Kir2.3 isoform confers pH sensitivity to heteromeric Kir2.1/Kir2.3 channels in HEK293 cells

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi et al. · Cell · 2001 · 998 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the <i>KCNJ2</i> Gene

Silvia G. Priori, Sandeep V. Pandit, Ilaria Rivolta et al. · Circulation Research · 2005 · 624 citations · Full text

Life Sciences, Cardiology, Genetics +17

Rectification of the Background Potassium Current

Faramarz H. Samie, Omer Berenfeld, Justus Anumonwo et al. · Circulation Research · 2001 · 295 citations

Medicine, Cardiology, Physiology +17

Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification

S.D. Pegan, Christine Arrabit, Wei Zhou et al. · Nature Neuroscience · 2005 · 288 citations

Life Sciences, Biochemistry, Molecular Biology +8

Binding of the Inward Rectifier K+ Channel Kir 2.3 to PSD-95 Is Regulated by Protein Kinase A Phosphorylation

Noam A. Cohen, Jay E. Brenman, Solomon H. Snyder et al. · Neuron · 1996 · 264 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17