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foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish.
Whitesell TR, Chrystal PW, Ryu JR, Munsie N, Grosse A, French CR, Workentine ML, Li R, Zhu LJ, Waskiewicz A, Lehmann OJ, Lawson ND, Childs SJ. Whitesell TR, et al. Among authors: french cr. Dev Biol. 2019 Sep 1;453(1):34-47. doi: 10.1016/j.ydbio.2019.06.005. Epub 2019 Jun 11. Dev Biol. 2019. PMID: 31199900 Free article.
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ. Chrystal PW, et al. Among authors: french cr. Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170. Genes (Basel). 2021. PMID: 33530637 Free PMC article.
Pbx homeodomain proteins pattern both the zebrafish retina and tectum.
French CR, Erickson T, Callander D, Berry KM, Koss R, Hagey DW, Stout J, Wuennenberg-Stapleton K, Ngai J, Moens CB, Waskiewicz AJ. French CR, et al. BMC Dev Biol. 2007 Jul 16;7:85. doi: 10.1186/1471-213X-7-85. BMC Dev Biol. 2007. PMID: 17634100 Free PMC article.
GDF6, a novel locus for a spectrum of ocular developmental anomalies.
Asai-Coakwell M, French CR, Berry KM, Ye M, Koss R, Somerville M, Mueller R, van Heyningen V, Waskiewicz AJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: french cr. Am J Hum Genet. 2007 Feb;80(2):306-15. doi: 10.1086/511280. Epub 2006 Dec 29. Am J Hum Genet. 2007. PMID: 17236135 Free PMC article.
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
Ye M, Berry-Wynne KM, Asai-Coakwell M, Sundaresan P, Footz T, French CR, Abitbol M, Fleisch VC, Corbett N, Allison WT, Drummond G, Walter MA, Underhill TM, Waskiewicz AJ, Lehmann OJ. Ye M, et al. Among authors: french cr. Hum Mol Genet. 2010 Jan 15;19(2):287-98. doi: 10.1093/hmg/ddp496. Epub 2009 Oct 28. Hum Mol Genet. 2010. PMID: 19864492
49 results