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Journal Abstract Search

225 related items for PubMed ID: 18974863

  • 1.
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  • 3. The plasma membrane calcium pump in the hearing process: physiology and pathology.
    Carafoli E.
    Sci China Life Sci; 2011 Aug; 54(8):686-90. PubMed ID: 21786191
    [Abstract] [Full Text] [Related]

  • 4. A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.
    Watson CJ, Tempel BL.
    Hear Res; 2013 Oct; 304():41-8. PubMed ID: 23792079
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  • 5. Hair cells, plasma membrane Ca²⁺ ATPase and deafness.
    Giacomello M, De Mario A, Primerano S, Brini M, Carafoli E.
    Int J Biochem Cell Biol; 2012 May; 44(5):679-83. PubMed ID: 22349217
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  • 6. A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
    Ficarella R, Di Leva F, Bortolozzi M, Ortolano S, Donaudy F, Petrillo M, Melchionda S, Lelli A, Domi T, Fedrizzi L, Lim D, Shull GE, Gasparini P, Brini M, Mammano F, Carafoli E.
    Proc Natl Acad Sci U S A; 2007 Jan 30; 104(5):1516-21. PubMed ID: 17234811
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  • 7. Two ENU-induced alleles of Atp2b2 cause deafness in mice.
    Carpinelli MR, Manning MG, Kile BT, Burt RA.
    PLoS One; 2013 Jan 30; 8(6):e67479. PubMed ID: 23826306
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  • 8. Identification of a novel point mutation of mouse Atp2b2 induced by N-ethyl-N-nitrosourea mutagenesis.
    Xu L, Wang Z, Xiong X, Gu X, Gao X, Gao X.
    Exp Anim; 2011 Jan 30; 60(1):71-8. PubMed ID: 21325754
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  • 9. A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness.
    Wong EY, Xu CY, Brahmachary M, Xu PX.
    PLoS One; 2016 Jan 30; 11(5):e0154984. PubMed ID: 27171474
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  • 10. Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice.
    Street VA, McKee-Johnson JW, Fonseca RC, Tempel BL, Noben-Trauth K.
    Nat Genet; 1998 Aug 30; 19(4):390-4. PubMed ID: 9697703
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  • 11. 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 30; 5(2):215-26. PubMed ID: 15357422
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  • 12. Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
    Washington JL, Pitts D, Wright CG, Erway LC, Davis RR, Alagramam K.
    Hear Res; 2005 Apr 30; 202(1-2):161-9. PubMed ID: 15811708
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  • 13. A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
    Longo-Guess CM, Gagnon LH, Cook SA, Wu J, Zheng QY, Johnson KR.
    Proc Natl Acad Sci U S A; 2005 May 31; 102(22):7894-9. PubMed ID: 15905332
    [Abstract] [Full Text] [Related]

  • 14. Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect.
    Giacomello M, De Mario A, Lopreiato R, Primerano S, Campeol M, Brini M, Carafoli E.
    Cell Calcium; 2011 Dec 31; 50(6):569-76. PubMed ID: 22047666
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  • 15. PMCA2 pump mutations and hereditary deafness.
    Bortolozzi M, Mammano F.
    Neurosci Lett; 2018 Jan 10; 663():18-24. PubMed ID: 29452611
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  • 16. Deafness causing neuroplastin missense variants fail to promote plasma membrane Ca2+-ATPase levels and Ca2+ transient regulation in brain neurons.
    Liang Y, Ormazabal-Toledo R, Yao S, Shi YS, Herrera-Molina R, Montag D, Lin X.
    J Biol Chem; 2024 Jul 10; 300(7):107474. PubMed ID: 38879011
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  • 17. Low endolymph calcium concentrations in deafwaddler2J mice suggest that PMCA2 contributes to endolymph calcium maintenance.
    Wood JD, Muchinsky SJ, Filoteo AG, Penniston JT, Tempel BL.
    J Assoc Res Otolaryngol; 2004 Jun 10; 5(2):99-110. PubMed ID: 15357414
    [Abstract] [Full Text] [Related]

  • 18. Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.
    Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB.
    J Neurocytol; 1999 Jun 10; 28(10-11):969-85. PubMed ID: 10900098
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  • 19. Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice.
    Parker A, Hardisty-Hughes RE, Wisby L, Joyce S, Brown SD.
    Mamm Genome; 2010 Dec 10; 21(11-12):565-76. PubMed ID: 21116635
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  • 20. Maintenance of neuronal size gradient in MNTB requires sound-evoked activity.
    Weatherstone JH, Kopp-Scheinpflug C, Pilati N, Wang Y, Forsythe ID, Rubel EW, Tempel BL.
    J Neurophysiol; 2017 Feb 01; 117(2):756-766. PubMed ID: 27881722
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