A/Prof Shireen Lamande
Honorary (Principal Fellow)
Department of Paediatrics
124 Scholarly works
1 Projects
HIGHLIGHTS
2025
Journal article
Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930 189C>T
DOI: 10.1093/brain/awaf1162025
Journal article
Failed cellular surveillance enables pathogenic matrix deposition in a COL2A1-related osteoarthritis
DOI: 10.1016/j.jbc.2025.1104362025
Journal article
Failed Cellular Surveillance Enables Pathogenic Matrix Deposition in a COL2A1 -Related Osteoarthritis.
DOI: 10.1101/2023.10.19.5627802025
Journal article
Viscoelasticity Can Be Tuned Through Covalent Incorporation of Chondroitin Sulphate in Allylated Gelatin Hydrogels
DOI: 10.1002/mabi.2024004222025
Journal article
Generation of an iPSC line (with isogenic control) from the PBMCs of a COL6A1 (c.1056 2T > A) Bethlem myopathy patient
DOI: 10.1016/j.scr.2025.1036732025
Journal article
Human iPSC-derived superficial-zone, deep-zone or hybrid chondrocyte organoids for osteochondral defect repair – first in-vivo study in rat
DOI: 10.1016/j.joca.2025.02.6802024
Journal article
10P Characterization of the severe phenotype of COL6-related dystrophy due to the recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930 189C>T
DOI: 10.1016/j.nmd.2024.07.217
RECENT SCHOLARLY WORKS
2024
Journal article
ER procollagen storage defect without coupled unfolded protein response drives precocious arthritis
DOI: 10.26508/lsa.2024028422024
Journal article
Benfotiamine improves dystrophic pathology and exercise capacity in mdx mice by reducing inflammation and fibrosis
DOI: 10.1093/hmg/ddae0662024
Journal article
The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930 189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.
DOI: 10.1101/2024.03.29.24304673
RECENT PROJECTS
Research Grant
Mutation Analysis of Type I Collagen Within Patients With Dentinogenesis Imperfecta