AbstractArginine residue at position 285 (R285) in the intracellular C-terminal domain of inward rectifier potassium channel Kir2.2 is conserved in many species, but missing in previously reported human Kir2.2 sequences. We here identified the human Kir2.2 gene in normal individuals, which contained R285 in the deduced amino-acid sequence (hKir2.2/R285). All 30 individuals we examined were homozygous for Kir2.2/R285 gene. The hKir2.2/R285 was electrophysiologically functional in both mammalian cells and Xenopus oocytes. However, the hKir2.2 missing R285 was functional only in Xenopus oocytes, but not in mammalian cells. Thus, R285 in Kir2.2 is important for its functional expression in mammalian cells
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...
A 2 P domain potassium channel expressed in eye, lung, and stomach, Kcnk8, has recently been identif...
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...
AbstractArginine residue at position 285 (R285) in the intracellular C-terminal domain of inward rec...
AbstractWe have identified several cDNAs for the human Kir5.1 subunit of inwardly rectifying K+ chan...
AbstractWe have cloned the human genes encoding the inwardly rectifying K+ (Kir) channel subunits, K...
AbstractA new member of the two transmembrane domain potassium (K+) channel family was identified an...
AbstractWe have identified several cDNAs for the human Kir5.1 subunit of inwardly rectifying K+ chan...
AbstractWe have cloned the human genes encoding the inwardly rectifying K+ (Kir) channel subunits, K...
AbstractWe have cloned a novel inward rectifier K+ channel (hIRK2) from a human frontal cortex cDNA ...
For many model organisms traditionally in use for cardiac electrophysiological studies, characteriza...
AbstractWe have cloned a novel inward rectifier K+ channel (hIRK2) from a human frontal cortex cDNA ...
Inward rectifying potassium: Kir) channels are important in regulating cellular excitability in orga...
AbstractA full-length K+ channel cDNA (RHK1) was isolated from a rat cardiac library using the polym...
Kir2.1, a strong inward rectifier potassium channel encoded by the KCNJ2 gene, is a key regulator of...
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...
A 2 P domain potassium channel expressed in eye, lung, and stomach, Kcnk8, has recently been identif...
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...
AbstractArginine residue at position 285 (R285) in the intracellular C-terminal domain of inward rec...
AbstractWe have identified several cDNAs for the human Kir5.1 subunit of inwardly rectifying K+ chan...
AbstractWe have cloned the human genes encoding the inwardly rectifying K+ (Kir) channel subunits, K...
AbstractA new member of the two transmembrane domain potassium (K+) channel family was identified an...
AbstractWe have identified several cDNAs for the human Kir5.1 subunit of inwardly rectifying K+ chan...
AbstractWe have cloned the human genes encoding the inwardly rectifying K+ (Kir) channel subunits, K...
AbstractWe have cloned a novel inward rectifier K+ channel (hIRK2) from a human frontal cortex cDNA ...
For many model organisms traditionally in use for cardiac electrophysiological studies, characteriza...
AbstractWe have cloned a novel inward rectifier K+ channel (hIRK2) from a human frontal cortex cDNA ...
Inward rectifying potassium: Kir) channels are important in regulating cellular excitability in orga...
AbstractA full-length K+ channel cDNA (RHK1) was isolated from a rat cardiac library using the polym...
Kir2.1, a strong inward rectifier potassium channel encoded by the KCNJ2 gene, is a key regulator of...
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...
A 2 P domain potassium channel expressed in eye, lung, and stomach, Kcnk8, has recently been identif...
The cardiac inwardly rectifying potassium current IK1 is responsible for stabilizing the resting mem...