Edinburgh Research Explorer

Dinesh Soares, PhD

(Former employee or visitor)

  1. 2020
  2. Translation elongation factor 1A2 (eEF1A2) is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

    Idigo, N., Soares, D. & Abbott, C. M., 31 Jan 2020, In: Bioscience reports.

    Research output: Contribution to journalArticlepeer-review

  3. 2018
  4. 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 journalArticlepeer-review

  5. 2017
  6. 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 journalArticlepeer-review

  7. 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 journalArticlepeer-review

  8. 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 journalArticlepeer-review

  9. 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 journalArticlepeer-review

  10. 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 journalArticlepeer-review

  11. 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 journalArticlepeer-review

  12. 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 journalArticlepeer-review

  13. 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 journalArticlepeer-review

  14. Pathogenic Mutations in Retinitis Pigmentosa 2 Predominantly Result in Loss of RP2 Protein Stability in Human and Zebrafish

    Liu, F., Qin, Y., Yu, S., Soares, D. C., Yang, L., Weng, J., Li, C., Gao, M., Lu, Z., Hu, X., Liu, X., Jiang, T., Liu, J. Y., Shu, X., Tang, Z. & Liu, M., 14 Apr 2017, In: Journal of Biological Chemistry.

    Research output: Contribution to journalArticlepeer-review

  15. Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

    Lu, Z., Hu, X., Liu, F., Soares, D. C., Liu, X., Yu, S., Gao, M., Han, S., Qin, Y., Li, C., Jiang, T., Luo, D., Guo, A-Y., Tang, Z. & Liu, M., 5 Apr 2017, In: Scientific Reports. 7, p. 46098

    Research output: Contribution to journalArticlepeer-review

  16. 2016
  17. Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability

    DDD study & Abbott, C. M., Jul 2016, In: Molecular Genetics & Genomic Medicine.

    Research output: Contribution to journalArticlepeer-review

  18. Condensin II mutation causes T cell lymphoma through tissue-specific genome instability

    Woodward, J., Taylor, G. C., Soares, D. C., Boyle, S., Sie, D., Read, D., Chathoth, K., Vukovic, M., Tarrats, N., Jamieson, D., Campbell, K. J., Blyth, K., Acosta, J. C., Ylstra, B., Arends, M. J., Kranc, K. R., Jackson, A. P., Bickmore, W. A. & Wood, A. J., 2016, In: Genes and Development. 30, 19, p. 2173-2186 14 p.

    Research output: Contribution to journalArticlepeer-review

  19. 2015
  20. Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target

    Li, D., Wei, T., Rawle, D. J., Qin, F., Wang, R., Soares, D. C., Jin, H., Sivakumaran, H., Lin, M-H., Spann, K., Abbott, C. M. & Harrich, D., 1 Dec 2015, In: Plos Pathogens. 11, 12, e1005289.

    Research output: Contribution to journalArticlepeer-review

  21. Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator Gene

    Raghupathy, R. K., Gautier, P., Soares, D. C., Wright, A. F. & Shu, X., 1 Oct 2015, In: Investigative Ophthalmology & Visual Science. 56, 11, p. 6255-64 10 p.

    Research output: Contribution to journalArticlepeer-review

  22. RPGR: its role in photoreceptor physiology, human disease, and future therapies

    Megaw, R., Soares, D. & Wright, A., Sep 2015, In: Experimental Eye Research. 138, p. 32-41 10 p.

    Research output: Contribution to journalArticlepeer-review

  23. Atypical Femoral Fracture in Osteoporosis Pseudoglioma Syndrome Associated With Two Novel Compound Heterozygous Mutations in LRP5

    Alonso, N., Soares, D. C., McCloskey, E., Summers, G. D., Ralston, S. H. & Gregson, C. L., Apr 2015, In: Journal of Bone and Mineral Research. 30, 4, p. 615-620

    Research output: Contribution to journalArticlepeer-review

  24. 2014
  25. Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

    Rainger, J., Pehlivan, D., Johansson, S., Bengani, H., Sanchez-Pulido, L., Williamson, K. A., Ture, M., Barker, H., Rosendahl, K., Spranger, J., Horn, D., Meynert, A., Floyd, J. A. B., Prescott, T., Anderson, C. A., Rainger, J. K., Karaca, E., Gonzaga-Jauregui, C., Jhangiani, S., Muzny, D. M. & 16 others, Seawright, A., Soares, D. C., Kharbanda, M., Murday, V., Finch, A., Gibbs, R. A., van Heyningen, V., Taylor, M. S., Yakut, T., Knappskog, P. M., Hurles, M. E., Ponting, C., Lupski, J. R., Houge, G., FitzPatrick, D. R. & UK10K, 5 Jun 2014, In: American Journal of Human Genetics. 94, 6, p. 915-923 9 p.

    Research output: Contribution to journalArticlepeer-review

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