Connection

Robert Gemmill to Carcinoma, Renal Cell

This is a "connection" page, showing publications Robert Gemmill has written about Carcinoma, Renal Cell.
Connection Strength

1.848
  1. Cholesterol and the development of clear-cell renal carcinoma. Curr Opin Pharmacol. 2012 Dec; 12(6):742-50.
    View in: PubMed
    Score: 0.388
  2. Obesity, cholesterol, and clear-cell renal cell carcinoma (RCC). Adv Cancer Res. 2010; 107:39-56.
    View in: PubMed
    Score: 0.323
  3. Synergistic growth inhibition by Iressa and Rapamycin is modulated by VHL mutations in renal cell carcinoma. Br J Cancer. 2005 Jun 20; 92(12):2266-77.
    View in: PubMed
    Score: 0.236
  4. Growth suppression induced by the TRC8 hereditary kidney cancer gene is dependent upon JAB1/CSN5. Oncogene. 2005 May 12; 24(21):3503-11.
    View in: PubMed
    Score: 0.234
  5. 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: 0.146
  6. 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: 0.108
  7. 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: 0.069
  8. Upstream signaling inhibition enhances rapamycin effect on growth of kidney cancer cells. Urology. 2007 Mar; 69(3):596-602.
    View in: PubMed
    Score: 0.066
  9. RING-dependent tumor suppression and G2/M arrest induced by the TRC8 hereditary kidney cancer gene. Oncogene. 2007 Apr 05; 26(16):2263-71.
    View in: PubMed
    Score: 0.064
  10. The TRC8 hereditary kidney cancer gene suppresses growth and functions with VHL in a common pathway. Oncogene. 2002 May 16; 21(22):3507-16.
    View in: PubMed
    Score: 0.048
  11. 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
  12. 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
  13. 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: 0.028
  14. Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndrome. Cancer Genet Cytogenet. 1989 Jun; 39(2):289-93.
    View in: PubMed
    Score: 0.019
  15. 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
  16. 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
  17. Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14. Cancer Genet Cytogenet. 1988 Mar; 31(1):75-82.
    View in: PubMed
    Score: 0.018
  18. Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL). Cancer Genet Cytogenet. 1994 Oct; 77(1):1-13.
    View in: PubMed
    Score: 0.007
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.