Found 38 results
Filters: Author is Lieberman, Raquel L  [Clear All Filters]
S. D. Orwig, Tan, Y. Lei, Grimster, N. P., Yu, Z., Powers, E. T., Kelly, J. W., and Lieberman, R. L., Binding of 3,4,5,6-tetrahydroxyazepanes to the acid-β-glucosidase active site: implications for pharmacological chaperone design for Gaucher disease., Biochemistry, vol. 50, no. 49, pp. 10647-57, 2011.
S. D. Orwig and Lieberman, R. L., Biophysical characterization of the olfactomedin domain of myocilin, an extracellular matrix protein implicated in inherited forms of glaucoma., PLoS One, vol. 6, no. 1, p. e16347, 2011.
J. C. Pai, Culver, J. A., Drury, J. E., Motani, R. S., Lieberman, R. L., and Maynard, J. A., Conversion of scFv peptide-binding specificity for crystal chaperone development., Protein Eng Des Sel, vol. 24, no. 5, pp. 419-28, 2011.
R. L. Lieberman, Culver, J. A., Entzminger, K. C., Pai, J. C., and Maynard, J. A., Crystallization chaperone strategies for membrane proteins., Methods, vol. 55, no. 4, pp. 293-302, 2011.
R. L. Lieberman, A Guided Tour of the Structural Biology of Gaucher Disease: Acid-β-Glucosidase and Saposin C, Enzyme Research, vol. 2011, 2011.
R. L. Lieberman, Sneak peak at galactocerebrosidase, Krabbe disease's lysosomal hydrolase., Proc Natl Acad Sci U S A, vol. 108, no. 37, pp. 15017-8, 2011.
N. J Burns, Turnage, K. C., Walker, C. A., and Lieberman, R. L., The stability of myocilin olfactomedin domain variants provides new insight into glaucoma as a protein misfolding disorder., Biochemistry, vol. 50, no. 26, pp. 5824-33, 2011.