BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

304 related articles for article (PubMed ID: 17675367)

  • 1. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome.
    Babcock M; Yatsenko S; Hopkins J; Brenton M; Cao Q; de Jong P; Stankiewicz P; Lupski JR; Sikela JM; Morrow BE
    Hum Mol Genet; 2007 Nov; 16(21):2560-71. PubMed ID: 17675367
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution.
    Babcock M; Pavlicek A; Spiteri E; Kashork CD; Ioshikhes I; Shaffer LG; Jurka J; Morrow BE
    Genome Res; 2003 Dec; 13(12):2519-32. PubMed ID: 14656960
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome.
    Pavlicek A; House R; Gentles AJ; Jurka J; Morrow BE
    Genome Res; 2005 Nov; 15(11):1487-95. PubMed ID: 16251458
    [TBL] [Abstract][Full Text] [Related]  

  • 4. AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.
    Babcock M; Yatsenko S; Stankiewicz P; Lupski JR; Morrow BE
    Genome Res; 2007 Apr; 17(4):451-60. PubMed ID: 17284672
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications.
    Torres-Juan L; Rosell J; Sánchez-de-la-Torre M; Fibla J; Heine-Suñer D
    BMC Med Genet; 2007 Apr; 8():14. PubMed ID: 17397557
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes.
    Spiteri E; Babcock M; Kashork CD; Wakui K; Gogineni S; Lewis DA; Williams KM; Minoshima S; Sasaki T; Shimizu N; Potocki L; Pulijaal V; Shanske A; Shaffer LG; Morrow BE
    Hum Mol Genet; 2003 Aug; 12(15):1823-37. PubMed ID: 12874103
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Concurrent microdeletion and duplication of 22q11.2.
    Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
    Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A common molecular basis for rearrangement disorders on chromosome 22q11.
    Edelmann L; Pandita RK; Spiteri E; Funke B; Goldberg R; Palanisamy N; Chaganti RS; Magenis E; Shprintzen RJ; Morrow BE
    Hum Mol Genet; 1999 Jul; 8(7):1157-67. PubMed ID: 10369860
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus.
    Edelmann L; Stankiewicz P; Spiteri E; Pandita RK; Shaffer L; Lupski JR; Morrow BE
    Genome Res; 2001 Feb; 11(2):208-17. PubMed ID: 11157784
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication and relocation of the functional DPY19L2 gene within low copy repeats.
    Carson AR; Cheung J; Scherer SW
    BMC Genomics; 2006 Mar; 7():45. PubMed ID: 16526957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The 22q11 low copy repeats are characterized by unprecedented size and structural variability.
    Demaerel W; Mostovoy Y; Yilmaz F; Vervoort L; Pastor S; Hestand MS; Swillen A; Vergaelen E; Geiger EA; Coughlin CR; Chow SK; McDonald-McGinn D; Morrow B; Kwok PY; Xiao M; Emanuel BS; Shaikh TH; Vermeesch JR
    Genome Res; 2019 Sep; 29(9):1389-1401. PubMed ID: 31481461
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Studies on karyotype evolution in higher primates in relation to human chromosome 14 and 9 by comparative mapping of immunoglobulin C epsilon genes with fluorescence in situ hybridization.
    Tanabe H
    Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku; 1999; (117):77-90. PubMed ID: 10859938
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysis.
    Shimojima K; Okamoto N; Inazu T; Yamamoto T
    J Hum Genet; 2011 Nov; 56(11):810-2. PubMed ID: 21866110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. AT-rich palindromes mediate the constitutional t(11;22) translocation.
    Edelmann L; Spiteri E; Koren K; Pulijaal V; Bialer MG; Shanske A; Goldberg R; Morrow BE
    Am J Hum Genet; 2001 Jan; 68(1):1-13. PubMed ID: 11095996
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
    Funke B; Pandita RK; Morrow BE
    Genomics; 2001 May; 73(3):264-71. PubMed ID: 11350118
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular phylogenetics of the hominoid Y chromosome.
    Samonte RV; Conte RA; Verma RS
    J Hum Genet; 1998; 43(3):185-6. PubMed ID: 9747032
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
    Thomas NS; Durkie M; Potts G; Sandford R; Van Zyl B; Youings S; Dennis NR; Jacobs PA
    Eur J Hum Genet; 2006 Jul; 14(7):831-7. PubMed ID: 16617304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of human specific gene duplications relative to other primates by array CGH and quantitative PCR.
    Armengol G; Knuutila S; Lozano JJ; Madrigal I; Caballín MR
    Genomics; 2010 Apr; 95(4):203-9. PubMed ID: 20153417
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids.
    Münch C; Kirsch S; Fernandes AM; Schempp W
    BMC Evol Biol; 2008 Oct; 8():269. PubMed ID: 18831734
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The 22q11.2 Low Copy Repeats.
    Vervoort L; Vermeesch JR
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421776
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.