sun, Sara A, Bird, Jonathan E, Nagy, Attila, Friedman, Thomas B, Takagi, Yasuharu, Sellers, James R

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Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 von Riazuddin, Saima, Belyantseva, Inna A, Giese, Arnaud P J, Lee, Kwanghyuk, Indzhykulian, Artur A, Nandamuri, Sri Pratima, Yousaf, Rizwan, Sinha, Ghanshyam P, Lee, Sue, Terrell, David, Hegde, Rashmi S, Ali, Rana A, Anwar, Saima, Andrade-Elizondo, Paula B, Sirmaci, Asli, Parise, Leslie V, Basit, Sulman, Wali, Abdul, Ayub, Muhammad, Ansar, Muhammad, Ahmad, Wasim, Khan, Shaheen N, Akram, Javed, Tekin, Mustafa, Riazuddin, Sheikh, Cook, Tiffany, Buschbeck, Elke K, Frolenkov, Gregory I, Leal, Suzanne M, Friedman, Thomas B, Ahmed, Zubair M

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Synthesis and Characterization of Titania−Graphene Nanocomposites von Lambert, Timothy N, Chavez, Carlos A, Hernandez-Sanchez, Bernadette, Lu, Ping, Bell, Nelson S, Ambrosini, Andrea, Friedman, Thomas, Boyle, Timothy J, Wheeler, David R, Huber, Dale L

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Modifier variant of METTL13 suppresses human GAB1-associated profound deafness von Yousaf, Rizwan, Ahmed, Zubair M, Giese, Arnaud Pj, Morell, Robert J, Lagziel, Ayala, Dabdoub, Alain, Wilcox, Edward R, Riazuddin, Sheikh, Friedman, Thomas B, Riazuddin, Saima

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Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness von Nakano, Yoko, Kelly, Michael C., Rehman, Atteeq U., Boger, Erich T., Morell, Robert J., Kelley, Matthew W., Friedman, Thomas B., Bánfi, Botond

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Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP von Babahosseini, Hesam, Belyantseva, Inna A., Yousaf, Rizwan, Tona, Risa, Hadi, Shadan, Inagaki, Sayaka, Wilson, Elizabeth, Kitajiri, Shin-ichiro, Frolenkov, Gregory I., Friedman, Thomas B., Cartagena-Rivera, Alexander X.

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Combined AAV-mediated gene replacement therapy improves auditory function in a mouse model of human DFNB42 deafness von Isgrig, Kevin, Cartagena-Rivera, Alexander X., Wang, Hong Jun, Grati, Mhamed, Fernandez, Katharine A., Friedman, Thomas B., Belyantseva, Inna A., Chien, Wade

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New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder von Faridi, Rabia, Rea, Alessandro, Fenollar-Ferrer, Cristina, O’Keefe, Raymond T., Gu, Shoujun, Munir, Zunaira, Khan, Asma Ali, Riazuddin, Sheikh, Hoa, Michael, Naz, Sadaf, Newman, William G., Friedman, Thomas B.

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Defective Gpsm2/Gαi3 signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndrome von Mauriac, Stephanie A., Hien, Yeri E., Bird, Jonathan E., Carvalho, Steve Dos-Santos, Peyroutou, Ronan, Lee, Sze Chim, Moreau, Maite M., Blanc, Jean-Michel, Gezer, Aysegul, Medina, Chantal, Thoumine, Olivier, Beer-Hammer, Sandra, Friedman, Thomas B., Rüttiger, Lukas, Forge, Andrew, Nürnberg, Bernd, Sans, Nathalie, Montcouquiol, Mireille

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ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points von Krey, Jocelyn F, Liu, Chang, Belyantseva, Inna A, Bateschell, Michael, Dumont, Rachel A, Goldsmith, Jennifer, Chatterjee, Paroma, Morrill, Rachel S, Fedorov, Lev M, Foster, Sarah, Kim, Jinkyung, Nuttall, Alfred L, Jones, Sherri M, Choi, Dongseok, Friedman, Thomas B, Ricci, Anthony J, Zhao, Bo, Barr-Gillespie, Peter G

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Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyn... von Morell, Robert J, Olszewski, Rafal, Tona, Risa, Leitess, Samuel, Wafa, Talah T, Taukulis, Ian, Schultz, Julie M, Thomason, Elizabeth J, Richards, Keri, Whitley, Brittany N, Hill, Connor, Saunders, Thomas, Starost, Matthew F, Fitzgerald, Tracy, Wilson, Elizabeth, Ohyama, Takahiro, Friedman, Thomas B, Hoa, Michael

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