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Letter: Autosomal assignment of the gene for the form of adenosine deaminase which is deficient in patients with combined immunodeficiency syndrome.

作者信息

Creagan R P, Tischfield J A, Nichols E A, Ruddle F H

出版信息

Lancet. 1973 Dec 22;2(7843):1449. doi: 10.1016/s0140-6736(73)92850-x.

DOI:10.1016/s0140-6736(73)92850-x
PMID:4128766
Abstract
摘要

相似文献

1
Letter: Autosomal assignment of the gene for the form of adenosine deaminase which is deficient in patients with combined immunodeficiency syndrome.信函:腺苷脱氨酶基因的常染色体定位,该酶在联合免疫缺陷综合征患者中缺乏。
Lancet. 1973 Dec 22;2(7843):1449. doi: 10.1016/s0140-6736(73)92850-x.
2
Adenosine deaminase deficiency in a child with severe combined immunodeficiency.一名患有严重联合免疫缺陷的儿童出现腺苷脱氨酶缺乏。
Clin Genet. 1973;4(4):344-7. doi: 10.1111/j.1399-0004.1973.tb01929.x.
3
Adenosine-deaminase deficiency and combined immunodeficiency syndrome.腺苷脱氨酶缺乏与联合免疫缺陷综合征
Lancet. 1972 Dec 16;2(7790):1316. doi: 10.1016/s0140-6736(72)92692-x.
4
Adenosine-deaminase deficiency and severe combined immunodeficiency syndrome.腺苷脱氨酶缺乏症与重症联合免疫缺陷综合征。
Lancet. 1973 Jun 16;1(7816):1393-4. doi: 10.1016/s0140-6736(73)91725-x.
5
Heterogeneity for adenosine deaminase deficiency: Expression of the enzyme in cultured skin fibroblasts and amniotic fluid cells.腺苷脱氨酶缺乏症的异质性:该酶在培养的皮肤成纤维细胞和羊水细胞中的表达。
Am J Hum Genet. 1975 Jan;27(1):46-52.
6
Molecular form of adenosine deaminase in severe combined immunodeficiency.重症联合免疫缺陷中腺苷脱氨酶的分子形式
Biochem Biophys Res Commun. 1974 Apr 8;57(3):590-5. doi: 10.1016/0006-291x(74)90587-7.
7
Adenosine deaminase isozymes in human tissues.人体组织中的腺苷脱氨酶同工酶。
Ann Hum Genet. 1971 Oct;35(2):207-19. doi: 10.1111/j.1469-1809.1956.tb01393.x.
8
Evidence for control of several different tissue-specific isozymes of adenosine deaminase by a single genetic locus.单一基因座控制腺苷脱氨酶几种不同组织特异性同工酶的证据。
Nat New Biol. 1973 Dec 19;246(155):200-2. doi: 10.1038/newbio246200a0.
9
Adenosine deaminase: demonstration of a "silent" gene associated with combined immunodeficiency disease.腺苷脱氨酶:与联合免疫缺陷病相关的“沉默”基因的证明。
Am J Hum Genet. 1974 Jan;26(1):103-7.
10
Severe combined immunodeficiency and adenosine deaminase deficiency.重症联合免疫缺陷与腺苷脱氨酶缺乏症
N Engl J Med. 1975 Apr 3;292(14):714-9. doi: 10.1056/NEJM197504032921402.

引用本文的文献

1
Animal model for immune dysfunction associated with adenosine deaminase deficiency.与腺苷脱氨酶缺乏相关的免疫功能障碍动物模型。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4899-903. doi: 10.1073/pnas.77.8.4899.
2
The biochemical basis of immunodeficiency disease.免疫缺陷疾病的生化基础。
Eur J Pediatr. 1980 Oct;135(1):13-20. doi: 10.1007/BF00445887.
3
Chromosome assignments of genes in man using mouse-human somatic cell hybrids: Cytoplasmic isocitrate dehydrogenase (IDH 1) and malate dehydrogenase (MDH 1) to chromosomes 2.
利用鼠 - 人杂交体细胞对人类基因进行染色体定位:细胞质异柠檬酸脱氢酶(IDH 1)和苹果酸脱氢酶(MDH 1)定位于第2号染色体。
Am J Hum Genet. 1974 Sep;26(5):604-13.
4
Heterogeneity for adenosine deaminase deficiency: Expression of the enzyme in cultured skin fibroblasts and amniotic fluid cells.腺苷脱氨酶缺乏症的异质性:该酶在培养的皮肤成纤维细胞和羊水细胞中的表达。
Am J Hum Genet. 1975 Jan;27(1):46-52.
5
A normal level of adenosine deaminase activity in the red cell lysates of carriers and patients with severe combined immunodeficiency disease.携带者和重症联合免疫缺陷病患者红细胞裂解物中腺苷脱氨酶活性的正常水平。
Proc Natl Acad Sci U S A. 1976 Jan;73(1):104-8. doi: 10.1073/pnas.73.1.104.
6
Evaluation of adenosine deaminase and other purine salvage pathway enzymes in horses with combined immunodeficiency.联合免疫缺陷马匹中腺苷脱氨酶及其他嘌呤补救途径酶的评估
Infect Immun. 1976 Mar;13(3):995-7. doi: 10.1128/iai.13.3.995-997.1976.
7
Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography.精氨基琥珀酸尿症:通过放射自显影片法将精氨基琥珀酸裂解酶基因定位于人类染色体7的pter至q22区域。
Proc Natl Acad Sci U S A. 1978 Dec;75(12):6159-62. doi: 10.1073/pnas.75.12.6159.