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GATA4 and GATA6 control mouse pancreas organogenesis
by
Soria, Bernat
, Carrasco, Manuel
, Rojas, Anabel
, Delgado, Irene
, Martín, Francisco
in
Animals
/ Binding Sites
/ Biomedical research
/ Cell Differentiation
/ Cell Division
/ Cell growth
/ Diabetes
/ Epithelial Cells - pathology
/ GATA4 Transcription Factor - deficiency
/ GATA4 Transcription Factor - genetics
/ GATA4 Transcription Factor - physiology
/ GATA6 Transcription Factor - deficiency
/ GATA6 Transcription Factor - genetics
/ GATA6 Transcription Factor - physiology
/ Gene Expression Regulation, Developmental - genetics
/ Genes
/ Genetic aspects
/ Genotype
/ Homeodomain Proteins - biosynthesis
/ Homeodomain Proteins - genetics
/ Hyperglycemia - congenital
/ Hyperglycemia - genetics
/ Mice
/ Mice, Knockout
/ Mice, Transgenic
/ Morphogenesis
/ Mutation
/ Organogenesis - genetics
/ Pancreas
/ Pancreas - abnormalities
/ Pancreas - embryology
/ Pancreas - pathology
/ Physiological aspects
/ Promoter Regions, Genetic - genetics
/ Protein Binding
/ Trans-Activators - biosynthesis
/ Trans-Activators - genetics
/ Transcription factors
/ Transcription, Genetic
/ Transgenic animals
2012
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GATA4 and GATA6 control mouse pancreas organogenesis
by
Soria, Bernat
, Carrasco, Manuel
, Rojas, Anabel
, Delgado, Irene
, Martín, Francisco
in
Animals
/ Binding Sites
/ Biomedical research
/ Cell Differentiation
/ Cell Division
/ Cell growth
/ Diabetes
/ Epithelial Cells - pathology
/ GATA4 Transcription Factor - deficiency
/ GATA4 Transcription Factor - genetics
/ GATA4 Transcription Factor - physiology
/ GATA6 Transcription Factor - deficiency
/ GATA6 Transcription Factor - genetics
/ GATA6 Transcription Factor - physiology
/ Gene Expression Regulation, Developmental - genetics
/ Genes
/ Genetic aspects
/ Genotype
/ Homeodomain Proteins - biosynthesis
/ Homeodomain Proteins - genetics
/ Hyperglycemia - congenital
/ Hyperglycemia - genetics
/ Mice
/ Mice, Knockout
/ Mice, Transgenic
/ Morphogenesis
/ Mutation
/ Organogenesis - genetics
/ Pancreas
/ Pancreas - abnormalities
/ Pancreas - embryology
/ Pancreas - pathology
/ Physiological aspects
/ Promoter Regions, Genetic - genetics
/ Protein Binding
/ Trans-Activators - biosynthesis
/ Trans-Activators - genetics
/ Transcription factors
/ Transcription, Genetic
/ Transgenic animals
2012
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GATA4 and GATA6 control mouse pancreas organogenesis
by
Soria, Bernat
, Carrasco, Manuel
, Rojas, Anabel
, Delgado, Irene
, Martín, Francisco
in
Animals
/ Binding Sites
/ Biomedical research
/ Cell Differentiation
/ Cell Division
/ Cell growth
/ Diabetes
/ Epithelial Cells - pathology
/ GATA4 Transcription Factor - deficiency
/ GATA4 Transcription Factor - genetics
/ GATA4 Transcription Factor - physiology
/ GATA6 Transcription Factor - deficiency
/ GATA6 Transcription Factor - genetics
/ GATA6 Transcription Factor - physiology
/ Gene Expression Regulation, Developmental - genetics
/ Genes
/ Genetic aspects
/ Genotype
/ Homeodomain Proteins - biosynthesis
/ Homeodomain Proteins - genetics
/ Hyperglycemia - congenital
/ Hyperglycemia - genetics
/ Mice
/ Mice, Knockout
/ Mice, Transgenic
/ Morphogenesis
/ Mutation
/ Organogenesis - genetics
/ Pancreas
/ Pancreas - abnormalities
/ Pancreas - embryology
/ Pancreas - pathology
/ Physiological aspects
/ Promoter Regions, Genetic - genetics
/ Protein Binding
/ Trans-Activators - biosynthesis
/ Trans-Activators - genetics
/ Transcription factors
/ Transcription, Genetic
/ Transgenic animals
2012
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Journal Article
GATA4 and GATA6 control mouse pancreas organogenesis
2012
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Overview
Recently, heterozygous mutations in GATA6 have been found in neonatal diabetic patients with failed pancreatic organogenesis. To investigate the roles of GATA4 and GATA6 in mouse pancreas organogenesis, we conditionally inactivated these genes within the pancreas. Single inactivation of either gene did not have a major impact on pancreas formation, indicating functional redundancy. However, double Gata4/Gata6 mutant mice failed to develop pancreata, died shortly after birth, and displayed hyperglycemia. Morphological defects in Gata4/Gata6 mutant pancreata were apparent during embryonic development, and the epithelium failed to expand as a result of defects in cell proliferation and differentiation. The number of multipotent pancreatic progenitors, including PDX1+ cells, was reduced in the Gata4/Gata6 mutant pancreatic epithelium. Remarkably, deletion of only 1 Gata6 allele on a Gata4 conditional knockout background severely reduced pancreatic mass. In contrast, a single WT allele of Gata4 in Gata6 conditional knockout mice was sufficient for normal pancreatic development, indicating differential contributions of GATA factors to pancreas formation. Our results place GATA factors at the top of the transcriptional network hierarchy controlling pancreas organogenesis.
Publisher
American Society for Clinical Investigation
Subject
/ Diabetes
/ Epithelial Cells - pathology
/ GATA4 Transcription Factor - deficiency
/ GATA4 Transcription Factor - genetics
/ GATA4 Transcription Factor - physiology
/ GATA6 Transcription Factor - deficiency
/ GATA6 Transcription Factor - genetics
/ GATA6 Transcription Factor - physiology
/ Gene Expression Regulation, Developmental - genetics
/ Genes
/ Genotype
/ Homeodomain Proteins - biosynthesis
/ Homeodomain Proteins - genetics
/ Mice
/ Mutation
/ Pancreas
/ Promoter Regions, Genetic - genetics
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