Somatic and germline mutations of the TSH receptor and thyroid diseases (Q34352820)

1 August 2017

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title

Somatic and germline mutations of the TSH receptor and thyroid diseases (English)

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1 August 2017

Corvilain B

1

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1 August 2017

Van Sande J

series ordinal

2

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1 August 2017

Dumont JE

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3

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1 August 2017

Vassart G

series ordinal

4

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1 August 2017

publication date

1 August 2001

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1 August 2017

published in

Clinical Endocrinology

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1 August 2017

volume

55

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1 August 2017

issue

2

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1 August 2017

page(s)

143-158

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Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland

1 August 2017

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Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Somatic and germline mutations of the TSH receptor gene in thyroid diseases

21 January 2018

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In Chinese hamster ovary K1 cells dog and human thyrotropin receptors activate both the cyclic AMP and the phosphatidylinositol 4,5-bisphosphate cascades in the presence of thyrotropin and the cyclic AMP cascade in its absence

21 January 2018

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21 January 2018

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21 January 2018

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Screening of Thyrotropin Receptor Mutations by Fine-Needle Aspiration Biopsy in Autonomous Functioning Thyroid Nodules in Multinodular Goiters

21 January 2018

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10.1046/J.1365-2265.2001.01365.X

21 January 2018

Identifiers

DOI

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1 August 2017

1 reference