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Number of items: 2.
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.
Wani, Sachin, Daroszewska, Anna, Salter, Donald M, van 't Hof, Rob J 
ORCID: 0000-0002-8193-6788, Ralston, Stuart H and Albagha, Omar ME
(2022)
The Paget's disease of bone risk gene <i>PML</i> is a negative regulator of osteoclast differentiation and bone resorption.
DISEASE MODELS & MECHANISMS, 15 (4).
dmm049318-.