Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia (Q43805190)

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scientific article published on 2 April 2013

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English	Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia	scientific article published on 2 April 2013

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scholarly article

1 reference

Europe PubMed Central

27 November 2017

Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia (English)

1 reference

Europe PubMed Central

27 November 2017

1 reference

based on heuristic

inferred from title

maturity-onset diabetes of the young

1 reference

based on heuristic

inferred from title

object named as

Sarah E Flanagan

4

0 references

object named as

Sian Ellard

5

0 references

Christine Bellanné-Chantelot

2

object named as

Christine Bellanne-Chantelot

1 reference

Europe PubMed Central

27 November 2017

author name string

Kevin Colclough

1

1 reference

Europe PubMed Central

27 November 2017

Cecile Saint-Martin

3

1 reference

Europe PubMed Central

27 November 2017

publication date

2 April 2013

1 reference

Europe PubMed Central

27 November 2017

1 reference

Europe PubMed Central

27 November 2017

34

1 reference

Europe PubMed Central

27 November 2017

5

1 reference

Europe PubMed Central

27 November 2017

669-685

1 reference

Europe PubMed Central

27 November 2017

A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian Indians.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Structure of the gene encoding hepatocyte nuclear factor 1 (HNF1)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Three novel mutations in MODY and its phenotype in three different Czech families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The A98V single nucleotide polymorphism (SNP) in hepatic nuclear factor 1 alpha (HNF-1alpha) is associated with insulin sensitivity and beta-cell function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Urine C-peptide creatinine ratio is a noninvasive alternative to the mixed-meal tolerance test in children and adults with type 1 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Urinary C-peptide creatinine ratio is a practical outpatient tool for identifying hepatocyte nuclear factor 1-{alpha}/hepatocyte nuclear factor 4-{alpha} maturity-onset diabetes of the young from long-duration type 1 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Bi-allelic inactivation of TCF1 in hepatic adenomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Analysis of protein dimerization and ligand binding of orphan receptor HNF4alpha

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Triple diabetes: coexistence of type 1 diabetes mellitus and a novel mutation in the gene responsible for MODY3 in an overweight adolescent

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Familial young-onset forms of diabetes related to HNF4A and rare HNF1A molecular aetiologies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Cloning and sequencing of cDNAs encoding the human hepatocyte nuclear factor 4 indicate the presence of two isoforms in human liver

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Disruption of the HNF-4 gene, expressed in visceral endoderm, leads to cell death in embryonic ectoderm and impaired gastrulation of mouse embryos

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Locus Reference Genomic sequences: an improved basis for describing human DNA variants.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Nomenclature for the description of human sequence variations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Crystal structure of the HNF4 alpha ligand binding domain in complex with endogenous fatty acid ligand

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Human hepatocyte nuclear factor 4 isoforms are encoded by distinct and differentially expressed genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations in hepatocyte nuclear factor-1beta and their related phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Prevalence ofHNF1A(MODY3) mutations in a Norwegian population (the HUNT2 Study)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The functional Thr130Ile and Val255Met polymorphisms of the hepatocyte nuclear factor-4alpha (HNF4A): gene associations with type 2 diabetes or altered beta-cell function among Danes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

MODY: history, genetics, pathophysiology, and clinical decision making

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A genetic switch in pancreatic beta-cells: implications for differentiation and haploinsufficiency.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1alpha (TCF1) promoter region in MODY patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1 alpha and glucokinase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Messenger RNA transcripts of the hepatocyte nuclear factor-1alpha gene containing premature termination codons are subject to nonsense-mediated decay

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Diabetes susceptibility in the Canadian Oji-Cree population is moderated by abnormal mRNA processing of HNF1A G319S transcripts

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Linkage of type 2 diabetes to the glucokinase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Novel P2 promoter-derived HNF4alpha isoforms with different N-terminus generated by alternate exon insertion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Spectrum of HNF1A somatic mutations in hepatocellular adenoma differs from that in patients with MODY3 and suggests genotoxic damage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Half of clinically defined maturity-onset diabetes of the young patients in Denmark do not have mutations in HNF4A, GCK, and TCF1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Prevalence of monogenic diabetes in young adults: a community-based, cross-sectional study in Oxfordshire, UK.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Identifying hepatic nuclear factor 1alpha mutations in children and young adults with a clinical diagnosis of type 1 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Naturally occurring mutations in the human HNF4alpha gene impair the function of the transcription factor to a varying degree

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Laron dwarfism and non-insulin-dependent diabetes mellitus in the Hnf-1alpha knockout mouse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Autoantigens IA-2 and GAD in Type I (insulin-dependent) diabetes

1 reference

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21 January 2018

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

C-peptide in the classification of diabetes in children and adolescents.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The polymorphism Gly574Ser in the transcription factor HNF-1alpha is not a marker of adult-onset ketosis-prone atypical diabetes in Afro-Caribbean patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Lipoprotein composition in HNF1A-MODY: differentiating between HNF1A-MODY and type 2 diabetes.

1 reference

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21 January 2018

High-sensitivity CRP discriminates HNF1A-MODY from other subtypes of diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Analysis of the rat hepatocyte nuclear factor (HNF) 1 gene promoter: synergistic activation by HNF4 and HNF1 proteins

1 reference

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21 January 2018

Hepatocyte nuclear factor-4alpha is essential for glucose-stimulated insulin secretion by pancreatic beta-cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

HNF-1alpha G574S is a functional variant with decreased transactivation activity.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function

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21 January 2018

Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics.

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21 January 2018

The clinical application of non-genetic biomarkers for differential diagnosis of monogenic diabetes

1 reference

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21 January 2018

Assessment of high-sensitivity C-reactive protein levels as diagnostic discriminator of maturity-onset diabetes of the young due to HNF1A mutations

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21 January 2018

C-peptide is the appropriate outcome measure for type 1 diabetes clinical trials to preserve beta-cell function: report of an ADA workshop, 21-22 October 2001.

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21 January 2018

Contrasting diabetes phenotypes associated with hepatocyte nuclear factor-1alpha and -1beta mutations

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21 January 2018

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

PAX4 mutations in Thais with maturity onset diabetes of the young

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21 January 2018

Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome

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21 January 2018

HNF1alpha controls renal glucose reabsorption in mouse and man.

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21 January 2018

Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice

1 reference

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21 January 2018

Control of ACAT2 liver expression by HNF4{alpha}: lesson from MODY1 patients

1 reference

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21 January 2018

Primer-site SNPs mask mutations.

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein

1 reference

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21 January 2018

Hepatocyte nuclear factor-1 alpha gene inactivation: cosegregation between liver adenomatosis and diabetes phenotypes in two maturity-onset diabetes of the young (MODY)3 families.

1 reference

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21 January 2018

Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levels

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21 January 2018

MLPA and MAPH: new techniques for detection of gene deletions

1 reference

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21 January 2018

'I don't feel like a diabetic any more': the impact of stopping insulin in patients with maturity onset diabetes of the young following genetic testing

1 reference

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21 January 2018

No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Molecular background and clinical characteristics of HNF1A MODY in a Polish population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Clinical application of 1,5-anhydroglucitol measurements in patients with hepatocyte nuclear factor-1alpha maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Evaluation of Apolipoprotein M Serum Concentration as a Biomarker of HNF-1alpha MODY

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Increased all-cause and cardiovascular mortality in monogenic diabetes as a result of mutations in the HNF1A gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The maturity-onset diabetes of the young (MODY1) transcription factor HNF4alpha regulates expression of genes required for glucose transport and metabolism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Different genes, different diabetes: lessons from maturity-onset diabetes of the young

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21 January 2018

Inferring causality and functional significance of human coding DNA variants

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A distant upstream promoter of the HNF-4alpha gene connects the transcription factors involved in maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

HNF-1alpha G319S, a transactivation-deficient mutant, is associated with altered dynamics of diabetes onset in an Oji-Cree community

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Improved prandial glucose control with lower risk of hypoglycemia with nateglinide than with glibenclamide in patients with maturity-onset diabetes of the young type 3.

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

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21 January 2018

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

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21 January 2018

Hepatic hepatocyte nuclear factor 4α is essential for maintaining triglyceride and cholesterol homeostasis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Identification of an endogenous ligand bound to a native orphan nuclear receptor

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21 January 2018

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Heterozygous ABCC8 mutations are a cause of MODY

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Identification of HNF1A-MODY and HNF4A-MODY in Irish families: Phenotypic characteristics and therapeutic implications

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21 January 2018

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection

1 reference

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21 January 2018

Maturity-onset diabetes of the young (MODY): how many cases are we missing?

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https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Association of CYP1B1 Germ Line Mutations with Hepatocyte Nuclear Factor 1 -Mutated Hepatocellular Adenoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Mutations in the hepatocyte nuclear factor-1α gene in Caucasian families originally classified as having Type I diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

21 January 2018

Familial liver adenomatosis associated with hepatocyte nuclear factor 1alpha inactivation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Neonatal hyperinsulinaemic hypoglycaemia and monogenic diabetes due to a heterozygous mutation of the HNF4A gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion and insertion mutations in short tandem repeats in the coding regions of human genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Liver and kidney function in Japanese patients with maturity-onset diabetes of the young

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

HNF1alpha mutations are present in half of clinically defined MODY patients in South-Brazilian individuals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Can complement factors 5 and 8 and transthyretin be used as biomarkers for MODY 1 (HNF4A-MODY) and MODY 3 (HNF1A-MODY)?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Islet autoantibodies can discriminate maturity-onset diabetes of the young (MODY) from Type 1 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of maturity-onset diabetes of the young mutations in Brazilian families with autosomal-dominant early-onset type 2 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of molecular genetics in transforming diagnosis of diabetes mellitus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotype/phenotype relationships in HNF-4alpha/MODY1: haploinsufficiency is associated with reduced apolipoprotein (AII), apolipoprotein (CIII), lipoprotein(a), and triglyceride levels

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of hepatocyte nuclear factor 4alpha (HNF4alpha) gene variants on the risk of type 2 diabetes: a meta-analysis in 49,577 individuals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Early-onset type-II diabetes mellitus (MODY4) linked to IPF1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Synergistic trans-activation of the human C-reactive protein promoter by transcription factor HNF-1 binding at two distinct sites.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

A Large-Scale Association Analysis of Common Variation of the HNF1 Gene With Type 2 Diabetes in the U.K. Caucasian Population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22279

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.22279

1 reference

Europe PubMed Central

27 November 2017

1 reference

Europe PubMed Central

27 November 2017

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