Bürer, Céline

ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components

Rohrbach, M., Spencer, H. L., Porter, L. F., Burkitt-Wright, E. M. M., Bürer, C., Janecke, A., Bakshi, M., Sillence, D., Al-Hussain, H., Baumgartner, M., et al. (2013) · Molecular Genetics and Metabolism

Connective tissue disorders researchCorneal surgery and disorders

Cited by 83

Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase

Blomgren, L. K. M., Huber, M., Mackinnon, S. R., Bürer, C., Baslé, A., Yue, W. W., Froese, D. S., & McCorvie, T. J. (2023) · Nature Communications

Folate and B Vitamins ResearchProtein Structure and Dynamics

Cited by 18