Acid starch gel electrophoresis and two dimensional immuno-electrophoresis have been used to recognize genetic variants of human 伪1-antitrypsin; 9 phenotypes have so far been found. They are inherited by a series of autosomal codominant alleles. One in 750 New Zealanders has a severe serum ...
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
【Osmosis】α-1抗胰蛋白酶缺乏症 Alpha-1 Antitrypsin Deficiency(中英字幕) 996 1 1:09 App 丝裂原活化蛋白激酶-MAPK(mitogen-activated protein kinase)-动画 16 -- 2:05 App 脂肪酸氧化缺乏 Fatty acid oxidation deficiency_PTH 8082 3 2:16 App 胰腺之歌(英文字幕) 757 -- 17:48 App (搬运油管...
So alpha-1 antitrypsin deficiency can lead to both emphysema and chronic bronchitis, the two types of chronic obstructive pulmonary disease, or COPD. 老慢支肺气肿,是否似成相识?不就是COPD嘛 Another, more common cause of COPD is smoking, and if someone with alpha-1 antitrypsin deficiency also s...
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...
alpha 1-Antitrypsin Deficiency α1抗胰蛋白酶缺乏症文献(pubmed) 以下为句子列表:英文: Purification and biological activity of recombinant thymosin alpha1中文: 重组胸腺素α1的分离纯化和活性测定 英文: The optimization of the recombinant thymosin alpha1’s fermentation conditions中文: 重组胸腺素α1在...
genetic model of alpha-1-antitrypsin deficiency. chinese.eurekalert.org 圣路易大学儿童医学系塔克曼博士(Jeffrey Teckma)所领导的研究团队,证实了甲一型胰蛋白酵素抑 制剂 缺陷 动 物模 式中有氧化压力的产生。 chinese.eurekalert.org [...] and registered as having originated from the Liberian Camp ...
Alpha-1-antitrypsinProteaseAntiproteaseLiver diseaseChronic obstructive pulmonary disease (COPDTwo disparate disease states—an adult form of emphysema and a childhood form of liver cirrhosis—have been linked to an inherited absence of this antienzyme. In their severe, homozygous forms, both conditions...
Alpha-1-antitrypsin deficiency (AATD) is a rare genetic disorder associated with the development of liver and lung disease. AAT is a 52-kD glycoprotein, produced mainly by hepatocytes and secreted into the blood. Agglomeration of the AAT-protein in hepatocytes can result in liver disease. Exposur...
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...