Molecular Vision, 1090-0535

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  1. 2010
  2. Mitogen-activated protein kinases in the porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Håkansson, G., Carpio, R., Gustafsson, L., Maria Thereza Perez & Malin Malmsjö, 2010, In : Molecular Vision. 16, p. 392-407

    Research output: Contribution to journalArticle

  3. 2009
  4. Protein kinase C in porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Gustafsson, L., Wackenfors, A., Fredrik Ghosh & Malin Malmsjö, 2009, In : Molecular Vision. 15, Apr 13, p. 737-746

    Research output: Contribution to journalArticle

  5. 2008
  6. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration

    Ahmed, Z. M., Kjellstrom, S., Haywood-Watson, R. J. L., Bush, R. A., Hampton, L. L., Battey, J. F., Riazuddin, S., Frolenkov, G., Sieving, P. A. & Friedman, T. B., 2008, In : Molecular Vision. 14, p. 2227-36 10 p.

    Research output: Contribution to journalArticle

  7. 2007
  8. Evidence against a blood derived origin for transforming growth factor beta induced protein in corneal disorders caused by mutations in the TGFBI gene

    Karring, H., Valnickova, Z., Thogersen, I. B., Hedegaard, C. J., Moller-Pedersen, T., Kristensen, T., Klintworth, G. K. & Enghild, J. J., 2007, In : Molecular Vision. 13, p. 997

    Research output: Contribution to journalArticle

  9. 2006
  10. The human cornea proteome: bioinformatic analyses indicate import of plasma proteins into the cornea

    Karring, H., Thogersen, I. B., Klintworth, G. K., Moller-Pedersen, T. & Enghild, J. J., 2006, In : Molecular Vision. 12, p. 451-460

    Research output: Contribution to journalReview article

  11. 2003
  12. Growth of the postnatal rat retina in vitro: Quantitative RT-PCR analyses of mRNA expression for photoreceptor proteins

    Liljekvist Soltic, I., Torngren, M., Magnus Abrahamson & Johansson, K., 2003, In : Molecular Vision. 9, 79, p. 657-664

    Research output: Contribution to journalArticle

  13. Mutation screening of patients with Leber congenital amaurosis or the enhanced S-cone syndrome reveals a lack of sequence variations in the NRL gene

    Acar, C., Mears, A., Yashar, B., Maheshwary, A., Sten Andréasson, Baldi, A., Sieving, P., Iannaccone, A., Musarella, M., Jacobson, S. & Swaroop, A., 2003, In : Molecular Vision. 9, 3-4, p. 14-17

    Research output: Contribution to journalArticle

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