Jeremy D. Bushman

Molecular defects of ATP-sensitive potassium channels in congenital hyperinsulinism

S. Shyng, Jeremy D. Bushman, E. Pratt, 2012 .

Optimized expression vector for ion channel studies in Xenopus oocytes and mammalian cells using alfalfa mosaic virus

Feyza Sancar, Kelly Christopherson, Jeremy D. Bushman, 2007, Pflügers Archiv - European Journal of Physiology.

A Kir6.2 Pore Mutation Causes Inactivation of ATP-Sensitive Potassium Channels by Disrupting PIP2-Dependent Gating

S. Shyng, Jeremy D. Bushman, Qing Zhou, 2013, PloS one.

A proton current associated with sour taste: distribution and functional properties

E. Liman, W. Ye, Jeremy D. Bushman, 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Study of a glycine hinge in ATP-sensitive potassium channels

Jeremy D. Bushman, 2012 .

The K+ channel KIR2.1 functions in tandem with proton influx to mediate sour taste transduction

M. Nelson, W. S. Chick, S. Kinnamon, 2015, Proceedings of the National Academy of Sciences.

A k-mer based transcriptomics approach for antisense drug discovery targeting the Ewing’s family of tumors

P. Iversen, J. Summerton, A. Annalora, 2018, Oncotarget.

Destabilization of ATP-sensitive Potassium Channel Activity by Novel KCNJ11 Mutations Identified in Congenital Hyperinsulinism*

C. Stanley, A. Ganguly, C. Macmullen, 2008, Journal of Biological Chemistry.

Characterization and Functional Restoration of a Potassium Channel Kir6.2 Pore Mutation Identified in Congenital Hyperinsulinism*

C. Stanley, S. Shyng, Jeremy D. Bushman, 2009, The Journal of Biological Chemistry.