Hakola, Panu

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts

Paloneva, J., Kestilä, M., Wu, J., Salminen, A., Böhling, T., Ruotsalainen, V., Hakola, P., Bakker, A. B. H., Phillips, J. H., Pekkarinen, P., et al. (2000) · Nature Genetics

Genomics and Rare DiseasesBone Metabolism and Diseases

Cited by 460

DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features

Paloneva, J., Mandelin, J., Kiialainen, A., Böhling, T., Prudlo, J., Hakola, P., Haltia, M., Konttinen, Y. T., & Peltonen, L. (2003) · The Journal of Experimental Medicine

Bone Metabolism and DiseasesImmunodeficiency and Autoimmune Disorders

Cited by 318