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Plos One|July 1, 2026
Determining optimal practices for foal weaning - A protocol for a systematic review and network meta-analysisNicole Cranston, Petra Buckley, Lorraine Rose, et al.
Bone|April 4, 2017
Open source software for semi-automated histomorphometry of bone resorption and formation parametersRob J van 't Hof, Lorraine Rose, Euphemie Bassonga, et al.
Aging & Mental Health|April 18, 2024
Psychological interventions designed to reduce relocation stress for older people transitioning into permanent residential aged care: a systematic scoping reviewShanna Fealy, Suzanne McLaren, Melissa Nott, et al.
Journal of Medical Radiation Sciences|March 17, 2026
Letter in Response to 'Standardised Request and Contrast Consent Forms to Enhance Clinical Learning in Radiography Education'Clare L Singh, Kelly Bentley-Spuur, Lorraine Rose, et al.
Nurse Educator|March 19, 2025
Success Strategies That Support First Nations Students in Undergraduate Nursing Programs: A Scoping ReviewLinda Deravin, Rebecca Keogh, Keden Montgomery, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 16, 2021
Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous MiceNerea Alonso, Sachin Wani, Lorraine Rose, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|March 26, 2016
Regulation of angiogenesis through the efficient delivery of microRNAs into endothelial cells using polyamine-coated carbon nanotubesAndrea Masotti, Mark R Miller, Antonella Celluzzi, et al.
Annals of the Rheumatic Diseases|October 8, 2013
Identification of small molecule inhibitors of RANKL and TNF signalling as anti-inflammatory and antiresorptive agents in miceEmmanuel Coste, Iain R Greig, Patrick Mollat, et al.
Disease Models & Mechanisms|August 30, 2018
Zoledronic acid prevents pagetic-like lesions and accelerated bone loss in the p62P394L mouse model of Paget's diseaseAnna Daroszewska, Lorraine Rose, Nadine Sarsam, et al.
Human Molecular Genetics|April 26, 2011
A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in miceAnna Daroszewska, Robert J van 't Hof, Javier A Rojas, et al.
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