Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes (Q34578534)

3 August 2017

title

Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes (English)

1 reference

3 August 2017

1 reference

Xiao-Hui Liao

1 reference

3 August 2017

Caterina Di Cosmo

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3 August 2017

Alexandra M Dumitrescu

1 reference

3 August 2017

Arturo Hernandez

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3 August 2017

Jacqueline Van Sande

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3 August 2017

Donald L St Germain

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3 August 2017

Roy E Weiss

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3 August 2017

Valerie Anne Galton

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3 August 2017

Samuel Refetoff

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3 August 2017

language of work or name

English

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publication date

1 February 2011

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3 August 2017

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inferred from page(s)

published in

Endocrinology

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3 August 2017

volume

152

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3 August 2017

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3 August 2017

page(s)

1180-1191

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Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion

3 August 2017

cites work

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Thyroglobulin gene mutations producing defective intracellular transport of thyroglobulin are associated with increased thyroidal type 2 iodothyronine deiodinase activity

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21285310

inferred from PubMed ID database lookup

12 December 2020

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Uncoupling protein-2 (UCP2): molecular and genetic studies

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

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Identifiers

DOI

10.1210/EN.2010-0900

1 reference

3 August 2017

1 reference

3 August 2017

1 reference