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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Mary F. Lyon

Medical Research Council

Mammalian Genetics Unit

Didcot

UK

[email]@har.mrc.ac.uk

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Affiliations

Medical Research Council, Mammalian Genetics Unit, Didcot, UK. 1998 - 2003
MRC Mammalian Genetics Unit, Harwell, Didcot, Oxon, United Kingdom. 2000 - 2003

References

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. Lyon, M.F., Jamieson, R.V., Perveen, R., Glenister, P.H., Griffiths, R., Boyd, Y., Glimcher, L.H., Favor, J., Munier, F.L., Black, G.C. Hum. Mol. Genet. (2003) [Pubmed]
James Neel and the doubling dose concept. Lyon, M.F. Mutat. Res. (2003) [Pubmed]
Transmission ratio distortion in mice. Lyon, M.F. Annu. Rev. Genet. (2003) [Pubmed]
The Lyon and the LINE hypothesis. Lyon, M.F. Semin. Cell Dev. Biol. (2003) [Pubmed]
A personal history of the mouse genome. Lyon, M.F. Annu. Rev. Genomics. Hum. Genet (2002) [Pubmed]
X-chromosome inactivation and human genetic disease. Lyon, M.F. Acta. Paediatr. Suppl (2002) [Pubmed]
Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions. Lyon, M.F., Schimenti, J.C., Evans, E.P. Genetics (2000) [Pubmed]
LINE-1 elements and X chromosome inactivation: a function for "junk" DNA?. Lyon, M.F. Proc. Natl. Acad. Sci. U.S.A. (2000) [Pubmed]
Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop). Lyon, M.F., Bogani, D., Boyd, Y., Guillot, P., Favor, J. Mol. Vis. (2000) [Pubmed]
X-chromosome inactivation: a repeat hypothesis. Lyon, M.F. Cytogenet. Cell Genet. (1998) [Pubmed]

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