BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 21681852)

  • 41. An analysis of the Kozak consensus in retinal genes and its relevance to gene therapy.
    McClements ME; Butt A; Piotter E; Peddle CF; MacLaren RE
    Mol Vis; 2021; 27():233-242. PubMed ID: 34012226
    [TBL] [Abstract][Full Text] [Related]  

  • 42. HAltORF: a database of predicted out-of-frame alternative open reading frames in human.
    Vanderperre B; Lucier JF; Roucou X
    Database (Oxford); 2012; 2012():bas025. PubMed ID: 22613085
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The Human Gene Mutation Database (HGMD) and its exploitation in the study of mutational mechanisms.
    Cooper DN; Stenson PD; Chuzhanova NA
    Curr Protoc Bioinformatics; 2006 Jan; Chapter 1():Unit 1.13. PubMed ID: 18428754
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genes within Genes in Bacterial Genomes.
    Meydan S; Vázquez-Laslop N; Mankin AS
    Microbiol Spectr; 2018 Jul; 6(4):. PubMed ID: 30003865
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity.
    Ball EV; Stenson PD; Abeysinghe SS; Krawczak M; Cooper DN; Chuzhanova NA
    Hum Mutat; 2005 Sep; 26(3):205-13. PubMed ID: 16086312
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The sequence flanking translational initiation site in protozoa.
    Yamauchi K
    Nucleic Acids Res; 1991 May; 19(10):2715-20. PubMed ID: 2041747
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Patterns and mutational signatures of tandem base substitutions causing human inherited disease.
    Chen JM; Férec C; Cooper DN
    Hum Mutat; 2013 Aug; 34(8):1119-30. PubMed ID: 23606422
    [TBL] [Abstract][Full Text] [Related]  

  • 48. TISdb: a database for alternative translation initiation in mammalian cells.
    Wan J; Qian SB
    Nucleic Acids Res; 2014 Jan; 42(Database issue):D845-50. PubMed ID: 24203712
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Natural variability of Kozak sequences correlates with function in a zebrafish model.
    Grzegorski SJ; Chiari EF; Robbins A; Kish PE; Kahana A
    PLoS One; 2014; 9(9):e108475. PubMed ID: 25248153
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A genome-wide survey of alternative translational initiation events in Homo sapiens.
    Zhang J; Cai J; Li Y
    Sci China C Life Sci; 2007 Jun; 50(3):423-8. PubMed ID: 17609900
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Low hanging fruit: a subset of human cSNPs is both highly non-uniform and predictable.
    Horvath MM; Fondon JW; Garner HR
    Gene; 2003 Jul; 312():197-206. PubMed ID: 12909356
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Feature selection for the prediction of translation initiation sites.
    Li GL; Leong TY
    Genomics Proteomics Bioinformatics; 2005 May; 3(2):73-83. PubMed ID: 16393144
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Recognition of translation initiation sites of eukaryotic genes based on an EM algorithm.
    Wang Y; Ou H; Guo F
    J Comput Biol; 2003; 10(5):699-708. PubMed ID: 14633394
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The human gene mutation database.
    Cooper DN; Ball EV; Krawczak M
    Nucleic Acids Res; 1998 Jan; 26(1):285-7. PubMed ID: 9399854
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Single base-pair substitutions in pathology and evolution: two sides to the same coin.
    Krawczak M; Cooper DN
    Hum Mutat; 1996; 8(1):23-31. PubMed ID: 8807332
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The Human Gene Mutation Database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution.
    Stenson PD; Ball EV; Mort M; Phillips AD; Shaw K; Cooper DN
    Curr Protoc Bioinformatics; 2012 Sep; Chapter 1():1.13.1-1.13.20. PubMed ID: 22948725
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
    Stenson PD; Mort M; Ball EV; Evans K; Hayden M; Heywood S; Hussain M; Phillips AD; Cooper DN
    Hum Genet; 2017 Jun; 136(6):665-677. PubMed ID: 28349240
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Translational enhancement by base editing of the Kozak sequence rescues haploinsufficiency.
    Ambrosini C; Destefanis E; Kheir E; Broso F; Alessandrini F; Longhi S; Battisti N; Pesce I; Dassi E; Petris G; Cereseto A; Quattrone A
    Nucleic Acids Res; 2022 Oct; 50(18):10756-10771. PubMed ID: 36165847
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Do inherited disease genes have distinguishing functional characteristics?
    Cooper DN; Mort M
    Genet Test Mol Biomarkers; 2010 Jun; 14(3):289-91. PubMed ID: 20367189
    [No Abstract]   [Full Text] [Related]  

  • 60. Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited disease.
    Casola C; Zekonyte U; Phillips AD; Cooper DN; Hahn MW
    Genome Res; 2012 Mar; 22(3):429-35. PubMed ID: 22090377
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.