Patients heterozygous for the Z gene (phenotype MZ) also have an increased incidence of emphysema, usually of later onset, but we have observed several cases under 40. The other manifestation of severe 伪-antitrypsin deficiency is liver disease. Three children studied had prolonged neonatal ...
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-1 antitrypsin 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...
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...
Liver disease in alpha 1-antitrypsin deficiency: a review. Am J Gastroenterol 2008;103:2136-2141.Fairbanks KD, Tavill AS (2008) Liver Disease in Alpha 1-Antitrypsin Deficiency: A Review. Am J Gastroenterol, 103: 2136-2141. Link: https://goo.gl/V2h8FA...
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...
Two 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 carry a grave prognosis. The question of increased risk to the heterozygote is ...
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-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-Liver Diseasecirrhosissialic acidcell transportalpha-1-antitrypsinantitrypsin sialyltransferasedoi:10.1111/j.1753-4887.1975.tb05102.xNoneJohn Wiley & Sons, Ltd.Nutrition Reviews