|
Civilization
|
I01.076.201.450.226 |
|
|
Hand-Assisted Laparoscopy
|
E01.370.388.250.520.500 |
|
|
Laparoscopy
|
E01.370.388.250.520 |
|
|
Glucosidases
|
D005959 |
[Enzymes that hydrolyze O-glucosyl-compounds. (Enzyme Nomenclature, 1992) EC 3.2.1.-.
] |
|
Dibucaine
|
D02.065.355 |
|
|
Glucosephosphate Dehydrogenase Deficiency
|
D005955 |
[A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.
] |
|
Glucose-6-Phosphate Isomerase
|
D005956 |
[A secreted form of glucose-6-phosphate isomerase.
, An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose 6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the enzyme is found in the cytoplasm and as a secreted protein. This secreted form of glucose-6-phosphate isomerase has been referred to as autocrine motility factor or neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR. Deficiency of the enzyme in humans is an autosomal recessive trait, which results in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.
] |
|
UTP-Glucose-1-Phosphate Uridylyltransferase
|
D005957 |
[An enzyme that catalyzes the formation of UDPglucose from UTP plus glucose 1-phosphate. EC 2.7.7.9.
] |
|
Iridoid Glycosides
|
D02.455.426.392.368.450.675.500.500 |
|
|
Glucosephosphates
|
D005958 |
|
|
Glucose Tolerance Test
|
D005951 |
[A test to determine the ability of an individual to maintain HOMEOSTASIS of BLOOD GLUCOSE. It includes measuring blood glucose levels in a fasting state, and at prescribed intervals before and after oral glucose intake (75 or 100 g) or intravenous infusion (0.5 g/kg).
] |
|
Glucose-6-Phosphatase
|
D005952 |
[An enzyme that catalyzes the conversion of D-glucose 6-phosphate and water to D-glucose and orthophosphate. EC 3.1.3.9.
] |
|
HIV Envelope Protein gp120
|
D12.776.964.775.325.164.249 |
|
|
Glycogen Storage Disease Type I
|
D005953 |
[An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
] |
|
Glucosephosphate Dehydrogenase
|
D005954 |
|
|
Cecum
|
A03.556.249.249.209 |
|
|
Glucose Solution, Hypertonic
|
D005950 |
[Solution that is usually 10 percent glucose but may be higher. An isotonic solution of glucose is 5 percent.
] |
|
Propionibacterium freudenreichii
|
B03.510.024.990.600.800 |
|
|
Trifolium
|
D029921 |
[A plant genus of the family FABACEAE.
] |
|
Erythema Nodosum
|
C20.543.206.380.375 |
|
