M. Regan
发表
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant‐negative, or hypomorphic alleles
Patrick R. Cushing,
Caroline L. Speck,
S. Griffey,
2007,
The EMBO journal.
A. Craig,
M. Regan,
J. Elegheert,
2017,
Neuron.
M. Regan,
Hiro Furukawa,
A. Romero-Hernandez,
2015,
Current opinion in structural biology.
M. Regan,
D. Liotta,
Zongjian Zhu,
2019,
Nature Communications.
L. Wollmuth,
Huan‐Xiang Zhou,
M. Regan,
2017,
The Journal of general physiology.
M. Regan,
T. Grant,
Hiro Furukawa,
2018,
Neuron.
N. Grigorieff,
M. Regan,
S. Traynelis,
2018
.
R. Dingledine,
M. Regan,
S. Traynelis,
2023,
ACS chemical neuroscience.
Qingyu Wu,
M. Regan,
D. Jackson,
2018,
PLoS genetics.
John H. Bushweller,
Edward E. Pryor,
David S. Cafiso,
2013,
Proceedings of the National Academy of Sciences.
Remy A. Yovanno,
M. Regan,
Hiro Furukawa,
2022,
Nature Communications.
M. Regan,
Hiro Furukawa,
E. Karakas,
2015,
Trends in biochemical sciences.
M. Regan,
Hiro Furukawa,
2016,
Neuron.
M. Regan,
Hiro Furukawa,
2019
.