Systemic membrane defect and the inhibition of lymphocyte capping in Duchenne Muscular Dystrophy
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference36 articles.
1. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker;Lancet,1985
2. Biochemistry of muscle membranes in Duchenne muscular dystrophy;Rowland;Muscle Nerve,1980
3. Systemic membrane defect in the proximal muscular dystrophies;Pickard;N Engl J Med,1978
4. The contribution of assays for lymphocyte capping and Creatine Kinase to detection of the Becker-type dystrophy trait;Goldsmith;Clin Chem,1980
5. Blind evaluation of lymphocyte capping in Duchenne muscular dystrophy;Goldsmith;Neurology,1984
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Altered expression, intracellular distribution and activity of lymphocyte calpain II in Duchenne muscular dystrophy;Clinica Chimica Acta;2006-11
2. Age-related studies of SIg, Leu-4 and concanavalin a receptor densities and capping in human lymphocytes;Mechanisms of Ageing and Development;1991-06
3. Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect;Human Genetics;1989-10
4. Oxidative stress and muscular dystrophy;Chemico-Biological Interactions;1989
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