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HLA and complement genetic markers in diabetic retinopathy.

作者信息

McCann V J, McCluskey J, Kay P H, Zilko P J, Christiansen F T, Dawkins R L

出版信息

Diabetologia. 1983 Mar;24(3):221. doi: 10.1007/BF00250171.

DOI:10.1007/BF00250171
PMID:6404683
Abstract
摘要

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1
HLA and complement genetic markers in diabetic retinopathy.糖尿病视网膜病变中的人类白细胞抗原和补体遗传标记
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2
Localization of the human MHC-linked complement genes between HLA-B and HLA-DR by using HLA mutant cell lines.利用HLA突变细胞系将人类MHC连锁补体基因定位在HLA - B和HLA - DR之间。
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Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.系统性红斑狼疮患者主要组织相容性复合体的家系研究：C4A和C4B无效等位基因在决定疾病易感性中的重要性。
Br Med J (Clin Res Ed). 1983 Feb 5;286(6363):425-8. doi: 10.1136/bmj.286.6363.425.
4
Rare variant of complement C4 is seen in high frequency in patients with primary glomerulonephritis.补体C4的罕见变异在原发性肾小球肾炎患者中高频出现。
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Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies.21-羟化酶基因座的遗传定位：小重组频率的估计
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DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population.芬兰人群中人类HLA连锁补体C4同种异型包括C4无效等位基因的DNA多态性。
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A major histocompatibility complex class III allotype (C4B 2) associated with primary biliary cirrhosis (PBC).
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Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes.用于准确测定人类补体C4A、C4B、C4长链、C4短链和RCCX模块拷贝数变异（CNV）的灵敏且特异的实时聚合酶链反应检测方法：对50名具有明确HLA基因型的近亲受试者C4 CNV的阐释
J Immunol. 2007 Sep 1;179(5):3012-25. doi: 10.4049/jimmunol.179.5.3012.

引用本文的文献

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Lipids, hyperreflective crystalline deposits and diabetic retinopathy: potential systemic and retinal-specific effect of lipid-lowering therapies.脂质、高反射性结晶沉积物和糖尿病视网膜病变：降脂治疗的潜在全身和视网膜特异性作用。
Diabetologia. 2022 Apr;65(4):587-603. doi: 10.1007/s00125-022-05655-z. Epub 2022 Feb 11.
2
Interleukin-1 receptor antagonist allele (IL1RN*2) associated with nephropathy in diabetes mellitus.白细胞介素-1受体拮抗剂等位基因（IL1RN*2）与糖尿病肾病相关。
Hum Genet. 1996 Mar;97(3):369-74. doi: 10.1007/BF02185776.
3
Extended major histocompatibility complex haplotypes in type I diabetes mellitus.

本文引用的文献

1
HLA association with diabetic retinopathy - fact or fancy.人类白细胞抗原与糖尿病视网膜病变的关联——事实还是臆想。
Diabetologia. 1981 May;20(5):585. doi: 10.1007/BF00252771.
2
Of genes and proliferative retinopathy.关于基因与增殖性视网膜病变
Diabetologia. 1981 Apr;20(4):506. doi: 10.1007/BF00253416.
3
Are HLA types or Bf alleles markers for diabetic retinopathy?人类白细胞抗原（HLA）类型或补体因子B（Bf）等位基因是糖尿病视网膜病变的标志物吗？
I型糖尿病中的扩展主要组织相容性复合体单倍型
J Clin Invest. 1984 Aug;74(2):449-54. doi: 10.1172/JCI111441.
4
Do genetic factors play a role in the pathogenesis of diabetic microangiopathy?遗传因素在糖尿病微血管病变的发病机制中起作用吗？
Diabetologia. 1984 Nov;27(5):487-92. doi: 10.1007/BF00290381.
5
Relation of gene expression (allotypes) of the fourth component of complement to insulin dependent diabetes and its microangiopathic complications.补体第四成分的基因表达（同种异型）与胰岛素依赖型糖尿病及其微血管并发症的关系。
Br Med J (Clin Res Ed). 1985 Jul 6;291(6487):9-10. doi: 10.1136/bmj.291.6487.9.
6
HLA-DR antigen association with proliferative diabetic retinopathy.人类白细胞抗原-DR抗原与增殖性糖尿病视网膜病变的关联。
Int Ophthalmol. 1985 Apr;8(1):33-5. doi: 10.1007/BF00136459.
7
Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.麸质敏感性肠病患者的扩展主要组织相容性复合体单倍型
J Clin Invest. 1987 Jan;79(1):251-6. doi: 10.1172/JCI112791.
Diabetologia. 1980 Oct;19(4):402-3. doi: 10.1007/BF00280528.
4
Genetic susceptibility to the development of retinopathy in insulin-dependent diabetics.胰岛素依赖型糖尿病患者发生视网膜病变的遗传易感性。
Diabetes. 1982 Mar;31(3):226-31. doi: 10.2337/diab.31.3.226.