Pekka Nieminen
Institute of Dentistry
Biomedicum
University of Helsinki
Helsinki
Finland
Name/email consistency: high
- Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location. Nieminen, P., Papagiannoulis-Lascarides, L., Waltimo-Siren, J., Ollila, P., Karjalainen, S., Arte, S., Veerkamp, J., Tallon Walton, V., Chimenos Küstner, E., Siltanen, T., Holappa, H., Lukinmaa, P.L., Alaluusua, S. J. Bone Miner. Res. (2011)
- Genetic basis of tooth agenesis. Nieminen, P. J. Exp. Zool. B Mol. Dev. Evol. (2009)
- MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia. Nieminen, P., Kotilainen, J., Aalto, Y., Knuutila, S., Pirinen, S., Thesleff, I. J. Dent. Res. (2003)
- Identification of a nonsense mutation in the PAX9 gene in molar oligodontia. Nieminen, P., Arte, S., Tanner, D., Paulin, L., Alaluusua, S., Thesleff, I., Pirinen, S. Eur. J. Hum. Genet. (2001)
- A graphical WWW-database on gene expression in tooth. Nieminen, P., Pekkanen, M., Aberg, T., Thesleff, I. Eur. J. Oral Sci. (1998)
