| alanine–glyoxylate transaminase |
[EC 2.6.1.44] an enzyme of the transferase class that catalyzes the transamination of glyoxylate to form glycine, using alanine as an amino group donor. Deficiency of the hepatic peroxisomal enzyme, an autosomal recessive trait, causes primary hyperoxaluria, type I.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| Alanson's a. |
circular amputation in which the stump is shaped like a hollow cone.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| Alanson's amputation |
see under amputation.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| alantin |
inulin.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| alanyl |
the acyl radical of alanine.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|