Curtis J. Layton, Ph.D.
Affiliations: | 2010 | Biochemistry | Duke University, Durham, NC |
Area:
Biochemistry, General BiophysicsGoogle:
"Curtis Layton"Mean distance: 7962.6
Parents
Sign in to add mentor| Homme W. Hellinga | grad student | 2010 | Duke | |
| (Analysis and redesign of protein-protein interactions: A hotspot-centric view.) | ||||
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Publications
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| Jarmoskaite I, Denny SK, Vaidyanathan PP, et al. (2019) A Quantitative and Predictive Model for RNA Binding by Human Pumilio Proteins. Molecular Cell |
| Layton CJ, McMahon PL, Greenleaf WJ. (2019) Large-Scale, Quantitative Protein Assays on a High-Throughput DNA Sequencing Chip. Molecular Cell. 73: 1075-1082.e4 |
| She R, Chakravarty AK, Layton CJ, et al. (2017) Comprehensive and quantitative mapping of RNA-protein interactions across a transcribed eukaryotic genome. Proceedings of the National Academy of Sciences of the United States of America |
| Buenrostro JD, Araya CL, Chircus LM, et al. (2014) Quantitative analysis of RNA-protein interactions on a massively parallel array reveals biophysical and evolutionary landscapes. Nature Biotechnology. 32: 562-8 |
| Layton CJ, Hellinga HW. (2011) Integration of cell-free protein coexpression with an enzyme-linked immunosorbent assay enables rapid analysis of protein-protein interactions directly from DNA. Protein Science : a Publication of the Protein Society. 20: 1432-8 |
| Layton CJ, Hellinga HW. (2011) Quantitation of protein-protein interactions by thermal stability shift analysis. Protein Science : a Publication of the Protein Society. 20: 1439-50 |
| Layton CJ, Hellinga HW. (2010) Thermodynamic analysis of ligand-induced changes in protein thermal unfolding applied to high-throughput determination of ligand affinities with extrinsic fluorescent dyes. Biochemistry. 49: 10831-41 |