Lymphocyte capping and carrier detection in Duchenne muscular dystrophy.
出版信息
Br Med J. 1978 Dec 9;2(6152):1589-90. doi: 10.1136/bmj.2.6152.1589.
Abstract
摘要
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Lymphocyte capping and carrier detection in Duchenne muscular dystrophy.杜氏肌营养不良症中的淋巴细胞帽化和载体检测
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An evaluation of lymphocyte capping in Duchenne muscular dystrophy.杜兴氏肌营养不良症中淋巴细胞帽化的评估。
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Human lymphocyte capping and the effect of lanthanum in Duchenne muscular dystrophy.人类淋巴细胞帽化及镧对杜氏肌营养不良症的影响。
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本文引用的文献
1
Mutation rate in Duchenne type of muscular dystrophy.杜兴氏型肌营养不良症的突变率
J Med Genet. 1970 Dec;7(4):334-7. doi: 10.1136/jmg.7.4.334.
2
Erythrocyte deformation in human muscular dystrophy.
Science. 1974 Apr 12;184(4133):165-6. doi: 10.1126/science.184.4133.165.
3
A new approach for carrier detection in Duchenne muscular dystrophy. Protein synthesis of muscle polyribosomes in vitro.
Neurology. 1971 Jul;21(7):703-9. doi: 10.1212/wnl.21.7.703.
4
Ouabain and erythrocyte-ghost adenosine triphosphatase. Effects in human muscular dystrophies.哇巴因与红细胞血影三磷酸腺苷酶。对人类肌肉营养不良症的影响。
Arch Neurol. 1971 Feb;24(2):187-90. doi: 10.1001/archneur.1971.00480320115012.
5
Duchenne dystrophy: electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber.杜兴氏肌营养不良症：电子显微镜检查结果表明肌纤维质膜存在基本或早期异常。
Neurology. 1975 Dec;25(12):1111-20. doi: 10.1212/wnl.25.12.1111.
6
Abnormalities of cell-membrane fluidity in the pathogenesis of disease.细胞膜流动性异常在疾病发病机制中的作用
N Engl J Med. 1977 Aug 18;297(7):371-7. doi: 10.1056/NEJM197708182970707.
7
Systemic membrane defect in the proximal muscular dystrophies.近端型肌营养不良症中的系统性膜缺陷。
N Engl J Med. 1978 Oct 19;299(16):841-6. doi: 10.1056/NEJM197810192991601.
8
Stages in fibre breakdown in Duchenne muscular dystrophy. An electron-microscopic study.杜兴氏肌营养不良症中纤维分解的阶段。一项电子显微镜研究。
J Neurol Sci. 1975 Feb;24(2):179-200. doi: 10.1016/0022-510x(75)90232-4.
9
Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetus.杜氏肌营养不良症的产前诊断：挽救正常男性胎儿。
Lancet. 1978 Jan 14;1(8055):90. doi: 10.1016/s0140-6736(78)90021-1.
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