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囊性纤维化患者血浆中激肽释放酶活性缺乏。

Deficiency of kallikrein activity in plasma of patients with cystic fibrosis.

作者信息

Rao G J, Posner L A, Nadler H L

出版信息

Science. 1972 Aug 18;177(4049):610-1. doi: 10.1126/science.177.4049.610.

Abstract

Total kallikrein activity and kallikrein activity inhibited by soybean trypsin inhibitor are significantly reduced in the plasma of patients with cystic fibrosis compared to age-matched controls. The level of the STI inhibited kallikrein activity in the plasma of heterozygotes was significantly different from that in either controls or affected children. However, the individual heterozygote could not be reliably identified in each case.

摘要

与年龄匹配的对照组相比,囊性纤维化患者血浆中的总激肽释放酶活性以及被大豆胰蛋白酶抑制剂抑制的激肽释放酶活性显著降低。杂合子血浆中被STI抑制的激肽释放酶活性水平与对照组或患病儿童的水平均有显著差异。然而,无法在每个病例中可靠地识别个体杂合子。

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