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Facial asymmetry tracks genetic diversity among Gorilla subspecies.
McGrath K, Eriksen AB, García-Martínez D, Galbany J, Gómez-Robles A, Massey JS, Fatica LM, Glowacka H, Arbenz-Smith K, Muvunyi R, Stoinski TS, Cranfield MR, Gilardi K, Shalukoma C, de Merode E, Gilissen E, Tocheri MW, McFarlin SC, Heuzé Y. McGrath K, et al. Among authors: heuze y. Proc Biol Sci. 2022 Feb 23;289(1969):20212564. doi: 10.1098/rspb.2021.2564. Epub 2022 Feb 23. Proc Biol Sci. 2022. PMID: 35193404 Free PMC article.
Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.
Heuzé Y, Martínez-Abadías N, Stella JM, Arnaud E, Collet C, García Fructuoso G, Alamar M, Lo LJ, Boyadjiev SA, Di Rocco F, Richtsmeier JT. Heuzé Y, et al. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):250-9. doi: 10.1002/bdra.23228. Epub 2014 Feb 27. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24578066 Free PMC article. Clinical Trial.
FGFR3 mutation causes abnormal membranous ossification in achondroplasia.
Di Rocco F, Biosse Duplan M, Heuzé Y, Kaci N, Komla-Ebri D, Munnich A, Mugniery E, Benoist-Lasselin C, Legeai-Mallet L. Di Rocco F, et al. Among authors: heuze y. Hum Mol Genet. 2014 Jun 1;23(11):2914-25. doi: 10.1093/hmg/ddu004. Epub 2014 Jan 12. Hum Mol Genet. 2014. PMID: 24419316
FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model.
Cornille M, Moriceau S, Khonsari RH, Heuzé Y, Loisay L, Boitez V, Morice A, Arnaud E, Collet C, Bensidhoum M, Kaci N, Boddaert N, Paternoster G, Rauschendorfer T, Werner S, Mansour SL, Di Rocco F, Oury F, Legeai-Mallet L. Cornille M, et al. Among authors: heuze y. J Exp Med. 2022 Apr 4;219(4):e20201879. doi: 10.1084/jem.20201879. Epub 2022 Mar 7. J Exp Med. 2022. PMID: 35254402 Free PMC article.
60 results