HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain
Michael A. Kalchman(University of British Columbia), Michael R. Hayden(University of British Columbia), Francis C. Lynn(University of British Columbia), Rona K. Graham(Université de Sherbrooke), Cheryl L. Wellington(University of British Columbia), Krista McCutcheon(University of British Columbia), Parsa Kazemi‐Esfarjani(University of British Columbia), Kazutoshi Nishiyama(The University of Tokyo), K. Nichol(University of British Columbia), Martina Metzler(University of Helsinki), R D Gietz(University of Manitoba), Y. Paul Goldberg(University of British Columbia), Ichiro Kanazawa(The University of Tokyo), Hiroshi Koide(Juntendo University)
Cited by 384
Related Papers
Huntington disease
|Nature Reviews Disease Primers|2015|1.6k
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
|Nature Genetics|2003|976
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
|Nature|1998|804
Vascular dysfunction—The disregarded partner of Alzheimer's disease
|Alzheimer s & Dementia|2019|721