261 related articles for article (PubMed ID: 22402448)
21. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Sheridan MB; Kato T; Haldeman-Englert C; Jalali GR; Milunsky JM; Zou Y; Klaes R; Gimelli G; Gimelli S; Gemmill RM; Drabkin HA; Hacker AM; Brown J; Tomkins D; Shaikh TH; Kurahashi H; Zackai EH; Emanuel BS
Am J Hum Genet; 2010 Aug; 87(2):209-18. PubMed ID: 20673865
[TBL] [Abstract][Full Text] [Related]
22. Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
Kogo H; Inagaki H; Ohye T; Kato T; Emanuel BS; Kurahashi H
Nucleic Acids Res; 2007; 35(4):1198-208. PubMed ID: 17264116
[TBL] [Abstract][Full Text] [Related]
23. Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.
Kurahashi H; Inagaki H; Yamada K; Ohye T; Taniguchi M; Emanuel BS; Toda T
J Biol Chem; 2004 Aug; 279(34):35377-83. PubMed ID: 15208332
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).
Ashley T; Gaeth AP; Inagaki H; Seftel A; Cohen MM; Anderson LK; Kurahashi H; Emanuel BS
Am J Hum Genet; 2006 Sep; 79(3):524-38. PubMed ID: 16909390
[TBL] [Abstract][Full Text] [Related]
26. Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.
Mishra D; Kato T; Inagaki H; Kosho T; Wakui K; Kido Y; Sakazume S; Taniguchi-Ikeda M; Morisada N; Iijima K; Fukushima Y; Emanuel BS; Kurahashi H
Mol Cytogenet; 2014; 7():55. PubMed ID: 25478009
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.
Hsiao MC; Piotrowski A; Alexander J; Callens T; Fu C; Mikhail FM; Claes KB; Messiaen L
Hum Mutat; 2014 Jul; 35(7):891-8. PubMed ID: 24760680
[TBL] [Abstract][Full Text] [Related]
29. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
Kurahashi H; Shaikh TH; Zackai EH; Celle L; Driscoll DA; Budarf ML; Emanuel BS
Am J Hum Genet; 2000 Sep; 67(3):763-8. PubMed ID: 10903930
[TBL] [Abstract][Full Text] [Related]
30. Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).
Kurahashi H; Shaikh TH; Hu P; Roe BA; Emanuel BS; Budarf ML
Hum Mol Genet; 2000 Jul; 9(11):1665-70. PubMed ID: 10861293
[TBL] [Abstract][Full Text] [Related]
31. Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11).
Debeer P; Mols R; Huysmans C; Devriendt K; Van de Ven WJ; Fryns JP
Clin Genet; 2002 Nov; 62(5):410-4. PubMed ID: 12431258
[TBL] [Abstract][Full Text] [Related]
32. Genetic variation affects de novo translocation frequency.
Kato T; Inagaki H; Yamada K; Kogo H; Ohye T; Kowa H; Nagaoka K; Taniguchi M; Emanuel BS; Kurahashi H
Science; 2006 Feb; 311(5763):971. PubMed ID: 16484486
[TBL] [Abstract][Full Text] [Related]
33. Marked contribution of alternative end-joining to chromosome-translocation-formation by stochastically induced DNA double-strand-breaks in G2-phase human cells.
Soni A; Siemann M; Pantelias GE; Iliakis G
Mutat Res Genet Toxicol Environ Mutagen; 2015 Nov; 793():2-8. PubMed ID: 26520366
[TBL] [Abstract][Full Text] [Related]
34. Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences.
Bacolla A; Tainer JA; Vasquez KM; Cooper DN
Nucleic Acids Res; 2016 Jul; 44(12):5673-88. PubMed ID: 27084947
[TBL] [Abstract][Full Text] [Related]
35. DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.
Kato T; Inagaki H; Tong M; Kogo H; Ohye T; Yamada K; Tsutsumi M; Emanuel BS; Kurahashi H
Mol Cytogenet; 2011 Sep; 4():18. PubMed ID: 21899780
[TBL] [Abstract][Full Text] [Related]
36. Alternative end-joining repair pathways are the ultimate backup for abrogated classical non-homologous end-joining and homologous recombination repair: Implications for the formation of chromosome translocations.
Iliakis G; Murmann T; Soni A
Mutat Res Genet Toxicol Environ Mutagen; 2015 Nov; 793():166-75. PubMed ID: 26520387
[TBL] [Abstract][Full Text] [Related]
37. Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.
Inagaki H; Ohye T; Kogo H; Tsutsumi M; Kato T; Tong M; Emanuel BS; Kurahashi H
Nat Commun; 2013; 4():1592. PubMed ID: 23481400
[TBL] [Abstract][Full Text] [Related]
38. Biochemical mechanisms of chromosomal translocations resulting from DNA double-strand breaks.
Povirk LF
DNA Repair (Amst); 2006 Sep; 5(9-10):1199-212. PubMed ID: 16822725
[TBL] [Abstract][Full Text] [Related]
39. Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription.
Ali H; Daser A; Dear P; Wood H; Rabbitts P; Rabbitts T
Genes Chromosomes Cancer; 2013 Apr; 52(4):402-9. PubMed ID: 23341332
[TBL] [Abstract][Full Text] [Related]
40. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
Chuzhanova N; Abeysinghe SS; Krawczak M; Cooper DN
Hum Mutat; 2003 Sep; 22(3):245-51. PubMed ID: 12938089
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
