Academic article
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Pavithram, Aishwarya; Zhang, Haichen; Maloney, Kristin A.
et al. (2024). In Vitro Functional Analysis Can Aid Precision Diagnostics of HNF1B-MODY. (external link)
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Brekke, Ranveig Seim; Svanbring, Anny Gravdal; Jellas, Khadija el
et al. (2024). Common single-base insertions in the VNTR of the carboxyl ester lipase (CEL) gene are benign and also likely to arise somatically in the exocrine pancreas. (external link)
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Svalastoga, Pernille; Kaci, Alba; Molnes, Janne
et al. (2023). Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes. (external link)
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Helgeland, Øyvind; Vaudel, Marc; Sole-Navais, Pol
et al. (2022). Characterization of the genetic architecture of infant and early childhood body mass index. (external link)
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Fjeld, Karianne; Svanbring, Anny Gravdal; Brekke, Ranveig Seim
et al. (2022). The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice. (external link)
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Jellas, Khadija el; Dušátková, Petra; Haldorsen, Ingfrid S.
et al. (2022). Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases. (external link)
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Kahraman, Sevim; Dirice, Ercument; Basile, Giorgio
et al. (2022). Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8. (external link)
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Tjora, Erling; Gravdal, Anny; Engjom, Trond
et al. (2021). Protein misfolding in combination with other risk factors in CEL-HYB1-mediated chronic pancreatitis. (external link)
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Svanbring, Anny Gravdal; Xiao, Xunjun; Cnop, Miriam
et al. (2021). The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity. (external link)
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Fjeld, Karianne; Masson, Emmanuelle; Lin, Jin-Huan
et al. (2020). Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis. (external link)
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Valvatne, Monica Dalva; Lavik, Ida Marie Kjærefjord; Jellas, Khadija el
et al. (2020). Pathogenic Carboxyl Ester Lipase (CEL) Variants Interact with the Normal CEL Protein in Pancreatic Cells. (external link)
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Jellas, Khadija el; Johansson, Bente Berg; Fjeld, Karianne
et al. (2018). The mucinous domain of pancreatic carboxyl-ester lipase (CEL) contains core 1/core 2 O-glycans that can be modified by ABO blood group determinants. (external link)
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Dalva, Monica; Jellas, Khadija el; Steine, Solrun
et al. (2017). Copy number variants and VNTR length polymorphisms of the carboxyl-ester lipase (CEL) gene as risk factors in pancreatic cancer. (external link)
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Johansson, Bente Berg; Fjeld, Karianne; Solheim, Marie Holm
et al. (2017). Nuclear import of glucokinase in pancreatic beta-cells is mediated by a nuclear localization signal and modulated by SUMOylation. (external link)
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Johansson, Bente Berg; Irgens, Henrik Underthun; Molnes, Janne
et al. (2017). Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry. (external link)
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Fjeld, Karianne; Weiss, Frank Ulrich; Lasher, Denise
et al. (2015). A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis. (external link)
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Irgens, Henrik Underthun; Fjeld, Karianne; Johansson, Bente Berg
et al. (2015). Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release. (external link)
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Torsvik, Janniche; Johansson, Bente Berg; Dalva, Monica
et al. (2014). Endocytosis of secreted carboxyl ester lipase in a syndrome of diabetes and pancreatic exocrine dysfunction. (external link)
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Negahdar, Maria; Aukrust, Ingvild; Molnes, Janne
et al. (2014). GCK-MODY diabetes as a protein misfolding disease: The mutation R275C promotes protein misfolding, self-association and cellular degradation. (external link)
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Irgens, Henrik Underthun; Molnes, Janne; Johansson, Bente Berg
et al. (2013). Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. (external link)
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Teo, Adrian K.K.; Windmueller, Rebecca; Johansson, Bente Berg
et al. (2013). Derivation of Human Induced Pluripotent Stem Cells from Patients with Maturity Onset Diabetes of the Young. (external link)
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Aukrust, Ingvild; Bjørkhaug, Lise; Negahdar, Maria
et al. (2013). SUMOylation of pancreatic glucokinase regulates its cellular stability and activity. (external link)
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Chudasama, Kishan Kumar; Winnay, Jonathan; Johansson, Stefan
et al. (2013). SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. (external link)
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Negahdar, Maria; Aukrust, Ingvild; Johansson, Bente Berg
et al. (2012). GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. (external link)
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Johansson, Bente Berg; Torsvik, Janniche; Bjørkhaug, Lise
et al. (2011). Diabetes and pancreatic exocrine dysfunction due to mutations in the carboxyl ester lipase gene-maturity onset diabetes of the young (CEL-MODY) A PROTEIN MISFOLDING DISEASE. (external link)
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Ardawatia, Vandana; Masià-Balagué, Miriam; Krakstad, Beate Fast
et al. (2011). Gα(12) binds to the N-terminal regulatory domain of p120(ctn), and downregulates p120(ctn) tyrosine phosphorylation induced by Src family kinases via a RhoA independent mechanism. (external link)
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Ardawatia, Vandana; Masià-Balagué, Miriam; Krakstad, Beate Fast
et al. (2011). G alpha(12) binds to the N-terminal regulatory domain of p120(ctn), and downregulates p120(ctn) tyrosine phosphorylation induced by Src family kinases via a RhoA independent mechanism. (external link)
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Johansson, Bente Berg; Minsaas, Laura; Aragay, Anna M.
(2005). Proteasome involvement in the degradation of the G(q) family of G alpha subunits. (external link)
Errata
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