Connection

Robert Gemmill to Translocation, Genetic

This is a "connection" page, showing publications Robert Gemmill has written about Translocation, Genetic.
Connection Strength

0.946
  1. The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8. Proc Natl Acad Sci U S A. 1998 Aug 04; 95(16):9572-7.
    View in: PubMed
    Score: 0.145
  2. Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation. Cancer Genet. 2014 Apr; 207(4):133-40.
    View in: PubMed
    Score: 0.107
  3. Isolation of a yeast artificial chromosome clone that spans the (12;16) translocation breakpoint characteristic of myxoid liposarcoma. Cancer Genet Cytogenet. 1992 Sep; 62(2):166-70.
    View in: PubMed
    Score: 0.096
  4. Putative apolipoprotein receptor gene (LRP, A2MR) is not rearranged in either myxoid liposarcoma or lipomas with translocations in 12q13-14. Cancer Genet Cytogenet. 1992 Jun; 60(2):125-30.
    View in: PubMed
    Score: 0.095
  5. Myxoid liposarcoma with t(12;16) (q13;p11) contains site-specific differences in methylation patterns surrounding a zinc-finger gene mapped to the breakpoint region on chromosome 12. Cancer Res. 1990 Dec 15; 50(24):7902-7.
    View in: PubMed
    Score: 0.086
  6. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Am J Hum Genet. 2010 Aug 13; 87(2):209-18.
    View in: PubMed
    Score: 0.083
  7. The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma. Mol Cancer. 2009 Jul 30; 8:52.
    View in: PubMed
    Score: 0.078
  8. A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma. Genes Chromosomes Cancer. 2007 Sep; 46(9):805-12.
    View in: PubMed
    Score: 0.068
  9. Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma. Genes Chromosomes Cancer. 1995 Mar; 12(3):224-8.
    View in: PubMed
    Score: 0.029
  10. Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B. Genes Chromosomes Cancer. 1994 Dec; 11(4):216-21.
    View in: PubMed
    Score: 0.028
  11. Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies. Cancer Genet Cytogenet. 1993 Nov; 71(1):15-21.
    View in: PubMed
    Score: 0.026
  12. Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint. Proc Natl Acad Sci U S A. 1993 Sep 15; 90(18):8509-13.
    View in: PubMed
    Score: 0.026
  13. Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Genomics. 1989 May; 4(4):518-29.
    View in: PubMed
    Score: 0.019
  14. A 1.5-megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma. Genomics. 1989 Jan; 4(1):28-35.
    View in: PubMed
    Score: 0.019
  15. Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. Cancer Genet Cytogenet. 1988 Mar; 31(1):69-73.
    View in: PubMed
    Score: 0.018
  16. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics. 1994 Jul 15; 22(2):319-26.
    View in: PubMed
    Score: 0.007
  17. Report of the first international workshop on human chromosome 12 mapping. Cytogenet Cell Genet. 1992; 61(4):243-51.
    View in: PubMed
    Score: 0.006
  18. A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome. Genomics. 1991 Sep; 11(1):93-102.
    View in: PubMed
    Score: 0.006
  19. The Philadelphia chromosome: a model of cancer and molecular cytogenetics. Cancer Genet Cytogenet. 1986 Mar 15; 21(2):129-46.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.