Lista de obras - Lise Bjørkhaug Gundersen

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry

artículo científico publicado en 2006

A novel SRC-2-dependent regulation of epithelial-mesenchymal transition in breast cancer cells

scientific article published on 23 July 2018

A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene

artículo científico publicado en 2000

Allosteric activation of human glucokinase by free polyubiquitin chains and its ubiquitin-dependent cotranslational proteasomal degradation

scientific article published on 08 June 2007

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population

artículo científico publicado en 2014

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

artículo científico publicado el 31 de mayo de 2011

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry

artículo científico publicado en 2008

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

artículo científico publicado en 2006

Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants

scientific article published on 01 April 2020

Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population

artículo científico publicado en 2016

Functional dissection of the HNF-1alpha transcription factor: a study on nuclear localization and transcriptional activation

artículo científico publicado en 2005

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway

artículo científico publicado en 2003

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism

artículo científico publicado en 2015

In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins

artículo científico publicado en 2017

MODY associated with two novel hepatocyte nuclear factor-1alpha loss-of-function mutations (P112L and Q466X)

scientific article published on 01 December 2000

Molecular diagnostics in diabetes mellitus

artículo científico publicado en 2005

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

artículo científico publicado en 2005

Neonatal diabetes mellitus due to complete glucokinase deficiency

artículo científico publicado en 2001

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

artículo científico publicado en 2017

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

artículo científico publicado en 2003

STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity

artículo científico publicado en 2014

SUMOylation of pancreatic glucokinase regulates its cellular stability and activity

artículo científico publicado en 2013

Structure-function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes

artículo científico publicado en 2016

The E3 SUMO ligase PIASγ is a novel interaction partner regulating the activity of diabetes associated hepatocyte nuclear factor-1α

artículo científico publicado en 2018

The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes

artículo científico publicado en 2017

The cAMP-dependent protein kinase downregulates glucose-6-phosphatase expression through RORα and SRC-2 coactivator transcriptional activity.

artículo científico publicado en 2015

Lista de obras de Lise Bjørkhaug Gundersen

35th Annual Meeting of the European Association for the Study of Diabetes

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry

A novel SRC-2-dependent regulation of epithelial-mesenchymal transition in breast cancer cells

A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene

Allosteric activation of human glucokinase by free polyubiquitin chains and its ubiquitin-dependent cotranslational proteasomal degradation

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population

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

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

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

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry

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

Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants

Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population

Functional dissection of the HNF-1alpha transcription factor: a study on nuclear localization and transcriptional activation

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

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

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism

In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins

MODY associated with two novel hepatocyte nuclear factor-1alpha loss-of-function mutations (P112L and Q466X)

Molecular diagnostics in diabetes mellitus

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

Neonatal diabetes mellitus due to complete glucokinase deficiency

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

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

STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity

SUMOylation of pancreatic glucokinase regulates its cellular stability and activity

Structure-function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes

The E3 SUMO ligase PIASγ is a novel interaction partner regulating the activity of diabetes associated hepatocyte nuclear factor-1α

The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes

The cAMP-dependent protein kinase downregulates glucose-6-phosphatase expression through RORα and SRC-2 coactivator transcriptional activity.