Oluf Borbye Pedersen

Oluf Borbye Pedersen

Professor

ORCID: 0000-0002-3321-3972

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  1. Published

    Search for variants of the gene-promoter and the potential phosphotyrosine encoding sequence of the insulin receptor substrate-2 gene : Evaluation of their relation with alterations in insulin secretion and insulin sensitivity. / Almind, K.; Frederiksen, S. K.; Bernal, D.; Hansen, T.; Ambye, L.; Urhammer, S.; Ekstrøm, C. T.; Berglund, L.; Reneland, R.; Lithell, H.; White, M. F.; Van Obberghen, E.; Pedersen, O.

    In: Diabetologia, Vol. 42, No. 10, 11.10.1999, p. 1244-1249.

    Research output: Contribution to journal › Journal article › Research › peer-review

  2. Published

    Mutational analysis of the coding regions of the genes encoding protein kinase B-alpha and -beta, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin : lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients. / Hansen, L; Fjordvang, H; Rasmussen, S K; Vestergaard, H; Echwald, Søren Morgenthaler; Hansen, T; Alessi, D; Shenolikar, S; Saltiel, A R; Barbetti, F; Pedersen, O.

    In: Diabetes, Vol. 48, No. 2, 02.1999, p. 403-7.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Intermediate Expansions of a GAA Repeat in the Frataxin Gene are not associated with Type 2 Diabetes or Altered Glucose-Induced ¿-cell function in Danish Caucasians. / Dalgaard, Louise Torp; Hansen, Torben; Urhammer, S.A.; Clausen, Jesper O.; Eiberg, Hans Rudolf Lytchoff; Pedersen, Oluf.

    In: Diabetes, No. 48, 1999, p. 914-917.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Implications of compound heterozygous insulin receptor mutations in congenital muscle fibre type disproportion myopathy for the receptor kinase activation. / Klein, H H; Müller, R; Vestergaard, H; Pedersen, O.

    In: Diabetologia, Vol. 42, No. 2, 02.1999, p. 245-9.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Alternative splicing of exon 17 and a missense mutation in exon 20 of the insulin receptor gene in two brothers with a novel syndrome of insulin resistance (congenital fiber-type disproportion myopathy). / Vorwerk, P; Christoffersen, C T; Müller, J; Vestergaard, H; Pedersen, O; De Meyts, P; Vestergaard, Henrik.

    In: Hormone Research, Vol. 52, No. 5, 1999, p. 211-20.

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 919113