List of works - Sarah L. Rea

A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype

scientific article published in July 2006

ALS-FTLD associated mutations of SQSTM1 impact on Keap1-Nrf2 signalling

scientific article published on 20 August 2016

An FTLD-associated SQSTM1 variant impacts Nrf2 and NF-κB signalling and is associated with reduced phosphorylation of p62

scientific article published on 04 April 2019

Bafilomycin A1 Attenuates Osteoclast Acidification and Formation, Accompanied by Increased Levels of SQSTM1/p62 Protein

scientific article published on 26 November 2015

Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease

scientific article published in November 2013

Disulfiram attenuates osteoclast differentiation in vitro: a potential antiresorptive agent

scientific article

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

scientific article

New insights into the role of sequestosome 1/p62 mutant proteins in the pathogenesis of Paget's disease of bone.

scientific article published on 23 April 2013

Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and function

scientific article

SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD.

scientific article published on 30 January 2014

Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding.

scientific article

Targeted sequencing of in familial Paget's disease of bone

scientific article published on 21 February 2019

The Changing Presentation of Paget's Disease of Bone in Australia, A High Prevalence Region.

scientific article published on 7 September 2017

The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone.

scientific article

The endoplasmic reticulum-associated protein, OS-9, behaves as a lectin in targeting the immature calcium-sensing receptor

scientific article published on 17 April 2017

The helix 1-3 loop in the glucocorticoid receptor LBD is a regulatory element for FKBP cochaperones.

scientific article

p62 overexpression induces TDP-43 cytoplasmic mislocalisation, aggregation and cleavage and neuronal death

scientific article published on 01 June 2021

List of works by Sarah L. Rea

A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype

ALS-FTLD associated mutations of SQSTM1 impact on Keap1-Nrf2 signalling

An FTLD-associated SQSTM1 variant impacts Nrf2 and NF-κB signalling and is associated with reduced phosphorylation of p62

Bafilomycin A1 Attenuates Osteoclast Acidification and Formation, Accompanied by Increased Levels of SQSTM1/p62 Protein

Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease

Disulfiram attenuates osteoclast differentiation in vitro: a potential antiresorptive agent

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

New insights into the role of sequestosome 1/p62 mutant proteins in the pathogenesis of Paget's disease of bone.

Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and function

SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD.

Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding.

Targeted sequencing of in familial Paget's disease of bone

The Changing Presentation of Paget's Disease of Bone in Australia, A High Prevalence Region.

The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone.

The endoplasmic reticulum-associated protein, OS-9, behaves as a lectin in targeting the immature calcium-sensing receptor

The helix 1-3 loop in the glucocorticoid receptor LBD is a regulatory element for FKBP cochaperones.

p62 overexpression induces TDP-43 cytoplasmic mislocalisation, aggregation and cleavage and neuronal death