Alpha-1抗胰蛋白酶缺乏症的英文名字是Alpha-1 antitrypsin deficiency。基因解码表明:Alpha-1抗胰蛋白酶缺乏症是一种遗传性疾病,与基因突变密切相关。Alpha-1抗胰蛋白酶是一种由SERPINA1基因编码的蛋白质,它在肝脏中合成并通过血液循环分布到全身。该蛋白质的主要功能是
网络抗胰蛋白酶缺乏 网络释义 1. 抗胰蛋白酶缺乏 α1-抗胰蛋白酶缺乏(alpha-l-antitrypsin deficiency)是一种伴有慢性肝脏病变的常染色体隐性遗传疾病,在儿童代谢性疾病中最为 … www.transplantation.org.cn|基于 1 个网页
Alpha-1 antitrypsin(抗胰蛋白酶)deficiency is a genetic disorder(遗传病)in which a protein called alpha-1antitrypsin is defective or absent, and it causes lung and liver disease. α抗胰蛋白酶缺乏症是一种遗传性疾病,患者体内的一种叫做α抗胰蛋白酶的蛋白质出现了问题或者含量减少了,最终导致肺和肝脏...
待解决 悬赏分:1 - 离问题结束还有 alpha-1-antitrypsin deficiency lessons from longevity问题补充:匿名 2013-05-23 12:21:38 α- 1抗胰蛋白酶缺乏症的教训,从长寿 匿名 2013-05-23 12:23:18 α1-抗胰蛋白酶缺陷从长寿教训 匿名 2013-05-23 12:24:58 α-1-抗胰蛋白酶缺乏教训从长寿 匿名 ...
Alpha 1 antitrypsin deficiencyemphysemachronic obstructive pulmonary diseaseaugmentation therapytreatmentgene therapyIntroduction: 伪-1-antitrypsin deficiency (AATD) is a rare hereditary disorder associated with early onset emphysema, chronic obstructive pulmonary disease, liver cirrhosis and panniculitis. The ...
Alpha-1 Antitrypsin Deficiency (A1AD) is a hereditary condition characterized by low levels of circulating alpha-antitrypsin (AAT) in plasma. It is the best understood genetic risk factor for the development of chronic obstructive pulmonary disease (COPD). The diagnosis of A1AD is under-recognized...
alpha-1-antitrypsin deficiency and pi typing问题补充:匿名 2013-05-23 12:21:38 α- 1 -抗胰蛋白酶缺乏症和PI打字 匿名 2013-05-23 12:23:18 α1-抗胰蛋白酶缺陷和有价证券投资打字 匿名 2013-05-23 12:24:58 α-1-抗胰蛋白酶缺乏和pi键入 匿名 2013-05-23 12:26:38 阿尔法-1-...
Feelings of isolation can be common among people diagnosed with a rare disease. But Dee Kroecker, who is living with the rare genetic condition Alpha 1 Antitrypsin Deficiency, wants newly diagnosed patients to know that they are not alone. ...
产品别名: Alpha-1-Antichymotrypsin; AACT-Alpha 1; AACT Alpha 1; SERPINA3; AACT; A1ACT; ACT; Alpha 1 Antichymotrypsin 1; Alpha 1 Antichymotrypsin 2; Alpha 1 Antichymotrypsin 3; Alpha 1 Antitrypsin Deficiency; Anti Elastase; Antichymotrypsin; Cell growth inhibiting gene 24/25 protein; Clade A ...
Alpha 1 antitrypsin deficiency (AATD)is a hereditary disorder first describedin 1963 as a genetic cause of chronicobstructive pulmonary disease (COPD).1AATD is characterized by low levels of alpha1 antitrypsin (AAT) allowing neutrophilelastase (NE) to destroy the elastin structureof the lung.2 Alt...