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Journal Abstract Search

372 related items for PubMed ID: 15292243

  • 1. Evaluation of the contribution of different ADAMs to tumor necrosis factor alpha (TNFalpha) shedding and of the function of the TNFalpha ectodomain in ensuring selective stimulated shedding by the TNFalpha convertase (TACE/ADAM17).
    Zheng Y, Saftig P, Hartmann D, Blobel C.
    J Biol Chem; 2004 Oct 08; 279(41):42898-906. PubMed ID: 15292243
    [Abstract] [Full Text] [Related]

  • 2. Selective roles for tumor necrosis factor alpha-converting enzyme/ADAM17 in the shedding of the epidermal growth factor receptor ligand family: the juxtamembrane stalk determines cleavage efficiency.
    Hinkle CL, Sunnarborg SW, Loiselle D, Parker CE, Stevenson M, Russell WE, Lee DC.
    J Biol Chem; 2004 Jun 04; 279(23):24179-88. PubMed ID: 15066986
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  • 5. Ectodomain shedding of TNF-alpha is enhanced by nardilysin via activation of ADAM proteases.
    Hiraoka Y, Yoshida K, Ohno M, Matsuoka T, Kita T, Nishi E.
    Biochem Biophys Res Commun; 2008 May 23; 370(1):154-8. PubMed ID: 18355445
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  • 6. Evidence for a critical role of the tumor necrosis factor alpha convertase (TACE) in ectodomain shedding of the p75 neurotrophin receptor (p75NTR).
    Weskamp G, Schlöndorff J, Lum L, Becherer JD, Kim TW, Saftig P, Hartmann D, Murphy G, Blobel CP.
    J Biol Chem; 2004 Feb 06; 279(6):4241-9. PubMed ID: 14638693
    [Abstract] [Full Text] [Related]

  • 7. Different ADAMs have distinct influences on Kit ligand processing: phorbol-ester-stimulated ectodomain shedding of Kitl1 by ADAM17 is reduced by ADAM19.
    Kawaguchi N, Horiuchi K, Becherer JD, Toyama Y, Besmer P, Blobel CP.
    J Cell Sci; 2007 Mar 15; 120(Pt 6):943-52. PubMed ID: 17344430
    [Abstract] [Full Text] [Related]

  • 8. Pro-tumor necrosis factor-alpha processing activity is tightly controlled by a component that does not affect notch processing.
    Merlos-Suárez A, Fernández-Larrea J, Reddy P, Baselga J, Arribas J.
    J Biol Chem; 1998 Sep 18; 273(38):24955-62. PubMed ID: 9733803
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  • 9. Short-term TNFα shedding is independent of cytoplasmic phosphorylation or furin cleavage of ADAM17.
    Schwarz J, Broder C, Helmstetter A, Schmidt S, Yan I, Müller M, Schmidt-Arras D, Becker-Pauly C, Koch-Nolte F, Mittrücker HW, Rabe B, Rose-John S, Chalaris A.
    Biochim Biophys Acta; 2013 Dec 18; 1833(12):3355-3367. PubMed ID: 24135057
    [Abstract] [Full Text] [Related]

  • 10. Angiotensin-converting enzyme 2 ectodomain shedding cleavage-site identification: determinants and constraints.
    Lai ZW, Hanchapola I, Steer DL, Smith AI.
    Biochemistry; 2011 Jun 14; 50(23):5182-94. PubMed ID: 21563828
    [Abstract] [Full Text] [Related]

  • 11. Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands.
    Sahin U, Weskamp G, Kelly K, Zhou HM, Higashiyama S, Peschon J, Hartmann D, Saftig P, Blobel CP.
    J Cell Biol; 2004 Mar 01; 164(5):769-79. PubMed ID: 14993236
    [Abstract] [Full Text] [Related]

  • 12. Tumor necrosis factor-alpha-converting enzyme (TACE/ADAM-17) mediates the ectodomain cleavage of intercellular adhesion molecule-1 (ICAM-1).
    Tsakadze NL, Sithu SD, Sen U, English WR, Murphy G, D'Souza SE.
    J Biol Chem; 2006 Feb 10; 281(6):3157-64. PubMed ID: 16332693
    [Abstract] [Full Text] [Related]

  • 13. Natural soluble interleukin-15Ralpha is generated by cleavage that involves the tumor necrosis factor-alpha-converting enzyme (TACE/ADAM17).
    Budagian V, Bulanova E, Orinska Z, Ludwig A, Rose-John S, Saftig P, Borden EC, Bulfone-Paus S.
    J Biol Chem; 2004 Sep 24; 279(39):40368-75. PubMed ID: 15215246
    [Abstract] [Full Text] [Related]

  • 14. Reactive oxygen species mediate tumor necrosis factor alpha-converting, enzyme-dependent ectodomain shedding induced by phorbol myristate acetate.
    Zhang Z, Oliver P, Lancaster JR, Schwarzenberger PO, Joshi MS, Cork J, Kolls JK.
    FASEB J; 2001 Feb 24; 15(2):303-5. PubMed ID: 11156944
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  • 15. Characterization of growth factor-induced serine phosphorylation of tumor necrosis factor-alpha converting enzyme and of an alternatively translated polypeptide.
    Fan H, Turck CW, Derynck R.
    J Biol Chem; 2003 May 16; 278(20):18617-27. PubMed ID: 12621058
    [Abstract] [Full Text] [Related]

  • 16. Catalytic properties of ADAM19.
    Chesneau V, Becherer JD, Zheng Y, Erdjument-Bromage H, Tempst P, Blobel CP.
    J Biol Chem; 2003 Jun 20; 278(25):22331-40. PubMed ID: 12682046
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  • 17. Metalloprotease-dependent protransforming growth factor-alpha ectodomain shedding in the absence of tumor necrosis factor-alpha-converting enzyme.
    Merlos-Suárez A, Ruiz-Paz S, Baselga J, Arribas J.
    J Biol Chem; 2001 Dec 21; 276(51):48510-7. PubMed ID: 11600492
    [Abstract] [Full Text] [Related]

  • 18. Regulated cell surface pro-EGF ectodomain shedding is a zinc metalloprotease-dependent process.
    Le Gall SM, Auger R, Dreux C, Mauduit P.
    J Biol Chem; 2003 Nov 14; 278(46):45255-68. PubMed ID: 12947092
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  • 19. ADAMs and protein disulfide isomerase: the key to regulated cell-surface protein ectodomain shedding?
    Bass R, Edwards DR.
    Biochem J; 2010 May 27; 428(3):e3-5. PubMed ID: 20504280
    [Abstract] [Full Text] [Related]

  • 20. Impaired trafficking and activation of tumor necrosis factor-alpha-converting enzyme in cell mutants defective in protein ectodomain shedding.
    Borroto A, Ruiz-Paz S, de la Torre TV, Borrell-Pages M, Merlos-Suarez A, Pandiella A, Blobel CP, Baselga J, Arribas J.
    J Biol Chem; 2003 Jul 11; 278(28):25933-9. PubMed ID: 12714588
    [Abstract] [Full Text] [Related]

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