How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining-Reference-Cited by-同舟云学术

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How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining

Published:2023-06 Issue:6 Volume:26 Page:106900
ISSN:2589-0042
Container-title:iScience
language:en
Short-container-title:iScience

Author:

Streb Patrick,Kowarz Eric,Benz Tamara,Reis Jennifer,Marschalek Rolf^ORCID

Funder

Wilhelm Sander-Stiftung

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference62 articles.

1. Fine structure of translocation breakpoints in leukemic blasts with chromosomal translocation t(4;11): the DNA damage-repair model of translocation;Reichel;Oncogene,1998

2. A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells;Gillert;Oncogene,1999

3. Frequent chromosomal translocations induced by DNA double-strand breaks;Richardson;Nature,2000

4. Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining;Ghezraoui;Mol. Cell,2014

5. Mechanisms driving chromosomal translocations: lost in time and space;Ramsden;Oncogene,2021

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