腺苷

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传代谢疾病。

Expressions of S-adenosylmethionine synthetase gene, arginase gene and oxidant stress related genes in myocardial tissue of normal and diabetic rats were assayed by DNA microarray.

在正常鼠和糖尿病鼠心肌组织中,以基因芯片技术测定S腺苷蛋氨合成酶、精氨酶及氧化应激相关基因的表达。