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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.

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).

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.

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).

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
(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).

This list was generated on Wed Sep 15 02:24:48 2021 BST.