自身免疫性甲状腺疾病中无主要基因：突尼斯一个大型家系的复杂分离分析和流行病学研究 - Suppr

No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree.

作者信息

Bougacha-Elleuch Noura, Ben Arab Saida, Rebai Ahmed, Mnif Mouna, Maalej Abdellatif, Charfi Nadia, Ben Lassouad Mohamed, Jouida Jomaa, Abid Mohamed, Ayadi Hammadi

机构信息

Unité Cibles pour le Diagnostic et la Thérapie, Centre de Biotechnologie Sfax, BP '1177' 3018, Universiteé de Sfax, Sfax, Tunisia.

出版信息

J Genet. 2011 Aug;90(2):333-7. doi: 10.1007/s12041-011-0064-z.

DOI:10.1007/s12041-011-0064-z

PMID:21869485

Abstract

摘要

相似文献

No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree.自身免疫性甲状腺疾病中无主要基因：突尼斯一个大型家系的复杂分离分析和流行病学研究

J Genet. 2011 Aug;90(2):333-7. doi: 10.1007/s12041-011-0064-z.

The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population.突尼斯人群中蛋白酪氨酸磷酸酶22基因R620W多态性与自身免疫性甲状腺疾病及类风湿关节炎的关系

Ann Hum Biol. 2009 May-Jun;36(3):342-9. doi: 10.1080/03014460902817968.

Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies.维生素D受体基因多态性与甲状腺自身免疫性疾病无关联：家族性及病例对照研究

J Clin Immunol. 2008 Jan;28(1):21-5. doi: 10.1007/s10875-007-9124-9. Epub 2007 Oct 18.

A full genome screening in a large Tunisian family affected with thyroid autoimmune disorders.对一个受甲状腺自身免疫性疾病影响的突尼斯大家族进行全基因组筛查。

Genes Immun. 2001 Apr;2(2):71-5. doi: 10.1038/sj.gene.6363736.

[Epidemiologic study of autoimmune thyroid disease in south Tunisia].[突尼斯南部自身免疫性甲状腺疾病的流行病学研究]

Ann Endocrinol (Paris). 2006 Dec;67(6):591-5. doi: 10.1016/s0003-4266(06)73012-8.

Association of CTLA-4 gene A-G polymorphism (IDDM12 locus) with acute-onset and insulin-depleted IDDM as well as autoimmune thyroid disease (Graves' disease and Hashimoto's thyroiditis) in the Japanese population.日本人群中细胞毒性T淋巴细胞相关抗原4（CTLA-4）基因A-G多态性（IDDM12位点）与急性起病及胰岛素缺乏型1型糖尿病以及自身免疫性甲状腺疾病（格雷夫斯病和桥本甲状腺炎）的关联

Diabetes. 1998 Jan;47(1):128-9. doi: 10.2337/diab.47.1.128.

[Autoimmune dysthyroidisms with autosomal recessive transmission: 25 cases].[常染色体隐性遗传的自身免疫性甲状腺疾病：25例]

Tunis Med. 1992 Dec;70(12):579-82.

Analysis of heat shock protein polymorphisms in a large family with autoimmune thyroid diseases.

Arch Inst Pasteur Tunis. 2000;77(1-4):23-4.

Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large Tunisian family.

Hum Immunol. 2001 Nov;62(11):1245-50. doi: 10.1016/s0198-8859(01)00316-0.

A thyroid hormone receptor beta gene polymorphism associated with Graves' disease.一种与格雷夫斯病相关的甲状腺激素受体β基因多态性。

J Mol Endocrinol. 1995 Dec;15(3):267-72. doi: 10.1677/jme.0.0150267.

引用本文的文献

Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.S292F甲状腺过氧化物酶（TPO）基因突变在三个突尼斯甲状腺激素合成障碍大家族中的分离：奠基者效应的证据

Eur J Pediatr. 2015 Nov;174(11):1491-501. doi: 10.1007/s00431-015-2550-4. Epub 2015 May 13.

A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction.突尼斯一个多代家族甲状腺自身免疫的20年临床与遗传学研究：基因相互作用的证据

Meta Gene. 2013 Dec 29;2:63-71. doi: 10.1016/j.mgene.2013.11.003. eCollection 2014 Dec.

本文引用的文献

A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.

Cytokine. 2008 Aug;43(2):110-3. doi: 10.1016/j.cyto.2008.01.018. Epub 2008 Jun 20.

A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.自身免疫性甲状腺疾病遗传结构的多基因座模型及其临床意义

Am J Hum Genet. 2008 Jun;82(6):1349-56. doi: 10.1016/j.ajhg.2008.04.017. Epub 2008 May 15.

Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.突尼斯人群自身免疫性甲状腺疾病白细胞介素基因多态性的关联分析。

Eur Cytokine Netw. 2007 Dec;18(4):196-200. doi: 10.1684/ecn.2007.0104. Epub 2007 Oct 26.

The genetic basis of thyroid autoimmunity.甲状腺自身免疫的遗传基础。

Thyroid. 2007 Oct;17(10):949-61. doi: 10.1089/thy.2007.0153.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.对14000例七种常见疾病患者及3000例共享对照进行全基因组关联研究。

Nature. 2007 Jun 7;447(7145):661-78. doi: 10.1038/nature05911.

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.通过全基因组分析得出的1型糖尿病四个新染色体区域的强关联。

Nat Genet. 2007 Jul;39(7):857-64. doi: 10.1038/ng2068. Epub 2007 Jun 6.

Evidence for linkage and association between autoimmune thyroid diseases and the 18q12-q21 region in a large Tunisian family.在一个大型突尼斯家族中自身免疫性甲状腺疾病与18q12 - q21区域之间的连锁和关联证据。

Int J Immunogenet. 2006 Feb;33(1):25-32. doi: 10.1111/j.1744-313X.2005.00554.x.

Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family.在一个突尼斯大家族中FKBP1B与甲状腺自身免疫性疾病之间关联的证据。

Autoimmunity. 2004 May;37(3):237-9. doi: 10.1080/08916930410001702478.

Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphism.突尼斯自身免疫性甲状腺疾病分离株中MHC基因分析：TNF -308基因多态性的影响

J Autoimmun. 2004 Aug;23(1):75-80. doi: 10.1016/j.jaut.2004.03.011.

Sibling recurrence risk in autoimmune thyroid disease.自身免疫性甲状腺疾病中的同胞复发风险。

Thyroid. 2003 Aug;13(8):761-4. doi: 10.1089/105072503768499653.

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No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree.

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