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NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets.
Bouveret R, Waardenberg AJ, Schonrock N, Ramialison M, Doan T, de Jong D, Bondue A, Kaur G, Mohamed S, Fonoudi H, Chen CM, Wouters MA, Bhattacharya S, Plachta N, Dunwoodie SL, Chapman G, Blanpain C, Harvey RP. Bouveret R, et al. Among authors: de jong d. Elife. 2015 Jul 6;4:e06942. doi: 10.7554/eLife.06942. Elife. 2015. PMID: 26146939 Free PMC article.
Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes.
Romeo S, Duim RA, Bridge JA, Mertens F, de Jong D, Dal Cin P, Wijers-Koster PM, Debiec-Rychter M, Sciot R, Rosenberg AE, Szuhai K, Hogendoorn PC. Romeo S, et al. Among authors: de jong d. Am J Pathol. 2010 Sep;177(3):1365-76. doi: 10.2353/ajpath.2010.091277. Epub 2010 Aug 9. Am J Pathol. 2010. PMID: 20696777 Free PMC article.
Fusion events lead to truncation of FOS in epithelioid hemangioma of bone.
van IJzendoorn DG, de Jong D, Romagosa C, Picci P, Benassi MS, Gambarotti M, Daugaard S, van de Sande M, Szuhai K, Bovée JV. van IJzendoorn DG, et al. Among authors: de jong d. Genes Chromosomes Cancer. 2015 Sep;54(9):565-74. doi: 10.1002/gcc.22269. Epub 2015 Jul 14. Genes Chromosomes Cancer. 2015. PMID: 26173738
921 results