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Austin Hopiavuori
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Homozygous expression of mutant ELOVL4 leads to seizures and death in a novel animal model of very long-chain fatty acid deficiency
BR Hopiavuori, F Deák, JL Wilkerson, RS Brush, NA Rocha-Hopiavuori, ...
Molecular Neurobiology 55, 1795-1813, 2018
322018
Investigation and restoration of BEST1 activity in patient-derived RPEs with dominant mutations
C Ji, Y Li, A Kittredge, A Hopiavuori, N Ward, P Yao, Y Fukuda, Y Zhang, ...
Scientific reports 9 (1), 19026, 2019
312019
Structural and functional characterization of the bestrophin-2 anion channel
AP Owji, Q Zhao, C Ji, A Kittredge, A Hopiavuori, Z Fu, N Ward, OB Clarke, ...
Nature structural & molecular biology 27 (4), 382-391, 2020
282020
Dual Ca2+-dependent gates in human Bestrophin1 underlie disease-causing mechanisms of gain-of-function mutations
C Ji, A Kittredge, A Hopiavuori, N Ward, S Chen, Y Fukuda, Y Zhang, ...
Communications Biology 2 (1), 240, 2019
162019
Expression and purification of mammalian bestrophin ion channels
A Kittredge, N Ward, A Hopiavuori, Y Zhang, T Yang
JoVE (Journal of Visualized Experiments), e57832, 2018
72018
Dual Ca [supercript 2+]-dependent gates in human Bestrophin1 underlie disease-causing mechanisms of g
C Ji, A Kittredge, A Hopiavuori, N Ward, S Chen, Y Fukuda, Y Zhang, ...
Commun. Biol. 2, 2019
2019
Dissecting the Structure and Function of Bestrophin Channels
A Kittredge, C Ji, A Hopiavuori, N Ward, S Chen, Y Fukuda, Y Zhang, ...
Biophysical Journal 116 (3), 399a-400a, 2019
2019
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Articles 1–7