BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

538 related articles for article (PubMed ID: 12368240)

  • 1. Retroelement distributions in the human genome: variations associated with age and proximity to genes.
    Medstrand P; van de Lagemaat LN; Mager DL
    Genome Res; 2002 Oct; 12(10):1483-95. PubMed ID: 12368240
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are important.
    Kvikstad EM; Makova KD
    Genome Res; 2010 May; 20(5):600-13. PubMed ID: 20219940
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The distribution of L1 and Alu retroelements in relation to GC content on human sex chromosomes is consistent with the ectopic recombination model.
    Abrusán G; Krambeck HJ
    J Mol Evol; 2006 Oct; 63(4):484-92. PubMed ID: 16955238
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alu and L1 retroelements are correlated with the tissue extent and peak rate of gene expression, respectively.
    Kim TM; Jung YC; Rhyu MG
    J Korean Med Sci; 2004 Dec; 19(6):783-92. PubMed ID: 15608386
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The insertional history of an active family of L1 retrotransposons in humans.
    Boissinot S; Entezam A; Young L; Munson PJ; Furano AV
    Genome Res; 2004 Jul; 14(7):1221-31. PubMed ID: 15197167
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recently integrated Alu retrotransposons are essentially neutral residents of the human genome.
    Cordaux R; Lee J; Dinoso L; Batzer MA
    Gene; 2006 May; 373():138-44. PubMed ID: 16527433
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The 5'-end transitional CpGs between the CpG islands and retroelements are hypomethylated in association with loss of heterozygosity in gastric cancers.
    Kim YH; Hong SJ; Jung YC; Kim SJ; Seo EJ; Choi SW; Rhyu MG
    BMC Cancer; 2006 Jul; 6():180. PubMed ID: 16827945
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exceptional diversity, non-random distribution, and rapid evolution of retroelements in the B73 maize genome.
    Baucom RS; Estill JC; Chaparro C; Upshaw N; Jogi A; Deragon JM; Westerman RP; Sanmiguel PJ; Bennetzen JL
    PLoS Genet; 2009 Nov; 5(11):e1000732. PubMed ID: 19936065
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Why are young and old repetitive elements distributed differently in the human genome?
    Belle EM; Webster MT; Eyre-Walker A
    J Mol Evol; 2005 Mar; 60(3):290-6. PubMed ID: 15871040
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Abundance, distribution, and transcriptional activity of repetitive elements in the maize genome.
    Meyers BC; Tingey SV; Morgante M
    Genome Res; 2001 Oct; 11(10):1660-76. PubMed ID: 11591643
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication, coclustering, and selection of human Alu retrotransposons.
    Jurka J; Kohany O; Pavlicek A; Kapitonov VV; Jurka MV
    Proc Natl Acad Sci U S A; 2004 Feb; 101(5):1268-72. PubMed ID: 14736919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clustering, duplication and chromosomal distribution of mouse SINE retrotransposons.
    Jurka J; Kohany O; Pavlicek A; Kapitonov VV; Jurka MV
    Cytogenet Genome Res; 2005; 110(1-4):117-23. PubMed ID: 16093663
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular reconstruction of extinct LINE-1 elements and their interaction with nonautonomous elements.
    Wagstaff BJ; Kroutter EN; Derbes RS; Belancio VP; Roy-Engel AM
    Mol Biol Evol; 2013 Jan; 30(1):88-99. PubMed ID: 22918960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Active Alu element "A-tails": size does matter.
    Roy-Engel AM; Salem AH; Oyeniran OO; Deininger L; Hedges DJ; Kilroy GE; Batzer MA; Deininger PL
    Genome Res; 2002 Sep; 12(9):1333-44. PubMed ID: 12213770
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A tissue-specific decrease in the pre-mRNA level of L1- and alu-containing alleles of human genes].
    Ustiugova SV; Amosova AL; Lebedev IuB; Sverdlov ED
    Bioorg Khim; 2006; 32(1):103-6. PubMed ID: 16523728
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The length of CpG islands is associated with the distribution of Alu and L1 retroelements.
    Kang MI; Rhyu MG; Kim YH; Jung YC; Hong SJ; Cho CS; Kim HS
    Genomics; 2006 May; 87(5):580-90. PubMed ID: 16488573
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Do genetic recombination and gene density shape the pattern of DNA elimination in rice long terminal repeat retrotransposons?
    Tian Z; Rizzon C; Du J; Zhu L; Bennetzen JL; Jackson SA; Gaut BS; Ma J
    Genome Res; 2009 Dec; 19(12):2221-30. PubMed ID: 19789376
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome.
    Greally JM
    Proc Natl Acad Sci U S A; 2002 Jan; 99(1):327-32. PubMed ID: 11756672
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Widespread occurrence of power-law distributions in inter-repeat distances shaped by genome dynamics.
    Klimopoulos A; Sellis D; Almirantis Y
    Gene; 2012 May; 499(1):88-98. PubMed ID: 22370293
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epigenetic control of retrotransposon expression in human embryonic stem cells.
    Macia A; Muñoz-Lopez M; Cortes JL; Hastings RK; Morell S; Lucena-Aguilar G; Marchal JA; Badge RM; Garcia-Perez JL
    Mol Cell Biol; 2011 Jan; 31(2):300-16. PubMed ID: 21041477
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.