[人类磷酸葡萄糖变位酶同工酶系统中的一种“新”表型] - Suppr

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超能文献

[A "new" phenotype in the isoenzyme system of the human phosphoglucomutases].

作者信息

Fiedler H, Pettenkofer H

出版信息

Blut. 1969 Mar;18(6):358-62. doi: 10.1007/BF01632122.

DOI:10.1007/BF01632122

PMID:5778712

Abstract

摘要

相似文献

[A "new" phenotype in the isoenzyme system of the human phosphoglucomutases].[人类磷酸葡萄糖变位酶同工酶系统中的一种“新”表型]

Blut. 1969 Mar;18(6):358-62. doi: 10.1007/BF01632122.

Red cell PGM1 (phosphoglucomutase) phenotyping by isoelectric focussing and starch gel electrophoresis in cases of disputed paternity in the United Kingdom. An evaluation of the results obtained in 95 cases.英国亲子鉴定案例中通过等电聚焦和淀粉凝胶电泳对红细胞磷酸葡萄糖变位酶1（PGM1）进行表型分析。对95个案例所获结果的评估。

Forensic Sci Int. 1979 Mar-Apr;13(2):87-92. doi: 10.1016/0379-0738(79)90268-8.

[On the value of phosphoglucomutase in paternity cases].

Beitr Gerichtl Med. 1969;25:216-21.

Isoenzymes of phosphoglucomutase from human red blood cells: isolation and kinetic properties.人红细胞磷酸葡萄糖变位酶的同工酶：分离与动力学性质

Prep Biochem. 1989;19(3):251-71. doi: 10.1080/10826068908544915.

[Further supplements to the Essen-Moller lg Y-X tables for the computation of probability of paternity from serological findings].

Z Immunitatsforsch Allerg Klin Immunol. 1969 Apr;137(4):320-32.

Genetics of the phosphoglucomutase (PGM) system of human red cells. Family-, mother-child- and association-studies.

Hum Hered. 1969;19(4):365-74. doi: 10.1159/000152240.

[Silent allele of the PGM1 system of erythrocytic phosphoglucomutase].

Soud Lek. 1981;26(4 Suppl):60-3.

[A "new" phenotype in the isoenzymesystem of human phosphoglucomutases (PGM10)].

Blut. 1968;18(1):33-4. doi: 10.1007/BF01632787.

Erythrocyte and leukocyte phosphoglucomutase in Chinese.中国人的红细胞和白细胞磷酸葡萄糖变位酶

Am J Hum Genet. 1968 Mar;20(2):101-6.

[Isoenzym polymorphism].[同工酶多态性]

Bibl Haematol. 1969;32:56-63.

引用本文的文献

Human neutral alpha-glucosidase C: genetic polymorphism including a "null" allele.人中性α-葡萄糖苷酶C：包括“无效”等位基因在内的基因多态性。

Am J Hum Genet. 1980 Jul;32(4):497-507.

Red cell phosphoglucomutase (PGM)-deficiency: hereditary defect of the PGM1-locus.红细胞磷酸葡萄糖变位酶（PGM）缺乏症：PGM1基因座的遗传性缺陷。

Eur J Pediatr. 1981 Mar;136(1):63-5. doi: 10.1007/BF00441713.

Erythrocyte phosphoglucomutase: a family study of a PGM1 deficient allele.

Hum Genet. 1984;67(3):306-8. doi: 10.1007/BF00291358.

[Forensic importance of spectrophotometric tests of the isoenzyme systems red cell acid phosphatase and glutamatic-pyruvic transaminase in settlement of paternity disputes (author's transl)].

Z Rechtsmed. 1974 Jun 18;74(3):177-80. doi: 10.1007/BF00200586.

Is the PGM1 locus subject to selection?磷酸葡萄糖变位酶-1（PGM1）基因座是否受到选择作用？

Humangenetik. 1973 Sep 20;19(3):247-52. doi: 10.1007/BF00278397.

Demonstration of the silent allele PGM01 in three families and description of a new variant.

Z Rechtsmed. 1973 Nov 23;73(3):207-17. doi: 10.1007/BF02116824.

[Enzyme activity of PGM1 in erythrocytes].[红细胞中PGM1的酶活性]

Z Rechtsmed. 1990;103(8):609-12. doi: 10.1007/BF01261426.

本文引用的文献

PHOSPHOGLUCOMUTASE POLYMORPHISM IN MAN.人类中的磷酸葡萄糖变位酶多态性

Nature. 1964 Nov 21;204:742-5. doi: 10.1038/204742a0.

The enzymatic reaction between ribose 1-phosphate and glucose 1, 6-diphosphate.磷酸核糖1与磷酸葡萄糖1,6二磷酸之间的酶促反应。

Arch Biochem Biophys. 1955 Oct;58(2):276-87. doi: 10.1016/0003-9861(55)90129-6.

[A "new" phenotype in the isoenzymesystem of human phosphoglucomutases (PGM10)].

Blut. 1968;18(1):33-4. doi: 10.1007/BF01632787.

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