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Page 1
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2.
Aten E, Brasz LC, Bornholdt D, Hooijkaas IB, Porteous ME, Sybert VP, Vermeer MH, Vossen RH, van der Wielen MJ, Bakker E, Breuning MH, Grzeschik KH, Oosterwijk JC, den Dunnen JT. Aten E, et al. Among authors: hooijkaas ib. Hum Mutat. 2010 Oct;31(10):1125-33. doi: 10.1002/humu.21335. Hum Mutat. 2010. PMID: 20672378
Conserved NPPB+ Border Zone Switches From MEF2- to AP-1-Driven Gene Program.
van Duijvenboden K, de Bakker DEM, Man JCK, Janssen R, Günthel M, Hill MC, Hooijkaas IB, van der Made I, van der Kraak PH, Vink A, Creemers EE, Martin JF, Barnett P, Bakkers J, Christoffels VM. van Duijvenboden K, et al. Among authors: hooijkaas ib. Circulation. 2019 Sep 9;140(10):864-879. doi: 10.1161/CIRCULATIONAHA.118.038944. Epub 2019 Jul 1. Circulation. 2019. PMID: 31259610
Genetic Dissection of a Super Enhancer Controlling the Nppa-Nppb Cluster in the Heart.
Man JCK, van Duijvenboden K, Krijger PHL, Hooijkaas IB, van der Made I, de Gier-de Vries C, Wakker V, Creemers EE, de Laat W, Boukens BJ, Christoffels VM. Man JCK, et al. Among authors: hooijkaas ib. Circ Res. 2021 Jan 8;128(1):115-129. doi: 10.1161/CIRCRESAHA.120.317045. Epub 2020 Oct 27. Circ Res. 2021. PMID: 33107387
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