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Tian-Lin Cheng - Publications

Affiliations: 
2008-2019 Institute of Neuroscience, Chinese Academy of Sciences, Shanghai, China 
 2020- Fudan university, Shanghai, Shanghai Shi, China 
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20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Wu SH, Li X, Qin DD, Zhang LH, Cheng TL, Chen ZF, Nie BB, Ren XF, Wu J, Wang WC, Hu YZ, Gu YL, Lv LB, Yin Y, Hu XT, et al. Corrigendum to "Induction of core symptoms of autism spectrum disorders by in vivo CRISPR/Cas9-based gene editing in the brain of adolescent rhesus monkeys" [Sci. Bull. 66(9) (2021) 937-946. Science Bulletin. PMID 36842864 DOI: 10.1016/j.scib.2023.02.025  0.493
2023 Zhang S, Song L, Yuan B, Zhang C, Cao J, Chen J, Qiu J, Tai Y, Chen J, Qiu Z, Zhao XM, Cheng TL. TadA reprogramming to generate potent miniature base editors with high precision. Nature Communications. 14: 413. PMID 36702845 DOI: 10.1038/s41467-023-36004-2  0.554
2023 Zhang S, Yuan B, Cao J, Song L, Chen J, Qiu J, Qiu Z, Zhao XM, Chen J, Cheng TL. TadA orthologs enable both cytosine and adenine editing of base editors. Nature Communications. 14: 414. PMID 36702837 DOI: 10.1038/s41467-023-36003-3  0.555
2020 Sun L, Chen R, Li L, Yuan B, Song K, Pan N, Cheng TL, Chang S, Lin K, He X, Wu Q, Xu F, Qiu Z, Wang X. Visualization and correction of social abnormalities-associated neural ensembles in adult MECP2 duplication mice. Science Bulletin. 65: 1192-1202. PMID 36659149 DOI: 10.1016/j.scib.2020.03.026  0.536
2020 Wu SH, Li X, Qin DD, Zhang LH, Cheng TL, Chen ZF, Nie BB, Ren XF, Wu J, Wang WC, Hu YZ, Gu YL, Lv LB, Yin Y, Hu XT, et al. Induction of core symptoms of autism spectrum disorder by in vivo CRISPR/Cas9-based gene editing in the brain of adolescent rhesus monkeys. Science Bulletin. 66: 937-946. PMID 36654241 DOI: 10.1016/j.scib.2020.12.017  0.585
2020 Li S, Yuan B, Cao J, Chen J, Chen J, Qiu J, Zhao XM, Wang X, Qiu Z, Cheng TL. Docking sites inside Cas9 for adenine base editing diversification and RNA off-target elimination. Nature Communications. 11: 5827. PMID 33203850 DOI: 10.1038/s41467-020-19730-9  0.527
2020 He X, Chen W, Liu Z, Yu G, Chen Y, Cai YJ, Sun L, Xu W, Zhong L, Gao C, Chen J, Zhang M, Yang S, Yao Y, Zhang Z, ... ... Cheng TL, et al. Efficient and risk-reduced genome editing using double nicks enhanced by bacterial recombination factors in multiple species. Nucleic Acids Research. PMID 32232370 DOI: 10.1093/nar/gkaa195  0.536
2020 Yu B, Yuan B, Dai JK, Cheng TL, Xia SN, He LJ, Yuan YT, Zhang YF, Xu HT, Xu FQ, Liang ZF, Qiu ZL. Reversal of Social Recognition Deficit in Adult Mice with MECP2 Duplication via Normalization of MeCP2 in the Medial Prefrontal Cortex. Neuroscience Bulletin. PMID 32144612 DOI: 10.1007/S12264-020-00467-W  0.563
2019 Cheng TL, Li S, Yuan B, Wang X, Zhou W, Qiu Z. Expanding C-T base editing toolkit with diversified cytidine deaminases. Nature Communications. 10: 3612. PMID 31399578 DOI: 10.1038/s41467-019-11562-6  0.487
2017 Cheng TL, Qiu Z. Long non-coding RNA tagging and expression manipulation via CRISPR/Cas9-mediated targeted insertion. Protein & Cell. PMID 28875452 DOI: 10.1007/s13238-017-0464-9  0.517
2017 Wen Z, Cheng TL, Li GZ, Sun SB, Yu SY, Zhang Y, Du YS, Qiu Z. Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation. Molecular Autism. 8: 43. PMID 28785396 DOI: 10.1186/s13229-017-0157-5  0.579
2017 Wen Z, Cheng TL, Yin DZ, Sun SB, Wang Z, Yu SY, Zhang Y, Qiu Z, Du YS. Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing. Neuroscience Bulletin. PMID 28283807 DOI: 10.1007/S12264-017-0119-0  0.517
2017 Cheng TL, Chen J, Wan H, Tang B, Tian W, Liao L, Qiu Z. Regulation of mRNA splicing by MeCP2 via epigenetic modifications in the brain. Scientific Reports. 7: 42790. PMID 28211484 DOI: 10.1038/srep42790  0.561
2016 Yuan B, Cheng TL, Yang K, Zhang X, Qiu Z. Autism-related protein MeCP2 regulates FGF13 expression and emotional behaviors. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 27916441 DOI: 10.1016/j.jgg.2016.10.004  0.511
2016 Lyu JW, Yuan B, Cheng TL, Qiu ZL, Zhou WH. Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs. Scientific Reports. 6: 20392. PMID 26843422 DOI: 10.1038/srep20392  0.593
2016 Liu Z, Li X, Zhang JT, Cai YJ, Cheng TL, Cheng C, Wang Y, Zhang CC, Nie YH, Chen ZF, Bian WJ, Zhang L, Xiao J, Lu B, Zhang YF, et al. Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2. Nature. PMID 26808898 DOI: 10.1038/Nature16533  0.583
2014 He LJ, Liu N, Cheng TL, Chen XJ, Li YD, Shu YS, Qiu ZL, Zhang XH. Conditional deletion of Mecp2 in parvalbumin-expressing GABAergic cells results in the absence of critical period plasticity. Nature Communications. 5: 5036. PMID 25297674 DOI: 10.1038/Ncomms6036  0.544
2014 Cheng TL, Qiu Z. MeCP2: multifaceted roles in gene regulation and neural development. Neuroscience Bulletin. 30: 601-9. PMID 25082535 DOI: 10.1007/s12264-014-1452-6  0.594
2014 Cheng TL, Wang Z, Liao Q, Zhu Y, Zhou WH, Xu W, Qiu Z. MeCP2 suppresses nuclear microRNA processing and dendritic growth by regulating the DGCR8/Drosha complex. Developmental Cell. 28: 547-60. PMID 24636259 DOI: 10.1016/j.devcel.2014.01.032  0.582
2013 Lv JW, Cheng TL, Qiu ZL, Zhou WH. Role of the PTEN signaling pathway in autism spectrum disorder. Neuroscience Bulletin. 29: 773-8. PMID 24136242 DOI: 10.1007/s12264-013-1382-3  0.559
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