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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

309 related items for PubMed ID: 15632083

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  • 5. 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
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  • 7. Mesenchymal stem cell transplantation accelerates hearing recovery through the repair of injured cochlear fibrocytes.
    Kamiya K, Fujinami Y, Hoya N, Okamoto Y, Kouike H, Komatsuzaki R, Kusano R, Nakagawa S, Satoh H, Fujii M, Matsunaga T.
    Am J Pathol; 2007 Jul 01; 171(1):214-26. PubMed ID: 17591967
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  • 8. Time course of auditory impairment in mice lacking the electroneutral sodium bicarbonate cotransporter NBC3 (slc4a7).
    Lopez IA, Acuna D, Galbraith G, Bok D, Ishiyama A, Liu W, Kurtz I.
    Brain Res Dev Brain Res; 2005 Nov 07; 160(1):63-77. PubMed ID: 16181686
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  • 9. Auditory function and cochlear morphology in the German waltzing guinea pig.
    Jin Z, Mannström P, Skjönsberg A, Järlebark L, Ulfendahl M.
    Hear Res; 2006 Sep 07; 219(1-2):74-84. PubMed ID: 16870368
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  • 10. 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 07; 5(2):215-26. PubMed ID: 15357422
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  • 11. [Intervention of spiral ligament fibrocytes in the metabolic regulation of the inner ear].
    García Berrocal JR, Méndez-Benegassi I, Martí C, Ramírez Camacho R.
    Acta Otorrinolaringol Esp; 2008 Dec 07; 59(10):494-9. PubMed ID: 19080786
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  • 12. Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter.
    Delpire E, Lu J, England R, Dull C, Thorne T.
    Nat Genet; 1999 Jun 07; 22(2):192-5. PubMed ID: 10369265
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  • 13. Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.
    Kitajiri S, Miyamoto T, Mineharu A, Sonoda N, Furuse K, Hata M, Sasaki H, Mori Y, Kubota T, Ito J, Furuse M, Tsukita S.
    J Cell Sci; 2004 Oct 01; 117(Pt 21):5087-96. PubMed ID: 15456848
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  • 14. Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV.
    Rickheit G, Maier H, Strenzke N, Andreescu CE, De Zeeuw CI, Muenscher A, Zdebik AA, Jentsch TJ.
    EMBO J; 2008 Nov 05; 27(21):2907-17. PubMed ID: 18833191
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  • 15. Morphological and functional alterations of the cochlea in apolipoprotein E gene deficient mice.
    Guo Y, Zhang C, Du X, Nair U, Yoo TJ.
    Hear Res; 2005 Oct 05; 208(1-2):54-67. PubMed ID: 16051453
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  • 16. Expression of the carrier protein apolipoprotein D in the mouse inner ear.
    Hildebrand MS, de Silva MG, Klockars T, Solares CA, Hirose K, Smith JD, Patel SC, Dahl HH.
    Hear Res; 2005 Feb 05; 200(1-2):102-14. PubMed ID: 15668042
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  • 17. LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice.
    Gamp AC, Tanaka Y, Lüllmann-Rauch R, Wittke D, D'Hooge R, De Deyn PP, Moser T, Maier H, Hartmann D, Reiss K, Illert AL, von Figura K, Saftig P.
    Hum Mol Genet; 2003 Mar 15; 12(6):631-46. PubMed ID: 12620969
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  • 18. The physiology of the normal and pathological cochlear neurones--some recent advances.
    Harrison RV.
    J Otolaryngol; 1985 Dec 15; 14(6):345-56. PubMed ID: 3908701
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  • 19. [Molecular biology of hearing].
    Stöver T, Diensthuber M.
    Laryngorhinootologie; 2011 Mar 15; 90 Suppl 1():S22-34. PubMed ID: 21523631
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  • 20. Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4.
    Boettger T, Hübner CA, Maier H, Rust MB, Beck FX, Jentsch TJ.
    Nature; 2002 Apr 25; 416(6883):874-8. PubMed ID: 11976689
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