Le Zhang

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Area:
Epigenetics
Google:
"Le Zhang"
Mean distance: 16.08 (cluster 11)
 
SNBCP
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Publications

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Zhang L, Ettou S, Khalid M, et al. (2018) Eed, a member of the Polycomb group, is required for nephron differentiation and the maintenance of nephron progenitor cells. Development (Cambridge, England)
Ma Q, Chen C, Deng P, et al. (2016) Extremely Low-Frequency Electromagnetic Fields Promote In Vitro Neuronal Differentiation and Neurite Outgrowth of Embryonic Neural Stem Cells via Up-Regulating TRPC1. Plos One. 11: e0150923
Zhang YL, Zhou Z, Han WW, et al. (2016) Oleanolic Acid Inhibiting the Differentiation of Neural Stem Cells into Astrocyte by Down-Regulating JAK/STAT Signaling Pathway. The American Journal of Chinese Medicine. 44: 103-17
Zhang L, An XP, Liu XR, et al. (2015) Characterization of the Transcriptional Complexity of the Receptive and Pre-receptive Endometria of Dairy Goats. Scientific Reports. 5: 14244
Lin CM, Ma JM, Zhang L, et al. (2015) Inhibition of Transient Receptor Potential Melastain 7 Enhances Apoptosis Induced by TRAIL in PC-3 cells. Asian Pacific Journal of Cancer Prevention : Apjcp. 16: 4469-75
Zhou Z, Zhang L, Xie B, et al. (2015) FOXC2 promotes chemoresistance in nasopharyngeal carcinomas via induction of epithelial mesenchymal transition. Cancer Letters. 363: 137-45
Duan WX, He MD, Mao L, et al. (2015) NiO nanoparticles induce apoptosis through repressing SIRT1 in human bronchial epithelial cells. Toxicology and Applied Pharmacology. 286: 80-91
Chong CM, Shen M, Zhou ZY, et al. (2014) Discovery of a benzofuran derivative (MBPTA) as a novel ROCK inhibitor that protects against MPP⁺-induced oxidative stress and cell death in SH-SY5Y cells. Free Radical Biology & Medicine. 74: 283-93
Ma Q, Deng P, Zhu G, et al. (2014) Extremely low-frequency electromagnetic fields affect transcript levels of neuronal differentiation-related genes in embryonic neural stem cells. Plos One. 9: e90041
Goffin D, Allen M, Zhang L, et al. (2012) Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses. Nature Neuroscience. 15: 274-83
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