Background: Huntington disease (HD) is caused by an expanded polyglutamine (polyQ) domain in huntingtin (htt), leading to aggregation. Results: Specific flanking sequences adjacent to the polyQ domain modulate htt aggregation on lipid bilayers. Conclusion: Lipid mediated htt aggregation may lead to membrane dysfunction in HD. Significance: Flanking sequences may play a role in membrane dysfunction associated with Huntington disease
The amino-terminal domain of huntingtin (Htt17), located immediately upstream of the decisive polygl...
Huntington’s disease (HD) is caused by the presence of an extended polyglutamine (polyQ) region at t...
Huntington’s Disease (HD) is a genetic, neurodegenerative disease characterized by an abnormal polyg...
Background: Huntington disease (HD) is caused by an expanded polyglutamine (polyQ) domain in hunting...
Background: Huntington disease (HD) is caused by an expanded polyglutamine (polyQ) domain in hunting...
Huntington’s Disease (HD) is a neurodegenerative disorder that is defined by the accumulation of n...
An expanded polyglutamine (Q) tract (>37Q) in huntingtin (htt) causes Huntington disease. Htt associ...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is caused by a polyglutamine (polyQ) domain that is expanded beyond a crit...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
The amino-terminal domain of huntingtin (Htt17), located immediately upstream of the decisive polygl...
Huntington’s disease (HD) is caused by the presence of an extended polyglutamine (polyQ) region at t...
Huntington’s Disease (HD) is a genetic, neurodegenerative disease characterized by an abnormal polyg...
Background: Huntington disease (HD) is caused by an expanded polyglutamine (polyQ) domain in hunting...
Background: Huntington disease (HD) is caused by an expanded polyglutamine (polyQ) domain in hunting...
Huntington’s Disease (HD) is a neurodegenerative disorder that is defined by the accumulation of n...
An expanded polyglutamine (Q) tract (>37Q) in huntingtin (htt) causes Huntington disease. Htt associ...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-re...
Huntington’s disease (HD) is caused by a polyglutamine (polyQ) domain that is expanded beyond a crit...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a c...
The amino-terminal domain of huntingtin (Htt17), located immediately upstream of the decisive polygl...
Huntington’s disease (HD) is caused by the presence of an extended polyglutamine (polyQ) region at t...
Huntington’s Disease (HD) is a genetic, neurodegenerative disease characterized by an abnormal polyg...