期刊文献+

Pendrin蛋白在甲状腺疾病中的研究进展

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出处 《中国实验诊断学》 北大核心 2010年第2期306-308,共3页 Chinese Journal of Laboratory Diagnosis
基金 吉林省科技厅资助(200705277)
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参考文献19

  • 1De La Vieja A, Ginter CS, Carrasco N. The Q267E mutation in tile sodium/iodide symporter(NIS) causes congenital iodide transport defect(ITD) by decreasing the NIS turnover number[J]. J Cell Sci, 2004,117(5) : 677.
  • 2De La Vieja A, Ginter CS, Carrasco N. Molecular analysis of a congenital iodide transport defect: G543E impairs maturation and trafficking of the Na +/I- ymporter[J]. Mol Endocrinol, 2005,19( 11 ) : 2847.
  • 3Pendred V. Deaf mutism and goitre[J]. Lancet, 1896,11 (3) : 532.
  • 4Sheffield VC, Kraiem Z, Beck JC, et al. Pendred syndrome maps to chromosome and is caused by an intrinsic defect in thyroid iodine organification [J]. Nat Genet, 1996,12(5) :424.
  • 5Coyle T, Coffey R, Armour JAL, et al. Pendred syndrome(goiter and sensorineural hearing loss)maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4[J].Nat Genet, 1996,12(5) :421.
  • 6Everett LA, Glaser B, Beck JC, et al. Pendred syndrome is caused by mutations in a putative sulphate transporter gene ( PDS ) [ J ]. Nat Genet, 1997, 17(6) :411.
  • 7Royaux IE, Suzuki K, Mori A, et al. Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-Scells[J]. Endocrinology, 2000,141 (2) : 839.
  • 8Scott DA, Wang R, Kreman TM, et al. The Pendred syndrome gene encodes a chloride-iodide transport protein[J]. Nat Genet, 1999,21(4):440.
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