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Epidemiology and Psychiatric Sciences|October 24, 2018
The impact of Recovery Colleges on mental health staff, services and societyA Crowther, A Taylor, R Toney, et al.
Human Molecular Genetics|October 15, 2009
Identical oligomeric and fibrillar structures captured from the brains of R6/2 and knock-in mouse models of Huntington's diseaseKirupa Sathasivam, Amin Lane, Justin Legleiter, et al.
Human Molecular Genetics|August 1, 1997
Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domainsJ Flint, G P Bates, K Clark, et al.
RNA Biology|October 21, 2021
Integrated multi-omics reveals common properties underlying stress granule and P-body formationChristopher J Kershaw, Michael G Nelson, Jennifer Lui, et al.
Annals of Neurology|February 9, 2002
Environmental enrichment slows disease progression in R6/2 Huntington's disease miceEmma Hockly, Patricia M Cordery, Benjamin Woodman, et al.
Neuroscience|October 19, 2000
Amyloid-like inclusions in Huntington's diseaseD P McGowan, W van Roon-Mom, H Holloway, et al.
Human Molecular Genetics|April 30, 2004
Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approachDavid G Hay, Kirupa Sathasivam, Sönke Tobaben, et al.
International Journal of Molecular Sciences|August 27, 2021
Transglutaminase 6 Is Colocalized and Interacts with Mutant Huntingtin in Huntington Disease Rodent Animal ModelsAnja Schulze-Krebs, Fabio Canneva, Judith Stemick, et al.
Nature Cell Biology|February 21, 2002
Arfaptin 2 regulates the aggregation of mutant huntingtin proteinPeter J Peters, Ke Ning, Felipe Palacios, et al.
The Journal of Urology|September 1, 1987
A prospective double-blind clinically controlled multicenter trial of sodium pentosanpolysulfate in the treatment of interstitial cystitis and related painful bladder diseaseM Holm-Bentzen, F Jacobsen, B Nerstrøm, et al.
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