PDX1, pancreatic and duodenal homeobox 1, 3651

N. diseases: 185; N. variants: 22
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE Patients with HNF4alpha and IPF1 mutations show a similar clinical picture to HNF1alpha although diabetes may be diagnosed later. 9472859 1998
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE This circumstance suggests that the mechanism of diabetes in these individuals may be due not only to reduced gene dosage, but also to a dominant negative inhibition of transcription of the insulin gene and other beta cell-specific genes regulated by the mutant IPF-1. 9649577 1998
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE The identification of mutations in hepatocyte nuclear factors-1alpha, -4alpha, -1beta and insulin promoter factor-1 in maturity onset diabetes of the young (MODY) has highlighted the role that transcription factors may have in the development of diabetes. 10230653 1999
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Mutations in the homeobox gene Ipf1/Pdx1 are linked to diabetes in both mouse and human. 11130726 2000
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE Unusual causes of diabetes have been identified, including autosomal dominant, single gene forms due to mutations of glucokinase, the hepatocyte nuclear factors, and insulin promoter factor 1. 11467342 2000
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE It should be emphasized that MODY comprises two discrete clinical syndromes: glucokinase diabetes and transcription factor diabetes, the latter of which results from mutations in the genes encoding hepatocyte nuclear factor (HNF)-1alpha, HNF-1beta, HNF-4alpha and insulin promoter factor-1. 11202217 2000
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE All of the five known MODY genes, HNF-4alpha, glucokinase, HNF-1alpha, HNF-1beta, and IPF1, were previously excluded as being the cause of diabetes in these families. 10868949 2000
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Heterozygous mutations in the gene result in impaired glucose tolerance and symptoms of diabetes as seen in MODY4 and late-onset Type II (non-insulin-dependent) diabetes mellitus. 11692168 2001
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE We carried out mutation screening of the IPF1 gene in 115 Scandinavian families with at least two members with onset of diabetes younger than 40 years. 11270685 2001
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE We demonstrate the significance of this alternative promoter in a large MODY family where a mutated IPF-1 binding site in the P2 promoter of the HNF-4alpha gene co-segregates with diabetes (LOD score 3.25). 11590126 2001
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Mutations in transcription factors that play a role in the development of the endocrine pancreas, such as insulin promoter factor-1 and NeuroD1/BETA2, have been associated with diabetes. 11246894 2001
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Whereas heterozygous mutations in islet-cell transcription factors such as IPF1/IDX-1/STF-1/PDX-1 and NEUROD1/BETA2 serve as a genetic cause of diabetes or glucose intolerance, we investigated the possibility of PAX6 gene mutations being a genetic factor common to aniridia and diabetes. 11756345 2002
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE The significance of the P2 promoter was shown by the identification of a mutation in the IPF-1 binding site of the alternative promoter which cosegregated with diabetes in a large MODY family. 12242469 2002
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE We screened 264 unrelated subjects with type 2 diabetes diagnosed before 40 yr of age and a family history of diabetes for mutations in the minimal promoter and coding region of the IPF-1 gene (IPF1). 14764823 2004
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Impairment of interactions between PDX-1 and p300 in pancreatic beta-cells may limit insulin production and lead to the development of diabetes. 15001545 2004
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE The D76N variant of PDX1 does not significantly alter insulin secretion or act as a high-risk susceptibility allele for late-onset type 2 diabetes as proposed previously, although we cannot exclude a minor role in increasing risk of diabetes. 15277425 2004
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE An earlier French study identified InsCCG243 as a cause of autosomal dominant diabetes. 17003361 2006
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 AlteredExpression disease BEFREE These results indicated that the Pdx1 functioned as a key regulator for maintenance of beta-cell function, at least in part, through controlling c-Myc expression and the loss of its regulatory function may be an alternative mechanism for beta-cell neogenesis and apoptosis found in diabetes. 17317781 2007
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Adult rat liver cells transdifferentiated with lentiviral IPF1 vectors reverse diabetes in mice: an ex vivo gene therapy approach. 17131142 2007
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Taken together, PDX-1 and MafA play a crucial role in inducing surrogate beta-cells and could be a therapeutic target for diabetes. 17449132 2007
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE This property of PDX-1 opens new strategies for the treatment of diabetes. 18360684 2008
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease BEFREE We found a novel mutation in the pancreatic and duodenal homeobox 1 gene (PDX1, IPF1) in the two patients, which segregated with diabetes in the homozygous state. 20009086 2010
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE These results establish Nix as a critical mediator of β cell apoptosis and programmed necrosis in Pdx1-deficient diabetes. 20978346 2010
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Targeting cyclophilin D and the mitochondrial permeability transition enhances beta-cell survival and prevents diabetes in Pdx1 deficiency. 20479245 2010
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 Biomarker disease BEFREE Several studies showed that stress can stimulate autophagy in β-cells: the number of autophagosomes is increased in different in vivo models for diabetes, such as db/db mice, mice fed high-fat diet, pdx-1 knockout mice, as well as in in vitro models of glucotoxicity and lipotoxicity. 21029295 2010