Red cell enzymes in trisomy 21.
作者信息
Pantelakis S N, Karaklis A G, Alexiou D, Vardas E, Valaes T
出版信息
Am J Hum Genet. 1970 Mar;22(2):184-93.
Abstract
摘要
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Red cell enzymes in trisomy 21.21三体综合征中的红细胞酶
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[Investigations of erythrocyte metabolism in trisomy 21 (author's transl)].
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Erythrocyte enzymes and glycolytic intermediates of high- and low-glutathione sheep.高谷胱甘肽和低谷胱甘肽绵羊的红细胞酶及糖酵解中间产物
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[Enzyme determination of erythrocytes of children with Down syndrome].[唐氏综合征患儿红细胞的酶测定]
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Quantitative measurement of enzymes.酶的定量测定
Ann Clin Lab Sci (1971). 1972 Jan-Feb;2(1):57-62.
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[Fanconi's anemia. Transformation into leukemia and erythrocyte metabolism findings].[范科尼贫血。向白血病的转化及红细胞代谢研究结果]
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引用本文的文献
1
Down syndrome is an oxidative phosphorylation disorder.唐氏综合征是一种氧化磷酸化障碍疾病。
Redox Biol. 2021 May;41:101871. doi: 10.1016/j.redox.2021.101871. Epub 2021 Jan 22.
2
Assignment of the human gene for liver-type 6-phosphofructokinase isozyme (PFKL) to chromosome 21 by using somatic cell hybrids and monoclonal anti-L antibody.利用体细胞杂种和抗L单克隆抗体将人类肝型6-磷酸果糖激酶同工酶（PFKL）基因定位于21号染色体。
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3738-42. doi: 10.1073/pnas.78.6.3738.
3
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.
4
Phosphofructokinase and chromosome 21.磷酸果糖激酶与21号染色体
Am J Hum Genet. 1972 Sep;24(5):533-43.
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Overproduction of human Cu/Zn-superoxide dismutase in transfected cells: extenuation of paraquat-mediated cytotoxicity and enhancement of lipid peroxidation.转染细胞中人类铜锌超氧化物歧化酶的过量表达：百草枯介导的细胞毒性减轻及脂质过氧化增强。
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Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody.利用体细胞杂种和抗L单克隆抗体将人肝型6-磷酸果糖激酶定位于染色体21q22.3
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Evidence for the lack of feedback regulation of gene activity and for the absence of subunit exchange between lactate dehydrogenase tetramers in vivo.体内基因活性缺乏反馈调节以及乳酸脱氢酶四聚体之间不存在亚基交换的证据。
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8
Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.基因剂量：红细胞酸性磷酸酶基因座定位于2号染色体的证据。
Proc Natl Acad Sci U S A. 1975 Nov;72(11):4526-30. doi: 10.1073/pnas.72.11.4526.
本文引用的文献
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EFFECT OF AGE ON THE ENZYME ACTIVITY IN ERYTHROCYTES.年龄对红细胞中酶活性的影响。
Proc Natl Acad Sci U S A. 1958 Jun;44(6):529-36. doi: 10.1073/pnas.44.6.529.
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A comparative study of hexokinase from yeast and animal tissues.酵母和动物组织中己糖激酶的比较研究。
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Types of thalassaemia-trait carriers as revealed by a study of their incidence in Greece.通过对希腊地中海贫血特征携带者发病率的研究揭示的携带者类型。
Br J Haematol. 1962 Jan;8:5-14. doi: 10.1111/j.1365-2141.1962.tb06489.x.
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LEUCOCYTE ALKALINE PHOSPHATASE IN KLINEFELTER'S SYNDROME.克兰费尔特综合征中的白细胞碱性磷酸酶
J Med Genet. 1965 Jun;2(2):112-5. doi: 10.1136/jmg.2.2.112.
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ACID-PHOSPHATASE ACTIVITY IN PARTIAL TRANSLOCATION-TRISOMY.
Lancet. 1965 Apr 3;1(7388):768. doi: 10.1016/s0140-6736(65)92134-3.
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ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
Lancet. 1965 Mar 6;1(7384):553. doi: 10.1016/s0140-6736(65)92057-x.
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PHOSPHOHEXOKINASE ACTIVITY OF ERYTHROCYTES IN MONGOLISM: ANOTHER POSSIBLE MARKER FOR CHROMOSOME 21.
Lancet. 1965 Feb 20;1(7382):412-4. doi: 10.1016/s0140-6736(65)90007-3.
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GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE ASSAY BY USE OF RADIOACTIVE GALACTOSE-1-PHOSPHATE.利用放射性半乳糖-1-磷酸进行半乳糖-1-磷酸尿苷转移酶测定
Clin Chim Acta. 1964 Oct;10:337-43. doi: 10.1016/0009-8981(64)90064-6.
10
CHROMOSOME-21 AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.21号染色体与阵发性夜间血红蛋白尿症
Blood. 1964 Aug;24:160-3.
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