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Journal Abstract Search


110 related items for PubMed ID: 7805033

  • 1. Homozygous deletions of the multiple tumor suppressor gene 1 in the progression of human astrocytomas.
    Walker DG, Duan W, Popovic EA, Kaye AH, Tomlinson FH, Lavin M.
    Cancer Res; 1995 Jan 01; 55(1):20-3. PubMed ID: 7805033
    [Abstract] [Full Text] [Related]

  • 2. Loci associated with malignant progression in astrocytomas: a candidate on chromosome 19q.
    von Deimling A, Bender B, Jahnke R, Waha A, Kraus J, Albrecht S, Wellenreuther R, Fassbender F, Nagel J, Menon AG.
    Cancer Res; 1994 Mar 15; 54(6):1397-401. PubMed ID: 8137236
    [Abstract] [Full Text] [Related]

  • 3. Malignant astrocytomas with homozygous CDKN2/p16 gene deletions have higher Ki-67 proliferation indices.
    Ono Y, Tamiya T, Ichikawa T, Kunishio K, Matsumoto K, Furuta T, Ohmoto T, Ueki K, Louis DN.
    J Neuropathol Exp Neurol; 1996 Oct 15; 55(10):1026-31. PubMed ID: 8857999
    [Abstract] [Full Text] [Related]

  • 4. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene.
    Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M.
    Clin Cancer Res; 2005 Feb 01; 11(3):1119-28. PubMed ID: 15709179
    [Abstract] [Full Text] [Related]

  • 5. The retinoblastoma gene is involved in malignant progression of astrocytomas.
    Henson JW, Schnitker BL, Correa KM, von Deimling A, Fassbender F, Xu HJ, Benedict WF, Yandell DW, Louis DN.
    Ann Neurol; 1994 Nov 01; 36(5):714-21. PubMed ID: 7979217
    [Abstract] [Full Text] [Related]

  • 6. Evidence for a tumor suppressor gene on chromosome 19q associated with human astrocytomas, oligodendrogliomas, and mixed gliomas.
    von Deimling A, Louis DN, von Ammon K, Petersen I, Wiestler OD, Seizinger BR.
    Cancer Res; 1992 Aug 01; 52(15):4277-9. PubMed ID: 1353411
    [Abstract] [Full Text] [Related]

  • 7. CDKN2 (p16/MTS1) gene deletion or CDK4 amplification occurs in the majority of glioblastomas.
    Schmidt EE, Ichimura K, Reifenberger G, Collins VP.
    Cancer Res; 1994 Dec 15; 54(24):6321-4. PubMed ID: 7987821
    [Abstract] [Full Text] [Related]

  • 8. Loss of heterozygosity on chromosome 10q associated with malignancy and prognosis in astrocytic tumors, and discovery of novel loss regions.
    Daido S, Takao S, Tamiya T, Ono Y, Terada K, Ito S, Ouchida M, Date I, Ohmoto T, Shimizu K.
    Oncol Rep; 2004 Oct 15; 12(4):789-95. PubMed ID: 15375501
    [Abstract] [Full Text] [Related]

  • 9. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
    Simoneau AR, Spruck CH, Gonzalez-Zulueta M, Gonzalgo ML, Chan MF, Tsai YC, Dean M, Steven K, Horn T, Jones PA.
    Cancer Res; 1996 Nov 01; 56(21):5039-43. PubMed ID: 8895761
    [Abstract] [Full Text] [Related]

  • 10. MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p.
    Ueki K, Rubio MP, Ramesh V, Correa KM, Rutter JL, von Deimling A, Buckler AJ, Gusella JF, Louis DN.
    Hum Mol Genet; 1994 Oct 01; 3(10):1841-5. PubMed ID: 7849711
    [Abstract] [Full Text] [Related]

  • 11. Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours.
    Miyakawa A, Ichimura K, Schmidt EE, Varmeh-Ziaie S, Collins VP.
    Br J Cancer; 2000 Feb 01; 82(3):543-9. PubMed ID: 10682663
    [Abstract] [Full Text] [Related]

  • 12. Homozygous deletions of the MTS1 gene are rare in non-astrocytic brain tumors.
    Walker DG, Duan W, Kaye AH, Lavin MF.
    Biochem Biophys Res Commun; 1995 Jun 15; 211(2):404-9. PubMed ID: 7794250
    [Abstract] [Full Text] [Related]

  • 13. Chromosome 9p deletions in invasive and noninvasive nonfunctional pituitary adenomas: the deleted region involves markers outside of the MTS1 and MTS2 genes.
    Farrell WE, Simpson DJ, Bicknell JE, Talbot AJ, Bates AS, Clayton RN.
    Cancer Res; 1997 Jul 01; 57(13):2703-9. PubMed ID: 9205080
    [Abstract] [Full Text] [Related]

  • 14. A common region of homozygous deletion in malignant human gliomas lies between the IFN alpha/omega gene cluster and the D9S171 locus.
    Ichimura K, Schmidt EE, Yamaguchi N, James CD, Collins VP.
    Cancer Res; 1994 Jun 15; 54(12):3127-30. PubMed ID: 8205529
    [Abstract] [Full Text] [Related]

  • 15. Evidence for the involvement of a potential second tumor suppressor gene on chromosome 17 distinct from p53 in malignant astrocytomas.
    Saxena A, Clark WC, Robertson JT, Ikejiri B, Oldfield EH, Ali IU.
    Cancer Res; 1992 Dec 01; 52(23):6716-21. PubMed ID: 1358438
    [Abstract] [Full Text] [Related]

  • 16. High frequency of p53 protein accumulation without p53 gene mutation in human juvenile pilocytic, low grade and anaplastic astrocytomas.
    Lang FF, Miller DC, Pisharody S, Koslow M, Newcomb EW.
    Oncogene; 1994 Mar 01; 9(3):949-54. PubMed ID: 8108140
    [Abstract] [Full Text] [Related]

  • 17. Molecular pathogenesis of pediatric astrocytic tumors.
    Nakamura M, Shimada K, Ishida E, Higuchi T, Nakase H, Sakaki T, Konishi N.
    Neuro Oncol; 2007 Apr 01; 9(2):113-23. PubMed ID: 17327574
    [Abstract] [Full Text] [Related]

  • 18. Chromosome 10 and 17 deletions and p53 gene mutations in Thai patients with astrocytomas.
    Put-Ti-Noi S, Petmitr S, Chanyavanich V, Sangruji T, Theerapuncharoen V, Hayashi K, Thangnipon W.
    Oncol Rep; 2004 Jan 01; 11(1):207-11. PubMed ID: 14654927
    [Abstract] [Full Text] [Related]

  • 19. The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumors.
    Frank S, Müller J, Plaschke J, Hahn M, Hampl J, Hampl M, Pistorius S, Schackert G, Schackert HK.
    Cancer Res; 1997 Jul 01; 57(13):2638-41. PubMed ID: 9205070
    [Abstract] [Full Text] [Related]

  • 20. Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas.
    Cairns P, Tokino K, Eby Y, Sidransky D.
    Cancer Res; 1995 Jan 15; 55(2):224-7. PubMed ID: 7812948
    [Abstract] [Full Text] [Related]


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