356 related articles for article (PubMed ID: 11095996)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.
Funke B; Edelmann L; McCain N; Pandita RK; Ferreira J; Merscher S; Zohouri M; Cannizzaro L; Shanske A; Morrow BE
Am J Hum Genet; 1999 Mar; 64(3):747-58. PubMed ID: 10053009
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Molecular cloning of a translocation breakpoint hotspot in 22q11.
Kurahashi H; Inagaki H; Hosoba E; Kato T; Ohye T; Kogo H; Emanuel BS
Genome Res; 2007 Apr; 17(4):461-9. PubMed ID: 17267815
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. Genomic disorders on 22q11.
McDermid HE; Morrow BE
Am J Hum Genet; 2002 May; 70(5):1077-88. PubMed ID: 11925570
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
