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Molecular Vision, ISSN 1090-0535, 2018, Volume 24, pp. 853 - 866
Purpose: Telocytes (TCs) are peculiar interstitial cells, characterized by their typical elongated and interconnected processes called telopodes. TCs are... 
PROGENITOR CELLS | NORMAL CONJUNCTIVA | PATHOGENESIS | SURVIVIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | JUNCTIONS | OPHTHALMOLOGY | CAJAL ICC | MESENCHYMAL STEM-CELLS | NESTIN EXPRESSION | INTERSTITIAL-CELLS | P53 | Immunohistochemistry | Antigens, CD34 - metabolism | Platelet Endothelial Cell Adhesion Molecule-1 - genetics | Vimentin - metabolism | Humans | Middle Aged | Actins - metabolism | Male | Vascular Endothelial Growth Factor A - metabolism | Conjunctiva - surgery | Proto-Oncogene Proteins c-kit - metabolism | Pterygium - genetics | Vascular Endothelial Growth Factor A - genetics | Formaldehyde | Actins - genetics | Conjunctiva - metabolism | Conjunctiva - pathology | S100 Proteins - genetics | Pterygium - surgery | Platelet Endothelial Cell Adhesion Molecule-1 - metabolism | Vimentin - genetics | Nestin - genetics | Aged, 80 and over | Adult | Female | Immunophenotyping - methods | Proto-Oncogene Proteins c-kit - genetics | Tissue Fixation | Telocytes - metabolism | Gene Expression | AC133 Antigen - genetics | Receptor, Platelet-Derived Growth Factor alpha - metabolism | S100 Proteins - metabolism | Pterygium - pathology | Telocytes - pathology | Conjunctiva - abnormalities | Laminin - genetics | Nestin - metabolism | Pterygium - metabolism | Receptor, Platelet-Derived Growth Factor alpha - genetics | AC133 Antigen - metabolism | Telocytes - classification | Aged | Laminin - metabolism | Antigens, CD34 - genetics | Index Medicus
Journal Article
Cellular Signalling, ISSN 0898-6568, 07/2015, Volume 27, Issue 7, pp. 1509 - 1516
IRF6 and RIPK4 are critical regulators of keratinocyte differentiation and their mutation cause the developmental syndromes Van der Woude syndrome (VWS) and... 
Protein degradation | IRF6 | Mutation | RIPK4 | Cleft lip/palate | TRANSCRIPTION FACTORS | REGULATORY FACTOR 6 | KERATINOCYTE DIFFERENTIATION | WOUDE SYNDROME PATIENTS | PROTEIN-KINASE | POPLITEAL PTERYGIUM SYNDROME | INDEPENDENT MANNER | CELL BIOLOGY | BARTSOCAS-PAPAS SYNDROME | C-ASSOCIATED KINASE | NF-KAPPA-B | Abnormalities, Multiple - metabolism | Abnormalities, Multiple - pathology | Lip - abnormalities | Phosphorylation | Humans | Transcriptional Activation | Interferon Regulatory Factors - metabolism | Knee - pathology | Half-Life | Knee - abnormalities | Cytoplasm - metabolism | JNK Mitogen-Activated Protein Kinases - metabolism | NF-kappa B - metabolism | Syndactyly - pathology | Mutation, Missense | Lip - metabolism | Cysts - metabolism | Cleft Lip - pathology | HEK293 Cells | Eye Abnormalities - metabolism | Protein-Serine-Threonine Kinases - metabolism | Lip - pathology | Protein Structure, Tertiary | Recombinant Fusion Proteins - biosynthesis | Cell Line | Promoter Regions, Genetic | Signal Transduction | Syndactyly - metabolism | Protein-Serine-Threonine Kinases - genetics | Interferon Regulatory Factors - genetics | Recombinant Fusion Proteins - chemistry | Cleft Lip - metabolism | Cysts - pathology | beta Catenin - metabolism | Eye Abnormalities - pathology | Cleft Palate - pathology | Recombinant Fusion Proteins - genetics | Cleft Palate - metabolism | Genetic aspects | Interferon | Biological response modifiers | Proteolysis | Protein kinases | Index Medicus
Journal Article
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 10/2018, Volume 59, Issue 12, pp. 5060 - 5066
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, pp. e97402 - e97402
Journal Article
Birth Defects Research, ISSN 2472-1727, 01/2017, Volume 109, Issue 2, pp. 169 - 179
Background: Single genetic variants can affect multiple tissues during development. Thus it is possible that disruption of shared gene regulatory networks... 
TFAP2A | mouse models | human genetics | CLP | spina bifida | embryonic development | orofacial clefts | Van der Woude Syndrome | cleft palate | neural tube defects | GRHL3 | popliteal pterygium syndrome | cleft lip | cleft lip and palate | IRF6 | Embryonic development | Cleft palate | Cleft lip | Neural tube defects | Orofacial clefts | Popliteal pterygium syndrome | Spina bifida | Mouse models | Human genetics | Cleft lip and palate | SKIN EPIDERMIS | WOUDE-SYNDROME | TUMOR-SUPPRESSOR ACTIVITY | DEVELOPMENTAL BIOLOGY | TOXICOLOGY | DEFECTS | IKK-ALPHA | AP-2 FACTORS | MICE LACKING | Vander Woude Syndrome | SYNDROMIC CLEFT-LIP | Abnormalities, Multiple - metabolism | Abnormalities, Multiple - pathology | Humans | Interferon Regulatory Factors - metabolism | Neural Tube Defects - genetics | Neural Tube Defects - pathology | Data Mining | Neural Tube Defects - metabolism | Cleft Palate - genetics | Gene Regulatory Networks | Transcription Factor AP-2 - metabolism | DNA-Binding Proteins - metabolism | Cleft Lip - pathology | Gene Expression Regulation, Developmental | Neural Tube - metabolism | Abnormalities, Multiple - genetics | Signal Transduction | Computational Biology | Embryonic Development - genetics | Interferon Regulatory Factors - genetics | Neurulation - genetics | Transcription Factors - genetics | Cleft Lip - metabolism | DNA-Binding Proteins - genetics | Transcription Factors - metabolism | Cleft Lip - genetics | Transcription Factor AP-2 - genetics | Animals | Organogenesis - genetics | Cleft Palate - pathology | Cleft Palate - metabolism | Mice | Mutation | Neural Tube - growth & development | Neural Tube - abnormalities | Index Medicus
Journal Article
Journal Article
Journal Article