A novel hypomorphic PDX1 mutation responsible for permanent neonatal diabetes with subclinical exocrine deficiency
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New insights from monogenic diabetes for "common" type 2 diabetesNeonatal diabetes: an expanding list of genes allows for improved diagnosis and treatmentGenetics and pathophysiology of neonatal diabetes mellitus.Mitochondrial regulation of β-cell function: maintaining the momentum for insulin releaseTranscription factor regulation of pancreatic organogenesis, differentiation and maturationRB regulates pancreas development by stabilizing Pdx1Neonatal diabetes mellitus: a model for personalized medicineWolcott-Rallison syndromeFunctional analysis of Rfx6 and mutant variants associated with neonatal diabetes.Permanent diabetes during the first year of life: multiple gene screening in 54 patientsResearch resource: the pdx1 cistrome of pancreatic islets.Tshz1 Regulates Pancreatic β-Cell Maturation.Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiencyBiallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiencyMonogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes.Insulin secretion impairment in Sirt6 knockout pancreatic β cells is mediated by suppression of the FoxO1-Pdx1-Glut2 pathwayIsolated Pancreatic Aplasia Due to a Hypomorphic PTF1A Mutation.Pancreatic agenesis with congenital diaphragmatic hernia and congenital heart disease: a case reportAnalysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.Permanent neonatal diabetes mellitus--the importance of diabetes differential diagnosis in neonates and infants.The role of pancreatic imaging in monogenic diabetes mellitus.Management of diabetes mellitus in infants.The endocrine pancreas: insights into development, differentiation, and diabetes.Pdx1 and USF transcription factors co-ordinately regulate Alx3 gene expression in pancreatic β-cells.Novel mutation in wolcott-rallison syndrome with variable expression in two omani siblingsDiabetic pdx1-mutant zebrafish show conserved responses to nutrient overload and anti-glycemic treatment.Differentiation of Human Mesenchymal Stem Cells into Insulin Producing Cells by Using A Lentiviral Vector Carrying PDX1.A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient.A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes.PDX1 -MODY and dorsal pancreatic agenesis: New phenotype of a rare disease.Epidemiology, clinical characteristics, and genetic etiology of neonatal diabetes in Japan
P2860
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P2860
A novel hypomorphic PDX1 mutation responsible for permanent neonatal diabetes with subclinical exocrine deficiency
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@ast
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@en
type
label
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@ast
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@en
prefLabel
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@ast
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@en
P2093
P2860
P356
P1433
P1476
A novel hypomorphic PDX1 mutat ...... ubclinical exocrine deficiency
@en
P2093
Anne Boland
Doris A Stoffers
Kathryn C Claiborn
Marc Nicolino
P2860
P304
P356
10.2337/DB09-1284
P407
P577
2009-12-15T00:00:00Z