The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification von Cross, Sally H., Mckie, Lisa, Hurd, Toby W., Riley, Sam, Wills, Jimi, Barnard, Alun R., Young, Fiona, MacLaren, Robert E., Jackson, Ian J.

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Novel gene function revealed by mouse mutagenesis screens for models of age-related disease von Potter, Paul K., Bowl, Michael R., Jeyarajan, Prashanthini, Wisby, Laura, Blease, Andrew, Goldsworthy, Michelle E., Simon, Michelle M., Greenaway, Simon, Michel, Vincent, Barnard, Alun, Aguilar, Carlos, Agnew, Thomas, Banks, Gareth, Blake, Andrew, Chessum, Lauren, Dorning, Joanne, Falcone, Sara, Goosey, Laurence, Harris, Shelley, Haynes, Andy, Heise, Ines, Hillier, Rosie, Hough, Tertius, Hoslin, Angela, Hutchison, Marie, King, Ruairidh, Kumar, Saumya, Lad, Heena V., Law, Gemma, MacLaren, Robert E., Morse, Susan, Nicol, Thomas, Parker, Andrew, Pickford, Karen, Sethi, Siddharth, Starbuck, Becky, Stelma, Femke, Cheeseman, Michael, Cross, Sally H., Foster, Russell G., Jackson, Ian J., Peirson, Stuart N., Thakker, Rajesh V., Vincent, Tonia, Scudamore, Cheryl, Wells, Sara, El-Amraoui, Aziz, Petit, Christine, Acevedo-Arozena, Abraham, Nolan, Patrick M., Cox, Roger, Mallon, Anne-Marie, Brown, Steve D. M.

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Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation von Lian, Gewei, Lu, Jie, Hu, Jianjun, Zhang, Jingping, Cross, Sally H, Ferland, Russell J, Sheen, Volney L

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Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice von Tolman, Nicholas G., Balasubramanian, Revathi, Macalinao, Danilo G., Kearney, Alison L., MacNicoll, Katharine H., Montgomery, Christa L., de Vries, Wilhelmine N., Jackson, Ian J., Cross, Sally H., Kizhatil, Krishnakumar, Nair, K. Saidas, John, Simon W. M.

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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function von Findlay, Amy S, Carter, Roderick N, Starbuck, Becky, McKie, Lisa, Nováková, Klára, Budd, Peter S, Keighren, Margaret A, Marsh, Joseph A, Cross, Sally H, Simon, Michelle M, Potter, Paul K, Morton, Nicholas M, Jackson, Ian J

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Cardiac malformations and midline skeletal defects in mice lacking filamin A von Hart, Alan W., Morgan, Joanne E., Schneider, Jürgen, West, Katrine, McKie, Lisa, Bhattacharya, Shoumo, Jackson, Ian J., Cross, Sally H.

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Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development von Webb, Tom R, Cross, Sally H, McKie, Lisa, Edgar, Ruth, Vizor, Lucie, Harrison, Jackie, Peters, Jo, Jackson, Ian J

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Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy von Van Agtmael, Tom, Schlötzer-Schrehardt, Ursula, McKie, Lisa, Brownstein, David G., Lee, Angela W., Cross, Sally H., Sado, Yoshikazu, Mullins, John J., Pöschl, Ernst, Jackson, Ian J.

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The methylated component of the Neurospora crassa genome von Selker, Eric U, Tountas, Nikolaos A, Cross, Sally H, Margolin, Brian S, Murphy, Jonathan G, Bird, Adrian P, Freitag, Michael

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The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells von Parker, Andrew, Cross, Sally H, Jackson, Ian J, Hardisty-Hughes, Rachel, Morse, Susan, Nicholson, George, Coghill, Emma, Bowl, Michael R, Brown, Steve D M

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Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse von Cross, Sally H, Mckie, Lisa, Keighren, Margaret, West, Katrine, Thaung, Caroline, Davey, Tracey, Soares, Dinesh C, Sanchez-Pulido, Luis, Jackson, Ian J

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A meckelin―filamin A interaction mediates ciliogenesis von ADAMS, Matthew, SIMMS, Roslyn J, BLAIR, Edward, CROSS, Sally H, SAYER, John A, JOHNSON, Colin A, ABDELHAMED, Zakia, DAWE, Helen R, SZYMANSKA, Katarzyna, LOGAN, Clare V, WHEWAY, Gabrielle, PITT, Eva, GULL, Keith, KNOWLES, Margaret A

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Purification of CpG islands using a methylated DNA binding column von Cross, Sally H, Charlton, Jillian A, Nan, Xinsheng, Bird, Adrian P

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Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function von Findlay, Amy S., McKie, Lisa, Keighren, Margaret, Clementson-Mobbs, Sharon, Sanchez-Pulido, Luis, Wells, Sara, Cross, Sally H., Jackson, Ian J.

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A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation von Cross, Sally H, Macalinao, Danilo G, McKie, Lisa, Rose, Lorraine, Kearney, Alison L, Rainger, Joe, Thaung, Caroline, Keighren, Margaret, Jadeja, Shalini, West, Katrine, Kneeland, Stephen C, Smith, Richard S, Howell, Gareth R, Young, Fiona, Robertson, Morag, van t' Hof, Rob, John, Simon W. M, Jackson, Ian J

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Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction von Jadeja, Shalini, Barnard, Alun R, McKie, Lisa, Cross, Sally H, White, Jacqueline K, Robertson, Morag, Budd, Peter S, MacLaren, Robert E, Jackson, Ian J

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CpG islands of chicken are concentrated on microchromosomes von McQueen, H.A. (Unversity of Edinburgh, Edinburgh, Scotland.), Fantes, J, Cross, S.H, Clark, V.H, Archibald, A.L, Bird, A.P

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CpG islands and genes von Cross, Sally H, Bird, Adrian P

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Genotype-Phenotype Correlation of Mouse Pde6b Mutations von Hart, Alan W, McKie, Lisa, Morgan, Joanne E, Gautier, Philippe, West, Katrine, Jackson, Ian J, Cross, Sally H

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A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected] von Cross, Sally H, Macalinao, Danilo G, McKie, Lisa, Rose, Lorraine, Kearney, Alison L, Rainger, Joe, Thaung, Caroline, Keighren, Margaret, Jadeja, Shalini, West, Katrine, Kneeland, Stephen C, Smith, Richard S, Howell, Gareth R, Young, Fiona, Robertson, Morag, van T' Hof, Rob, John, Simon W M, Jackson, Ian J

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