Sharpe, Paul T.

An Aneuploid Mouse Strain Carrying Human Chromosome 21 with down Syndrome Phenotypes.

O'Doherty, A., Ruf, S., Mulligan, C., Hildreth, V., Errington, M. L., Cooke, S., Sesay, A., Modino, S., Vanes, L., Hernandez, D., et al. (2005) · Science

Down syndrome and intellectual disability researchGenomic variations and chromosomal abnormalities

Cited by 434

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Headon, D. J., Emmal, S. A., Ferguson, B. M., Tucker, A. S., Justice, M. J., Sharpe, P. T., Zonana, J., & Overbeek, P. A. (2001) · Nature

dental development and anomaliesHair Growth and Disorders

Cited by 378

Craniofacial Development

Depew, M. J., Tucker, A. S., & Sharpe, P. T. (2002) · Mouse Development

Developmental Biology and Gene RegulationCraniofacial Disorders and Treatments

Cited by 259

Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis.

Tucker, A. S., Headon, D. J., Schneider, P., Ferguson, B. M., Overbeek, P., Tschopp, J., & Sharpe, P. T. (2000) · Development

dental development and anomaliesDevelopmental Biology and Gene Regulation

Cited by 211

The activation level of the TNF family receptor, Edar, determines cusp number and tooth number during tooth development.

Tucker, A. S., Headon, D. J., Courtney, J.-M., Overbeek, P., & Sharpe, P. T. (2004) · Developmental Biology

dental development and anomaliesDevelopmental Biology and Gene Regulation

Cited by 146

Mesenchymal stem cells inhibit T-cell function through conserved induction of cellular stress

Laing, A. G., Fanelli, G., Ramirez-Valdez, A., Lechler, R. I., Lombardi, G., & Sharpe, P. T. (2019) · PLOS ONE

Mesenchymal stem cell researchT-cell and B-cell Immunology

Cited by 59

Shape and volume of craniofacial cavities in intentional skull deformations

Khonsari, R. H., Friess, M., Nysjö, J., Odri, G., Malmberg, F., Nyström, I., Messo, E., Hirsch, J. M., Cabanis, E. A. M., Kunzelmann, K. H., et al. (2013) · American Journal of Physical Anthropology

Forensic Anthropology and Bioarchaeology StudiesCraniofacial Disorders and Treatments

Cited by 25

Dlx homeobox gene family expression in osteoclasts

Lézot, F., Thomas, B. L., Blin‐Wakkach, C., Castaneda, B., Bolanos, A., Hotton, D., Sharpe, P. T., Heymann, D., Carles, G. F., Grigoriadis, A. E., et al. (2010) · Journal of Cellular Physiology

Bone Metabolism and DiseasesDevelopmental Biology and Gene Regulation

Cited by 24

Overactivation of the NF‐κB pathway impairs molar enamel formation

Yamada, A., Kawasaki, M., Miake, Y., Yamada, Y., Blackburn, J., Kawasaki, K., Trakanant, S., Nagai, T., Nihara, J., Kudo, T., et al. (2020) · Oral Diseases

dental development and anomaliesBone and Dental Protein Studies

Cited by 9