Connection

Robert Gemmill to Female

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

0.157
  1. The neuropilin 2 isoform NRP2b uniquely supports TGF?-mediated progression in lung cancer. Sci Signal. 2017 01 17; 10(462).
    View in: PubMed
    Score: 0.029
  2. Induction of E-cadherin in lung cancer and interaction with growth suppression by histone deacetylase inhibition. J Thorac Oncol. 2009 Dec; 4(12):1455-65.
    View in: PubMed
    Score: 0.018
  3. MYC and EIF3H Coamplification significantly improve response and survival of non-small cell lung cancer patients (NSCLC) treated with gefitinib. J Thorac Oncol. 2009 Apr; 4(4):472-8.
    View in: PubMed
    Score: 0.017
  4. 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: 0.011
  5. Isoforms of Neuropilin-2 Denote Unique Tumor-Associated Macrophages in Breast Cancer. Front Immunol. 2022; 13:830169.
    View in: PubMed
    Score: 0.011
  6. Molecular definition of a small amplification domain within 3q26 in tumors of cervix, ovary, and lung. Cancer Genet Cytogenet. 2000 Feb; 117(1):9-18.
    View in: PubMed
    Score: 0.009
  7. Neuropilin-2 Is upregulated in lung cancer cells during TGF-?1-induced epithelial-mesenchymal transition. Cancer Res. 2013 Dec 01; 73(23):7111-21.
    View in: PubMed
    Score: 0.006
  8. Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma, pancreatic and lung cancer based on in vitro assessments of the combination. Invest New Drugs. 2012 Dec; 30(6):2303-17.
    View in: PubMed
    Score: 0.005
  9. Report of the Second International Workshop on Human Chromosome 3 mapping. Cytogenet Cell Genet. 1991; 57(4):162-6.
    View in: PubMed
    Score: 0.005
  10. Gene expression profiling identifies inflammation and angiogenesis as distinguishing features of canine hemangiosarcoma. BMC Cancer. 2010 Nov 09; 10:619.
    View in: PubMed
    Score: 0.005
  11. 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: 0.005
  12. 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: 0.004
  13. Semaphorin SEMA3F affects multiple signaling pathways in lung cancer cells. Cancer Res. 2007 Sep 15; 67(18):8708-15.
    View in: PubMed
    Score: 0.004
  14. 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: 0.004
  15. Y chromosome--specific DNA sequences in Turner-syndrome mosaicism. Am J Hum Genet. 1987 Aug; 41(2):157-67.
    View in: PubMed
    Score: 0.004
  16. Selective suppression of in vivo tumorigenicity by semaphorin SEMA3F in lung cancer cells. Neoplasia. 2005 May; 7(5):457-65.
    View in: PubMed
    Score: 0.003
  17. High-throughput tissue microarray analysis used to evaluate biology and prognostic significance of the E-cadherin pathway in non-small-cell lung cancer. J Clin Oncol. 2002 May 15; 20(10):2417-28.
    View in: PubMed
    Score: 0.003
  18. Mutations of the beta- and gamma-catenin genes are uncommon in human lung, breast, kidney, cervical and ovarian carcinomas. Br J Cancer. 2001 Jul 06; 85(1):64-8.
    View in: PubMed
    Score: 0.003
  19. Angiogenic squamous dysplasia in bronchi of individuals at high risk for lung cancer. Clin Cancer Res. 2000 May; 6(5):1616-25.
    View in: PubMed
    Score: 0.002
  20. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet. 1997 Sep; 17(1):65-70.
    View in: PubMed
    Score: 0.002
  21. A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia loci. Eur J Hum Genet. 1997 May-Jun; 5(3):171-4.
    View in: PubMed
    Score: 0.002
  22. The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. Am J Hum Genet. 1996 Dec; 59(6):1328-36.
    View in: PubMed
    Score: 0.002
  23. 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: 0.002
  24. Report of the first international workshop on human chromosome 12 mapping. Cytogenet Cell Genet. 1992; 61(4):243-51.
    View in: PubMed
    Score: 0.001
  25. 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: 0.001
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.