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HD protein, human

Known as: Huntington disease protein, human, HTT protein, human, Huntingtin 
Huntingtin (3144 aa, ~348 kDa) is encoded by the human HTT gene. This protein may be involved in the regulation of vesicular transport.
National Institutes of Health

Papers overview

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Review
2018
Review
2018
: Huntington's Disease (HD) is a progressive neurodegenerative disorder. It is an autosomal dominant disorder that is categorized… 
2013
2013
Huntington’s disease is associated with NMDA receptor dysfunction, but how the expanded polyglutamine repeat in the huntingtin… 
2013
2013
Huntington’s disease is associated with NMDA receptor dysfunction, but how the expanded polyglutamine repeat in the huntingtin… 
2011
2011
Combining experiments and calculations makes it possible to measure the prognostic value of toxic protein species in the cell. 
2009
2009
Huntington’s disease (HD) is a purely genetic neurodegenerative disorder affecting approximately 1 in 10,000 people. It is most… 
2005
2005
Huntington’s disease is a neurodegenerative disorder, caused by mutations in the huntingtin (htt) protein that result in expanded…