Selected publications

Huh SH*, Warchol ME, Ornitz DM*. Cochlear progenitor number is controlled through mesenchymal FGF receptor signaling, eLife. 2015 Apr 27;4. doi: 10.7554/eLife.05921.  *Correspondence.

Kim JY, Lee RH, Kim TM, Kim DW, Jeon YJ, Huh SH, OH SY, Kyba M, Kataoka H, Choi K, Ornitz DM, Chae JI, Park C. OVOL2 is a critical regulator of ER71 in generating FLK+ cells, hematopoietic and endothelial cells from embryonic stem cells, Blood. 2014 Nov 6;124(19):2948-52.

Chen Z, Huang J, Liu Y, Dattilo LK, Huh SH, Ornitz D, Beebe DC. FGF signaling activates a Sox9-Sox10 pathway for the formation and branching morphogenesis of mouse ocular glands, Development. 2014 Jul;141(13):2691-701.

Huh SH*, Närhi K*, Lindfors PH, Häärä O, Yang L, Ornitz DM**, Mikkola ML**. FGF20 governs formation of primary and secondary dermal condensations in developing hair follicles, Genes&Development 2013 Feb; 27: 450-458 *Equal contribution, **Correspondence. Evaluated by Faculty of 1000.

Lin C, Yin Y, Bell SM, Veith GM, Chen H, Huh SH, Ornitz DM, Ma L. Delineating a Conserved Genetic Cassette Promoting Outgrowth of Body Appendages. PLoS Genet. 9(1): e1003231.

Häärä O, Harjunmaa E, Lindfors PH, Huh SH, Fliniaux I, Åberg T, Jernvall J, Ornitz DM, Mikkola ML, Thesleff I. Ectodysplasin regulates activator-inhibitor balance in murine tooth development through Fgf20 signaling, Development 2012 Sep;139(17):3189-99.

Barak H*, Huh SH*, Chen S, Jeanpierre S, Martinovic J, Parisot M, Bole-Feysot C, Nitschké P, Salomon R, Antignac C, Ornitz DM**, Kopan R**. FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man, Dev. Cell. 2012 Jun 22(6):1191-1207 *Equal contribution, **Correspondence. Previewed in ‘Dev.Cell.’ Featured in Cover Page. Evaluated by Faculty of 1000.

Huh SH, Jones J, Warchol ME, Ornitz DM. Differentiation of the lateral compartment of the cochlea    requires a temporally restricted FGF20 signal, PLoS Biology 10(1): e1001231. Highlighted in ‘Nature’. Evaluated by Faculty of 1000.

Huh SH and Ornitz DM. b-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1, Development 2010 Apr;137(7):1137-47.

Yin Y, White AC, Huh SH, Hilton MJ, Kanazawa H, Long F, Ornitz DM. An FGF-WNT gene regulatory network controls lung mesenchyme development. Dev. Biol. 2008 Jul 15;319(2):426-36.

Complete list of publications