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.

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy

Gorvin, C. M., Hannan, F. M., Howles, S. A., Babinsky, V. N., Piret, S. E., Rogers, A., Freidin, A. J., Stewart, M., Paudyal, A., Hough, T. A., Nesbit, M. A., Wells, S., Vincent, T. L., Brown, S. D., Cox, R. D., Thakker, R. V.

(2017) , JCI Insight , 2 , e91103

10.1172/jci.insight.91103

PMC5291742

View Full Paper


Does age matter? The impact of rodent age on study outcomes

Jackson, S. J., Andrews, N., Ball, D., Bellantuono, I., Gray, J., Hachoumi, L., Holmes, A., Latcham, J., Petrie, A., Potter, P., Rice, A., Ritchie, A., Stewart, M., Strepka, C., Yeoman, M., Chapman, K.

(2017) , Lab Anim , 51 , 160-169

10.1177/0023677216653984

PMC5367550

View Full Paper


Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxiety

Moir, L., Bochukova, E. G., Dumbell, R., Banks, G., Bains, R. S., Nolan, P. M., Scudamore, C., Simon, M., Watson, K. A., Keogh, J., Henning, E., Hendricks, A., O'Rahilly, S., Barroso, I., UK10K consortium, Sullivan, A. E., Bersten, D. C., Whitelaw, M. L., Kirsch, S., Bentley, E., Farooqi, I. S., Cox, R. D.

(2017) , Mol Metabol , 6 , 1419-1428

http://dx.doi.org/10.1016/j.molmet.2017.08.006

View Full Paper


Cinacalcet corrects hypercalcemia in mice with an inactivating Galpha11 mutation

Howles, S. A., Hannan, F. M., Gorvin, C. M., Piret, S. E., Paudyal, A., Stewart, M., Hough, T. A., Nesbit, M. A., Wells, S., Brown, S. D., Cox, R. D., Thakker, R. V.

(2017) , JCI Insight , 2 , e96540

10.1172/jci.insight.96540

View Full Paper


Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features

Santiago-Sim, T., Burrage, L. C., Ebstein, F., Tokita, M. J., Miller, M., Bi, W., Braxton, A. A., Rosenfeld, J. A., Shahrour, M., Lehmann, A., Cogne, B., Kury, S., Besnard, T., Isidor, B., Bezieau, S., Hazart, I., Nagakura, H., Immken, L. L., Littlejohn, R. O., Roeder, E., Kara, B., Hardies, K., Weckhuysen, S., May, P., Lemke, J. R., Elpeleg, O., Abu-Libdeh, B., James, K. N., Silhavy, J. L., Issa, M. Y., Zaki, M. S., Gleeson, J. G., Seavitt, J. R., Dickinson, M. E., Ljungberg, M. C., Wells, S., Johnson, S. J., Teboul, L., Eng, C. M., Yang, Y., Kloetzel, P. M., Heaney, J. D., Walkiewicz, M. A.

(2017) , Am J Hum Genet , 100 , 676-688

10.1016/j.ajhg.2017.03.001

PMC5384096

View Full Paper


1 15 16 17 18 19 22