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Journal Abstract Search

140 related items for PubMed ID: 8557252

  • 21.
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  • 23. Frequency and distribution of NF2 mutations in schwannomas.
    Jacoby LB, MacCollin M, Barone R, Ramesh V, Gusella JF.
    Genes Chromosomes Cancer; 1996 Sep; 17(1):45-55. PubMed ID: 8889506
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  • 26. Impairment of cell adhesion by expression of the mutant neurofibromatosis type 2 (NF2) genes which lack exons in the ERM-homology domain.
    Koga H, Araki N, Takeshima H, Nishi T, Hirota T, Kimura Y, Nakao M, Saya H.
    Oncogene; 1998 Aug 20; 17(7):801-10. PubMed ID: 9779996
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  • 27. A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected].
    Kluwe L, Pulst SM, Köppen J, Mautner VF.
    Hum Genet; 1995 Apr 20; 95(4):443-6. PubMed ID: 7705843
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  • 28. Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.
    Paganini I, Capone GL, Vitte J, Sestini R, Putignano AL, Giovannini M, Papi L.
    J Neurooncol; 2018 Mar 20; 137(1):33-38. PubMed ID: 29230670
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  • 29. Segmental neurofibromatosis type 2: discriminating two hit from four hit in a patient presenting multiple schwannomas confined to one limb.
    Castellanos E, Bielsa I, Carrato C, Rosas I, Solanes A, Hostalot C, Amilibia E, Prades J, Roca-Ribas F, Lázaro C, Blanco I, Serra E, NF2 Multidisciplinary Clinics HUGTiP-ICO-IMPPC.
    BMC Med Genomics; 2015 Jan 24; 8():2. PubMed ID: 25739810
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  • 30. NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH.
    Szijan I, Rochefort D, Bruder C, Surace E, Machiavelli G, Dalamon V, Cotignola J, Ferreiro V, Campero A, Basso A, Dumanski JP, Rouleau GA.
    Neuromolecular Med; 2003 Jan 24; 3(1):41-52. PubMed ID: 12665675
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  • 31. 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 24; 95(3):347-51. PubMed ID: 7868131
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  • 33. Molecular genetics alterations and tumor behavior of sporadic vestibular schwannoma from the People's Republic of China.
    Bian LG, Tirakotai W, Sun QF, Zhao WG, Shen JK, Luo QZ.
    J Neurooncol; 2005 Jul 24; 73(3):253-60. PubMed ID: 15980976
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  • 35. Screening for large mutations of the NF2 gene.
    Kluwe L, Nygren AO, Errami A, Heinrich B, Matthies C, Tatagiba M, Mautner V.
    Genes Chromosomes Cancer; 2005 Apr 24; 42(4):384-91. PubMed ID: 15645494
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  • 36. PTEN is not altered in sporadic vestibular schwannomas.
    Mawrin C, Kirches E, Boltze C, Dietzmann K.
    Histopathology; 2002 Jun 24; 40(6):526-30. PubMed ID: 12047763
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  • 37. Genetics of familial and non-familial skull base tumours.
    Irving RM, Moffat DA, Maher ER.
    Clin Otolaryngol Allied Sci; 1995 Feb 24; 20(1):5-11. PubMed ID: 7788935
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  • 38. Molecular characterization of chromosome 22 deletions in schwannomas.
    Bijlsma EK, Brouwer-Mladin R, Bosch DA, Westerveld A, Hulsebos TJ.
    Genes Chromosomes Cancer; 1992 Oct 24; 5(3):201-5. PubMed ID: 1384671
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  • 39. Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes.
    Kluwe L, Bayer S, Baser ME, Hazim W, Haase W, Fünsterer C, Mautner VF.
    Hum Genet; 1996 Nov 24; 98(5):534-8. PubMed ID: 8882871
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  • 40. Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin.
    De Vitis LR, Tedde A, Vitelli F, Ammannati F, Mennonna P, Bono P, Grammatico B, Grammatico P, Radice P, Bigozzi U, Montali E, Papi L.
    Hum Genet; 1996 May 24; 97(5):638-41. PubMed ID: 8655145
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