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 *

237 related articles for article (PubMed ID: 25324539)

  • 1. 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]  

  • 2. 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]  

  • 3. The role of gene conversion in preserving rearrangement hotspots in the human genome.
    Fawcett JA; Innan H
    Trends Genet; 2013 Oct; 29(10):561-8. PubMed ID: 23953668
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 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. 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]  

  • 7. Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans.
    Uddin M; Sturge M; Peddle L; O'Rielly DD; Rahman P
    PLoS One; 2011; 6(12):e28853. PubMed ID: 22194928
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
    Dittwald P; Gambin T; Szafranski P; Li J; Amato S; Divon MY; Rodríguez Rojas LX; Elton LE; Scott DA; Schaaf CP; Torres-Martinez W; Stevens AK; Rosenfeld JA; Agadi S; Francis D; Kang SH; Breman A; Lalani SR; Bacino CA; Bi W; Milosavljevic A; Beaudet AL; Patel A; Shaw CA; Lupski JR; Gambin A; Cheung SW; Stankiewicz P
    Genome Res; 2013 Sep; 23(9):1395-409. PubMed ID: 23657883
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination.
    Lindsay SJ; Khajavi M; Lupski JR; Hurles ME
    Am J Hum Genet; 2006 Nov; 79(5):890-902. PubMed ID: 17033965
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detecting non-allelic homologous recombination from high-throughput sequencing data.
    Parks MM; Lawrence CE; Raphael BJ
    Genome Biol; 2015 Apr; 16(1):72. PubMed ID: 25886137
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome.
    Li J; Harris RA; Cheung SW; Coarfa C; Jeong M; Goodell MA; White LD; Patel A; Kang SH; Shaw C; Chinault AC; Gambin T; Gambin A; Lupski JR; Milosavljevic A
    PLoS Genet; 2012; 8(5):e1002692. PubMed ID: 22615578
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over.
    Liu P; Lacaria M; Zhang F; Withers M; Hastings PJ; Lupski JR
    Am J Hum Genet; 2011 Oct; 89(4):580-8. PubMed ID: 21981782
    [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. Mechanisms for recurrent and complex human genomic rearrangements.
    Liu P; Carvalho CM; Hastings PJ; Lupski JR
    Curr Opin Genet Dev; 2012 Jun; 22(3):211-20. PubMed ID: 22440479
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletions.
    Hillmer M; Wagner D; Summerer A; Daiber M; Mautner VF; Messiaen L; Cooper DN; Kehrer-Sawatzki H
    Hum Mol Genet; 2016 Feb; 25(3):484-96. PubMed ID: 26614388
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders.
    Mosley TJ; Johnston HR; Cutler DJ; Zwick ME; Mulle JG
    BMC Med Genomics; 2021 Jun; 14(1):154. PubMed ID: 34107974
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human genomic disorders.
    Sankaranarayanan K; Wassom JS
    Mutat Res; 2005 Oct; 578(1-2):333-70. PubMed ID: 16084534
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history.
    Kim PM; Lam HY; Urban AE; Korbel JO; Affourtit J; Grubert F; Chen X; Weissman S; Snyder M; Gerstein MB
    Genome Res; 2008 Dec; 18(12):1865-74. PubMed ID: 18842824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies.
    Ma R; Deng L; Xia Y; Wei X; Cao Y; Guo R; Zhang R; Guo J; Liang D; Wu L
    Sci Rep; 2017 Mar; 7():44446. PubMed ID: 28322228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.