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 *

244 related articles for article (PubMed ID: 19271239)

  • 1. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.
    D'Angelo CS; Gajecka M; Kim CA; Gentles AJ; Glotzbach CD; Shaffer LG; Koiffmann CP
    Hum Genet; 2009 Jun; 125(5-6):551-63. PubMed ID: 19271239
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.
    Woodward KJ; Cundall M; Sperle K; Sistermans EA; Ross M; Howell G; Gribble SM; Burford DC; Carter NP; Hobson DL; Garbern JY; Kamholz J; Heng H; Hodes ME; Malcolm S; Hobson GM
    Am J Hum Genet; 2005 Dec; 77(6):966-87. PubMed ID: 16380909
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.
    Gajecka M; Pavlicek A; Glotzbach CD; Ballif BC; Jarmuz M; Jurka J; Shaffer LG
    Hum Genet; 2006 Nov; 120(4):519-26. PubMed ID: 16847692
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
    Ballif BC; Wakui K; Gajecka M; Shaffer LG
    Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
    Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
    Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.
    Luo Y; Hermetz KE; Jackson JM; Mulle JG; Dodd A; Tsuchiya KD; Ballif BC; Shaffer LG; Cody JD; Ledbetter DH; Martin CL; Rudd MK
    Hum Mol Genet; 2011 Oct; 20(19):3769-78. PubMed ID: 21729882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.
    Lee JA; Inoue K; Cheung SW; Shaw CA; Stankiewicz P; Lupski JR
    Hum Mol Genet; 2006 Jul; 15(14):2250-65. PubMed ID: 16774974
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1.
    Gajecka M; Glotzbach CD; Shaffer LG
    Chromosome Res; 2006; 14(3):277-82. PubMed ID: 16628498
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions.
    Ballif BC; Gajecka M; Shaffer LG
    Chromosome Res; 2004; 12(2):133-41. PubMed ID: 15053483
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication.
    Linardopoulou EV; Williams EM; Fan Y; Friedman C; Young JM; Trask BJ
    Nature; 2005 Sep; 437(7055):94-100. PubMed ID: 16136133
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
    Gajecka M; Glotzbach CD; Jarmuz M; Ballif BC; Shaffer LG
    Eur J Hum Genet; 2006 Dec; 14(12):1255-62. PubMed ID: 16941016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.
    Yatsenko SA; Brundage EK; Roney EK; Cheung SW; Chinault AC; Lupski JR
    Hum Mol Genet; 2009 Jun; 18(11):1924-36. PubMed ID: 19293338
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
    Ou Z; Stankiewicz P; Xia Z; Breman AM; Dawson B; Wiszniewska J; Szafranski P; Cooper ML; Rao M; Shao L; South ST; Coleman K; Fernhoff PM; Deray MJ; Rosengren S; Roeder ER; Enciso VB; Chinault AC; Patel A; Kang SH; Shaw CA; Lupski JR; Cheung SW
    Genome Res; 2011 Jan; 21(1):33-46. PubMed ID: 21205869
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.
    Bauters M; Van Esch H; Friez MJ; Boespflug-Tanguy O; Zenker M; Vianna-Morgante AM; Rosenberg C; Ignatius J; Raynaud M; Hollanders K; Govaerts K; Vandenreijt K; Niel F; Blanc P; Stevenson RE; Fryns JP; Marynen P; Schwartz CE; Froyen G
    Genome Res; 2008 Jun; 18(6):847-58. PubMed ID: 18385275
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nonrecurrent 17p11.2p12 Rearrangement Events that Result in Two Concomitant Genomic Disorders: The PMP22-RAI1 Contiguous Gene Duplication Syndrome.
    Yuan B; Harel T; Gu S; Liu P; Burglen L; Chantot-Bastaraud S; Gelowani V; Beck CR; Carvalho CM; Cheung SW; Coe A; Malan V; Munnich A; Magoulas PL; Potocki L; Lupski JR
    Am J Hum Genet; 2015 Nov; 97(5):691-707. PubMed ID: 26544804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.
    Dave BJ; Hess MM; Pickering DL; Zaleski DH; Pfeifer AL; Weisenburger DD; Armitage JO; Sanger WG
    Clin Cancer Res; 1999 Jun; 5(6):1401-9. PubMed ID: 10389925
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
    Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
    Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements.
    Emanuel BS
    Dev Disabil Res Rev; 2008; 14(1):11-8. PubMed ID: 18636632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
    Weckselblatt B; Hermetz KE; Rudd MK
    Genome Res; 2015 Jul; 25(7):937-47. PubMed ID: 26070663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.