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 *

98 related articles for article (PubMed ID: 22659238)

  • 21. Introducing dAUTObase: a first step towards the global scale geoepidemiology of autoimmune syndromes and diseases.
    Gkantouna VA; Kambouris ME; Viennas ES; Ioannou ZM; Paraskevas M; Lagoumintzis G; Zagoriti Z; Patrinos GP; Tzimas GE; Poulas K
    Bioinformatics; 2015 Feb; 31(4):581-6. PubMed ID: 25332376
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. PathJam: a new service for integrating biological pathway information.
    Glez-Peña D; Reboiro-Jato M; Domínguez R; Gómez-López G; Pisano DG; Fdez-Riverola F
    J Integr Bioinform; 2010 Oct; 7(1):. PubMed ID: 20980714
    [TBL] [Abstract][Full Text] [Related]  

  • 24. BIAS: Bioinformatics Integrated Application Software.
    Finak G; Godin N; Hallett M; Pepin F; Rajabi Z; Srivastava V; Tang Z
    Bioinformatics; 2005 Apr; 21(8):1745-6. PubMed ID: 15572471
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.
    Patrinos GP; van Baal S; Petersen MB; Papadakis MN
    Hum Mutat; 2005 Apr; 25(4):327-33. PubMed ID: 15776445
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization data.
    Chi B; DeLeeuw RJ; Coe BP; MacAulay C; Lam WL
    BMC Bioinformatics; 2004 Feb; 5():13. PubMed ID: 15040819
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CSVS, a crowdsourcing database of the Spanish population genetic variability.
    Peña-Chilet M; Roldán G; Perez-Florido J; Ortuño FM; Carmona R; Aquino V; Lopez-Lopez D; Loucera C; Fernandez-Rueda JL; Gallego A; García-Garcia F; González-Neira A; Pita G; Núñez-Torres R; Santoyo-López J; Ayuso C; Minguez P; Avila-Fernandez A; Corton M; Moreno-Pelayo MÁ; Morin M; Gallego-Martinez A; Lopez-Escamez JA; Borrego S; Antiñolo G; Amigo J; Salgado-Garrido J; Pasalodos-Sanchez S; Morte B; ; Carracedo Á; Alonso Á; Dopazo J
    Nucleic Acids Res; 2021 Jan; 49(D1):D1130-D1137. PubMed ID: 32990755
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.
    Polvi A; Linturi H; Varilo T; Anttonen AK; Byrne M; Fokkema IF; Almusa H; Metzidis A; Avela K; Aula P; Kestilä M; Muilu J
    Hum Mutat; 2013 Nov; 34(11):1458-66. PubMed ID: 23904198
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase).
    Georgitsi M; Patrinos GP
    Methods Mol Biol; 2013; 1015():321-36. PubMed ID: 23824866
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China.
    Wang L; Aikemu A; Yibulayin A; Du S; Geng T; Wang B; Zhang Y; Jin T; Yang J
    BMC Genet; 2015 Jun; 16():66. PubMed ID: 26091847
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.
    Patrinos GP; Giardine B; Riemer C; Miller W; Chui DH; Anagnou NP; Wajcman H; Hardison RC
    Nucleic Acids Res; 2004 Jan; 32(Database issue):D537-41. PubMed ID: 14681476
    [TBL] [Abstract][Full Text] [Related]  

  • 32. SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access.
    Amigo J; Salas A; Phillips C; Carracedo A
    BMC Bioinformatics; 2008 Oct; 9():428. PubMed ID: 18847484
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Databases for neurogenetics: introduction, overview, and challenges.
    Sobrido MJ; Cacheiro P; Carracedo A; Bertram L
    Hum Mutat; 2012 Sep; 33(9):1311-4. PubMed ID: 22890789
    [TBL] [Abstract][Full Text] [Related]  

  • 34. ETHNOS : A versatile electronic tool for the development and curation of national genetic databases.
    van Baal S; Zlotogora J; Lagoumintzis G; Gkantouna V; Tzimas I; Poulas K; Tsakalidis A; Romeo G; Patrinos GP
    Hum Genomics; 2010 Jun; 4(5):361-8. PubMed ID: 20650823
    [TBL] [Abstract][Full Text] [Related]  

  • 35. AlleleRetain: a program to assess management options for conserving allelic diversity in small, isolated populations.
    Weiser EL; Grueber CE; Jamieson IG
    Mol Ecol Resour; 2012 Nov; 12(6):1161-7. PubMed ID: 22925629
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gigwa-Genotype investigator for genome-wide analyses.
    Sempéré G; Philippe F; Dereeper A; Ruiz M; Sarah G; Larmande P
    Gigascience; 2016 Jun; 5():25. PubMed ID: 27267926
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Allele Catalog Tool: a web-based interactive tool for allele discovery and analysis.
    Chan YO; Dietz N; Zeng S; Wang J; Flint-Garcia S; Salazar-Vidal MN; Škrabišová M; Bilyeu K; Joshi T
    BMC Genomics; 2023 Mar; 24(1):107. PubMed ID: 36899307
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Exploratory visual analysis of pharmacogenomic results.
    Reif DM; Dudek SM; Shaffer CM; Wang J; Moore JH
    Pac Symp Biocomput; 2005; ():296-307. PubMed ID: 15759635
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Near East University Genetic Mutation Database (NEU-GD): The first mutation database of Northern Cyprus.
    Ergoren MC; Pirzada RH; Arici M; Serakinci N
    Gene; 2015 Oct; 571(1):145-8. PubMed ID: 26183225
    [TBL] [Abstract][Full Text] [Related]  

  • 40. GeneDive: A gene interaction search and visualization tool to facilitate precision medicine.
    Previde P; Thomas B; Wong M; Mallory EK; Petkovic D; Altman RB; Kulkarni A
    Pac Symp Biocomput; 2018; 23():590-601. PubMed ID: 29218917
    [TBL] [Abstract][Full Text] [Related]  

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