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A pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activity.

作者信息

Yoshida A, Motulsky A G

出版信息

Am J Hum Genet. 1969 Sep;21(5):486-98.

PMID:5822291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1706557/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/67223ab2d77e/ajhg00383-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/138d21e26da3/ajhg00383-0078-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/72701dab749e/ajhg00383-0080-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/bbae618ff74f/ajhg00383-0080-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/67223ab2d77e/ajhg00383-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/138d21e26da3/ajhg00383-0078-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/72701dab749e/ajhg00383-0080-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/bbae618ff74f/ajhg00383-0080-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/1706557/67223ab2d77e/ajhg00383-0082-a.jpg

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本文引用的文献

1
A 'silent' pseudo-cholinesterase gene.一个“沉默”的拟胆碱酯酶基因。
Nature. 1962 Feb 10;193:561-2. doi: 10.1038/193561a0.
2
Some statistical data on atypical cholinesterase of human serum.一些关于人血清非典型胆碱酯酶的统计数据。
Ann Hum Genet. 1959 Jul;23:239-50. doi: 10.1111/j.1469-1809.1959.tb01467.x.
3
ACUTE INTERMITTENT PORPHYRIA: THE FIRST "OVERPRODUCTION DISEASE" LOCALIZED TO A SPECIFIC ENZYME.急性间歇性卟啉症:第一种定位到特定酶的“产量过剩疾病”。
琥珀胆碱——从1906年至今一种现代药物的发展历程。
Med Hist. 1982 Apr;26(2):145-68. doi: 10.1017/s0025727300041132.
4
Immunological comparison of the usual and atypical human serum cholinesterase phenotypes.正常与非典型人类血清胆碱酯酶表型的免疫学比较。
Biochem Genet. 1983 Feb;21(1-2):93-108.
5
Human skin collagenase in recessive dystrophic epidermolysis bullosa. Purification of a mutant enzyme from fibroblast cultures.隐性营养不良性大疱性表皮松解症中的人皮肤胶原酶。从成纤维细胞培养物中纯化一种突变酶。
J Clin Invest. 1982 Jun;69(6):1373-83. doi: 10.1172/jci110577.
6
Enhanced biosynthesis of human skin collagenase in fibroblast cultures from recessive dystrophic epidermolysis bullosa.隐性营养不良性大疱性表皮松解症成纤维细胞培养物中人类皮肤胶原酶生物合成增强。
J Clin Invest. 1980 Aug;66(2):176-87. doi: 10.1172/JCI109842.
7
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Humangenetik. 1970;9(3):246-8. doi: 10.1007/BF00279235.
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Fabry's disease: the search for a regulator gene mutation in man.法布里病:人类调节基因突变的探寻
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High dihydrofolate reductase levels in Diplococcus pneumoniae after mutation in the structural gene: biochemical and immunological evidence for increased synthesis.结构基因突变后肺炎双球菌中二氢叶酸还原酶水平升高:合成增加的生化及免疫学证据
J Bacteriol. 1971 May;106(2):318-24. doi: 10.1128/jb.106.2.318-324.1971.
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Ann Hum Genet. 1963 Jun;26:359-82. doi: 10.1111/j.1469-1809.1963.tb01335.x.