These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

337 related items for PubMed ID: 7951231

  • 1. Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.
    Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM.
    Hum Mol Genet; 1994 Jun; 3(6):885-91. PubMed ID: 7951231
    [Abstract] [Full Text] [Related]

  • 2. 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; 3(1):147-51. PubMed ID: 8162016
    [Abstract] [Full Text] [Related]

  • 3. Analysis of mutations in the SCH gene in schwannomas.
    Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ.
    Genes Chromosomes Cancer; 1994 Sep; 11(1):7-14. PubMed ID: 7529050
    [Abstract] [Full Text] [Related]

  • 4. Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas).
    Welling DB.
    Laryngoscope; 1998 Feb; 108(2):178-89. PubMed ID: 9473065
    [Abstract] [Full Text] [Related]

  • 5. Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma.
    Irving RM, Moffat DA, Hardy DG, Barton DE, Xuereb JH, Maher ER.
    Hum Mol Genet; 1994 Feb; 3(2):347-50. PubMed ID: 8004107
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. cDNA microarray analysis of vestibular schwannomas.
    Welling DB, Lasak JM, Akhmametyeva E, Ghaheri B, Chang LS.
    Otol Neurotol; 2002 Sep; 23(5):736-48. PubMed ID: 12218628
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. The neurofibromatosis 2 (NF2) tumor suppressor gene encodes multiple alternatively spliced transcripts.
    Pykett MJ, Murphy M, Harnish PR, George DL.
    Hum Mol Genet; 1994 Apr; 3(4):559-64. PubMed ID: 8069298
    [Abstract] [Full Text] [Related]

  • 12. Exon scanning for mutation of the NF2 gene in schwannomas.
    Jacoby LB, MacCollin M, Louis DN, Mohney T, Rubio MP, Pulaski K, Trofatter JA, Kley N, Seizinger B, Ramesh V.
    Hum Mol Genet; 1994 Mar; 3(3):413-9. PubMed ID: 8012353
    [Abstract] [Full Text] [Related]

  • 13. Mutational analysis of patients with neurofibromatosis 2.
    MacCollin M, Ramesh V, Jacoby LB, Louis DN, Rubio MP, Pulaski K, Trofatter JA, Short MP, Bove C, Eldridge R.
    Am J Hum Genet; 1994 Aug; 55(2):314-20. PubMed ID: 7913580
    [Abstract] [Full Text] [Related]

  • 14. Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas.
    Kluwe L, Mautner V, Heinrich B, Dezube R, Jacoby LB, Friedrich RE, MacCollin M.
    J Med Genet; 2003 Feb; 40(2):109-14. PubMed ID: 12566519
    [Abstract] [Full Text] [Related]

  • 15. Functional analysis of neurofibromatosis 2 (NF2) missense mutations.
    Gutmann DH, Hirbe AC, Haipek CA.
    Hum Mol Genet; 2001 Jul 01; 10(14):1519-29. PubMed ID: 11448944
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The mouse homologue of the neurofibromatosis type 2 gene is highly conserved.
    Claudio JO, Marineau C, Rouleau GA.
    Hum Mol Genet; 1994 Jan 01; 3(1):185-90. PubMed ID: 8162023
    [Abstract] [Full Text] [Related]

  • 18. Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosis.
    Jacoby LB, MacCollin M, Parry DM, Kluwe L, Lynch J, Jones D, Gusella JF.
    Neurogenetics; 1999 Apr 01; 2(2):101-8. PubMed ID: 10369886
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 20. A point mutation associated with a severe phenotype of neurofibromatosis 2.
    MacCollin M, Braverman N, Viskochil D, Ruttledge M, Davis K, Ojemann R, Gusella J, Parry DM.
    Ann Neurol; 1996 Sep 01; 40(3):440-5. PubMed ID: 8797533
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.