BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 16845470)

  • 1. A de novo deafwaddler mutation of Pmca2 arising in ES cells and hitchhiking with a targeted modification of the Pparg gene.
    Tsai YS; Pendse A; Moy SS; Mohri I; Perez A; Crawley JN; Suzuki K; Maeda N
    Mamm Genome; 2006 Jul; 17(7):716-22. PubMed ID: 16845470
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia.
    McCullough BJ; Tempel BL
    Hear Res; 2004 Sep; 195(1-2):90-102. PubMed ID: 15350283
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of the deafwaddler mutant of the rat plasma membrane calcium-ATPase 2.
    Penheiter AR; Filoteo AG; Croy CL; Penniston JT
    Hear Res; 2001 Dec; 162(1-2):19-28. PubMed ID: 11707348
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2.
    Kozel PJ; Friedman RA; Erway LC; Yamoah EN; Liu LH; Riddle T; Duffy JJ; Doetschman T; Miller ML; Cardell EL; Shull GE
    J Biol Chem; 1998 Jul; 273(30):18693-6. PubMed ID: 9668038
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PMCA2 mutation causes structural changes in the auditory system in deafwaddler mice.
    Dodson HC; Charalabapoulou M
    J Neurocytol; 2001 Apr; 30(4):281-92. PubMed ID: 11875276
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Plasma membrane calcium ATPase deficiency causes neuronal pathology in the spinal cord: a potential mechanism for neurodegeneration in multiple sclerosis and spinal cord injury.
    Kurnellas MP; Nicot A; Shull GE; Elkabes S
    FASEB J; 2005 Feb; 19(2):298-300. PubMed ID: 15576480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Effects of PMCA2 mutation on DPOAE amplitudes and latencies in deafwaddler mice.
    Konrad-Martin D; Norton SJ; Mascher KE; Tempel BL
    Hear Res; 2001 Jan; 151(1-2):205-220. PubMed ID: 11124466
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modification of human hearing loss by plasma-membrane calcium pump PMCA2.
    Schultz JM; Yang Y; Caride AJ; Filoteo AG; Penheiter AR; Lagziel A; Morell RJ; Mohiddin SA; Fananapazir L; Madeo AC; Penniston JT; Griffith AJ
    N Engl J Med; 2005 Apr; 352(15):1557-64. PubMed ID: 15829536
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 5(2):99-110. PubMed ID: 15357414
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Atp2b2, encoding plasma membrane Ca2+-ATPase type 2, (PMCA2) exhibits tissue-specific first exon usage in hair cells, neurons, and mammary glands of mice.
    Silverstein RS; Tempel BL
    Neuroscience; 2006 Aug; 141(1):245-57. PubMed ID: 16675132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 19(4):390-4. PubMed ID: 9697703
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A point mutation in a plasma membrane Ca(2+)-ATPase gene causes deafness in Wriggle Mouse Sagami.
    Takahashi K; Kitamura K
    Biochem Biophys Res Commun; 1999 Aug; 261(3):773-8. PubMed ID: 10441500
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Optimized proteomic analysis of a mouse model of cerebellar dysfunction using amine-specific isobaric tags.
    Hu J; Qian J; Borisov O; Pan S; Li Y; Liu T; Deng L; Wannemacher K; Kurnellas M; Patterson C; Elkabes S; Li H
    Proteomics; 2006 Aug; 6(15):4321-34. PubMed ID: 16800037
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Insertion of an intracisternal A particle retrotransposon element in plasma membrane calcium ATPase 2 gene attenuates its expression and produces an ataxic phenotype in joggle mutant mice.
    Sun XY; Chen ZY; Hayashi Y; Kanou Y; Takagishi Y; Oda S; Murata Y
    Gene; 2008 Mar; 411(1-2):94-102. PubMed ID: 18280673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression and immunolocalization of plasma membrane calcium ATPase isoforms in human corneal epithelium.
    Talarico EF; Kennedy BG; Marfurt CF; Loeffler KU; Mangini NJ
    Mol Vis; 2005 Mar; 11():169-78. PubMed ID: 15765049
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The role of the calcium transporter protein plasma membrane calcium ATPase PMCA2 in cerebellar Purkinje neuron function.
    Empson RM; Akemann W; Knöpfel T
    Funct Neurol; 2010; 25(3):153-8. PubMed ID: 21232211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.
    Parker LL; Gao J; Zuo J
    Brain Res; 2006 May; 1091(1):235-42. PubMed ID: 16630581
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Plasma membrane Ca2+-ATPase expression in the human lens.
    Marian MJ; Li H; Borchman D; Paterson CA
    Exp Eye Res; 2005 Jul; 81(1):57-64. PubMed ID: 15978255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypes of SERCA and PMCA knockout mice.
    Prasad V; Okunade GW; Miller ML; Shull GE
    Biochem Biophys Res Commun; 2004 Oct; 322(4):1192-203. PubMed ID: 15336967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular alterations in the cerebellum of the plasma membrane calcium ATPase 2 (PMCA2)-null mouse indicate abnormalities in Purkinje neurons.
    Kurnellas MP; Lee AK; Li H; Deng L; Ehrlich DJ; Elkabes S
    Mol Cell Neurosci; 2007 Feb; 34(2):178-88. PubMed ID: 17150372
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.