Henrik Fagman
Department of Medical Chemistry and Cell Biology
Institute of Biomedicine
Sahlgrenska Academy at Göteborg University
SE-40530
Sweden
Name/email consistency: high
- The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning. Fagman, H., Liao, J., Westerlund, J., Andersson, L., Morrow, B.E., Nilsson, M. Hum. Mol. Genet. (2007)
- The developing mouse thyroid: embryonic vessel contacts and parenchymal growth pattern during specification, budding, migration, and lobulation. Fagman, H., Andersson, L., Nilsson, M. Dev. Dyn. (2006)
- Genetic deletion of sonic hedgehog causes hemiagenesis and ectopic development of the thyroid in mouse. Fagman, H., Grände, M., Gritli-Linde, A., Nilsson, M. Am. J. Pathol. (2004)
- Expression of classical cadherins in thyroid development: maintenance of an epithelial phenotype throughout organogenesis. Fagman, H., Grände, M., Edsbagge, J., Semb, H., Nilsson, M. Endocrinology (2003)
- Nuclear accumulation of full-length and truncated adenomatous polyposis coli protein in tumor cells depends on proliferation. Fagman, H., Larsson, F., Arvidsson, Y., Meuller, J., Nordling, M., Martinsson, T., Helmbrecht, K., Brabant, G., Nilsson, M. Oncogene (2003)