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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 (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-.