Search Results - "Søvik, Oddmund" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry

Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry

by Johansson, Bente B., Irgens, Henrik U., Molnes, Janne, Sztromwasser, Paweł, Aukrust, Ingvild, Juliusson, Petur B., Søvik, Oddmund, Levy, Shawn, Skrivarhaug, Torild, Joner, Geir, Molven, Anders, Johansson, Stefan, Njølstad, Pål R.
Published in Diabetologia (01.04.2017)

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One hundred years of insulin

One hundred years of insulin

by Søvik, Oddmund
Published in Tidsskrift for den Norske Lægeforening (15.12.2020)

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Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes

Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes

by Molven, Anders, Ringdal, Monika, Nordbø, Anita M, Raeder, Helge, Støy, Julie, Lipkind, Gregory M, Steiner, Donald F, Philipson, Louis H, Bergmann, Ines, Aarskog, Dagfinn, Undlien, Dag E, Joner, Geir, Søvik, Oddmund, Bell, Graeme I, Njølstad, Pål R
Published in Diabetes (New York, N.Y.) (01.04.2008)

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Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations

Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations

by Pearson, Ewan R, Flechtner, Isabelle, Njølstad, Pål R, Malecki, Maciej T, Flanagan, Sarah E, Larkin, Brian, Ashcroft, Frances M, Klimes, Iwar, Codner, Ethel, Iotova, Violeta, Slingerland, Annabelle S, Shield, Julian, Robert, Jean-Jacques, Holst, Jens J, Clark, Penny M, Ellard, Sian, Søvik, Oddmund, Polak, Michel, Hattersley, Andrew T
Published in The New England journal of medicine (03.08.2006)

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Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

by Holm, Pål I, Sbarra, Véronique, Njølstad, Pål Rasmus, Sagen, Jørn V, Ræder, Helge, Mas, Eric, Søvik, Oddmund, Nermoen, Ingrid, Molven, Anders, Johansson, Stefan, Aksnes, Lage, Bjørkhaug, Lise, Haldorsen, Ingfrid S, Eide, Stig Å, Lombardo, Dominique, Grevle, Louise
Published in Nature genetics (01.01.2006)

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Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

by MOLVEN, Anders, MATRE, Guri E, DURAN, Marinus, WANDERS, Ronald J, RISHAUG, Unni, NJØLSTAD, Pal R, JELLUM, Egil, SØVIK, Oddmund
Published in Diabetes (New York, N.Y.) (01.01.2004)

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Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy

by SAGEN, Jørn V, RAEDER, Helge, GLOYN, Anna L, HATTERSLEY, Andrew T, MOLVEN, Anders, SØVIK, Oddmund, NJØLSTAD, Pal R, HATHOUT, Eba, SHEHADEH, Naim, GUDMUNDSSON, Kolbeinn, BAEVRE, Halvor, ABUELO, Dianne, PHORNPHUTKUL, Chanika, MOLNES, Janne, BELL, Graeme I
Published in Diabetes (New York, N.Y.) (01.10.2004)

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The Coping Styles of Adolescents With Type 1 Diabetes Are Associated With Degree of Metabolic Control

The Coping Styles of Adolescents With Type 1 Diabetes Are Associated With Degree of Metabolic Control

by Marit Graue, Tore Wentzel-Larsen, Edvin Bru, Berit Rokne Hanestad, Oddmund Søvik
Published in Diabetes care (01.06.2004)

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Pancreatic Lipomatosis Is a Structural Marker in Nondiabetic Children With Mutations in Carboxyl-Ester Lipase

Pancreatic Lipomatosis Is a Structural Marker in Nondiabetic Children With Mutations in Carboxyl-Ester Lipase

by RAEDER, Helge, HALDORSEN, Ingfrid S, ERSLAND, Lars, GRFÜNER, Renate, TAXT, Torfinn, SØVIK, Oddmund, MOLVEN, Anders, NJØLSTAD, Pal R
Published in Diabetes (New York, N.Y.) (01.02.2007)

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Glycogenin-2 Is Dispensable for Liver Glycogen Synthesis and Glucagon-Stimulated Glucose Release

Glycogenin-2 Is Dispensable for Liver Glycogen Synthesis and Glucagon-Stimulated Glucose Release

by Irgens, Henrik U, Fjeld, Karianne, Johansson, Bente B, Ringdal, Monika, Immervoll, Heike, Leh, Sabine, Søvik, Oddmund, Johansson, Stefan, Molven, Anders, Njølstad, Pål R
Published in The journal of clinical endocrinology and metabolism (01.05.2015)

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SUMOylation of Pancreatic Glucokinase Regulates Its Cellular Stability and Activity[S]

SUMOylation of Pancreatic Glucokinase Regulates Its Cellular Stability and Activity[S]

by Aukrust, Ingvild, Bjørkhaug, Lise, Negahdar, Maria, Molnes, Janne, Johansson, Bente B., MÜller, Yvonne, Haas, Wilhelm, Gygi, Steven P., Søvik, Oddmund, Flatmark, Torgeir, Kulkarni, Rohit N., Njølstad, Pål R.
Published in The Journal of biological chemistry (22.02.2013)

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Spatiotemporal Trends and Age-Period-Cohort Modeling of the Incidence of Type 1 Diabetes Among Children Aged <15 Years in Norway 1973–1982 and 1989–2003

Spatiotemporal Trends and Age-Period-Cohort Modeling of the Incidence of Type 1 Diabetes Among Children Aged <15 Years in Norway 1973–1982 and 1989–2003

by AAMODT, Geir, STENE, Lars C, NJOLSTAD, Pal R, SOVIK, Oddmund, JONER, Geir
Published in Diabetes care (01.04.2007)

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Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4α (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4α (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

by JOHANSSON, Stefan, RAEDER, Helge, EIDE, Stig A, MIDTHJELL, Kristian, HVEEM, Kristian, SØVIK, Oddmund, MOLVEN, Anders, NJØLSTAD, Pal Rasmus
Published in Diabetes (New York, N.Y.) (01.12.2007)

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Permanent neonatal diabetes caused by glucokinase deficiency: Inborn error of the glucose-insulin signaling pathway

Permanent neonatal diabetes caused by glucokinase deficiency: Inborn error of the glucose-insulin signaling pathway

by NJØLSTAD, Pal R, SAGEN, Jørn V, SØVIK, Oddmund, MATSCHINSKY, Franz M, BJØRKHAUG, Lise, ODILI, Stella, SHEHADEH, Naim, BAKRY, Doua, SARICI, S. Umit, ALPAY, Faruk, MOLNES, Janne, MOLVEN, Anders
Published in Diabetes (New York, N.Y.) (01.11.2003)

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From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation

From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation

by SAGEN, Jørn V, ODILI, Stella, YI HAN, GRIMSBY, Joseph, TAUB, Rebecca, MOLVEN, Anders, SØVIK, Oddmund, NJØLSTAD, Pal R, MATSCHINSKY, Franz M, BJØRKHAUG, Lise, ZELENT, Dorothy, BUETTGER, Carol, KWAGH, Jae, STANLEY, Charles, DAHL-JØRGENSEN, Knut, DE BEAUFORT, Carine, BELL, Graeme I
Published in Diabetes (New York, N.Y.) (01.06.2006)

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Binding of ATP at the active site of human pancreatic glucokinase - nucleotide-induced conformational changes with possible implications for its kinetic cooperativity

Binding of ATP at the active site of human pancreatic glucokinase - nucleotide-induced conformational changes with possible implications for its kinetic cooperativity

by Molnes, Janne, Teigen, Knut, Aukrust, Ingvild, Bjørkhaug, Lise, Søvik, Oddmund, Flatmark, Torgeir, Njølstad, Pål Rasmus
Published in The FEBS journal (01.07.2011)

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Catalytic activation of human glucokinase by substrate binding – residue contacts involved in the binding of D‐glucose to the super‐open form and conformational transitions

Catalytic activation of human glucokinase by substrate binding – residue contacts involved in the binding of D‐glucose to the super‐open form and conformational transitions

by Molnes, Janne, Bjørkhaug, Lise, Søvik, Oddmund, Njølstad, Pål R., Flatmark, Torgeir
Published in The FEBS journal (01.05.2008)

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Co‐occurrence of vitamin D‐dependent rickets type 1 and phenylketonuria

Co‐occurrence of vitamin D‐dependent rickets type 1 and phenylketonuria

by Søvik, Oddmund, Boman, Helge
Published in Acta Paediatrica (01.05.2008)

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GCK-MODY diabetes as a protein misfolding disease: The mutation R275C promotes protein misfolding, self-association and cellular degradation

GCK-MODY diabetes as a protein misfolding disease: The mutation R275C promotes protein misfolding, self-association and cellular degradation

by Negahdar, Maria, Aukrust, Ingvild, Molnes, Janne, Solheim, Marie H., Johansson, Bente B., Sagen, Jørn V., Dahl-Jørgensen, Knut, Kulkarni, Rohit N., Søvik, Oddmund, Flatmark, Torgeir, Njølstad, Pål R., Bjørkhaug, Lise
Published in Molecular and cellular endocrinology (25.01.2014)

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Allosteric Activation of Human Glucokinase by Free Polyubiquitin Chains and Its Ubiquitin-dependent Cotranslational Proteasomal Degradation

Allosteric Activation of Human Glucokinase by Free Polyubiquitin Chains and Its Ubiquitin-dependent Cotranslational Proteasomal Degradation

by Bjørkhaug, Lise, Molnes, Janne, Søvik, Oddmund, Njølstad, Paål Rasmus, Flatmark, Torgeir
Published in The Journal of biological chemistry (03.08.2007)

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