Results 201 to 210 of about 6,546,213 (228)
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Mutant huntingtin protein expression and blood–spinal cord barrier dysfunction in huntington disease
Annals of Neurology, 2017G. Sciacca, F. Cicchetti
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The isolation and characterization of Huntingtin interacting proteins
2009Huntington Disease (HD) is an autosomal dominant, neurodegenerative disorder with onset normally occurring at around 40 years of age. This devastating disease is the result of the expression of a polyglutamine tract greater than 35 in a protein with unknown function.
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HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease
Neurobiology of Disease, 2021Manuel Seefelder +2 more
exaly
Protein–protein interactions of huntingtin in the hippocampus
Molecular Biology, 2017A. L. Proskura +3 more
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The Role of Low Complexity Regions in Protein Interaction Modes: An Illustration in Huntingtin
International Journal of Molecular Sciences, 2021Kristina Kastano +2 more
exaly
Selective Expression of Huntingtin-associated Protein 1 in β-Cells of the Rat Pancreatic Islets
Journal of Histochemistry and Cytochemistry, 2010He Li
exaly
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein
Nature Biotechnology, 2010P. Bauer +10 more
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Immunohistochemical Localization of Huntingtin-associated Protein 1 in Endocrine System of the Rat
Journal of Histochemistry and Cytochemistry, 2005Xiao-Jiang Li
exaly