Jing Wang, M.D., Ph.D.
Affiliations: | Harbin Medical University, China | Harbin Medical University, China, Haerbin Shi, Heilongjiang Sheng, China |
Area:
ElectrophysiologyGoogle:
"Jing Wang"Mean distance: 15.49 (cluster 6) | S | N | B | C | P |
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Publications
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| Zhang H, Liu T, Zhang Z, et al. (2016) Integrated Proteogenomic Characterization of Human High-Grade Serous Ovarian Cancer. Cell |
| Mertins P, Mani DR, Ruggles KV, et al. (2016) Proteogenomics connects somatic mutations to signalling in breast cancer. Nature. 534: 55-62 |
| Mertins P, Mani, Ruggles K, et al. (2016) Abstract IA29: Proteogenomic and phosphoproteomic analysis of breast cancer Molecular Cancer Research. 14 |
| Qian J, Hassanein M, Hoeksema MD, et al. (2015) The RNA binding protein FXR1 is a new driver in the 3q26-29 amplicon and predicts poor prognosis in human cancers. Proceedings of the National Academy of Sciences of the United States of America. 112: 3469-74 |
| Zhang B, Wang J, Wang X, et al. (2014) Proteogenomic characterization of human colon and rectal cancer. Nature. 513: 382-7 |
| Burrage LC, Tang S, Wang J, et al. (2014) Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 gene. Molecular Genetics and Metabolism. 113: 207-12 |
| Halvey PJ, Wang X, Wang J, et al. (2014) Proteogenomic analysis reveals unanticipated adaptations of colorectal tumor cells to deficiencies in DNA mismatch repair. Cancer Research. 74: 387-97 |
| Chanprasert S, Wang J, Weng SW, et al. (2013) Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene. Molecular Genetics and Metabolism. 110: 153-61 |
| Wang J, Duncan D, Shi Z, et al. (2013) WEB-based GEne SeT AnaLysis Toolkit (WebGestalt): update 2013. Nucleic Acids Research. 41: W77-83 |
| Tang S, Wang J, Zhang VW, et al. (2013) Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects. Human Mutation. 34: 882-93 |