Mellis, David
University of Aberdeen
2 papers on CoChat
Most cited papers
- Verified
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
Guerrini, M. M., Sobacchi, C., Cassani, B., Abinun, M., Kilic, S. S., Pangrazio, A., Moratto, D., Mazzolari, E., Clayton-Smith, J., Orchard, P., et al. (2008) · The American Journal of Human Genetics
Bone Metabolism and DiseasesImmunodeficiency and Autoimmune Disorders
Cited by 309
- Verified
New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis
Crockett, J. C., Mellis, D. J., Scott, D. I., & Helfrich, M. H. (2011) · Osteoporosis International
Bone Metabolism and DiseasesOsteomyelitis and Bone Disorders Research
Cited by 143
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