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 *

183 related articles for article (PubMed ID: 24327335)

  • 1. 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]  

  • 2. Hydroxyurea induces de novo copy number variants in human cells.
    Arlt MF; Ozdemir AC; Birkeland SR; Wilson TE; Glover TW
    Proc Natl Acad Sci U S A; 2011 Oct; 108(42):17360-5. PubMed ID: 21987784
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Replication stress and mechanisms of CNV formation.
    Arlt MF; Wilson TE; Glover TW
    Curr Opin Genet Dev; 2012 Jun; 22(3):204-10. PubMed ID: 22365495
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.
    Arlt MF; Rajendran S; Birkeland SR; Wilson TE; Glover TW
    PLoS Genet; 2012 Sep; 8(9):e1002981. PubMed ID: 23028374
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effects of hydroxyurea on CNV induction in the mouse germline.
    Arlt MF; Rajendran S; Holmes SN; Wang K; Bergin IL; Ahmed S; Wilson TE; Glover TW
    Environ Mol Mutagen; 2018 Oct; 59(8):698-714. PubMed ID: 30218578
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.
    Arlt MF; Mulle JG; Schaibley VM; Ragland RL; Durkin SG; Warren ST; Glover TW
    Am J Hum Genet; 2009 Mar; 84(3):339-50. PubMed ID: 19232554
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large transcription units unify copy number variants and common fragile sites arising under replication stress.
    Wilson TE; Arlt MF; Park SH; Rajendran S; Paulsen M; Ljungman M; Glover TW
    Genome Res; 2015 Feb; 25(2):189-200. PubMed ID: 25373142
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencing.
    Arlt MF; Ozdemir AC; Birkeland SR; Lyons RH; Glover TW; Wilson TE
    Genetics; 2011 Mar; 187(3):675-83. PubMed ID: 21212237
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Contrasting mechanisms of de novo copy number mutagenesis suggest the existence of different classes of environmental copy number mutagens.
    Conover HN; Argueso JL
    Environ Mol Mutagen; 2016 Jan; 57(1):3-9. PubMed ID: 26247157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA Copy Number Variations as Markers of Mutagenic Impact.
    Hovhannisyan G; Harutyunyan T; Aroutiounian R; Liehr T
    Int J Mol Sci; 2019 Sep; 20(19):. PubMed ID: 31554154
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.
    Du H; Jolly A; Grochowski CM; Yuan B; Dawood M; Jhangiani SN; Li H; Muzny D; Fatih JM; Coban-Akdemir Z; Carlin ME; Scheuerle AE; Witzl K; Posey JE; Pendleton M; Harrington E; Juul S; Hastings PJ; Bi W; Gibbs RA; Sedlazeck FJ; Lupski JR; Carvalho CMB; Liu P
    Genome Med; 2022 Oct; 14(1):122. PubMed ID: 36303224
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle.
    Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP
    BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of copy number variations induced by ultrashort electron beam radiation in human leukocytes in vitro.
    Harutyunyan T; Hovhannisyan G; Sargsyan A; Grigoryan B; Al-Rikabi AH; Weise A; Liehr T; Aroutiounian R
    Mol Cytogenet; 2019; 12():18. PubMed ID: 31131024
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay.
    Park SH; Bennett-Baker P; Ahmed S; Arlt MF; Ljungman M; Glover TW; Wilson TE
    Nucleic Acids Res; 2021 Jul; 49(13):7507-7524. PubMed ID: 34181717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing.
    Onsongo G; Baughn LB; Bower M; Henzler C; Schomaker M; Silverstein KA; Thyagarajan B
    J Mol Diagn; 2016 Nov; 18(6):872-881. PubMed ID: 27597741
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.