Table 6_NETSseq reveals inflammatory and aging mechanisms in distinct cell types, driving cerebellar decline in ataxia telangiectasia.xlsx

<p>Ataxia–telangiectasia (A–T) is a rare, autosomal recessive, multisystem disorder caused by mutations in the Ataxia–Telangiectasia Mutated (ATM) gene and is characterized by a devastating and progressive neurological pathology. The cellular and molecular changes driving the neurological abno...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Giuliano G. Stirparo (22152931) (author)
مؤلفون آخرون: Xiao Xu (112147) (author), Toni Thompson (22152934) (author), Keith Page (18059237) (author), Jenna R. M. Harvey (16871248) (author), David Cadwalladr (22152937) (author), Jason Lawrence (841133) (author), Russell J. Burley (22152940) (author), Joel Juvvanapudi (22152943) (author), Megan Roberts (9908672) (author), Daniel F. Barker (22152949) (author), Victoria Mulligan (16871251) (author), Chloe Sherlock (22152952) (author), Marina Lizio (185917) (author), Louisa Christie (22152955) (author), Mani Mudaliar (22152958) (author), Steven Sheardown (16986259) (author), Brad Margus (22152961) (author), Craig Thompson (151910) (author), Louise Dickson (14708571) (author), Nicola L. Brice (10660712) (author), Mark B. Carlton (22152964) (author), Justin A. C. Powell (16986256) (author), Lee A. Dawson (2467774) (author)
منشور في: 2025
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