Cystic fibrosis protein, a confirmed diagnostic marker for detecting heterozygote carriers: significance in relation to future screening and to a proposed primary defect in alpha 2-macroglobulin. - Suppr | 超能文献

Cystic fibrosis protein, a confirmed diagnostic marker for detecting heterozygote carriers: significance in relation to future screening and to a proposed primary defect in alpha 2-macroglobulin.

作者信息

Wilson G B

出版信息

Pediatr Res. 1979 Sep;13(9):1079-81. doi: 10.1203/00006450-197909000-00028.

DOI:10.1203/00006450-197909000-00028

PMID:92006

Abstract

摘要

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Cystic fibrosis protein, a confirmed diagnostic marker for detecting heterozygote carriers: significance in relation to future screening and to a proposed primary defect in alpha 2-macroglobulin.

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Cystic fibrosis alpha 2-macroglobulin protease interaction in vitro.囊性纤维化α2-巨球蛋白蛋白酶的体外相互作用

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Normal subunit cleavage of alpha-2-macroglobulin in cystic fibrosis.囊性纤维化中α-2-巨球蛋白的正常亚基裂解

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Identification of cystic fibrosis homozygotes and heterozygotes by isoelectric focusing of serum proteins.

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Decreased sialic acid and altered binding to lectins of purified alpha 2-macroglobulin from patients with cystic fibrosis.囊性纤维化患者纯化的α2-巨球蛋白的唾液酸减少以及与凝集素的结合改变。

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Synthesis and secretion of cystic fibrosis ciliary dyskinesia substances by purified subpopulations of leukocytes.白细胞纯化亚群对囊性纤维化纤毛运动障碍物质的合成与分泌。

J Clin Invest. 1980 Nov;66(5):1010-9. doi: 10.1172/JCI109929.

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Cystic fibrosis ciliary dyskinesia substances and pulmonary disease. Effects of ciliary dyskinesia substances on neutrophil movement in vitro.囊性纤维化纤毛运动障碍物质与肺部疾病。纤毛运动障碍物质对体外中性粒细胞运动的影响。

J Clin Invest. 1981 Jul;68(1):171-83. doi: 10.1172/jci110233.

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Controlled trial of serum isoelectric focusing in the detection of the cystic fibrosis gene.

Hum Genet. 1982;60(1):30-1. doi: 10.1007/BF00281259.