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Journal Abstract Search


2513 related items for PubMed ID: 7669741

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  • 3. Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas.
    Lekanne Deprez RH, Bianchi AB, Groen NA, Seizinger BR, Hagemeijer A, van Drunen E, Bootsma D, Koper JW, Avezaat CJ, Kley N.
    Am J Hum Genet; 1994 Jun; 54(6):1022-9. PubMed ID: 7911002
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  • 5. Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.
    Ng HK, Lau KM, Tse JY, Lo KW, Wong JH, Poon WS, Huang DP.
    Neurosurgery; 1995 Oct; 37(4):764-73. PubMed ID: 8559307
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  • 7. Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas.
    Papi L, De Vitis LR, Vitelli F, Ammannati F, Mennonna P, Montali E, Bigozzi U.
    Hum Genet; 1995 Mar; 95(3):347-51. PubMed ID: 7868131
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  • 8. Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma.
    Harada T, Irving RM, Xuereb JH, Barton DE, Hardy DG, Moffat DA, Maher ER.
    J Neurosurg; 1996 May; 84(5):847-51. PubMed ID: 8622160
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  • 9. [A new tumor suppressor gene responsible for type 2 neurofibromatosis is inactivated in neurinoma and meningioma].
    Sanson M.
    Rev Neurol (Paris); 1996 Jan; 152(1):1-10. PubMed ID: 8729390
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  • 13. Calpain-dependent proteolysis of NF2 protein: involvement in schwannomas and meningiomas.
    Kimura Y, Saya H, Nakao M.
    Neuropathology; 2000 Sep; 20(3):153-60. PubMed ID: 11132929
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  • 14. Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomas.
    Huynh DP, Mautner V, Baser ME, Stavrou D, Pulst SM.
    J Neuropathol Exp Neurol; 1997 Apr; 56(4):382-90. PubMed ID: 9100669
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  • 15. Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.
    Wellenreuther R, Kraus JA, Lenartz D, Menon AG, Schramm J, Louis DN, Ramesh V, Gusella JF, Wiestler OD, von Deimling A.
    Am J Pathol; 1995 Apr; 146(4):827-32. PubMed ID: 7717450
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  • 16. Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
    Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP.
    Nat Genet; 1994 Feb; 6(2):180-4. PubMed ID: 8162072
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  • 17. Allelic status of 1p, 14q, and 22q and NF2 gene mutations in sporadic schwannomas.
    Leone PE, Bello MJ, Mendiola M, Kusak ME, De Campos JM, Vaquero J, Sarasa JL, Pestana A, Rey JA.
    Int J Mol Med; 1998 May; 1(5):889-92. PubMed ID: 9852312
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  • 18. Tight association of loss of merlin expression with loss of heterozygosity at chromosome 22q in sporadic meningiomas.
    Ueki K, Wen-Bin C, Narita Y, Asai A, Kirino T.
    Cancer Res; 1999 Dec 01; 59(23):5995-8. PubMed ID: 10606247
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  • 19. Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas.
    De Vitis LR, Tedde A, Vitelli F, Ammannati F, Mennonna P, Bigozzi U, Montali E, Papi L.
    Hum Genet; 1996 May 01; 97(5):632-7. PubMed ID: 8655144
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  • 20. Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.
    Hansson CM, Buckley PG, Grigelioniene G, Piotrowski A, Hellström AR, Mantripragada K, Jarbo C, Mathiesen T, Dumanski JP.
    BMC Genomics; 2007 Jan 12; 8():16. PubMed ID: 17222329
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