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Journal Abstract Search

130 related items for PubMed ID: 3865620

  • 1. Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17.
    Sheer D, Sheppard DM, le Beau M, Rowley JD, San Roman C, Solomon E.
    Ann Hum Genet; 1985 Jul; 49(3):167-71. PubMed ID: 3865620
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  • 2. Precise localization of NF1 to 17q11.2 by balanced translocation.
    Ledbetter DH, Rich DC, O'Connell P, Leppert M, Carey JC.
    Am J Hum Genet; 1989 Jan; 44(1):20-4. PubMed ID: 2491776
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  • 3. A human c-erbA oncogene homologue is closely proximal to the chromosome 17 breakpoint in acute promyelocytic leukemia.
    Dayton AI, Selden JR, Laws G, Dorney DJ, Finan J, Tripputi P, Emanuel BS, Rovera G, Nowell PC, Croce CM.
    Proc Natl Acad Sci U S A; 1984 Jul; 81(14):4495-9. PubMed ID: 6589608
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  • 4. The nerve growth factor receptor gene is at human chromosome region 17q12-17q22, distal to the chromosome 17 breakpoint in acute leukemias.
    Huebner K, Isobe M, Chao M, Bothwell M, Ross AH, Finan J, Hoxie JA, Sehgal A, Buck CR, Lanahan A.
    Proc Natl Acad Sci U S A; 1986 Mar; 83(5):1403-7. PubMed ID: 3006050
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  • 5. Translocation of the p53 gene in t(15;17) in acute promyelocytic leukaemia.
    Le Beau MM, Westbrook CA, Diaz MO, Rowley JD, Oren M.
    Nature; 1986 Mar; 316(6031):826-8. PubMed ID: 3929142
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  • 6. Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22).
    Morris CM, Bowen J, Fitzgerald PH.
    Hum Genet; 1989 Mar; 81(4):339-42. PubMed ID: 2703237
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  • 9. Human c-erbB-2 remains on chromosome 17 in band q21 in the 15;17 translocation associated with acute promyelocytic leukemia.
    Kaneko Y, Homma C, Maseki N, Sakurai M, Toyoshima K, Yamamoto T.
    Jpn J Cancer Res; 1987 Jan; 78(1):16-9. PubMed ID: 3102433
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  • 11. Localization of c-Ha-ras-1 oncogene in the t(7p-;11p+) abnormality of two cases with myeloid leukemia.
    Mise K, Abe S, Sato Y, Miura Y, Sasaki M.
    Cancer Genet Cytogenet; 1987 Dec; 29(2):191-9. PubMed ID: 3315181
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  • 13. A variant t(X;15)(p11;q22) translocation in acute promyelocytic leukemia.
    Srivastava A, Heerema N, Lauer RC, Nahreini P, Boswell HS, Hoffman R, Antony AC.
    Cancer Genet Cytogenet; 1987 Nov; 29(1):65-74. PubMed ID: 3478130
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  • 14. The role of the c-mos gene in the 8;21 translocation in human acute myeloblastic leukemia.
    Diaz MO, Le Beau MM, Rowley JD, Drabkin HA, Patterson D.
    Science; 1985 Aug 23; 229(4715):767-9. PubMed ID: 3860954
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  • 15. Translocation breakpoint mapping: molecular and cytogenetic studies of chromosome 22.
    Emanuel BS, Nowell PC, McKeon C, Croce CM, Israel MA.
    Cancer Genet Cytogenet; 1986 Jan 01; 19(1-2):81-92. PubMed ID: 3455663
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