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Sonam Parakh

Macquarie University

21

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Protein disulphide isomerase (PDI) is protective against several types of DNA damage, including that induced by amyotrophic lateral sclerosis-associated mutant TDP-43 in neuronal cells/ in vitro models

2021 bioRxiv
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Mitochondrial associated ER membrane (MAM) compartment and its dysregulation in Amyotrophic lateral sclerosis (ALS).

2021 Seminars in Cell & Developmental Biology
- Sonam Parakh
- Julie D. Atkin
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Mutant Cyclin F Impedes COPII Vesicle-Mediated ER-Golgi Trafficking and ER-Associated Degradation, Inducing ER Stress and Golgi Fragmentation in ALS/FTD

2021
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Emerging Evidence Highlighting the Importance of Redox Dysregulation in the Pathogenesis of Amyotrophic Lateral Sclerosis (ALS).

2021 Frontiers in Cellular Neuroscience
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Protein disulphide isomerase (PDI) is protective against amyotrophic lateral sclerosis (ALS)-related mutant Fused in Sarcoma (FUS) in in vitro models.

2021 Scientific Reports
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The redox activity of protein disulphide isomerase (PDI) inhibits ALS phenotypes in cellular and zebrafish models.

2020 iScience
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Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations

2020 Molecular Neurodegeneration
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The Cysteine (Cys) Residues Cys-6 and Cys-111 in Mutant Superoxide Dismutase 1 (SOD1) A4V Are Required for Induction of Endoplasmic Reticulum Stress in Amyotrophic Lateral Sclerosis.

2020 Journal of Molecular Neuroscience
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Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress

2019 Cellular and Molecular Life Sciences
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ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis

2018 Human Molecular Genetics
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Citations (16)