Research in cystic fibrosis (second of three parts).

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作者信息

di Sant'Agnese P A, Davis P B

出版信息

N Engl J Med. 1976 Sep 2;295(10):534-41. doi: 10.1056/NEJM197609022951005.

DOI:10.1056/NEJM197609022951005

PMID:781536

Abstract

摘要

相似文献

Research in cystic fibrosis (second of three parts).

N Engl J Med. 1976 Sep 2;295(10):534-41. doi: 10.1056/NEJM197609022951005.

Recent advances in cystic fibrosis research.囊性纤维化研究的最新进展。

Birth Defects Orig Artic Ser. 1976;12(6):197-212.

Cultured cells in cystic fibrosis research: A review.囊性纤维化研究中的培养细胞：综述

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Cystic fibrosis. A dilemma in the metabolic pathogenesis of genetic disease.囊性纤维化。遗传性疾病代谢发病机制中的一个难题。

Arch Pathol Lab Med. 1976 Jan;100(1):7-11.

Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis.囊性纤维化患者汗腺中氯化物吸收减少导致生物电位升高。

N Engl J Med. 1983 May 19;308(20):1185-9. doi: 10.1056/NEJM198305193082002.

Suggestion of an abnormal anion exchange mechanism in sweat glands of cystic fibrosis patients.囊性纤维化患者汗腺中异常阴离子交换机制的推测。

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Microperfusion study of the sweat gland abnormality in cystic fibrosis.囊性纤维化汗腺异常的微灌注研究

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Human reabsorptive sweat duct in primary cell culture. Cellular mechanisms of ion transport and their regulation with special reference to cystic fibrosis.原代细胞培养中的人重吸收性汗腺导管。离子转运的细胞机制及其调节，特别提及囊性纤维化。

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Cystic fibrosis of the pancreas. A generalised disturbance of water and electrolyte movement in exocrine tissues.

Lancet. 1968 Mar 2;1(7540):455-60.

Cystic fibrosis o the pancreas. A generalised disturbance of water and electrolyte movement in exocrine tissues.胰腺囊性纤维化。外分泌组织中水电解质运动的全身性紊乱。

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引用本文的文献

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.

Mitochondrial NADH dehydrogenase in cystic fibrosis: enzyme kinetics in cultured fibroblasts.囊性纤维化中的线粒体NADH脱氢酶：培养成纤维细胞中的酶动力学

Am J Hum Genet. 1982 Nov;34(6):846-52.

Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants.对患有囊性纤维化的婴儿和对照婴儿气管黏膜下腺发育的定量评估。

Am J Pathol. 1982 Mar;106(3):303-11.

Utilization of human respiratory secretions by mucoid Pseudomonas aeruginosa of cystic fibrosis origin.源自囊性纤维化的黏液型铜绿假单胞菌对人呼吸道分泌物的利用。

Infect Immun. 1982 Aug;37(2):662-9. doi: 10.1128/iai.37.2.662-669.1982.

Cloning and expression in Pseudomonas aeruginosa of a gene involved in the production of alginate.铜绿假单胞菌中一个参与藻酸盐产生的基因的克隆与表达

J Bacteriol. 1984 Jun;158(3):1115-21. doi: 10.1128/jb.158.3.1115-1121.1984.

Cystic fibrosis.囊性纤维化

Postgrad Med J. 1984 Mar;60(701):225-33. doi: 10.1136/pgmj.60.701.225.

Diseases of the respiratory system: Bronchiectasis and cystic fibrosis.呼吸系统疾病：支气管扩张症和囊性纤维化。

Br Med J. 1978 Apr 15;1(6118):971-3. doi: 10.1136/bmj.1.6118.971.

Serotypes and antibiotic susceptibilities of Pseudomonas aeruginosa isolates from single sputa of cystic fibrosis patients.来自囊性纤维化患者单次痰液的铜绿假单胞菌分离株的血清型及抗生素敏感性

J Clin Microbiol. 1979 Jan;9(1):72-8. doi: 10.1128/jcm.9.1.72-78.1979.

R-factor inheritance and plasmid content in mucoid Pseudomonas aeruginosa.

Infect Immun. 1978 Nov;22(2):530-9. doi: 10.1128/iai.22.2.530-539.1978.

Mitrochondrial NADH dehydrogenase in cystic fibrosis.囊性纤维化中的线粒体NADH脱氢酶

Proc Natl Acad Sci U S A. 1979 Jun;76(6):2979-83. doi: 10.1073/pnas.76.6.2979.

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