Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice.
Tong, Xiaoping
Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice. [electronic resource] - Nature neuroscience May 2014 - 694-703 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1546-1726
10.1038/nn.3691 doi
Age Factors
Animals
Astrocytes--metabolism
Corpus Striatum--physiopathology
Disease Models, Animal
Green Fluorescent Proteins--genetics
HEK293 Cells
Hindlimb Suspension--physiology
Humans
Huntingtin Protein
Huntington Disease--genetics
In Vitro Techniques
Locomotion--genetics
Mice
Mice, Inbred C57BL
Mice, Transgenic
Nerve Tissue Proteins--genetics
Neurons--metabolism
Nuclear Proteins--genetics
Potassium Channels, Inwardly Rectifying--deficiency
Survival Analysis
Trinucleotide Repeats--genetics
Kcnj10 Channel
Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice. [electronic resource] - Nature neuroscience May 2014 - 694-703 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1546-1726
10.1038/nn.3691 doi
Age Factors
Animals
Astrocytes--metabolism
Corpus Striatum--physiopathology
Disease Models, Animal
Green Fluorescent Proteins--genetics
HEK293 Cells
Hindlimb Suspension--physiology
Humans
Huntingtin Protein
Huntington Disease--genetics
In Vitro Techniques
Locomotion--genetics
Mice
Mice, Inbred C57BL
Mice, Transgenic
Nerve Tissue Proteins--genetics
Neurons--metabolism
Nuclear Proteins--genetics
Potassium Channels, Inwardly Rectifying--deficiency
Survival Analysis
Trinucleotide Repeats--genetics
Kcnj10 Channel