Berdal, Ariane

Msx2 −/− transgenic mice develop compound amelogenesis imperfecta, dentinogenesis imperfecta and periodental osteopetrosis

Aïoub, M., Lézot, F., Molla, M., Castaneda, B., Robert, B., Goubin, G., Néfussi, J. R., & Berdal, A. (2007) · Bone

dental development and anomaliesBone Metabolism and Diseases

Cited by 91

Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders

de La Dure‐Molla, M., Fournier, B. P., Manzanares, M. C., Acevedo, A. C., Hennekam, R. C., Friedlander, L., Boy‐Lefèvre, M., Kerner, S., Toupenay, S., Garrec, P., et al. (2019) · American Journal of Medical Genetics Part A

dental development and anomaliesCleft Lip and Palate Research

Cited by 85

MSX2 in ameloblast cell fate and activity

Babajko, S., de La Dure-Molla, M., Jedeon, K., & Berdal, A. (2015) · Frontiers in Physiology

dental development and anomaliesBone and Dental Protein Studies

Cited by 40

Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study

Friedlander, L., Berdal, A., Boizeau, P., Licht, B. A., Manière, M.-C., Picard, A., Azzis, O., Vazquez, M.-P., Alberti, C., & Molla, M. D. L. D. (2019) · Orphanet Journal of Rare Diseases

Dental Health and Care Utilizationdental development and anomalies

Cited by 30

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

Role of RANKL (TNFSF11)-Dependent Osteopetrosis in the Dental Phenotype of Msx2 Null Mutant Mice

Castaneda, B., Simon, Y., Ferbus, D., Robert, B., Chesneau, J., Mueller, C., Berdal, A., & Lézot, F. (2013) · PLoS ONE

Bone Metabolism and Diseasesdental development and anomalies

Cited by 15