Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yeonjoo Chung"'
Autor:
Joana G Marques, Berkley E Gryder, Blaz Pavlovic, Yeonjoo Chung, Quy A Ngo, Fabian Frommelt, Matthias Gstaiger, Young Song, Katharina Benischke, Dominik Laubscher, Marco Wachtel, Javed Khan, Beat W Schäfer
Publikováno v:
eLife, Vol 9 (2020)
The NuRD complex subunit CHD4 is essential for fusion-positive rhabdomyosarcoma (FP-RMS) survival, but the mechanisms underlying this dependency are not understood. Here, a NuRD-specific CRISPR screen demonstrates that FP-RMS is particularly sensitiv
Externí odkaz:
https://doaj.org/article/d33cd1744564400abf93c1226f3c6a09
Autor:
Yeonjoo Chung, Ho Park
Publikováno v:
Journal of Korea Research Association of International Commerce. 19:71-88
Autor:
Young K. Song, Joana G. Marques, Beat W. Schäfer, Katharina Benischke, Quy A. Ngo, Dominik Laubscher, Berkley E. Gryder, Marco Wachtel, Matthias Gstaiger, Blaz Pavlovic, Javed Khan, Fabian Frommelt, Yeonjoo Chung
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db95c34c9e6de4da7d3d38f2c5869ccd
https://doi.org/10.7554/elife.54993.sa2
https://doi.org/10.7554/elife.54993.sa2
Autor:
Blaz Pavlovic, Javed Khan, Yeonjoo Chung, Marco Wachtel, Young K. Song, Beat W. Schäfer, Quy A. Ngo, Joana G. Marques, Matthias Gstaiger, Fabian Frommelt, Berkley E. Gryder, Dominik Laubscher, Katharina Benischke
Publikováno v:
eLife, Vol 9 (2020)
eLife
eLife, 9
eLife
eLife, 9
The NuRD complex subunit CHD4 is essential for fusion-positive rhabdomyosarcoma (FP-RMS) survival, but the mechanisms underlying this dependency are not understood. Here, a NuRD-specific CRISPR screen demonstrates that FP-RMS is particularly sensitiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf9b081301749f709d71b7bba0d1d825
Autor:
Yeonjoo Chung, Beat W. Schäfer, Joana G. Marques, Marco Wachtel, Berkley E. Gryder, Blaz Pavlovic, Quy A. Ngo, Javed Khan
Publikováno v:
Cancer Research. 80:PO-009
Cancer-specific chromosomal aberrations producing chimeric fusion genes are recurrently found in pediatric sarcomas. Fusion positive rhabdomyosarcoma (FP-RMS) and Ewing sarcoma (ES) are two rare but lethal pediatric malignancies driven by such chromo