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 *

406 related articles for article (PubMed ID: 19514061)

  • 21. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
    Charzewska A; Obersztyn E; Hoffman-Zacharska D; Lenart J; PoznaƄski J; Bal J
    Cleft Palate Craniofac J; 2015 Sep; 52(5):e161-7. PubMed ID: 25489771
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Combining learning and constraints for genome-wide protein annotation.
    Teso S; Masera L; Diligenti M; Passerini A
    BMC Bioinformatics; 2019 Jun; 20(1):338. PubMed ID: 31208327
    [TBL] [Abstract][Full Text] [Related]  

  • 23. MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum.
    Bader I; Decker E; Mayr JA; Lunzer V; Koch J; Boltshauser E; Sperl W; Pietsch P; Ertl-Wagner B; Bolz H; Bergmann C; Rittinger O
    Eur J Med Genet; 2016 Aug; 59(8):386-91. PubMed ID: 27377014
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation.
    Chu D; Wei L
    BMC Cancer; 2019 Apr; 19(1):359. PubMed ID: 30991970
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Human non-synonymous SNPs: server and survey.
    Ramensky V; Bork P; Sunyaev S
    Nucleic Acids Res; 2002 Sep; 30(17):3894-900. PubMed ID: 12202775
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Tool for rapid annotation of microbial SNPs (TRAMS): a simple program for rapid annotation of genomic variation in prokaryotes.
    Reumerman RA; Tucker NP; Herron PR; Hoskisson PA; Sangal V
    Antonie Van Leeuwenhoek; 2013 Sep; 104(3):431-4. PubMed ID: 23828175
    [TBL] [Abstract][Full Text] [Related]  

  • 27. GO functional similarity clustering depends on similarity measure, clustering method, and annotation completeness.
    Liu M; Thomas PD
    BMC Bioinformatics; 2019 Mar; 20(1):155. PubMed ID: 30917779
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A structural bioinformatics approach to the analysis of nonsynonymous single nucleotide polymorphisms (nsSNPs) and their relation to disease.
    Worth CL; Bickerton GR; Schreyer A; Forman JR; Cheng TM; Lee S; Gong S; Burke DF; Blundell TL
    J Bioinform Comput Biol; 2007 Dec; 5(6):1297-318. PubMed ID: 18172930
    [TBL] [Abstract][Full Text] [Related]  

  • 29. NegGOA: negative GO annotations selection using ontology structure.
    Fu G; Wang J; Yang B; Yu G
    Bioinformatics; 2016 Oct; 32(19):2996-3004. PubMed ID: 27318205
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A relation based measure of semantic similarity for Gene Ontology annotations.
    Sheehan B; Quigley A; Gaudin B; Dobson S
    BMC Bioinformatics; 2008 Nov; 9():468. PubMed ID: 18983678
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome).
    Orrico A; Galli L; Falciani M; Bracci M; Cavaliere ML; Rinaldi MM; Musacchio A; Sorrentino V
    FEBS Lett; 2000 Aug; 478(3):216-20. PubMed ID: 10930571
    [TBL] [Abstract][Full Text] [Related]  

  • 32. HashGO: hashing gene ontology for protein function prediction.
    Yu G; Zhao Y; Lu C; Wang J
    Comput Biol Chem; 2017 Dec; 71():264-273. PubMed ID: 29031869
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An evaluation of GO annotation retrieval for BioCreAtIvE and GOA.
    Camon EB; Barrell DG; Dimmer EC; Lee V; Magrane M; Maslen J; Binns D; Apweiler R
    BMC Bioinformatics; 2005; 6 Suppl 1(Suppl 1):S17. PubMed ID: 15960829
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Interspecies gene function prediction using semantic similarity.
    Yu G; Luo W; Fu G; Wang J
    BMC Syst Biol; 2016 Dec; 10(Suppl 4):121. PubMed ID: 28155711
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.
    Capriotti E; Arbiza L; Casadio R; Dopazo J; Dopazo H; Marti-Renom MA
    Hum Mutat; 2008 Jan; 29(1):198-204. PubMed ID: 17935148
    [TBL] [Abstract][Full Text] [Related]  

  • 37. UniProt genomic mapping for deciphering functional effects of missense variants.
    McGarvey PB; Nightingale A; Luo J; Huang H; Martin MJ; Wu C;
    Hum Mutat; 2019 Jun; 40(6):694-705. PubMed ID: 30840782
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.
    Pal LR; Moult J
    J Mol Biol; 2015 Jul; 427(13):2271-89. PubMed ID: 25937569
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Predicting functions of maize proteins using graph convolutional network.
    Zhou G; Wang J; Zhang X; Guo M; Yu G
    BMC Bioinformatics; 2020 Dec; 21(Suppl 16):420. PubMed ID: 33323113
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.
    Barenboim M; Masso M; Vaisman II; Jamison DC
    Proteins; 2008 Jun; 71(4):1930-9. PubMed ID: 18186470
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.