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腺苷脱氨酶在腺苷脱氨酶严重联合免疫缺陷病(ADA - SCID)中的表达基本缺陷。II. 在人 - 中国仓鼠细胞杂合子中检测到ADA - CRM的缺乏。

Basic defect in the expression of adenosine deaminase in ADA-SCID disease. II. Deficiency of ADA-CRM detected in heterozygote human-Chinese hamster cell hybrids.

作者信息

Herbschleb-Voogt E, Scholten J W, Meera Khan P

出版信息

Hum Genet. 1983;63(2):121-5. doi: 10.1007/BF00291530.

DOI:10.1007/BF00291530
PMID:6840756
Abstract

A specific competitive radioimmunoassay (RIA) was employed to quantify human adenosine deaminase molecules produced in human-Chinese hamster somatic cell hybrids. Studies on a set of hybrids in which the normal and aberrant expressions of adenosine deaminase (assigned earlier to human chromosome 20) were segregating, have demonstrated that in the patient with ADA-SCID disease reported by Herbschleb-Voogt et al. (1981 a), the deficiency of ADA activity was associated with a comparable deficiency of adenosine deaminase specific immuno-crossreacting material (ADA-CRM).

摘要

采用一种特定的竞争性放射免疫测定法(RIA)来定量检测人 - 中国仓鼠体细胞杂种中产生的人腺苷脱氨酶分子。对一组杂种进行的研究表明,在Herbschleb - Voogt等人(1981年a)报道的患有ADA - SCID疾病的患者中,腺苷脱氨酶(先前定位于人类20号染色体)正常和异常表达正在分离,ADA活性的缺乏与腺苷脱氨酶特异性免疫交叉反应物质(ADA - CRM)的相应缺乏有关。

相似文献

1
Basic defect in the expression of adenosine deaminase in ADA-SCID disease. II. Deficiency of ADA-CRM detected in heterozygote human-Chinese hamster cell hybrids.腺苷脱氨酶在腺苷脱氨酶严重联合免疫缺陷病(ADA - SCID)中的表达基本缺陷。II. 在人 - 中国仓鼠细胞杂合子中检测到ADA - CRM的缺乏。
Hum Genet. 1983;63(2):121-5. doi: 10.1007/BF00291530.
2
Basic defect in the expression of adenosine deaminase in ADA- SCID disease investigated through the cells of an obligate heterozygote.通过一名 obligate 杂合子的细胞研究腺苷脱氨酶在腺苷脱氨酶严重联合免疫缺陷病(ADA - SCID)中的表达基本缺陷。
Hum Genet. 1981;56(3):379-86. doi: 10.1007/BF00274697.
3
Basic molecular defect in ADA-SCID.
Adv Exp Med Biol. 1984;165 Pt A:381-4. doi: 10.1007/978-1-4684-4553-4_75.
4
Somatic cell genetics of adenosine deaminase expression and severe combined immunodeficiency disease in humans.人类腺苷脱氨酶表达与严重联合免疫缺陷病的体细胞遗传学
Proc Natl Acad Sci U S A. 1980 Jul;77(7):4211-5. doi: 10.1073/pnas.77.7.4211.
5
Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.患有严重联合免疫缺陷的人类细胞中腺苷脱氨酶(ADA)缺乏是由于ADA蛋白异常所致。
Nucleic Acids Res. 1984 Jan 25;12(2):1015-24. doi: 10.1093/nar/12.2.1015.
6
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybrids.人20号染色体上决定腺苷脱氨酶(ADA)基因座定位的确认:人-中国仓鼠体细胞杂种中ADA与免疫性血小板减少症(ITP)可能的同线性数据。
Cytogenet Cell Genet. 1976;16(1-5):159-60. doi: 10.1159/000130579.
7
A gene on human chromosome 6 functions in assembly of tissue-specific adenosine deaminase isozymes.人类6号染色体上的一个基因在组织特异性腺苷脱氨酶同工酶的组装中发挥作用。
Proc Natl Acad Sci U S A. 1978 Aug;75(8):3876-80. doi: 10.1073/pnas.75.8.3876.
8
Regional assignment of ADA and ITPA to mouse chromosome 2 (C1----ter). A demonstration of the conserved linkage of enzyme and proto-oncogene loci.腺苷脱氨酶(ADA)和次黄嘌呤-鸟嘌呤磷酸核糖转移酶(ITPA)在小鼠2号染色体(着丝粒----端粒)上的区域定位。酶基因座与原癌基因座保守连锁的证明。
J Hered. 1984 May-Jun;75(3):175-80. doi: 10.1093/oxfordjournals.jhered.a109907.
9
Radioimmunochemical quantitation of human adenosine deaminase.人腺苷脱氨酶的放射免疫化学定量分析
J Clin Invest. 1979 Sep;64(3):798-803. doi: 10.1172/JCI109526.
10
Mutations in the human adenosine deaminase gene that affect protein structure and RNA splicing.影响蛋白质结构和RNA剪接的人类腺苷脱氨酶基因突变。
Proc Natl Acad Sci U S A. 1987 Aug;84(16):5947-51. doi: 10.1073/pnas.84.16.5947.

引用本文的文献

1
Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.患有严重联合免疫缺陷的人类细胞中腺苷脱氨酶(ADA)缺乏是由于ADA蛋白异常所致。
Nucleic Acids Res. 1984 Jan 25;12(2):1015-24. doi: 10.1093/nar/12.2.1015.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Standardization of hemoglobinometry. II. The hemiglobincyanide method.血红蛋白测定法的标准化。II. 高铁氰化血红蛋白法。
Clin Chim Acta. 1961 Jul;6:538-44. doi: 10.1016/0009-8981(61)90145-0.
3
Human adenosine deaminase and its binding protein in normal and adenosine deaminase-deficient fibroblast cell strains.正常及腺苷脱氨酶缺陷型成纤维细胞株中的人腺苷脱氨酶及其结合蛋白
J Biol Chem. 1980 Jun 25;255(12):5681-7.
4
Basic defect in the expression of adenosine deaminase in ADA- SCID disease investigated through the cells of an obligate heterozygote.通过一名 obligate 杂合子的细胞研究腺苷脱氨酶在腺苷脱氨酶严重联合免疫缺陷病(ADA - SCID)中的表达基本缺陷。
Hum Genet. 1981;56(3):379-86. doi: 10.1007/BF00274697.
5
Immunoreactive protein in adenosine deaminase deficient human lymphoblast cell lines.腺苷脱氨酶缺陷型人淋巴母细胞系中的免疫反应性蛋白。
J Biol Chem. 1982 Mar 25;257(6):3211-7.
6
Identification of human thymus-leukemia-associated antigen as a low-molecular-weight form of adenosine deaminase.鉴定人类胸腺白血病相关抗原为腺苷脱氨酶的一种低分子量形式。
J Natl Cancer Inst. 1980 May;64(5):1077-83.
7
The genetic defect in the various types of human beta-galactosidase deficiency.人类各种类型β-半乳糖苷酶缺乏症中的基因缺陷。
Hum Genet. 1980 Feb;53(2):241-7. doi: 10.1007/BF00273505.
8
Thalassemia revisited.再谈地中海贫血
Cell. 1982 May;29(1):7-9. doi: 10.1016/0092-8674(82)90084-8.
9
Adenosine deaminase complexing protein (ADCP): a transformation sensitive protein with potentials of a cancer marker.腺苷脱氨酶复合蛋白(ADCP):一种对转化敏感且具有癌症标志物潜力的蛋白质。
Anticancer Res. 1983 Mar-Apr;3(2):95-100.
10
Assignment of adenosine deaminase complexing protein (ADCP) gene(s) to human chromosome 2 in rodent-human somatic cell hybrids.在啮齿动物-人类体细胞杂种中将腺苷脱氨酶复合蛋白(ADCP)基因定位到人类第2号染色体上。
Hum Genet. 1981;59(4):317-23. doi: 10.1007/BF00295464.