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...
Saved in:
Main Authors: | Namrata Jayanth, Gurvan Mahé, Matthew Campbell, Mike Lipkin, Shushant Jain, Rhea van de Bospoort, Jennifer Thornton, Brad Margus, David F. Fischer |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-01-01
|
Series: | SLAS Discovery |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2472555224000625 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Long-term safety of dexamethasone sodium phosphate encapsulated in autologous erythrocytes in pediatric patients with ataxia telangiectasia
by: Mary Kay Koenig, et al.
Published: (2025-01-01) -
Clinical-cognitive Characterization of Spinocerebellar Ataxia Type 2
by: Alberto Caballero Laguna, et al.
Published: (2021-09-01) -
ATM in immunobiology: From lymphocyte development to cancer immunotherapy
by: Ji-Hoon Lee
Published: (2025-02-01) -
Exploring neuropsychiatric symptoms in Friedreich ataxia
by: Simona Karamazovova, et al.
Published: (2024-11-01) -
Depression and Associated Factors Among Patients with Spinocerebellar Ataxia
by: Sirivipa Jekpoo, et al.
Published: (2025-01-01)