Promote Scientific Collaboration
Access to Unique Applications and Tools
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
- Sad news from the SIGNAL study: pepinemab does not influence HD symptoms
- Working as a team: Changes in brain development mean some brain regions may be slacking off
- Caution urged for the use of gene-editing technology CRISPR
- HD and Histamines: Targeting Hybrid Receptors to Quiet Stressful Brain Talk
- Changing jobs: converting other cell types into neurons
- Critical Impact of Different Conserved Endoplasmic Retention Motifs and Dopamine Receptor Interacting Proteins (DRIPs) on Intracellular Localization and Trafficking of the D2 Dopamine Receptor (D2-R) Isoforms.
- The Role of Vesicle Trafficking Defects in the Pathogenesis of Prion and Prion-Like Disorders.
- Structural brain correlates of dementia in Huntington's disease.
- Inconsistencies in histone acetylation patterns among different HD model systems and HD post-mortem brains.
- pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC model.
- Texas Original Compassionate Cultivation Introduces Patient- and Doctor-Driven Medical ...
- Music on the Vine raises awareness of Huntington's Disease
- 12-year veteran of the NYPD forced out after not being allowed to use prescribed medical cannabis
- Genentech Presents New 2-Year Data for Evrysdi (risdiplam) in Infants With Type 1 Spinal ...
- Roche presents new 2-year data for Evrysdi (risdiplam) in infants with Type 1 spinal muscular ...