从一名患有碘有机化缺陷的家族性甲状腺肿中溶解出的缺陷性甲状腺过氧化物酶。 - Suppr

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超能文献

A defective thyroid peroxidase solubilized from a familial goiter with iodine organification defect.

作者信息

Pommier J, Tourniaire J, Dème D, Chalendar D, Bornet H, Nunez J

出版信息

J Clin Endocrinol Metab. 1974 Jul;39(1):69-80. doi: 10.1210/jcem-39-1-69.

DOI:10.1210/jcem-39-1-69

PMID:4835124

Abstract

摘要

相似文献

A defective thyroid peroxidase solubilized from a familial goiter with iodine organification defect.从一名患有碘有机化缺陷的家族性甲状腺肿中溶解出的缺陷性甲状腺过氧化物酶。

J Clin Endocrinol Metab. 1974 Jul;39(1):69-80. doi: 10.1210/jcem-39-1-69.

Peroxidase deficiency in familial goiter with iodide organification defect.伴有碘有机化缺陷的家族性甲状腺肿中的过氧化物酶缺乏症。

N Engl J Med. 1971 Dec 16;285(25):1394-8. doi: 10.1056/NEJM197112162852502.

Thyroid iodine organification defects: a case with lack of thyroglobulin iodination and a case without any peroxidase activity.甲状腺碘有机化缺陷：一例缺乏甲状腺球蛋白碘化的病例和一例无任何过氧化物酶活性的病例。

J Clin Endocrinol Metab. 1976 Feb;42(2):319-29. doi: 10.1210/jcem-42-2-319.

Normal peroxidase activity in Pendred's syndrome.

J Clin Endocrinol Metab. 1973 Mar;36(3):522-30. doi: 10.1210/jcem-36-3-522.

Abnormal thyroid peroxidase causing iodide organification defect.

J Clin Endocrinol Metab. 1972 Apr;34(4):607-16. doi: 10.1210/jcem-34-4-607.

Peroxidase defect in congenital goiter with complete organification block.

J Clin Endocrinol Metab. 1973 Feb;36(2):347-57. doi: 10.1210/jcem-36-2-347.

Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidase.伴有部分碘有机化缺陷、甲状腺球蛋白缺乏及甲状腺过氧化物酶水平升高的家族性甲状腺肿

Clin Endocrinol (Oxf). 1977 Jan;6(1):27-39. doi: 10.1111/j.1365-2265.1977.tb01993.x.

The concentration of peroxidase in normal and adenomatous human thyroid tissue with special reference to patients with Pendred's syndrome.

Acta Endocrinol (Copenh). 1973 Feb;72(2):272-8. doi: 10.1530/acta.0.0720272.

Congenital goitre and hypothyroidism with impaired iodide organification and high thyroid peroxidase concentration.先天性甲状腺肿和甲状腺功能减退伴碘有机化受损及甲状腺过氧化物酶浓度升高。

Clin Endocrinol (Oxf). 1979;11(2):123-39. doi: 10.1111/j.1365-2265.1979.tb03058.x.

Thyroid peroxidase and thyroxine biosynthesis.

Recent Prog Horm Res. 1970;26:189-247. doi: 10.1016/b978-0-12-571126-5.50009-1.

引用本文的文献

Association of peroxidase enzyme defect and low thyroglobulin content in a case of endemic cretinism.地方性克汀病一例中过氧化物酶缺陷与甲状腺球蛋白含量低的关联

J Endocrinol Invest. 1985 Jun;8(3):257-62. doi: 10.1007/BF03348489.

Autoantibodies to the thyroid microsomal/thyroid peroxidase antigen are polyclonal and directed to several distinct antigenic sites.甲状腺微粒体/甲状腺过氧化物酶抗原的自身抗体是多克隆的，且针对几个不同的抗原位点。

Immunology. 1988 May;64(1):23-9.

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.鉴定人类甲状腺过氧化物酶基因编码序列中导致先天性甲状腺肿的一种突变。

J Clin Invest. 1992 Oct;90(4):1200-4. doi: 10.1172/JCI115981.

Deficient thyroid peroxidase causing organification defect and goitrous hypothyroidism.甲状腺过氧化物酶缺乏导致有机化缺陷和甲状腺肿性甲状腺功能减退。

J Endocrinol Invest. 1979 Oct-Dec;2(4):353-7. doi: 10.1007/BF03349333.

Partial and total iodide organification defect in different sibships in a kindred.一个家族中不同同胞关系的部分和完全碘有机化缺陷

Am J Hum Genet. 1977 Mar;29(2):142-8.

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