219 related articles for article (PubMed ID: 16909390)
1. 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]
2. 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]
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. 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]
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. 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]
7. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
Armstrong SJ; Goldman AS; Speed RM; Hultén MA
Am J Hum Genet; 2000 Sep; 67(3):601-9. PubMed ID: 10936106
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. Chromosomal translocations mediated by palindromic DNA.
Kurahashi H; Inagaki H; Ohye T; Kogo H; Kato T; Emanuel BS
Cell Cycle; 2006 Jun; 5(12):1297-303. PubMed ID: 16760666
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.
Kurahashi H; Shaikh T; Takata M; Toda T; Emanuel BS
Am J Hum Genet; 2003 Mar; 72(3):733-8. PubMed ID: 12557125
[TBL] [Abstract][Full Text] [Related]
20. Meiotic Chromosome Contacts as a Plausible Prelude for Robertsonian Translocations.
Matveevsky S; Kolomiets O; Bogdanov A; Alpeeva E; Bakloushinskaya I
Genes (Basel); 2020 Apr; 11(4):. PubMed ID: 32252399
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
