Search filters

List of works by Pål R Njølstad

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

article

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

article

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

article

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

scientific article

A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma.

scientific article published on 15 January 2009

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes

article

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

scientific 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

scientific article published on June 2006

A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes.

scientific article

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

scientific article published on 01 July 2006

A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young ⬇️

scientific article published on 01 August 1998

A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes

scientific article published on 21 November 2013

A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta

scientific article

A pathway to insulin independence in newborns and infants with diabetes

scientific article published in August 2011

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

scientific article published on 16 March 2015

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

scientific article published on 01 June 2000

A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity

scientific article published on 01 October 2019

A zebrafish engrailed-like homeobox sequence expressed during embryogenesis

scientific article

A zebrafish homeobox-containing gene with embryonic transcription

scientific article

A zebrafish homologue of the murine Hox-2.1 gene

scientific article

Absence of diabetes and pancreatic exocrine dysfunction in a transgenic model of carboxyl-ester lipase-MODY (maturity-onset diabetes of the young).

scientific article

Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometry

scientific article

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation

scientific article published in May 2008

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

scientific article

All-cause mortality in a nationwide cohort of childhood-onset diabetes in Norway 1973-2013.

scientific article published on 14 May 2015

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

scientific article published on 08 June 2007

An Egyptian case of congenital hyperinsulinism of infancy due to a novel mutation in KCNJ11 encoding Kir6.2 and response to octreotide

scientific article

An Egyptian family with H syndrome due to a novel mutation inSLC29A3illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis ⬇️

scientific article published on September 18, 2012

Antibiotics, acetaminophen and infections during prenatal and early life in relation to type 1 diabetes

scientific article published on 01 October 2018

Are family factors universally related to metabolic outcomes in adolescents with Type 1 diabetes?

scientific article

Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis

scientific article

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

scientific article

Assessment of exocrine pancreatic function by secretin-stimulated magnetic resonance cholangiopancreaticography and diffusion-weighted imaging in healthy controls

scientific article published on 6 May 2013

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

scientific article published on June 2014

Asthma, steroid inhalation and growth

scientific article published in January 2001

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

scientific article published on May 31, 2011

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations

article

Carboxyl-ester lipase maturity-onset diabetes of the young is associated with development of pancreatic cysts and upregulated MAPK signaling in secretin-stimulated duodenal fluid

scientific article published on 23 September 2013

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

scientific article

Causes of death in childhood-onset Type 1 diabetes: long-term follow-up

scientific article published on 21 March 2016

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

scientific article published on 20 January 2020

Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children ⬇️

scientific article published on August 20, 2012

Clinical characteristics of mutation carriers in a large family with glucokinase diabetes (MODY2).

scientific article published in August 2005

Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management

scientific article

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function

scientific article

Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes

scientific article published on 15 April 2016

Contributions to the MODY5 phenotype

scientific article published on 01 November 2002

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

scientific article published on 11 October 2016

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins

scientific article published on 13 June 2009

De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features

scientific article published on July 2007

De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features

scientific article published on 23 January 2009

Derivation of human induced pluripotent stem cells from patients with maturity onset diabetes of the young

scientific article published on 10 January 2013

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

scientific article

Diabetes genetics. A seventh sense for the successful sequel of 'come together'. "The genotypes and phenotypes of diabetes". Bergen, Norway. April 22-26, 2009. 2nd meeting of 'EASD Study Group on Genetics of Diabetes' and 44th annual meeting of the

scientific article published on 06 July 2009

Diagnosis and treatment of congenital hyperinsulinism--to Paris at any price?

scientific article published in February 2001

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

scientific article published on 9 April 2008

Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus

scientific article published in August 2005

Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies

scientific article

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

scholarly article by Pamela Bowman et al published August 2018 in The Lancet: Diabetes & Endocrinology

Endocytosis of secreted carboxyl ester lipase in a syndrome of diabetes and pancreatic exocrine dysfunction

scientific article published on 25 August 2014

Enlarged nephrons and severe nondiabetic nephropathy in hepatocyte nuclear factor-1beta (HNF-1beta) mutation carriers

scientific article published in September 2003

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 23 January 2018

Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study) ⬇️

scientific article published on February 4, 2011

Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas

scientific article published on 19 April 2013

Exome sequencing and genetic testing for MODY.

scientific article

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

scientific article

FTO, type 2 diabetes, and weight gain throughout adult life: a meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies

scientific article published on 11 March 2011

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation

scientific article

Familial non-immune hydrops fetalis and congenital pulmonary lymphangiectasia

scientific article published on 01 June 1998

Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up.

scientific article published on 24 April 2011

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

scientific article published on 01 June 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

scientific article

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

scientific article published on 01 November 2005

Functional effects of mutations at F35 in the NH2-terminus of Kir6.2 (KCNJ11), causing neonatal diabetes, and response to sulfonylurea therapy

scientific article published in June 2006

Functional evaluation of sixteen SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitro

scientific article published on 02 September 2020

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

scientific article published on 31 August 2013

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

scientific article

Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study).

scientific article published on 24 April 2008

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

article

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

scientific article published on 3 January 2018

Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth

scientific article published on 01 October 2019

Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene

scientific article published on April 1991

Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release

scientific article published on 9 March 2015

HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease

scientific article published on 19 July 2011

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

scientific article published on 01 February 2003

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

scientific article published on 2 October 2015

Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family

scientific article published in November 2002

Hyperexcitability to sulphonylurea in MODY3 ⬇️

scientific article published on May 1, 1998

IRX5 regulates adipocyte amyloid precursor protein and mitochondrial respiration in obesity

scientific article published on 11 December 2018

ISPAD Clinical Practice Consensus Guidelines 2006-2007. The diagnosis and management of monogenic diabetes in children

scientific article published on 01 December 2006

ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents

scientific article published on 01 October 2018

In situ hybridization patterns of zebrafish homeobox genes homologous to Hox-2.1 and En-2 of mouse

scientific article published on 01 December 1988

Infant Feeding and Risk of Type 1 Diabetes in Two Large Scandinavian Birth Cohorts

scientific article published on 9 May 2017

Infant Growth and Risk of Childhood-Onset Type 1 Diabetes in Children From 2 Scandinavian Birth Cohorts

scientific article

Inhibition of the PI 3-kinase pathway disrupts the unfolded protein response and reduces sensitivity to ER stress-dependent apoptosis

scientific article published on 03 August 2020

Insights from Monogenic Diabetes

Intellectual Disability in KATP Channel Neonatal Diabetes

scientific article published on 13 January 2020

Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes

scientific article published on 06 September 2019

Iris Malformation and Anterior Segment Dysgenesis in Mice and Humans With a Mutation in PI 3-Kinase

scientific article

Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes

scientific article published on 22 February 2008

Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions

scientific journal article

Lack of pancreatic body and tail in HNF1B mutation carriers

scientific article published on 01 July 2008

Length of Variable Numbers of Tandem Repeats in the Carboxyl Ester Lipase (CEL) Gene May Confer Susceptibility to Alcoholic Liver Cirrhosis but Not Alcoholic Chronic Pancreatitis

scientific article

Lipase gene fusion: a new route to chronic pancreatitis

scientific article

Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3

scientific article

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

scientific article

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

scientific article published on 01 December 2000

Management of neonatal and infancy-onset diabetes mellitus

scientific article published on January 2007

Maternal and Neonatal Vitamin D Status are not Associated With Risk of Childhood Type 1 Diabetes: A Scandinavian Case-Cohort Study

scientific article published on 23 November 2017

Maternal and Newborn Vitamin D-Binding Protein, Vitamin D Levels, Vitamin D Receptor Genotype, and Childhood Type 1 Diabetes

scientific article published on 28 January 2019

Maternal and child gluten intake and association with type 1 diabetes: The Norwegian Mother and Child Cohort Study

scientific article published on 02 March 2020

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

scientific article published on 01 May 2019

Maternal microchimerism in cord blood and risk of childhood-onset type 1 diabetes

scientific article published on 19 June 2019

Medium chain acyl-CoA dehydrogenase deficiency and fatal valproate toxicity

scientific article published on February 1997

Metabolic outcomes in young children with type 1 diabetes differ between treatment centers: the Hvidoere Study in Young Children 2009.

scientific article published on 10 September 2012

Mice Carrying a Dominant-Negative Human PI 3-Kinase Mutation are Protected From Obesity and Hepatic Steatosis But Not Diabetes.

scientific article

Molecular diagnostics in diabetes mellitus

scientific article published in November 2005

Molecular genetic diagnostics in syndromes associated with the RAS/MAPK signalling pathway

scientific article published in November 2009

Mutations in HNF1A result in marked alterations of plasma glycan profile

scientific article published on 28 December 2012

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

scientific article

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

scientific article published on 17 September 2009

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes

scientific article

Neonatal diabetes mellitus due to complete glucokinase deficiency

scientific article published in May 2001

Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations

scientific article published on 10 June 2008

Non-insulin dependent diabetes in children and adolescents

scientific article published on March 10, 1998

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

scientific article published on 12 October 2020

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

scientific article

PI3-kinase mutation linked to insulin and growth factor resistance in vivo

scientific article published on 14 March 2016

Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3

article published in 2007

Pancreatic function in carboxyl-ester lipase knockout mice

scientific article

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase

scientific article published on 01 February 2007

Papillary thyroid carcinoma: a multivariate analysis of prognostic factors including an evaluation of the p-TNM staging system

scientific article published on November 1, 1992

Parental Smoking and Risk of Childhood-onset Type 1 Diabetes

scientific article published on 01 November 2018

Paternal and maternal obesity but not gestational weight gain is associated with type 1 diabetes

scientific article published on 5 February 2018

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

scientific article published on 18 January 2020

PathwayMatcher: proteoform-centric network construction enables fine-granularity multiomics pathway mapping

scientific article published on 01 August 2019

PeptideMapper: Efficient and Versatile Amino Acid Sequence and Tag Mapping

scientific article

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

scientific article published in November 2003

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

scientific article published in October 2004

Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children

scientific article

Plasma immunological markers in pregnancy and cord blood: A possible link between macrophage chemo-attractants and risk of childhood type 1 diabetes

scientific article published on 20 December 2017

Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes

scientific article

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents

scientific article published on 10 August 2020

Prenatal iron exposure and childhood type 1 diabetes.

scientific article published on 13 June 2018

Preserved insulin response to tolbutamide in hepatocyte nuclear factor-1alpha mutation carriers

scientific article published in April 2005

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

scientific article published on 27 April 2013

Primary structure, developmentally regulated expression and potential duplication of the zebrafish homeobox gene ZF-21.

scientific article published on October 1988

Prospective Associations of Systemic and Urinary Choline Metabolites with Incident Type 2 Diabetes

scientific article

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 22 December 2017

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 16 March 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 01 July 2019

Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)

Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young.

scientific article

Reduced prevalence of late-diabetic complications in MODY3 with early diagnosis

scientific article published on 01 August 2002

Roadmap for a precision-medicine initiative in the Nordic region

scientific article published on 01 June 2019

Role of molecular genetics in transforming diagnosis of diabetes mellitus

scientific article published on April 2011

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

scientific article published on 27 June 2013

SUMOylation of pancreatic glucokinase regulates its cellular stability and activity

scientific article published on 7 January 2013

Secretin-stimulated MRI assessment of exocrine pancreatic function in patients with cystic fibrosis and healthy controls

scientific article published on 10 November 2016

Sequence analysis of the zebrafish hox-B5/B6 region

scientific article published on April 1993

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 19 December 2017

Serum Acylcarnitines and Risk of Cardiovascular Death and Acute Myocardial Infarction in Patients With Stable Angina Pectoris

scientific article published on 03 February 2017

Severe pancreatic dysfunction but compensated nutritional status in monogenic pancreatic disease caused by carboxyl-ester lipase mutations

scientific article published in October 2013

Sonographic pancreas echogenicity in cystic fibrosis compared to exocrine pancreatic function and pancreas fat content at Dixon-MRI

scientific article published on 26 July 2018

Spatial Environment Affects HNF4A Mutation-Specific Proteome Signatures and Cellular Morphology in hiPSC-Derived β-Like Cells

scientific article published on 01 April 2022

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.

scientific article published on April 2007

Structure and early embryonic expression of the zebrafish engrailed-2 gene

scientific article

Structure and neural expression of a zebrafish homeobox sequence

scientific article

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

scientific article published on 8 February 2016

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

scientific article

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations

scientific article published in August 2006

Tailored medicine or narcissomics? ⬇️

scientific article published on 01 September 2012

Target setting in intensive insulin management is associated with metabolic control: the Hvidoere childhood diabetes study group centre differences study 2005.

scientific article published on 6 November 2009

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

scientific article published on 2 December 2016

Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes.

scientific article published on 20 November 2017

The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey)

scientific article published on 18 May 2015

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

scientific article published in Scientific Reports

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

scientific article

The Hypoglycemic Phenotype Is Islet Cell-Autonomous in Short-Chain Hydroxyacyl-CoA Dehydrogenase-Deficient Mice

scientific article published on 07 March 2016

The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal development.

scientific article

The diagnosis and management of monogenic diabetes in children and adolescents

scientific article published on September 2009

The diagnosis and management of monogenic diabetes in children and adolescents

article by Oscar Rubio-Cabezas et al published September 2014 in Pediatric Diabetes

The genetic abnormality in the beta cell determines the response to an oral glucose load

scientific article published in March 2002

The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

The homeobox factor Irx3 maintains adipogenic identity

scientific article published on 18 November 2019

The kynurenine:tryptophan ratio as a predictor of incident type 2 diabetes mellitus in individuals with coronary artery disease

scientific article published on 13 June 2017

The molecular function of oncogenes

scientific article

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

scientific article published in Journal of Biological Chemistry

The number of tandem repeats in the carboxyl-ester lipase (CEL) gene as a risk factor in alcoholic and idiopathic chronic pancreatitis

article

The role of pancreatic imaging in monogenic diabetes mellitus

scientific article

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

scientific article published on 5 December 2017

The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.

scientific article published in May 2009

The zebrafish homeobox gene hox-2.2: transcription unit, potential regulatory regions and in situ localization of transcripts

scientific article published on February 1990

The zebrafish homeobox gene hox[zf-114]: primary structure, expression pattern and evolutionary aspects

scientific article published on June 1, 1992

Thyroid carcinoma: results from surgical treatment in 211 consecutive patients

scientific article published on 01 September 1991

To test, or not to test: time for a MODY calculator? ⬇️

scientific article published on 02 March 2012

Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes

scientific article published on 01 June 2006

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

scientific article published on 01 December 2021

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

scientific article published on 02 September 2019

Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome

scientific article

[Progress in diabetes genetics]

scientific article published on 01 June 2010

[The homeo box--a genetic key to fetal development]

scientific article published on 01 May 1993

Paulina is supported by:

About Paulina

Help