Julie Atkin

Macquarie University

Australia

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Articles (17)

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2025

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2025

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2025

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2024

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2020

Collaborators (26)

Marta Vidal

Macquarie University

AUSTRALIA

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Sina Shadfar

Macquarie University

AUSTRALIA

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Ian Blair

Macquarie University

AUSTRALIA

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Cyril Jones Jagaraj

Macquarie University

AUSTRALIA

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Angela Laird

Macquarie University

AUSTRALIA

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Dominic Rowe

Macquarie University

AUSTRALIA

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Natalie Grima

Macquarie University

AUSTRALIA

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Sonam Parakh

Macquarie University

AUSTRALIA

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Amanda Wright

Macquarie University

AUSTRALIA

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Prachi Mehta

Macquarie University

AUSTRALIA

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Mary-Louise Rogers

Flinders University

AUSTRALIA

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Stephanie Rayner

Macquarie University

AUSTRALIA

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Julie Hunter

Macquarie University

AUSTRALIA

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Flora Cheng

Macquarie University

AUSTRALIA

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Fabiha Farzana

Macquarie University

AUSTRALIA

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Saravanabavan Sayanthooran

Macquarie University

AUSTRALIA

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Anand Deva

Macquarie University

AUSTRALIA

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Luan Luu

Macquarie University

AUSTRALIA

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Emily Don

Macquarie University

AUSTRALIA

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Shu Yang

Macquarie University

AUSTRALIA

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Marco Morsch

Macquarie University

AUSTRALIA

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Sharlynn Wu

Macquarie University

AUSTRALIA

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Kelly Jacobs

Macquarie University

AUSTRALIA

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Anna Konopka

Flinders University

AUSTRALIA

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Lezanne Ooi

University of Wollongong

AUSTRALIA

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Albert Lee

Macquarie University

AUSTRALIA

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Julie Atkin

Research Interests

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Articles (17)

The redox activity of protein disulphide isomerase functions in non-homologous end-joining repair to prevent DNA damage

A slower-progressing TDP-43 rNLS8 mouse model for ALS

Pathological forms of TDP-43 in amyotrophic lateral sclerosis (ALS) promote aberrant telomere elongation

Protein disulfide isomerase endoplasmic reticulum protein 57 (ERp57) is protective against ALS-associated mutant TDP-43 in neuronal cells

C9orf72-associated dipeptide repeat expansions perturb ER-golgi vesicular trafficking, inducing golgi fragmentation and ER stress, in ALS/FTD

Molecular hallmarks of ageing in amyotrophic lateral sclerosis

Redox dysregulation as a driver for DNA damage and its relationship to neurodegenerative diseases

ALS/FTD-associated mutation in cyclin F inhibits ER-Golgi trafficking, inducing ER stress, ERAD and Golgi fragmentation

TDP-43 is a ubiquitylation substrate of the SCFcyclin F complex

The role of DNA damage in neural plasticity in physiology and neurodegeneration

DNA damage, defective DNA repair, and neurodegeneration in amyotrophic lateral sclerosis

The Complex Mechanisms by Which Neurons Die Following DNA Damage in Neurodegenerative Diseases

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

Riluzole does not ameliorate disease caused by cytoplasmic TDP-43 in a mouse model of amyotrophic lateral sclerosis

The mitochondrial-associated ER membrane (MAM) compartment and its dysregulation in amyotrophic lateral sclerosis (ALS)

Emerging evidence highlighting the importance of redox dysregulation in the pathogenesis of amyotrophic lateral sclerosis (ALS)

Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress

Collaborators (26)

Marta Vidal

Sina Shadfar

Ian Blair

Cyril Jones Jagaraj

Angela Laird

Dominic Rowe

Natalie Grima

Sonam Parakh

Amanda Wright

Prachi Mehta

Mary-Louise Rogers

Stephanie Rayner

Julie Hunter

Flora Cheng

Fabiha Farzana

Saravanabavan Sayanthooran

Anand Deva

Luan Luu

Emily Don

Shu Yang

Marco Morsch

Sharlynn Wu

Kelly Jacobs

Anna Konopka

Lezanne Ooi

Albert Lee

Make your next move.