通过易位检测21三体综合征中的铜/锌超氧化物歧化酶活性。 - Suppr

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Copper/zinc superoxide dismutase activity in trisomy 21 by translocation.

作者信息

Garber P, Sinet P M, Jerome H, Lejeune J

出版信息

Lancet. 1979 Oct 27;2(8148):914-5. doi: 10.1016/s0140-6736(79)92745-4.

DOI:10.1016/s0140-6736(79)92745-4

PMID:91020

Abstract

摘要

相似文献

Copper/zinc superoxide dismutase activity in trisomy 21 by translocation.通过易位检测21三体综合征中的铜/锌超氧化物歧化酶活性。

Lancet. 1979 Oct 27;2(8148):914-5. doi: 10.1016/s0140-6736(79)92745-4.

Copper/zinc superoxide dismutase (SOD-1) activity in regular trisomy 21, trisomy 21 by translocation and mosaic trisomy 21.

Clin Genet. 1982 Oct;22(4):160-4. doi: 10.1111/j.1399-0004.1982.tb01429.x.

Dismutase activity in translocation trisomy.易位三体中的歧化酶活性。

Lancet. 1979 Jan;1(8107):105. doi: 10.1016/s0140-6736(79)90095-3.

The level of superoxide dismutase in erythrocytes of children with Down syndrome (trisomy G and unbalanced translocation G 21/22).唐氏综合征患儿（G组三体及G 21/22不平衡易位）红细胞中超氧化物歧化酶的水平。

Acta Biol Med Ger. 1977;36(5-6):779-82.

Immunoreactive copper-zinc superoxide-dismutase (SOD-1) in mosaic trisomy 21 and normal subjects.

Acta Paediatr Scand. 1984 May;73(3):341-4. doi: 10.1111/j.1651-2227.1994.tb17745.x.

Selenium, zinc and copper in Down's syndrome (trisomy 21): blood levels and relations with glutathione peroxidase and superoxide dismutase.

Clin Chim Acta. 1983 Sep 30;133(2):209-14. doi: 10.1016/0009-8981(83)90406-0.

Atypical Down syndrome and partial trisomy 21.非典型唐氏综合征与21号染色体部分三体性

Clin Genet. 1983 Aug;24(2):97-102. doi: 10.1111/j.1399-0004.1983.tb02219.x.

Lack of position effect on the activity of SODCu/Zn gene in subjects with 21/D and 21/G Robertsonian translocations.21/D和21/G罗伯逊易位患者中SODCu/Zn基因活性缺乏位置效应。

Hum Genet. 1981;57(2):203-4. doi: 10.1007/BF00282023.

Letter: Superoxide dismutase in Down syndrome.信件：唐氏综合征中的超氧化物歧化酶

Lancet. 1975 Jul 5;2(7923):42-3. doi: 10.1016/s0140-6736(75)92996-7.

Regular trisomy 21 not accompanied by increased copper-zinc superoxide dismutase (SOD1) activity.

Clin Genet. 1988 Jan;33(1):11-9. doi: 10.1111/j.1399-0004.1988.tb04259.x.

引用本文的文献

Normal superoxide dismutase-1 (SOD-1) activity with deletion of chromosome band 21q21 supports localization of SOD-1 locus to 21q22.正常超氧化物歧化酶1（SOD-1）活性伴21号染色体21q21带缺失支持SOD-1基因座定位于21q22。

Hum Genet. 1983;64(3):271-2. doi: 10.1007/BF00279408.

A case of 21q-syndrome with half normal SOD-1 activity.一例超氧化物歧化酶-1（SOD-1）活性半正常的21号染色体长臂缺失综合征病例。

Hum Genet. 1983;64(2):200-2. doi: 10.1007/BF00327128.

Lack of position effect on the activity of SODCu/Zn gene in subjects with 21/D and 21/G Robertsonian translocations.21/D和21/G罗伯逊易位患者中SODCu/Zn基因活性缺乏位置效应。

Hum Genet. 1981;57(2):203-4. doi: 10.1007/BF00282023.

The levels of superoxide dismutase, catalase, and carbonic anhydrase in erythrocytes of patients with Down's syndrome.唐氏综合征患者红细胞中超氧化物歧化酶、过氧化氢酶和碳酸酐酶的水平。

Klin Wochenschr. 1984 Mar 15;62(6):287-8. doi: 10.1007/BF01721891.

Human Cu/Zn superoxide dismutase gene family: molecular structure and characterization of four Cu/Zn superoxide dismutase-related pseudogenes.人类铜/锌超氧化物歧化酶基因家族：四个与铜/锌超氧化物歧化酶相关的假基因的分子结构与特征

Proc Natl Acad Sci U S A. 1986 Jun;83(11):3619-23. doi: 10.1073/pnas.83.11.3619.

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