Associated Papers
A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
Kırkgöz T et al.
Frontiers in Genetics, 2022
Genetic disorders associated with the RANKL/OPG/RANK pathway.
Xue JY et al.
Journal of Bone and Mineral Metabolism, 2021
Dysosteosclerosis is also caused by TNFRSF11A mutation.
Guo L et al.
Journal of Human Genetics, 2018
RANK receptor oligomerisation in the regulation of NFκB signalling.
Das S et al.
Journal of Molecular Endocrinology, 2014
New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis.
Crockett JC et al.
Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the Usa, 2011
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations.
Guerrini MM et al.
American Journal of Human Genetics, 2008
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