| Albright, Fuller | <person> Physician, 1900-1969. See: Albright's disease, Albright's syndrome, Albright's hereditary osteodystrophy, Forbes-Albright syndrome, McCune-Albright syndrome. (05 Mar 2000) |
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| albuginea | Tough white fibrous tissue. The tunica albuginea of the testis, for example, is the layer of dense whitish inelastic tissue that surrounds the testis. (12 Dec 1998) |
| albugineotomy | Incision into any tunica albuginea. Origin: albuginea + G. Tome, cutting (05 Mar 2000) |
| albugineous | 1. Resembling boiled white of egg. 2. Relating to any tunica albuginea. Origin: L. Albugineus, fr. Albugo, white spot (05 Mar 2000) |
| albugo | Origin: L, whiteness, fr. Albus white. <medicine> Same as Leucoma. Source: Websters Dictionary (01 Mar 1998) |
| album | 1. A white tablet on which anything was inscribed, as a list of names, etc. 2. A register for visitors' names; a visitors' book. 3. A blank book, in which to insert autographs sketches, memorial writing of friends, photographs, etc. Origin: L, neut. Of albus white: cf. F. Album. Cf. Alb. Source: Websters Dictionary (01 Mar 1998) |
| album graecum | Dung of dogs or hyenas, which becomes white by exposure to air. It is used in dressing leather, and was formerly used in medicine. Origin: L, Greek white. Source: Websters Dictionary (01 Mar 1998) |
| albumen | 1. The white of an egg. 2. <botany> Nourishing matter stored up within the integuments of the seed in many plants, but not incorporated in the embryo. It is the floury part in corn, wheat, and like grains, the oily part in poppy seeds, the fleshy part in the cocoanut, etc. 3. <chemistry> Same as Albumin. Origin: L, fr. Albus white. Source: Websters Dictionary (01 Mar 1998) |
| albumin | 1. <chemistry> Any protein that is soluble in water and moderately concentrated salt solutions and is coagulable by heat. Found in egg whites, blood, lymph, and other tissues and fluids. 2. <biochemistry> Serum albumin, the major plasma protein (approximately 60 per cent of the total), which is responsible for much of the plasma colloidal osmotic pressure and serves as a transport protein carrying large organic anions, such as fatty acids, bilirubin and many drugs and also carrying certain hormones, such as cortisol and thyroxine, when their specific binding globulins are saturated. Albumin is synthesised in the liver. Low serum levels occur in protein malnutrition, active inflammation and serious hepatic and renal disease. (31 Jan 2000) |
| albumin A | The normal or common type of human serum albumin. (05 Mar 2000) |
| albumin B | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Ghent | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Mexico | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Naskapi | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Reading | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |