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Genes and autoimmune diseases - a complex inheritance.基因与自身免疫性疾病——复杂的遗传关系
MedGenMed. 2004 Dec 8;6(4):18.
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[Pathogenetic features of autoimmune disorders].[自身免疫性疾病的发病机制特点]
Orv Hetil. 2007 Apr 8;148 Suppl 1:12-6. doi: 10.1556/OH.2007.28028.
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Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus.X连锁基因CCDC22中rs2294020与自身免疫性疾病易感性的关联，重点关注系统性红斑狼疮。
Immunol Lett. 2017 Jan;181:58-62. doi: 10.1016/j.imlet.2016.11.011. Epub 2016 Nov 22.
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The critical role of epigenetics in systemic lupus erythematosus and autoimmunity.表观遗传学在系统性红斑狼疮和自身免疫中的关键作用。
J Autoimmun. 2016 Nov;74:118-138. doi: 10.1016/j.jaut.2016.06.020. Epub 2016 Jul 6.
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Systemic lupus erythematosus, autoimmunity, sex and inheritance.系统性红斑狼疮、自身免疫、性别与遗传。
N Engl J Med. 1979 Oct 11;301(15):838-9. doi: 10.1056/NEJM197910113011510.
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Omics studies: their use in diagnosis and reclassification of SLE and other systemic autoimmune diseases.组学研究：其在系统性红斑狼疮及其他系统性自身免疫性疾病的诊断和重新分类中的应用
Rheumatology (Oxford). 2017 Apr 1;56(suppl_1):i78-i87. doi: 10.1093/rheumatology/kew339.
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The crossroads of autoimmunity and immunodeficiency: Lessons from polygenic traits and monogenic defects.自身免疫与免疫缺陷的交叉点：多基因性状和单基因缺陷的启示。
J Allergy Clin Immunol. 2016 Jan;137(1):3-17. doi: 10.1016/j.jaci.2015.11.004.
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[Dermatoglyphic investigations in respect to the genetic basis of autoimmune diseases (author's transl)].关于自身免疫性疾病遗传基础的皮纹学研究（作者译）
Wien Klin Wochenschr. 1975 Jan 10;87(1):33-5.
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Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes.荟萃分析证实 FCGR3B 缺失在自身免疫表型中起作用。
Hum Mol Genet. 2012 May 15;21(10):2370-6. doi: 10.1093/hmg/dds039. Epub 2012 Feb 14.
引用本文的文献
1
Therapeutic potential of natural coumarins in autoimmune diseases with underlying mechanisms.天然香豆素类化合物在潜在机制相关自身免疫性疾病中的治疗潜力。
Front Immunol. 2024 Oct 31;15:1432846. doi: 10.3389/fimmu.2024.1432846. eCollection 2024.
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Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity.病态序列提示微生物肽与自身抗原之间存在分子模拟：引发自身免疫的一种可能性。
Front Microbiol. 2017 Oct 9;8:1938. doi: 10.3389/fmicb.2017.01938. eCollection 2017.
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Interferon regulatory factor signaling in autoimmune disease.自身免疫性疾病中的干扰素调节因子信号传导
Cytokine. 2017 Oct;98:15-26. doi: 10.1016/j.cyto.2017.02.006. Epub 2017 Mar 7.
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Familial Aggregation and Segregation Analysis in Families Presenting Autoimmunity, Polyautoimmunity, and Multiple Autoimmune Syndrome.自身免疫性疾病、多发性自身免疫性疾病和多重自身免疫综合征患者家庭中的家族聚集性和分离分析
J Immunol Res. 2015;2015:572353. doi: 10.1155/2015/572353. Epub 2015 Nov 30.
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DLA class II alleles are associated with risk for canine symmetrical lupoid onychodystrophy [corrected](SLO).DLA Ⅱ类等位基因与犬对称性狼疮甲营养不良（已更正）（SLO）的发病风险相关。
PLoS One. 2010 Aug 23;5(8):e12332. doi: 10.1371/journal.pone.0012332.
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Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex.全基因组关联作图鉴定出多个犬类系统性红斑狼疮相关疾病复合性状的位点。
Nat Genet. 2010 Mar;42(3):250-4. doi: 10.1038/ng.525. Epub 2010 Jan 31.
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MHC class II polymorphism is associated with a canine SLE-related disease complex.主要组织相容性复合体II类多态性与犬类系统性红斑狼疮相关疾病复合体有关。
Immunogenetics. 2009 Aug;61(8):557-64. doi: 10.1007/s00251-009-0387-6. Epub 2009 Jul 28.
本文引用的文献
1
Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23.系统性红斑狼疮基因组扫描：支持1q23、2q33、16q12 - 13和17q21 - 23处的连锁关系，以及3p24、10q23 - 24、13q32和18q22 - 23处的新证据。
Arthritis Rheum. 2004 Oct;50(10):3203-10. doi: 10.1002/art.20511.
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Current advances in the human lupus genetics.人类狼疮遗传学的当前进展。
Curr Rheumatol Rep. 2004 Oct;6(5):391-8. doi: 10.1007/s11926-004-0014-3.
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Update on human systemic lupus erythematosus genetics.人类系统性红斑狼疮遗传学的最新进展。
Curr Opin Rheumatol. 2004 Sep;16(5):513-21. doi: 10.1097/01.bor.0000132648.62680.81.
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Comparison of differentially expressed genes in T lymphocytes between human autoimmune disease and murine models of autoimmune disease.人类自身免疫性疾病与自身免疫性疾病小鼠模型中T淋巴细胞差异表达基因的比较。
Clin Immunol. 2004 Sep;112(3):225-30. doi: 10.1016/j.clim.2004.03.017.
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Co-localization of differentially expressed genes and shared susceptibility loci in human autoimmunity.人类自身免疫中差异表达基因与共享易感位点的共定位
Genet Epidemiol. 2004 Sep;27(2):162-72. doi: 10.1002/gepi.20013.
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Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.蛋白酪氨酸磷酸酶PTPN22的R620W多态性与人类系统性红斑狼疮的遗传关联。
Am J Hum Genet. 2004 Sep;75(3):504-7. doi: 10.1086/423790. Epub 2004 Jul 23.
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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.增强复杂疾病的连锁分析：高密度基因分型评估
Hum Mol Genet. 2004 Sep 1;13(17):1943-9. doi: 10.1093/hmg/ddh202. Epub 2004 Jul 6.
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A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.编码蛋白酪氨酸磷酸酶（PTPN22）的基因中的一个错义单核苷酸多态性与类风湿性关节炎相关。
Am J Hum Genet. 2004 Aug;75(2):330-7. doi: 10.1086/422827. Epub 2004 Jun 18.
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Expression levels for many genes in human peripheral blood cells are highly sensitive to ex vivo incubation.人类外周血细胞中许多基因的表达水平对体外培养高度敏感。
Genes Immun. 2004 Aug;5(5):347-53. doi: 10.1038/sj.gene.6364098.
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Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.多发性硬化症中与17号染色体17q11上NOS2A基因座的连锁与关联
Ann Neurol. 2004 Jun;55(6):793-800. doi: 10.1002/ana.20092.
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