Connection

Robert Gemmill to Molecular Sequence Data

This is a "connection" page, showing publications Robert Gemmill has written about Molecular Sequence Data.
Connection Strength

0.322
  1. 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: 0.056
  2. 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: 0.050
  3. 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: 0.041
  4. 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: 0.032
  5. YAC contigs covering an 8-megabase region of 3p deleted in the small-cell lung cancer cell line U2020. Genomics. 1995 Jan 01; 25(1):19-28.
    View in: PubMed
    Score: 0.025
  6. Dinucleotide repeat polymorphism (D3S1776) on human chromosome 3p. Hum Mol Genet. 1994 May; 3(5):841.
    View in: PubMed
    Score: 0.024
  7. 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: 0.023
  8. 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: 0.018
  9. DEF-3(g16/NY-LU-12), an RNA binding protein from the 3p21.3 homozygous deletion region in SCLC. Oncogene. 1999 Apr 22; 18(16):2589-97.
    View in: PubMed
    Score: 0.008
  10. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet. 1997 Sep; 17(1):65-70.
    View in: PubMed
    Score: 0.007
  11. Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B. Hum Mol Genet. 1997 Feb; 6(2):193-203.
    View in: PubMed
    Score: 0.007
  12. Molecular cytogenetic characterization and physical mapping of 12q13-15 amplification in human cancers. Genes Chromosomes Cancer. 1996 Dec; 17(4):205-14.
    View in: PubMed
    Score: 0.007
  13. Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorin. Oncogene. 1996 Mar 21; 12(6):1289-97.
    View in: PubMed
    Score: 0.007
  14. Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats. Chromosome Res. 1994 Nov; 2(6):423-7.
    View in: PubMed
    Score: 0.006
  15. 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: 0.006
  16. Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library. Am J Hum Genet. 1992 Aug; 51(2):263-72.
    View in: PubMed
    Score: 0.005
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.