<p><b>(A)</b> Measurement of the capacitance of the distal dendritic arbor (C<sub>2</sub>) reveals dendritic degeneration starting at five weeks of age in ATXN1[82Q] Purkinje neurons. <b>(B)</b> Measurement of the capacitance of the soma and proximal dendrite (C<sub>1</sub>) reveals no change in ATXN1[82Q] Purkinje neurons. <b>(C and D)</b> Evaluation of published RNA sequencing data [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0198040#pone.0198040.ref024" target="_blank">24</a>] for all voltage-gated ion channel genes reveals altered expression of several subfamilies of ion channel genes in ATXN1[82Q] mice at five weeks of age <b>(C)</b> and twelve weeks of age <b>(D)</b>. Only ion channel genes where a statistica...
Abnormal cell excitability is commonly seen in neurodegenerative diseases. However, the roles of exc...
Age-related hearing loss (AHL) is the most common sensory disorder in the elderly population, and th...
Down syndrome (DS), which is due to triplication of chromosome 21, is constantly associated with int...
Purkinje neuron dendritic degeneration precedes cell loss in cerebellar ataxia, but the basis for de...
<p><b>(A)</b> Representative dendritic whole-cell patch clamp recordings from a fifteen week old wil...
<p><b>(A)</b> Representative traces from Purkinje neurons at five weeks of age where dendritic calci...
<p><b>(A)</b> Representative image of dendritic patch clamp recording configuration with patch pipet...
Selective neuronal vulnerability in neurodegenerative disease is poorly understood. Using the ATXN1[...
<p><b>(A)</b> Representative images at the cerebellar primary fissure in wild-type mice, ATXN1[82Q] ...
Neuronal atrophy in neurodegenerative diseases is commonly viewed as an early event in a continuum t...
Input from the sensory organs is required to pattern neurons into topographical maps during developm...
<p><b>A:</b> MBP<sup>+</sup> myelin sheaths (green) enclose type I SGNs in Rosenthal's canal of the ...
SummarySmall-conductance Ca2+-activated K+ channels (SK channels) modulate excitability and curtail ...
Adult neural stem/precursor cells (NPCs) play a pivotal role in neuronal plasticity throughout life....
Staggerer (Rorasg/sg) is an autosomal mutation in an orphan nuclear hormone receptor gene, RORalpha,...
Abnormal cell excitability is commonly seen in neurodegenerative diseases. However, the roles of exc...
Age-related hearing loss (AHL) is the most common sensory disorder in the elderly population, and th...
Down syndrome (DS), which is due to triplication of chromosome 21, is constantly associated with int...
Purkinje neuron dendritic degeneration precedes cell loss in cerebellar ataxia, but the basis for de...
<p><b>(A)</b> Representative dendritic whole-cell patch clamp recordings from a fifteen week old wil...
<p><b>(A)</b> Representative traces from Purkinje neurons at five weeks of age where dendritic calci...
<p><b>(A)</b> Representative image of dendritic patch clamp recording configuration with patch pipet...
Selective neuronal vulnerability in neurodegenerative disease is poorly understood. Using the ATXN1[...
<p><b>(A)</b> Representative images at the cerebellar primary fissure in wild-type mice, ATXN1[82Q] ...
Neuronal atrophy in neurodegenerative diseases is commonly viewed as an early event in a continuum t...
Input from the sensory organs is required to pattern neurons into topographical maps during developm...
<p><b>A:</b> MBP<sup>+</sup> myelin sheaths (green) enclose type I SGNs in Rosenthal's canal of the ...
SummarySmall-conductance Ca2+-activated K+ channels (SK channels) modulate excitability and curtail ...
Adult neural stem/precursor cells (NPCs) play a pivotal role in neuronal plasticity throughout life....
Staggerer (Rorasg/sg) is an autosomal mutation in an orphan nuclear hormone receptor gene, RORalpha,...
Abnormal cell excitability is commonly seen in neurodegenerative diseases. However, the roles of exc...
Age-related hearing loss (AHL) is the most common sensory disorder in the elderly population, and th...
Down syndrome (DS), which is due to triplication of chromosome 21, is constantly associated with int...