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Oncogene, ISSN 1476-5594, 2007, Volume 26, Issue 49, pp. 6979 - 6988
Epithelial to mesenchymal transition (EMT) is implicated in the progression of primary tumours towards metastasis andis likely caused by a pathological activation of transcription factors regulating EMT in embryonic development... 
Epithelial to mesenchymal transition | Transcription | Epithelial polarity | Invasion | Cell adhesion | epithelial polarity | METASTASIS | transcription | FACTOR SNAIL | BIOCHEMISTRY & MOLECULAR BIOLOGY | VITAMIN-D-RECEPTOR | E-CADHERIN | MESENCHYMAL TRANSITION | BETA-CATENIN | CANCER | SLUG | CELL BIOLOGY | invasion | ONCOLOGY | cell adhesion | GENETICS & HEREDITY | epithelial to mesenchymal transition | EXPRESSION | Cell Polarity | Colonic Neoplasms - genetics | Nucleoside-Phosphate Kinase - genetics | Cadherins - metabolism | Cytoskeletal Proteins - antagonists & inhibitors | Membrane Glycoproteins - metabolism | Oligonucleotide Array Sequence Analysis | Cytoskeletal Proteins - genetics | Homeodomain Proteins - metabolism | Humans | Middle Aged | Immunoblotting | Gene Expression Profiling | Colonic Neoplasms - metabolism | Breast Neoplasms - metabolism | Membrane Glycoproteins - antagonists & inhibitors | Chromatin Immunoprecipitation | Neoplasm Invasiveness - pathology | Adult | Cytoskeletal Proteins - metabolism | Cell Differentiation | Membrane Proteins - metabolism | Tumor Cells, Cultured | Snail Family Transcription Factors | Promoter Regions, Genetic | Epithelium - pathology | Epithelium - metabolism | Membrane Proteins - genetics | Down-Regulation | Nucleoside-Phosphate Kinase - antagonists & inhibitors | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Disease Progression | Homeodomain Proteins - genetics | Membrane Glycoproteins - genetics | Transcription Factors - metabolism | Breast Neoplasms - genetics | Membrane Proteins - antagonists & inhibitors | Breast Neoplasms - pathology | Colonic Neoplasms - pathology | Aged | Microscopy, Fluorescence | Nucleoside-Phosphate Kinase - metabolism | Zinc Finger E-box-Binding Homeobox 1 | Cancer cells | Physiological aspects | Genetic aspects | Research | DNA binding proteins | Health aspects | Proteins | Oncology | Gene expression | Colorectal cancer | Cell adhesion & migration | Tumors
Journal Article
PloS one, ISSN 1932-6203, 2017, Volume 12, Issue 7, p. e0177962
Adult neural crest stem-derived cells (NCSC) are of extraordinary high plasticity and promising candidates for use in regenerative medicine. Several locations... 
PROGENITOR CELLS | MESENCHYMAL STROMAL CELLS | STEM-CELLS | TRUNK | MULTIDISCIPLINARY SCIENCES | PERIODONTAL-LIGAMENT | ONTOGENY | GENERATION | SKIN-DERIVED PRECURSORS | DIFFERENTIATION | MELANOCYTES | RNA-Binding Proteins - genetics | Humans | Adipose Tissue - cytology | Melanocytes - metabolism | Neurons - cytology | Receptors, Nerve Growth Factor - metabolism | Neural Stem Cells - cytology | Schwann Cells - cytology | Neural Crest - metabolism | Adipose Tissue - metabolism | Mesenchymal Stromal Cells - cytology | Snail Family Transcription Factors - genetics | Melanocytes - cytology | Nestin - genetics | Adult | Female | Cell Differentiation | Neurons - metabolism | Dermis - cytology | Nuclear Proteins - genetics | Biomarkers - metabolism | SOX9 Transcription Factor - metabolism | Gene Expression | Neural Crest - cytology | Dermis - metabolism | Snail Family Transcription Factors - metabolism | Microinjections | Bone Marrow Cells - cytology | Neural Crest - growth & development | Mesenchymal Stromal Cells - metabolism | Nuclear Proteins - metabolism | Schwann Cells - metabolism | Transcription Factor Brn-3A - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | Receptors, Nerve Growth Factor - genetics | Nerve Tissue Proteins - metabolism | Nestin - metabolism | Animals | Transcription Factor Brn-3A - genetics | Twist-Related Protein 1 - genetics | Twist-Related Protein 1 - metabolism | Neural Stem Cells - metabolism | SOX9 Transcription Factor - genetics | Bone Marrow Cells - metabolism | Mesenchymal Stem Cell Transplantation | RNA-Binding Proteins - metabolism | Adipose tissues | Comparative analysis | Skin | Neurosciences | Nestin | Adipose tissue | Leukocyte migration | Laboratories | Sox9 protein | Dermis | Melanocytes | Nervous system | Human tissues | Regeneration (physiology) | Cell adhesion & migration | Msi1 protein | Plasticity (neural) | Ethics | Immunology | Pathways | Surgery | Bone marrow | Hair | Hematology | Neurons | Tissue engineering | Schwann cells | Brn-3 protein | Gene expression | Embryos | Neural crest | Medicine | Regeneration | Human performance | Stromal cells | Stem cells | Cell migration | Dental pulp
Journal Article
Nature (London), ISSN 1476-4687, 2010, Volume 463, Issue 7283, pp. 958 - 962
Heterozygous mutations in the gene encoding the CHD (chromo-domain helicase DNA-binding domain) member CHD7, an ATP-dependent chromatin remodeller homologous... 
NETWORK | COMPLEX | PROTEIN | CHROMATIN | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | TRANSCRIPTION | POLYMERASE-II | MUTATIONS | EXPRESSION | CHARGE-SYNDROME | Embryonic Stem Cells - metabolism | Embryo, Nonmammalian - cytology | Embryonic Stem Cells - cytology | Xenopus Proteins - genetics | Humans | Multipotent Stem Cells - metabolism | Embryo, Nonmammalian - metabolism | Embryo, Nonmammalian - embryology | DNA-Binding Proteins - deficiency | Neural Crest - metabolism | Xenopus Proteins - chemistry | DNA-Binding Proteins - metabolism | Gene Expression Regulation, Developmental | Transcription, Genetic | Cell Differentiation | Xenopus laevis - genetics | DNA Helicases - genetics | Snail Family Transcription Factors | SOX9 Transcription Factor - metabolism | Cell Line | DNA Helicases - chemistry | Neural Crest - cytology | Xenopus laevis - embryology | Chromosomal Proteins, Non-Histone - metabolism | DNA Helicases - deficiency | Transcription Factors - genetics | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Syndrome | Chromosomal Proteins, Non-Histone - genetics | Transcription Factors - metabolism | Cell Lineage | DNA Helicases - metabolism | Animals | Xenopus Proteins - deficiency | Multipotent Stem Cells - cytology | Neural Crest - embryology | Xenopus laevis - metabolism | Twist-Related Protein 1 - genetics | Protein Binding | Xenopus Proteins - metabolism | Enhancer Elements, Genetic - genetics | Twist-Related Protein 1 - metabolism | SOX9 Transcription Factor - genetics | Cell Movement | Chromatin | Drosophila | Polybrominated biphenyls | Physiological aspects | Genetic aspects | Research | Structure | Embryonic stem cells | Helicases | Proteins | Labeling | Evacuations & rescues | Cell adhesion & migration | Human | Peripheral nervous system | Genes | Charge | Bones | Activation | Numerical control | Gene expression
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2010, Volume 107, Issue 35, pp. 15449 - 15454
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, p. e0150635
Transcription factors are key molecules that finely tune gene expression in response to injury... 
REPAIR | EMBRYO | REGENERATION | MULTIDISCIPLINARY SCIENCES | DEFICIENT | TUMOR | MICE | MECHANISMS | DIFFERENTIATION | EXPRESSION | CELL | Cadherins - metabolism | Skin - metabolism | Vimentin - metabolism | Keratin-16 - genetics | Male | Green Fluorescent Proteins - genetics | Epithelial-Mesenchymal Transition - genetics | Skin - injuries | Matrix Metalloproteinase 9 - metabolism | Forkhead Transcription Factors - metabolism | Matrix Metalloproteinase 9 - genetics | Vimentin - genetics | Female | Wound Healing - genetics | Cadherins - genetics | Snail Family Transcription Factors | Genes, Reporter | Green Fluorescent Proteins - metabolism | Signal Transduction | Mice, Inbred C57BL | Gene Expression Regulation | Keratin-16 - metabolism | Mice, Transgenic | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Transcription Factors - metabolism | Keratinocytes - pathology | Animals | Keratinocytes - metabolism | Wounds, Penetrating - pathology | Mice | Wounds, Penetrating - metabolism | Keratin | Care and treatment | Wound healing | Genes | Stem cells | Genetic engineering | Skin | DNA binding proteins | Gene expression | Wounds and injuries | Vimentin | Flow cytometry | Transcription factors | Tongue | Mesenchyme | Dermis | Follicles | E-cadherin | Western blotting | Thymus | Proteins | Genotype & phenotype | Animal reproduction | N-Cadherin | Animal tissues | Fibroblasts | Extracellular matrix | Localization | Growth factors | Injuries | Injury analysis | Food | Hair | Cytokines | Transgenic mice | Keratinocytes | Epidermis | Mammals | Epithelium | Gelatinase B | Wounding | Scars | Immunofluorescence
Journal Article
Journal Article
Journal Article
BMC cancer, ISSN 1471-2407, 2016, Volume 16, Issue 1, p. 53
Journal Article
PLoS genetics, ISSN 1553-7404, 2018, Volume 14, Issue 2, p. e1007167
Journal Article