Edinburgh Research Explorer

Dinesh Soares, PhD

(Former employee or visitor)

  1. 2020
  2. 2018
  3. Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodeling

    Lyraki, R., Lokaj, M., Soares, D. C., Little, A., Vermeren, M., Marsh, J. A., Wittinghofer, A. & Hurd, T., 12 Jan 2018, In : Journal of Cell Science.

    Research output: Contribution to journalArticle

  4. 2017
  5. A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells

    Johnston, C. J. C., Smyth, D., Kodali, R. B., White, M. P. J., Harcus, Y., Filbey, K. J., Hewitson, J. P., Hinck, C. S., Ivens, A., Kemter, A. M., Kildemoes, A. O., Le Bihan, T., Soares, D., Anderton, S. M., Brenn, T., Wigmore, S. J., Woodcock, H., Chambers, R. C., Hinck, A. P., McSorley, H. J. & 1 others, Maizels, R., 23 Nov 2017, In : Nature Communications. 8, 13 p., 1741.

    Research output: Contribution to journalArticle

  6. HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33

    Osbourn, M., Soares, D. C., Vacca, F., Cohen, E. S., Scott, I. C., Gregory, W. F., Smyth, D. J., Toivakka, M., Kemter, A. M., Le Bihan, T., Wear, M., Hoving, D., Filbey, K. J., Hewitson, J. P., Henderson, H., Gonzàlez-cìscar, A., Errington, C., Vermeren, S., Astier, A. L., Wallace, W. A. & 4 others, Schwarze, J., Ivens, A. C., Maizels, R. M. & McSorley, H. J., 17 Oct 2017, In : Immunity. 47, 4, p. 739-751.e5 18 p.

    Research output: Contribution to journalArticle

  7. Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration

    Stanton, C. M., Borooah, S., Drake, C., Marsh, J. A., Campbell, S., Lennon, A., Soares, D. C., Vallabh, N. A., Sahni, J., Cideciyan, A. V., Dhillon, B., Vitart, V., Jacobson, S. G., Wright, A. F. & Hayward, C., 22 Sep 2017, In : Scientific Reports. 7, 1, p. 12147

    Research output: Contribution to journalArticle

  8. A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma

    Rainger, J., Williamson, K., Soares, D., Truch, J., Thekkedath Kurian, D., Gillessen-Kaesbach, G., Seawright, A., Prendergast, J., Halachev, M., Wheeler, A., McTeir, L., Gill, A., Van Heyningen, V., Davey, M., UK10K & FitzPatrick, D. R., Aug 2017, In : Human Mutation. 38, 8, p. 942-946

    Research output: Contribution to journalArticle

  9. Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

    Teng, S., Thomson, P. A., Mccarthy, S., Kramer, M., Muller, S., Lihm, J., Morris, S., Soares, D. C., Hennah, W., Harris, S., Camargo, L. M., Malkov, V., Mcintosh, A. M., Millar, J. K., Blackwood, D. H., Evans, K. L., Deary, I. J., Porteous, D. J. & Mccombie, W. R., 20 Jun 2017, In : Molecular Psychiatry.

    Research output: Contribution to journalArticle

  10. SAF-A Regulates Interphase Chromosome Structure through Oligomerization with Chromatin-Associated RNAs

    Nozawa, R-S., Boteva, L., Soares, D. C., Naughton, C., Dun, A. R., Buckle, A., Ramsahoye, B., Bruton, P. C., Saleeb, R. S., Arnedo, M., Hill, B., Duncan, R. R., Maciver, S. K. & Gilbert, N., 15 Jun 2017, In : Cell. 169, 7, p. 1214-1227.e18 22 p.

    Research output: Contribution to journalArticle

  11. PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins

    Hall, E. A., Nahorski, M. S., Murray, L. M., Shaheen, R., Perkins, E., Dissanayake, K. N., Kristaryanto, Y., Jones, R., Vogt, J., Rivagorda, M., Handley, M. T., Mali, G. R., Quidwai, T., Soares, D. C., Keighren, M. A., Mckie, L., Mort, R. L., Gammoh, N., Garcia-munoz, A., Davey, T. & 15 others, Vermeren, M., Walsh, D., Budd, P., Aligianis, I. A., Faqeih, E., Quigley, A. J., Jackson, I. J., Kulathu, Y., Jackson, M., Ribchester, R. R., Von Kriegsheim, A., Alkuraya, F. S., Woods, C. G., Maher, E. R. & Mill, P., 4 May 2017, In : American Journal of Human Genetics.

    Research output: Contribution to journalArticle

  12. A Structural Organization for Disrupted in Schizophrenia 1, Identified by High-Throughput Screening, Reveals Distinctly Folded Regions Which Are Bisected by Mental Illness-Related Mutations

    Yerabham, A. S. K., Mas, P. J., Decker, C., Soares, D. C., Weiergräber, O. H., Nagel-Steger, L., Willbold, D., Hart, D. J., Bradshaw, N. J. & Korth, C., 21 Apr 2017, In : Journal of Biological Chemistry.

    Research output: Contribution to journalArticle

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