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animals (225) 225
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foregut (186) 186
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endoderm (126) 126
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endoderm - embryology (26) 26
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multidisciplinary sciences (26) 26
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Annual Review of Cell and Developmental Biology, ISSN 1081-0706, 11/2009, Volume 25, Issue 1, pp. 221 - 251
The endoderm germ layer contributes to the respiratory and gastrointestinal tracts and to all of their associated organs. Over the past decade, studies in... 
Nodal | Pancreas | Digestive system | Intestine | Liver | Foregut | digestive system | intestine | VISCERAL ENDODERM | NODAL SIGNALS | liver | DEFINITIVE ENDODERM | DEVELOPMENTAL BIOLOGY | nodal | BETA-CATENIN | MOUSE EMBRYO | foregut | RETINOIC ACID | PRIMITIVE-STREAK | WNT/BETA-CATENIN | pancreas | EMBRYONIC STEM-CELLS | LIVER DEVELOPMENT | Animals | Endoderm - physiology | Humans | Vertebrates - embryology | Organogenesis
Journal Article
STEM CELLS, ISSN 1066-5099, 11/2016, Volume 34, Issue 11, pp. 2635 - 2647
As known from model organisms, such as frog, fish, mouse, and chicken, the anterior–posterior patterning of the definitive endoderm (DE) into distinct domains... 
Human embryonic stem cells | Pancreatic duodenal endoderm | Anterior‐posterior patterning | Differentiation | Definitive endoderm | Anterior-posterior patterning | ORGAN FORMATION | ZEBRAFISH | VIVO | FOREGUT ENDODERM | ACTIVIN | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Anteriorposterior patterning | MORPHOGENESIS | IN-VITRO | XENOPUS | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | PANCREATIC PROGENITORS | HEMATOLOGY | EXPRESSION | Hepatocyte Nuclear Factor 3-beta - genetics | Bone Morphogenetic Protein 4 - genetics | Homeodomain Proteins - metabolism | Human Embryonic Stem Cells - cytology | Humans | Fibroblast Growth Factor 2 - pharmacology | Mesoderm - drug effects | Activins - metabolism | Mesoderm - cytology | Bone Morphogenetic Protein 4 - metabolism | Wnt3 Protein - genetics | SOXB1 Transcription Factors - metabolism | Immunomagnetic Separation | SOXB1 Transcription Factors - genetics | Endoderm - cytology | Gene Expression Regulation, Developmental | Human Embryonic Stem Cells - drug effects | Trans-Activators - genetics | Fibroblast Growth Factor 2 - metabolism | Wnt3 Protein - metabolism | Cell Differentiation | Wnt Signaling Pathway | Tretinoin - pharmacology | Hepatocyte Nuclear Factor 3-beta - metabolism | Cell Line | Human Embryonic Stem Cells - metabolism | beta Catenin - metabolism | Bone Morphogenetic Protein 4 - pharmacology | Homeodomain Proteins - genetics | beta Catenin - genetics | Endoderm - metabolism | Wnt3 Protein - pharmacology | Transforming Growth Factor beta - pharmacology | Transforming Growth Factor beta - genetics | Activins - pharmacology | Fibroblast Growth Factor 2 - genetics | Endoderm - drug effects | Trans-Activators - metabolism | Activins - genetics | Mesoderm - metabolism | Body Patterning - genetics | Transforming Growth Factor beta - metabolism | Bone morphogenetic proteins | Transforming growth factors | Embryonic stem cells | Analysis | Tretinoin | Embryos | Rodents | Stem cells | Pattern formation | Fibroblast growth factor | Wnt protein | Embryo cells | Mesoderm | Stem cell transplantation | Organisms | CDX2 protein | β-catenin | Inhibition | Pancreas | Endoderm | trans-Retinoic acid | Fibroblast growth factor 2 | Bone morphogenetic protein 4 | Inhibitors | Acids | Ligands | Activin | Retinoic acid | Foregut | Pluripotency
Journal Article
Development, ISSN 0950-1991, 07/2007, Volume 134, Issue 13, pp. 2521 - 2531
Sox2 is expressed in developing foregut endoderm, with highest levels in the future esophagus and anterior stomach. By contrast, Nkx2.1 (Titf1) is expressed... 
Metaplasia | Sox2 | Mouse embryo | Mutant | p63 | Tracheoesophageal fistula | Foregut development | Nkx2.1 | foregut development | metaplasia | STOMACH DEVELOPMENT | tracheoesophageal fistula | GASTROINTESTINAL-TRACT | mouse embryo | LUNG MORPHOGENESIS | CELL-PROLIFERATION | DEVELOPMENTAL BIOLOGY | CHICKEN-EMBRYO | BARRETTS-ESOPHAGUS | EPITHELIAL-MESENCHYMAL INTERACTIONS | CAUSE ANOPHTHALMIA | mutant | TRANSCRIPTIONAL REGULATION | MOLECULAR-MECHANISMS | Thyroid Nuclear Factor 1 | Tracheoesophageal Fistula - embryology | Transcription Factors - deficiency | Esophageal Atresia - pathology | DNA-Binding Proteins - metabolism | Time Factors | Endoderm - cytology | Esophageal Atresia - embryology | Gene Expression Regulation, Developmental | Nuclear Proteins - deficiency | Body Patterning | Trans-Activators - genetics | Cell Differentiation | Esophageal Atresia - genetics | Fibroblast Growth Factor 10 - genetics | Nuclear Proteins - genetics | SOXB1 Transcription Factors | Fibroblast Growth Factor 10 - metabolism | Tracheoesophageal Fistula - pathology | Digestive System - metabolism | Mice, Inbred C57BL | Nuclear Proteins - metabolism | Digestive System - embryology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Esophageal Atresia - metabolism | Endoderm - metabolism | Tracheoesophageal Fistula - metabolism | Transcription Factors - metabolism | Phenotype | Animals | Tracheoesophageal Fistula - genetics | Trans-Activators - metabolism | Mice
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 10/2017, Volume 232, Issue 10, pp. 2616 - 2625
Human‐induced pluripotent stem cells (hiPSCs) can potentially serve as an invaluable source for cell replacement therapy and allow the creation of patient‐ and... 
HUMAN ES CELLS | OCT4 | IN-VITRO | PHYSIOLOGY | DISEASE | LINEAGE | EFFICIENT DIFFERENTIATION | IPS CELLS | CELL BIOLOGY | Humans | Diabetes Mellitus, Type 1 - metabolism | SOXB1 Transcription Factors - metabolism | Teratoma - metabolism | Octamer Transcription Factor-3 - genetics | Insulin-Secreting Cells - metabolism | Transfection | SOXB1 Transcription Factors - genetics | Gene Expression Regulation, Developmental | Kruppel-Like Transcription Factors - metabolism | Endoderm - pathology | Cell Differentiation | Insulin Secretion | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | Induced Pluripotent Stem Cells - pathology | Signal Transduction | Feeder Cells | Cells, Cultured | Diabetes Mellitus, Type 1 - pathology | Diabetes Mellitus, Type 1 - genetics | Genotype | Cell Separation - methods | Fibroblasts - pathology | Proto-Oncogene Proteins c-myc - metabolism | Endoderm - metabolism | Organogenesis | Cell Lineage | Insulin - metabolism | Phenotype | Teratoma - pathology | Animals | Mice, Nude | Octamer Transcription Factor-3 - metabolism | Glucose - metabolism | Teratoma - genetics | Mice | Proto-Oncogene Proteins c-myc - genetics | Insulin-Secreting Cells - pathology | Kruppel-Like Transcription Factors - genetics | Diabetics | Care and treatment | Developmental biology | Stem cells | Transplantation | Drug discovery | Glucose | Web sites | Insulin | Dextrose | Incompatibility | Therapy | Transcription factors | Human influences | Diabetes mellitus | Embryos | Beta cells | Secretory vesicles | Immunology | Granular materials | Granules | Diabetes | Pancreas | Differentiation | In vitro methods and tests | Endoderm | Foregut | Pluripotency | Index Medicus
Journal Article
Cell Stem Cell, ISSN 1934-5909, 04/2012, Volume 10, Issue 4, pp. 355 - 361
The lung is composed of numerous epithelial lineages that arise from the anterior foregut endoderm. This review discusses how insights into the signaling... 
SOX2 | IDENTITY | MORPHOGENESIS | EPITHELIUM | ROLES | FOREGUT | BETA | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Animals | Pluripotent Stem Cells - cytology | Endoderm - cytology | Humans | Pluripotent Stem Cells - physiology | Endoderm - embryology | Lung - embryology | Signal Transduction - physiology | Lung - cytology | Cell Differentiation - physiology
Journal Article
Journal Article