about
C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal traffickingCellular uptake of self-assembled cationic peptide-DNA complexes: multifunctional role of the enhancer chloroquine.Phosphorylation of hnRNP K by cyclin-dependent kinase 2 controls cytosolic accumulation of TDP-43.CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.TDP-43: a DNA and RNA binding protein with roles in neurodegenerative diseases.Ubiquilin 2: a component of the ubiquitin-proteasome system with an emerging role in neurodegeneration.TDP-43 mutations causing amyotrophic lateral sclerosis are associated with altered expression of RNA-binding protein hnRNP K and affect the Nrf2 antioxidant pathway.Cyclin F: A component of an E3 ubiquitin ligase complex with roles in neurodegeneration and cancer.Fused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding protein.Casein kinase II phosphorylation of cyclin F at serine 621 regulates the Lys48-ubiquitylation E3 ligase activity of the SCF(cyclin F) complex.Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy.Evaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological Features.C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking.ERp57 is protective against mutant SOD1-induced cellular pathology in Amyotrophic Lateral Sclerosis.DNA nanoclew templated spherical nucleic acids for siRNA delivery.A novelTARDBPinsertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosisMutation analysis of the optineurin gene in familial amyotrophic lateral sclerosisThe characterization of a novel dendritic system for gene delivery by isothermal titration calorimetryThe mRNA-based reprogramming of fibroblasts from a SOD1E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 miceTheme 3 In vitro experimental modelsAmyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stressGeneration and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNFS621G familial amyotrophic lateral sclerosis patient using mRNA reprogramming
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description
researcher ORCID ID=0000-0002-4847-9263
@en
name
Shu Yang
@ast
Shu Yang
@en
Shu Yang
@es
Shu Yang
@nl
type
label
Shu Yang
@ast
Shu Yang
@en
Shu Yang
@es
Shu Yang
@nl
prefLabel
Shu Yang
@ast
Shu Yang
@en
Shu Yang
@es
Shu Yang
@nl
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P1153
36674281500
P31
P496
0000-0002-4847-9263