We are building and sharing the most comprehensive clinical, genetic, molecular & biochemical assessment of ALS, while openly sharing the results with the global research community.
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ANSWER ALS reposted this
We are excited to partner with ANSWER ALS to integrate the AD Workbench with their Neuromine Data Portal. By providing a unified, single access platform for data sharing and analysis, this integration will enable researchers to save time and resources while enhancing the depth of their research by allowing cross-referencing of disease pathways and genetic data. Read more here: https://lnkd.in/eUtw4V9q
Announcing a Major Collaboration to Advance Neurological Research: Answer ALS and the Alzheimer’s Disease Data Initiative (AD Data Initiative) are joining forces to strengthen research capabilities in neurological diseases. By integrating the AD Workbench with the Neuromine Data Portal, this partnership establishes a comprehensive resource for researchers tackling Alzheimer’s and ALS. This unified platform combines the expertise and data from two leading organizations, offering researchers a powerful tool to accelerate discoveries that benefit millions affected by these conditions. For more info go to 👉
Today is Giving Tuesday. Support accelerating ALS research by donating to Answer ALS. Together, we are expanding the search for answers and changing the future of ALS.
This Thanksgiving, let's take a moment to cherish our loved ones, especially those facing the challenges of ALS. Their strength inspires us every day as we work tirelessly to find a cure. Together, we can make a difference in their lives and honor their courage www.answerals.org
ALS research needs your support on Giving Tuesday! Save the date, December 3rd to contribute to the cause and help us advance breakthroughs in understanding and treating ALS. Every donation counts!
Join us on Giving Tuesday, December 3rd in supporting the fight against ALS. Every contribution to Answer ALS helps advance research and bring hope to those affected by this disease.
Breaking News Answer ALS Releases World's Largest ALS Patient-Based iPSC and Bio Data Repository An unprecedented resource, created with Cedars-Sinai, to accelerate ALS research and drive development of targeted therapies globally Learn more at:
🚨 Breaking News 🚨 Answer ALS Releases World's Largest ALS Patient-Based iPSC and Bio Data Repository An unprecedented resource, created with Cedars-Sinai, to accelerate ALS research and drive development of targeted therapies globally Learn more at: https://pxl.to/56z6qxd #AnswerALS #Cedars-Sinai #together #TheDataIsHere
If you’re in Chicago for the Society for Neuroscience meeting, please stop by our booth 1615! We would love to talk about how the data and samples form over 1000 people with ALS are freely accessible on the Neuromine data portal. #Together
Join us in honoring the 10th Anniversary of the Ice Bucket Challenge with a chance to win tickets to the Game Changer Gala, Super Bowl week in New Orleans! In 2014, Pete Frates and Pat Quinn sparked a viral ALS fundraising campaign by encouraging people to pour ice on themselves, donate, and then challenge others to do the same. 10 years later, instead of asking people to cover themselves in ice, we are challenging people to give $50 "ice cubes" for an opportunity to WIN: Two tickets and a hotel stay for the 2025 Game Changer Gala, February 4-5, 2025. For Gala details: www.GameChangerGala.com We are extending the campaign for 30 days, so grab your chance to win at the link below until September 28th! https://lnkd.in/ggegzB4T