|
Ferrozine
|
D005297 |
[A ferroin compound that forms a stable magenta-colored solution with the ferrous ion. The complex has an absorption peak at 562 nm and is used as a reagent and indicator for iron.
] |
|
Purple Membrane
|
A11.284.149.648 |
|
|
Mastectomy, Modified Radical
|
E04.466.678.476 |
|
|
Ferric Compounds
|
D005290 |
[Inorganic or organic compounds containing trivalent iron.
] |
|
Ferrichrome
|
D005291 |
[A cyclic peptide consisting of three residues of delta-N-hydroxy-delta-N-acetylornithine. It acts as an iron transport agent in Ustilago sphaerogena.
] |
|
Monoamine Oxidase Inhibitors
|
D27.505.519.389.616 |
|
|
Ferricyanides
|
D005292 |
[Inorganic salts of the hypothetical acid, H3Fe(CN)6.
] |
|
Optic Atrophy, Autosomal Dominant
|
D029241 |
[Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.
] |
|
Cardiomyopathy, Alcoholic
|
C14.280.238.057 |
|
|
Ferritins
|
D005293 |
[Iron-containing proteins that are widely distributed in animals, plants, and microorganisms. Their major function is to store IRON in a nontoxic bioavailable form. Each ferritin molecule consists of ferric iron in a hollow protein shell (APOFERRITINS) made of 24 subunits of various sequences depending on the species and tissue types.
] |
|
Optic Atrophy, Hereditary, Leber
|
D029242 |
[A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))
] |
|
Information Management
|
L01.399 |
|
|
Health Policy
|
I01.655.500.608.400 |
|
|
Cola
|
D030221 |
[A plant genus of the family STERCULIACEAE. This is the source of the kola nut which contains CAFFEINE and is used in popular beverages.
] |
|
Poly(ADP-ribose) Polymerase Inhibitors
|
D000067856 |
[Chemicals and drugs that inhibit the action of POLY(ADP-RIBOSE)POLYMERASES.
] |
|
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
|
D019860 |
[This enzyme is a lymphoid-specific src family tyrosine kinase that is critical for T-cell development and activation. Lck is associated with the cytoplasmic domains of CD4, CD8 and the beta-chain of the IL-2 receptor, and is thought to be involved in the earliest steps of TCR-mediated T-cell activation.
] |
|
Enterochromaffin-like Cells
|
D019861 |
[Neuroendocrine cells in the glands of the GASTRIC MUCOSA. They produce HISTAMINE and peptides such as CHROMOGRANINS. ECL cells respond to GASTRIN by releasing histamine which acts as a paracrine stimulator of the release of HYDROCHLORIC ACID from the GASTRIC PARIETAL CELLS.
] |
|
Hereditary Complement Deficiency Diseases
|
C20.673.795.500 |
|
|
Fat Necrosis
|
D005218 |
[A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol.
] |
|
Lentiviruses, Equine
|
B04.820.650.589.520 |
|
