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
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 Deficiency Family Study Α1-抗胰蛋白酶缺乏症慢性阻塞性肺疾病慢性阻塞性肺病遗传性疾病家系世界卫生组织COPD摘要:生命科学:英文版OsorioRaquelFemandesHelenaCafofoTomasiaClementeHelenaFialhoLicinio
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 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...
Tips for Those Newly Diagnosed with Alpha 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 ...
待解决 悬赏分:1 - 离问题结束还有 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 ...
ALPHA 1 ANTITRYPSIN DEFICIENCY IN THE PATHOGENESIS (OF BRONCHOPULMONARY DYSPLASIABronchopulmonary Dysplasia (BPD) is a major cause of neonatal respiratory morbidity and mortality. The pathophysiology of BPD may be related to an absence of the antiprotease alpha 1 anti-trypsin (αLat) in pulmonary ...