Research supported by MLC
The MLC supports the work of many research groups across a diverse range of disease areas, including hearing loss, type 2 diabetes, sex determination, neurodegeneration and circadian function, to name a few. Such support can include detailed phenotyping in addition to generation and husbandry of mutant mouse lines.
Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock
Bafna, A., Banks, G., Hastings, M. H., Nolan, P. M.
Cysteine-lowering treatment with mesna against obesity: Proof of concept and results from a human phase I, dose-finding study
Vinknes, K. J. Olsen, T. Zare, H. K. Bastani, N. E. Stolt, E. Dahl, A. F. Cox, R. D. Refsum, H. Retterstol, K. Asberg, A. Elshorbagy, A.
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout
Bai, Y., Bentley, L., Ma, C., Naveenan, N., Cleak, J., Wu, Y., Simon, M. M., Westerberg, H., Cañas, R. C., Horner, N., Pandey, R., Paphiti, K., Schulze, U., Mianné, J., Hough, T., Teboul, L., de Baaij, J. H. F., Cox, R. D.
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6
Jones, E., Hill, E., Linehan, J., Nazari, T., Caulder, A., Codner, G. F., Hutchison, M., Mackenzie, M., Farmer, M., Coysh, T., De Oliveira, M. W., Al-Doujaily, H., Sandberg, M., Viré, E., Cunningham, T. J., Asante, E. A., Brandner, S., Collinge, J., Mead, S.
Absence of Embigin accelerates hearing loss and causes sub-viability, brain and heart defects in C57BL/6N mice due to interaction with Cdh23(ahl)
Newton, S., Aguilar, C., Bunton-Stasyshyn, R. K., Flook, M., Stewart, M., Marcotti, W., Brown, S., Bowl, M. R.