Edinburgh Research Explorer

Dr Sally Cross

Senior Scientist

  1. 2020
  2. Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

    Findlay, A., McKie, L., Keighren, M., Clementson-Mobbs, S., Sanchez-Pulido, L., Wells, S., Cross, S. & Jackson, I., 16 Jan 2020, In : Scientific Reports.

    Research output: Contribution to journalArticle

  3. 2019
  4. Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects In the Mouse

    Cross, S., McKie, L., Keighren, M., West, K., Thaung, C., Davey, T., Soares, D. C., Sanchez-Pulido, L. & Jackson, I., 1 Jul 2019, In : Investigative Ophthalmology & Visual Science.

    Research output: Contribution to journalArticle

  5. 2018
  6. Mouse Idh3a Mutations Cause Retinal Degeneration and Reduced Mitochondrial Function

    Findlay, A., Carter, R., Starbuck, B., McKie, L., Novakova, K., Budd, P. S., Keighren, M., Marsh, J., Cross, S., Simon, M., Potter, P., Morton, N. & Jackson, I., Dec 2018, In : Disease Models & Mechanisms.

    Research output: Contribution to journalArticle

  7. 2016
  8. Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

    Potter, P. K., Bowl, M. R., Jeyarajan, P., Wisby, L., Blease, A., Goldsworthy, M. E., Simon, M. M., Greenaway, S., Michel, V., Barnard, A., Aguilar, C., Agnew, T., Banks, G., Blake, A., Chessum, L., Dorning, J., Falcone, S., Goosey, L., Harris, S., Haynes, A. & 33 others, Heise, I., Hillier, R., Hough, T., Hoslin, A., Hutchison, M., King, R., Kumar, S., Lad, H. V., Law, G., MacLaren, R. E., Morse, S., Nicol, T., Parker, A., Pickford, K., Sethi, S., Starbuck, B., Stelma, F., Cheeseman, M., Cross, S. H., Foster, R. G., Jackson, I. J., Peirson, S. N., Thakker, R. V., Vincent, T., Scudamore, C., Wells, S., El-Amraoui, A., Petit, C., Acevedo-Arozena, A., Nolan, P. M., Cox, R., Mallon, A-M. & Brown, S. D. M., 18 Aug 2016, In : Nature Communications. 7, 12444.

    Research output: Contribution to journalArticle

  9. 2015
  10. The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells

    Parker, A., Cross, S. H., Jackson, I. J., Hardisty-Hughes, R., Morse, S., Nicholson, G., Coghill, E., Bowl, M. R. & Brown, S. D. M., 5 Nov 2015, In : Disease Models & Mechanisms. 8, 12, p. 1555-1568

    Research output: Contribution to journalArticle

  11. Mouse Slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction

    Jadeja, S., Barnard, A. R., McKie, L., Cross, S. H., Sanger Mouse Genetics Project, S. M. G. P., Robertson, M., Budd, P. S., MacLaren, R. E. & Jackson, I. J., May 2015, In : Investigative Ophthalmology & Visual Science. 56, 5

    Research output: Contribution to journalArticle

  12. 2014
  13. A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation

    Cross, S. H., Macalinao, D. G., McKie, L., Rose, L., Kearney, A. L., Rainger, J., Thaung, C., Keighren, M., Jadeja, S., West, K., Kneeland, S. C., Smith, R. S., Howell, G. R., Young, F., Robertson, M., van T' Hof, R., John, S. W. M. & Jackson, I. J., 8 May 2014, In : PLoS Genetics. 10, 5, e1004359.

    Research output: Contribution to journalArticle

  14. 2012
  15. Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation

    Lian, G., Lu, J., Hu, J., Zhang, J., Cross, S. H., Ferland, R. J. & Sheen, V. L., 30 May 2012, In : Journal of Neuroscience. 32, 22, p. 7672-84 13 p.

    Research output: Contribution to journalArticle

  16. A meckelin-filamin A interaction mediates ciliogenesis

    Adams, M., Simms, R. J., Abdelhamed, Z., Dawe, H. R., Szymanska, K., Logan, C. V., Wheway, G., Pitt, E., Gull, K., Knowles, M. A., Blair, E., Cross, S. H., Sayer, J. A. & Johnson, C. A., 2012, In : Human Molecular Genetics. 21, 6, p. 1272-86 15 p.

    Research output: Contribution to journalArticle

  17. Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases

    Douvaras, P., Liu, W., Mort, R. L., McKie, L., West, K. M., Cross, S. H., Morley, S. D. & West, J. D., 2012, In : BMC Research Notes. 5, p. 122

    Research output: Contribution to journalArticle

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