Y. B. Liu

Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

William B Dobyns, Allison Brashear, L. Ozelius, 2015, Epilepsia.

Impaired AQP2 trafficking in Fxyd1 knockout mice: A role for FXYD1 in regulated vesicular transport

R. Bouley, K. Sweadner, E. Arystarkhova, 2017, PloS one.

Hyperplasia of Pancreatic Beta Cells and Improved Glucose Tolerance in Mice Deficient in the FXYD2 Subunit of Na,K-ATPase*

J. Kaplan, G. Kidder, K. Sweadner, 2013, The Journal of Biological Chemistry.

Oxidative inhibition of the vascular Na+-K+ pump via NADPH oxidase-dependent β1-subunit glutathionylation: implications for angiotensin II-induced vascular dysfunction.

G. Figtree, R. Weisbrod, R. Cohen, 2013, Free radical biology & medicine.

A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1

K. Khodakhah, A. Brashear, T. Hampton, 2015, eLife.

Paradoxical activation of the sodium chloride cotransporter (NCC) without hypertension in kidney deficient in a regulatory subunit of Na,K‐ATPase, FXYD2

R. Bouley, A. McDonough, K. Sweadner, 2014, Physiological reports.