Elevate HD-Related
Scientific Research
Promote Scientific Collaboration
Access to Unique Applications and Tools
Disseminate Data
HDinHD: Open Source Science for the HD Research Community
The goal of HDinHD is to foster and support a collaborative community united in its drive to accelerate the development of therapeutics that will delay the onset and/or ameliorate the effects of Huntington’s disease. HDinHD seeks to achieve this through:
- Sharing HD-related primary scientific data
- Sharing analyses and computational models built from HD-related scientific data
- Providing browsing and data interrogation tools over both primary and analyzed data that facilitate data exploration and hypothesis generation
- Building a forum for HD researchers to highlight their data, tools, know-how and insight to the community
The HDinHD website is currently a joint development effort by CHDI and UCLA, through the laboratory of Dr. Giovanni Coppola. As you will see when you Register for access, HDinHD highlights data and tools provided by the broader community. If you are interested in Contributing Data to HDinHD, suggest links to other HD-related scientific data or websites, or would otherwise like to provide Feedback to us, we encourage you to do so. HDinHD is for the community; please help us tailor and grow HDinHD in a direction that can make a difference to your research, and ultimately, to improve the lives of HD families.
Latest news and publications from around the HD Ecosystem
HDBuzz
- New collaboration seeks to speed Huntington’s disease drug licensing
- HDSA’s Q&A on the latest huntingtin-lowering update from Ionis and Roche
- Exciting Experiments in “Open Science” by Huntington’s Researchers
- The structure of the protein that causes Huntington’s disease, revealed
- Huntington’s disease therapeutics conference 2018 – day 3
Literature
- Understanding patient-reported outcome measures in Huntington disease: at what point is cognitive impairment related to poor measurement reliability?
- Mechanism of neuroprotection by trehalose: controversy surrounding autophagy induction.
- The Neuropsychology of Huntington’s Disease.
- Unconventional Secretion and Intercellular Transfer of Mutant Huntingtin.
- Intravenous immunoglobulin ameliorates motor and cognitive deficits and neuropathology in R6/2 mouse model of Huntington’s disease by decreasing mutant huntingtin protein level and normalizing NF-κB signaling pathway.
News
- North-east neurological centre shines light on what people can do
- Family dig up dark inheritance after father used alcohol to hide symptoms
- Family dig up dark inheritance after father used alcohol to hide symptoms
- Research undermines medical marijuana claims
- Invasive Brain Monitoring Device Market Latest Trends, Phenomena Growth
