Mary F. Lyon, PhD, FRS, DSc

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Nag N, Peterson K, Wyatt K, et al. (2007) Endogenous retroviral insertion in Cryge in the mouse No3 cataract mutant. Genomics. 89: 512-20
Lyon M. (2007) X-chromosome inactivation and human genetic disease. Acta Paediatrica. 91: 107-112
Lyon MF. (2006) Do LINEs have a role in X-chromosome inactivation? Journal of Biomedicine & Biotechnology. 2006: 59746
Hough TA, Bogani D, Cheeseman MT, et al. (2004) Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification. Proceedings of the National Academy of Sciences of the United States of America. 101: 13566-71
Lyon MF. (2004) Vertebrate Sex Chromosomes. Edited by N. TAKAGI. S. Karger AG. 2003. 352 pages. ISBN 3 8055 7637 4. Price $138.25 (hardback). Genetics Research. 83: 67-68
Lyon MF. (2003) The Lyon and the LINE hypothesis. Seminars in Cell & Developmental Biology. 14: 313-8
Lyon MF. (2003) Transmission ratio distortion in mice. Annual Review of Genetics. 37: 393-408
Lyon MF, Jamieson RV, Perveen R, et al. (2003) A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding Human Molecular Genetics. 12: 585-594
Hayes C, Rump A, Cadman MR, et al. (2001) A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35. Genomics. 78: 197-205
Lyon MF. (2000) LINE-1 elements and X chromosome inactivation: A function for 'junk' DNA? Proceedings of the National Academy of Sciences of the United States of America. 97: 6248-6249