Institutionen för medicinska vetenskaper

Publikationer

PubMed Anders Vahlquist

PubMed Hans Törmä

Utvalda publikationer

  1. Dalin F, Adamus G, Yang S, Landgren E, Palle J, Hallgren Å, Frost BM, Hugosson T, Landegren N, Eriksson D, Andréasson S, Tabbara KF, Kämpe O, Alimohammadi M. Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy. Ophthalmology.123:1401-4, 2016.
  2. Blokzijl A, Chen LE, Gustafsdottir SM, Vuu J, Ullenhag G, Kämpe O, Landegren U, Kamali-Moghaddam M, Hedstrand H. Elevated Levels of SOX10 in Serum from Vitiligo and Melanoma Patients, Analyzed by Proximity Ligation Assay. PLoS One. 11(4):e0154214, 2016
  3. Hellström Pigg M, Bygum A, Gånemo A, Virtanen M, Brandrup F, Zimmer AD, Hotz A, Vahlquist A, Fischer J. Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients. Acta Derm Venereol. 96: 932-937. 2016.
  4. Punga AR, Eriksson A, Alimohammadi M. Regional diffusion of botulinum toxin in facial muscles: a randomised double-blind study and a consideration for clinical studies with split-face design. Acta Derm Venereol. 95:948-5, 2015
  5. Hagforsen E, Paivandy A, Lampinen M, Weström S, Calounova G, Melo FR, Rollman O, Pejler G. Ablation of human skin mast cells in situ by lysosomotropic agents. Exp Dermatol. 24:516-21, 2015
  6. Grönberg A, Mahlapuu M, Ståhle M, Whately-Smith C, Rollman O. Treatment with LL-37 is safe and effective in enhancing healing of hard-to-heal venous leg ulcers: a randomized, placebo-controlled clinical trial. Wound Repair Regen. 22:613-21, 2014
  7. Li H, Vahlquist A, Törmä H. Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis. J Dermatol Sci 69:195-201, 2013
  8. Li H, Loriè EP, Fischer J, Vahlquist A, Törmä H. The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis. J Invest Dermatol. 132:2368-75, 2012
  9. Winge, M.C., Hoppe, T., Berne, B., Vahlquist, A., Nordenskjöld, M., Bradley, M., and Törmä, H. The filaggrin genotype determines functional and molecular alterations in the skin of patients with atopic dermatitis and ichthyosis vulgaris. PLoS One.; 6: e28254, 2011
  10. Dahlqvist, J, Klar, J, Tiwari, N, Schuster, J, Törmä, H, Pujol, R, van Steensel, M, Brinkhuijzen, T, Gijezen, L, Chaves, A, Tadini, G, Vahlquist, A, Dahl, N. A single-nucleotide deletion in the POMP 5’ UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis. Am J Hum Genet 86, 596-603, 2010
  11. Klar J, Schweiger M, Zimmerman R, Zechner R, Li H, Törmä H, Vahlquist A, Bouadjar B, Dahl N, Fischer J. Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome. Am J Hum Genet 85: 248-253, 2009