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489 related items for PubMed ID: 8379998

  • 1. Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2.
    Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B.
    Nature; 1993 Jun 10; 363(6429):515-21. PubMed ID: 8379998
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  • 2. The neurofibromatosis type 2 gene product, schwannomin, suppresses growth of NIH 3T3 cells.
    Lutchman M, Rouleau GA.
    Cancer Res; 1995 Jun 01; 55(11):2270-4. PubMed ID: 7757975
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  • 3. [Molecular-genetic aspects of neurofibromatosis].
    Hulsebos TJ.
    Ned Tijdschr Geneeskd; 1997 Mar 29; 141(13):620-3. PubMed ID: 9190537
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  • 4. [Neurofibromatosis type 2 (NF2)].
    Araki N, Takeshima H, Saya H.
    Gan To Kagaku Ryoho; 1997 Sep 29; 24(11):1427-31. PubMed ID: 9309136
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  • 5. Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.
    Bianchi AB, Hara T, Ramesh V, Gao J, Klein-Szanto AJ, Morin F, Menon AG, Trofatter JA, Gusella JF, Seizinger BR.
    Nat Genet; 1994 Feb 29; 6(2):185-92. PubMed ID: 8162073
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  • 11. Molecular characterization of germline NF2 gene rearrangements.
    Legoix P, Sarkissian HD, Cazes L, Giraud S, Sor F, Rouleau GA, Lenoir G, Thomas G, Zucman-Rossi J.
    Genomics; 2000 Apr 01; 65(1):62-6. PubMed ID: 10777666
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  • 12. Neurofibromatosis type 2 and von Hippel-Lindau disease: from gene cloning to function.
    Kley N, Whaley J, Seizinger BR.
    Glia; 1995 Nov 01; 15(3):297-307. PubMed ID: 8586465
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  • 13. Frequent mutations of NF2 and allelic loss from chromosome band 22q12 in malignant mesothelioma: evidence for a two-hit mechanism of NF2 inactivation.
    Cheng JQ, Lee WC, Klein MA, Cheng GZ, Jhanwar SC, Testa JR.
    Genes Chromosomes Cancer; 1999 Mar 01; 24(3):238-42. PubMed ID: 10451704
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  • 14. The neurofibromatosis type 2 gene is inactivated in schwannomas.
    Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA.
    Hum Mol Genet; 1994 Jan 01; 3(1):147-51. PubMed ID: 8162016
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  • 15. Neurofibromatosis 2 antisense oligodeoxynucleotides induce reversible inhibition of schwannomin synthesis and cell adhesion in STS26T and T98G cells.
    Huynh DP, Pulst SM.
    Oncogene; 1996 Jul 04; 13(1):73-84. PubMed ID: 8700556
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  • 16. Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line.
    Nishioka M, Kohno T, Takahashi M, Niki T, Yamada T, Sone S, Yokota J.
    Oncogene; 2000 Dec 14; 19(54):6251-60. PubMed ID: 11175339
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  • 18. Identification of new members of the Gas2 and Ras families in the 22q12 chromosome region.
    Zucman-Rossi J, Legoix P, Thomas G.
    Genomics; 1996 Dec 15; 38(3):247-54. PubMed ID: 8975699
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