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费尔蒂综合征中的补体C4B无效等位基因。

Complement C4B-null alleles in Felty's syndrome.

作者信息

Thomson W, Sanders P A, Davis M, Davidson J, Dyer P A, Grennan D M

机构信息

University of Manchester, Rheumatic Diseases Centre, Hope Hospital, Salford, United Kingdom.

出版信息

Arthritis Rheum. 1988 Aug;31(8):984-9. doi: 10.1002/art.1780310807.

DOI:10.1002/art.1780310807
PMID:3261591
Abstract

C4A and C4B allotypes were compared in 20 patients with Felty's syndrome (FS), 52 patients with rheumatoid arthritis (RA), and 55 control subjects. Nineteen of the FS patients had HLA-DR4. A C4B-null allele was more frequent in the patients with FS (60%) than in either the RA patients (15%) or the control subjects (26%). Only the differences between patients with FS and those with RA remained statistically significant when DR4 positive subjects were compared. The C4B null allele may identify individuals within the rheumatoid population who are at risk of developing particular systemic complications.

摘要

对20例费尔蒂综合征(FS)患者、52例类风湿关节炎(RA)患者和55名对照者的C4A和C4B同种异型进行了比较。19例FS患者携带HLA - DR4。FS患者中C4B无效等位基因的频率(60%)高于RA患者(15%)或对照者(26%)。当比较DR4阳性受试者时,只有FS患者与RA患者之间的差异具有统计学意义。C4B无效等位基因可能有助于识别类风湿人群中具有发生特定全身并发症风险的个体。

相似文献

1
Complement C4B-null alleles in Felty's syndrome.费尔蒂综合征中的补体C4B无效等位基因。
Arthritis Rheum. 1988 Aug;31(8):984-9. doi: 10.1002/art.1780310807.
2
DQw7 and the C4B null allele in rheumatoid arthritis and Felty's syndrome.类风湿关节炎和费尔蒂综合征中的DQw7与C4B无效等位基因。
Ann Rheum Dis. 1990 Dec;49(12):976-9. doi: 10.1136/ard.49.12.976.
3
DQ beta polymorphism and genetic susceptibility to Felty's syndrome.DQβ多态性与费尔蒂综合征的遗传易感性
Arthritis Rheum. 1988 Aug;31(8):990-4. doi: 10.1002/art.1780310808.
4
Molecular characterisation of C4 null alleles found in Felty's syndrome.在费尔蒂综合征中发现的C4无效等位基因的分子特征分析。
Ann Rheum Dis. 1990 Oct;49(10):763-7. doi: 10.1136/ard.49.10.763.
5
Studies of a C2 DNA polymorphism in RA, Felty's and normal subjects.对类风湿关节炎、费尔蒂综合征患者及正常受试者的C2基因多态性研究。
Exp Clin Immunogenet. 1990;7(1):64-8.
6
Immunogenetic heterogeneity in rheumatoid disease as illustrated by different MHC associations (DQ, Dw and C4) in articular and extra-articular subsets.类风湿病中的免疫遗传异质性,如关节和关节外亚组中不同的主要组织相容性复合体关联(DQ、Dw和C4)所示。
Br J Rheumatol. 1991 Feb;30(1):5-9. doi: 10.1093/rheumatology/30.1.5.
7
HLA-DP in rheumatoid arthritis.
Tissue Antigens. 1988 Feb;31(2):83-9. doi: 10.1111/j.1399-0039.1988.tb02068.x.
8
TAP2D is associated with HLA-B44 and DR4 and may contribute to rheumatoid arthritis and Felty's syndrome susceptibility.TAP2D与HLA - B44和DR4相关,可能与类风湿性关节炎和费尔蒂综合征易感性有关。
Clin Exp Rheumatol. 1996 Jan-Feb;14(1):67-70.
9
Haplotypes bearing HLA-A, -B, and -DR: Bf and C4 genes in rheumatoid arthritis families.类风湿关节炎家族中携带HLA - A、- B和 - DR:Bf及C4基因的单倍型。
Tissue Antigens. 1989 Jan;33(1):21-9. doi: 10.1111/j.1399-0039.1989.tb01673.x.
10
Association of rheumatoid arthritis with a dominant DR1/Dw4/Dw14 sequence motif, but not with T cell receptor beta chain gene alleles or haplotypes.类风湿性关节炎与显性DR1/Dw4/Dw14序列基序相关,但与T细胞受体β链基因等位基因或单倍型无关。
Arthritis Rheum. 1991 Nov;34(11):1416-24. doi: 10.1002/art.1780341112.

引用本文的文献

1
Prognostic significance of complement alleles Bf and C4 in early rheumatoid arthritis.补体等位基因Bf和C4在早期类风湿关节炎中的预后意义
Clin Rheumatol. 1996 Nov;15(6):594-8. doi: 10.1007/BF02238550.
2
Genes associated with rheumatoid arthritis and mild inflammatory arthritis. I. Major histocompatibility complex class I, II, and III allotypes.与类风湿性关节炎和轻度炎症性关节炎相关的基因。I. 主要组织相容性复合体I类、II类和III类同种异型。
Ann Rheum Dis. 1990 Apr;49(4):219-24. doi: 10.1136/ard.49.4.219.
3
Effects of C4 null alleles and homoduplications on quantitative expression of C4A and C4B.
C4无效等位基因和同型重复对C4A和C4B定量表达的影响。
Clin Exp Immunol. 1992 Apr;88(1):163-8. doi: 10.1111/j.1365-2249.1992.tb03057.x.