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 *

203 related articles for article (PubMed ID: 23259534)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.
    Conrad DF; Bird C; Blackburne B; Lindsay S; Mamanova L; Lee C; Turner DJ; Hurles ME
    Nat Genet; 2010 May; 42(5):385-91. PubMed ID: 20364136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
    Vissers LE; Bhatt SS; Janssen IM; Xia Z; Lalani SR; Pfundt R; Derwinska K; de Vries BB; Gilissen C; Hoischen A; Nesteruk M; Wisniowiecka-Kowalnik B; Smyk M; Brunner HG; Cheung SW; van Kessel AG; Veltman JA; Stankiewicz P
    Hum Mol Genet; 2009 Oct; 18(19):3579-93. PubMed ID: 19578123
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy number variants are produced in response to low-dose ionizing radiation in cultured cells.
    Arlt MF; Rajendran S; Birkeland SR; Wilson TE; Glover TW
    Environ Mol Mutagen; 2014 Mar; 55(2):103-13. PubMed ID: 24327335
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing.
    Yilmaz F; Gurusamy U; Mosley TJ; Hallast P; Kim K; Mostovoy Y; Purcell RH; Shaikh TH; Zwick ME; Kwok PY; Lee C; Mulle JG
    Genome Med; 2023 May; 15(1):35. PubMed ID: 37165454
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Single-cell copy number variant detection reveals the dynamics and diversity of adaptation.
    Lauer S; Avecilla G; Spealman P; Sethia G; Brandt N; Levy SF; Gresham D
    PLoS Biol; 2018 Dec; 16(12):e3000069. PubMed ID: 30562346
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization.
    Nazaryan-Petersen L; Eisfeldt J; Pettersson M; Lundin J; Nilsson D; Wincent J; Lieden A; Lovmar L; Ottosson J; Gacic J; Mäkitie O; Nordgren A; Vezzi F; Wirta V; Käller M; Hjortshøj TD; Jespersgaard C; Houssari R; Pignata L; Bak M; Tommerup N; Lundberg ES; Tümer Z; Lindstrand A
    PLoS Genet; 2018 Nov; 14(11):e1007780. PubMed ID: 30419018
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Decoding NF1 Intragenic Copy-Number Variations.
    Hsiao MC; Piotrowski A; Callens T; Fu C; Wimmer K; Claes KB; Messiaen L
    Am J Hum Genet; 2015 Aug; 97(2):238-49. PubMed ID: 26189818
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
    Verdin H; D'haene B; Beysen D; Novikova Y; Menten B; Sante T; Lapunzina P; Nevado J; Carvalho CM; Lupski JR; De Baere E
    PLoS Genet; 2013; 9(3):e1003358. PubMed ID: 23516377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
    Newman S; Hermetz KE; Weckselblatt B; Rudd MK
    Am J Hum Genet; 2015 Feb; 96(2):208-20. PubMed ID: 25640679
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.
    Abyzov A; Li S; Kim DR; Mohiyuddin M; Stütz AM; Parrish NF; Mu XJ; Clark W; Chen K; Hurles M; Korbel JO; Lam HY; Lee C; Gerstein MB
    Nat Commun; 2015 Jun; 6():7256. PubMed ID: 26028266
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Elevated variant density around SV breakpoints in germline lineage lends support to error-prone replication hypothesis.
    Dhokarh D; Abyzov A
    Genome Res; 2016 Jul; 26(7):874-81. PubMed ID: 27216746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synaptonemal Complex-Deficient
    Miller DE
    G3 (Bethesda); 2020 Feb; 10(2):525-537. PubMed ID: 31882405
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Drosophila duplication hotspots are associated with late-replicating regions of the genome.
    Cardoso-Moreira M; Emerson JJ; Clark AG; Long M
    PLoS Genet; 2011 Nov; 7(11):e1002340. PubMed ID: 22072977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.