199 related articles for article (PubMed ID: 12557125)
21. 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]
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. Double strand breaks (DSBs) as indicators of genomic instability in PATRR-mediated translocations.
Correll-Tash S; Lilley B; Salmons Iv H; Mlynarski E; Franconi CP; McNamara M; Woodbury C; Easley CA; Emanuel BS
Hum Mol Genet; 2021 Feb; 29(24):3872-3881. PubMed ID: 33258468
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 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]
28. 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]
29. 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]
30. 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]
31. 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]
32. A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2.
Bengesser K; Cooper DN; Steinmann K; Kluwe L; Chuzhanova NA; Wimmer K; Tatagiba M; Tinschert S; Mautner VF; Kehrer-Sawatzki H
Hum Mutat; 2010 Jun; 31(6):742-51. PubMed ID: 20506354
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication.
Kehrer-Sawatzki H; Assum G; Hameister H
Hum Genet; 2002 Oct; 111(4-5):465-7; author reply 468-9. PubMed ID: 12384794
[TBL] [Abstract][Full Text] [Related]
35. cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene.
Cawthon RM; Andersen LB; Buchberg AM; Xu GF; O'Connell P; Viskochil D; Weiss RB; Wallace MR; Marchuk DA; Culver M
Genomics; 1991 Mar; 9(3):446-60. PubMed ID: 1903357
[TBL] [Abstract][Full Text] [Related]
36. Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2).
Arai E; Ikeuchi T; Nakamura Y
Hum Mol Genet; 1994 Jun; 3(6):937-9. PubMed ID: 7951241
[TBL] [Abstract][Full Text] [Related]
37. Decoding NF1 Intragenic Copy-Number Variations.
Hsiao MC; Piotrowski A; Callens T; Fu C; Wimmer K; Claes KB; Messiaen L
Am J Hum Genet; 2015 Aug; 97(2):238-49. PubMed ID: 26189818
[TBL] [Abstract][Full Text] [Related]
38. Precise localization of NF1 to 17q11.2 by balanced translocation.
Ledbetter DH; Rich DC; O'Connell P; Leppert M; Carey JC
Am J Hum Genet; 1989 Jan; 44(1):20-4. PubMed ID: 2491776
[TBL] [Abstract][Full Text] [Related]
39. Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.
Jenne DE; Tinschert S; Reimann H; Lasinger W; Thiel G; Hameister H; Kehrer-Sawatzki H
Am J Hum Genet; 2001 Sep; 69(3):516-27. PubMed ID: 11468690
[TBL] [Abstract][Full Text] [Related]
40. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]