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Genetics in Medicine
Vig, A. and Poulter, J.A. and Ottaviani, D. and Tavares, E. and Toropova, K. and Tracewska, A.M. and Mollica, A. and Kang, J. and Kehelwathugoda, O. and Paton, T. and Maynes, J.T. and Wheway, G. and Arno, G. and Genomics England Research, C. and Khan, K.N. and McKibbin, M. and Toomes, C. and Ali, M. and Di Scipio, M. and Li, S. and Ellingford, J. and Black, G. and Webster, A. and Rydzanicz, M. and Stawiński, P. and Płoski, R. and Vincent, A. and Cheetham, M.E. and Inglehearn, C.F. and Roberts, Anthony J. and Heon, E. (2020) DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration. Genetics in Medicine 22 (12), pp. 2041-2051. ISSN 1530-0366.
Nature Structural & Molecular Biology
Toropova, K. and Zalyte, R. and Mukhopadhyay, A.G. and Mladenov, M. and Carter, A.P. and Roberts, Anthony J. (2019) Structure of the dynein-2 complex and its assembly with intraflagellar transport trains. Nature Structural & Molecular Biology 26 (9), pp. 823-829. ISSN 1545-9993.
Toropova, K. and Mladenov, M. and Roberts, Anthony (2017) Intraflagellar transport dynein is autoinhibited by trapping of its mechanical and track-binding elements. Nature Structural & Molecular Biology 24 , pp. 461-468. ISSN 1545-9993.