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Journal Abstract Search

754 related items for PubMed ID: 15357422

  • 1. Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice.
    Dou H, Vazquez AE, Namkung Y, Chu H, Cardell EL, Nie L, Parson S, Shin HS, Yamoah EN.
    J Assoc Res Otolaryngol; 2004 Jun; 5(2):215-26. PubMed ID: 15357422
    [Abstract] [Full Text] [Related]

  • 2. Auditory and vestibular defects in the circling (ci2) rat mutant.
    Kaiser A, Fedrowitz M, Ebert U, Zimmermann E, Hedrich HJ, Wedekind D, Löscher W.
    Eur J Neurosci; 2001 Oct; 14(7):1129-42. PubMed ID: 11683905
    [Abstract] [Full Text] [Related]

  • 3. [Mice lacking of voltage-gated L-type calcium channel alpha1D subunit have impaired sinoatrial node function and caused deafness].
    Chu H, Zhou X, Song H, Cui Y, Xiong H, Zhou L.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 May; 21(10):468-72. PubMed ID: 17650821
    [Abstract] [Full Text] [Related]

  • 4. Cav1.3 (alpha1D) Ca2+ currents in neonatal outer hair cells of mice.
    Michna M, Knirsch M, Hoda JC, Muenkner S, Langer P, Platzer J, Striessnig J, Engel J.
    J Physiol; 2003 Dec 15; 553(Pt 3):747-58. PubMed ID: 14514878
    [Abstract] [Full Text] [Related]

  • 5. Localization of efferent neurotransmitters in the inner ear of the homozygous Bronx waltzer mutant mouse.
    Kong WJ, Scholtz AW, Hussl B, Kammen-Jolly K, Schrott-Fischer A.
    Hear Res; 2002 May 15; 167(1-2):136-55. PubMed ID: 12117537
    [Abstract] [Full Text] [Related]

  • 6. Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
    Platzer J, Engel J, Schrott-Fischer A, Stephan K, Bova S, Chen H, Zheng H, Striessnig J.
    Cell; 2000 Jul 07; 102(1):89-97. PubMed ID: 10929716
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  • 8. Structure and function of the adult inner ear in the mouse following prenatal irradiation.
    Hultcrantz M.
    Scand Audiol Suppl; 1985 Jul 07; 24():1-24. PubMed ID: 3879375
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  • 10. Developmental expression of Ca(v)1.3 (alpha1d) calcium channels in the mouse inner ear.
    Hafidi A, Dulon D.
    Brain Res Dev Brain Res; 2004 Jun 21; 150(2):167-75. PubMed ID: 15158080
    [Abstract] [Full Text] [Related]

  • 11. Targeted disruption of otog results in deafness and severe imbalance.
    Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ.
    Nat Genet; 2000 Feb 21; 24(2):139-43. PubMed ID: 10655058
    [Abstract] [Full Text] [Related]

  • 12. Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness.
    Kharkovets T, Dedek K, Maier H, Schweizer M, Khimich D, Nouvian R, Vardanyan V, Leuwer R, Moser T, Jentsch TJ.
    EMBO J; 2006 Feb 08; 25(3):642-52. PubMed ID: 16437162
    [Abstract] [Full Text] [Related]

  • 13. Deafness due to degeneration of cochlear neurons in caspase-3-deficient mice.
    Morishita H, Makishima T, Kaneko C, Lee YS, Segil N, Takahashi K, Kuraoka A, Nakagawa T, Nabekura J, Nakayama K, Nakayama KI.
    Biochem Biophys Res Commun; 2001 Jun 01; 284(1):142-9. PubMed ID: 11374883
    [Abstract] [Full Text] [Related]

  • 14. Sox10 Gene Is Required for the Survival of Saccular and Utricular Hair Cells in a Porcine Model.
    Qi JC, Jiang QQ, Ma L, Yuan SL, Sun W, Yu LS, Guo WW, Yang SM.
    Mol Neurobiol; 2022 Jun 01; 59(6):3323-3335. PubMed ID: 35249166
    [Abstract] [Full Text] [Related]

  • 15. Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder.
    Jones SM, Robertson NG, Given S, Giersch AB, Liberman MC, Morton CC.
    Hear Res; 2011 Feb 01; 272(1-2):42-8. PubMed ID: 21073934
    [Abstract] [Full Text] [Related]

  • 16. Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.
    Williams LH, Miller KA, Dahl HH, Manji SS.
    Hear Res; 2013 May 01; 299():53-62. PubMed ID: 23485424
    [Abstract] [Full Text] [Related]

  • 17. Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.
    Delprat B, Ruel J, Guitton MJ, Hamard G, Lenoir M, Pujol R, Puel JL, Brabet P, Hamel CP.
    Mol Cell Biol; 2005 Jan 01; 25(2):847-53. PubMed ID: 15632083
    [Abstract] [Full Text] [Related]

  • 18. Ca2+-binding protein 2 inhibits Ca2+-channel inactivation in mouse inner hair cells.
    Picher MM, Gehrt A, Meese S, Ivanovic A, Predoehl F, Jung S, Schrauwen I, Dragonetti AG, Colombo R, Van Camp G, Strenzke N, Moser T.
    Proc Natl Acad Sci U S A; 2017 Feb 28; 114(9):E1717-E1726. PubMed ID: 28183797
    [Abstract] [Full Text] [Related]

  • 19. Downregulation of Cav1.3 calcium channel expression in the cochlea is associated with age-related hearing loss in C57BL/6J mice.
    Chen J, Chu H, Xiong H, Yu Y, Huang X, Zhou L, Chen Q, Bing D, Liu Y, Wang S, Cui Y.
    Neuroreport; 2013 Apr 17; 24(6):313-7. PubMed ID: 23470431
    [Abstract] [Full Text] [Related]

  • 20. Gata3 is required for the functional maturation of inner hair cells and their innervation in the mouse cochlea.
    Bardhan T, Jeng JY, Waldmann M, Ceriani F, Johnson SL, Olt J, Rüttiger L, Marcotti W, Holley MC.
    J Physiol; 2019 Jul 17; 597(13):3389-3406. PubMed ID: 31069810
    [Abstract] [Full Text] [Related]

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