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Connection

Michael Thirman to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications Michael Thirman has written about In Situ Hybridization, Fluorescence.
  1. Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13.1) in acute myeloid leukemia. Proc Natl Acad Sci U S A. 1994 Dec 06; 91(25):12110-4.
    View in: PubMed
    Score: 0.025
  2. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood. 1993 Jul 15; 82(2):547-51.
    View in: PubMed
    Score: 0.023
  3. Analysis of the t(6;11)(q27;q23) in leukemia shows a consistent breakpoint in AF6 in three patients and in the ML-2 cell line. Genes Chromosomes Cancer. 1996 Apr; 15(4):206-16.
    View in: PubMed
    Score: 0.007
  4. Abnormalities of chromosome band 11q23 and the MLL gene in pediatric myelomonocytic and monoblastic leukemias. Identification of the t(9;11) as an indicator of long survival. J Pediatr Hematol Oncol. 1995 Nov; 17(4):277-83.
    View in: PubMed
    Score: 0.007
  5. Detection of 11q23/MLL rearrangements in infant leukemias with fluorescence in situ hybridization and molecular analysis. Leukemia. 1995 Aug; 9(8):1299-304.
    View in: PubMed
    Score: 0.007
  6. U937 cell line has a t(10;11)(p13-14;q14-21) rather than a deletion of 11q. Genes Chromosomes Cancer. 1995 Jul; 13(3):217-8.
    View in: PubMed
    Score: 0.007
  7. Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization. Genes Chromosomes Cancer. 1993 Aug; 7(4):204-8.
    View in: PubMed
    Score: 0.006
Connection Strength

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