B. Johansson

发表

Protein misfolding in combination with other risk factors in CEL-HYB1-mediated chronic pancreatitis.

A. Molven, M. Cnop, G. Dimcevski, 2020, European journal of gastroenterology & hepatology.

The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity

A. Molven, P. Njølstad, M. Cnop, 2021, The Journal of biological chemistry.

The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity

A. Molven, P. Njølstad, M. Cnop, 2020, bioRxiv.

Pathogenic Carboxyl Ester Lipase (CEL) Variants Interact with the Normal CEL Protein in Pancreatic Cells

A. Molven, P. Njølstad, R. Waldron, 2020, Cells.

Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8

A. Molven, E. Dirice, S. Kahraman, 2022, Nature Metabolism.

The role of the carboxyl ester lipase (CEL) gene in pancreatic disease.

A. Molven, P. Njølstad, S. Johansson, 2017, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Nuclear import of glucokinase in pancreatic beta-cells is mediated by a nuclear localization signal and modulated by SUMOylation

P. Njølstad, T. Flatmark, N. Wierup, 2017, Molecular and Cellular Endocrinology.

GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation.

A. Molven, P. Njølstad, O. Søvik, 2012, Biochimica et biophysica acta.

Endocytosis of Secreted Carboxyl Ester Lipase in a Syndrome of Diabetes and Pancreatic Exocrine Dysfunction*

A. Molven, P. Njølstad, S. Johansson, 2014, The Journal of Biological Chemistry.

Characterization of the genetic architecture of infant and early childhood body mass index

O. Andreassen, P. Njølstad, B. Jacobsson, 2022, Nature Metabolism.

SUMOylation of Pancreatic Glucokinase Regulates Its Cellular Stability and Activity*

S. Gygi, P. Njølstad, O. Søvik, 2013, The Journal of Biological Chemistry.

SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling.

Stefan Johansson, Ingfrid Haldorsen, Pål Rasmus Njølstad, 2013, American journal of human genetics.

The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice

A. Molven, P. Njølstad, K. Fjeld, 2022, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis

P. Bugert, R. Grützmann, M. Scholz, 2015, Nature Genetics.

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

S. Levy, A. Molven, P. Njølstad, 2017, Diabetologia.

Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

A. Molven, P. Njølstad, O. Søvik, 2013, Diabetologia.

Proteasome involvement in the degradation of the Gq family of Gα subunits

B. Johansson, A. Aragay, L. Minsaas, 2005 .

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

A. Molven, P. Njølstad, H. Immervoll, 2018, The Journal of Biological Chemistry.

Copy number variants and VNTR length polymorphisms of the carboxyl-ester lipase (CEL) gene as risk factors in pancreatic cancer.

A. Molven, P. Njølstad, H. Immervoll, 2017, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

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.

A. Lewis, B. Johansson, E. Spriet, 2011, Experimental cell research.

Characterization of the genetic architecture of BMI in infancy and early childhood reveals age-specific effects and implicates pathways involved in Mendelian obesity

O. Andreassen, P. Njølstad, B. Jacobsson, 2021, medRxiv.

Diabetes and Pancreatic Exocrine Dysfunction Due to Mutations in the Carboxyl Ester Lipase Gene-Maturity Onset Diabetes of the Young (CEL-MODY)

A. Molven, P. Njølstad, T. Flatmark, 2011, The Journal of Biological Chemistry.

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

P. Njølstad, O. Søvik, T. Flatmark, 2014, Molecular and Cellular Endocrinology.

GCK-MODY diabetes as a protein misfolding disease : The mutation R 275 C promotes protein misfolding

P. Njølstad, O. Søvik, T. Flatmark, 2013 .

Derivation of Human Induced Pluripotent Stem Cells from Patients with Maturity Onset Diabetes of the Young*

Rohit N Kulkarni, P. Njølstad, E. Dirice, 2013, The Journal of Biological Chemistry.

Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases

L. Groop, A. Molven, P. Njølstad, 2021, The Journal of clinical endocrinology and metabolism.

Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis.

A. Molven, P. Njølstad, Z. Liao, 2020, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Proteasome involvement in the degradation of the G(q) family of Galpha subunits.

B. Johansson, A. Aragay, L. Minsaas, 2005, The FEBS journal.

Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes

E. Søfteland, Eivind Valen, A. Molven, 2023, Diabetologia.