促甲状腺激素受体胞外段基因突变与Graves病的相关研究

Study on association between the mutation in extracellular domain of TSH receptor gene and Graves′ disease

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作者戴亚丽施秉银薛明战李雪萍高慧何岚王毅马秀萍袁育康

出处《中华内分泌代谢杂志》 CAS CSCD 北大核心 2002年第2期131-132,共2页 Chinese Journal of Endocrinology and Metabolism

基金国家自然科学基金资助项目 (3 95 70 674)

关键词突眼性甲状腺肿促甲状腺素受体基因突变

参考文献5

1Bahn RS,Dutton CM,Heufelder AE,et al.A genomic point mutation in the extracellular domain of the thyrotropin receptor in patients with Graves′ophthalmopathy[].The Journal of Clinical Endocrinology.1994
2Misrahi M,Loosfelt H,Atger M,et al.Cloning, sequencing and expression of human TSH receptor[].Biochemical and Biophysical Research Communications.1990
3Kaczur V,Szalai C,Falus A,et al.Polymorphism of the 52 triplet gene ( nucleotide 253 ) of the TSH receptor in Basedow-Graves′ patients and in healthy controls[].Orvosi Hetilap.1997
4Simananen J,Kinch A,Westermark K,et al.Analysis of mutations in exon 1 of the human thyrotropin receptor gene: high frequency of the D36H and P52T polymorphic variants[].Thyroid.1999
5Nagayama Y,Kaufmam KD,Seto P,et al.Molecular cloning,sequence and functional expression of the cDNA for the human thyrotropin receptor[].Biochemical and Biophysical Research Communications.1989

中华内分泌代谢杂志

2002年第2期

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