Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症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疾病。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症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
定S腺苷蛋氨酸合成酶、精氨酸酶及氧化应激相关基因的表达。
声明:以上例句、词分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不
表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
二酸血症是由于
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性代谢疾病。
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,
因芯片技术测定S腺苷蛋氨酸合成酶、精氨酸酶及氧化应激相关
因的表达。
:
上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙酸血症是由于甲基丙
酶A变位酶或其
酶腺苷钴胺素缺陷所致
一种遗传性代谢疾病。
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腺苷蛋氨酸合成酶、精氨酸酶及氧化应激相关基因
。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其内容亦不代
本软件
观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰A变位
或
腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
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腺苷蛋氨酸合成
、精氨酸
及
激相关基因的表达。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
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。
声明:以上例句、词类均由互联网资源自动生成,部
未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二血症是由于甲基丙二酰辅
A变位
或其辅
腺
素缺陷所致的一种遗传性代谢疾病。
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
蛋
合成
、精
及氧化应激相关基因的表达。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰酶A变位酶
酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
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腺苷蛋氨酸合成酶、精氨酸酶及氧
相关基因的表达。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲酸血症是由于甲
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性代谢疾病。
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
因芯片技术测定S腺苷蛋氨酸合成酶、精氨酸酶及氧化应激相关
因的表
。
:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表
内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症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性代谢。
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.
正常
鼠和糖尿
鼠心肌组织中,以基
技术测定S腺苷蛋氨酸合成酶、精氨酸酶及氧化应激相关基
的表达。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。