Works by Raphael, Yehoash


Results: 51
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    From gene identification to gene therapy.

    Published in:
    2002
    By:
    • Kanzaki, Sho;
    • Kawamoto, Kohei;
    • Oh, Seung-Ha;
    • Stöver, Timo;
    • Suzuki, Mitsuya;
    • Ishimoto, Shinichi;
    • Yagi, Masao;
    • Miller, Josef M.;
    • Lomax, Margaret I.;
    • Raphael, Yehoash;
    • Stöver, Timo
    Publication type:
    journal article
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    Grxcr2 is required for stereocilia morphogenesis in the cochlea.

    Published in:
    PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201713
    By:
    • Avenarius, Matthew R.;
    • Jung, Jae-Yun;
    • Askew, Charles;
    • Jones, Sherri M.;
    • Hunker, Kristina L.;
    • Azaiez, Hela;
    • Rehman, Atteeq U.;
    • Schraders, Margit;
    • Najmabadi, Hossein;
    • Kremer, Hannie;
    • Smith, Richard J. H.;
    • Géléoc, Gwenaëlle S. G.;
    • Dolan, David F.;
    • Raphael, Yehoash;
    • Kohrman, David C.
    Publication type:
    Article
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    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 Loss.

    Published in:
    Journal of Neuroscience, 2004, v. 24, n. 7, p. 1772, doi. 10.1523/JNEUROSCI.5063-03.2004
    By:
    • Nair, Thankam S.;
    • Kozma, Kelley E.;
    • Hoefling, Nickoleta L.;
    • Kommareddi, Pavan K.;
    • Yo Ueda, Pavan K.;
    • Tzy-Wen Gong, Pavan K.;
    • Lomax, Margaret I.;
    • Lansford, Christopher D.;
    • Telian, Steven A.;
    • Satar, Bulent;
    • Arts, H. Alexander;
    • El-Kashlan, Hussam K.;
    • Berryhill, Wayne E.;
    • Raphael, Yehoash;
    • Carey, Thomas E.
    Publication type:
    Article
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    COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

    Published in:
    2011
    By:
    • Heeringa, Saskia F.;
    • Chernin, Gil;
    • Chaki, Moumita;
    • Weibin Zhou;
    • Sloan, Alexis J.;
    • Ziming Ji;
    • Xie, Letian X.;
    • Salviati, Leonardo;
    • Hurd, Toby W.;
    • Vega-Warner, Virginia;
    • Killen, Paul D.;
    • Raphael, Yehoash;
    • Ashraf, Shazia;
    • Ovunc, Bugsu;
    • Schoeb, Dominik S.;
    • McLaughlin, Heather M.;
    • Airik, Rannar;
    • Vlangos, Christopher N.;
    • Gbadegesin, Rasheed;
    • Hinkes, Bernward
    Publication type:
    journal article
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    Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

    Published in:
    Human Molecular Genetics, 2003, v. 12, n. 16, p. 2049, doi. 10.1093/hmg/ddg210
    By:
    • Ben-Yosef, Tamar;
    • Belyantseva, Inna A.;
    • Saunders, Thomas L.;
    • Hughes, Elizabeth D.;
    • Kawamoto, Kohei;
    • Van Itallie, Christina M.;
    • Beyer, Lisa A.;
    • Halsey, Kärin;
    • Gardner, Donald J.;
    • Wilcox, Edward R.;
    • Rasmussen, Julia;
    • Anderson, James M.;
    • Dolan, David F.;
    • Forge, Andrew;
    • Raphael, Yehoash;
    • Camper, Sally A.;
    • Friedman, Thomas B.
    Publication type:
    Article
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    Cochlear Health and Cochlear-implant Function.

    Published in:
    JARO - Journal of the Association for Research in Otolaryngology, 2023, v. 24, n. 1, p. 5, doi. 10.1007/s10162-022-00882-y
    By:
    • Schvartz-Leyzac, Kara C.;
    • Colesa, Deborah J.;
    • Swiderski, Donald L.;
    • Raphael, Yehoash;
    • Pfingst, Bryan E.
    Publication type:
    Article
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