AbstractAndersen's syndrome is caused by mutations in the potassium channel Kir2.1, a major determinant of resting membrane potential. The clinical features of this disease illustrate the importance of a stable resting membrane potential for many cell functions
BACKGROUND Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the An...
Andersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic feat...
We describe here how ion-channel dysfunction in p-cells is associated with the pa thogenesis of a po...
AbstractAndersen's syndrome is caused by mutations in the potassium channel Kir2.1, a major determin...
International audienceAndersen's syndrome (AS) is a rare autosomal disorder that has been defined by...
AbstractInwardly rectifying K+ (Kir) channels are important regulators of resting membrane potential...
The ubiquitously expressed family of inward rectifier potassium (KIR) channels, encoded by KCNJ gene...
AbstractAndersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorp...
Inwardly rectifying potassium (Kir) channels control cell membrane K+ fluxes and electrical signalli...
Abstract Background Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to ...
Background: Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the Ande...
My research focuses on understanding the mechanisms of eukaryotic inwardly rectifying potassium chan...
INTRODUCTION: K(+) channels allow the passive and selective transport of K(+) ions through the membr...
Andersen’s syndrome, which is characterized by periodic paralysis, cardiac arrhythmias and dysmorphi...
Inward rectifier potassium channels of the Kir2 subfamily are important determinants of the electric...
BACKGROUND Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the An...
Andersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic feat...
We describe here how ion-channel dysfunction in p-cells is associated with the pa thogenesis of a po...
AbstractAndersen's syndrome is caused by mutations in the potassium channel Kir2.1, a major determin...
International audienceAndersen's syndrome (AS) is a rare autosomal disorder that has been defined by...
AbstractInwardly rectifying K+ (Kir) channels are important regulators of resting membrane potential...
The ubiquitously expressed family of inward rectifier potassium (KIR) channels, encoded by KCNJ gene...
AbstractAndersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorp...
Inwardly rectifying potassium (Kir) channels control cell membrane K+ fluxes and electrical signalli...
Abstract Background Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to ...
Background: Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the Ande...
My research focuses on understanding the mechanisms of eukaryotic inwardly rectifying potassium chan...
INTRODUCTION: K(+) channels allow the passive and selective transport of K(+) ions through the membr...
Andersen’s syndrome, which is characterized by periodic paralysis, cardiac arrhythmias and dysmorphi...
Inward rectifier potassium channels of the Kir2 subfamily are important determinants of the electric...
BACKGROUND Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the An...
Andersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic feat...
We describe here how ion-channel dysfunction in p-cells is associated with the pa thogenesis of a po...
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