KATNAL1 regulation of sertoli cell microtubule dynamics is essential for spermiogenesis and male fertility von Smith, Lee B, Milne, Laura, Nelson, Nancy, Eddie, Sharon, Brown, Pamela, Atanassova, Nina, O'Bryan, Moira K, O'Donnell, Liza, Rhodes, Danielle, Wells, Sara, Napper, Diane, Nolan, Patrick, Lalanne, Zuzanna, Cheeseman, Michael, Peters, Josephine

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Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study von Medina-Gomez, Carolina, Felix, Janine Frédérique, Estrada, Karol, Peters, Marjoline Josephine, Herrera, Lizbeth, Kruithof, Claudia Jeanette, Duijts, Liesbeth, Hofman, Albert, van Duijn, Cornelia Marja, Uitterlinden, Andreas Gerardus, Jaddoe, Vincent Wilfred Vishal, Rivadeneira, Fernando

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The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1α, encoded by the Eef1a2 gene von Chambers, Doreen M., Peters, Josephine, Abbott, Catherine M.

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An Imprinted Transcript, Antisense to Nesp, Adds Complexity to the Cluster of Imprinted Genes at the Mouse Gnas Locus von Wroe, Stephanie F., Kelsey, Gavin, Skinner, Judith A., Bodle, Dorothy, Ball, Simon T., Beechey, Colin V., Peters, Josephine, Williamson, Christine M.

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Interactions Between Imprinting Effects in the Mouse von Cattanach, Bruce M, Beechey, Colin V, Peters, Josephine

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Progressive Loss of Motor Neuron Function in Wasted Mice: Effects of a Spontaneous Null Mutation in the Gene for the eEF1A2 Translation Factor von Newbery, Helen J., Gillingwater, Thomas H., Dharmasaroja, Permphan, Peters, Josephine, Wharton, Stephen B., Thomson, Derek, Ribchester, Richard R., Abbott, Catherine M.

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Identification of Imprinted Loci by Methylation-Sensitive Representational Difference Analysis: Application to Mouse Distal Chromosome 2 von Kelsey, Gavin, Bodle, Dorothy, Miller, Howard J., Beechey, Colin V., Coombes, Candice, Peters, Josephine, Williamson, Christine M.

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Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation von Clapcott, Steven J, Peters, Josephine, Orban, Paul C, Brambilla, Riccardo, Graham, Chris F

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Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice von Pennisi, David, Gardner, Jennifer, Chambers, Doreen, Hosking, Brett, Peters, Josephine, Muscat, George, Abbott, Catherine, Koopman, Peter

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An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus von Wroe, Stephanie F., Kelsey, Gavin, Skinner, Judith A., Bodle, Dorothy, Ball, Simon T., Beechey, Colin V., Peters, Josephine, Williamson, Christine M.

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The Lethal Mutation of the Mouse Wasted (wst) is a Deletion that Abolishes Expression of a Tissue-Specific Isoform of Translation Elongation Factor 1α , Encoded by the Eefla2 Gene von Chambers, Doreen M., Peters, Josephine, Abbott, Catherine M.

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Informatics for mutagenesis: the design of Mutabase—a distributed data recording system for animal husbandry, mutagenesis, and phenotypic analysis von Strivens, Mark A, Selley, Rachel L, Greenaway, Simon J, Hewitt, Mazda, Liu, Xinhong, Battershill, Kirstin, McCormack, Stefan L, Pickford, Karen A, Vizor, Lucie, Nolan, Patrick M, Hunter, A. Jacqueline, Peters, Josephine, Brown, Stephen D.M

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Demonstration of Autoimmunity in the Tight Skin-2 Mouse: A Model for Scleroderma von Gentiletti, Julieta, McCloskey, Laura J, Artlett, Carol M, Peters, Josephine, Jimenez, Sergio A, Christner, Paul J

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A comparison of 24micro metre and 6cm star-formation tracers in the spiral galaxy M83 von Peters, Josephine

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Interactions between imprinting effects in ths mouse von Cattanach, Bruce M, Beechey, Colin V, Peters, Josephine

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Two imprinted gene mutations : three phenotypes von CATTANACH, Bruce M, PETERS, Josephine, BALL, Simon, RASBERRY, Carol

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Collagen Dysregulation in the Dermis of the Sagg/+ Mouse: A Loose Skin Model von Christner, Paul J., Gentiletti, Julieta, Peters, Josephine, Ball, Simon T., Yamauchi, Mitsuo, Atsawasuwan, Phimon, Beason, David P., Soslowsky, Louis J., Birk, David E.

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Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study von Medina-Gomez, Carolina, Felix, Janine Frédérique, Estrada, Karol, Peters, Marjoline Josephine, Herrera, Lizbeth, Kruithof, Claudia Jeanette, Duijts, Liesbeth, Hofman, Albert, van Duijn, Cornelia Marja, Uitterlinden, Andreas Gerardus, Jaddoe, Vincent Wilfred Vishal, Rivadeneira, Fernando

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Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2 von Kikyo, N, Williamson, C M, John, R M, Barton, S C, Beechey, C V, Ball, S T, Cattanach, B M, Surani, M A, Peters, J

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Novel phenotypes identified by plasma biochemical screening in the mouse von Hough, Tertius A, Nolan, Patrick M, Tsipouri, Vicky, Toye, Ayo A, Gray, Ian C, Goldsworthy, Michelle, Moir, Lee, Cox, Roger D, Clements, Sian, Glenister, Peter H, Wood, John, Selley, Rachael L, Strivens, Mark A, Vizor, Lucie, McCormack, Stefan L, Peters, Josephine, Fisher, Elizabeth M, Spurr, Nigel, Rastan, Sohaila, Martin, Joanne E, Brown, Steve D M, Hunter, A Jacqueline

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