Similar articles for PMID: 21565790

Year	Number of Results
1947	1
1970	1
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1993	1
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1997	2
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1999	2
2000	1
2002	2
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2004	1
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2007	8
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2009	4
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2012	5
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2014	9
2015	13
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2018	11
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2020	11
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2024	0

1

Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.

De Marco G, Agretti P, Montanelli L, Di Cosmo C, Bagattini B, De Servi M, Ferrarini E, Dimida A, Freitas Ferreira AC, Molinaro A, Ceccarelli C, Brozzi F, Pinchera A, Vitti P, Tonacchera M. De Marco G, et al. J Clin Endocrinol Metab. 2011 Aug;96(8):E1335-9. doi: 10.1210/jc.2010-2467. Epub 2011 May 11. J Clin Endocrinol Metab. 2011. PMID: 21565790

2

Identification and functional studies of two new dual-oxidase 2 (DUOX2) mutations in a child with congenital hypothyroidism and a eutopic normal-size thyroid gland.

Tonacchera M, De Marco G, Agretti P, Montanelli L, Di Cosmo C, Freitas Ferreira AC, Dimida A, Ferrarini E, Ramos HE, Ceccarelli C, Brozzi F, Pinchera A, Vitti P. Tonacchera M, et al. J Clin Endocrinol Metab. 2009 Nov;94(11):4309-14. doi: 10.1210/jc.2009-0426. Epub 2009 Sep 29. J Clin Endocrinol Metab. 2009. PMID: 19789206

3

High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.

Jin HY, Heo SH, Kim YM, Kim GH, Choi JH, Lee BH, Yoo HW. Jin HY, et al. Horm Res Paediatr. 2014;82(4):252-60. doi: 10.1159/000362235. Epub 2014 Sep 20. Horm Res Paediatr. 2014. PMID: 25248169

4

A novel homozygous missense mutation of the dual oxidase 2 (DUOX2) gene in an adult patient with large goiter.

Ohye H, Fukata S, Hishinuma A, Kudo T, Nishihara E, Ito M, Kubota S, Amino N, Ieiri T, Kuma K, Miyauchi A. Ohye H, et al. Thyroid. 2008 May;18(5):561-6. doi: 10.1089/thy.2007.0258. Thyroid. 2008. PMID: 18426362

5

Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program.

Maruo Y, Takahashi H, Soeda I, Nishikura N, Matsui K, Ota Y, Mimura Y, Mori A, Sato H, Takeuchi Y. Maruo Y, et al. J Clin Endocrinol Metab. 2008 Nov;93(11):4261-7. doi: 10.1210/jc.2008-0856. Epub 2008 Sep 2. J Clin Endocrinol Metab. 2008. PMID: 18765513

6

Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect.

Varela V, Rivolta CM, Esperante SA, Gruñeiro-Papendieck L, Chiesa A, Targovnik HM. Varela V, et al. Clin Chem. 2006 Feb;52(2):182-91. doi: 10.1373/clinchem.2005.058321. Epub 2005 Dec 1. Clin Chem. 2006. PMID: 16322276

7

Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis.

Belforte FS, Citterio CE, Testa G, Olcese MC, Sobrero G, Miras MB, Targovnik HM, Rivolta CM. Belforte FS, et al. Mol Cell Endocrinol. 2016 Jan 5;419:172-84. doi: 10.1016/j.mce.2015.10.014. Epub 2015 Oct 24. Mol Cell Endocrinol. 2016. PMID: 26506010

8

High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.

Matsuo K, Tanahashi Y, Mukai T, Suzuki S, Tajima T, Azuma H, Fujieda K. Matsuo K, et al. J Pediatr Endocrinol Metab. 2016 Jul 1;29(7):807-12. doi: 10.1515/jpem-2015-0400. J Pediatr Endocrinol Metab. 2016. PMID: 27166716

9

Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes.

Wang F, Lu K, Yang Z, Zhang S, Lu W, Zhang L, Liu S, Yan S. Wang F, et al. Clin Endocrinol (Oxf). 2014 Sep;81(3):452-7. doi: 10.1111/cen.12469. Epub 2014 May 19. Clin Endocrinol (Oxf). 2014. PMID: 24735383

10

Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism.

Hoste C, Rigutto S, Van Vliet G, Miot F, De Deken X. Hoste C, et al. Hum Mutat. 2010 Apr;31(4):E1304-19. doi: 10.1002/humu.21227. Hum Mutat. 2010. PMID: 20187165

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