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Journal Abstract Search

174 related items for PubMed ID: 16368689

  • 1. Isoform specificity of ankyrin-B: a site in the divergent C-terminal domain is required for intramolecular association.
    Abdi KM, Mohler PJ, Davis JQ, Bennett V.
    J Biol Chem; 2006 Mar 03; 281(9):5741-9. PubMed ID: 16368689
    [Abstract] [Full Text] [Related]

  • 2. The ankyrin-B C-terminal domain determines activity of ankyrin-B/G chimeras in rescue of abnormal inositol 1,4,5-trisphosphate and ryanodine receptor distribution in ankyrin-B (-/-) neonatal cardiomyocytes.
    Mohler PJ, Gramolini AO, Bennett V.
    J Biol Chem; 2002 Mar 22; 277(12):10599-607. PubMed ID: 11781319
    [Abstract] [Full Text] [Related]

  • 3. Isoform specificity among ankyrins. An amphipathic alpha-helix in the divergent regulatory domain of ankyrin-b interacts with the molecular co-chaperone Hdj1/Hsp40.
    Mohler PJ, Hoffman JA, Davis JQ, Abdi KM, Kim CR, Jones SK, Davis LH, Roberts KF, Bennett V.
    J Biol Chem; 2004 Jun 11; 279(24):25798-804. PubMed ID: 15075330
    [Abstract] [Full Text] [Related]

  • 4. Ankyrin-B targets beta2-spectrin to an intracellular compartment in neonatal cardiomyocytes.
    Mohler PJ, Yoon W, Bennett V.
    J Biol Chem; 2004 Sep 17; 279(38):40185-93. PubMed ID: 15262991
    [Abstract] [Full Text] [Related]

  • 5. Inositol 1,4,5-trisphosphate receptor localization and stability in neonatal cardiomyocytes requires interaction with ankyrin-B.
    Mohler PJ, Davis JQ, Davis LH, Hoffman JA, Michaely P, Bennett V.
    J Biol Chem; 2004 Mar 26; 279(13):12980-7. PubMed ID: 14722080
    [Abstract] [Full Text] [Related]

  • 6. Obscurin targets ankyrin-B and protein phosphatase 2A to the cardiac M-line.
    Cunha SR, Mohler PJ.
    J Biol Chem; 2008 Nov 14; 283(46):31968-80. PubMed ID: 18782775
    [Abstract] [Full Text] [Related]

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  • 8. The membrane-binding domain of ankyrin contains four independently folded subdomains, each comprised of six ankyrin repeats.
    Michaely P, Bennett V.
    J Biol Chem; 1993 Oct 25; 268(30):22703-9. PubMed ID: 8226780
    [Abstract] [Full Text] [Related]

  • 9. Ankyrin-G and beta2-spectrin collaborate in biogenesis of lateral membrane of human bronchial epithelial cells.
    Kizhatil K, Yoon W, Mohler PJ, Davis LH, Hoffman JA, Bennett V.
    J Biol Chem; 2007 Jan 19; 282(3):2029-37. PubMed ID: 17074766
    [Abstract] [Full Text] [Related]

  • 10. Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles.
    Bagnato P, Barone V, Giacomello E, Rossi D, Sorrentino V.
    J Cell Biol; 2003 Jan 20; 160(2):245-53. PubMed ID: 12527750
    [Abstract] [Full Text] [Related]

  • 11. Structure of the ZU5-ZU5-UPA-DD tandem of ankyrin-B reveals interaction surfaces necessary for ankyrin function.
    Wang C, Yu C, Ye F, Wei Z, Zhang M.
    Proc Natl Acad Sci U S A; 2012 Mar 27; 109(13):4822-7. PubMed ID: 22411828
    [Abstract] [Full Text] [Related]

  • 12. Revisiting ankyrin-InsP3 receptor interactions: ankyrin-B associates with the cytoplasmic N-terminus of the InsP3 receptor.
    Kline CF, Cunha SR, Lowe JS, Hund TJ, Mohler PJ.
    J Cell Biochem; 2008 Jul 01; 104(4):1244-53. PubMed ID: 18275062
    [Abstract] [Full Text] [Related]

  • 13. AnkB, a periplasmic ankyrin-like protein in Pseudomonas aeruginosa, is required for optimal catalase B (KatB) activity and resistance to hydrogen peroxide.
    Howell ML, Alsabbagh E, Ma JF, Ochsner UA, Klotz MG, Beveridge TJ, Blumenthal KM, Niederhoffer EC, Morris RE, Needham D, Dean GE, Wani MA, Hassett DJ.
    J Bacteriol; 2000 Aug 01; 182(16):4545-56. PubMed ID: 10913088
    [Abstract] [Full Text] [Related]

  • 14. Heterologous C-terminal sequences disrupt transcriptional activation and oncogenesis by p59v-rel.
    Diehl JA, Hannink M.
    J Virol; 1993 Dec 01; 67(12):7161-71. PubMed ID: 8230438
    [Abstract] [Full Text] [Related]

  • 15. Novel UNC-44 AO13 ankyrin is required for axonal guidance in C. elegans, contains six highly repetitive STEP blocks separated by seven potential transmembrane domains, and is localized to neuronal processes and the periphery of neural cell bodies.
    Otsuka AJ, Boontrakulpoontawee P, Rebeiz N, Domanus M, Otsuka D, Velamparampil N, Chan S, Vande Wyngaerde M, Campagna S, Cox A.
    J Neurobiol; 2002 Mar 01; 50(4):333-49. PubMed ID: 11891667
    [Abstract] [Full Text] [Related]

  • 16. Identification of a critical ankyrin-binding loop on the cytoplasmic domain of erythrocyte membrane band 3 by crystal structure analysis and site-directed mutagenesis.
    Chang SH, Low PS.
    J Biol Chem; 2003 Feb 28; 278(9):6879-84. PubMed ID: 12482869
    [Abstract] [Full Text] [Related]

  • 17. Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation.
    Nicolas V, Le Van Kim C, Gane P, Birkenmeier C, Cartron JP, Colin Y, Mouro-Chanteloup I.
    J Biol Chem; 2003 Jul 11; 278(28):25526-33. PubMed ID: 12719424
    [Abstract] [Full Text] [Related]

  • 18. Hydrophobic residues in small ankyrin 1 participate in binding to obscurin.
    Willis CD, Oashi T, Busby B, Mackerell AD, Bloch RJ.
    Mol Membr Biol; 2012 Mar 11; 29(2):36-51. PubMed ID: 22416964
    [Abstract] [Full Text] [Related]

  • 19. Identification of Ank(G107), a muscle-specific ankyrin-G isoform.
    Gagelin C, Constantin B, Deprette C, Ludosky MA, Recouvreur M, Cartaud J, Cognard C, Raymond G, Kordeli E.
    J Biol Chem; 2002 Apr 12; 277(15):12978-87. PubMed ID: 11796721
    [Abstract] [Full Text] [Related]

  • 20. Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain.
    Peters LL, John KM, Lu FM, Eicher EM, Higgins A, Yialamas M, Turtzo LC, Otsuka AJ, Lux SE.
    J Cell Biol; 1995 Jul 12; 130(2):313-30. PubMed ID: 7615634
    [Abstract] [Full Text] [Related]

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