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PLoS genetics, ISSN 1553-7390, 2011, Volume 7, Issue 7, pp. e1002114 - e1002114
Journal Article
OPHTHALMIC GENETICS, ISSN 1381-6810, 2017, Volume 38, Issue 6, pp. 580 - 583
Journal Article
Cell Stem Cell, ISSN 1934-5909, 10/2018, Volume 23, Issue 4, pp. 501 - 515.e7
Tracheal and esophageal disorders are prevalent in humans and difficult to accurately model in mice. We therefore established a three-dimensional organoid... 
foregut | Sox2 | esophagus | organoid | MORPHOGENESIS | PROGENITORS | WNT/BETA-CATENIN | LUNG SPECIFICATION | IN-VIVO | CAUSE ANOPHTHALMIA | MOUSE | ANTERIOR FOREGUT ENDODERM | VERTEBRATE ENDODERM DEVELOPMENT | DIFFERENTIATION | CELL & TISSUE ENGINEERING | CELL BIOLOGY
Journal Article
Birth Defects Research Part A - Clinical and Molecular Teratology, ISSN 1542-0752, 03/2012, Volume 94, Issue 3, pp. 147 - 152
BACKGROUND Infants with anophthalmia and microphthalmia frequently have other associated congenital anomalies. The reported frequency and types of associated... 
An/microphthalmia | Birth defects | Anophthalmia | Eye malformations | Congenital anomalies | Microphthalmia | eye malformations | COLOBOMA MAC | SYSTEM | DEFECTS | microphthalmia | ANOMALIES | anophthalmia | SOX2 CAUSE ANOPHTHALMIA | DESCRIPTIVE EPIDEMIOLOGY | DEVELOPMENTAL BIOLOGY | congenital anomalies | birth defects | CONGENITAL EYE MALFORMATIONS | CONSECUTIVE BIRTHS | TOXICOLOGY | MUTATIONS | HOMEOBOX GENE | Chromosome Disorders - epidemiology | Congenital Abnormalities - epidemiology | Polycystic Kidney Diseases - diagnosis | Trisomy | Prevalence | Encephalocele - epidemiology | Humans | Infant | Microphthalmos - epidemiology | CHARGE Syndrome - epidemiology | Congenital Abnormalities - diagnosis | Spine - abnormalities | Abnormalities, Multiple - epidemiology | Amniotic Band Syndrome - epidemiology | Chromosome Disorders - diagnosis | Amniotic Band Syndrome - diagnosis | Trachea - abnormalities | Ciliary Motility Disorders - epidemiology | Encephalocele - diagnosis | France - epidemiology | CHARGE Syndrome - diagnosis | Esophagus - abnormalities | Anal Canal - abnormalities | Limb Deformities, Congenital - diagnosis | Kidney - abnormalities | Limb Deformities, Congenital - epidemiology | Abnormalities, Multiple - diagnosis | Chromosomes, Human, Pair 13 | Heart Defects, Congenital - epidemiology | Ciliary Motility Disorders - diagnosis | Heart Defects, Congenital - diagnosis | Trisomy 13 Syndrome | Polycystic Kidney Diseases - epidemiology | Anophthalmos - epidemiology | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 08/2013, Volume 110, Issue 32, pp. E3017 - E3026
Journal Article
JOURNAL OF CLINICAL INVESTIGATION, ISSN 0021-9738, 09/2006, Volume 116, Issue 9, pp. 2442 - 2455
The transcription factor SOX2 is expressed most notably in the developing CNS and placodes, where it plays critical roles in embryogenesis. Heterozygous de... 
NUCLEAR-LOCALIZATION | MEDICINE, RESEARCH & EXPERIMENTAL | ESOPHAGEAL ATRESIA | SEX REVERSAL | GENE | SOX2 CAUSE ANOPHTHALMIA | MESSENGER-RNA DECAY | SRY | BILATERAL ANOPHTHALMIA | MOLECULAR-BASIS | GROWTH-HORMONE DEFICIENCY
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 | Index Medicus
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 03/2014, Volume 81, Issue 2, pp. 133 - 138
Journal Article
Developmental Biology, ISSN 0012-1606, 09/2013, Volume 381, Issue 2, pp. 491 - 501
Journal Article
Mechanisms of Development, ISSN 0925-4773, 2009, Volume 126, Issue 1, pp. 42 - 55
Journal Article