2013年论文

1. Dongrong Chen, Xujia, Jing Zhang, Wenxia Sun, Weizhi He, Hengyi Jiang, Alastair I. H. Murchie*. Riboswitch control of Aminoglycoside Antibiotic Resistance. Cell. 2013;152:68-81  
2. Zhao, D., Zou, S., Liu, Y., Zhou, X., Mo, Y., Wang, P., Xu, Y., Dong, B., Xiong, Y*.,Lei, Q-Y*., and Guan K-L*. Lysine-5 Acetylation Negatively Regulates Lactate Dehydrogenase A and Is Decreased in PancreaticCancer. Cancer Cell. 2013; 23: 464-476
3. Lv, L., Xu, Y-P., Zhao, D., Li, F-L., Wang, W., Sasaki N., Jiang, Y., Zhou, X., Li, T-T., Guan, K-L*.,Lei, Q-Y*.,and Xiong*, Y. Mitogenic and oncogenic stimulation of K433 acetylation promote PKM2 protein kinase activity and nuclear localization. Molecular Cell . 2013; 52: 340-352  
4. Lin,R., Ren, T., Gao, X., Zhou, X., Li, T., Xiong, Y., Guan, K-L., Lei, Q-Y*.  Acetylation Stabilizes ATP-citrate Lyase to Promote Lipid Biosynthesis and Tumor Growth. Molecular Cell. 2013; 51: 506–518  
5. Shu-wen Qian, Yan Tang, Xi Li, Yuan Liu, You-you Zhang, Hai-yan Huang, Rui-Dan  Xue, Hao-yong Yu, Liang Guo, Hui-di Gao, Yan Liu, Xia Sun, Yi-ming Li, Wei-Ping Jia, Qi-Qun Tang*. BMP4-mediated brown fat-like changes in white adipose tissue alter glucose and energy homeostasis. ProcNatlAcadSci USA. 2013; 110(9):E798-807  
6. SH Zhang, S Zhang, L Chen, G Cheng, JS. Mruk, L Zhu, SP. Kunapuli, Z Ding*. Tumor vascular disrupting agent DMXAA inhibits platelet activation and thrombosis via inhibition of TXA2 signaling and phosphodiesterase. J ThrombHaemost 2013; 11(10): 1855 - 66
7. S Zhang, J Ye, Y Zhang, X Xu, J Liu, SH Zhang, SP Kunapuli, Z Ding*. P2Y12 protects platelets from apoptosis via PI3k-dependent Bak/Bax inactivation. J ThrombHaemost 2013; 11: 149 - 160
8. Yang Liu, Ya-Dong Zhang, Liang Guo, Hai-Yan Huang, HaoZhu,Jia-XinHuang, Yuan Liu, Shui-RongZhou, Yong-Jun Dang, Xi Li, Qi-QunTang*. Protein Inhibitor of Activated STAT 1 (PIAS1) Is Identified as the SUMO E3 Ligase of CCAAT/Enhancer-Binding Protein β (C/EBPβ) during Adipogenesis.Mol Cell Biol.2013 Nov;33(22):4606-17
9. Liang Guo, Jia-Xin Huang,Yang Liu,Xi Li,Shui-Rong Zhou, Shu-Wen Qian, Yuan Liu, Hao Zhu, Hai-Yan Huang, Yong-Jun Dang, Qi-Qun Tang*. Transactivation of Atg4b by C/EBPβ promotes autophagy to facilitate adipogenesis. Mol Cell Biol. 2013; 33(16):3180-90  
10. Shan-Shan Wang, Hai-Yan Huang, Su-Zhen Chen, Xi Li, Yuan Liu, Wen-Ting Zhang,Qi-QunTang*.Early growth response 2 (Egr2) plays opposing roles in committing C3H10T1/2 stem cells to adipocytes and smooth muscle-like cells.Int J Biochem Cell Biol. 2013; 45(8):1825-32  
11. Shan-Shan Wang, Hai-Yan Huang, Su-Zhen Chen, Xi Li, Wen-Ting Zhang, Qi-QunTang*. Gdf6 induces commitment of pluripotent mesenchymal C3H10T1/2 cells to the adipocyte lineage. FEBS J. 2013Jun; 280(11):2644-51
12. Shu-fen Li, Liang Guo, Shu-wen Qian, Yuan Liu, You-You Zhang, Zhi-Chun Zhang, Yue Zhao, Jian-Yong Shou, Qi-Qun Tang, Xi Li*. G9a is transactivated by C/EBPβ to facilitate mitotic clonal expansion during 3T3-L1 preadipocytedifferentiation. Am JPhysiolEndocrinolMetab.
 2013;  304(9):E990-998  
13. Yuan Liu, Zhi-Chun Zhang,Shu-Wen Qian, You-you Zhang,Hai-yan Huang, Yan Tang,Liang Guo, Xi Li, and Qi-Qun Tang*. MicroRNA-140 promotes adipocyte lineage commitment of C3H10T1/2 pluripotent stem cell via targeting Osteopetrosis-associated transmembrane protein 1. J. Biol. Chem. 2013; 288(12):8222-30
14. Hai-Yan Huang, Su-Zhen Chen, Wen-Ting Zhang, Shan-Shan Wang, Yang Liu, Xi Li, Xia Sun, Yi-Ming Li, Bo Wen,Qun-Ying Lei,Qi-Qun Tang*. Induction of EMT-like response by BMP4 via up-regulation of lysyl oxidase is required for adipocyte lineage commitment. Stem Cell Research. 2013; 10(3): 278-287  
15. Wang Y, Chen Y, Tian F, Zhang J, Song Z, Wu Y, Han X, Hu W, Ma D, Cram D, Cheng W. Maternal Mosaicism Is a Significant Contributor to Discordant Sex Chromosomal Aneuploidies Associated with Noninvasive Prenatal Testing.ClinChem. 2013 Nov 5. [Epub ahead of print]
16. Sheng W, Qian Y, Wang H, Ma X, Zhang P, Diao L, An Q, Chen L, Ma D*, Huang G*. DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.BMC Med Genomics. 2013 Nov 1;6(1):46.  
17. Xu F, Wang YL, Chang JJ, Du SC, Diao L, Jiang N, Wang H, Ma D*, Zhang J*.Mammalian sterile 20-like kinase 1/2 inhibit Wnt/β-catenin signaling pathway by directly binding Casein kinase 1 epsilon.Biochem J. 2013 Nov 4. [Epub ahead of print]  
18. Wu Y, Ma XJ, Wang HJ, Li WC, Chen L, Ma D, Huang GY. Expression of Cx43-related microRNAs in patients with tetralogy of Fallot.World J Pediatr.2013 Oct 21. [Epub ahead of print]
19. Jin Zhang, Yingying Du, Fei Xu, Cheng Xu, Huijun Wang, Shanshan Deng, Tianyu Zhang, Duan Ma*. miRNA Deregulation in Right Ventricular Outflow Tract Myocardium of Non-syndromic Tetralogy of Fallot. Canadian Journal of Cardiology. 2013 Oct 18.
20. Yang L, Zhan GD, Ding JJ, Wang HJ, Ma D, Huang GY, Zhou WH.Psychiatric illness and intellectual disability in the prader-willi syndrome with different molecular defects - a meta analysis.PLoS One. 2013;8(8):e72640.
21. Wang Y, Zhu J, Chen Y, Lu S, Chen B, Zhao X, Wu Y, Han X, Ma D, Liu Z, Cram D, Cheng W. Two cases of placental T21 mosaicism: challenging the detection limits of non-invasive prenatal testing.PrenatDiagn. 2013 Aug 8:1-4.
22. Lin J, Zhao CB, Lu JH, Wang HJ, Zhu WH, Xi JY, Lu J, Luo SS, Ma D, Wang Y, Xiao BG, Lu CZ. Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS. Mitochondrial DNA. 2013 Jul 8. [Epub ahead of print]
23. Wei Sheng, YanyanQian, Huijun Wang, Xiaojing Ma, Ping Zhang, Long Chen, Duan Ma*, Guoying Huang*. Association between mRNA levels of DNMT1, DNMT3A, DNMT3B, MBD2 and LINE-1 methylation status in infants with tetralogy of Fallot. International Journal of Molecular Medicine. 2013 Jul 2.doi: 10.3892/ijmm.2013.1427. [Epub ahead of print]  
24. Zhang YL, Wang LN, Zhou WH, Zhang J, Wang HJ, Jiang Q, Deng SS, Li WH, Wang L, Li HW, Mao ZH, Ma D*. Tissue factor pathway inhibitor-2: A novel gene involved in zebrafish central nervous system development. Developemntal Biology.2013 Jun 22. [Epub ahead of print]  
25. Meng Y, Ma X, Zhang J, Wang H, Ma D, Huang G. The Genotype and Expression of the TGFβ2 Gene in Children With Congenital Conotruncal Defects.PediatrCardiol. 2013 May 28. [Epub ahead of print]  
26. Ting W, Yanyan Q, Jian H, Keqin H, Duan M*. The Relationship Between Insulin Resistance and CpG Island Methylation of LMNA Gene in Polycystic Ovary Syndrome.Cell Biochemistry and Biophysics. April 2013  
27. Yao G, Chen D, Wang H, Li S, Zhang J, Feng Z, Guo L, Yang Z, Yang S, Sun C, Zhang X, Ma D*. Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss. Acta Otolaryngol. 2013 May 3. [Epub ahead of print]  
28. Pan J, Ma D, Sun F, Liang W, Liu R, Shen W, Wang H, Ji Y, Hu R, Liu R, Luo X, Shi H. Over-expression of TFPI-2 promotes atherosclerotic plaque stability by inhibiting MMPs in apoE-/- mice. Int J Cardiol. 2013 Apr 19. [Epub ahead of print]  
29. Xu C, Wang H, He H, Zheng F, Chen Y, Zhang J, Lin X, Ma D*, Zhang H*. Low expression of TFPI-2 associated with poor survival outcome in patients with breast cancer. BMC Cancer. 2013 Mar 15;13(1):118. [Epub ahead of print]
30. Yao G, Li S, Chen D, Wang H, Zhang J, Feng Z, Guo L, Yang Z, Yang S, Sun C, Zhang X, Ma D*. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct. Int J PediatrOtorhinolaryngol. 2013;77(4):544-9
31. Xie K, Jin B, Li Y, Luo X, Zhu J, Ma D*, Shi H*. Modulating Autophagy Improves Cardiac Function in a Rat Model of Early-Stage Dilated Cardiomyopathy. Cardiology. 2013;125(1):60-68.
32. Sang Q, Yan X, Wang H, Feng R, Fei X, Ma D, Xing Q, Li Q, Zhao X, Jin L, He L, Li H, Wang L. Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11). PLoS One. 2013; 8(1):e55178
33. Li J, Cao Y, Ma XJ, Wang HJ, Zhang J, Luo X, Chen W, Wu Y, Meng Y, Zhang J, Yuan Y, Ma D*, Huang GY. Roles of miR-1-1 and miR-181c in ventricular septal defects. Int J Cardiol. 2013 Jan 23
34. Wu D, Chen Y, Xu C, Wang K, Wang H, Zheng F, Ma D*, Wang G*. Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in chinesevelocardiofacial syndrome patients. PLoS One. 2013; 8(1):e54404  
35. Li CL, Hao SJ, Wang HJ, Jin L, Qing FH, Zheng FY, Zhang P, Chen L, Ma D*, Zhang TY*. MicroRNA expression profiling and target genes study in congenital microtia. Int J PediatrOtorhinolaryngol. 2013;77(4):483-7.

版权所有:复旦大学代谢分子医学教育部重点实验室  技术支持:维程信息  电话:(021) 54237739
通讯地址:上海市医学院路138号238信箱  邮编:200032  Email:fenziyixue@yahoo.cn  传真:(021) 64033738