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Development, ISSN 0950-1991, 11/2004, Volume 131, Issue 22, pp. 5539 - 5550
Radial glial cells derive from neuroepithelial cells, and both cell types are identified as neural stem cells. Neural stem cells are known to change their... 
Basal lamina | Radial glia | Tight junction | Neuroepithelium | Adherens junction | bHLH | neuroepithelium | radial glia | TUBE | CYCLIN D1 | MOUSE | NOTCH | DEVELOPMENTAL BIOLOGY | TIGHT JUNCTIONS | adherens junction | basal lamina | MICE | CHICKEN BRAIN | EXPRESSION | tight junction | N-CADHERIN | BASEMENT-MEMBRANE | Spinal Cord - abnormalities | Transcription Factor HES-1 | Spinal Cord - metabolism | Neuroglia - pathology | Homeodomain Proteins - metabolism | Nerve Tissue Proteins - deficiency | Nervous System - metabolism | Eye Abnormalities - embryology | Stem Cells - cytology | Stem Cells - metabolism | DNA-Binding Proteins - deficiency | DNA-Binding Proteins - metabolism | Neuroglia - cytology | In Situ Hybridization | Time Factors | Gene Expression Regulation, Developmental | Cell Differentiation | Spinal Cord - cytology | Nervous System - embryology | Eye Abnormalities - metabolism | Repressor Proteins - metabolism | Basic Helix-Loop-Helix Transcription Factors | Nervous System - cytology | Microscopy, Electron, Scanning | Basement Membrane - abnormalities | Repressor Proteins - genetics | DNA-Binding Proteins - genetics | Eye Abnormalities - genetics | Mutation - genetics | Basement Membrane - metabolism | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Mice, Knockout | Nerve Tissue Proteins - metabolism | Spinal Cord - embryology | Animals | Basement Membrane - embryology | Neuroglia - metabolism | Mice | Index Medicus
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 05/2013, Volume 22, Issue 10, pp. 2024 - 2040
Journal Article
Journal Article
Cell Metabolism, ISSN 1550-4131, 2008, Volume 7, Issue 3, pp. 258 - 268
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2012, Volume 180, Issue 6, pp. 2230 - 2239
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 11/2014, Volume 17, Issue 6, pp. 491 - 495
Journal Article
Eye (Basingstoke), ISSN 0950-222X, 04/2015, Volume 29, Issue 4, pp. 492 - 498
Purpose To describe a cohort of patients with congenital eyelid coloboma, to identify associated ocular and craniofacial abnormalities, and to establish any... 
PATHOGENESIS | OPHTHALMOLOGY | FACIAL CLEFTS | Coloboma - embryology | Humans | Eyelids - abnormalities | Abnormalities, Multiple | Child, Preschool | Infant | Male | Coloboma - epidemiology | Syndrome | Incidence | Young Adult | Eye Abnormalities - pathology | Adolescent | Adult | Craniofacial Abnormalities - pathology | Female | Retrospective Studies | Child | Infant, Newborn | Index Medicus | Clinical Study
Journal Article
Development, ISSN 0950-1991, 03/2010, Volume 137, Issue 5, pp. 725 - 734
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, pp. e44975 - e44975
Joubert syndrome and related diseases (JSRD) are developmental cerebello-oculo-renal syndromes with phenotypes including cerebellar hypoplasia, retinal... 
RETINAL DEGENERATION | LEBER CONGENITAL AMAUROSIS | MUTATIONS CAUSE | TRANSITION ZONE | SYNDROME-RELATED DISORDERS | MULTIDISCIPLINARY SCIENCES | CILIOPATHY | MICE | NPHP6 GENE | CENTROSOMAL PROTEIN | MECKEL-GRUBER-SYNDROME | Brain - embryology | Kidney - embryology | Genomics | Humans | Eye Abnormalities - embryology | Retina - embryology | Cerebellum - abnormalities | Kidney Diseases, Cystic - embryology | Neoplasm Proteins - metabolism | Brain - metabolism | Kidney - metabolism | Gene Expression Regulation, Developmental | Antigens, Neoplasm - metabolism | Conserved Sequence | Kidney Diseases, Cystic - genetics | Neoplasm Proteins - genetics | Cerebellar Diseases - embryology | Antigens, Neoplasm - genetics | Cell Line | Abnormalities, Multiple | Eye Abnormalities - genetics | Organ Specificity | Centrosome - metabolism | Protein Transport | Animals | Cerebellar Diseases - genetics | Adaptor Proteins, Signal Transducing - genetics | Retina - abnormalities | Mice | Evolution, Molecular | Embryonic development | Gene mutations | Joubert syndrome | Physiological aspects | Development and progression | Genetic aspects | Research | Choroid plexus | Cerebellum | Brain | Syngeneic grafts | Congenital defects | Epithelial cells | Genes | Biological evolution | Central nervous system | Evolutionary genetics | Retina | Nervous system | Neurodevelopmental disorders | Tissues | Defects | Recruitment | Proteins | Ethics | Genotype & phenotype | Hypoplasia | Congenital diseases | Nephronophthisis | Developmental biology | Fetuses | Organs | Gene expression | Embryos | Medicine | Environmental science | Retinal degeneration | Mutation | Kidney diseases | Dystrophy | Position (location) | Kidney transplantation | Index Medicus
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 2012, Volume 122, Issue 4, pp. 1233 - 1245
Cilia are highly specialized microtubule-based organelles that have pivotal roles in numerous biological processes, including transducing sensory signals.... 
JOUBERT-SYNDROME | RETINAL DEGENERATION | MEDICINE, RESEARCH & EXPERIMENTAL | INTRAFLAGELLAR TRANSPORT MOTORS | KUPFFERS VESICLE | LEBER CONGENITAL AMAUROSIS | ZEBRAFISH MODEL | BARDET-BIEDL-SYNDROME | PLANAR CELL POLARITY | NPHP6 GENE | PRIMARY CILIUM | Group II Chaperonins - physiology | Microtubule-Associated Proteins - genetics | Chaperonins - deficiency | Humans | Eye Abnormalities - embryology | Ear - embryology | Molecular Sequence Data | Sensation Disorders - pathology | Zebrafish - embryology | Genetic Complementation Test | Olfactory Receptor Neurons - ultrastructure | Group II Chaperonins - genetics | DNA Mutational Analysis | Gene Expression Regulation, Developmental | Nuclear Proteins - deficiency | HEK293 Cells | Cilia - ultrastructure | Bardet-Biedl Syndrome - genetics | Microtubule-Associated Proteins - deficiency | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Amino Acid Sequence | Antigens, Neoplasm - genetics | Chaperonins - physiology | Group II Chaperonins - deficiency | Ear - abnormalities | Mice, Inbred C57BL | Photoreceptor Connecting Cilium - ultrastructure | Leber Congenital Amaurosis - genetics | Eye Abnormalities - genetics | Zebrafish - genetics | Zebrafish Proteins - physiology | Microtubule-Associated Proteins - physiology | Protein Interaction Mapping | Sequence Homology, Amino Acid | Hair Cells, Auditory - ultrastructure | Sequence Alignment | Zebrafish Proteins - deficiency | Animals | Alleles | Sensation Disorders - prevention & control | Mice | Nuclear Proteins - physiology | Sensation Disorders - genetics | Zebrafish Proteins - genetics | Chaperonins - genetics | Allelomorphism | Gene mutations | Cilia and ciliary motion | Photoreceptors | Genetic aspects | Properties | Identification and classification | Index Medicus | Abridged Index Medicus
Journal Article