Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jianrong Wu"'
Autor:
Elizabeth Stewart, Ross Goshorn, Cori Bradley, Lyra M. Griffiths, Claudia Benavente, Nathaniel R. Twarog, Gregory M. Miller, William Caufield, Burgess B. Freeman III, Armita Bahrami, Alberto Pappo, Jianrong Wu, Amos Loh, Åsa Karlström, Chris Calabrese, Brittney Gordon, Lyudmila Tsurkan, M. Jason Hatfield, Philip M. Potter, Scott E. Snyder, Suresh Thiagarajan, Abbas Shirinifard, Andras Sablauer, Anang A. Shelat, Michael A. Dyer
Publikováno v:
Cell Reports, Vol 9, Iss 3, Pp 829-840 (2014)
Ewing sarcoma (EWS) is a tumor of the bone and soft tissue that primarily affects adolescents and young adults. With current therapies, 70% of patients with localized disease survive, but patients with metastatic or recurrent disease have a poor outc
Externí odkaz:
https://doaj.org/article/40a0e6c6da1444659221f51065bf900e
Autor:
Xiang Chen, Armita Bahrami, Alberto Pappo, John Easton, James Dalton, Erin Hedlund, David Ellison, Sheila Shurtleff, Gang Wu, Lei Wei, Matthew Parker, Michael Rusch, Panduka Nagahawatte, Jianrong Wu, Shenghua Mao, Kristy Boggs, Heather Mulder, Donald Yergeau, Charles Lu, Li Ding, Michael Edmonson, Chunxu Qu, Jianmin Wang, Yongjin Li, Fariba Navid, Najat C. Daw, Elaine R. Mardis, Richard K. Wilson, James R. Downing, Jinghui Zhang, Michael A. Dyer
Publikováno v:
Cell Reports, Vol 7, Iss 1, Pp 104-112 (2014)
Pediatric osteosarcoma is characterized by multiple somatic chromosomal lesions, including structural variations (SVs) and copy number alterations (CNAs). To define the landscape of somatic mutations in pediatric osteosarcoma, we performed whole-geno
Externí odkaz:
https://doaj.org/article/40f55a27461a4869b9e264b8b60dc172
Autor:
Heather L. Mulder, Najat C. Daw, James R. Downing, Charles Lu, Panduka Nagahawatte, Shenghua Mao, Jianmin Wang, Richard K. Wilson, Li Ding, Alberto S. Pappo, Yongjin Li, Kristy Boggs, Xiang Chen, Gang Wu, Donald Yergeau, Michael N. Edmonson, Michael Rusch, Matthew Parker, Jinghui Zhang, David H. Ellison, Armita Bahrami, Sheila A. Shurtleff, Elaine R. Mardis, Fariba Navid, Jianrong Wu, James T. Dalton, Michael A. Dyer, Erin Hedlund, John Easton, Lei Wei, Chunxu Qu
Publikováno v:
Cell Reports, Vol 7, Iss 1, Pp 104-112 (2014)
Osteosarcoma is a neoplasm of mesenchymal origin with features of osteogenic differentiation. Patients with recurrent or metastatic disease have a very poor prognosis. To define the landscape of somatic mutations in pediatric osteosarcoma, we perform