Hasil Pencarian - Magnus D Vigeland

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  1. 1
    QuickPed: an online tool for drawing pedigrees and analysing relatedness

    QuickPed: an online tool for drawing pedigrees and analysing relatedness oleh Magnus D. Vigeland

    Diterbitkan 2022-06-01
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  2. 2
    Joint DNA-based disaster victim identification

    Joint DNA-based disaster victim identification oleh Magnus D. Vigeland, Thore Egeland

    Diterbitkan 2021-07-01
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  3. 3
    The use of segregation analysis in interpretation of sequence variants in SMAD3: A case report

    The use of segregation analysis in interpretation of sequence variants in SMAD3: A case report oleh Aleksandra Ratajska, Magnus D. Vigeland, Katrine Verena Wirgenes, Kirsten Krohg‐Sørensen, Benedicte Paus

    Diterbitkan 2023-02-01
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  4. 4
    Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis.

    Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis. oleh Toni C Berger, Magnus D Vigeland, Hanne S Hjorthaug, Lars Etholm, Cecilie G Nome, Erik Taubøll, Kjell Heuser, Kaja K Selmer

    Diterbitkan 2019-01-01
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  5. 5
    DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes.

    DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes. oleh Kristina Gervin, Magnus D Vigeland, Morten Mattingsdal, Martin Hammerø, Heidi Nygård, Anne O Olsen, Ingunn Brandt, Jennifer R Harris, Dag E Undlien, Robert Lyle

    Diterbitkan 2012-01-01
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  6. 6
    Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study

    Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study oleh Markus K.H. Wiedmann, Ingunn V. Steinsvåg, Tovy Dinh, Magnus D. Vigeland, Pål G. Larsson, Hanne Hjorthaug, Ying Sheng, Inger-Lise Mero, Kaja K. Selmer

    Diterbitkan 2023-01-01
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  7. 7
    Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

    Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease oleh Sigrid Aslaksen, Sigrid Aslaksen, Paal Methlie, Paal Methlie, Paal Methlie, Magnus D. Vigeland, Magnus D. Vigeland, Dag E. Jøssang, Anette B. Wolff, Anette B. Wolff, Ying Sheng, Bergithe E. Oftedal, Bergithe E. Oftedal, Beate Skinningsrud, Dag E. Undlien, Dag E. Undlien, Kaja K. Selmer, Kaja K. Selmer, Eystein S. Husebye, Eystein S. Husebye, Eystein S. Husebye, Eirik Bratland, Eirik Bratland

    Diterbitkan 2019-09-01
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  8. 8
    Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

    Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease oleh Sigrid Aslaksen, Anette B. Wolff, Magnus D. Vigeland, Lars Breivik, Ying Sheng, Bergithe E. Oftedal, Haydee Artaza, Beate Skinningsrud, Dag E. Undlien, Kaja K. Selmer, Eystein S. Husebye, Eirik Bratland

    Diterbitkan 2019-04-01
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  9. 9
    Differential Glial Activation in Early Epileptogenesis—Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus

    Differential Glial Activation in Early Epileptogenesis—Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus oleh Toni C. Berger, Toni C. Berger, Magnus D. Vigeland, Hanne S. Hjorthaug, Cecilie G. Nome, Erik Taubøll, Erik Taubøll, Kaja K. Selmer, Kaja K. Selmer, Kaja K. Selmer, Kjell Heuser, Kjell Heuser

    Diterbitkan 2020-11-01
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