The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway

by Zakia A. Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, Christopher F. Inglehearn, Carmel Toomes, Colin A. Johnson, Daniel J. Jagger
Published 2015-06-01

The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickens.

by Hemanth Tummala, Stewart Fleming, Paul M Hocking, Daniel Wehner, Zahid Naseem, Manir Ali, Christopher F Inglehearn, Nikolai Zhelev, Douglas H Lester
Published 2011-01-01

A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities

by Claire E. L. Smith, Claire E. L. Smith, Jennifer Kirkham, Peter F. Day, Peter F. Day, Francesca Soldani, Esther J. McDerra, Esther J. McDerra, James A. Poulter, Christopher F. Inglehearn, Alan J. Mighell, Alan J. Mighell, Steven J. Brookes
Published 2017-05-01