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Number of items: 5.

Loveridge, Carolyn J, van't Hof, Rob J, Charlesworth, Gemma, King, Ayala, Tan, Ee Hong, Rose, Lorraine, Daroszewska, Anna ORCID: 0000-0002-6692-6610, Prior, Amanda, Ahmad, Imran, Welsh, Michelle
et al (show 6 more authors) (2017) Analysis of Nkx3.1: Cre-driven Erk5 deletion reveals a profound spinal deformity which is linked to increased osteoclast activity. SCIENTIFIC REPORTS, 7 (1). 13241-.

Cross, Sally H, Macalinao, Danilo G, Mckie, Lisa, Rose, Lorraine, Kearney, Alison L, Rainger, Joe, Thaung, Caroline, Keighren, Margaret, Jadeja, Shalini, West, Katrine
et al (show 8 more authors) (2014) A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation. PLOS GENETICS, 10 (5). e1004359-.

Alonso, Nerea, Wani, Sachin, Rose, Lorraine, van't Hof, Rob J, Ralston, Stuart H and Albagha, Omar ME
(2021) Insertion mutation in Tnfrsf11a causes a Paget's disease‐like phenotype in heterozygous mice and osteopetrosis in homozygous mice. Journal of Bone and Mineral Research, 36 (7). pp. 1376-1386.

Rainger, Joe, Keighren, Margaret, Keene, Douglas R, Charbonneau, Noe L, Rainger, Jacqueline K, Fisher, Malcolm, Mella, Sebastien, Huang, Jeffrey T-J, Rose, Lorraine, van't Hof, Rob
et al (show 3 more authors) (2013) A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse. PLOS GENETICS, 9 (12). e1003998-.

Daroszewska, Anna ORCID: 0000-0002-6692-6610, Rose, Lorraine, Sarsam, Nadine, Charlesworth, Gemma, Prior, Amanda, Rose, Kenneth, Ralston, Stuart H and van 't Hof, Robert J ORCID: 0000-0002-8193-6788
(2018) Zoledronic acid prevents pagetic-like lesions and accelerated bone loss in the p62(P394L) mouse model of Paget's disease. Disease Models and Mechanisms, 11 (9). dmm035576-.

This list was generated on Sat Sep 30 02:40:50 2023 BST.