S. Miller

发表

Site-Selective N-Methylation of Peptides on Solid Support

T. Scanlan, S. Miller, 1997 .

oNBS−SPPS: A New Method for Solid-Phase Peptide Synthesis

T. Scanlan, S. Miller, 1998 .

Robust light emission from cyclic alkylaminoluciferin substrates for firefly luciferase.

Stephen C. Miller, G. R. Reddy, S. Miller, 2010, Journal of the American Chemical Society.

A synthetic luciferin improves bioluminescence imaging in live mice

Jennifer A. Prescher, Stephen C. Miller, Miranda A. Paley, 2014, Nature Methods.

Firefly Luciferase Mutants Allow Substrate-Selective Bioluminescence Imaging in the Mouse Brain.

D. M. Mofford, S. Miller, Spencer T. Adams, 2016, Angewandte Chemie.

Lessons Learned from Luminous Luciferins and Latent Luciferases.

D. M. Mofford, S. Miller, Spencer T. Adams, 2018, ACS chemical biology.

Labeling Tetracysteine‐Tagged Proteins with a SplAsH of Color: A Modular Approach to Bis‐Arsenical Fluorophores

S. Miller, A. Bhunia, 2007, Chembiochem : a European journal of chemical biology.

Synthesis of near-IR fluorescent oxazine dyes with esterase-labile sulfonate esters.

S. Miller, Steven M. Pauff, 2011, Organic letters.

Silicon functionalization expands the repertoire of Si-rhodamine fluorescent probes

Xincai Ji, S. Miller, Desaboini Nageswara Rao, 2022, Chemical science.

Reductively-labile sulfonate ester protecting groups that are rapidly cleaved by physiological glutathione.

S. Miller, Adam Choi, 2017, Organic & biomolecular chemistry.

Enzymatic promiscuity and the evolution of bioluminescence

S. Miller, Spencer T. Adams, 2019, The FEBS journal.

A trifluoroacetic acid-labile sulfonate protecting group and its use in the synthesis of a near-IR fluorophore.

S. Miller, Steven M. Pauff, 2013, The Journal of organic chemistry.

Profiling sulfonate ester stability: identification of complementary protecting groups for sulfonates.

S. Miller, 2010, The Journal of organic chemistry.

Design and application of esterase-labile sulfonate protecting groups.

S. Miller, Laert Rusha, 2011, Chemical communications.

Latent luciferase activity in the fruit fly revealed by a synthetic luciferin

S. Miller, D. M. Mofford, G. R. Reddy, 2014, Proceedings of the National Academy of Sciences.

Beyond D-luciferin: expanding the scope of bioluminescence imaging in vivo.

S. Miller, Spencer T. Adams, 2014, Current opinion in chemical biology.

Bioluminescence imaging in mice with synthetic luciferin analogues.

Xincai Ji, S. Miller, Spencer T. Adams, 2020, Methods in enzymology.

Luciferase Activity of Insect Fatty Acyl-CoA Synthetases with Synthetic Luciferins.

D. M. Mofford, G. R. Reddy, S. Miller, 2017, ACS Chemical Biology.

Rapid Access to a Broad Range of 6'-Substituted Firefly Luciferin Analogues Reveals Surprising Emitters and Inhibitors.

S. Miller, Spencer T. Adams, Kate L. Liebmann, 2017, Organic letters.

Sulfonamides Are an Overlooked Class of Electron Donors in Luminogenic Luciferins and Fluorescent Dyes.

S. Miller, Spencer T. Adams, Kate L. Liebmann, 2018, Organic letters.

Aminoluciferins Extend Firefly Luciferase Bioluminescence into the Near-Infrared and Can Be Preferred Substrates over d-Luciferin

D. M. Mofford, G. R. Reddy, S. Miller, 2014, Journal of the American Chemical Society.

Palladium-Mediated Synthesis of a Near-Infrared Fluorescent K+ Sensor.

W. R. Kobertz, H. Bandara, S. Miller, 2017, The Journal of organic chemistry.

Supplemental Information Identification of Mutant Firefly Luciferases that Efficiently Utilize Aminoluciferins

Katryn R. Harwood, D. M. Mofford, G. R. Reddy, 2011 .

A biocompatible in vivo ligation reaction and its application for noninvasive bioluminescent imaging of protease activity in living mice.

D. Hanahan, M. Bogyo, Ke Cheng, 2013, ACS chemical biology.

Coupling between trans/cis proline isomerization and protein stability in staphylococcal nuclease

J. R. Somoza, J. Markley, K. Prehoda, 1996, Protein science : a publication of the Protein Society.

Methods for Detecting PER2:LUCIFERASE Bioluminescence Rhythms in Freely Moving Mice

D. Weaver, M. Harrington, V. van der Vinne, 2021, Journal of biological rhythms.

Methods for detecting PER2::LUCIFERASE bioluminescence rhythms in freely moving mice

D. Weaver, M. Harrington, V. van der Vinne, 2020, bioRxiv.

Luciferin Amides Enable in Vivo Bioluminescence Detection of Endogenous Fatty Acid Amide Hydrolase Activity

D. M. Mofford, G. R. Reddy, G. S. Kiran, 2015, Journal of the American Chemical Society.

Luciferins behave like drugs.

D. M. Mofford, S. Miller, 2015, ACS chemical neuroscience.

Leveraging a Small‐Molecule Modification to Enable the Photoactivation of Rho GTPases

Katryn R. Harwood, S. Miller, 2009, Chembiochem : a European journal of chemical biology.

Firefly luciferin methyl ester illuminates the activity of multiple serine hydrolases.

S. Miller, Innus Mohammad, Kate L Liebmann, 2023, Chemical communications.

FruitFire: a luciferase based on a fruit fly metabolic enzyme

C. Schiffer, M. Bohn, S. Miller, 2023, bioRxiv.

Computational investigation into the fluorescence of luciferin analogues

Thom Vreven, Stephen C. Miller, T. Vreven, 2018, J. Comput. Chem..

Silicon Substitution in Oxazine Dyes Yields Near-Infrared Azasiline Fluorophores That Absorb and Emit beyond 700 nm.

S. Miller, Adam Choi, 2018, Organic letters.