Zheng Xiang

Affiliations: 
University of California, San Francisco, San Francisco, CA 
Google:
"Zheng Xiang"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Zhang Y, Du Y, Li M, et al. (2020) Activity-based Genetically Encoded Fluorescent and Luminescent Probes for Detecting Formaldehyde in Living Cells. Angewandte Chemie (International Ed. in English)
Chen XH, Xiang Z, Hu YS, et al. (2014) Genetically encoding an electrophilic amino acid for protein stapling and covalent binding to native receptors. Acs Chemical Biology. 9: 1956-61
Xiang Z, Lacey VK, Ren H, et al. (2014) Proximity-enabled protein crosslinking through genetically encoding haloalkane unnatural amino acids. Angewandte Chemie (International Ed. in English). 53: 2190-3
Xiang Z, Ren H, Hu YS, et al. (2014) Erratum: Adding an unnatural covalent bond to proteins through proximity-enhanced bioreactivity Nature Methods. 11: 210-210
Coin I, Katritch V, Sun T, et al. (2013) Genetically encoded chemical probes in cells reveal the binding path of urocortin-I to CRF class B GPCR. Cell. 155: 1258-69
Kang JY, Kawaguchi D, Coin I, et al. (2013) In vivo expression of a light-activatable potassium channel using unnatural amino acids. Neuron. 80: 358-70
Xiang Z, Ren H, Hu YS, et al. (2013) Adding an unnatural covalent bond to proteins through proximity-enhanced bioreactivity. Nature Methods. 10: 885-8
Parrish AR, She X, Xiang Z, et al. (2012) Expanding the genetic code of Caenorhabditis elegans using bacterial aminoacyl-tRNA synthetase/tRNA pairs. Acs Chemical Biology. 7: 1292-302
Johnson DB, Xu J, Shen Z, et al. (2011) RF1 knockout allows ribosomal incorporation of unnatural amino acids at multiple sites. Nature Chemical Biology. 7: 779-86
Xiang Z, Wang L. (2011) Enantiospecific synthesis of genetically encodable fluorescent unnatural amino acid L-3-(6-acetylnaphthalen-2-ylamino)-2-aminopropanoic acid. The Journal of Organic Chemistry. 76: 6367-71
See more...