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Page 1
Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures.
Coyac BR, Hoac B, Chafey P, Falgayrac G, Slimani L, Rowe PS, Penel G, Linglart A, McKee MD, Chaussain C, Bardet C. Coyac BR, et al. Among authors: bardet c. J Dent Res. 2018 Feb;97(2):184-191. doi: 10.1177/0022034517728497. Epub 2017 Sep 7. J Dent Res. 2018. PMID: 28880715 Free PMC article.
MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia.
Salmon B, Bardet C, Khaddam M, Naji J, Coyac BR, Baroukh B, Letourneur F, Lesieur J, Decup F, Le Denmat D, Nicoletti A, Poliard A, Rowe PS, Huet E, Vital SO, Linglart A, McKee MD, Chaussain C. Salmon B, et al. Among authors: bardet c. PLoS One. 2013;8(2):e56749. doi: 10.1371/journal.pone.0056749. Epub 2013 Feb 22. PLoS One. 2013. PMID: 23451077 Free PMC article.
Wnt Acts as a Prosurvival Signal to Enhance Dentin Regeneration.
Hunter DJ, Bardet C, Mouraret S, Liu B, Singh G, Sadoine J, Dhamdhere G, Smith A, Tran XV, Joy A, Rooker S, Suzuki S, Vuorinen A, Miettinen S, Chaussain C, Helms JA. Hunter DJ, et al. Among authors: bardet c. J Bone Miner Res. 2015 Jul;30(7):1150-9. doi: 10.1002/jbmr.2444. J Bone Miner Res. 2015. PMID: 25556760 Free article.
[Diseases revealed by the mouth].
Opsahl-Vital S, Gaucher C, Bardet C, Courson F, Linglart A, Chaussain C. Opsahl-Vital S, et al. Among authors: bardet c. Arch Pediatr. 2015 May;22(5 Suppl 1):151-2. doi: 10.1016/S0929-693X(15)30075-0. Arch Pediatr. 2015. PMID: 26112566 French. No abstract available.
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation.
Bardet C, Courson F, Wu Y, Khaddam M, Salmon B, Ribes S, Thumfart J, Yamaguti PM, Rochefort GY, Figueres ML, Breiderhoff T, Garcia-Castaño A, Vallée B, Le Denmat D, Baroukh B, Guilbert T, Schmitt A, Massé JM, Bazin D, Lorenz G, Morawietz M, Hou J, Carvalho-Lobato P, Manzanares MC, Fricain JC, Talmud D, Demontis R, Neves F, Zenaty D, Berdal A, Kiesow A, Petzold M, Menashi S, Linglart A, Acevedo AC, Vargas-Poussou R, Müller D, Houillier P, Chaussain C. Bardet C, et al. J Bone Miner Res. 2016 Mar;31(3):498-513. doi: 10.1002/jbmr.2726. Epub 2015 Oct 20. J Bone Miner Res. 2016. PMID: 26426912 Free article.
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.
Yamaguti PM, Neves FA, Hotton D, Bardet C, de La Dure-Molla M, Castro LC, Scher MD, Barbosa ME, Ditsch C, Fricain JC, de La Faille R, Figueres ML, Vargas-Poussou R, Houillier P, Chaussain C, Babajko S, Berdal A, Acevedo AC. Yamaguti PM, et al. Among authors: bardet c. J Med Genet. 2017 Jan;54(1):26-37. doi: 10.1136/jmedgenet-2016-103956. Epub 2016 Aug 16. J Med Genet. 2017. PMID: 27530400
54 results