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Journal Abstract Search

258 related items for PubMed ID: 12579316

  • 21. Plasminogen activation in neurofibromatosis 2-associated and sporadic schwannomas.
    Sirén V, Antinheimo JP, Jääskeläinen J, Böhling T, Carpén O, Vaheri A.
    Acta Neurochir (Wien); 2004 Feb; 146(2):111-8. PubMed ID: 14963743
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  • 22. Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas.
    von Haken MS, White EC, Daneshvar-Shyesther L, Sih S, Choi E, Kalra R, Cogen PH.
    Genes Chromosomes Cancer; 1996 Sep; 17(1):37-44. PubMed ID: 8889505
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  • 23. Frequent genomic imbalances in chromosomes 17, 19, and 22q in peripheral nerve sheath tumours detected by comparative genomic hybridization analysis.
    Koga T, Iwasaki H, Ishiguro M, Matsuzaki A, Kikuchi M.
    J Pathol; 2002 May; 197(1):98-107. PubMed ID: 12081210
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  • 24. Microsatellite analysis of recurrent vestibular schwannoma (acoustic neuroma) following stereotactic radiosurgery.
    Lee DJ, Maseyesva B, Westra W, Long D, Niparko JK, Califano J.
    Otol Neurotol; 2006 Feb; 27(2):213-9. PubMed ID: 16436992
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  • 25. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
    Espinosa AB, Mackintosh C, Maíllo A, Gutierrez L, Sousa P, Merino M, Ortiz J, de Alava E, Orfao A, Tabernero MD.
    Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
    [Abstract] [Full Text] [Related]

  • 26. High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.
    Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Sainio M, Hung G, Mathiesen T, Möller C, Pulst SM, Harder H, Heiberg A, Honda M, Niimura M, Sahlén S, Blennow E, Albertson DG, Pinkel D, Dumanski JP.
    Hum Mol Genet; 2001 Feb 01; 10(3):271-82. PubMed ID: 11159946
    [Abstract] [Full Text] [Related]

  • 27. Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.
    Díaz de Ståhl T, Hartmann C, de Bustos C, Piotrowski A, Benetkiewicz M, Mantripragada KK, Tykwinski T, von Deimling A, Dumanski JP.
    Genes Chromosomes Cancer; 2005 Oct 01; 44(2):161-9. PubMed ID: 15945096
    [Abstract] [Full Text] [Related]

  • 28. Somatic neurofibromatosis type 2 gene mutations and growth characteristics in vestibular schwannoma.
    Irving RM, Harada T, Moffat DA, Hardy DG, Whittaker JL, Xuereb JH, Maher ER.
    Am J Otol; 1997 Nov 01; 18(6):754-60. PubMed ID: 9391673
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  • 34. Universal absence of merlin, but not other ERM family members, in schwannomas.
    Stemmer-Rachamimov AO, Xu L, Gonzalez-Agosti C, Burwick JA, Pinney D, Beauchamp R, Jacoby LB, Gusella JF, Ramesh V, Louis DN.
    Am J Pathol; 1997 Dec 01; 151(6):1649-54. PubMed ID: 9403715
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