178 related articles for article (PubMed ID: 20673865)
1. 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]
2. Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.
Kato T; Franconi CP; Sheridan MB; Hacker AM; Inagakai H; Glover TW; Arlt MF; Drabkin HA; Gemmill RM; Kurahashi H; Emanuel BS
Cancer Genet; 2014 Apr; 207(4):133-40. PubMed ID: 24813807
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.
Tong M; Kato T; Yamada K; Inagaki H; Kogo H; Ohye T; Tsutsumi M; Wang J; Emanuel BS; Kurahashi H
Hum Mol Genet; 2010 Jul; 19(13):2630-7. PubMed ID: 20392709
[TBL] [Abstract][Full Text] [Related]
5. Long AT-rich palindromes and the constitutional t(11;22) breakpoint.
Kurahashi H; Emanuel BS
Hum Mol Genet; 2001 Nov; 10(23):2605-17. PubMed ID: 11726547
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Chromosomal translocations and palindromic AT-rich repeats.
Kato T; Kurahashi H; Emanuel BS
Curr Opin Genet Dev; 2012 Jun; 22(3):221-8. PubMed ID: 22402448
[TBL] [Abstract][Full Text] [Related]
8. A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.
Gotter AL; Shaikh TH; Budarf ML; Rhodes CH; Emanuel BS
Hum Mol Genet; 2004 Jan; 13(1):103-15. PubMed ID: 14613967
[TBL] [Abstract][Full Text] [Related]
9. A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.
Gotter AL; Nimmakayalu MA; Jalali GR; Hacker AM; Vorstman J; Conforto Duffy D; Medne L; Emanuel BS
Genome Res; 2007 Apr; 17(4):470-81. PubMed ID: 17351131
[TBL] [Abstract][Full Text] [Related]
10. Palindrome-mediated chromosomal translocations in humans.
Kurahashi H; Inagaki H; Ohye T; Kogo H; Kato T; Emanuel BS
DNA Repair (Amst); 2006 Sep; 5(9-10):1136-45. PubMed ID: 16829213
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.
Edelmann L; Spiteri E; McCain N; Goldberg R; Pandita RK; Duong S; Fox J; Blumenthal D; Lalani SR; Shaffer LG; Morrow BE
Am J Hum Genet; 1999 Dec; 65(6):1608-16. PubMed ID: 10577914
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
Dufke A; Mayrhofer H; Enders H; Kaiser P; Leipoldt M
Cytogenet Cell Genet; 2001; 93(3-4):168-70. PubMed ID: 11528107
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
