220 related articles for article (PubMed ID: 11726547)
21. The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.
Kurahashi H; Inagaki H; Ohye T; Kogo H; Tsutsumi M; Kato T; Tong M; Emanuel BS
Clin Genet; 2010 Oct; 78(4):299-309. PubMed ID: 20507342
[TBL] [Abstract][Full Text] [Related]
22. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.
Shaikh TH; Budarf ML; Celle L; Zackai EH; Emanuel BS
Am J Hum Genet; 1999 Dec; 65(6):1595-607. PubMed ID: 10577913
[TBL] [Abstract][Full Text] [Related]
23. The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.
Tapia-Páez I; Kost-Alimova M; Hu P; Roe BA; Blennow E; Fedorova L; Imreh S; Dumanski JP
Hum Genet; 2001 Aug; 109(2):167-77. PubMed ID: 11511922
[TBL] [Abstract][Full Text] [Related]
24. Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.
Willett-Brozick JE; Savul SA; Richey LE; Baysal BE
Hum Genet; 2001 Aug; 109(2):216-23. PubMed ID: 11511928
[TBL] [Abstract][Full Text] [Related]
25. Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint.
Kurahashi H; Shaikh TH; Emanuel BS
Hum Mol Genet; 2000 Nov; 9(18):2727-32. PubMed ID: 11063731
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Molecular characterization of the genomic breakpoint junction in a t(11;22) translocation in Ewing sarcoma.
Obata K; Hiraga H; Nojima T; Yoshida MC; Abe S
Genes Chromosomes Cancer; 1999 May; 25(1):6-15. PubMed ID: 10221334
[TBL] [Abstract][Full Text] [Related]
29. Paternal origin of the de novo constitutional t(11;22)(q23;q11).
Ohye T; Inagaki H; Kogo H; Tsutsumi M; Kato T; Tong M; Macville MV; Medne L; Zackai EH; Emanuel BS; Kurahashi H
Eur J Hum Genet; 2010 Jul; 18(7):783-7. PubMed ID: 20179746
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.
Inagaki H; Ohye T; Kogo H; Yamada K; Kowa H; Shaikh TH; Emanuel BS; Kurahashi H
Hum Mutat; 2005 Oct; 26(4):332-42. PubMed ID: 16116616
[TBL] [Abstract][Full Text] [Related]
33. Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Shaikh TH; O'Connor RJ; Pierpont ME; McGrath J; Hacker AM; Nimmakayalu M; Geiger E; Emanuel BS; Saitta SC
Genome Res; 2007 Apr; 17(4):482-91. PubMed ID: 17351135
[TBL] [Abstract][Full Text] [Related]
34. Fine mapping of the constitutional translocation t(11;22)(q23;q11).
Tapia-Páez I; O'Brien KP; Kost-Alimova M; Sahlén S; Kedra D; Bruder CE; Andersson B; Roe BA; Hu P; Imreh S; Blennow E; Dumanski JP
Hum Genet; 2000 May; 106(5):506-16. PubMed ID: 10914680
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. 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]
38. [Palindromic sequence-mediated de novo chromosome translocation in sperm samples derived from normal and oligospermic males].
Wen T; Zhang JS; Ci J; Zhao YH; Fei X; Wu B; Li L
Zhonghua Nan Ke Xue; 2007 Aug; 13(8):675-80. PubMed ID: 17918702
[TBL] [Abstract][Full Text] [Related]
39. The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event.
Correll-Tash S; Conlin L; Mininger BA; Lilley B; Mennuti MT; Emanuel BS
Cytogenet Genome Res; 2018; 156(4):185-190. PubMed ID: 30566958
[TBL] [Abstract][Full Text] [Related]
40. Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.
Kurahashi H; Inagaki H; Kato T; Hosoba E; Kogo H; Ohye T; Tsutsumi M; Bolor H; Tong M; Emanuel BS
Hum Mol Genet; 2009 Sep; 18(18):3397-406. PubMed ID: 19520744
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
