These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

84 related articles for article (PubMed ID: 19921752)

  • 21. BAliBASE 3.0: latest developments of the multiple sequence alignment benchmark.
    Thompson JD; Koehl P; Ripp R; Poch O
    Proteins; 2005 Oct; 61(1):127-36. PubMed ID: 16044462
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases.
    Claustres M; Horaitis O; Vanevski M; Cotton RG
    Genome Res; 2002 May; 12(5):680-8. PubMed ID: 11997335
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
    Tan EC; Loh M; Chuon D; Lim YP
    Hum Mutat; 2006 Mar; 27(3):232-5. PubMed ID: 16429432
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Detailed computational study of p53 and p16: using evolutionary sequence analysis and disease-associated mutations to predict the functional consequences of allelic variants.
    Greenblatt MS; Beaudet JG; Gump JR; Godin KS; Trombley L; Koh J; Bond JP
    Oncogene; 2003 Feb; 22(8):1150-63. PubMed ID: 12606942
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Missense mutations of human homeoboxes: A review.
    D'Elia AV; Tell G; Paron I; Pellizzari L; Lonigro R; Damante G
    Hum Mutat; 2001 Nov; 18(5):361-74. PubMed ID: 11668629
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The novel human SHOX allelic variant database.
    Niesler B; Röth R; Wilke S; Fujimura F; Fischer C; Rappold G
    Hum Mutat; 2007 Oct; 28(10):933-8. PubMed ID: 17726696
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MitoRes: a resource of nuclear-encoded mitochondrial genes and their products in Metazoa.
    Catalano D; Licciulli F; Turi A; Grillo G; Saccone C; D'Elia D
    BMC Bioinformatics; 2006 Jan; 7():36. PubMed ID: 16433928
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The SAAPdb web resource: a large-scale structural analysis of mutant proteins.
    Hurst JM; McMillan LE; Porter CT; Allen J; Fakorede A; Martin AC
    Hum Mutat; 2009 Apr; 30(4):616-24. PubMed ID: 19191322
    [TBL] [Abstract][Full Text] [Related]  

  • 29. GeneTools--application for functional annotation and statistical hypothesis testing.
    Beisvag V; Jünge FK; Bergum H; Jølsum L; Lydersen S; Günther CC; Ramampiaro H; Langaas M; Sandvik AK; Laegreid A
    BMC Bioinformatics; 2006 Oct; 7():470. PubMed ID: 17062145
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The human SHOX mutation database.
    Niesler B; Fischer C; Rappold GA
    Hum Mutat; 2002 Nov; 20(5):338-41. PubMed ID: 12402330
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 'PACLIMS': a component LIM system for high-throughput functional genomic analysis.
    Donofrio N; Rajagopalon R; Brown D; Diener S; Windham D; Nolin S; Floyd A; Mitchell T; Galadima N; Tucker S; Orbach MJ; Patel G; Farman M; Pampanwar V; Soderlund C; Lee YH; Dean RA
    BMC Bioinformatics; 2005 Apr; 6():94. PubMed ID: 15826298
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotology of disease-linked proteins.
    Myers JK; Beihoffer LA; Sanders CR
    Hum Mutat; 2005 Jan; 25(1):90-7. PubMed ID: 15580569
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors.
    Banerjee-Basu S; Baxevanis AD
    Proteins; 2004 Mar; 54(4):639-47. PubMed ID: 14997560
    [TBL] [Abstract][Full Text] [Related]  

  • 34. KD4v: Comprehensible Knowledge Discovery System for Missense Variant.
    Luu TD; Rusu A; Walter V; Linard B; Poidevin L; Ripp R; Moulinier L; Muller J; Raffelsberger W; Wicker N; Lecompte O; Thompson JD; Poch O; Nguyen H
    Nucleic Acids Res; 2012 Jul; 40(Web Server issue):W71-5. PubMed ID: 22641855
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Knowledge discovery in variant databases using inductive logic programming.
    Nguyen H; Luu TD; Poch O; Thompson JD
    Bioinform Biol Insights; 2013; 7():119-31. PubMed ID: 23589683
    [TBL] [Abstract][Full Text] [Related]  

  • 36. GFINDer: genetic disease and phenotype location statistical analysis and mining of dynamically annotated gene lists.
    Masseroli M; Galati O; Pinciroli F
    Nucleic Acids Res; 2005 Jul; 33(Web Server issue):W717-23. PubMed ID: 15980570
    [TBL] [Abstract][Full Text] [Related]  

  • 37. MISCAST: MIssense variant to protein StruCture Analysis web SuiTe.
    Iqbal S; Hoksza D; Pérez-Palma E; May P; Jespersen JB; Ahmed SS; Rifat ZT; Heyne HO; Rahman MS; Cottrell JR; Wagner FF; Daly MJ; Campbell AJ; Lal D
    Nucleic Acids Res; 2020 Jul; 48(W1):W132-W139. PubMed ID: 32402084
    [TBL] [Abstract][Full Text] [Related]  

  • 38. ChemProt-3.0: a global chemical biology diseases mapping.
    Kringelum J; Kjaerulff SK; Brunak S; Lund O; Oprea TI; Taboureau O
    Database (Oxford); 2016; 2016():. PubMed ID: 26876982
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutation@A Glance: an integrative web application for analysing mutations from human genetic diseases.
    Hijikata A; Raju R; Keerthikumar S; Ramabadran S; Balakrishnan L; Ramadoss SK; Pandey A; Mohan S; Ohara O
    DNA Res; 2010 Jun; 17(3):197-208. PubMed ID: 20360267
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cancer3D: understanding cancer mutations through protein structures.
    Porta-Pardo E; Hrabe T; Godzik A
    Nucleic Acids Res; 2015 Jan; 43(Database issue):D968-73. PubMed ID: 25392415
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.