NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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P1476

NCOR1 modulates erythroid disorders caused by mutations of thyroid hormone receptor α1.

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P2093

Cho Rong Han

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Sheue-Yann Cheng

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Sunmi Park

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P2860

Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta

Resistance to thyroid hormone due to defective thyroid receptor alpha

From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications

Transcriptional regulation of erythropoiesis: an affair involving multiple partners

Combinatorial roles of the nuclear receptor corepressor in transcription and development

Functions of thyroid hormone receptors in mice.

A targeted dominant negative mutation of the thyroid hormone alpha 1 receptor causes increased mortality, infertility, and dwarfism in mice.

The interaction between nuclear receptor corepressor and histone deacetylase 3 regulates both positive and negative thyroid hormone action in vivo.

Thyroid hormone receptor α mutation causes a severe and thyroxine-resistant skeletal dysplasia in female mice.

Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone.

P2888

s41598-017-18409-4

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18080

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P31

scholarly article

P356

10.1038/S41598-017-18409-4

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P407

English

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P478

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P577

2017-12-22T00:00:00Z

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P698

29273766

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P932

5741760

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