Search Results - Kofod‐Olsen, E.

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  1. 1
    Innate DNA sensing is impaired in HIV patients and IFI16 expression correlates with chronic immune activation

    Innate DNA sensing is impaired in HIV patients and IFI16 expression correlates with chronic immune activation by Nissen, S. K., Højen, J. F., Andersen, K. L. D., Kofod‐Olsen, E., Berg, R. K., Paludan, S. R., Østergaard, L., Jakobsen, M. R., Tolstrup, M., Mogensen, T. H.

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  2. 2
    Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis

    Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis by Mørk, N, Kofod-Olsen, E, Sørensen, K B, Bach, E, Ørntoft, T F, Østergaard, L, Paludan, S R, Christiansen, M, Mogensen, T H

    Published in Genes and immunity
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  3. 3
    Human Herpesvirus 6B Induces Phenotypic Maturation Without IL-10 and IL-12p70 Production in Dendritic Cells

    Human Herpesvirus 6B Induces Phenotypic Maturation Without IL-10 and IL-12p70 Production in Dendritic Cells by Bertelsen, L.B, Petersen, C.C, Kofod-Olsen, E, Øster, B, Höllsberg, P, Agger, R, Hokland, M

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  4. 4
    Human Herpesvirus 6B Induces Phenotypic Maturation Without IL-10 and IL-12p70 Production in Dendritic Cells: HHV-6B Induces Partial Maturation of DC

    Human Herpesvirus 6B Induces Phenotypic Maturation Without IL-10 and IL-12p70 Production in Dendritic Cells: HHV-6B Induces Partial Maturation of DC by Bertelsen, L. B., Petersen, C. C., Kofod-Olsen, E., Øster, B., Höllsberg, P., Agger, R., Hokland, M.

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  5. 5
    Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO

    Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO by Jørgensen, Sofie E., MS, Bøttger, Pernille, PhD, Kofod-Olsen, Emil, PhD, Holm, Mette, MD, PhD, Mørk, Nanna, MD, Ørntoft, Torben F., MD, PhD, Sørensen, Uffe B.S., PhD, Bernth-Jensen, Jens Magnus, MD, Herlin, Troels, MD, DMSc, Veirum, Jens, MD, PhD, Larsen, Carsten S., MD, DMSc, Østergaard, Lars, MD, DMSc, Hartmann, Rune, PhD, Christiansen, Mette, PhD, Mogensen, Trine H., MD, PhD, DMSc

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  6. 6
    Functional IRF3 deficiency in a patient with herpes simplex encephalitis

    Functional IRF3 deficiency in a patient with herpes simplex encephalitis by Andersen, Line Lykke, Mørk, Nanna, Reinert, Line S, Kofod-Olsen, Emil, Narita, Ryo, Jørgensen, Sofie E, Skipper, Kristian A, Höning, Klara, Gad, Hans Henrik, Østergaard, Lars, Ørntoft, Torben F, Hornung, Veit, Paludan, Søren R, Mikkelsen, Jacob Giehm, Fujita, Takashi, Christiansen, Mette, Hartmann, Rune, Mogensen, Trine H

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  7. 7
    Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO

    Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO by Jørgensen, Sofie E, Bøttger, Pernille, Kofod-Olsen, Emil, Holm, Mette, Mørk, Nanna, Ørntoft, Torben F, Sørensen, Uffe B S, Bernth-Jensen, Jens Magnus, Herlin, Troels, Veirum, Jens, Larsen, Carsten S, Østergaard, Lars, Hartmann, Rune, Christiansen, Mette, Mogensen, Trine H

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