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BioMed Research International, ISSN 2314-6133, 2014, Volume 2014, pp. 495091 - 14
Journal Article
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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
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 10/2012, Volume 123, Issue 1, pp. 44 - 59
NeuroD1 encodes a basic helix‐loop‐helix transcription factor involved in the development of neural and endocrine structures, including the retina and pineal... 
transcriptome profiling | microarray | retina | NeuroD1 | pineal gland | gene expression | NUCLEAR IMPORT | S-ANTIGEN | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL FATE | NEUROSCIENCES | RETINAL PHOTORECEPTOR | LEBER CONGENITAL AMAUROSIS | MEKA PHOSDUCIN | MOUSE MODEL | TRANSCRIPTION FACTOR | EXPRESSION | GLAND | Opsins - genetics | Pineal Gland - metabolism | Pineal Gland - ultrastructure | Cell Survival - genetics | Bromodeoxyuridine | RNA, Messenger - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Retina - cytology | Microarray Analysis | Pineal Gland - cytology | Basic Helix-Loop-Helix Transcription Factors - deficiency | Mucoproteins - genetics | Electroretinography | Microscopy, Electron, Transmission | Photoreceptor Cells, Vertebrate - ultrastructure | Basic Helix-Loop-Helix Transcription Factors - genetics | Gene Expression Regulation - genetics | Mice, Inbred C57BL | Mice, Knockout | Transcription Factors - metabolism | Animals | Analysis of Variance | Mucoproteins - deficiency | Opsins - metabolism | Mice | Photoreceptor Cells, Vertebrate - metabolism | Adaptor Proteins, Signal Transducing - metabolism | Retinal Degeneration - pathology | Genetic research | Anopheles | Genetic transcription | Ophthalmology | Analysis | Genes | Studies | Gene expression | Neurons | Recombination | Transcription factors | retinal degeneration | Pineal gland | Homeostasis | Retina | Rod outer segment membranes | Gene deletion | Survival | Cre recombinase | Promoters | Beta2 protein | Electroretinograms | Pinealocytes | DNA microarrays | Photoreceptors | Helix-loop-helix proteins | Age
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