25 Q. Zhao, C. Ren, L. Liu, J. Chen, Y. Shao, N. Sun, R. Sun, Y. Kong, X. Ding, X. Zhang, Y. Xu, B. Yang, Q. Yin,* X. Yang*;B. Jiang*, J Med Chemy, 2019, 62, 9281-9298.
24 Huang, R.; Zhu W.; Wu Y.; Chen, J. K.; Yu, J. H.; Jiang, B.*;Chen, H. L.*; Chen, W. Z.*,A novel mass spectrometry-cleavable, phosphate-based enrichableand multi-targeting protein cross-linkerChem. Sci., 2019, 10, 6443-6447.
23 Qiu, X.; Sun, N.; Kong, Y.; Li, Y.; Yang, X.*; Jiang, B.*, Chemoselective Synthesis of Lenalidomide-Based PROTAC Library Using Alkylation Reaction. Org Lett2019, 21 (10), 3838-3841.
22 Huang, R.; Li, Z. H.; Yu, J. H.; Chen, H. L.*; Jiang, B.*,H2O‑Regulated Chemoselectivity in Oxa- Versus Aza-Michael Reactions,Org. Lett., 2019, 21, 4159-4162.
22 Huang, R.; Li, Z. H.; Sheng, Y.; Yu, J. H.; Wu, Y.; Zhan, Y. X.; Chen, H. L.*; Jiang, B.*, N-Methyl- N-phenylvinylsulfonamides for Cysteine-Selective Conjugation,Org. Lett., 2018, 20, 6526-6529.
21 Huang, R.; Li, Z. H.; Ren, P. L.; Chen, W. Z.; Kuang, Y. Y.; Chen, J. K.; Zhan, Y. X.; Chen, H. L.*; Jiang, B.*,N‐Phenyl‐N‐aceto‐vinylsulfonamides as Efficient and Chemoselective Handles for N‐Terminal Modification of Peptides and Proteins,Eur. J. Org. Chem.2018, 829-836.
20 Li, Z. H.; Huang, R.; Xu, H. T.; Chen, J. K.; Zhan, Y. X.; Zhou, X. H.; Chen, H. L.*; Jiang, B.* Divinylsulfonamides as Specific Linkers for Stapling Disulfide Bonds in Peptides Org. Lett., 2017, 19, 4972–4975
19 Chen, H. L.*; Huang, R.; Li, Z. H.; Zhu, W.; Chen, J. K.; Zhan, Y. X.; Jiang, B.* Selective lysine modification of native peptides via aza-Michael addition, Org. Biomol. Chem.2017, 15, 7339 – 7345
18 Liu, X. Y.; Xu, H. T.; Zhan, Y. X.; Ma, P. X.*; Chen, H. L.*; Jiang, B.* Tris(2-carboxyethyl)phosphine promotes hydrolysis of imonoboronates Tetrahedron Lett., 2017, 58, 3101-3106
17 Wang, H.; Zhou, F.; Ren, G.R.; Zheng, Q. H.; Chen, H. L.; Gao, B.; Klivansky, L.; Liu, Y.; Wu, B.; Xiu, Q. F.; Lu, J. M.; Sharpless, K. B.; Wu, P. SuFEx-Based Polysulfonate Formation from Ethenesulfonyl Fluoride-Amine Adducts Angew Chem Int Ed Engl; 2017, 56, 11203 –11208.
16 Chen, H. L.*; Han, C. J.; Wu, J.; Liu, X. Y.; Zhan, Y. X.; Chen, J. K.; Chen, Y. K.; Gu, R. N.; Zhang, L.; Chen, S. S.; Jia, J.; Zhen, X. C.; Zheng, L. T.*; Jiang, B.* Accessible Method for the Development of Novel Sterol Analogues with Dipeptide-like Side Chains That Act as Neuroinflammation Inhibitors ACS Chem. Neurosci.2016, 7, 305-315.
15. Mao D., Dr. Liang Y., Liu Y., Zhou X., Ma J., Prof. Jiang B.*, Prof. Liu J.*, Prof. Ma D.*, Acid-Labile Acyclic Cucurbit[n]uril Molecular Containers for Controlled Release - Angewandte Chemie International Edition DOI: 10.1002/anie.201707164
14. Liu J. and Shui S.L. (2016) Delivery methods for site-specific nucleases: Achieving the full potential of therapeutic gene editing. J Control Release 244(Pt A):83-97 doi: 10.1016/j.jconrel.2016.11.014.
13. Gaj T., Sirk S.J., Shui S.-l., and Liu J. (2016) Genome-Editing Technologies: Principles and Applications. Cold Spring Harbor Perspectives in Biology:a023754 doi: 10.1101/cshperspect.a023754.
12. Liu S.S., Wei X., Ji Q., Xin X., Jiang B*., and Liu J*. (2016) A facile and efficient transposon mutagenesis method for generation of multi-codon deletions in protein sequences. J Biotechnol 227:27-34 doi: 10.1016/j.jbiotec.2016.03.038.
11. ChenH., Han C., Wu J., Liu X., Zhan Y., Chen J., Chen Y., Gu R., Zhang L., Chen S.,Jia J., Zhen X., Zheng L.T., and Jiang B. (2016) Accessible Method for theDevelopment of Novel Sterol Analogues with Dipeptide-like Side Chains That Actas Neuroinflammation Inhibitors. ACS ChemNeurosci 7(3):305-315 doi: 10.1021/acschemneuro.5b00256.
10.Liu J., Gaj T., Yang Y., Wang N., Shui S., Kim S., Kanchiswamy C.N., Kim J.S., and Barbas C.F., 3rd (2015) Efficient delivery of nuclease proteins for genome editing in human stem cells and primary cells. Nat Protoc 10(11):1842-1859 doi: 10.1038/nprot.2015.117.
9. (Review article in Chinese)Pang X.N.,Hong X., Wei X., Chen X.W., Liu J.*, and Chen D.F.*(2015). Research progress inphysicochemical characteristics of lactoferrin and its recombinant expressionsystems.Hereditas (Beijing),37(9): 873-884 doi: 10.16288/j.yczz.15-146 (庞晓楠, 弘笑, 魏璇, 陈喜文, 刘佳*, 陈德富*(2015). 乳铁蛋白的理化性质及其重组表达系统的研究进展. 遗传, 37(9): 873-884 doi: 10.16288/j.yczz.15-146)
8. Sun Y., Liu J., Jiang X., Sun T., Liu L., Zhang X., Ding S., Li J., Zhuang Y., Wang Y., and Wang R. (2015) One-Step Synthesis of Chiral Oxindole-type Analogues with Potent Anti-inflammatory and Analgesic Activities. Sci Rep 5:13699 doi: 10.1038/srep13699.
7. Liu S.S., Wei X., Dong X., Xu L., Liu J., and Jiang B. (2015) Structural plasticity of green fluorescent protein to amino acid deletions and fluorescence rescue by folding-enhancing mutations. BMC Biochem 16(1):17 doi: 10.1186/s12858-015-0046-5.
6. Wu J., Du J., Gu R., Zhang L., Zhen X., Li Y., Chen H., Jiang B., and Zheng L. (2015) Inhibition of neuroinflammation by synthetic androstene derivatives incorporating amino acid methyl esters on activated BV-2 microglia. ChemMedChem 10(4):610-616 doi: 10.1002/cmdc.201500027.
5. Liu J., Gaj T., Wallen M.C., and Barbas C.F., 3rd (2015) Improved cell-penetrating zinc-finger nuclease proteins for precision genome engineering. Mol Ther Nucleic Acids 4:e232 doi: 10.1038/mtna.2015.6.
4. Gaj T. and Liu J. (2015) Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains. J Vis Exp (97) doi: 10.3791/52814.
3. Liu, J., Sun, Y., Zhang, X., Liang, X., Wu, Y., Wang, Y. and Jiang, X. (2014) Spirooxindoles, a potential novel class of anti-inflammatory agents. Inflamm. Cell Signal. 1: e372 doi: 10.14800/ics.372.
2. Lin Y., Qiu Y., Xu C., Liu Q., Peng B., Kaufmann G.F., Chen X., Lan B., Wei C., Lu D., Zhang Y., Guo Y., Lu Z., Jiang B., Edgington T.S., and Guo F. (2014) Functional role of asparaginyl endopeptidase ubiquitination by TRAF6 in tumor invasion and metastasis. J Natl Cancer Inst 106(4):dju012 doi: 10.1093/jnci/dju012.
1. Jiang B., Li M.M., Xing P., and Huang Z.G. (2013) A concise formal synthesis of (-)-hamigeran B.Org Lett 15(4):871-873 doi: 10.1021/ol400030a.
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