Degenerative diseases genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy24

Photoreceptor Cells, Vertebrate Fundus Oculi Retina Retinal Pigment Epithelium Pigment Epithelium of Eye Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Lumbar Vertebrae Muscle, Skeletal Chromosomes, Human, Pair 4 Cells, Cultured Cervical Vertebrae Rod Cell Outer Segment Cell Line X Chromosome Mitochondria Brain Induced Pluripotent Stem Cells Inclusion Bodies Stem Cells Chromosomes, Human, Pair 5 Neurons Cartilage, Articular

Organisms5

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL Mice, Knockout Mice, Transgenic

Diseases59

Retinal Dystrophies Retinal Degeneration Muscular Dystrophies Myotonic Dystrophy Retinitis Pigmentosa Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Retinal Diseases Genetic Diseases, Inborn Disease Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Eye Diseases, Hereditary Spinal Diseases Blindness Muscular Dystrophy, Facioscapulohumeral Macular Degeneration Bardet-Biedl Syndrome Microphthalmos Night Blindness Alstrom Syndrome Syndrome Disease Models, Animal Muscular Dystrophy, Emery-Dreifuss Kidney Diseases, Cystic Spinal Osteophytosis Usher Syndromes Optic Atrophy, Hereditary, Leber Intervertebral Disc Degeneration Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Neurodegenerative Diseases Optic Disk Drusen Spondylosis Gyrate Atrophy Intellectual Disability Abnormalities, Multiple Muscular Dystrophy, Oculopharyngeal Intervertebral Disc Displacement Reflex Sympathetic Dystrophy Genetic Predisposition to Disease Muscular Atrophy, Spinal Vision Disorders Hepatolenticular Degeneration Vitelliform Macular Dystrophy Huntington Disease Osteoarthritis Spinal Stenosis Nerve Degeneration Neuromuscular Diseases Radiculopathy Alzheimer Disease Machado-Joseph Disease Myotonic Disorders Menkes Kinky Hair Syndrome Neoplasms

Chemicals and Drugs30

cis-trans-Isomerases Eye Proteins Peripherins Dystrophin Rhodopsin Nerve Tissue Proteins Codon, Nonsense Proteins Genetic Markers Carrier Proteins Sarcoglycans Lipofuscin Membrane Proteins Dystroglycans Utrophin Intermediate Filament Proteins ATP-Binding Cassette Transporters Rod Opsins Antioxidants Guanylate Cyclase DNA, Mitochondrial Amyloid DNA Thymopoietins DNA Primers Polyphenols RNA, Messenger Reactive Oxygen Species Collagen Type VI Receptor Protein-Tyrosine Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Electroretinography Pedigree DNA Mutational Analysis Chromosome Mapping Visual Acuity Disease Models, Animal Fluorescein Angiography Genetic Testing Polymerase Chain Reaction Heteroduplex Analysis Tomography, Optical Coherence Injections, Intraocular Visual Field Tests Spinal Fusion Ophthalmoscopy Sequence Analysis, DNA Stem Cell Transplantation Models, Genetic Heterozygote Detection Immunohistochemistry Protein Interaction Mapping Decompression, Surgical Genetic Therapy Models, Biological Blotting, Western Amino Acid Substitution Genetic Association Studies Genome-Wide Association Study Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Reproducibility of Results Magnetic Resonance Imaging

Psychiatry and Psychology6

Visual Acuity Visual Fields Intellectual Disability Huntington Disease Alzheimer Disease Vision, Ocular

Phenomena and Processes60

Genes, Recessive Consanguinity Mutation Genetic Linkage Phenotype Genes, Dominant Lod Score Mutation, Missense Exome Dark Adaptation Visual Acuity Exons Haplotypes Base Sequence Codon, Nonsense Homozygote Genetic Markers Heterozygote Amino Acid Sequence Genotype Visual Fields Frameshift Mutation Polymorphism, Single-Stranded Conformational Oxidative Stress Aging Chromosomes, Human, Pair 4 Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genome, Human Trinucleotide Repeat Expansion Light Alleles Linkage Disequilibrium Point Mutation Gene Expression Regulation Genetic Heterogeneity Cell Differentiation X Chromosome Protein Interaction Maps Cell Survival Gene Regulatory Networks Signal Transduction Time Factors Regeneration Vision, Ocular Amino Acid Substitution Genetic Structures Gene Expression Longevity Diet Genetic Vectors Apoptosis Founder Effect Chromosomes, Human, Pair 5 Fluorescence Genes Algorithms Lipid Peroxidation DNA Damage Penetrance

Disciplines and Occupations3

Computational Biology Immunohistochemistry Genetics, Medical

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Databases, Genetic Algorithms

Health Care4

Genetic Testing Age of Onset Genome-Wide Association Study Reproducibility of Results

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

Retinal Dystrophies Retinal Degeneration Muscular Dystrophies Myotonic Dystrophy Retinitis Pigmentosa Leber Congenital Amaurosis Muscular Dystrophy, Duchenne cis-trans-Isomerases Electroretinography Eye Proteins Corneal Dystrophies, Hereditary Pedigree Photoreceptor Cells, Vertebrate Muscular Dystrophy, Animal Fundus Oculi Retinal Diseases Retina Genes, Recessive Consanguinity Mutation Genetic Diseases, Inborn Disease Fuchs' Endothelial Dystrophy Retinal Pigment Epithelium Laurence-Moon Syndrome Eye Diseases, Hereditary DNA Mutational Analysis Pigment Epithelium of Eye Genetic Linkage Phenotype Peripherins Photoreceptor Cells Chromosome Mapping Spinal Diseases Blindness Muscular Dystrophy, Facioscapulohumeral Genes, Dominant Macular Degeneration Dystrophin Retinal Rod Photoreceptor Cells Bardet-Biedl Syndrome Molecular Sequence Data Rhodopsin Microphthalmos Night Blindness Retinal Cone Photoreceptor Cells Nerve Tissue Proteins Lod Score Mutation, Missense Exome Alstrom Syndrome Dark Adaptation Syndrome Visual Acuity Exons Haplotypes Disease Models, Animal Muscular Dystrophy, Emery-Dreifuss Kidney Diseases, Cystic Fluorescein Angiography Spinal Osteophytosis Mice, Inbred mdx Base Sequence Codon, Nonsense Usher Syndromes Optic Atrophy, Hereditary, Leber Proteins Lumbar Vertebrae Homozygote Intervertebral Disc Degeneration Genetic Markers Genetic Testing Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Heterozygote Carrier Proteins Amino Acid Sequence Neurodegenerative Diseases Optic Disk Drusen Sarcoglycans Age of Onset Lipofuscin Membrane Proteins Spondylosis Rats, Mutant Strains Genotype Polymerase Chain Reaction Muscle, Skeletal Gyrate Atrophy Mice, Inbred C57BL Visual Fields Frameshift Mutation Polymorphism, Single-Stranded Conformational Heteroduplex Analysis Intellectual Disability Abnormalities, Multiple Tomography, Optical Coherence Injections, Intraocular Muscular Dystrophy, Oculopharyngeal

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