TRANSMISSION RATIO DISTORTION IN MICE von Lyon, Mary F

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Activating Calcium-Sensing Receptor Mutation in the Mouse Is Associated with Cataracts and Ectopic Calcification von Hough, Tertius A., Bogani, Debora, Cheeseman, Michael T., Favor, Jack, Nesbit, M. Andrew, Thakker, Rajesh V., Lyon, Mary F.

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LINE-1 Elements and X Chromosome Inactivation: A Function for "Junk" DNA? von Lyon, Mary F.

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The Lyon and the LINE hypothesis von Lyon, Mary F

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X-chromosome inactivation von Lyon, Mary F

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Elucidating mouse transmission ratio distortion von Lyon, Mary F

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No longer 'all-or-none' von Lyon, Mary F

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A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract von Steele Jr, Ernest C., Lyon, Mary F., Favor, Jack, Guillot, Pascale V., Boyd, Yvonne, Church, Robert L.

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An 85-kb Tandem Triplication in the Slow Wallerian Degeneration (Wlds) Mouse von Coleman, Michael P., Conforti, Laura, Buckmaster, E. Anne, Tarlton, Andrea, Ewing, Robert M., Brown, Michael C., Lyon, Mary F., Perry, V. Hugh

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Do LINEs have a role in X-chromosome inactivation? von Lyon, Mary F

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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 von Lyon, Mary F., Jamieson, Robyn V., Perveen, Rahat, Glenister, Peter H., Griffiths, Robert, Boyd, Yvonne, Glimcher, Laurie H., Favor, Jack, Munier, Francis L., Black, Graeme C. M.

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A Personal History of the Mouse Genome von Lyon, Mary F

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major brain isoform of Kif1b lacks the putative mitochondria-binding domain von Conforti, Laura, Buckmaster, E. Anne, Tarlton, Andrea, Brown, Michael C, Lyon, Mary F, Perry, V. Hugh, Coleman, Michael P

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death von Hagiwara, N, Klewer, S E, Samson, R A, Erickson, D T, Lyon, M F, Brilliant, M H

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Pinpointing the centre von Lyon, Mary F

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A Very Large Protein with Diverse Functional Motifs is Deficient in rjs (Runty, Jerky, Sterile) Mice von 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.

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The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes von Gardner, John M., Nakatsu, Yoshimichi, Gondo, Yoichi, Lee, Susan, Lyon, Mary F., King, Richard A., Brilliant, Murray H.

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Some Milestones in the History of X-Chromosome Inactivation von Lyon, Mary F

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James Neel and the doubling dose concept von Lyon, Mary F.

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Dynamic changes in paternal X-chromosome activity during imprinted X-chromosome inactivation in mice von Patrat, Catherine, Okamoto, Ikuhiro, Diabangouaya, Patricia, Vialon, Vivian, Le Baccon, Patricia, Chow, Jennifer, Heard, Edith

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