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Tariq O Faquih, N Ahmad Aziz, Sarah L Gardiner, Ruifang Li-Gao, Renée de Mutsert, Yuri Milaneschi, Stella Trompet, J Wouter Jukema, Frits R Rosendaal, Astrid van Hylckama Vlieg, Ko Willems van Dijk, Dennis O Mook-Kanamori

Human molecular genetics 2023;32(10):1741-1752

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Role of chaperone-mediated autophagy in degrading Huntington's disease-associated huntingtin protein.

Lin Qi, Xing-Ding Zhang

Acta biochimica et biophysica Sinica 2014;46(2):83-91

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Probing the Huntingtin 1-17 membrane anchor on a phospholipid bilayer by using all-atom simulations.

Sébastien Côté, Normand Mousseau, Burkhard Bechinger, Evgeniy S Salnikov, Vincent Binette

Biophysical journal 2016;108(5):1187-98

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Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study.

E Ray Dorsey

PloS one 2012;7(2):e29522

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Results for ""Huntingtin Protein""[mesh_terms]

Recent Microscopy Advances and the Applications to Huntington's Disease Research.

The Mystery of EVP4593: Perspectives of the Quinazoline-Derived Compound in the Treatment of Huntington's Disease and Other Human Pathologies.

Possible role of mitochondrial permeability transition pore in the pathogenesis of Huntington disease.

Glucose transportation in the brain and its impairment in Huntington disease: one more shade of the energetic metabolism failure?

Atomistic mechanisms of huntingtin N-terminal fragment insertion on a phospholipid bilayer revealed by molecular dynamics simulations.

Imaging specific proteins in living cells with small unnatural amino acid attached Raman reporters.

Lipid Composition Drives Mutant Huntingtin Dimerization and Membrane Association: Insights from Computational Simulations.

Genetics and neuropathology of Huntington's disease.

Anti-amyloid potential of some phytochemicals against Aβ-peptide and α-synuclein, tau, prion, and Huntingtin protein.

Therapeutic Update on Huntington's Disease: Symptomatic Treatments and Emerging Disease-Modifying Therapies.

Huntington disease: pathogenesis, biomarkers, and approaches to experimental therapeutics.

Normal range CAG repeat size variations in the HTT gene are associated with an adverse lipoprotein profile partially mediated by body mass index.

Role of chaperone-mediated autophagy in degrading Huntington's disease-associated huntingtin protein.

Probing the Huntingtin 1-17 membrane anchor on a phospholipid bilayer by using all-atom simulations.

Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study.

Results for
""Huntingtin Protein""[mesh_terms]