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Journal Abstract Search

396 related items for PubMed ID: 9668168

  • 1. Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1.
    Klose A, Ahmadian MR, Schuelke M, Scheffzek K, Hoffmeyer S, Gewies A, Schmitz F, Kaufmann D, Peters H, Wittinghofer A, Nürnberg P.
    Hum Mol Genet; 1998 Aug; 7(8):1261-8. PubMed ID: 9668168
    [Abstract] [Full Text] [Related]

  • 2. Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1.
    Hirata Y, Brems H, Suzuki M, Kanamori M, Okada M, Morita R, Llano-Rivas I, Ose T, Messiaen L, Legius E, Yoshimura A.
    J Biol Chem; 2016 Feb 12; 291(7):3124-34. PubMed ID: 26635368
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  • 3. Ras-GTP regulation is not altered in cultured melanocytes with reduced levels of neurofibromin derived from patients with neurofibromatosis 1 (NF1).
    Griesser J, Kaufmann D, Eisenbarth I, Bäuerle C, Krone W.
    Biol Chem Hoppe Seyler; 1995 Feb 12; 376(2):91-101. PubMed ID: 7794530
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  • 4. Structural analysis of the GAP-related domain from neurofibromin and its implications.
    Scheffzek K, Ahmadian MR, Wiesmüller L, Kabsch W, Stege P, Schmitz F, Wittinghofer A.
    EMBO J; 1998 Aug 03; 17(15):4313-27. PubMed ID: 9687500
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  • 5. Neurofibromin GTPase-activating protein-related domains restore normal growth in Nf1-/- cells.
    Hiatt KK, Ingram DA, Zhang Y, Bollag G, Clapp DW.
    J Biol Chem; 2001 Mar 09; 276(10):7240-5. PubMed ID: 11080503
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  • 6. A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activity.
    Andersen LB, Ballester R, Marchuk DA, Chang E, Gutmann DH, Saulino AM, Camonis J, Wigler M, Collins FS.
    Mol Cell Biol; 1993 Jan 09; 13(1):487-95. PubMed ID: 8417346
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  • 7. Pathogenic Mutations Associated with Legius Syndrome Modify the Spred1 Surface and Are Involved in Direct Binding to the Ras Inactivator Neurofibromin.
    Führer S, Tollinger M, Dunzendorfer-Matt T.
    J Mol Biol; 2019 Sep 06; 431(19):3889-3899. PubMed ID: 31401120
    [Abstract] [Full Text] [Related]

  • 8. [Genetics of type 1 neurofibromatosis].
    Garavelli L, Donadio A, Sigorini M, Grassi L, Banchini G.
    Acta Biomed Ateneo Parmense; 2000 Sep 06; 71(3-4):89-95. PubMed ID: 11424621
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  • 9. The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21.
    Martin GA, Viskochil D, Bollag G, McCabe PC, Crosier WJ, Haubruck H, Conroy L, Clark R, O'Connell P, Cawthon RM.
    Cell; 1990 Nov 16; 63(4):843-9. PubMed ID: 2121370
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  • 10. Identification and characterization of the neurofibromatosis type 1 protein product.
    DeClue JE, Cohen BD, Lowy DR.
    Proc Natl Acad Sci U S A; 1991 Nov 15; 88(22):9914-8. PubMed ID: 1946460
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  • 19. Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) gene.
    Thomas L, Richards M, Mort M, Dunlop E, Cooper DN, Upadhyaya M.
    Hum Mutat; 2012 Dec 15; 33(12):1687-96. PubMed ID: 22807134
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  • 20. Loss of neurofibromin is associated with activation of RAS/MAPK and PI3-K/AKT signaling in a neurofibromatosis 1 astrocytoma.
    Lau N, Feldkamp MM, Roncari L, Loehr AH, Shannon P, Gutmann DH, Guha A.
    J Neuropathol Exp Neurol; 2000 Sep 15; 59(9):759-67. PubMed ID: 11005256
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