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Items: 1 to 20 of 88

1.

Translocation mapping exposes the risky lifestyle of B cells.

McCord RP, Dekker J.

Cell. 2011 Sep 30;147(1):20-2. doi: 10.1016/j.cell.2011.09.005.

2.

DNA damage defines sites of recurrent chromosomal translocations in B lymphocytes.

Hakim O, Resch W, Yamane A, Klein I, Kieffer-Kwon KR, Jankovic M, Oliveira T, Bothmer A, Voss TC, Ansarah-Sobrinho C, Mathe E, Liang G, Cobell J, Nakahashi H, Robbiani DF, Nussenzweig A, Hager GL, Nussenzweig MC, Casellas R.

Nature. 2012 Feb 7;484(7392):69-74. doi: 10.1038/nature10909.

3.

Translocations in normal B cells and cancers: insights from new technical approaches.

Chiarle R.

Adv Immunol. 2013;117:39-71. doi: 10.1016/B978-0-12-410524-9.00002-5. Review.

PMID:
23611285
4.

Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements.

Inagaki H, Kato T, Tsutsumi M, Ouchi Y, Ohye T, Kurahashi H.

Front Genet. 2016 Jul 12;7:125. doi: 10.3389/fgene.2016.00125. eCollection 2016. Review.

5.
6.

Genome organization influences partner selection for chromosomal rearrangements.

Wijchers PJ, de Laat W.

Trends Genet. 2011 Feb;27(2):63-71. doi: 10.1016/j.tig.2010.11.001. Epub 2010 Dec 7. Review.

PMID:
21144612
7.

Translocation-capture sequencing reveals the extent and nature of chromosomal rearrangements in B lymphocytes.

Klein IA, Resch W, Jankovic M, Oliveira T, Yamane A, Nakahashi H, Di Virgilio M, Bothmer A, Nussenzweig A, Robbiani DF, Casellas R, Nussenzweig MC.

Cell. 2011 Sep 30;147(1):95-106. doi: 10.1016/j.cell.2011.07.048.

8.

Chromosomal translocations induced at specified loci in human stem cells.

Brunet E, Simsek D, Tomishima M, DeKelver R, Choi VM, Gregory P, Urnov F, Weinstock DM, Jasin M.

Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10620-5. doi: 10.1073/pnas.0902076106. Epub 2009 Jun 23.

9.

Recurrent chromosomal rearrangements at bands 8q24 and 11q13 in gastric cancer as detected by multicolor spectral karyotyping.

Yamashita Y, Nishida K, Okuda T, Nomura K, Matsumoto Y, Mitsufuji S, Horiike S, Hata H, Sakakura C, Hagiwara A, Yamagishi H, Taniwaki M.

World J Gastroenterol. 2005 Sep 7;11(33):5129-35.

10.

Formation of complex and unstable chromosomal translocations in yeast.

Schmidt KH, Viebranz E, Doerfler L, Lester C, Rubenstein A.

PLoS One. 2010 Aug 9;5(8):e12007. doi: 10.1371/journal.pone.0012007.

11.

Complex oncogenic translocations with gene amplification are initiated by specific DNA breaks in lymphocytes.

Wright SM, Woo YH, Alley TL, Shirley BJ, Akeson EC, Snow KJ, Maas SA, Elwell RL, Foreman O, Mills KD.

Cancer Res. 2009 May 15;69(10):4454-60. doi: 10.1158/0008-5472.CAN-08-4515. Epub 2009 May 12.

12.

Chromosomal translocations caused by either pol32-dependent or pol32-independent triparental break-induced replication.

Ruiz JF, Gómez-González B, Aguilera A.

Mol Cell Biol. 2009 Oct;29(20):5441-54. doi: 10.1128/MCB.00256-09. Epub 2009 Aug 3.

13.

The role of mechanistic factors in promoting chromosomal translocations found in lymphoid and other cancers.

Zhang Y, Gostissa M, Hildebrand DG, Becker MS, Boboila C, Chiarle R, Lewis S, Alt FW.

Adv Immunol. 2010;106:93-133. doi: 10.1016/S0065-2776(10)06004-9. Review.

14.

Characterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing data.

Xu C, Zhang J, Wang YP, Deng HW, Li J.

Genome Biol Evol. 2014 Oct 27;6(11):3015-24. doi: 10.1093/gbe/evu234.

15.

Three-dimensional genome architecture influences partner selection for chromosomal translocations in human disease.

Engreitz JM, Agarwala V, Mirny LA.

PLoS One. 2012;7(9):e44196. doi: 10.1371/journal.pone.0044196. Epub 2012 Sep 28.

16.
17.

Mechanisms that promote and suppress chromosomal translocations in lymphocytes.

Gostissa M, Alt FW, Chiarle R.

Annu Rev Immunol. 2011;29:319-50. doi: 10.1146/annurev-immunol-031210-101329. Review.

PMID:
21219174
18.

3D view of chromosomes, DNA damage, and translocations.

Schwartz M, Hakim O.

Curr Opin Genet Dev. 2014 Apr;25:118-25. doi: 10.1016/j.gde.2013.12.008. Epub 2014 Mar 12. Review.

PMID:
24632298
19.

Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites.

Burrow AA, Williams LE, Pierce LC, Wang YH.

BMC Genomics. 2009 Jan 30;10:59. doi: 10.1186/1471-2164-10-59.

20.

Microhomology directs diverse DNA break repair pathways and chromosomal translocations.

Villarreal DD, Lee K, Deem A, Shim EY, Malkova A, Lee SE.

PLoS Genet. 2012;8(11):e1003026. doi: 10.1371/journal.pgen.1003026. Epub 2012 Nov 8.

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