An Artificial Cofactor Catalyzing the Baylis‐Hillman Reaction with Designed Streptavidin as Protein Host

por Lechner, Horst, Emann, Vincent R., Breuning, M., Höcker, Birte
Publicado 2021

Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes.

por Moerland, E., Breuning, M. H., Cornelisse, C. J., Cleton-Jansen, A. M.
Publicado 1997

Genetic counselling and the intention to undergo prophylactic mastectomy: effects of a breast cancer risk assessment

por van Dijk, S, Otten, W, Zoeteweij, M W, Timmermans, D R M, van Asperen, C J, Breuning, M H, Tollenaar, R A E M, Kievit, J
Publicado 2003

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

por Hannes, F D, Sharp, A J, Mefford, H C, de Ravel, T, Ruivenkamp, C A, Breuning, M H, Fryns, J-P, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R C, Cooper, G M, Regan, R, Knight, S J L, Eichler, E E, Vermeesch, J R
Publicado 2009

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects

por van der Linde, I. H. M., Hiemstra, Y. L., Bökenkamp, R., van Mil, A. M., Breuning, M. H., Ruivenkamp, C., ten Broeke, S. W., Veldkamp, R. F., van Waning, J. I., van Slegtenhorst, M. A., van Spaendonck-Zwarts, K. Y., Lekanne Deprez, R. H., Herkert, J. C., Boven, L., van der Zwaag, P. A., Jongbloed, J. D. H., Bootsma, M., Barge-Schaapveld, D. Q. C. M.
Publicado 2017