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PUBMED FOR HANDHELDS

Journal Abstract Search

550 related items for PubMed ID: 28209736

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  • 2. Conditional deletion of pejvakin in adult outer hair cells causes progressive hearing loss in mice.
    Harris SL, Kazmierczak M, Pangršič T, Shah P, Chuchvara N, Barrantes-Freer A, Moser T, Schwander M.
    Neuroscience; 2017 Mar 06; 344():380-393. PubMed ID: 28089576
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  • 4. Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation.
    Cheng YF, Tsai YH, Huang CY, Lee YS, Chang PC, Lu YC, Hsu CJ, Wu CC.
    Biochem Biophys Res Commun; 2020 Nov 19; 532(4):675-681. PubMed ID: 32917362
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  • 5. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.
    Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C.
    Nat Genet; 2006 Jul 19; 38(7):770-8. PubMed ID: 16804542
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  • 6. The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.
    Vogl C, Butola T, Haag N, Hausrat TJ, Leitner MG, Moutschen M, Lefèbvre PP, Speckmann C, Garrett L, Becker L, Fuchs H, Hrabe de Angelis M, Nietzsche S, Kessels MM, Oliver D, Kneussel M, Kilimann MW, Strenzke N.
    EMBO Rep; 2017 Nov 19; 18(11):2015-2029. PubMed ID: 28893864
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  • 7. Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage.
    Defourny J, Aghaie A, Perfettini I, Avan P, Delmaghani S, Petit C.
    Proc Natl Acad Sci U S A; 2019 Apr 16; 116(16):8010-8017. PubMed ID: 30936319
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  • 8. Stereocilia fusion pathology in the cochlear outer hair cells at the nanoscale level.
    Ikäheimo K, Leinonen S, Lankinen T, Lindahl M, Saarma M, Pirvola U.
    J Physiol; 2024 Aug 16; 602(16):3995-4025. PubMed ID: 39037943
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  • 10. A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
    Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, Wiltshire T, Smith RJ, Tarantino LM, Müller U.
    J Neurosci; 2007 Feb 28; 27(9):2163-75. PubMed ID: 17329413
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  • 11. Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.
    Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N, Perfettini I, Zelles T, Aller M, Meyer A, Emptoz A, Giraudet F, Leibovici M, Dartevelle S, Soubigou G, Thiry M, Vizi ES, Safieddine S, Hardelin JP, Avan P, Petit C.
    Cell; 2015 Nov 05; 163(4):894-906. PubMed ID: 26544938
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  • 12. ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points.
    Krey JF, Liu C, Belyantseva IA, Bateschell M, Dumont RA, Goldsmith J, Chatterjee P, Morrill RS, Fedorov LM, Foster S, Kim J, Nuttall AL, Jones SM, Choi D, Friedman TB, Ricci AJ, Zhao B, Barr-Gillespie PG.
    J Cell Biol; 2022 Apr 04; 221(4):. PubMed ID: 35175278
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  • 14. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
    Nakanishi H, Kurima K, Pan B, Wangemann P, Fitzgerald TS, Géléoc GS, Holt JR, Griffith AJ.
    Sci Rep; 2018 Aug 14; 8(1):12125. PubMed ID: 30108230
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  • 19. CTCF is required for maintenance of auditory hair cells and hearing function in the mouse cochlea.
    Ma JH, Kim HP, Bok J, Shin JO.
    Biochem Biophys Res Commun; 2018 Sep 18; 503(4):2646-2652. PubMed ID: 30107916
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  • 20. A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function.
    Francis SP, Krey JF, Krystofiak ES, Cui R, Nanda S, Xu W, Kachar B, Barr-Gillespie PG, Shin JB.
    J Neurosci; 2015 Feb 04; 35(5):1999-2014. PubMed ID: 25653358
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