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Component deficiencies. 2. The fourth component.

作者信息

Hauptmann G, Goetz J, Uring-Lambert B, Grosshans E

出版信息

Prog Allergy. 1986;39:232-49.

PMID:3562465
Abstract
摘要

相似文献

1
Component deficiencies. 2. The fourth component.
Prog Allergy. 1986;39:232-49.
2
Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.一名患有额顶部线状硬皮病的患者及其家族中补体第四成分（C4）和第二成分（C2）存在不完全功能缺陷。缺陷由一个与人类白细胞抗原系统不连锁的基因决定。
Exp Clin Immunogenet. 1996;13(2):104-11.
3
Hereditary C4 deficiency--genetic studies and linkage to HLA.遗传性C4缺乏症——遗传学研究及其与HLA的连锁关系
Transplant Proc. 1979 Dec;11(4):1710-2.
4
HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency.用于补体C4缺乏症产前诊断的培养羊膜细胞的HLA分型
Clin Genet. 1980 Sep;18(3):197-200. doi: 10.1111/j.1399-0004.1980.tb00871.x.
5
Deficiency of the fourth component of complement (C4): a family case.补体第四成分（C4）缺乏：一个家族病例
Intern Med. 1994 Aug;33(8):508-11.
6
C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency.C4多态性与HLA连锁：对一个遗传性C4缺乏症家族的研究
Clin Immunol Immunopathol. 1981 Sep;20(3):354-60. doi: 10.1016/0090-1229(81)90146-x.
7
[Systemic lupus erythematosus in hereditary complement 4 deficiency].
Hautarzt. 1984 Jan;35(1):27-32.
8
Molecular studies of the fourth component of complement (C4) in glomerulonephritis.肾小球肾炎中补体第四成分（C4）的分子研究
Semin Nephrol. 1989 Mar;9(1):102-6.
9
Selective depression of the C4 component of complement: evidence for an association with genetic deficiency of C4 and dermatologic diseases.补体C4成分的选择性抑制：与C4基因缺陷和皮肤病关联的证据。
Diagn Immunol. 1983;1(1):49-55.
10
Chido, Rodgers, and C4 deficiency.奇多、罗杰斯与C4缺乏症
Transplant Proc. 1979 Dec;11(4):1941-3.

引用本文的文献

1
Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism.人类感染性免疫先天缺陷：从免疫系统到整个机体。
Curr Opin Immunol. 2019 Aug;59:88-100. doi: 10.1016/j.coi.2019.03.008. Epub 2019 May 20.
2
Clinical Features of Hereditary and Mast Cell-mediated Angioedema Focusing on the Differential Diagnosis in Japanese Patients.遗传性和肥大细胞介导的血管性水肿的临床特征：聚焦于日本患者的鉴别诊断
Intern Med. 2018 Feb 1;57(3):319-324. doi: 10.2169/internalmedicine.8624-16. Epub 2017 Nov 1.
3
Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.
高加索人中人类补体成分C4A和C4B的缺陷以及RP-C4-CYP21-TNX（RCCX）模块长度变异的杂合性。RCCX基因多样性对主要组织相容性复合体相关疾病的影响。
J Exp Med. 2000 Jun 19;191(12):2183-96. doi: 10.1084/jem.191.12.2183.
4
Quantitative analysis of C4Ab and C4Bb binding to the C3b/C4b receptor (CR1, CD35).C4Ab和C4Bb与C3b/C4b受体（CR1，CD35）结合的定量分析。
Clin Exp Immunol. 1997 Nov;110(2):310-6. doi: 10.1111/j.1365-2249.1997.tb08333.x.
5
Complement deficiency and immune complex disease.补体缺陷与免疫复合物疾病
Springer Semin Immunopathol. 1994;15(4):397-416. doi: 10.1007/BF01837367.
6
Expression of MHC class I determinants on erythrocytes of SLE patients.系统性红斑狼疮患者红细胞上主要组织相容性复合体I类决定簇的表达。
Clin Exp Immunol. 1987 Aug;69(2):368-74.
7
Immunopathologic studies of cutaneous lupus erythematosus.皮肤红斑狼疮的免疫病理学研究。
J Clin Immunol. 1988 Jul;8(4):223-33. doi: 10.1007/BF00916550.
8
C4 concentrations and C4 deficiency alleles in systemic lupus erythematosus.系统性红斑狼疮中的C4浓度及C4缺陷等位基因
Ann Rheum Dis. 1989 Jul;48(7):600-4. doi: 10.1136/ard.48.7.600.
9
Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis.通过脉冲场凝胶电泳直接观察补体C4和21-羟化酶基因座的基因组织。
J Exp Med. 1989 May 1;169(5):1803-18. doi: 10.1084/jem.169.5.1803.
10
Differences in the metabolism of C4 isotypes in patients with complement activation.补体激活患者中C4同种型代谢的差异。
Clin Exp Immunol. 1989 Oct;78(1):49-53.