LINE-1 elements and X chromosome inactivation: A function for “junk” DNA?

Por Lyon, Mary F.
Publicado em 2000

Introduction by the Chairman

Por Lyon, Mary F.
Publicado em 1974

Hereditary absence of otoliths in the house mouse

Por Lyon, Mary F.
Publicado em 1951

Do LINEs Have a Role in X-Chromosome Inactivation?

Por Lyon, Mary F.
Publicado em 2006

Sex Chromatin and Gene Action in the Mammalian X-Chromosome

Por Lyon, Mary F.
Publicado em 1962

Foam-cell Reticulosis of Mice: An Inherited Condition Resembling Gaucher's and Niemann-Pick Diseases

Por Lyon, Mary F., Hulse, E. V., Rowe, C. E.
Publicado em 1965

Morphogenesis of Doublefoot (Dbf), a mouse mutant with polydactyly and craniofacial defects

Por HAYES, CHRISTOPHER, LYON, MARY F., MORRISS-KAY, GILLIAN M.
Publicado em 1998

Sox6 is a candidate gene for p(100H) myopathy, heart block, and sudden neonatal death

Por Hagiwara, Nobuko, Klewer, Scott E., Samson, Ricardo A., Erickson, Drew T., Lyon, Mary F., Brilliant, Murray H.
Publicado em 2000

Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification

Por Hough, Tertius A., Bogani, Debora, Cheeseman, Michael T., Favor, Jack, Nesbit, M. Andrew, Thakker, Rajesh V., Lyon, Mary F.
Publicado em 2004

An 85-kb tandem triplication in the slow Wallerian degeneration (Wld(s)) mouse

Por Coleman, Michael P., Conforti, Laura, Buckmaster, E. Anne, Tarlton, Andrea, Ewing, Robert M., Brown, Michael C., Lyon, Mary F., Perry, V. Hugh
Publicado em 1998

A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice

Por Lehman, Anne L., Nakatsu, Yoshimichi, Ching, Ada, Bronson, Roderick T., Oakey, Rebecca J., Keiper-Hrynko, Natalie, Finger, Joshua N., Durham-Pierre, Donna, Horton, Daniel B., Newton, J Michael, Lyon, Mary F., Brilliant, Murray H.
Publicado em 1998