BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 16079246)

  • 1. Building a tree of knowledge: analysis of bitter molecules.
    Rodgers S; Busch J; Peters H; Christ-Hazelhof E
    Chem Senses; 2005 Sep; 30(7):547-57. PubMed ID: 16079246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterizing bitterness: identification of key structural features and development of a classification model.
    Rodgers S; Glen RC; Bender A
    J Chem Inf Model; 2006; 46(2):569-76. PubMed ID: 16562985
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chemical database mining through entropy-based molecular similarity assessment of randomly generated structural fragment populations.
    Batista J; Bajorath J
    J Chem Inf Model; 2007; 47(1):59-68. PubMed ID: 17238249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Representation of chemical information in OASIS centralized 3D database for existing chemicals.
    Nikolov N; Grancharov V; Stoyanova G; Pavlov T; Mekenyan O
    J Chem Inf Model; 2006; 46(6):2537-51. PubMed ID: 17125194
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Random reduction in fingerprint bit density improves compound recall in search calculations using complex reference molecules.
    Wang Y; Geppert H; Bajorath J
    Chem Biol Drug Des; 2008 Jun; 71(6):511-7. PubMed ID: 18466274
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sensory activity, chemical structure, and synthesis of Maillard generated bitter-tasting 1-oxo-2,3-dihydro-1H-indolizinium-6-olates.
    Frank O; Jezussek M; Hofmann T
    J Agric Food Chem; 2003 Apr; 51(9):2693-9. PubMed ID: 12696959
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of the key bitter compounds in our daily diet is a prerequisite for the understanding of the hTAS2R gene polymorphisms affecting food choice.
    Hofmann T
    Ann N Y Acad Sci; 2009 Jul; 1170():116-25. PubMed ID: 19686121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deep understanding of structure-solubility relationship for a diverse set of organic compounds using matched molecular pairs.
    Zhang L; Zhu H; Mathiowetz A; Gao H
    Bioorg Med Chem; 2011 Oct; 19(19):5763-70. PubMed ID: 21906951
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Positive selection drives the evolution of bat bitter taste receptor genes.
    Zhou Y; Dong D; Zhang S; Zhao H
    Biochem Genet; 2009 Apr; 47(3-4):207-15. PubMed ID: 19242789
    [TBL] [Abstract][Full Text] [Related]  

  • 10. RelACCS-FP: a structural minimalist approach to fingerprint design.
    Hu Y; Lounkine E; Batista J; Bajorath J
    Chem Biol Drug Des; 2008 Nov; 72(5):341-9. PubMed ID: 19012570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Single neurons in the nucleus of the solitary tract respond selectively to bitter taste stimuli.
    Geran LC; Travers SP
    J Neurophysiol; 2006 Nov; 96(5):2513-27. PubMed ID: 16899635
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structure determination and sensory analysis of bitter-tasting 4-vinylcatechol oligomers and their identification in roasted coffee by means of LC-MS/MS.
    Frank O; Blumberg S; Kunert C; Zehentbauer G; Hofmann T
    J Agric Food Chem; 2007 Mar; 55(5):1945-54. PubMed ID: 17269788
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Graph theoretical similarity approach to compare molecular electrostatic potentials.
    Marín RM; Aguirre NF; Daza EE
    J Chem Inf Model; 2008 Jan; 48(1):109-18. PubMed ID: 18166018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Automatic perception of organic molecules based on essential structural information.
    Zhao Y; Cheng T; Wang R
    J Chem Inf Model; 2007; 47(4):1379-85. PubMed ID: 17530839
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diversity analysis of 14 156 molecules tested by the National Cancer Institute for anti-HIV activity using the quantitative structure-activity relational expert system MCASE.
    Klopman G; Tu M
    J Med Chem; 1999 Mar; 42(6):992-8. PubMed ID: 10090782
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structure-activity models of chemical carcinogens: state of the art, and new directions.
    Benigni R; Bossa C
    Ann Ist Super Sanita; 2006; 42(2):118-26. PubMed ID: 17033131
    [TBL] [Abstract][Full Text] [Related]  

  • 17. yaInChI: modified InChI string scheme for line notation of chemical structures.
    Cho YS; No KT; Cho KH
    SAR QSAR Environ Res; 2012; 23(3-4):237-55. PubMed ID: 22468774
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mammalian bitter taste perception.
    Behrens M; Meyerhof W
    Results Probl Cell Differ; 2009; 47():203-20. PubMed ID: 19145413
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Toward an improved clustering of large data sets using maximum common substructures and topological fingerprints.
    Böcker A
    J Chem Inf Model; 2008 Nov; 48(11):2097-107. PubMed ID: 18956832
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structural determination of large molecules through the reassembly of optimized fragments.
    Lee JG; Lee YS; Roland C
    J Mol Graph Model; 2008 Oct; 27(3):364-75. PubMed ID: 18644742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.