BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 11030147)

  • 1. Structure and function of the C-terminal hypervariable region of K-Ras4B in plasma membrane targetting and transformation.
    Welman A; Burger MM; Hagmann J
    Oncogene; 2000 Sep; 19(40):4582-91. PubMed ID: 11030147
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lipid-binding characteristics of the polybasic carboxy-terminal sequence of K-ras4B.
    Leventis R; Silvius JR
    Biochemistry; 1998 May; 37(20):7640-8. PubMed ID: 9585579
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Solution structure and functional analysis of the cysteine-rich C1 domain of kinase suppressor of Ras (KSR).
    Zhou M; Horita DA; Waugh DS; Byrd RA; Morrison DK
    J Mol Biol; 2002 Jan; 315(3):435-46. PubMed ID: 11786023
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Membrane-mediated induction and sorting of K-Ras microdomain signaling platforms.
    Weise K; Kapoor S; Denter C; Nikolaus J; Opitz N; Koch S; Triola G; Herrmann A; Waldmann H; Winter R
    J Am Chem Soc; 2011 Feb; 133(4):880-7. PubMed ID: 21141956
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pivotal Advance: Phospholipids determine net membrane surface charge resulting in differential localization of active Rac1 and Rac2.
    Magalhaes MA; Glogauer M
    J Leukoc Biol; 2010 Apr; 87(4):545-55. PubMed ID: 19955208
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The cytoplasmic amino-terminus of the Latent Membrane Protein-1 of Epstein-Barr Virus: relationship between transmembrane orientation and effector functions of the carboxy-terminus and transmembrane domain.
    Coffin WF; Erickson KD; Hoedt-Miller M; Martin JM
    Oncogene; 2001 Aug; 20(38):5313-30. PubMed ID: 11536044
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel determinants of H-Ras plasma membrane localization and transformation.
    Willumsen BM; Cox AD; Solski PA; Der CJ; Buss JE
    Oncogene; 1996 Nov; 13(9):1901-9. PubMed ID: 8934536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transforming activity of ras proteins translocated to the plasma membrane by a myristoylation sequence from the src gene product.
    Lacal PM; Pennington CY; Lacal JC
    Oncogene; 1988 Jun; 2(6):533-7. PubMed ID: 2455265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mechanisms of membrane binding of small GTPase K-Ras4B farnesylated hypervariable region.
    Jang H; Abraham SJ; Chavan TS; Hitchinson B; Khavrutskii L; Tarasova NI; Nussinov R; Gaponenko V
    J Biol Chem; 2015 Apr; 290(15):9465-77. PubMed ID: 25713064
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Electrical properties of plasma membrane modulate subcellular distribution of K-Ras.
    Gomez GA; Daniotti JL
    FEBS J; 2007 May; 274(9):2210-28. PubMed ID: 17388810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. S-Acylation and plasma membrane targeting of the farnesylated carboxyl-terminal peptide of N-ras in mammalian fibroblasts.
    Schroeder H; Leventis R; Rex S; Schelhaas M; Nägele E; Waldmann H; Silvius JR
    Biochemistry; 1997 Oct; 36(42):13102-9. PubMed ID: 9335573
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The C-terminal domain of TRPV4 is essential for plasma membrane localization.
    Becker D; Müller M; Leuner K; Jendrach M
    Mol Membr Biol; 2008 Feb; 25(2):139-51. PubMed ID: 18307101
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Does lens intrinsic membrane protein MP19 contain a membrane-targeting signal?
    Chen T; Li X; Yang Y; Erdene AG; Church RL
    Mol Vis; 2003 Dec; 9():735-46. PubMed ID: 14735063
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Hypervariable Region of K-Ras4B Governs Molecular Recognition and Function.
    Abdelkarim H; Banerjee A; Grudzien P; Leschinsky N; Abushaer M; Gaponenko V
    Int J Mol Sci; 2019 Nov; 20(22):. PubMed ID: 31739603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rit, a non-lipid-modified Ras-related protein, transforms NIH3T3 cells without activating the ERK, JNK, p38 MAPK or PI3K/Akt pathways.
    Rusyn EV; Reynolds ER; Shao H; Grana TM; Chan TO; Andres DA; Cox AD
    Oncogene; 2000 Sep; 19(41):4685-94. PubMed ID: 11032018
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Carcinogenesis and its mechanism of mutant-type[12Asp]K-ras4B gene].
    Gui LM; Wei LH; Zhang YM; Wang JL; Wang Y; Chen Y; Ma DL
    Ai Zheng; 2002 Jan; 21(1):33-8. PubMed ID: 12500394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distinct functional domains of STP-C488 of herpesvirus saimiri.
    Jung JU; Desrosiers RC
    Virology; 1994 Nov; 204(2):751-8. PubMed ID: 7941343
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of choline kinase activity by Ras proteins involves Ral-GDS and PI3K.
    Ramírez de Molina A; Penalva V; Lucas L; Lacal JC
    Oncogene; 2002 Jan; 21(6):937-46. PubMed ID: 11840339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The defective transforming phenotype of c-Jun Ala(63/73) is rescued by mutation of the C-terminal phosphorylation site.
    Bost F; Caron L; Vial E; Montreau N; Marchetti I; Dejong V; Defize L; Castellazzi M; Binétruy B
    Oncogene; 2001 Nov; 20(50):7425-9. PubMed ID: 11704873
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An extended bipartite nuclear localization signal in Smad4 is required for its nuclear import and transcriptional activity.
    Xiao Z; Latek R; Lodish HF
    Oncogene; 2003 Feb; 22(7):1057-69. PubMed ID: 12592392
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.