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Sodium-Phosphate Cotransporter Proteins, Type III
|
D12.776.157.530.450.625.625.875 |
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Medicare Part B
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N03.706.615.699 |
|
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Origin Recognition Complex
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D051738 |
[The origin recognition complex is a multi-subunit DNA-binding protein that initiates DNA REPLICATION in eukaryotes.
] |
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Retinal Vein Occlusion
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D012170 |
[Blockage of the RETINAL VEIN. Those at high risk for this condition include patients with HYPERTENSION; DIABETES MELLITUS; ATHEROSCLEROSIS; and other CARDIOVASCULAR DISEASES.
] |
|
Microphthalmia-Associated Transcription Factor
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D051739 |
[A basic helix-loop-helix leucine zipper transcription factor that regulates the CELL DIFFERENTIATION and development of a variety of cell types including MELANOCYTES; OSTEOCLASTS; and RETINAL PIGMENT EPITHELIUM. Mutations in MITF protein have been associated with OSTEOPETROSIS and WAARDENBURG SYNDROME.
] |
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Arachnoid Cysts
|
C10.500.142.100 |
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Retinal Vessels
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D012171 |
[The blood vessels which supply and drain the RETINA.
] |
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Retinaldehyde
|
D012172 |
[A carotenoid-derived diterpene that is a constituent of visual pigments. It is the oxidized form of retinol which functions as the active component of the visual cycle. It is bound to the protein opsin forming the complex rhodopsin. When stimulated by visible light, the retinal component of the rhodopsin complex undergoes isomerization at the 11-position of the double bond to the cis-form; this is reversed in "dark" reactions to return to the native trans-configuration.
] |
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Hyperopia
|
C11.744.479 |
|
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Receptor, EphA7
|
D036141 |
[An eph family receptor found widely expressed in embryo tissues, including the NERVOUS SYSTEM. In the BRAIN high levels of EphA7 expression occurs in the anterior tectum, medulla, RHOMBENCEPHALON, and SUBCOMMISSURAL ORGAN. Several isoforms of the protein occur due to multiple alternative spicing of the EphA7 mRNA.
] |
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Laboratory Personnel
|
M01.526.502 |
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Hypobetalipoproteinemia, Familial, Apolipoprotein B
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C18.452.584.500.875.440.750 |
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Thiourea
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D02.886.904 |
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Radiation Dosage
|
G01.750.740 |
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Radiation Effects
|
G01.750.745 |
|
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Retinal Degeneration
|
D012162 |
[A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304)
] |
|
Retinal Detachment
|
D012163 |
[Separation of the inner layers of the retina (neural retina) from the pigment epithelium. Retinal detachment occurs more commonly in men than in women, in eyes with degenerative myopia, in aging and in aphakia. It may occur after an uncomplicated cataract extraction, but it is seen more often if vitreous humor has been lost during surgery. (Dorland, 27th ed; Newell, Ophthalmology: Principles and Concepts, 7th ed, p310-12).
] |
|
Retinal Diseases
|
D012164 |
[Diseases involving the RETINA.
] |
|
Retinal Ganglion Cells
|
D012165 |
[Neurons of the innermost layer of the retina, the internal plexiform layer. They are of variable sizes and shapes, and their axons project via the OPTIC NERVE to the brain. A small subset of these cells act as photoreceptors with projections to the SUPRACHIASMATIC NUCLEUS, the center for regulating CIRCADIAN RHYTHM.
] |
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Radiation Exposure
|
G01.750.748 |
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