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Wenchao Wang
Researcher at Hefei Institutes of Physical Science
Publications - 123
Citations - 2331
Wenchao Wang is an academic researcher from Hefei Institutes of Physical Science. The author has contributed to research in topics: Prodrug & Kinase. The author has an hindex of 20, co-authored 107 publications receiving 1849 citations. Previous affiliations of Wenchao Wang include Harvard University & Indiana University.
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Journal ArticleDOI
Activated ALK Collaborates with MYCN in Neuroblastoma Pathogenesis
Shizhen Zhu,Jeong-Soo Lee,Feng Guo,Jimann Shin,Antonio R. Perez-Atayde,Jeffery L. Kutok,Scott J. Rodig,Donna Neuberg,Daniel Helman,Hui Feng,Rodney A. Stewart,Wenchao Wang,Rani E. George,Rani E. George,John P. Kanki,A. Thomas Look,A. Thomas Look +16 more
TL;DR: A transgenic zebrafish model of neuroblastoma is generated in which MYCN-induced tumors arise from a subpopulation of neuroblasts that migrate into the adrenal medulla analog following organogenesis, and coexpression of activated ALK with MYCN in this model triples the disease penetrance and markedly accelerates tumor onset.
Journal ArticleDOI
The ALK(F1174L) mutation potentiates the oncogenic activity of MYCN in neuroblastoma.
Teeara Berry,William Luther,Namrata Bhatnagar,Yann Jamin,Evon Poon,Takaomi Sanda,De-Sheng Pei,Bandana Sharma,Winston R. Vetharoy,Albert Hallsworth,Zai Ahmad,Karen Barker,Lisa A. Moreau,Hannah Webber,Wenchao Wang,Qingsong Liu,Antonio R. Perez-Atayde,Scott J. Rodig,Nai-Kong V. Cheung,Florence I. Raynaud,Bengt Hallberg,Simon P. Robinson,Nathanael S. Gray,Andrew D.J. Pearson,Andrew D.J. Pearson,Suzanne A. Eccles,Louis Chesler,Louis Chesler,Rani E. George +28 more
TL;DR: Combined treatment with the ATP-competitive mTOR inhibitor Torin2 overcame the resistance of ALK(F1174L)/MYCN tumors to crizotinib and suggested a strategy for improving targeted therapy for ALK-positive neuroblastoma.
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H3K27me and PRC2 transmit a memory of repression across generations and during development
TL;DR: It is demonstrated that H3K27me and PRC2 each contribute to epigenetically transmitting the memory of repression across generations and during development.
Journal ArticleDOI
Regulation of the different chromatin states of autosomes and X chromosomes in the germ line of C. elegans.
TL;DR: It is proposed that all four MES proteins participate in X-chromosome silencing, and that the role of MES-4 is to exclude repressors from the autosomes, thus enabling efficient repression of the Xs.
Journal ArticleDOI
synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival
Lisa N. Petrella,Wenchao Wang,Caroline A. Spike,Andreas Rechtsteiner,Valerie Reinke,Susan Strome,Susan Strome +6 more
TL;DR: It is shown that, when grown at high temperature, a majority of synMuv B mutants irreversibly arrest at the L1 stage, revealing that arrest is caused by somatic cells possessing a germline-like chromatin state.