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Connection

Graeme Bell to Exons

This is a "connection" page, showing publications Graeme Bell has written about Exons.
Connection Strength

0.466
  1. Mutations in the hepatocyte nuclear factor-1alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4. Diabetes. 1997 Mar; 46(3):528-35.
    View in: PubMed
    Score: 0.124
  2. Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1. Gene. 2005 Jan 03; 344:143-59.
    View in: PubMed
    Score: 0.053
  3. No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY. Diabetologia. 2000 Aug; 43(8):1064-9.
    View in: PubMed
    Score: 0.039
  4. A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene. Diabetologia. 2000 Jun; 43(6):818-9.
    View in: PubMed
    Score: 0.039
  5. Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1) Nature. 1996 Dec 05; 384(6608):458-60.
    View in: PubMed
    Score: 0.030
  6. Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. PLoS One. 2015; 10(11):e0142130.
    View in: PubMed
    Score: 0.028
  7. Dinucleotide repeat polymorphism in the NEC2 gene. Hum Mol Genet. 1993 Nov; 2(11):1983.
    View in: PubMed
    Score: 0.025
  8. Organization of the human GLUT2 (pancreatic beta-cell and hepatocyte) glucose transporter gene. Diabetes. 1993 May; 42(5):773-7.
    View in: PubMed
    Score: 0.024
  9. Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene. Diabetologia. 1993 Feb; 36(2):170-1.
    View in: PubMed
    Score: 0.023
  10. Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation. Diabetes. 1992 Nov; 41(11):1436-45.
    View in: PubMed
    Score: 0.023
  11. Structure and transcription of the human m3 muscarinic receptor gene. Am J Respir Cell Mol Biol. 2002 Mar; 26(3):298-305.
    View in: PubMed
    Score: 0.011
  12. Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM. Diabetologia. 1997 Apr; 40(4):473-5.
    View in: PubMed
    Score: 0.008
  13. Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption. J Clin Invest. 1996 Nov 15; 98(10):2398-402.
    View in: PubMed
    Score: 0.008
  14. Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity. Diabetologia. 1995 Dec; 38(12):1466-74.
    View in: PubMed
    Score: 0.007
  15. Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics. 1995 Jun 10; 27(3):520-5.
    View in: PubMed
    Score: 0.007
  16. Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA. Mol Pharmacol. 1994 May; 45(5):854-60.
    View in: PubMed
    Score: 0.006
  17. Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family. Diabetologia. 1993 May; 36(5):433-7.
    View in: PubMed
    Score: 0.006
  18. Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes. Nat Genet. 1992 Oct; 2(2):153-6.
    View in: PubMed
    Score: 0.006
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.