Bente B. Johansson

Bergen, 5021, Norway

Last Updated: 09/26/2026

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Found 27 publications

HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childhood Diabetes Registry: Clinical Insights and Prevalence Informed by Genetic and Functional Evaluation.

HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childhood Diabetes Registry: Clinical Insights and Prevalence Informed by Genetic and Functional Evaluation.

Journal: International journal of molecular sciences

Published: February 24, 2026

MODY Mutations in Transcription Factors HNF1A and HNF1B Affect the Production of Interferon Signaling Proteins: Evidence at the Proteome Level.

MODY Mutations in Transcription Factors HNF1A and HNF1B Affect the Production of Interferon Signaling Proteins: Evidence at the Proteome Level.

Journal: Proteomics

Published: January 05, 2026

Author Correction: Characterization of the genetic architecture of infant and early childhood body mass index.

Author Correction: Characterization of the genetic architecture of infant and early childhood body mass index.

Journal: Nature metabolism

Published: February 10, 2024

In Vitro Functional Analysis Can Aid Precision Diagnostics of HNF1B-MODY.

In Vitro Functional Analysis Can Aid Precision Diagnostics of HNF1B-MODY.

Journal: The Journal of molecular diagnostics : JMD

Published: January 03, 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.

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.

Journal: Human molecular genetics

Published: November 24, 2023

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

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

Journal: Diabetologia

Published: February 11, 2023

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

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

Journal: Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]

Published: July 07, 2022

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

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

Journal: The Journal of clinical endocrinology and metabolism

Published: June 25, 2021

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

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

Journal: Nature metabolism

Published: May 26, 2021

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

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

Journal: Nature metabolism

Published: January 07, 2021

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

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

Journal: The Journal of biological chemistry

Published: December 22, 2020

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

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

Journal: European journal of gastroenterology & hepatology

Published: October 20, 2020

Showing 1-12 of 27

Last Updated: 09/26/2026