BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 8399217)

  • 1. Analysis of the palmitoylation and membrane targeting domain of neuromodulin (GAP-43) by site-specific mutagenesis.
    Liu Y; Fisher DA; Storm DR
    Biochemistry; 1993 Oct; 32(40):10714-9. PubMed ID: 8399217
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Palmitylation of neuromodulin (GAP-43) is not required for phosphorylation by protein kinase C.
    Chapman ER; Estep RP; Storm DR
    J Biol Chem; 1992 Dec; 267(35):25233-8. PubMed ID: 1460023
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The role of palmitoylation of the guanine nucleotide binding protein G11 alpha in defining interaction with the plasma membrane.
    McCallum JF; Wise A; Grassie MA; Magee AI; Guzzi F; Parenti M; Milligan G
    Biochem J; 1995 Sep; 310 ( Pt 3)(Pt 3):1021-7. PubMed ID: 7575398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intracellular sorting of neuromodulin (GAP-43) mutants modified in the membrane targeting domain.
    Liu Y; Fisher DA; Storm DR
    J Neurosci; 1994 Oct; 14(10):5807-17. PubMed ID: 7931546
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Palmitoylation of luteinizing hormone/human choriogonadotropin receptors in transfected cells. Abolition of palmitoylation by mutation of Cys-621 and Cys-622 residues in the cytoplasmic tail increases ligand-induced internalization of the receptor.
    Kawate N; Menon KM
    J Biol Chem; 1994 Dec; 269(48):30651-8. PubMed ID: 7982985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Palmitoylation of bovine opsin and its cysteine mutants in COS cells.
    Karnik SS; Ridge KD; Bhattacharya S; Khorana HG
    Proc Natl Acad Sci U S A; 1993 Jan; 90(1):40-4. PubMed ID: 8419942
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Palmitoylation of either Cys-3 or Cys-5 is required for the biological activity of the Lck tyrosine protein kinase.
    Yurchak LK; Sefton BM
    Mol Cell Biol; 1995 Dec; 15(12):6914-22. PubMed ID: 8524258
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeting of neuromodulin (GAP-43) fusion proteins to growth cones in cultured rat embryonic neurons.
    Liu YC; Chapman ER; Storm DR
    Neuron; 1991 Mar; 6(3):411-20. PubMed ID: 1825782
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of the palmitoylation domain of SNAP-25.
    Lane SR; Liu Y
    J Neurochem; 1997 Nov; 69(5):1864-9. PubMed ID: 9349529
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of the calmodulin binding domain of neuromodulin. Functional significance of serine 41 and phenylalanine 42.
    Chapman ER; Au D; Alexander KA; Nicolson TA; Storm DR
    J Biol Chem; 1991 Jan; 266(1):207-13. PubMed ID: 1824693
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations of the alpha 2A-adrenergic receptor that eliminate detectable palmitoylation do not perturb receptor-G-protein coupling.
    Kennedy ME; Limbird LE
    J Biol Chem; 1993 Apr; 268(11):8003-11. PubMed ID: 8385131
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Amino acid residues 24-31 but not palmitoylation of cysteines 30 and 45 are required for membrane anchoring of glutamic acid decarboxylase, GAD65.
    Shi Y; Veit B; Baekkeskov S
    J Cell Biol; 1994 Mar; 124(6):927-34. PubMed ID: 8132714
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Purification and characterization of a brain-specific protein kinase C substrate, neurogranin (p17). Identification of a consensus amino acid sequence between neurogranin and neuromodulin (GAP43) that corresponds to the protein kinase C phosphorylation site and the calmodulin-binding domain.
    Baudier J; Deloulme JC; Van Dorsselaer A; Black D; Matthes HW
    J Biol Chem; 1991 Jan; 266(1):229-37. PubMed ID: 1824695
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The 5-hydroxytryptamine(4a) receptor is palmitoylated at two different sites, and acylation is critically involved in regulation of receptor constitutive activity.
    Ponimaskin EG; Heine M; Joubert L; Sebben M; Bickmeyer U; Richter DW; Dumuis A
    J Biol Chem; 2002 Jan; 277(4):2534-46. PubMed ID: 11706023
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Palmitoylation negative mutants of murine G11 alpha have decreased ability to interact with the plasma membrane when expressed in COS-1 cells.
    McCallum JF; Wise A; Parenti M; Milligan G
    Biochem Soc Trans; 1995 Feb; 23(1):9S. PubMed ID: 7758810
    [No Abstract]   [Full Text] [Related]  

  • 19. A novel N-terminal motif for palmitoylation of G-protein alpha subunits.
    Parenti M; ViganĂ³ MA; Newman CM; Milligan G; Magee AI
    Biochem J; 1993 Apr; 291 ( Pt 2)(Pt 2):349-53. PubMed ID: 8484716
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mass spectrometric analysis of GAP-43/neuromodulin reveals the presence of a variety of fatty acylated species.
    Liang X; Lu Y; Neubert TA; Resh MD
    J Biol Chem; 2002 Sep; 277(36):33032-40. PubMed ID: 12105219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.