PubMed for id: 389434

Year	Number of Results
2002	1
2003	3
2004	3
2005	1
2006	2
2007	2
2008	3
2009	1
2010	1
2011	2
2012	1
2014	4
2015	4
2017	2
2018	2
2019	3
2023	1
2024	0

1

Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).

Shareef R, Furman A, Watanabe Y, Bruellman R, Abdullah MA, Dumitresu AM, Refetoff S, Bertolini A, Borsò M, Saba A, Zucchi R, Weiss RE. Shareef R, et al. Thyroid. 2023 Feb;33(2):261-266. doi: 10.1089/thy.2022.0492. Thyroid. 2023. PMID: 36633921 Free PMC article.

2

Redox control of iodotyrosine deiodinase.

Hu J, Su Q, Schlessman JL, Rokita SE. Hu J, et al. Protein Sci. 2019 Jan;28(1):68-78. doi: 10.1002/pro.3479. Epub 2018 Oct 17. Protein Sci. 2019. PMID: 30052294 Free PMC article.

3

Active Site Binding Is Not Sufficient for Reductive Deiodination by Iodotyrosine Deiodinase.

Ingavat N, Kavran JM, Sun Z, Rokita SE. Ingavat N, et al. Biochemistry. 2017 Feb 28;56(8):1130-1139. doi: 10.1021/acs.biochem.6b01308. Epub 2017 Feb 16. Biochemistry. 2017. PMID: 28157283 Free PMC article.

4

Rapid kinetics of dehalogenation promoted by iodotyrosine deiodinase from human thyroid.

Bobyk KD, Ballou DP, Rokita SE. Bobyk KD, et al. Biochemistry. 2015 Jul 28;54(29):4487-94. doi: 10.1021/acs.biochem.5b00410. Epub 2015 Jul 20. Biochemistry. 2015. PMID: 26151430 Free PMC article.

5

Iodotyrosine deiodinase defect identified via genome-wide approach.

Burniat A, Pirson I, Vilain C, Kulik W, Afink G, Moreno-Reyes R, Corvilain B, Abramowicz M. Burniat A, et al. J Clin Endocrinol Metab. 2012 Jul;97(7):E1276-83. doi: 10.1210/jc.2011-3314. Epub 2012 Apr 24. J Clin Endocrinol Metab. 2012. PMID: 22535972

6

[Biochemical characteristics of iodperoxidase activity of human saliva].

Belevich VK, Senchuk VV. Belevich VK, et al. Biomed Khim. 2011 Mar-Apr;57(2):187-94. doi: 10.18097/pbmc20115702187. Biomed Khim. 2011. PMID: 21870604 Russian.

7

Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mutations.

Moreno JC, Visser TJ. Moreno JC, et al. Mol Cell Endocrinol. 2010 Jun 30;322(1-2):91-8. doi: 10.1016/j.mce.2010.03.010. Epub 2010 Mar 16. Mol Cell Endocrinol. 2010. PMID: 20298747 Review.

8

Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.

Afink G, Kulik W, Overmars H, de Randamie J, Veenboer T, van Cruchten A, Craen M, Ris-Stalpers C. Afink G, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4894-901. doi: 10.1210/jc.2008-0865. Epub 2008 Sep 2. J Clin Endocrinol Metab. 2008. PMID: 18765512

9

Mutations in the iodotyrosine deiodinase gene and hypothyroidism.

Moreno JC, Klootwijk W, van Toor H, Pinto G, D'Alessandro M, Lèger A, Goudie D, Polak M, Grüters A, Visser TJ. Moreno JC, et al. N Engl J Med. 2008 Apr 24;358(17):1811-8. doi: 10.1056/NEJMoa0706819. N Engl J Med. 2008. PMID: 18434651 Free article.

10

Characterisation of DEHAL1 expression in thyroid pathologies.

Krause K, Karger S, Gimm O, Sheu SY, Dralle H, Tannapfel A, Schmid KW, Dupuy C, Fuhrer D. Krause K, et al. Eur J Endocrinol. 2007 Mar;156(3):295-301. doi: 10.1530/EJE-06-0596. Eur J Endocrinol. 2007. PMID: 17322488

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