Erika A. Bosman

Catweasel mice: A novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome

Elizabeth Quint, Helmut Fuchs, Karen P. Steel, 2009, Developmental biology.

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1

Jacqueline K. White, K. Steel, C. Podrini, 2012, Mammalian Genome.

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.

K. Steel, P. Scambler, K. Devriendt, 2009, The Journal of clinical investigation.

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.

K. Steel, E. Bosman, A. Penn, 2005, Human molecular genetics.

Study of smell and reproductive organs in a mouse model for CHARGE syndrome

K. Steel, C. V. van Ravenswaaij-Arts, J. Bergman, 2009, European Journal of Human Genetics.

Expression of the inhibitory Smad7 in early mouse development and upregulation during embryonic vasculogenesis

M. Goumans, C. Mummery, D. Huylebroeck, 2000, Developmental dynamics : an official publication of the American Association of Anatomists.

Transforming growth factor β signalling in vitro and in vivo: activin ligand–receptor interaction, Smad5 in vasculogenesis, and repression of target genes by the δEF1/ZEB-related SIP1 in the vertebrate embryo

L. Nelles, D. Huylebroeck, K. Verschueren, 2001, Molecular and Cellular Endocrinology.

Smad5 determines murine amnion fate through the control of bone morphogenetic protein expression and signalling levels

E. Bosman, D. Huylebroeck, L. Schoonjans, 2006, Development.