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Genome Research|April 4, 2019
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALSSahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Nature Neuroscience|July 31, 2019
RPS25 is required for efficient RAN translation of C9orf72 and other neurodegenerative disease-associated nucleotide repeatsShizuka B Yamada, Tania F Gendron, Teresa Niccoli, et al.
American Journal of Human Genetics|August 5, 2020
Evolution of a Human-Specific Tandem Repeat Associated with ALSMeredith M Course, Kathryn Gudsnuk, Samuel N Smukowski, et al.
Neuron|June 21, 2016
Activation of HIPK2 Promotes ER Stress-Mediated Neurodegeneration in Amyotrophic Lateral SclerosisSebum Lee, Yulei Shang, Stephanie A Redmond, et al.
Human Genetics|April 15, 2019
Variants in KIAA0825 underlie autosomal recessive postaxial polydactylyIrfan Ullah, Naseebullah Kakar, Isabelle Schrauwen, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Aberrant phase separation is a common killing strategy of positively charged peptides in biology and human diseaseSteven Boeynaems, X Rosa Ma, Vivian Yeong, et al.
Nature|August 27, 2010
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALSAndrew C Elden, Hyung-Jun Kim, Michael P Hart, et al.
Brain : a Journal of Neurology|June 28, 2024
Frontotemporal lobar degeneration targets brain regions linked to expression of recently evolved genesLorenzo Pasquini, Felipe L Pereira, Sahba Seddighi, et al.
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