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Journal Abstract Search

264 related items for PubMed ID: 16912075

  • 1. Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle.
    Ito D, Koshino I, Arashiki N, Adachi H, Tomihari M, Tamahara S, Kurogi K, Amano T, Ono K, Inaba M.
    J Cell Sci; 2006 Sep 01; 119(Pt 17):3602-12. PubMed ID: 16912075
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  • 2. Lumenal localization in the endoplasmic reticulum of the C-terminal tail of an AE1 mutant responsible for hereditary spherocytosis in cattle.
    Ito D, Otsuka Y, Koshino I, Inaba M.
    Jpn J Vet Res; 2007 Feb 01; 54(4):191-7. PubMed ID: 17405356
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  • 3. Protein 4.2 interaction with hereditary spherocytosis mutants of the cytoplasmic domain of human anion exchanger 1.
    Bustos SP, Reithmeier RA.
    Biochem J; 2011 Jan 15; 433(2):313-22. PubMed ID: 21039340
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  • 4. The forced aggresome formation of a bovine anion exchanger 1 (AE1) mutant through association with δF508-cystic fibrosis transmembrane conductance regulator upon proteasome inhibition in HEK293 cells.
    Adachi H, Kurooka T, Otsu W, Inaba M.
    Jpn J Vet Res; 2010 Aug 15; 58(2):101-10. PubMed ID: 20715420
    [Abstract] [Full Text] [Related]

  • 5. Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis.
    Quilty JA, Cordat E, Reithmeier RA.
    Biochem J; 2002 Dec 15; 368(Pt 3):895-903. PubMed ID: 12227829
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  • 8. Structure and stability of hereditary spherocytosis mutants of the cytosolic domain of the erythrocyte anion exchanger 1 protein.
    Bustos SP, Reithmeier RA.
    Biochemistry; 2006 Jan 24; 45(3):1026-34. PubMed ID: 16411779
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  • 9. Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger.
    Quilty JA, Reithmeier RA.
    Traffic; 2000 Dec 24; 1(12):987-98. PubMed ID: 11208088
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  • 10. Dominant and recessive distal renal tubular acidosis mutations of kidney anion exchanger 1 induce distinct trafficking defects in MDCK cells.
    Cordat E, Kittanakom S, Yenchitsomanus PT, Li J, Du K, Lukacs GL, Reithmeier RA.
    Traffic; 2006 Feb 24; 7(2):117-28. PubMed ID: 16420521
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  • 12. Palmitoylation is not required for trafficking of human anion exchanger 1 to the cell surface.
    Cheung JC, Reithmeier RA.
    Biochem J; 2004 Mar 15; 378(Pt 3):1015-21. PubMed ID: 14640982
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  • 13. Human anion exchanger1 mutations and distal renal tubular acidosis.
    Yenchitsomanus PT.
    Southeast Asian J Trop Med Public Health; 2003 Sep 15; 34(3):651-8. PubMed ID: 15115146
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  • 14. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.
    Inaba M, Yawata A, Koshino I, Sato K, Takeuchi M, Takakuwa Y, Manno S, Yawata Y, Kanzaki A, Sakai J, Ban A, Ono K, Maede Y.
    J Clin Invest; 1996 Apr 15; 97(8):1804-17. PubMed ID: 8621763
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  • 17. Molecular physiology of SLC4 anion exchangers.
    Alper SL.
    Exp Physiol; 2006 Jan 15; 91(1):153-61. PubMed ID: 16239253
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  • 19. Dominant-negative effects of episodic ataxia type 2 mutations involve disruption of membrane trafficking of human P/Q-type Ca2+ channels.
    Jeng CJ, Sun MC, Chen YW, Tang CY.
    J Cell Physiol; 2008 Feb 15; 214(2):422-33. PubMed ID: 17654512
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