X-linked severe combined immunodeficiency disease and the gamma c receptor component: prospects for molecular diagnosis.
作者信息
Farner N L, Voss S D, Sondel P M
机构信息
Department of Human Oncology, University of Wisconsin, Madison 53792, USA.
出版信息
Clin Diagn Lab Immunol. 1995 Sep;2(5):518-23. doi: 10.1128/cdli.2.5.518-523.1995.
Abstract
摘要
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本文引用的文献
1
The IL-2 receptor complex: its structure, function, and target genes.白细胞介素-2受体复合物：其结构、功能及靶基因。
Annu Rev Immunol. 1993;11:245-68. doi: 10.1146/annurev.iy.11.040193.001333.
2
The IL-2/IL-2 receptor system: a current overview.白细胞介素-2/白细胞介素-2受体系统：当前概述
Cell. 1993 Apr 9;73(1):5-8. doi: 10.1016/0092-8674(93)90152-g.
3
Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans.白细胞介素-2受体γ链突变导致人类X连锁重症联合免疫缺陷。
Cell. 1993 Apr 9;73(1):147-57. doi: 10.1016/0092-8674(93)90167-o.
4
Lowest dose interleukin-2 immunotherapy.最低剂量白细胞介素-2免疫疗法。
Blood. 1993 Mar 15;81(6):1414-23.
5
Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients.重症联合免疫缺陷：117例患者临床表现及预后的回顾性单中心研究
J Pediatr. 1993 Oct;123(4):564-72. doi: 10.1016/s0022-3476(05)80951-5.
6
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.白细胞介素-2受体γ链定位于Xq13.1，在X连锁重症联合免疫缺陷病（SCIDX1）中发生突变。
Hum Mol Genet. 1993 Aug;2(8):1099-104. doi: 10.1093/hmg/2.8.1099.
7
Fine mapping of the human SCIDX1 locus at Xq12-13.1.人类Xq12 - 13.1处重症联合免疫缺陷X1（SCIDX1）基因座的精细定位。
Hum Mol Genet. 1993 Jun;2(6):651-4. doi: 10.1093/hmg/2.6.651.
8
Immunodeficiency disorders.
Pediatr Rev. 1993 Jun;14(6):226-36. doi: 10.1542/pir.14-6-226.
9
X-linked immunodeficiencies.X连锁免疫缺陷病
Adv Hum Genet. 1993;21:107-44. doi: 10.1007/978-1-4615-3010-7_2.
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