BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 12949242)

  • 1. ADAM-17-independent shedding of L-selectin.
    Walcheck B; Alexander SR; St Hill CA; Matala E
    J Leukoc Biol; 2003 Sep; 74(3):389-94. PubMed ID: 12949242
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regulation of membrane metalloproteolytic cleavage of L-selectin (CD62l) by the epidermal growth factor domain.
    Zhao L; Shey M; Farnsworth M; Dailey MO
    J Biol Chem; 2001 Aug; 276(33):30631-40. PubMed ID: 11375402
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 15(2):303-5. PubMed ID: 11156944
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tissue inhibitor of metalloproteinases-3 inhibits shedding of L-selectin from leukocytes.
    Borland G; Murphy G; Ager A
    J Biol Chem; 1999 Jan; 274(5):2810-5. PubMed ID: 9915814
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The cytoplasmic domains of TNFalpha-converting enzyme (TACE/ADAM17) and L-selectin are regulated differently by p38 MAPK and PKC to promote ectodomain shedding.
    Killock DJ; Ivetić A
    Biochem J; 2010 May; 428(2):293-304. PubMed ID: 20331435
    [TBL] [Abstract][Full Text] [Related]  

  • 6. L-selectin shedding is independent of its subsurface structures and topographic distribution.
    Fors BP; Goodarzi K; von Andrian UH
    J Immunol; 2001 Oct; 167(7):3642-51. PubMed ID: 11564777
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of the rapid proteolytic shedding of murine L-selectin.
    Zhao LC; Edgar JB; Dailey MO
    Dev Immunol; 2001; 8(3-4):267-77. PubMed ID: 11785676
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ADAM17 but not ADAM10 mediates tumor necrosis factor-alpha and L-selectin shedding from leukocyte membranes.
    Condon TP; Flournoy S; Sawyer GJ; Baker BF; Kishimoto TK; Bennett CF
    Antisense Nucleic Acid Drug Dev; 2001 Apr; 11(2):107-16. PubMed ID: 11334139
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 279(39):40368-75. PubMed ID: 15215246
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ADAM17 deficiency by mature neutrophils has differential effects on L-selectin shedding.
    Li Y; Brazzell J; Herrera A; Walcheck B
    Blood; 2006 Oct; 108(7):2275-9. PubMed ID: 16735599
    [TBL] [Abstract][Full Text] [Related]  

  • 11. L-selectin: mechanisms and physiological significance of ectodomain cleavage.
    Smalley DM; Ley K
    J Cell Mol Med; 2005; 9(2):255-66. PubMed ID: 15963248
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The transmembrane domain of TACE regulates protein ectodomain shedding.
    Li X; Pérez L; Pan Z; Fan H
    Cell Res; 2007 Dec; 17(12):985-98. PubMed ID: 18040288
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CD93 is rapidly shed from the surface of human myeloid cells and the soluble form is detected in human plasma.
    Bohlson SS; Silva R; Fonseca MI; Tenner AJ
    J Immunol; 2005 Jul; 175(2):1239-47. PubMed ID: 16002728
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TACE/ADAM-17 enzymatic activity is increased in response to cellular stimulation.
    Doedens JR; Mahimkar RM; Black RA
    Biochem Biophys Res Commun; 2003 Aug; 308(2):331-8. PubMed ID: 12901873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stimulated shedding of vascular cell adhesion molecule 1 (VCAM-1) is mediated by tumor necrosis factor-alpha-converting enzyme (ADAM 17).
    Garton KJ; Gough PJ; Philalay J; Wille PT; Blobel CP; Whitehead RH; Dempsey PJ; Raines EW
    J Biol Chem; 2003 Sep; 278(39):37459-64. PubMed ID: 12878595
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diverse cell surface protein ectodomains are shed by a system sensitive to metalloprotease inhibitors.
    Arribas J; Coodly L; Vollmer P; Kishimoto TK; Rose-John S; Massagué J
    J Biol Chem; 1996 May; 271(19):11376-82. PubMed ID: 8626692
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Selenium supplementation induces metalloproteinase-dependent L-selectin shedding from monocytes.
    Ahrens I; Ellwanger C; Smith BK; Bassler N; Chen YC; Neudorfer I; Ludwig A; Bode C; Peter K
    J Leukoc Biol; 2008 Jun; 83(6):1388-95. PubMed ID: 18305178
    [TBL] [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; 278(46):45255-68. PubMed ID: 12947092
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 281(6):3157-64. PubMed ID: 16332693
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The disintegrin-like metalloproteinase ADAM10 is involved in constitutive cleavage of CX3CL1 (fractalkine) and regulates CX3CL1-mediated cell-cell adhesion.
    Hundhausen C; Misztela D; Berkhout TA; Broadway N; Saftig P; Reiss K; Hartmann D; Fahrenholz F; Postina R; Matthews V; Kallen KJ; Rose-John S; Ludwig A
    Blood; 2003 Aug; 102(4):1186-95. PubMed ID: 12714508
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.