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Journal Abstract Search


291 related items for PubMed ID: 9519875

  • 21. Construction of a 5-Mb YAC contig from the putative 10q25 tumor-suppressor region for glioblastomas.
    Albarosa R, Finocchiaro G, Chiariello E, Russo G, Susani L, Vezzoni P, Zucchi I.
    Genomics; 1997 May 01; 41(3):345-9. PubMed ID: 9169131
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  • 22. Molecular analysis of P16(Ink4)/CDKN2 and P15(INK4B)/MTS2 genes in primary human testicular germ cell tumors.
    Heidenreich A, Gaddipati JP, Moul JW, Srivastava S.
    J Urol; 1998 May 01; 159(5):1725-30. PubMed ID: 9554401
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  • 23. Molecular characterization of a novel human brain tumor-associated gene BR-3.
    Weil KC, Berge MS, Sehgal A.
    Anticancer Res; 2002 May 01; 22(3):1467-74. PubMed ID: 12168825
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  • 26. Loss of heterozygosity of a locus on 17p13.3, independent of p53, is associated with higher grades of astrocytic tumours.
    Chattopadhyay P, Rathore A, Mathur M, Sarkar C, Mahapatra AK, Sinha S.
    Oncogene; 1997 Aug 14; 15(7):871-4. PubMed ID: 9266974
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  • 27. [Expression of fibroblast growth factor receptors (FGFRs) mRNA in human astrocytomas].
    Yamada SM, Bruner JM, Berger MS, Morrison RS.
    No To Shinkei; 1996 Apr 14; 48(4):363-70. PubMed ID: 8679334
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  • 28. Loss of heterozygosity for loci on chromosome 17p in human malignant astrocytoma.
    Fults D, Tippets RH, Thomas GA, Nakamura Y, White R.
    Cancer Res; 1989 Dec 01; 49(23):6572-7. PubMed ID: 2573417
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  • 29. 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
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  • 31. Molecular characterization of areas with low grade tumor or satellitosis in human malignant astrocytomas.
    Leenstra S, Troost D, Westerveld A, Bosch DA, Hulsebos TJ.
    Cancer Res; 1992 Mar 15; 52(6):1568-72. PubMed ID: 1311634
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  • 32. DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours.
    Mollenhauer J, Wiemann S, Scheurlen W, Korn B, Hayashi Y, Wilgenbus KK, von Deimling A, Poustka A.
    Nat Genet; 1997 Sep 15; 17(1):32-9. PubMed ID: 9288095
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  • 33. Molecular pathogenesis of pediatric astrocytic tumors.
    Nakamura M, Shimada K, Ishida E, Higuchi T, Nakase H, Sakaki T, Konishi N.
    Neuro Oncol; 2007 Apr 15; 9(2):113-23. PubMed ID: 17327574
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  • 36. Structural and functional evidence for the presence of tumor suppressor genes on the short arm of chromosome 10 in human gliomas.
    Kon H, Sonoda Y, Kumabe T, Yoshimoto T, Sekiya T, Murakami Y.
    Oncogene; 1998 Jan 15; 16(2):257-63. PubMed ID: 9464544
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  • 37. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.
    Filippova GN, Lindblom A, Meincke LJ, Klenova EM, Neiman PE, Collins SJ, Doggett NA, Lobanenkov VV.
    Genes Chromosomes Cancer; 1998 May 15; 22(1):26-36. PubMed ID: 9591631
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  • 39. A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer.
    Schmid M, Sen M, Rosenbach MD, Carrera CJ, Friedman H, Carson DA.
    Oncogene; 2000 Nov 23; 19(50):5747-54. PubMed ID: 11126361
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