BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 8206991)

  • 1. Dual myristylation and palmitylation of Src family member p59fyn affects subcellular localization.
    Alland L; Peseckis SM; Atherton RE; Berthiaume L; Resh MD
    J Biol Chem; 1994 Jun; 269(24):16701-5. PubMed ID: 8206991
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid plasma membrane anchoring of newly synthesized p59fyn: selective requirement for NH2-terminal myristoylation and palmitoylation at cysteine-3.
    van't Hof W; Resh MD
    J Cell Biol; 1997 Mar; 136(5):1023-35. PubMed ID: 9060467
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Palmitylation of an amino-terminal cysteine motif of protein tyrosine kinases p56lck and p59fyn mediates interaction with glycosyl-phosphatidylinositol-anchored proteins.
    Shenoy-Scaria AM; Gauen LK; Kwong J; Shaw AS; Lublin DM
    Mol Cell Biol; 1993 Oct; 13(10):6385-92. PubMed ID: 8413237
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Myristylation and palmitylation of Src family members: the fats of the matter.
    Resh MD
    Cell; 1994 Feb; 76(3):411-3. PubMed ID: 8313462
    [No Abstract]   [Full Text] [Related]  

  • 5. The N-terminal SH4 region of the Src family kinase Fyn is modified by methylation and heterogeneous fatty acylation: role in membrane targeting, cell adhesion, and spreading.
    Liang X; Lu Y; Wilkes M; Neubert TA; Resh MD
    J Biol Chem; 2004 Feb; 279(9):8133-9. PubMed ID: 14660555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cysteine3 of Src family protein tyrosine kinase determines palmitoylation and localization in caveolae.
    Shenoy-Scaria AM; Dietzen DJ; Kwong J; Link DC; Lublin DM
    J Cell Biol; 1994 Jul; 126(2):353-63. PubMed ID: 7518463
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Palmitoylation of multiple Src-family kinases at a homologous N-terminal motif.
    Koegl M; Zlatkine P; Ley SC; Courtneidge SA; Magee AI
    Biochem J; 1994 Nov; 303 ( Pt 3)(Pt 3):749-53. PubMed ID: 7980442
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple features of the p59fyn src homology 4 domain define a motif for immune-receptor tyrosine-based activation motif (ITAM) binding and for plasma membrane localization.
    Timson Gauen LK; Linder ME; Shaw AS
    J Cell Biol; 1996 Jun; 133(5):1007-15. PubMed ID: 8655574
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutagenesis of palmitoylation sites in endothelial nitric oxide synthase identifies a novel motif for dual acylation and subcellular targeting.
    Robinson LJ; Michel T
    Proc Natl Acad Sci U S A; 1995 Dec; 92(25):11776-80. PubMed ID: 8524847
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amino-terminal palmitate or polybasic domain can provide required second signal to myristate for membrane binding of p56lck.
    Kwong J; Lublin DM
    Biochem Biophys Res Commun; 1995 Feb; 207(2):868-76. PubMed ID: 7864883
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Iodinated fatty acids as probes for myristate processing and function. Incorporation into pp60v-src.
    Peseckis SM; Deichaite I; Resh MD
    J Biol Chem; 1993 Mar; 268(7):5107-14. PubMed ID: 8444887
    [TBL] [Abstract][Full Text] [Related]  

  • 12. N-terminally myristoylated Ras proteins require palmitoylation or a polybasic domain for plasma membrane localization.
    Cadwallader KA; Paterson H; Macdonald SG; Hancock JF
    Mol Cell Biol; 1994 Jul; 14(7):4722-30. PubMed ID: 8007974
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Palmitylation of Src family tyrosine kinases regulates functional interaction with a B cell substrate.
    Saouaf SJ; Wolven A; Resh MD; Bolen JB
    Biochem Biophys Res Commun; 1997 May; 234(2):325-9. PubMed ID: 9177269
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Members of the src family of nonreceptor tyrosine kinases share a common mechanism for membrane binding.
    Silverman L; Sudol M; Resh MD
    Cell Growth Differ; 1993 Jun; 4(6):475-82. PubMed ID: 8373732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. N-terminal fatty acylation of the alpha-subunit of the G-protein Gi1: only the myristoylated protein is a substrate for palmitoylation.
    Galbiati F; Guzzi F; Magee AI; Milligan G; Parenti M
    Biochem J; 1994 Nov; 303 ( Pt 3)(Pt 3):697-700. PubMed ID: 7980434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of covalently bound amino-terminal myristic acid in endothelial nitric oxide synthase.
    Liu J; Sessa WC
    J Biol Chem; 1994 Apr; 269(16):11691-4. PubMed ID: 7512951
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dual fatty acylation of p59(Fyn) is required for association with the T cell receptor zeta chain through phosphotyrosine-Src homology domain-2 interactions.
    van't Hof W; Resh MD
    J Cell Biol; 1999 Apr; 145(2):377-89. PubMed ID: 10209031
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Palmitoylation of G protein-coupled receptor kinase, GRK6. Lipid modification diversity in the GRK family.
    Stoffel RH; Randall RR; Premont RT; Lefkowitz RJ; Inglese J
    J Biol Chem; 1994 Nov; 269(45):27791-4. PubMed ID: 7961702
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparison of src-family cDNAs reveals distinct mechanisms underlying focus formation in transfected fibroblasts.
    Sartor O; McLellan CA; Chiueh T
    J Biol Chem; 1992 Oct; 267(29):21044-51. PubMed ID: 1383216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Targeting of a G alpha subunit (Gi1 alpha) and c-Src tyrosine kinase to caveolae membranes: clarifying the role of N-myristoylation.
    Song KS; Sargiacomo M; Galbiati F; Parenti M; Lisanti MP
    Cell Mol Biol (Noisy-le-grand); 1997 May; 43(3):293-303. PubMed ID: 9193783
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.