Press Releases

Adrestia Therapeutics Partners with Patient Advocacy Groups to Further A-T Research

Feb 8, 2023 Comments Off on Adrestia Therapeutics Partners with Patient Advocacy Groups to Further A-T Research
Apr 13 @ 9:38 am

The A-T Children’s Project is excited to be part of this A-T research initiative. Please see the following press release from Adrestia Therapeutics:

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A-T Families Providing Data to Researchers

Jul 14, 2017 Comments Off on A-T Families Providing Data to Researchers
Apr 13 @ 9:38 am
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LONG TIME ADVISORS ELECTED TO THE NATIONAL ACADEMY OF SCIENCES

Sep 13, 2016 Comments Off on LONG TIME ADVISORS ELECTED TO THE NATIONAL ACADEMY OF SCIENCES
Apr 13 @ 9:38 am

Two of our long time scientific advisors have been elected to the prestigious National Academy of Sciences, one of the highest honors bestowed upon research scientists. Nathaniel Heintz, PhD Nathaniel (Nat) Heintz is the James and Marilyn Simons Professor and head of the Laboratory of Molecular Biology at The Rockefeller…

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FAMILIES OF ATAXIA-TELANGIECTASIA PATIENTS WORLDWIDE LAUNCH NEW DATA PLATFORM TO EMPOWER RESEARCHERS

Jun 29, 2016 Comments Off on FAMILIES OF ATAXIA-TELANGIECTASIA PATIENTS WORLDWIDE LAUNCH NEW DATA PLATFORM TO EMPOWER RESEARCHERS
Apr 13 @ 9:38 am
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ATW2015 INCLUDES SESSIONS ON NEUROGENERATION AND NON-TRADITIONAL ROLES OF THE A-T PROTEIN

Nov 1, 2015 Comments Off on ATW2015 INCLUDES SESSIONS ON NEUROGENERATION AND NON-TRADITIONAL ROLES OF THE A-T PROTEIN
Apr 13 @ 9:38 am

Scientists and clinicians from around the world traveled to Beijing, China in October to share information at the 2015 A-T Workshop, a meeting co-sponsored by the A-T Children’s Project and held at the Capital Normal University. Beyond primarily discussing DNA repair roles of the ATM protein as in the past,…

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RECURSION PHARMACEUTICALS ANNOUNCES FUNDING SUPPORT FOR ATAXIA-TELANGIECTASIA

Apr 6, 2015 Comments Off on RECURSION PHARMACEUTICALS ANNOUNCES FUNDING SUPPORT FOR ATAXIA-TELANGIECTASIA
Apr 13 @ 9:38 am

Press Release from Recursion Pharmaceuticals

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Unravelling Nerve-cell Death in Rare Children’s Disease

Mar 27, 2014 Comments Off on Unravelling Nerve-cell Death in Rare Children’s Disease
Apr 13 @ 9:38 am

From the Sanford-Burnham Medical Research Institute Press Release: Researchers discover mutations in a protein that plays a role in the body’s DNA repair system—similar to what’s observed in the rare children’s disease ataxia-telangiectasia. The discovery provides an approach to identifying therapies that will resuscitate the broken DNA repair mechanism. Newswise…

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