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nkx2.1 (124) 124
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Journal Article
Journal of Neuroscience, ISSN 0270-6474, 01/2018, Volume 38, Issue 5, pp. 1100 - 1113
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 11/2018, Volume 505, Issue 4, pp. 1027 - 1031
In non-small lung cancer, the expression of the transcription factor TTF-1/Nkx2.1 correlates with the presence of EGFR mutations, therefore TTF-1/Nkx2.1... 
LRIG1 | β-catenin | TTF-1/Nkx2.1 | EGFR | Non-small cell lung cancer | LR1G1 | beta-catenin | SURVIVAL | PROTEIN | BIOMARKER | BIOCHEMISTRY & MOLECULAR BIOLOGY | TTF-1 | DEPENDENCY | BIOPHYSICS | GENE-EXPRESSION
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 Neuroscience, ISSN 0270-6474, 03/2004, Volume 24, Issue 11, pp. 2612 - 2622
Journal Article
Neuron, ISSN 0896-6273, 2010, Volume 65, Issue 3, pp. 328 - 340
Interneurons in the cerebral cortex regulate cortical functions through the actions of distinct subgroups that express parvalbumin, somatostatin, or... 
STEMCELL | DEVBIO | MOLNEURO | GREEN FLUORESCENT PROTEIN | FOREBRAIN | ROLES | GSH2 | MICE | SPECIFICATION | EXPRESSION | NEUROSCIENCES | SHH MUTATIONS | MOUSE TELENCEPHALON | GENE-FUNCTION | Interneurons - physiology | Thyroid Nuclear Factor 1 | Embryo, Mammalian | Homeodomain Proteins - metabolism | Hedgehog Proteins - metabolism | Parvalbumins - metabolism | Green Fluorescent Proteins - genetics | Cerebral Cortex - cytology | Hedgehog Proteins - genetics | Eye Proteins - genetics | Nuclear Proteins - genetics | Somatostatin - metabolism | Gene Expression Regulation, Developmental - physiology | Telencephalon - cytology | Animals, Genetically Modified | Mice, Inbred C57BL | Nuclear Proteins - metabolism | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Embryonic Stem Cells - physiology | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | S100 Calcium Binding Protein G - metabolism | Transcription Factors - metabolism | Animals | Calbindin 2 | Eye Proteins - metabolism | Signal Transduction - physiology | Mice | Medical colleges | Bipolar disorder | Hypothalamic hormones | Neurons | Developmental biology | Studies | Kinases | Medical research | Smo signaling | medial ganglionic eminence | ZEG Cre reporter mouse | Cre-loxP | Gli1 | Nkx2.1 | ventral telencephalon | caudal ganglionic eminence | Ptch1 | Six3 | transcription factor GSX2 | interneuron subgroups markers - parvalbumin, somatostatin, calretinin | cortical development
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e83 - e90
In October 2016, the American Association for Cancer Research held a meeting of international childhood cancer predisposition syndrome experts to evaluate the... 
GENOTYPE-PHENOTYPE CORRELATION | RUBINSTEIN-TAYBI-SYNDROME | SOTOS-SYNDROME | ONCOLOGY | SCHINZEL-GIEDION-SYNDROME | CAUSE NOONAN | JUVENILE MYELOMONOCYTIC LEUKEMIA | GERM-CELL TUMOR | OF-FUNCTION MUTATIONS | CLINICAL-FEATURES | FACTOR-I TITF-1/NKX2.1 | Abnormalities, Multiple - pathology | Neoplastic Syndromes, Hereditary - pathology | Craniofacial Abnormalities - epidemiology | Sotos Syndrome - epidemiology | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - pathology | Nails, Malformed - pathology | Intellectual Disability - genetics | Noonan Syndrome - pathology | Neoplastic Syndromes, Hereditary - epidemiology | Rubinstein-Taybi Syndrome - genetics | Congenital Hypothyroidism - genetics | Abnormalities, Multiple - epidemiology | Craniofacial Abnormalities - pathology | Thyroid Nuclear Factor 1 - genetics | Neoplastic Syndromes, Hereditary - genetics | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Intellectual Disability - epidemiology | Colorectal Neoplasms - epidemiology | Hand Deformities, Congenital - epidemiology | Sotos Syndrome - genetics | Costello Syndrome - pathology | Sotos Syndrome - pathology | Risk Factors | Intellectual Disability - pathology | Brain Neoplasms - genetics | Rubinstein-Taybi Syndrome - pathology | Noonan Syndrome - genetics | Nails, Malformed - genetics | Costello Syndrome - epidemiology | Costello Syndrome - genetics | Hand Deformities, Congenital - genetics | Nails, Malformed - epidemiology | Rubinstein-Taybi Syndrome - epidemiology | Congenital Hypothyroidism - pathology | Noonan Syndrome - epidemiology | Mutation | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics | Colorectal Neoplasms - pathology | Congenital Hypothyroidism - epidemiology | Hand Deformities, Congenital - pathology | Brain Neoplasms - epidemiology | Brain | Physical examinations | Brain tumors | Health problems | Disorders | Health risks | Aciduria | Risk | Infants | Patients | K-Ras protein | Surveillance | Children | Health risk assessment | Thyroid transcription factor 1 | Metabolic disorders | Cancer
Journal Article
Neuropediatrics, ISSN 0174-304X, 08/2018, Volume 49, Issue 4, pp. 246 - 255
Abstract Objective  This article elucidates a clinical and genetic approach to pediatric early-onset chorea in patients with normal neuroimaging. Methods  We... 
Original Article | GNAO1 | NKX2.1 | OPA3 | pediatric chorea | ADCY5 | BENIGN HEREDITARY CHOREA | ACIDURIA TYPE-III | 3-METHYLGLUTACONIC ACIDURIA | CHILDHOOD | CLINICAL NEUROLOGY | FAMILIAL DYSKINESIA | DE-NOVO MUTATIONS | MOVEMENT-DISORDER | OPTIC ATROPHY SYNDROME | PEDIATRICS | OPA3 GENE
Journal Article
Journal Article