人类甲状腺素结合球蛋白缺乏症。一项遗传学研究。 - Suppr

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Human thyroxine-binding globulin deficiency. A genetic study.

作者信息

Marshall J S, Levy R P, Steinberg A G

出版信息

N Engl J Med. 1966 Jun 30;274(26):1469-73. doi: 10.1056/NEJM196606302742604.

DOI:10.1056/NEJM196606302742604

PMID:4957281

Abstract

摘要

相似文献

Human thyroxine-binding globulin deficiency. A genetic study.人类甲状腺素结合球蛋白缺乏症。一项遗传学研究。

N Engl J Med. 1966 Jun 30;274(26):1469-73. doi: 10.1056/NEJM196606302742604.

Familial thyroxine-binding globulin deficiency.家族性甲状腺素结合球蛋白缺乏症。

Br Med J. 1970 Jul 4;3(5713):27-9. doi: 10.1136/bmj.3.5713.27.

Effect of sulfonylurea drugs on the binding of triiodothyronine and thyroxine to thyroxine-binding globulin.磺脲类药物对三碘甲状腺原氨酸和甲状腺素与甲状腺素结合球蛋白结合的影响。

J Clin Endocrinol Metab. 1968 Nov;28(11):1605-10. doi: 10.1210/jcem-28-11-1605.

Inherited abnormality of thyroxine-binding globulin with no demonstrable thyroxine-binding activity and high serum levels of denatured thyroxine-binding globulin.甲状腺素结合球蛋白的遗传性异常，无明显甲状腺素结合活性，血清中变性甲状腺素结合球蛋白水平升高。

N Engl J Med. 1986 Mar 13;314(11):694-9. doi: 10.1056/NEJM198603133141107.

[Effect of l-triiodothyronine and d-thyroxine on the binding of thyroid hormones by serum proteins and on blood lipids in hypothyroidism].

Vnitr Lek. 1968 Dec;14(12):1150-3.

[A family with hereditary increase in thyroxine-binding globulin].[一个甲状腺素结合球蛋白遗传性增加的家族]

Dtsch Med Wochenschr. 1972 Feb 11;97(6):194-6. doi: 10.1055/s-0028-1107324.

[Chemical and radiochemical methods of studying the transport-organic stage of iodine metabolism].[研究碘代谢转运-有机阶段的化学和放射化学方法]

Med Radiol (Mosk). 1974 Apr;19(4):83-8.

Hereditary increased thyroxine-binding-globulin capacity.

Mayo Clin Proc. 1972 Oct;47(10):720-4.

Effects of variations of thyroxine-binding globulin capacity on the disappearance of triiodothyronine from the plasma.

J Clin Endocrinol Metab. 1969 Dec;29(12):1601-7. doi: 10.1210/jcem-29-12-1601.

Abnormal thyroxine and triiodothyronine concentration in the blood due to familial disorders in the thyroxine-binding globulin concentration.由于甲状腺素结合球蛋白浓度的家族性疾病导致血液中甲状腺素和三碘甲状腺原氨酸浓度异常。

Ned Tijdschr Geneeskd. 1974 Jul 20;118(29):1115-21.

引用本文的文献

Novel frameshift mutation causes early termination of the thyroxine-binding globulin protein and complete thyroxine-binding globulin deficiency in a Chinese family: A case report.新型移码突变导致中国一个家族中甲状腺素结合球蛋白蛋白提前终止及甲状腺素结合球蛋白完全缺乏：一例报告

World J Clin Cases. 2019 Nov 26;7(22):3887-3894. doi: 10.12998/wjcc.v7.i22.3887.

Genetic polymorphism of thyroxin-binding globulin (TBG) in the Pacific area.太平洋地区甲状腺素结合球蛋白（TBG）的基因多态性

Am J Hum Genet. 1984 May;36(3):646-54.

Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.一名纯合子女性中遗传性X染色体连锁甲状腺素结合球蛋白（TBG）缺乏症。

J Endocrinol Invest. 1980 Oct-Dec;3(4):349-52. doi: 10.1007/BF03349369.

Growth retardation and thyroxine-binding globulin deficiency.生长发育迟缓与甲状腺素结合球蛋白缺乏症

Arch Dis Child. 1971 Feb;46(245):115-7. doi: 10.1136/adc.46.245.115.

Studies on human thyroxine-binding globulin (TBG). I. Purification of TBG and immunologic studies on the relationship between TBG from normal persons and those with TBG "deficiency".关于人甲状腺素结合球蛋白（TBG）的研究。I. TBG的纯化以及关于正常人的TBG与TBG“缺乏”者的TBG之间关系的免疫学研究。

J Clin Invest. 1969 Mar;48(3):508-15. doi: 10.1172/JCI106008.

Thyroid-binding globulin deficiency in a patient with Beckwith's syndrome.一名患有贝克威思综合征患者的甲状腺结合球蛋白缺乏症。

Calif Med. 1973 Apr;118(4):63-6.

X-chromosome linked inheritance of decreased thyroxine-binding globulin.甲状腺素结合球蛋白降低的X染色体连锁遗传

Arch Dis Child. 1972 Aug;47(254):635-8. doi: 10.1136/adc.47.254.635.

The genetic polymorphism of the thyroxine-binding globulin (TBG).甲状腺素结合球蛋白（TBG）的基因多态性。

Humangenetik. 1972;14(2):85-94. doi: 10.1007/BF00273290.

Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups.家族性甲状腺素结合球蛋白缺乏症：与Xg血型的连锁研究

J Med Genet. 1974 Sep;11(3):271-4. doi: 10.1136/jmg.11.3.271.

Study of four new kindreds with inherited thyroxine-binding globulin abnormalities. Possible mutations of a single gene locus.对四个患有遗传性甲状腺素结合球蛋白异常的新家族的研究。单个基因位点的可能突变。

J Clin Invest. 1972 Apr;51(4):848-67. doi: 10.1172/JCI106880.

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