Hao Qian, Ph.D.

Affiliations: 
2007-2013 Institute of Biophysics, Chinese Academy of Sciences, Beijing, Beijing Shi, China 
 2013-2021 CMM University of California, San Diego, La Jolla, CA 
 2021- School of Medicine University of Electronic Science and Technology of China, Chengdu Shi, Sichuan Sheng, China 
Area:
Interaction between neurons and oligodendrocytes
Website:
https://faculty.uestc.edu.cn/qianhao/zh_CN/index.htm
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"Hao Qian"
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Mean distance: 106866
 
Cross-listing: Chemistry Tree

Parents

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Jin-Hui Wang grad student 2007-2013
Xiang-Dong Fu post-doc 2013-2021 (Chemistry Tree)
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Publications

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Hao Y, Hu J, Xue Y, et al. (2023) Reply to: Ptbp1 deletion does not induce astrocyte-to-neuron conversion. Nature. 618: E8-E13
Qian H, Fu XD. (2021) Brain Repair by Cell Replacement via In Situ Neuronal Reprogramming. Annual Review of Genetics
Qian H, Kang X, Hu J, et al. (2020) Author Correction: Reversing a model of Parkinson's disease with in situ converted nigral neurons. Nature
Qian H, Kang X, Hu J, et al. (2020) Reversing a model of Parkinson's disease with in situ converted nigral neurons. Nature. 582: 550-556
Hu J, Qian H, Xue Y, et al. (2018) PTB/nPTB: master regulators of neuronal fate in mammals. Biophysics Reports. 4: 204-214
Chen L, Chen JY, Huang YJ, et al. (2018) The Augmented R-Loop Is a Unifying Mechanism for Myelodysplastic Syndromes Induced by High-Risk Splicing Factor Mutations. Molecular Cell. 69: 412-425.e6
Chen L, Chen JY, Zhang X, et al. (2017) R-ChIP Using Inactive RNase H Reveals Dynamic Coupling of R-loops with Transcriptional Pausing at Gene Promoters. Molecular Cell
Yang Z, Chen N, Ge R, et al. (2017) Functional compatibility between Purkinje cell axon branches and their target neurons in the cerebellum. Oncotarget. 8: 72424-72437
Xue Y, Qian H, Hu J, et al. (2016) Sequential regulatory loops as key gatekeepers for neuronal reprogramming in human cells. Nature Neuroscience
Zhang ZN, Freitas BC, Qian H, et al. (2016) Layered hydrogels accelerate iPSC-derived neuronal maturation and reveal migration defects caused by MeCP2 dysfunction. Proceedings of the National Academy of Sciences of the United States of America
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