BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

84 related articles for article (PubMed ID: 19921752)

  • 1. SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases.
    Friedrich A; Garnier N; Gagnière N; Nguyen H; Albou LP; Biancalana V; Bettler E; Deléage G; Lecompte O; Muller J; Moras D; Mandel JL; Toursel T; Moulinier L; Poch O
    Hum Mutat; 2010 Feb; 31(2):127-35. PubMed ID: 19921752
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ProCMD: a database and 3D web resource for protein C mutants.
    D'Ursi P; Marino F; Caprera A; Milanesi L; Faioni EM; Rovida E
    BMC Bioinformatics; 2007 Mar; 8 Suppl 1(Suppl 1):S11. PubMed ID: 17430555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Décrypthon grid - grid resources dedicated to neuromuscular disorders.
    Bard N; Bolze R; Caron E; Desprez F; Heymann M; Friedrich A; Moulinier L; Nguyen NH; Poch O; Toursel T
    Stud Health Technol Inform; 2010; 159():124-33. PubMed ID: 20543432
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An interactive web-tool for molecular analyses links naturally occurring mutation data with three-dimensional structures of the rhodopsin-like glycoprotein hormone receptors.
    Kleinau G; Kreuchwig A; Worth CL; Krause G
    Hum Mutat; 2010 Jun; 31(6):E1519-25. PubMed ID: 20513138
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic disease.
    Terp BN; Cooper DN; Christensen IT; Jørgensen FS; Bross P; Gregersen N; Krawczak M
    Hum Mutat; 2002 Aug; 20(2):98-109. PubMed ID: 12124990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool.
    Saunders RE; Perkins SJ
    Hum Mutat; 2008 Mar; 29(3):333-44. PubMed ID: 18058827
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Missense mutations in transmembrane domains of proteins: phenotypic propensity of polar residues for human disease.
    Partridge AW; Therien AG; Deber CM
    Proteins; 2004 Mar; 54(4):648-56. PubMed ID: 14997561
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LySDB - Lysozyme Structural DataBase.
    Mohan KS; Das S; Chockalingam C; Shanthi V; Sekar K
    Acta Crystallogr D Biol Crystallogr; 2004 Mar; 60(Pt 3):597-600. PubMed ID: 14993706
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods.
    Thusberg J; Vihinen M
    Hum Mutat; 2009 May; 30(5):703-14. PubMed ID: 19267389
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations.
    Saunders RE; Goodship TH; Zipfel PF; Perkins SJ
    Hum Mutat; 2006 Jan; 27(1):21-30. PubMed ID: 16281287
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
    Capriotti E; Calabrese R; Casadio R
    Bioinformatics; 2006 Nov; 22(22):2729-34. PubMed ID: 16895930
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TOPOFIT-DB, a database of protein structural alignments based on the TOPOFIT method.
    Leslin CM; Abyzov A; Ilyin VA
    Nucleic Acids Res; 2007 Jan; 35(Database issue):D317-21. PubMed ID: 17065464
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases.
    van Driel MA; Cuelenaere K; Kemmeren PP; Leunissen JA; Brunner HG; Vriend G
    Nucleic Acids Res; 2005 Jul; 33(Web Server issue):W758-61. PubMed ID: 15980578
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MSV3d: database of human MisSense Variants mapped to 3D protein structure.
    Luu TD; Rusu AM; Walter V; Ripp R; Moulinier L; Muller J; Toursel T; Thompson JD; Poch O; Nguyen H
    Database (Oxford); 2012; 2012():bas018. PubMed ID: 22491796
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The human FOXL2 mutation database.
    Beysen D; Vandesompele J; Messiaen L; De Paepe A; De Baere E
    Hum Mutat; 2004 Sep; 24(3):189-93. PubMed ID: 15300845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A phylogenetic approach to assessing the significance of missense mutations in disease genes.
    Santibáñez Koref MF; Gangeswaran R; Santibáñez Koref IP; Shanahan N; Hancock JM
    Hum Mutat; 2003 Jul; 22(1):51-8. PubMed ID: 12815593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bioinformatic analysis of protein structure-function relationships: case study of leukocyte elastase (ELA2) missense mutations.
    Thusberg J; Vihinen M
    Hum Mutat; 2006 Dec; 27(12):1230-43. PubMed ID: 16986121
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency.
    Saunders RE; Shiltagh N; Gomez K; Mellars G; Cooper C; Perry DJ; Tuddenham EG; Perkins SJ
    Thromb Haemost; 2009 Aug; 102(2):287-301. PubMed ID: 19652879
    [TBL] [Abstract][Full Text] [Related]  

  • 19. UMD (Universal mutation database): a generic software to build and analyze locus-specific databases.
    Béroud C; Collod-Béroud G; Boileau C; Soussi T; Junien C
    Hum Mutat; 2000; 15(1):86-94. PubMed ID: 10612827
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MyHits: a new interactive resource for protein annotation and domain identification.
    Pagni M; Ioannidis V; Cerutti L; Zahn-Zabal M; Jongeneel CV; Falquet L
    Nucleic Acids Res; 2004 Jul; 32(Web Server issue):W332-5. PubMed ID: 15215405
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.