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Neurology. Genetics|December 13, 2021
Confirming Pathogenicity of the F386L PSEN1 Variant in a South Asian Family With Early-Onset Alzheimer DiseaseSarah J Eger, Yann Le Guen, Raiyan R Khan, et al.
Nature Genetics|March 7, 2018
CRISPR-Cas9 screens in human cells and primary neurons identify modifiers of C9ORF72 dipeptide-repeat-protein toxicityNicholas J Kramer, Michael S Haney, David W Morgens, et al.
Nature|October 7, 2021
Neurotoxic reactive astrocytes induce cell death via saturated lipidsKevin A Guttenplan, Maya K Weigel, Priya Prakash, et al.
Cell|September 26, 2002
Hop is an unusual homeobox gene that modulates cardiac developmentFabian Chen, Hyun Kook, Rita Milewski, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Cryptic splicing in synaptic and membrane excitability genes links TDP-43 loss to neuronal dysfunctionCaiwei Guo, Kuchuan Chen, Sarat C Vatsavayai, et al.
Molecular Cell|June 9, 2023
Poly(A)-binding protein is an ataxin-2 chaperone that regulates biomolecular condensatesSteven Boeynaems, Yanniv Dorone, Yanrong Zhuang, et al.
Molecular Biology and Evolution|January 22, 2021
The Hunt for Ancient Prions: Archaeal Prion-Like Domains Form Amyloid-Based Epigenetic ElementsTomasz Zajkowski, Michael D Lee, Shamba S Mondal, et al.
Neurology. Genetics|February 6, 2025
A 3'UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated With Increased Risk for FTLD-TDPAugustine Chemparathy, Yann Le Guen, Yi Zeng, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
An emergent disease-associated motor neuron state precedes cell death in a mouse model of ALSOlivia Gautier, Jacob A Blum, Thao P Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
A 3'UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated with Increased Risk for FTLD-TDPAugustine Chemparathy, Yann Le Guen, Yi Zeng, et al.
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