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 *

191 related articles for article (PubMed ID: 10810082)

  • 1. Structure of chromosomal duplicons and their role in mediating human genomic disorders.
    Ji Y; Eichler EE; Schwartz S; Nicholls RD
    Genome Res; 2000 May; 10(5):597-610. PubMed ID: 10810082
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.
    Kriek M; White SJ; Szuhai K; Knijnenburg J; van Ommen GJ; den Dunnen JT; Breuning MH
    Eur J Hum Genet; 2006 Feb; 14(2):180-9. PubMed ID: 16391556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human.
    Ji Y; Rebert NA; Joslin JM; Higgins MJ; Schultz RA; Nicholls RD
    Genome Res; 2000 Mar; 10(3):319-29. PubMed ID: 10720573
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome.
    Paulis M; Bensi M; Moralli D; De Carli L; Raimondi E
    Genomics; 2006 Jun; 87(6):747-57. PubMed ID: 16597496
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL; Fantes JA; Mewborn SK; Huang B; Ledbetter DH
    Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 duplicons.
    Khan WA; Knoll JH; Rogan PK
    Mol Cytogenet; 2011 Aug; 4(1):15. PubMed ID: 21824424
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
    Pujana MA; Nadal M; Gratacòs M; Peral B; Csiszar K; González-Sarmiento R; Sumoy L; Estivill X
    Genome Res; 2001 Jan; 11(1):98-111. PubMed ID: 11156619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes.
    Lupski JR; Stankiewicz P
    PLoS Genet; 2005 Dec; 1(6):e49. PubMed ID: 16444292
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recent segmental duplications in the human genome.
    Bailey JA; Gu Z; Clark RA; Reinert K; Samonte RV; Schwartz S; Adams MD; Myers EW; Li PW; Eichler EE
    Science; 2002 Aug; 297(5583):1003-7. PubMed ID: 12169732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic rearrangements in inherited disease and cancer.
    Chen JM; Cooper DN; Férec C; Kehrer-Sawatzki H; Patrinos GP
    Semin Cancer Biol; 2010 Aug; 20(4):222-33. PubMed ID: 20541013
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture.
    Mehan MR; Freimer NB; Ophoff RA
    Hum Genomics; 2004 Aug; 1(5):335-44. PubMed ID: 15588494
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genomic basis of disease, mechanisms and assays for genomic disorders.
    Stankiewicz P; Lupski JR
    Genome Dyn; 2006; 1():1-16. PubMed ID: 18724050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons.
    Pujana MA; Nadal M; Guitart M; Armengol L; Gratacòs M; Estivill X
    Eur J Hum Genet; 2002 Jan; 10(1):26-35. PubMed ID: 11896453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human subtelomeric duplicon structure and organization.
    Ambrosini A; Paul S; Hu S; Riethman H
    Genome Biol; 2007; 8(7):R151. PubMed ID: 17663781
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.
    Armengol L; Pujana MA; Cheung J; Scherer SW; Estivill X
    Hum Mol Genet; 2003 Sep; 12(17):2201-8. PubMed ID: 12915466
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome architecture, rearrangements and genomic disorders.
    Stankiewicz P; Lupski JR
    Trends Genet; 2002 Feb; 18(2):74-82. PubMed ID: 11818139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.
    Jiang Z; Tang H; Ventura M; Cardone MF; Marques-Bonet T; She X; Pevzner PA; Eichler EE
    Nat Genet; 2007 Nov; 39(11):1361-8. PubMed ID: 17922013
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Segment duplications in the human genome].
    Lakrua ME; Oparina NIu; Mashkova TD
    Mol Biol (Mosk); 2003; 37(2):212-20. PubMed ID: 12723468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus.
    Maggiolini FAM; Cantsilieris S; D'Addabbo P; Manganelli M; Coe BP; Dumont BL; Sanders AD; Pang AWC; Vollger MR; Palumbo O; Palumbo P; Accadia M; Carella M; Eichler EE; Antonacci F
    PLoS Genet; 2019 Mar; 15(3):e1008075. PubMed ID: 30917130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.