信函：新生儿黄疸与红细胞酸性磷酸酶表型 - Suppr

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Letter: Neonatal jaundice and erythrocyte-acid-phosphatase phenotype.

作者信息

Bottini E, Scacchi R, Gloria-Bottini F, Mortera J, Palmarino R, Carapella-De-Luca E, Lapi A S, Nodari C

出版信息

Lancet. 1976 Apr 24;1(7965):918. doi: 10.1016/s0140-6736(76)92148-6.

DOI:10.1016/s0140-6736(76)92148-6

PMID:58192

Abstract

摘要

相似文献

Letter: Neonatal jaundice and erythrocyte-acid-phosphatase phenotype.信函：新生儿黄疸与红细胞酸性磷酸酶表型

Lancet. 1976 Apr 24;1(7965):918. doi: 10.1016/s0140-6736(76)92148-6.

Is there a role of erythrocyte acid phosphatase polymorphism in intrauterine development?红细胞酸性磷酸酶多态性在子宫内发育中起作用吗？

Am J Hum Genet. 1980 Sep;32(5):764-7.

Interaction at clinical level between erythrocyte acid phosphatase and adenosine deaminase genetic polymorphisms.红细胞酸性磷酸酶与腺苷脱氨酶基因多态性在临床水平上的相互作用。

Hum Genet. 1989 Jun;82(3):213-5. doi: 10.1007/BF00291156.

Erythrocyte acid phosphatase polymorphism and haemolysis.红细胞酸性磷酸酶多态性与溶血

J Med Genet. 1972 Dec;9(4):434-5. doi: 10.1136/jmg.9.4.434.

The genetic component of quantitative perinatal variables. An analysis of relations between erythrocyte acid phosphatase phenotype and birth weight, gestational age and serum bilirubin level in the first days of life.

J Perinat Med. 1980;8(1):42-7.

[Erythrocyte enzyme activity in newborn infants with hyperbilirubinemia].[高胆红素血症新生儿的红细胞酶活性]

Akush Ginekol (Sofiia). 1981;20(5):361-5.

[Influence of exchange transfusion on the type of erythrocyte acid phosphatase].[换血疗法对红细胞酸性磷酸酶类型的影响]

Kinderarztl Prax. 1972 Nov;40(11):514-22.

Neonatal hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency.新生儿高胆红素血症与葡萄糖-6-磷酸脱氢酶缺乏症

Isr J Med Sci. 1973 Nov-Dec;9(11):1547-52.

[Hereditary erythrocyte enzymopathies in newborn infants with hyperbilirubinemia].[高胆红素血症新生儿中的遗传性红细胞酶病]

Bol Med Hosp Infant Mex. 1985 Aug;42(8):466-9.

Transitory hyperbilirubinaemia: no relationship of red cell metabolism to serum bilirubin?短暂性高胆红素血症：红细胞代谢与血清胆红素无关？

Acta Paediatr Scand. 1976 Jan;65(1):125-6. doi: 10.1111/j.1651-2227.1976.tb04419.x.

引用本文的文献

ACP1 and human adaptability. 1. Association with common diseases: a case-control study.酸性磷酸酶1与人类适应性。1. 与常见疾病的关联：一项病例对照研究。

Hum Genet. 1995 Dec;96(6):629-37. doi: 10.1007/BF00210290.

Haptoglobin development in newborn infants from diabetic mothers.

Experientia. 1994 Jul 15;50(7):687-90. doi: 10.1007/BF01952875.

Characterization of ACP1TIC-1, an electrophoretic variant of erythrocyte acid phosphatase restricted to the Ticuna Indians of central Amazonas.红细胞酸性磷酸酶电泳变异体ACP1TIC - 1的特征分析，该变异体仅限于亚马逊中部的提库纳印第安人。

Am J Hum Genet. 1980 Nov;32(6):898-907.

Is there a role of erythrocyte acid phosphatase polymorphism in intrauterine development?红细胞酸性磷酸酶多态性在子宫内发育中起作用吗？

Am J Hum Genet. 1980 Sep;32(5):764-7.

ACP1GUA-1--a low-activity variant of human erythrocyte acid phosphatase: association with increased glutathione reductase activity.ACP1GUA - 1——人类红细胞酸性磷酸酶的一种低活性变体：与谷胱甘肽还原酶活性增加相关

Am J Hum Genet. 1982 May;34(3):425-33.

Studies of the purine analog associated modulation of human erythrocyte acid phosphatase activity.嘌呤类似物对人红细胞酸性磷酸酶活性的相关调节研究。

Mol Cell Biochem. 1985 Mar;66(2):127-36. doi: 10.1007/BF00220780.

Hum Genet. 1989 Jun;82(3):213-5. doi: 10.1007/BF00291156.

Role of genetic variability in neonatal jaundice. A prospective study on full-term, blood group-compatible infants.基因变异性在新生儿黄疸中的作用。一项针对足月、血型匹配婴儿的前瞻性研究。

Experientia. 1991 Dec 1;47(11-12):1218-21. doi: 10.1007/BF01918389.

Phenotype dependence in the inhibition of red cell acid phosphatase (ACP) by folates.叶酸对红细胞酸性磷酸酶（ACP）抑制作用中的表型依赖性。

Am J Hum Genet. 1978 Sep;30(5):553-60.

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