Audrey G. Ragagnin
2 Technology Place
North Ryde, NSW 2109, Australia
North Ryde, NSW 2109, Australia
Last Updated: 09/26/2026
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Found 13 publications
Cofilin hyperphosphorylation triggers TDP-43 pathology in sporadic amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: July 31, 2025
C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD.
Journal: Molecular neurobiology
Published: December 22, 2022
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations.
Journal: Molecular neurodegeneration
Published: October 20, 2019
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: August 01, 2019
Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress.
Journal: Cellular and molecular life sciences : CMLS
Published: April 09, 2019
Rab-dependent cellular trafficking and amyotrophic lateral sclerosis.
Journal: Critical reviews in biochemistry and molecular biology
Published: February 12, 2019
ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
Journal: Human molecular genetics
Published: November 06, 2017
Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy.
Journal: Cellular and molecular life sciences : CMLS
Published: March 13, 2017
Casein kinase II phosphorylation of cyclin F at serine 621 regulates the Lys48-ubiquitylation E3 ligase activity of the SCF(cyclin F) complex.
Journal: Open biology
Published: March 09, 2017
Last Updated: 09/26/2026