Therapeutic candidate targeting retinitis pigmentosa. Medical search. Frequent questions

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Anatomy20

Photoreceptor Cells, Vertebrate Retina Cell Line, Tumor Fundus Oculi Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Cells, Cultured X Chromosome Retinal Photoreceptor Cell Outer Segment Fovea Centralis Photoreceptor Connecting Cilium Macula Lutea Cilia Rod Cell Outer Segment Retinal Pigment Epithelium Retinal Bipolar Cells Chromosomes, Human, Pair 19 Pigment Epithelium of Eye Retinal Photoreceptor Cell Inner Segment

Organisms3

Mice, Inbred C57BL Rats, Transgenic Dependovirus

Diseases24

Retinitis Pigmentosa Cytomegalovirus Retinitis Disease Models, Animal Retinitis Retinal Degeneration Genetic Diseases, X-Linked Usher Syndromes Night Blindness Blindness Eye Diseases, Hereditary Retinal Diseases Laurence-Moon Syndrome Leber Congenital Amaurosis Vision Disorders Retinal Dysplasia Optic Atrophy, Hereditary, Leber Ataxia Eye Infections, Viral Retinal Dystrophies Bardet-Biedl Syndrome Syndrome Vision, Low Optic Atrophies, Hereditary Optic Disk Drusen

Chemicals and Drugs17

Eye Proteins Rhodopsin Peripherins Cyclic Nucleotide Phosphodiesterases, Type 6 Rod Opsins IMP Dehydrogenase Carbonic Anhydrase IV Ribonucleoprotein, U4-U6 Small Nuclear Tetraspanins Intermediate Filament Proteins Opsins cis-trans-Isomerases Codon, Nonsense Carrier Proteins Foscarnet Arrestin Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Electroretinography Disease Models, Animal Pedigree Visual Acuity DNA Mutational Analysis Visual Field Tests Fluorescein Angiography Tomography, Optical Coherence Chromosome Mapping Sequence Analysis, DNA Polymerase Chain Reaction Vision Tests Ophthalmoscopy Visual Prosthesis Ophthalmoscopes Electrooculography Genetic Testing

Psychiatry and Psychology5

Visual Acuity Visual Fields Sensory Thresholds Phosphenes Vision, Ocular

Phenomena and Processes33

Genes, Dominant Genes, Recessive Cell Proliferation Dark Adaptation Signal Transduction Visual Acuity Visual Fields Mutation Genetic Linkage Consanguinity X Chromosome Exons Mutation, Missense Homozygote Phenotype Lod Score Polymorphism, Single-Stranded Conformational Amino Acid Sequence Base Sequence Frameshift Mutation Genes, X-Linked Heterozygote Phosphenes Codon, Nonsense Vision, Ocular Genotype Point Mutation Light RNA Splicing Haplotypes Microsatellite Repeats Genetic Heterogeneity Chromosomes, Human, Pair 19

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Health Care1

Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Health Care

Retinitis Pigmentosa Cytomegalovirus Retinitis Electroretinography Eye Proteins Disease Models, Animal Rhodopsin Retinitis Retinal Degeneration Genes, Dominant Photoreceptor Cells, Vertebrate Pedigree Genes, Recessive Mice, Inbred C57BL Retina Cell Line, Tumor Peripherins Genetic Diseases, X-Linked Cell Proliferation Dark Adaptation Fundus Oculi Signal Transduction Photoreceptor Cells Visual Acuity Cyclic Nucleotide Phosphodiesterases, Type 6 Retinal Rod Photoreceptor Cells Visual Fields Usher Syndromes Retinal Cone Photoreceptor Cells Mutation Cells, Cultured Genetic Linkage Night Blindness DNA Mutational Analysis Rod Opsins Consanguinity Blindness Visual Field Tests X Chromosome Exons Mutation, Missense Molecular Sequence Data Eye Diseases, Hereditary Fluorescein Angiography Tomography, Optical Coherence Homozygote IMP Dehydrogenase Chromosome Mapping Retinal Diseases Laurence-Moon Syndrome Carbonic Anhydrase IV Phenotype Lod Score Leber Congenital Amaurosis Ribonucleoprotein, U4-U6 Small Nuclear Tetraspanins Retinal Photoreceptor Cell Outer Segment Fovea Centralis Polymorphism, Single-Stranded Conformational Vision Disorders Intermediate Filament Proteins Photoreceptor Connecting Cilium Sensory Thresholds Amino Acid Sequence Opsins Base Sequence Frameshift Mutation Genes, X-Linked cis-trans-Isomerases Retinal Dysplasia Macula Lutea Optic Atrophy, Hereditary, Leber Heterozygote Sequence Analysis, DNA Ataxia Phosphenes Eye Infections, Viral Codon, Nonsense Polymerase Chain Reaction Vision, Ocular Retinal Dystrophies Genotype Bardet-Biedl Syndrome Syndrome Vision Tests Cilia Point Mutation Ophthalmoscopy Vision, Low Rats, Transgenic Visual Prosthesis Light Carrier Proteins Rod Cell Outer Segment Ophthalmoscopes Optic Atrophies, Hereditary RNA Splicing Electrooculography Haplotypes Microsatellite Repeats Foscarnet

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