胰腺囊性纤维化患者汗液和血清中的α-淀粉酶活性。
ALPHA-Amylase activity in sweat and serum of patients with cystic fibrosis of the pancreas.
作者信息
Nikolaejek W P, Emrich H M
出版信息
Eur J Pediatr. 1976 Jul 12;122(4):289-91. doi: 10.1007/BF00481509.
PMID:939232
Abstract
The hypothesis by Doggett and Harrison, according to which alpha-amylase is the pathogenic factor of the exocrinopathy in cystic fibrosis (C.F.), is investigated. No elevation of alpha-amylase in sweat and serum of C.F. patients, as compared with controls of similar age, is observed. It is concluded that the "C.F. factor" cannot be identified with alpha-amylase.
摘要
对多格特和哈里森的假说进行了研究，该假说认为α-淀粉酶是囊性纤维化（C.F.）外分泌病的致病因素。与年龄相仿的对照组相比，未观察到C.F.患者汗液和血清中α-淀粉酶升高。得出的结论是，“C.F.因子”不能等同于α-淀粉酶。
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引用本文的文献
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本文引用的文献
1
Sodium transport: inhibitory factor in sweat of patients with cystic fibrosis.
Science. 1967 Oct 6;158(3797):135-6. doi: 10.1126/science.158.3797.135.
2
Studies on the mechanism of inhibition of sodium transport in cystic fibrosis of the pancreas.
Pediatr Res. 1968 Sep;2(5):378-84. doi: 10.1203/00006450-196809000-00007.
3
[Separation of different compounds in sweat, depending upon sweat flow rate].
Pflugers Arch Gesamte Physiol Menschen Tiere. 1966;290(4):298-310.
4
Cystic fibrosis: in vivo reversal of the ciliostatic character of serum and parotid secretions by heparin.
Nat New Biol. 1973 Jun 20;243(129):250-1. doi: 10.1038/newbio243250a0.
5
A sodium transport inhibitory factor in the saliva of patients with cystic fibrosis of the pancreas.
Pediatr Res. 1967 Nov;1(6):436-42. doi: 10.1203/00006450-196711000-00002.
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