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New insights into the role of matrix metalloproteinase 3 (MMP3) in bone.
Jehan F, Zarka M, de la Houssaye G, Veziers J, Ostertag A, Cohen-Solal M, Geoffroy V. Jehan F, et al. Among authors: de la houssaye g. FASEB Bioadv. 2022 Jun 15;4(8):524-538. doi: 10.1096/fba.2021-00092. eCollection 2022 Aug. FASEB Bioadv. 2022. PMID: 35949513 Free PMC article.
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.
Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL. Schorderet DF, et al. Among authors: de la houssaye g. Am J Hum Genet. 2008 May;82(5):1178-84. doi: 10.1016/j.ajhg.2008.03.007. Am J Hum Genet. 2008. PMID: 18423520 Free PMC article.
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M. Dansault A, et al. Among authors: de la houssaye g. Mol Vis. 2007 Apr 2;13:511-23. Mol Vis. 2007. PMID: 17417613 Free PMC article.
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M. Vieira V, et al. Among authors: de la houssaye g. Mol Vis. 2006 Dec 1;12:1448-60. Mol Vis. 2006. PMID: 17167399 Free article.