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Journal Abstract Search

330 related items for PubMed ID: 11275983

  • 1. Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.
    Lamszus K, Lachenmayer L, Heinemann U, Kluwe L, Finckh U, Höppner W, Stavrou D, Fillbrandt R, Westphal M.
    Int J Cancer; 2001 Mar 15; 91(6):803-8. PubMed ID: 11275983
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  • 2. Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas.
    Ebert C, von Haken M, Meyer-Puttlitz B, Wiestler OD, Reifenberger G, Pietsch T, von Deimling A.
    Am J Pathol; 1999 Aug 15; 155(2):627-32. PubMed ID: 10433955
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  • 3. 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 15; 17(1):37-44. PubMed ID: 8889505
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  • 4. Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.
    Kraus JA, de Millas W, Sörensen N, Herbold C, Schichor C, Tonn JC, Wiestler OD, von Deimling A, Pietsch T.
    Acta Neuropathol; 2001 Jul 15; 102(1):69-74. PubMed ID: 11547953
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  • 6. Human ependymomas reveal frequent deletions on chromosomes 6 and 9.
    Huang B, Starostik P, Schraut H, Krauss J, Sörensen N, Roggendorf W.
    Acta Neuropathol; 2003 Oct 15; 106(4):357-62. PubMed ID: 12898154
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  • 7. Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas.
    Rubio MP, Correa KM, Ramesh V, MacCollin MM, Jacoby LB, von Deimling A, Gusella JF, Louis DN.
    Cancer Res; 1994 Jan 01; 54(1):45-7. PubMed ID: 8261460
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  • 8. Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas.
    Rousseau-Merck M, Versteege I, Zattara-Cannoni H, Figarella D, Lena G, Aurias A, Vagner-Capodano AM.
    Cancer Genet Cytogenet; 2000 Sep 01; 121(2):223-7. PubMed ID: 11063814
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  • 10. Frequent type 2 neurofibromatosis gene transcript mutations in sporadic intramedullary spinal cord ependymomas.
    Birch BD, Johnson JP, Parsa A, Desai RD, Yoon JT, Lycette CA, Li YM, Bruce JN.
    Neurosurgery; 1996 Jul 01; 39(1):135-40. PubMed ID: 8805149
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  • 11. A family with spinal anaplastic ependymoma: evidence of loss of chromosome 22q in tumor.
    Yokota T, Tachizawa T, Fukino K, Teramoto A, Kouno J, Matsumoto K, Emi M.
    J Hum Genet; 2003 Jul 01; 48(11):598-602. PubMed ID: 14566482
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  • 12. Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray.
    Ammerlaan AC, de Bustos C, Ararou A, Buckley PG, Mantripragada KK, Verstegen MJ, Hulsebos TJ, Dumanski JP.
    Genes Chromosomes Cancer; 2005 Aug 01; 43(4):329-38. PubMed ID: 15880457
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  • 18. Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas.
    Slavc I, MacCollin MM, Dunn M, Jones S, Sutton L, Gusella JF, Biegel JA.
    Int J Cancer; 1995 Aug 22; 64(4):243-7. PubMed ID: 7657387
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