BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

795 related articles for article (PubMed ID: 27825302)

  • 1. Arabidopsis thaliana population analysis reveals high plasticity of the genomic region spanning MSH2, AT3G18530 and AT3G18535 genes and provides evidence for NAHR-driven recurrent CNV events occurring in this location.
    Zmienko A; Samelak-Czajka A; Kozlowski P; Szymanska M; Figlerowicz M
    BMC Genomics; 2016 Nov; 17(1):893. PubMed ID: 27825302
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AthCNV: A Map of DNA Copy Number Variations in the Arabidopsis Genome.
    Zmienko A; Marszalek-Zenczak M; Wojciechowski P; Samelak-Czajka A; Luczak M; Kozlowski P; Karlowski WM; Figlerowicz M
    Plant Cell; 2020 Jun; 32(6):1797-1819. PubMed ID: 32265262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
    Peng Z; Zhou W; Fu W; Du R; Jin L; Zhang F
    Hum Mol Genet; 2015 Mar; 24(5):1225-33. PubMed ID: 25324539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MLPA-Based Analysis of Copy Number Variation in Plant Populations.
    Samelak-Czajka A; Marszalek-Zenczak M; Marcinkowska-Swojak M; Kozlowski P; Figlerowicz M; Zmienko A
    Front Plant Sci; 2017; 8():222. PubMed ID: 28270823
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination.
    Campbell IM; Gambin T; Dittwald P; Beck CR; Shuvarikov A; Hixson P; Patel A; Gambin A; Shaw CA; Rosenfeld JA; Stankiewicz P
    BMC Biol; 2014 Sep; 12():74. PubMed ID: 25246103
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification.
    Du R; Lu C; Jiang Z; Li S; Ma R; An H; Xu M; An Y; Xia Y; Jin L; Wang X; Zhang F
    J Hum Genet; 2012 Aug; 57(8):545-51. PubMed ID: 22673690
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Highly Specific Genome-Wide Association Study Integrated with Transcriptome Data Reveals the Contribution of Copy Number Variations to Specialized Metabolites in Arabidopsis thaliana Accessions.
    Shirai K; Matsuda F; Nakabayashi R; Okamoto M; Tanaka M; Fujimoto A; Shimizu M; Shinozaki K; Seki M; Saito K; Hanada K
    Mol Biol Evol; 2017 Dec; 34(12):3111-3122. PubMed ID: 28961930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.
    Cardoso-Moreira M; Arguello JR; Clark AG
    Genome Biol; 2012 Dec; 13(12):R119. PubMed ID: 23259534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
    Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
    BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.
    Startek M; Szafranski P; Gambin T; Campbell IM; Hixson P; Shaw CA; Stankiewicz P; Gambin A
    Nucleic Acids Res; 2015 Feb; 43(4):2188-98. PubMed ID: 25613453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variation shapes genome diversity in Arabidopsis over immediate family generational scales.
    DeBolt S
    Genome Biol Evol; 2010 Jul; 2():441-53. PubMed ID: 20624746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The impact and origin of copy number variations in the Oryza species.
    Bai Z; Chen J; Liao Y; Wang M; Liu R; Ge S; Wing RA; Chen M
    BMC Genomics; 2016 Mar; 17():261. PubMed ID: 27025496
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
    Gu S; Yuan B; Campbell IM; Beck CR; Carvalho CM; Nagamani SC; Erez A; Patel A; Bacino CA; Shaw CA; Stankiewicz P; Cheung SW; Bi W; Lupski JR
    Hum Mol Genet; 2015 Jul; 24(14):4061-77. PubMed ID: 25908615
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.
    Waszak SM; Hasin Y; Zichner T; Olender T; Keydar I; Khen M; Stütz AM; Schlattl A; Lancet D; Korbel JO
    PLoS Comput Biol; 2010 Nov; 6(11):e1000988. PubMed ID: 21085617
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Easy One-Step Amplification and Labeling Procedure for Copy Number Variation Detection.
    Blesa S; Olivares MD; Alic AS; Serrano A; Lendinez V; González-Albert V; Olivares L; Martínez-Hervás S; Juanes JM; Marín P; Real JT; Navarro B; García-García AB; Chaves FJ; Ivorra C
    Clin Chem; 2020 Mar; 66(3):463-473. PubMed ID: 32068788
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differences in the intraspecies copy number variation of Arabidopsis thaliana conserved and nonconserved miRNA genes.
    Samelak-Czajka A; Wojciechowski P; Marszalek-Zenczak M; Figlerowicz M; Zmienko A
    Funct Integr Genomics; 2023 Apr; 23(2):120. PubMed ID: 37036577
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hecaton: reliably detecting copy number variation in plant genomes using short read sequencing data.
    Wijfjes RY; Smit S; de Ridder D
    BMC Genomics; 2019 Nov; 20(1):818. PubMed ID: 31699036
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impact of the loss of AtMSH2 on double-strand break-induced recombination between highly diverged homeologous sequences in Arabidopsis thaliana germinal tissues.
    Lafleuriel J; Degroote F; Depeiges A; Picard G
    Plant Mol Biol; 2007 Apr; 63(6):833-46. PubMed ID: 17294256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Origins and breakpoint analyses of copy number variations: up close and personal.
    van Binsbergen E
    Cytogenet Genome Res; 2011; 135(3-4):271-6. PubMed ID: 21846967
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 40.