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Drug repurposing screen for the rare disease ataxia-telangiectasia

Ataxia Telangiectasia (A-T) is a rare, autosomal recessive genetic disorder characterized by a variety of symptoms, including progressive neurodegeneration, telangiectasia, immunodeficiency, and an increased susceptibility to cancer. It is caused by bi-allelic mutations impacting a gene encoding a s...

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Principais autores: Namrata Jayanth, Gurvan Mahé, Matthew Campbell, Mike Lipkin, Shushant Jain, Rhea van de Bospoort, Jennifer Thornton, Brad Margus, David F. Fischer
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2025-01-01
Serier:SLAS Discovery
Fag:
Drug repurposing screen
HTS
DNA damage
Rare disease
Ataxia-telangiectasia
Neurodegeneration
Online adgang:http://www.sciencedirect.com/science/article/pii/S2472555224000625
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