7
References
1. Conn, P.J., et al., Opportunities and challenges
in the discovery of allosteric modulators of
GPCRs for treating CNS disorders. Nat Rev
Drug Discov, 2014. 13(9): p. 692-708.
2. Wootten, D., A. Christopoulos, and P.M. Sexton,
Emerging paradigms in GPCR allostery:
implications for drug discovery. Nat Rev Drug
Discov, 2013. 12(8): p. 630-44.
3. Zheng, X., et al., Expression, stabilization and
purification of membrane proteins via diverse
protein synthesis systems and detergents
involving cell-free associated with self-assembly
peptide surfactants. Biotechnol Adv, 2014.
32(3): p. 564-74.
4. Chiu, M.L., et al., Over-expression,
solubilization, and purification of G protein-
coupled receptors for structural biology. Comb
Chem High Throughput Screen, 2008. 11(6): p.
439-62.
5. Walter, E.G. and D.E. Taylor, Comparison of
tellurite resistance determinants from the IncP
alpha plasmid RP4Ter and the IncHII plasmid
pHH1508a. J Bacteriol, 1989. 171(4): p. 2160-5.
6. Turner, R.J., D.E. Taylor, and J.H. Weiner,
Expression of Escherichia coli TehA gives
resistance to antiseptics and disinfectants
similar to that conferred by multidrug resistance
efflux pumps. Antimicrob Agents Chemother,
1997. 41(2): p. 440-4.
7. Chen, Y.H., et al., Homologue structure of the
SLAC1 anion channel for closing stomata in
leaves. Nature, 2010. 467(7319): p. 1074-80.
8. Maierhofer, T., et al., A Single-Pore Residue
Renders the Arabidopsis Root Anion Channel
SLAH2 Highly Nitrate Selective. Plant Cell,
2014. 26(6): p. 2554-2567.
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