Items where authors include "Fraser, W.D."

Article

Tattersall, L. orcid.org/0000-0001-8835-0627, Shah, K.M. orcid.org/0000-0001-9909-6409, Lath, D.L. et al. (11 more authors) (2021) The P2RX7B splice variant modulates osteosarcoma cell behaviour and metastatic properties. Journal of Bone Oncology, 31. 100398.

Cronin, O. orcid.org/0000-0002-1365-9942, Forsyth, L., Goodman, K. et al. (39 more authors) (2019) Zoledronate in the prevention of Paget's (ZiPP) : protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget's disease of bone. BMJ Open, 9 (9). e030689.

Gregson, C.L., Wheeler, L., Hardcastle, S.A. et al. (18 more authors) (2016) Mutations in known monogenic high bone mass loci only explain a small proportion of high bone mass cases. Journal of Bone and Mineral Research, 31 (3). pp. 640-649. ISSN 0884-0431

Dancer, R.C., Parekh, D., Lax, S. et al. (19 more authors) (2015) Vitamin D deficiency contributes directly to the acute respiratory distress syndrome (ARDS). Thorax, 70 (7). pp. 617-624. ISSN 0040-6376

Loh, N.Y., Bentley, L., Dimke, H. et al. (17 more authors) (2013) Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5. PLoS ONE, 8 (1). e55412. ISSN 1932-6203

Gartland, A. orcid.org/0000-0002-3712-2437, Skarratt, K.K., Hocking, L.J. et al. (7 more authors) (2012) Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal women. European Journal of Human Genetics, 20 (5). pp. 559-564. ISSN 1018-4813